Eleazar Eskin

Title(s)Professor, Computer Science
SchoolHenry Samueli School of Engineering and Applied Science
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    Other Positions
    Title(s)Professor, Human Genetics

    Title(s)Professor, Computational Medicine


    Collapse Research 
    Collapse Research Activities and Funding
    Computational Genomics Summer Institute and Mentoring Network
    NIH R25GM135043May 1, 2020 - Apr 30, 2025
    Role: Principal Investigator
    Undergraduate Research Experiences in Neurogenetics and Neurogenomics
    NIH R25NS115554Dec 15, 2019 - Nov 30, 2024
    Role: Principal Investigator
    Genetic pathways for impulsivity and drug reinforcement: DNA and transcriptome variation in mice
    NIH U01DA041602Sep 15, 2017 - May 31, 2022
    Role: Co-Principal Investigator
    Undergraduate Research Experience in Neuropsychiatric Genomics
    NIH R25MH109172Feb 1, 2016 - Nov 30, 2021
    Role: Co-Principal Investigator
    Mathematical and Computational Approaches in High-Throughput Genomics Training
    NIH R25GM112625Sep 1, 2015 - Jun 30, 2021
    Role: Principal Investigator
    Correcting for Population Structure in Gene-by-Environment Interaction Studies
    NIH R01ES022282Sep 1, 2013 - Jun 30, 2018
    Role: Principal Investigator
    Discovering the Genetic Basis of Hypertension
    NIH K25HL080079Jun 1, 2006 - May 31, 2012
    Role: Principal Investigator

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. A comprehensive benchmarking of WGS-based deletion structural variant callers. Brief Bioinform. 2022 07 18; 23(4). Sarwal V, Niehus S, Ayyala R, Kim M, Sarkar A, Chang S, Lu A, Rajkumar N, Darfci-Maher N, Littman R, Chhugani K, Soylev A, Comarova Z, Wesel E, Castellanos J, Chikka R, Distler MG, Eskin E, Flint J, Mangul S. PMID: 35753701; PMCID: PMC9294411.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimals
    2. Bruins-in-Genomics: Evaluation of the impact of a UCLA undergraduate summer program in computational biology on participating students. PLoS One. 2022; 17(5):e0268861. Coller HA, Beggs S, Andrews S, Maloy J, Chiu A, Sankararaman S, Pellegrini M, Freimer N, Johnson T, Papp J, Eskin E, Hoffmann A. PMID: 35622842; PMCID: PMC9140266.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    3. Critical Assessment of Metagenome Interpretation: the second round of challenges. Nat Methods. 2022 04; 19(4):429-440. Meyer F, Fritz A, Deng ZL, Koslicki D, Lesker TR, Gurevich A, Robertson G, Alser M, Antipov D, Beghini F, Bertrand D, Brito JJ, Brown CT, Buchmann J, Buluç A, Chen B, Chikhi R, Clausen PTLC, Cristian A, Dabrowski PW, Darling AE, Egan R, Eskin E, Georganas E, Goltsman E, Gray MA, Hansen LH, Hofmeyr S, Huang P, Irber L, Jia H, Jørgensen TS, Kieser SD, Klemetsen T, Kola A, Kolmogorov M, Korobeynikov A, Kwan J, LaPierre N, Lemaitre C, Li C, Limasset A, Malcher-Miranda F, Mangul S, Marcelino VR, Marchet C, Marijon P, Meleshko D, Mende DR, Milanese A, Nagarajan N, Nissen J, Nurk S, Oliker L, Paoli L, Peterlongo P, Piro VC, Porter JS, Rasmussen S, Rees ER, Reinert K, Renard B, Robertsen EM, Rosen GL, Ruscheweyh HJ, Sarwal V, Segata N, Seiler E, Shi L, Sun F, Sunagawa S, Sørensen SJ, Thomas A, Tong C, Trajkovski M, Tremblay J, Uritskiy G, Vicedomini R, Wang Z, Wang Z, Wang Z, Warren A, Willassen NP, Yelick K, You R, Zeller G, Zhao Z, Zhu S, Zhu J, Garrido-Oter R, Gastmeier P, Hacquard S, Häußler S, Khaledi A, Maechler F, Mesny F, Radutoiu S, Schulze-Lefert P, Smit N, Strowig T, Bremges A, Sczyrba A, McHardy AC. PMID: 35396482; PMCID: PMC9007738.
      View in: PubMed   Mentions: 6     Fields:    Translation:Cells
    4. Genomic epidemiology of the Los Angeles COVID-19 outbreak and the early history of the B.1.43 strain in the USA. BMC Genomics. 2022 Apr 04; 23(1):260. Guo L, Boocock J, Hilt EE, Chandrasekaran S, Zhang Y, Munugala C, Sathe L, Alexander N, Arboleda VA, Flint J, Eskin E, Luo C, Yang S, Garner OB, Yin Y, Bloom JS, Kruglyak L. PMID: 35379194; PMCID: PMC8978495.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCellsPHPublic Health
    5. Robust Mendelian randomization in the presence of residual population stratification, batch effects and horizontal pleiotropy. Nat Commun. 2022 03 01; 13(1):1093. Cinelli C, LaPierre N, Hill BL, Sankararaman S, Eskin E. PMID: 35232963; PMCID: PMC8888767.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    6. Identifying causal variants by fine mapping across multiple studies. PLoS Genet. 2021 09; 17(9):e1009733. LaPierre N, Taraszka K, Huang H, He R, Hormozdiari F, Eskin E. PMID: 34543273; PMCID: PMC8491908.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    7. Massively scaled-up testing for SARS-CoV-2 RNA via next-generation sequencing of pooled and barcoded nasal and saliva samples. Nat Biomed Eng. 2021 07; 5(7):657-665. Bloom JS, Sathe L, Munugala C, Jones EM, Gasperini M, Lubock NB, Yarza F, Thompson EM, Kovary KM, Park J, Marquette D, Kay S, Lucas M, Love T, Sina Booeshaghi A, Brandenberg OF, Guo L, Boocock J, Hochman M, Simpkins SW, Lin I, LaPierre N, Hong D, Zhang Y, Oland G, Choe BJ, Chandrasekaran S, Hilt EE, Butte MJ, Damoiseaux R, Kravit C, Cooper AR, Yin Y, Pachter L, Garner OB, Flint J, Eskin E, Luo C, Kosuri S, Kruglyak L, Arboleda VA. PMID: 34211145.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    8. MARS: leveraging allelic heterogeneity to increase power of association testing. Genome Biol. 2021 04 30; 22(1):128. Hormozdiari F, Jung J, Eskin E, J Joo JW. PMID: 33931127; PMCID: PMC8086090.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    9. Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease. Cell. 2021 05 13; 184(10):2633-2648.e19. de Goede OM, Nachun DC, Ferraro NM, Gloudemans MJ, Rao AS, Smail C, Eulalio TY, Aguet F, Ng B, Xu J, Barbeira AN, Castel SE, Kim-Hellmuth S, Park Y, Scott AJ, Strober BJ, GTEx Consortium, Brown CD, Wen X, Hall IM, Battle A, Lappalainen T, Im HK, Ardlie KG, Mostafavi S, Quertermous T, Kirkegaard K, Montgomery SB. PMID: 33864768; PMCID: PMC8651477.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
    10. Swab-Seq: A high-throughput platform for massively scaled up SARS-CoV-2 testing. medRxiv. 2021 Mar 09. Bloom JS, Sathe L, Munugala C, Jones EM, Gasperini M, Lubock NB, Yarza F, Thompson EM, Kovary KM, Park J, Marquette D, Kay S, Lucas M, Love T, Booeshaghi AS, Brandenberg OF, Guo L, Boocock J, Hochman M, Simpkins SW, Lin I, LaPierre N, Hong D, Zhang Y, Oland G, Choe BJ, Chandrasekaran S, Hilt EE, Butte MJ, Damoiseaux R, Kravit C, Cooper AR, Yin Y, Pachter L, Garner OB, Flint J, Eskin E, Luo C, Kosuri S, Kruglyak L, Arboleda VA. PMID: 32909008; PMCID: PMC7480060.
      View in: PubMed   Mentions:
    11. Pre-existing conditions in Hispanics/Latinxs that are COVID-19 risk factors. iScience. 2021 Mar 19; 24(3):102188. Chang TS, Ding Y, Freund MK, Johnson R, Schwarz T, Yabu JM, Hazlett C, Chiang JN, Wulf DA, UCLA Precision Health Data Discovery Repository Working Group, Geschwind DH, Butte MJ, Pasaniuc B. PMID: 33615196; PMCID: PMC7879099.
      View in: PubMed   Mentions: 4  
    12. PLEIO: a method to map and interpret pleiotropic loci with GWAS summary statistics. Am J Hum Genet. 2021 01 07; 108(1):36-48. Lee CH, Shi H, Pasaniuc B, Eskin E, Han B. PMID: 33352115; PMCID: PMC7820744.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    13. Genetic determinants of ammonia-induced acute lung injury in mice. Am J Physiol Lung Cell Mol Physiol. 2021 01 01; 320(1):L41-L62. Bein K, Ganguly K, Martin TM, Concel VJ, Brant KA, Di YPP, Upadhyay S, Fabisiak JP, Vuga LJ, Kaminski N, Kostem E, Eskin E, Prows DR, Jang AS, Leikauf GD. PMID: 33050709; PMCID: PMC7847062.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansAnimalsCells
    14. A machine learning algorithm to increase COVID-19 inpatient diagnostic capacity. PLoS One. 2020; 15(9):e0239474. Goodman-Meza D, Rudas A, Chiang JN, Adamson PC, Ebinger J, Sun N, Botting P, Fulcher JA, Saab FG, Brook R, Eskin E, An U, Kordi M, Jew B, Balliu B, Chen Z, Hill BL, Rahmani E, Halperin E, Manuel V. PMID: 32960917; PMCID: PMC7508387.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCellsPHPublic Health
    15. The GTEx Consortium atlas of genetic regulatory effects across human tissues. Science. 2020 09 11; 369(6509):1318-1330. GTEx Consortium. PMID: 32913098; PMCID: PMC7737656.
      View in: PubMed   Mentions: 448     Fields:    Translation:Humans
    16. Determinants of telomere length across human tissues. Science. 2020 09 11; 369(6509). Demanelis K, Jasmine F, Chen LS, Chernoff M, Tong L, Delgado D, Zhang C, Shinkle J, Sabarinathan M, Lin H, Ramirez E, Oliva M, Kim-Hellmuth S, Stranger BE, Lai TP, Aviv A, Ardlie KG, Aguet F, Ahsan H, GTEx Consortium, Doherty JA, Kibriya MG, Pierce BL. PMID: 32913074; PMCID: PMC8108546.
      View in: PubMed   Mentions: 68     Fields:    Translation:HumansCells
    17. The impact of sex on gene expression across human tissues. Science. 2020 09 11; 369(6509). Oliva M, Muñoz-Aguirre M, Kim-Hellmuth S, Wucher V, Gewirtz ADH, Cotter DJ, Parsana P, Kasela S, Balliu B, Viñuela A, Castel SE, Mohammadi P, Aguet F, Zou Y, Khramtsova EA, Skol AD, Garrido-Martín D, Reverter F, Brown A, Evans P, Gamazon ER, Payne A, Bonazzola R, Barbeira AN, Hamel AR, Martinez-Perez A, Soria JM, GTEx Consortium, Pierce BL, Stephens M, Eskin E, Dermitzakis ET, Segrè AV, Im HK, Engelhardt BE, Ardlie KG, Montgomery SB, Battle AJ, Lappalainen T, Guigó R, Stranger BE. PMID: 32913072; PMCID: PMC8136152.
      View in: PubMed   Mentions: 70     Fields:    Translation:HumansCells
    18. A vast resource of allelic expression data spanning human tissues. Genome Biol. 2020 09 11; 21(1):234. Castel SE, Aguet F, Mohammadi P, GTEx Consortium, Ardlie KG, Lappalainen T. PMID: 32912332; PMCID: PMC7488534.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    19. Cell type-specific genetic regulation of gene expression across human tissues. Science. 2020 09 11; 369(6509). Kim-Hellmuth S, Aguet F, Oliva M, Muñoz-Aguirre M, Kasela S, Wucher V, Castel SE, Hamel AR, Viñuela A, Roberts AL, Mangul S, Wen X, Wang G, Barbeira AN, Garrido-Martín D, Nadel BB, Zou Y, Bonazzola R, Quan J, Brown A, Martinez-Perez A, Soria JM, GTEx Consortium, Getz G, Dermitzakis ET, Small KS, Stephens M, Xi HS, Im HK, Guigó R, Segrè AV, Stranger BE, Ardlie KG, Lappalainen T. PMID: 32913075; PMCID: PMC8051643.
      View in: PubMed   Mentions: 51     Fields:    Translation:HumansCells
    20. Transcriptomic signatures across human tissues identify functional rare genetic variation. Science. 2020 09 11; 369(6509). Ferraro NM, Strober BJ, Einson J, Abell NS, Aguet F, Barbeira AN, Brandt M, Bucan M, Castel SE, Davis JR, Greenwald E, Hess GT, Hilliard AT, Kember RL, Kotis B, Park Y, Peloso G, Ramdas S, Scott AJ, Smail C, Tsang EK, Zekavat SM, Ziosi M, TOPMed Lipids Working Group, Ardlie KG, Assimes TL, Bassik MC, Brown CD, Correa A, Hall I, Im HK, Li X, Natarajan P, GTEx Consortium, Lappalainen T, Mohammadi P, Montgomery SB, Battle A. PMID: 32913073; PMCID: PMC7646251.
      View in: PubMed   Mentions: 31     Fields:    Translation:HumansCells
    21. A Quantitative Proteome Map of the Human Body. Cell. 2020 10 01; 183(1):269-283.e19. Jiang L, Wang M, Lin S, Jian R, Li X, Chan J, Dong G, Fang H, Robinson AE, GTEx Consortium, Snyder MP. PMID: 32916130; PMCID: PMC7575058.
      View in: PubMed   Mentions: 50     Fields:    Translation:HumansCells
    22. Metalign: efficient alignment-based metagenomic profiling via containment min hash. Genome Biol. 2020 09 10; 21(1):242. LaPierre N, Alser M, Eskin E, Koslicki D, Mangul S. PMID: 32912225; PMCID: PMC7488264.
      View in: PubMed   Mentions: 6     Fields:    
    23. Author Correction: Profiling immunoglobulin repertoires across multiple human tissues using RNA sequencing. Nat Commun. 2020 09 04; 11(1):4499. Mandric I, Rotman J, Yang HT, Strauli N, Montoya DJ, Van Der Wey W, Ronas JR, Statz B, Yao D, Petrova V, Zelikovsky A, Spreafico R, Shifman S, Zaitlen N, Rossetti M, Ansel KM, Eskin E, Mangul S. PMID: 32887888; PMCID: PMC7474053.
      View in: PubMed   Mentions:    Fields:    
    24. Correction to: Improving the usability and comprehensiveness of microbial databases. BMC Biol. 2020 07 28; 18(1):92. Loeffler C, Karlsberg A, Martin LS, Eskin E, Koslicki D, Mangul S. PMID: 32723395; PMCID: PMC7389812.
      View in: PubMed   Mentions: 1     Fields:    
    25. Profiling immunoglobulin repertoires across multiple human tissues using RNA sequencing. Nat Commun. 2020 06 19; 11(1):3126. Mandric I, Rotman J, Yang HT, Strauli N, Montoya DJ, Van Der Wey W, Ronas JR, Statz B, Yao D, Petrova V, Zelikovsky A, Spreafico R, Shifman S, Zaitlen N, Rossetti M, Ansel KM, Eskin E, Mangul S. PMID: 32561710; PMCID: PMC7305308.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    26. Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma. Nat Commun. 2020 04 15; 11(1):1776. Han Y, Jia Q, Jahani PS, Hurrell BP, Pan C, Huang P, Gukasyan J, Woodward NC, Eskin E, Gilliland FD, Akbari O, Hartiala JA, Allayee H. PMID: 32296059; PMCID: PMC7160128.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansAnimalsCells
    27. Improving the usability and comprehensiveness of microbial databases. BMC Biol. 2020 04 07; 18(1):37. Loeffler C, Karlsberg A, Martin LS, Eskin E, Koslicki D, Mangul S. PMID: 32264902; PMCID: PMC7140547.
      View in: PubMed   Mentions: 5     Fields:    Translation:AnimalsCells
    28. Benchmarking of computational error-correction methods for next-generation sequencing data. Genome Biol. 2020 03 17; 21(1):71. Mitchell K, Brito JJ, Mandric I, Wu Q, Knyazev S, Chang S, Martin LS, Karlsberg A, Gerasimov E, Littman R, Hill BL, Wu NC, Yang HT, Hsieh K, Chen L, Littman E, Shabani T, Enik G, Yao D, Sun R, Schroeder J, Eskin E, Zelikovsky A, Skums P, Pop M, Mangul S. PMID: 32183840; PMCID: PMC7079412.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    29. A Unifying Framework for Imputing Summary Statistics in Genome-Wide Association Studies. J Comput Biol. 2020 03; 27(3):418-428. Wu Y, Eskin E, Sankararaman S. PMID: 32053016; PMCID: PMC7081249.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    30. A GWAS approach identifies Dapp1 as a determinant of air pollution-induced airway hyperreactivity. PLoS Genet. 2019 12; 15(12):e1008528. Maazi H, Hartiala JA, Suzuki Y, Crow AL, Shafiei Jahani P, Lam J, Patel N, Rigas D, Han Y, Huang P, Eskin E, Lusis AJ, Gilliland FD, Akbari O, Allayee H. PMID: 31869344; PMCID: PMC6944376.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansAnimals
    31. Leveraging allelic imbalance to refine fine-mapping for eQTL studies. PLoS Genet. 2019 12; 15(12):e1008481. Zou J, Hormozdiari F, Jew B, Castel SE, Lappalainen T, Ernst J, Sul JH, Eskin E. PMID: 31834882; PMCID: PMC6952111.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    32. Genomic GPS: using genetic distance from individuals to public data for genomic analysis without disclosing personal genomes. Genome Biol. 2019 08 27; 20(1):175. Kim K, Baik H, Jang CS, Roh JK, Eskin E, Han B. PMID: 31455387; PMCID: PMC6712716.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    33. Profiling allele-specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage. Nat Neurosci. 2019 09; 22(9):1521-1532. Lee C, Kang EY, Gandal MJ, Eskin E, Geschwind DH. PMID: 31455884; PMCID: PMC6750256.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    34. A linear mixed model approach to gene expression-tumor aneuploidy association studies. Sci Rep. 2019 08 16; 9(1):11944. Yao DW, Balanis NG, Eskin E, Graeber TG. PMID: 31420589; PMCID: PMC6697733.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    35. Cell-type-specific resolution epigenetics without the need for cell sorting or single-cell biology. Nat Commun. 2019 07 31; 10(1):3417. Rahmani E, Schweiger R, Rhead B, Criswell LA, Barcellos LF, Eskin E, Rosset S, Sankararaman S, Halperin E. PMID: 31366909; PMCID: PMC6668473.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansCells
    36. Challenges and recommendations to improve the installability and archival stability of omics computational tools. PLoS Biol. 2019 06; 17(6):e3000333. Mangul S, Mosqueiro T, Abdill RJ, Duong D, Mitchell K, Sarwal V, Hill B, Brito J, Littman RJ, Statz B, Lam AK, Dayama G, Grieneisen L, Martin LS, Flint J, Eskin E, Blekhman R. PMID: 31220077; PMCID: PMC6605654.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    37. MiCoP: microbial community profiling method for detecting viral and fungal organisms in metagenomic samples. BMC Genomics. 2019 Jun 06; 20(Suppl 5):423. LaPierre N, Mangul S, Alser M, Mandric I, Wu NC, Koslicki D, Eskin E. PMID: 31167634; PMCID: PMC6551237.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansAnimalsCells
    38. Systematic benchmarking of omics computational tools. Nat Commun. 2019 03 27; 10(1):1393. Mangul S, Martin LS, Hill BL, Lam AK, Distler MG, Zelikovsky A, Eskin E, Flint J. PMID: 30918265; PMCID: PMC6437167.
      View in: PubMed   Mentions: 41     Fields:    Translation:Humans
    39. How bioinformatics and open data can boost basic science in countries and universities with limited resources. Nat Biotechnol. 2019 03; 37(3):324-326. Mangul S, Martin LS, Langmead B, Sanchez-Galan JE, Toma I, Hormozdiari F, Pevzner P, Eskin E. PMID: 30833765.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    40. Improving the usability and archival stability of bioinformatics software. Genome Biol. 2019 02 27; 20(1):47. Mangul S, Martin LS, Eskin E, Blekhman R. PMID: 30813962; PMCID: PMC6391762.
      View in: PubMed   Mentions: 25     Fields:    
    41. Population structure in genetic studies: Confounding factors and mixed models. PLoS Genet. 2018 12; 14(12):e1007309. Sul JH, Martin LS, Eskin E. PMID: 30589851; PMCID: PMC6307707.
      View in: PubMed   Mentions: 41     Fields:    Translation:HumansAnimals
    42. Word and Sentence Embedding Tools to Measure Semantic Similarity of Gene Ontology Terms by Their Definitions. J Comput Biol. 2019 01; 26(1):38-52. Duong D, Ahmad WU, Eskin E, Chang KW, Li JJ. PMID: 30383443; PMCID: PMC6350067.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansAnimals
    43. Improving Imputation Accuracy by Inferring Causal Variants in Genetic Studies. J Comput Biol. 2019 11; 26(11):1203-1213. Wu Y, Hormozdiari F, Joo JWJ, Eskin E. PMID: 30272994; PMCID: PMC6856942.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    44. BayesCCE: a Bayesian framework for estimating cell-type composition from DNA methylation without the need for methylation reference. Genome Biol. 2018 09 21; 19(1):141. Rahmani E, Schweiger R, Shenhav L, Wingert T, Hofer I, Gabel E, Eskin E, Halperin E. PMID: 30241486; PMCID: PMC6151042.
      View in: PubMed   Mentions: 20     Fields:    Translation:Cells
    45. Finding associated variants in genome-wide association studies on multiple traits. Bioinformatics. 2018 07 01; 34(13):i467-i474. Gai L, Eskin E. PMID: 29949991; PMCID: PMC6022769.
      View in: PubMed   Mentions: 3     Fields:    
    46. Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation. Nat Genet. 2018 07; 50(7):956-967. Gamazon ER, Segrè AV, van de Bunt M, Wen X, Xi HS, Hormozdiari F, Ongen H, Konkashbaev A, Derks EM, Aguet F, Quan J, GTEx Consortium, Nicolae DL, Eskin E, Kellis M, Getz G, McCarthy MI, Dermitzakis ET, Cox NJ, Ardlie KG. PMID: 29955180; PMCID: PMC6248311.
      View in: PubMed   Mentions: 171     Fields:    Translation:Humans
    47. Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits. Nat Genet. 2018 07; 50(7):1041-1047. Hormozdiari F, Gazal S, van de Geijn B, Finucane HK, Ju CJ, Loh PR, Schoech A, Reshef Y, Liu X, O'Connor L, Gusev A, Eskin E, Price AL. PMID: 29942083; PMCID: PMC6030458.
      View in: PubMed   Mentions: 55     Fields:    Translation:Humans
    48. An integrated -omics analysis of the epigenetic landscape of gene expression in human blood cells. BMC Genomics. 2018 Jun 19; 19(1):476. Kennedy EM, Goehring GN, Nichols MH, Robins C, Mehta D, Klengel T, Eskin E, Smith AK, Conneely KN. PMID: 29914364; PMCID: PMC6006777.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    49. An Association Mapping Framework To Account for Potential Sex Difference in Genetic Architectures. Genetics. 2018 07; 209(3):685-698. Kang EY, Lee CH, Furlotte NA, Joo JWJ, Kostem E, Zaitlen N, Eskin E, Han B. PMID: 29752291; PMCID: PMC6028251.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    50. Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia. Transl Psychiatry. 2018 05 10; 8(1):96. Olde Loohuis LM, Mangul S, Ori APS, Jospin G, Koslicki D, Yang HT, Wu T, Boks MP, Lomen-Hoerth C, Wiedau-Pazos M, Cantor RM, de Vos WM, Kahn RS, Eskin E, Ophoff RA. PMID: 29743478; PMCID: PMC5943399.
      View in: PubMed   Mentions: 37     Fields:    Translation:Humans
    51. Involving undergraduates in genomics research to narrow the education-research gap. Nat Biotechnol. 2018 04 05; 36(4):369-371. Mangul S, Martin LS, Eskin E. PMID: 29621227.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    52. ROP: dumpster diving in RNA-sequencing to find the source of 1 trillion reads across diverse adult human tissues. Genome Biol. 2018 02 15; 19(1):36. Mangul S, Yang HT, Strauli N, Gruhl F, Porath HT, Hsieh K, Chen L, Daley T, Christenson S, Wesolowska-Andersen A, Spreafico R, Rios C, Eng C, Smith AD, Hernandez RD, Ophoff RA, Santana JR, Levanon EY, Woodruff PG, Burchard E, Seibold MA, Shifman S, Eskin E, Zaitlen N. PMID: 29548336; PMCID: PMC5857127.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansCells
    53. Computational pan-genomics: status, promises and challenges. Brief Bioinform. 2018 01 01; 19(1):118-135. Computational Pan-Genomics Consortium. PMID: 27769991; PMCID: PMC5862344.
      View in: PubMed   Mentions: 70     Fields:    Translation:Humans
    54. An ancestry-based approach for detecting interactions. Genet Epidemiol. 2018 02; 42(1):49-63. Park DS, Eskin I, Kang EY, Gamazon ER, Eng C, Gignoux CR, Galanter JM, Burchard E, Ye CJ, Aschard H, Eskin E, Halperin E, Zaitlen N. PMID: 29114909; PMCID: PMC6065511.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    55. Genetic variation and gene expression across multiple tissues and developmental stages in a nonhuman primate. Nat Genet. 2017 Dec; 49(12):1714-1721. Jasinska AJ, Zelaya I, Service SK, Peterson CB, Cantor RM, Choi OW, DeYoung J, Eskin E, Fairbanks LA, Fears S, Furterer AE, Huang YS, Ramensky V, Schmitt CA, Svardal H, Jorgensen MJ, Kaplan JR, Villar D, Aken BL, Flicek P, Nag R, Wong ES, Blangero J, Dyer TD, Bogomolov M, Benjamini Y, Weinstock GM, Dewar K, Sabatti C, Wilson RK, Jentsch JD, Warren W, Coppola G, Woods RP, Freimer NB. PMID: 29083405; PMCID: PMC5714271.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansAnimals
    56. Loci associated with skin pigmentation identified in African populations. Science. 2017 11 17; 358(6365). Crawford NG, Kelly DE, Hansen MEB, Beltrame MH, Fan S, Bowman SL, Jewett E, Ranciaro A, Thompson S, Lo Y, Pfeifer SP, Jensen JD, Campbell MC, Beggs W, Hormozdiari F, Mpoloka SW, Mokone GG, Nyambo T, Meskel DW, Belay G, Haut J, NISC Comparative Sequencing Program, Rothschild H, Zon L, Zhou Y, Kovacs MA, Xu M, Zhang T, Bishop K, Sinclair J, Rivas C, Elliot E, Choi J, Li SA, Hicks B, Burgess S, Abnet C, Watkins-Chow DE, Oceana E, Song YS, Eskin E, Brown KM, Marks MS, Loftus SK, Pavan WJ, Yeager M, Chanock S, Tishkoff SA. PMID: 29025994; PMCID: PMC5759959.
      View in: PubMed   Mentions: 92     Fields:    Translation:HumansAnimalsCellsPHPublic Health
    57. Landscape of X chromosome inactivation across human tissues. Nature. 2017 10 11; 550(7675):244-248. Tukiainen T, Villani AC, Yen A, Rivas MA, Marshall JL, Satija R, Aguirre M, Gauthier L, Fleharty M, Kirby A, Cummings BB, Castel SE, Karczewski KJ, Aguet F, Byrnes A, GTEx Consortium, Laboratory, Data Analysis &Coordinating Center (LDACC)—Analysis Working Group, Statistical Methods groups—Analysis Working Group, Enhancing GTEx (eGTEx) groups, NIH Common Fund, NIH/NCI, NIH/NHGRI, NIH/NIMH, NIH/NIDA, Biospecimen Collection Source Site—NDRI, Biospecimen Collection Source Site—RPCI, Biospecimen Core Resource—VARI, Brain Bank Repository—University of Miami Brain Endowment Bank, Leidos Biomedical—Project Management, ELSI Study, Genome Browser Data Integration &Visualization—EBI, Genome Browser Data Integration &Visualization—UCSC Genomics Institute, University of California San, Lappalainen T, Regev A, Ardlie KG, Hacohen N, MacArthur DG. PMID: 29022598; PMCID: PMC5685192.
      View in: PubMed   Mentions: 290     Fields:    Translation:HumansCells
    58. Genetic effects on gene expression across human tissues. Nature. 2017 10 11; 550(7675):204-213. GTEx Consortium, Laboratory, Data Analysis &Coordinating Center (LDACC)—Analysis Working Group, Statistical Methods groups—Analysis Working Group, Enhancing GTEx (eGTEx) groups, NIH Common Fund, NIH/NCI, NIH/NHGRI, NIH/NIMH, NIH/NIDA, Biospecimen Collection Source Site—NDRI, Biospecimen Collection Source Site—RPCI, Biospecimen Core Resource—VARI, Brain Bank Repository—University of Miami Brain Endowment Bank, Leidos Biomedical—Project Management, ELSI Study, Genome Browser Data Integration &Visualization—EBI, Genome Browser Data Integration &Visualization—UCSC Genomics Institute, University of California San, Lead analysts:, Laboratory, Data Analysis &Coordinating Center (LDACC):, NIH program management:, Biospecimen collection:, Pathology:, eQTL manuscript working group:, Battle A, Brown CD, Engelhardt BE, Montgomery SB. PMID: 29022597; PMCID: PMC5776756.
      View in: PubMed   Mentions: 1239     Fields:    Translation:HumansCells
    59. The impact of rare variation on gene expression across tissues. Nature. 2017 10 11; 550(7675):239-243. Li X, Kim Y, Tsang EK, Davis JR, Damani FN, Chiang C, Hess GT, Zappala Z, Strober BJ, Scott AJ, Li A, Ganna A, Bassik MC, Merker JD, GTEx Consortium, Laboratory, Data Analysis &Coordinating Center (LDACC)—Analysis Working Group, Statistical Methods groups—Analysis Working Group, Enhancing GTEx (eGTEx) groups, NIH Common Fund, NIH/NCI, NIH/NHGRI, NIH/NIMH, NIH/NIDA, Biospecimen Collection Source Site—NDRI, Biospecimen Collection Source Site—RPCI, Biospecimen Core Resource—VARI, Brain Bank Repository—University of Miami Brain Endowment Bank, Leidos Biomedical—Project Management, ELSI Study, Genome Browser Data Integration &Visualization—EBI, Genome Browser Data Integration &Visualization—UCSC Genomics Institute, University of California San, Hall IM, Battle A, Montgomery SB. PMID: 29022581; PMCID: PMC5877409.
      View in: PubMed   Mentions: 99     Fields:    Translation:Humans
    60. Identifying cis-mediators for trans-eQTLs across many human tissues using genomic mediation analysis. Genome Res. 2017 11; 27(11):1859-1871. Yang F, Wang J, GTEx Consortium, Pierce BL, Chen LS. PMID: 29021290; PMCID: PMC5668943.
      View in: PubMed   Mentions: 29     Fields:    Translation:Humans
    61. Co-expression networks reveal the tissue-specific regulation of transcription and splicing. Genome Res. 2017 11; 27(11):1843-1858. Saha A, Kim Y, Gewirtz ADH, Jo B, Gao C, McDowell IC, GTEx Consortium, Engelhardt BE, Battle A. PMID: 29021288; PMCID: PMC5668942.
      View in: PubMed   Mentions: 75     Fields:    Translation:HumansCells
    62. Dynamic landscape and regulation of RNA editing in mammals. Nature. 2017 10 11; 550(7675):249-254. Tan MH, Li Q, Shanmugam R, Piskol R, Kohler J, Young AN, Liu KI, Zhang R, Ramaswami G, Ariyoshi K, Gupte A, Keegan LP, George CX, Ramu A, Huang N, Pollina EA, Leeman DS, Rustighi A, Goh YPS, GTEx Consortium, Laboratory, Data Analysis &Coordinating Center (LDACC)—Analysis Working Group, Statistical Methods groups—Analysis Working Group, Enhancing GTEx (eGTEx) groups, NIH Common Fund, NIH/NCI, NIH/NHGRI, NIH/NIMH, NIH/NIDA, Biospecimen Collection Source Site—NDRI, Biospecimen Collection Source Site—RPCI, Biospecimen Core Resource—VARI, Brain Bank Repository—University of Miami Brain Endowment Bank, Leidos Biomedical—Project Management, ELSI Study, Genome Browser Data Integration &Visualization—EBI, Genome Browser Data Integration &Visualization—UCSC Genomics Institute, University of California San, Chawla A, Del Sal G, Peltz G, Brunet A, Conrad DF, Samuel CE, O'Connell MA, Walkley CR, Nishikura K, Li JB. PMID: 29022589; PMCID: PMC5723435.
      View in: PubMed   Mentions: 204     Fields:    Translation:HumansAnimalsCells
    63. Incorporation of Biological Knowledge Into the Study of Gene-Environment Interactions. Am J Epidemiol. 2017 Oct 01; 186(7):771-777. Ritchie MD, Davis JR, Aschard H, Battle A, Conti D, Du M, Eskin E, Fallin MD, Hsu L, Kraft P, Moore JH, Pierce BL, Bien SA, Thomas DC, Wei P, Montgomery SB. PMID: 28978191; PMCID: PMC5860556.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansAnimals
    64. Increasing the power of meta-analysis of genome-wide association studies to detect heterogeneous effects. Bioinformatics. 2017 Jul 15; 33(14):i379-i388. Lee CH, Eskin E, Han B. PMID: 28881976; PMCID: PMC5870848.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    65. Applying meta-analysis to genotype-tissue expression data from multiple tissues to identify eQTLs and increase the number of eGenes. Bioinformatics. 2017 Jul 15; 33(14):i67-i74. Duong D, Gai L, Snir S, Kang EY, Han B, Sul JH, Eskin E. PMID: 28881962; PMCID: PMC5870567.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    66. Addressing the Digital Divide in Contemporary Biology: Lessons from Teaching UNIX. Trends Biotechnol. 2017 10; 35(10):901-903. Mangul S, Martin LS, Hoffmann A, Pellegrini M, Eskin E. PMID: 28720283.
      View in: PubMed   Mentions: 7     Fields:    
    67. Selection in Europeans on Fatty Acid Desaturases Associated with Dietary Changes. Mol Biol Evol. 2017 06 01; 34(6):1307-1318. Buckley MT, Racimo F, Allentoft ME, Jensen MK, Jonsson A, Huang H, Hormozdiari F, Sikora M, Marnetto D, Eskin E, Jørgensen ME, Grarup N, Pedersen O, Hansen T, Kraft P, Willerslev E, Nielsen R. PMID: 28333262; PMCID: PMC5435082.
      View in: PubMed   Mentions: 32     Fields:    Translation:Humans
    68. Widespread Allelic Heterogeneity in Complex Traits. Am J Hum Genet. 2017 May 04; 100(5):789-802. Hormozdiari F, Zhu A, Kichaev G, Ju CJ, Segrè AV, Joo JWJ, Won H, Sankararaman S, Pasaniuc B, Shifman S, Eskin E. PMID: 28475861; PMCID: PMC5420356.
      View in: PubMed   Mentions: 33     Fields:    Translation:Humans
    69. IPED2: Inheritance Path Based Pedigree Reconstruction Algorithm for Complicated Pedigrees. IEEE/ACM Trans Comput Biol Bioinform. 2017 Sep-Oct; 14(5):1094-1103. He D, Wang Z, Parida L, Eskin E. PMID: 28368828.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    70. HapIso: An Accurate Method for the Haplotype- Specific Isoforms Reconstruction From Long Single-Molecule Reads. IEEE Trans Nanobioscience. 2017 03; 16(2):108-115. Mangul S, Yang TH, Hormozdiari F, Dainis AM, Tseng E, Ashley EA, Zelikovsky A, Eskin E. PMID: 28328508.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    71. Correcting for cell-type heterogeneity in DNA methylation: a comprehensive evaluation. Nat Methods. 2017 02 28; 14(3):218-219. Rahmani E, Zaitlen N, Baran Y, Eng C, Hu D, Galanter J, Oh S, Burchard EG, Eskin E, Zou J, Halperin E. PMID: 28245214; PMCID: PMC5548185.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansCells
    72. Simultaneous Modeling of Disease Status and Clinical Phenotypes To Increase Power in Genome-Wide Association Studies. Genetics. 2017 03; 205(3):1041-1047. Bilow M, Crespo F, Pan Z, Eskin E, Eyheramendy S. PMID: 28132020; PMCID: PMC5340321.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    73. Long Single-Molecule Reads Can Resolve the Complexity of the Influenza Virus Composed of Rare, Closely Related Mutant Variants. J Comput Biol. 2017 Jun; 24(6):558-570. Artyomenko A, Wu NC, Mangul S, Eskin E, Sun R, Zelikovsky A. PMID: 27901586; PMCID: PMC5467126.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    74. Colocalization of GWAS and eQTL Signals Detects Target Genes. Am J Hum Genet. 2016 Dec 01; 99(6):1245-1260. Hormozdiari F, van de Bunt M, Segrè AV, Li X, Joo JWJ, Bilow M, Sul JH, Sankararaman S, Pasaniuc B, Eskin E. PMID: 27866706; PMCID: PMC5142122.
      View in: PubMed   Mentions: 215     Fields:    Translation:Humans
    75. Efficient and Accurate Multiple-Phenotype Regression Method for High Dimensional Data Considering Population Structure. Genetics. 2016 Dec; 204(4):1379-1390. Joo JW, Kang EY, Org E, Furlotte N, Parks B, Hormozdiari F, Lusis AJ, Eskin E. PMID: 27770036; PMCID: PMC5161272.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimals
    76. Chromosome conformation elucidates regulatory relationships in developing human brain. Nature. 2016 10 27; 538(7626):523-527. Won H, de la Torre-Ubieta L, Stein JL, Parikshak NN, Huang J, Opland CK, Gandal MJ, Sutton GJ, Hormozdiari F, Lu D, Lee C, Eskin E, Voineagu I, Ernst J, Geschwind DH. PMID: 27760116; PMCID: PMC5358922.
      View in: PubMed   Mentions: 225     Fields:    Translation:HumansCells
    77. The Genetic Architecture of Noise-Induced Hearing Loss: Evidence for a Gene-by-Environment Interaction. G3 (Bethesda). 2016 10 13; 6(10):3219-3228. Lavinsky J, Ge M, Crow AL, Pan C, Wang J, Salehi P, Myint A, Eskin E, Allayee H, Lusis AJ, Friedman RA. PMID: 27520957; PMCID: PMC5068943.
      View in: PubMed   Mentions: 11     Fields:    Translation:AnimalsCells
    78. Discovering Single Nucleotide Polymorphisms Regulating Human Gene Expression Using Allele Specific Expression from RNA-seq Data. Genetics. 2016 11; 204(3):1057-1064. Kang EY, Martin LJ, Mangul S, Isvilanonda W, Zou J, Ben-David E, Han B, Lusis AJ, Shifman S, Eskin E. PMID: 27765809; PMCID: PMC5105841.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    79. Improved methods for multi-trait fine mapping of pleiotropic risk loci. Bioinformatics. 2017 01 15; 33(2):248-255. Kichaev G, Roytman M, Johnson R, Eskin E, Lindström S, Kraft P, Pasaniuc B. PMID: 27663501; PMCID: PMC5254076.
      View in: PubMed   Mentions: 48     Fields:    Translation:Humans
    80. The Genetic Basis of Host Preference and Resting Behavior in the Major African Malaria Vector, Anopheles arabiensis. PLoS Genet. 2016 09; 12(9):e1006303. Main BJ, Lee Y, Ferguson HM, Kreppel KS, Kihonda A, Govella NJ, Collier TC, Cornel AJ, Eskin E, Kang EY, Nieman CC, Weakley AM, Lanzaro GC. PMID: 27631375; PMCID: PMC5025075.
      View in: PubMed   Mentions: 41     Fields:    Translation:HumansAnimalsPHPublic Health
    81. Hypothalamic transcriptomes of 99 mouse strains reveal trans eQTL hotspots, splicing QTLs and novel non-coding genes. Elife. 2016 09 13; 5. Hasin-Brumshtein Y, Khan AH, Hormozdiari F, Pan C, Parks BW, Petyuk VA, Piehowski PD, Brümmer A, Pellegrini M, Xiao X, Eskin E, Smith RD, Lusis AJ, Smith DJ. PMID: 27623010; PMCID: PMC5053804.
      View in: PubMed   Mentions: 20     Fields:    Translation:AnimalsCells
    82. ForestPMPlot: A Flexible Tool for Visualizing Heterogeneity Between Studies in Meta-analysis. G3 (Bethesda). 2016 07 07; 6(7):1793-8. Kang EY, Park Y, Li X, Segrè AV, Han B, Eskin E. PMID: 27194809; PMCID: PMC4938634.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansAnimals
    83. Using genomic annotations increases statistical power to detect eGenes. Bioinformatics. 2016 06 15; 32(12):i156-i163. Duong D, Zou J, Hormozdiari F, Sul JH, Ernst J, Han B, Eskin E. PMID: 27307612; PMCID: PMC4908356.
      View in: PubMed   Mentions: 7     Fields:    
    84. Imputing Phenotypes for Genome-wide Association Studies. Am J Hum Genet. 2016 Jul 07; 99(1):89-103. Hormozdiari F, Kang EY, Bilow M, Ben-David E, Vulpe C, McLachlan S, Lusis AJ, Han B, Eskin E. PMID: 27292110; PMCID: PMC5005435.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansAnimals
    85. Fast and Accurate Construction of Confidence Intervals for Heritability. Am J Hum Genet. 2016 06 02; 98(6):1181-1192. Schweiger R, Kaufman S, Laaksonen R, Kleber ME, März W, Eskin E, Rosset S, Halperin E. PMID: 27259052; PMCID: PMC4908190.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    86. Characterization of Expression Quantitative Trait Loci in Pedigrees from Colombia and Costa Rica Ascertained for Bipolar Disorder. PLoS Genet. 2016 05; 12(5):e1006046. Peterson CB, Service SK, Jasinska AJ, Gao F, Zelaya I, Teshiba TM, Bearden CE, Cantor RM, Reus VI, Macaya G, López-Jaramillo C, Bogomolov M, Benjamini Y, Eskin E, Coppola G, Freimer NB, Sabatti C. PMID: 27176483; PMCID: PMC4866754.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    87. The Hybrid Mouse Diversity Panel: a resource for systems genetics analyses of metabolic and cardiovascular traits. J Lipid Res. 2016 06; 57(6):925-42. Lusis AJ, Seldin MM, Allayee H, Bennett BJ, Civelek M, Davis RC, Eskin E, Farber CR, Hui S, Mehrabian M, Norheim F, Pan C, Parks B, Rau CD, Smith DJ, Vallim T, Wang Y, Wang J. PMID: 27099397; PMCID: PMC4878195.
      View in: PubMed   Mentions: 73     Fields:    Translation:HumansAnimalsCells
    88. Multiple testing correction in linear mixed models. Genome Biol. 2016 Apr 01; 17:62. Joo JW, Hormozdiari F, Han B, Eskin E. PMID: 27039378; PMCID: PMC4818520.
      View in: PubMed   Mentions: 25     Fields:    Translation:HumansAnimals
    89. Sparse PCA corrects for cell type heterogeneity in epigenome-wide association studies. Nat Methods. 2016 05; 13(5):443-5. Rahmani E, Zaitlen N, Baran Y, Eng C, Hu D, Galanter J, Oh S, Burchard EG, Eskin E, Zou J, Halperin E. PMID: 27018579; PMCID: PMC5548182.
      View in: PubMed   Mentions: 95     Fields:    Translation:HumansCells
    90. Accounting for Population Structure in Gene-by-Environment Interactions in Genome-Wide Association Studies Using Mixed Models. PLoS Genet. 2016 Mar; 12(3):e1005849. Sul JH, Bilow M, Yang WY, Kostem E, Furlotte N, He D, Eskin E. PMID: 26943367; PMCID: PMC4778803.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    91. Correction: Genetic Architecture of Atherosclerosis in Mice: A Systems Genetics Analysis of Common Inbred Strains. PLoS Genet. 2016 Mar; 12(3):e1005913. Bennett BJ, Davis RC, Civelek M, Orozco L, Wu J, Qi H, Pan C, Sevag Packard RR, Eskin E, Yan M, Kirchgessner T, Wang Z, Li X, Gregory JC, Hazen SL, Gargalovic PS, Lusis AJ. PMID: 26934746; PMCID: PMC4775237.
      View in: PubMed   Mentions: 3     Fields:    
    92. A general framework for meta-analyzing dependent studies with overlapping subjects in association mapping. Hum Mol Genet. 2016 05 01; 25(9):1857-66. Han B, Duong D, Sul JH, de Bakker PI, Eskin E, Raychaudhuri S. PMID: 26908615; PMCID: PMC4986332.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansAnimals
    93. Genetic Architecture of Atherosclerosis in Mice: A Systems Genetics Analysis of Common Inbred Strains. PLoS Genet. 2015 Dec; 11(12):e1005711. Bennett BJ, Davis RC, Civelek M, Orozco L, Wu J, Qi H, Pan C, Packard RR, Eskin E, Yan M, Kirchgessner T, Wang Z, Li X, Gregory JC, Hazen SL, Gargalovic PS, Lusis AJ. PMID: 26694027; PMCID: PMC4687930.
      View in: PubMed   Mentions: 65     Fields:    Translation:HumansAnimalsCells
    94. The Genetic Architecture of Hearing Impairment in Mice: Evidence for Frequency-Specific Genetic Determinants. G3 (Bethesda). 2015 Sep 04; 5(11):2329-39. Crow AL, Ohmen J, Wang J, Lavinsky J, Hartiala J, Li Q, Li X, Salehide P, Eskin E, Pan C, Lusis AJ, Allayee H, Friedman RA. PMID: 26342000; PMCID: PMC4632053.
      View in: PubMed   Mentions: 11     Fields:    Translation:Animals
    95. Genetic and environmental control of host-gut microbiota interactions. Genome Res. 2015 Oct; 25(10):1558-69. Org E, Parks BW, Joo JW, Emert B, Schwartzman W, Kang EY, Mehrabian M, Pan C, Knight R, Gunsalus R, Drake TA, Eskin E, Lusis AJ. PMID: 26260972; PMCID: PMC4579341.
      View in: PubMed   Mentions: 136     Fields:    Translation:Animals
    96. High-Density Genotypes of Inbred Mouse Strains: Improved Power and Precision of Association Mapping. G3 (Bethesda). 2015 Jul 28; 5(10):2021-6. Rau CD, Parks B, Wang Y, Eskin E, Simecek P, Churchill GA, Lusis AJ. PMID: 26224782; PMCID: PMC4592984.
      View in: PubMed   Mentions: 23     Fields:    Translation:Animals
    97. Quantitative analysis of 3-dimensional facial soft tissue photographic images: technical methods and clinical application. Prog Orthod. 2015; 16:21. Nanda V, Gutman B, Bar E, Alghamdi S, Tetradis S, Lusis AJ, Eskin E, Moon W. PMID: 26133934; PMCID: PMC4488234.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    98. Identification of causal genes for complex traits. Bioinformatics. 2015 Jun 15; 31(12):i206-13. Hormozdiari F, Kichaev G, Yang WY, Pasaniuc B, Eskin E. PMID: 26072484; PMCID: PMC4542778.
      View in: PubMed   Mentions: 34     Fields:    Translation:HumansAnimals
    99. Correction: Genome-Wide Association Study Identifies Nox3 as a Critical Gene for Susceptibility to Noise-Induced Hearing Loss. PLoS Genet. 2015 Jun; 11(6):e1005293. Lavinsky J, Crow AL, Pan C, Wang J, Aaron KA, Ho MK, Li Q, Salehide P, Myint A, Monges-Hernadez M, Eskin E, Allayee H, Lusis AJ, Friedman RA. PMID: 26068505; PMCID: PMC4465750.
      View in: PubMed   Mentions: 2     Fields:    
    100. The Genetic Landscape of Hematopoietic Stem Cell Frequency in Mice. Stem Cell Reports. 2015 Jul 14; 5(1):125-38. Zhou X, Crow AL, Hartiala J, Spindler TJ, Ghazalpour A, Barsky LW, Bennett BJ, Parks BW, Eskin E, Jain R, Epstein JA, Lusis AJ, Adams GB, Allayee H. PMID: 26050929; PMCID: PMC4618249.
      View in: PubMed   Mentions: 11     Fields:    Translation:AnimalsCells
    101. Accurate and fast multiple-testing correction in eQTL studies. Am J Hum Genet. 2015 Jun 04; 96(6):857-68. Sul JH, Raj T, de Jong S, de Bakker PI, Raychaudhuri S, Ophoff RA, Stranger BE, Eskin E, Han B. PMID: 26027500; PMCID: PMC4457958.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    102. Genome-wide association study identifies nox3 as a critical gene for susceptibility to noise-induced hearing loss. PLoS Genet. 2015 Apr; 11(4):e1005094. Lavinsky J, Crow AL, Pan C, Wang J, Aaron KA, Ho MK, Li Q, Salehide P, Myint A, Monges-Hernadez M, Eskin E, Allayee H, Lusis AJ, Friedman RA. PMID: 25880434; PMCID: PMC4399881.
      View in: PubMed   Mentions: 28     Fields:    Translation:Animals
    103. Gene-Gene Interactions Detection Using a Two-stage Model. J Comput Biol. 2015 Jun; 22(6):563-76. Wang Z, Sul JH, Snir S, Lozano JA, Eskin E. PMID: 25871811; PMCID: PMC4449719.
      View in: PubMed   Mentions: 2     Fields:    
    104. Efficient multiple-trait association and estimation of genetic correlation using the matrix-variate linear mixed model. Genetics. 2015 May; 200(1):59-68. Furlotte NA, Eskin E. PMID: 25724382; PMCID: PMC4423381.
      View in: PubMed   Mentions: 29     Fields:    Translation:Humans
    105. Genome-wide association study of NMDA receptor coagonists in human cerebrospinal fluid and plasma. Mol Psychiatry. 2015 Dec; 20(12):1557-64. Luykx JJ, Bakker SC, Visser WF, Verhoeven-Duif N, Buizer-Voskamp JE, den Heijer JM, Boks MP, Sul JH, Eskin E, Ori AP, Cantor RM, Vorstman J, Strengman E, DeYoung J, Kappen TH, Pariama E, van Dongen EP, Borgdorff P, Bruins P, de Koning TJ, Kahn RS, Ophoff RA. PMID: 25666758.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    106. Heritability of periodontal bone loss in mice. J Periodontal Res. 2015 Dec; 50(6):730-6. Hiyari S, Atti E, Camargo PM, Eskin E, Lusis AJ, Tetradis S, Pirih FQ. PMID: 25581386; PMCID: PMC4499504.
      View in: PubMed   Mentions: 12     Fields:    Translation:AnimalsCells
    107. A spatial haplotype copying model with applications to genotype imputation. J Comput Biol. 2015 May; 22(5):451-62. Yang WY, Hormozdiari F, Eskin E, Pasaniuc B. PMID: 25526526; PMCID: PMC4425418.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    108. Memory efficient assembly of human genome. J Bioinform Comput Biol. 2015 Apr; 13(2):1550008. Hormozdiari F, Eskin E. PMID: 25603998.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimals
    109. IPED2X: a robust pedigree reconstruction algorithm for complicated pedigrees. J Bioinform Comput Biol. 2014 Dec; 12(6):1442007. He D, Eskin E. PMID: 25553812.
      View in: PubMed   Mentions: 2     Fields:    
    110. Spatial localization of recent ancestors for admixed individuals. G3 (Bethesda). 2014 Nov 03; 4(12):2505-18. Yang WY, Platt A, Chiang CW, Eskin E, Novembre J, Pasaniuc B. PMID: 25371484; PMCID: PMC4267945.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    111. Integrating functional data to prioritize causal variants in statistical fine-mapping studies. PLoS Genet. 2014 Oct; 10(10):e1004722. Kichaev G, Yang WY, Lindstrom S, Hormozdiari F, Eskin E, Price AL, Kraft P, Pasaniuc B. PMID: 25357204; PMCID: PMC4214605.
      View in: PubMed   Mentions: 206     Fields:    Translation:Humans
    112. Identifying causal variants at loci with multiple signals of association. Genetics. 2014 Oct; 198(2):497-508. Hormozdiari F, Kostem E, Kang EY, Pasaniuc B, Eskin E. PMID: 25104515; PMCID: PMC4196608.
      View in: PubMed   Mentions: 182     Fields:    Translation:Humans
    113. Privacy preserving protocol for detecting genetic relatives using rare variants. Bioinformatics. 2014 Jun 15; 30(12):i204-11. Hormozdiari F, Joo JW, Wadia A, Guan F, Ostrosky R, Sahai A, Eskin E. PMID: 24931985; PMCID: PMC4058916.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    114. Accurate viral population assembly from ultra-deep sequencing data. Bioinformatics. 2014 Jun 15; 30(12):i329-37. Mangul S, Wu NC, Mancuso N, Zelikovsky A, Sun R, Eskin E. PMID: 24932001; PMCID: PMC4058922.
      View in: PubMed   Mentions: 20     Fields:    Translation:Cells
    115. Allele-specific expression and eQTL analysis in mouse adipose tissue. BMC Genomics. 2014 Jun 13; 15:471. Hasin-Brumshtein Y, Hormozdiari F, Martin L, van Nas A, Eskin E, Lusis AJ, Drake TA. PMID: 24927774; PMCID: PMC4089026.
      View in: PubMed   Mentions: 29     Fields:    Translation:Animals
    116. Effectively identifying regulatory hotspots while capturing expression heterogeneity in gene expression studies. Genome Biol. 2014 Apr 07; 15(4):r61. Joo JW, Sul JH, Han B, Ye C, Eskin E. PMID: 24708878; PMCID: PMC4053820.
      View in: PubMed   Mentions: 20     Fields:    Translation:AnimalsCells
    117. Identifying genetic relatives without compromising privacy. Genome Res. 2014 Apr; 24(4):664-72. He D, Furlotte NA, Hormozdiari F, Joo JW, Wadia A, Ostrovsky R, Sahai A, Eskin E. PMID: 24614977; PMCID: PMC3975065.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    118. Genome-wide association study for age-related hearing loss (AHL) in the mouse: a meta-analysis. J Assoc Res Otolaryngol. 2014 Jun; 15(3):335-52. Ohmen J, Kang EY, Li X, Joo JW, Hormozdiari F, Zheng QY, Davis RC, Lusis AJ, Eskin E, Friedman RA. PMID: 24570207; PMCID: PMC4010595.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansAnimals
    119. Genetic implication of a novel thiamine transporter in human hypertension. J Am Coll Cardiol. 2014 Apr 22; 63(15):1542-55. Zhang K, Huentelman MJ, Rao F, Sun EI, Corneveaux JJ, Schork AJ, Wei Z, Waalen J, Miramontes-Gonzalez JP, Hightower CM, Maihofer AX, Mahata M, Pastinen T, Ehret GB, International Consortium for Blood Pressure Genome-Wide Association Studies, Schork NJ, Eskin E, Nievergelt CM, Saier MH, O'Connor DT. PMID: 24509276; PMCID: PMC3992204.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    120. Diversity, differentiation, and linkage disequilibrium: prospects for association mapping in the malaria vector Anopheles arabiensis. G3 (Bethesda). 2014 Jan 10; 4(1):121-31. Marsden CD, Lee Y, Kreppel K, Weakley A, Cornel A, Ferguson HM, Eskin E, Lanzaro GC. PMID: 24281424; PMCID: PMC3887528.
      View in: PubMed   Mentions: 19     Fields:    Translation:AnimalsPHPublic Health
    121. Meta-analysis identifies gene-by-environment interactions as demonstrated in a study of 4,965 mice. PLoS Genet. 2014 Jan; 10(1):e1004022. Kang EY, Han B, Furlotte N, Joo JW, Shih D, Davis RC, Lusis AJ, Eskin E. PMID: 24415945; PMCID: PMC3886926.
      View in: PubMed   Mentions: 23     Fields:    Translation:Animals
    122. Fast pairwise IBD association testing in genome-wide association studies. Bioinformatics. 2014 Jan 15; 30(2):206-13. Han B, Kang EY, Raychaudhuri S, de Bakker PI, Eskin E. PMID: 24158599; PMCID: PMC3892684.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    123. eALPS: estimating abundance levels in pooled sequencing using available genotyping data. J Comput Biol. 2013 Nov; 20(11):861-77. Eskin I, Hormozdiari F, Conde L, Riby J, Skibola CF, Eskin E, Halperin E. PMID: 24144111; PMCID: PMC4013753.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    124. IPED: inheritance path-based pedigree reconstruction algorithm using genotype data. J Comput Biol. 2013 Oct; 20(10):780-91. He D, Wang Z, Han B, Parida L, Eskin E. PMID: 24093229; PMCID: PMC3791035.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    125. Efficiently identifying significant associations in genome-wide association studies. J Comput Biol. 2013 Oct; 20(10):817-30. Kostem E, Eskin E. PMID: 24033261; PMCID: PMC3791046.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    126. Analysis of allele-specific expression in mouse liver by RNA-Seq: a comparison with Cis-eQTL identified using genetic linkage. Genetics. 2013 Nov; 195(3):1157-66. Lagarrigue S, Martin L, Hormozdiari F, Roux PF, Pan C, van Nas A, Demeure O, Cantor R, Ghazalpour A, Eskin E, Lusis AJ. PMID: 24026101; PMCID: PMC3813844.
      View in: PubMed   Mentions: 29     Fields:    Translation:Animals
    127. Functional genomic assessment of phosgene-induced acute lung injury in mice. Am J Respir Cell Mol Biol. 2013 Sep; 49(3):368-83. Leikauf GD, Concel VJ, Bein K, Liu P, Berndt A, Martin TM, Ganguly K, Jang AS, Brant KA, Dopico RA, Upadhyay S, Cario C, Di YP, Vuga LJ, Kostem E, Eskin E, You M, Kaminski N, Prows DR, Knoell DL, Fabisiak JP. PMID: 23590305; PMCID: PMC3824050.
      View in: PubMed   Mentions: 8     Fields:    Translation:AnimalsCells
    128. Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data. Bioinformatics. 2013 Sep 15; 29(18):2245-52. Yang WY, Hormozdiari F, Wang Z, He D, Pasaniuc B, Eskin E. PMID: 23825370; PMCID: PMC3753566.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    129. Effectively identifying eQTLs from multiple tissues by combining mixed model and meta-analytic approaches. PLoS Genet. 2013 Jun; 9(6):e1003491. Sul JH, Han B, Ye C, Choi T, Eskin E. PMID: 23785294; PMCID: PMC3681686.
      View in: PubMed   Mentions: 54     Fields:    Translation:Animals
    130. Rare variant association testing under low-coverage sequencing. Genetics. 2013 Jul; 194(3):769-79. Navon O, Sul JH, Han B, Conde L, Bracci PM, Riby J, Skibola CF, Eskin E, Halperin E. PMID: 23636738; PMCID: PMC3697979.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    131. Improving the accuracy and efficiency of partitioning heritability into the contributions of genomic regions. Am J Hum Genet. 2013 Apr 04; 92(4):558-64. Kostem E, Eskin E. PMID: 23561845; PMCID: PMC3617385.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    132. Mixed models can correct for population structure for genomic regions under selection. Nat Rev Genet. 2013 Apr; 14(4):300. Sul JH, Eskin E. PMID: 23438871.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    133. CNVeM: copy number variation detection using uncertainty of read mapping. J Comput Biol. 2013 Mar; 20(3):224-36. Wang Z, Hormozdiari F, Yang WY, Halperin E, Eskin E. PMID: 23421794; PMCID: PMC3590897.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimalsCells
    134. Genome-wide association mapping of blood cell traits in mice. Mamm Genome. 2013 Apr; 24(3-4):105-18. Davis RC, van Nas A, Bennett B, Orozco L, Pan C, Rau CD, Eskin E, Lusis AJ. PMID: 23417284; PMCID: PMC3933005.
      View in: PubMed   Mentions: 28     Fields:    Translation:AnimalsCells
    135. Limited RNA editing in exons of mouse liver and adipose. Genetics. 2013 Apr; 193(4):1107-15. Lagarrigue S, Hormozdiari F, Martin LJ, Lecerf F, Hasin Y, Rau C, Hagopian R, Xiao Y, Yan J, Drake TA, Ghazalpour A, Eskin E, Lusis AJ. PMID: 23410828; PMCID: PMC3606090.
      View in: PubMed   Mentions: 15     Fields:    Translation:AnimalsCells
    136. Hap-seq: an optimal algorithm for haplotype phasing with imputation using sequencing data. J Comput Biol. 2013 Feb; 20(2):80-92. He D, Han B, Eskin E. PMID: 23383995; PMCID: PMC3576919.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    137. Genome reassembly with high-throughput sequencing data. BMC Genomics. 2013; 14 Suppl 1:S8. Parrish N, Sudakov B, Eskin E. PMID: 23368744; PMCID: PMC3549812.
      View in: PubMed   Mentions:    Fields:    Translation:Animals
    138. Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid. Mol Psychiatry. 2014 Feb; 19(2):228-34. Luykx JJ, Bakker SC, Lentjes E, Neeleman M, Strengman E, Mentink L, DeYoung J, de Jong S, Sul JH, Eskin E, van Eijk K, van Setten J, Buizer-Voskamp JE, Cantor RM, Lu A, van Amerongen M, van Dongen EP, Keijzers P, Kappen T, Borgdorff P, Bruins P, Derks EM, Kahn RS, Ophoff RA. PMID: 23319000.
      View in: PubMed   Mentions: 31     Fields:    Translation:HumansCells
    139. Genetic control of obesity and gut microbiota composition in response to high-fat, high-sucrose diet in mice. Cell Metab. 2013 Jan 08; 17(1):141-52. Parks BW, Nam E, Org E, Kostem E, Norheim F, Hui ST, Pan C, Civelek M, Rau CD, Bennett BJ, Mehrabian M, Ursell LK, He A, Castellani LW, Zinker B, Kirby M, Drake TA, Drevon CA, Knight R, Gargalovic P, Kirchgessner T, Eskin E, Lusis AJ. PMID: 23312289; PMCID: PMC3545283.
      View in: PubMed   Mentions: 248     Fields:    Translation:HumansAnimals
    140. Systems genetic analysis of osteoblast-lineage cells. PLoS Genet. 2012; 8(12):e1003150. Calabrese G, Bennett BJ, Orozco L, Kang HM, Eskin E, Dombret C, De Backer O, Lusis AJ, Farber CR. PMID: 23300464; PMCID: PMC3531492.
      View in: PubMed   Mentions: 31     Fields:    Translation:HumansAnimalsCells
    141. Hap-seqX: expedite algorithm for haplotype phasing with imputation using sequence data. Gene. 2013 Apr 10; 518(1):2-6. He D, Eskin E. PMID: 23269365.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    142. The Minnesota Center for Twin and Family Research genome-wide association study. Twin Res Hum Genet. 2012 Dec; 15(6):767-74. Miller MB, Basu S, Cunningham J, Eskin E, Malone SM, Oetting WS, Schork N, Sul JH, Iacono WG, McGue M. PMID: 23363460; PMCID: PMC3561927.
      View in: PubMed   Mentions: 54     Fields:    Translation:HumansCTClinical Trials
    143. Genome-wide association studies in mice. Nat Rev Genet. 2012 Nov; 13(11):807-17. Flint J, Eskin E. PMID: 23044826; PMCID: PMC3625632.
      View in: PubMed   Mentions: 102     Fields:    Translation:AnimalsCells
    144. Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits. Mamm Genome. 2012 Oct; 23(9-10):680-92. Ghazalpour A, Rau CD, Farber CR, Bennett BJ, Orozco LD, van Nas A, Pan C, Allayee H, Beaven SW, Civelek M, Davis RC, Drake TA, Friedman RA, Furlotte N, Hui ST, Jentsch JD, Kostem E, Kang HM, Kang EY, Joo JW, Korshunov VA, Laughlin RE, Martin LJ, Ohmen JD, Parks BW, Pellegrini M, Reue K, Smith DJ, Tetradis S, Wang J, Wang Y, Weiss JN, Kirchgessner T, Gargalovic PS, Eskin E, Lusis AJ, LeBoeuf RC. PMID: 22892838; PMCID: PMC3586763.
      View in: PubMed   Mentions: 79     Fields:    Translation:Animals
    145. Genome-wide association study of Tourette's syndrome. Mol Psychiatry. 2013 Jun; 18(6):721-8. Scharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon E, Edlund CK, Service SK, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, Davis LK, Han B, Crane J, Moorjani P, Crenshaw AT, Parkin MA, Reus VI, Lowe TL, Rangel-Lugo M, Chouinard S, Dion Y, Girard S, Cath DC, Smit JH, King RA, Fernandez TV, Leckman JF, Kidd KK, Kidd JR, Pakstis AJ, State MW, Herrera LD, Romero R, Fournier E, Sandor P, Barr CL, Phan N, Gross-Tsur V, Benarroch F, Pollak Y, Budman CL, Bruun RD, Erenberg G, Naarden AL, Lee PC, Weiss N, Kremeyer B, Berrío GB, Campbell DD, Cardona Silgado JC, Ochoa WC, Mesa Restrepo SC, Muller H, Valencia Duarte AV, Lyon GJ, Leppert M, Morgan J, Weiss R, Grados MA, Anderson K, Davarya S, Singer H, Walkup J, Jankovic J, Tischfield JA, Heiman GA, Gilbert DL, Hoekstra PJ, Robertson MM, Kurlan R, Liu C, Gibbs JR, Singleton A, North American Brain Expression Consortium, Hardy J, UK Human Brain Expression Database, Strengman E, Ophoff RA, Wagner M, Moessner R, Mirel DB, Posthuma D, Sabatti C, Eskin E, Conti DV, Knowles JA, Ruiz-Linares A, Rouleau GA, Purcell S, Heutink P, Oostra BA, McMahon WM, Freimer NB, Cox NJ, Pauls DL. PMID: 22889924; PMCID: PMC3605224.
      View in: PubMed   Mentions: 77     Fields:    Translation:HumansCells
    146. "Good enough solutions" and the genetics of complex diseases. Circ Res. 2012 Aug 03; 111(4):493-504. Weiss JN, Karma A, MacLellan WR, Deng M, Rau CD, Rees CM, Wang J, Wisniewski N, Eskin E, Horvath S, Qu Z, Wang Y, Lusis AJ. PMID: 22859671; PMCID: PMC3428228.
      View in: PubMed   Mentions: 46     Fields:    Translation:HumansAnimals
    147. Mapping genetic variants associated with beta-adrenergic responses in inbred mice. PLoS One. 2012; 7(7):e41032. Hersch M, Peter B, Kang HM, Schüpfer F, Abriel H, Pedrazzini T, Eskin E, Beckmann JS, Bergmann S, Maurer F. PMID: 22859963; PMCID: PMC3409184.
      View in: PubMed   Mentions: 6     Fields:    Translation:AnimalsCells
    148. High-resolution association mapping of atherosclerosis loci in mice. Arterioscler Thromb Vasc Biol. 2012 Aug; 32(8):1790-8. Bennett BJ, Orozco L, Kostem E, Erbilgin A, Dallinga M, Neuhaus I, Guan B, Wang X, Eskin E, Lusis AJ. PMID: 22723443; PMCID: PMC3519423.
      View in: PubMed   Mentions: 12     Fields:    Translation:Animals
    149. Incorporating prior information into association studies. Bioinformatics. 2012 Jun 15; 28(12):i147-53. Darnell G, Duong D, Han B, Eskin E. PMID: 22689754; PMCID: PMC3371867.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    150. Integrated computational and experimental analysis of the neuroendocrine transcriptome in genetic hypertension identifies novel control points for the cardiometabolic syndrome. Circ Cardiovasc Genet. 2012 Aug 01; 5(4):430-40. Friese RS, Ye C, Nievergelt CM, Schork AJ, Mahapatra NR, Rao F, Napolitan PS, Waalen J, Ehret GB, Munroe PB, Schmid-Schönbein GW, Eskin E, O'Connor DT. PMID: 22670052; PMCID: PMC3467001.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansAnimalsCells
    151. Improved linear mixed models for genome-wide association studies. Nat Methods. 2012 May 30; 9(6):525-6. Listgarten J, Lippert C, Kadie CM, Davidson RI, Eskin E, Heckerman D. PMID: 22669648; PMCID: PMC3597090.
      View in: PubMed   Mentions: 150     Fields:    Translation:Humans
    152. A model-based approach for analysis of spatial structure in genetic data. Nat Genet. 2012 May 20; 44(6):725-31. Yang WY, Novembre J, Eskin E, Halperin E. PMID: 22610118; PMCID: PMC3592563.
      View in: PubMed   Mentions: 80     Fields:    Translation:Humans
    153. Genome-wide association mapping with longitudinal data. Genet Epidemiol. 2012 Jul; 36(5):463-71. Furlotte NA, Eskin E, Eyheramendy S. PMID: 22581622; PMCID: PMC3625633.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    154. Increasing association mapping power and resolution in mouse genetic studies through the use of meta-analysis for structured populations. Genetics. 2012 Jul; 191(3):959-67. Furlotte NA, Kang EY, Van Nas A, Farber CR, Lusis AJ, Eskin E. PMID: 22505625; PMCID: PMC3389987.
      View in: PubMed   Mentions: 8     Fields:    Translation:Animals
    155. Interpreting meta-analyses of genome-wide association studies. PLoS Genet. 2012; 8(3):e1002555. Han B, Eskin E. PMID: 22396665; PMCID: PMC3291559.
      View in: PubMed   Mentions: 71     Fields:    Translation:Humans
    156. Fatigue risk management in the workplace. J Occup Environ Med. 2012 Feb; 54(2):231-58. Lerman SE, Eskin E, Flower DJ, George EC, Gerson B, Hartenbaum N, Hursh SR, Moore-Ede M, American College of Occupational and Environmental Medicine Presidential Task Force on Fatigue Risk . PMID: 22269988.
      View in: PubMed   Mentions: 43     Fields:    Translation:Humans
    157. Increasing power of groupwise association test with likelihood ratio test. J Comput Biol. 2011 Nov; 18(11):1611-24. Sul JH, Han B, Eskin E. PMID: 21919745; PMCID: PMC3216097.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    158. Mouse genomic variation and its effect on phenotypes and gene regulation. Nature. 2011 Sep 14; 477(7364):289-94. Keane TM, Goodstadt L, Danecek P, White MA, Wong K, Yalcin B, Heger A, Agam A, Slater G, Goodson M, Furlotte NA, Eskin E, Nellåker C, Whitley H, Cleak J, Janowitz D, Hernandez-Pliego P, Edwards A, Belgard TG, Oliver PL, McIntyre RE, Bhomra A, Nicod J, Gan X, Yuan W, van der Weyden L, Steward CA, Bala S, Stalker J, Mott R, Durbin R, Jackson IJ, Czechanski A, Guerra-Assunção JA, Donahue LR, Reinholdt LG, Payseur BA, Ponting CP, Birney E, Flint J, Adams DJ. PMID: 21921910; PMCID: PMC3276836.
      View in: PubMed   Mentions: 867     Fields:    Translation:Animals
    159. Assembly of non-unique insertion content using next-generation sequencing. BMC Bioinformatics. 2011; 12 Suppl 6:S3. Parrish N, Hormozdiari F, Eskin E. PMID: 21989261; PMCID: PMC3194191.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansAnimalsCells
    160. Genotyping common and rare variation using overlapping pool sequencing. BMC Bioinformatics. 2011; 12 Suppl 6:S2. He D, Zaitlen N, Pasaniuc B, Eskin E, Halperin E. PMID: 21989232; PMCID: PMC3194190.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    161. Mixed-model coexpression: calculating gene coexpression while accounting for expression heterogeneity. Bioinformatics. 2011 Jul 01; 27(13):i288-94. Furlotte NA, Kang HM, Ye C, Eskin E. PMID: 21685083; PMCID: PMC3117390.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimals
    162. Comparative analysis of proteome and transcriptome variation in mouse. PLoS Genet. 2011 Jun; 7(6):e1001393. Ghazalpour A, Bennett B, Petyuk VA, Orozco L, Hagopian R, Mungrue IN, Farber CR, Sinsheimer J, Kang HM, Furlotte N, Park CC, Wen PZ, Brewer H, Weitz K, Camp DG, Pan C, Yordanova R, Neuhaus I, Tilford C, Siemers N, Gargalovic P, Eskin E, Kirchgessner T, Smith DJ, Smith RD, Lusis AJ. PMID: 21695224; PMCID: PMC3111477.
      View in: PubMed   Mentions: 270     Fields:    Translation:AnimalsCells
    163. Random-effects model aimed at discovering associations in meta-analysis of genome-wide association studies. Am J Hum Genet. 2011 May 13; 88(5):586-98. Han B, Eskin E. PMID: 21565292; PMCID: PMC3146723.
      View in: PubMed   Mentions: 272     Fields:    Translation:Humans
    164. Identification and functional validation of the novel antimalarial resistance locus PF10_0355 in Plasmodium falciparum. PLoS Genet. 2011 Apr; 7(4):e1001383. Van Tyne D, Park DJ, Schaffner SF, Neafsey DE, Angelino E, Cortese JF, Barnes KG, Rosen DM, Lukens AK, Daniels RF, Milner DA, Johnson CA, Shlyakhter I, Grossman SR, Becker JS, Yamins D, Karlsson EK, Ndiaye D, Sarr O, Mboup S, Happi C, Furlotte NA, Eskin E, Kang HM, Hartl DL, Birren BW, Wiegand RC, Lander ES, Wirth DF, Volkman SK, Sabeti PC. PMID: 21533027; PMCID: PMC3080868.
      View in: PubMed   Mentions: 54     Fields:    Translation:Animals
    165. Efficient algorithms for tandem copy number variation reconstruction in repeat-rich regions. Bioinformatics. 2011 Jun 01; 27(11):1513-20. He D, Hormozdiari F, Furlotte N, Eskin E. PMID: 21505028; PMCID: PMC3102223.
      View in: PubMed   Mentions: 10     Fields:    Translation:AnimalsCells
    166. Mouse genome-wide association and systems genetics identify Asxl2 as a regulator of bone mineral density and osteoclastogenesis. PLoS Genet. 2011 Apr; 7(4):e1002038. Farber CR, Bennett BJ, Orozco L, Zou W, Lira A, Kostem E, Kang HM, Furlotte N, Berberyan A, Ghazalpour A, Suwanwela J, Drake TA, Eskin E, Wang QT, Teitelbaum SL, Lusis AJ. PMID: 21490954; PMCID: PMC3072371.
      View in: PubMed   Mentions: 79     Fields:    Translation:AnimalsCells
    167. Increasing power of genome-wide association studies by collecting additional single-nucleotide polymorphisms. Genetics. 2011 Jun; 188(2):449-60. Kostem E, Lozano JA, Eskin E. PMID: 21467568; PMCID: PMC3122306.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    168. Gene networks associated with conditional fear in mice identified using a systems genetics approach. BMC Syst Biol. 2011 Mar 16; 5:43. Park CC, Gale GD, de Jong S, Ghazalpour A, Bennett BJ, Farber CR, Langfelder P, Lin A, Khan AH, Eskin E, Horvath S, Lusis AJ, Ophoff RA, Smith DJ. PMID: 21410935; PMCID: PMC3070648.
      View in: PubMed   Mentions: 51     Fields:    Translation:AnimalsCells
    169. An optimal weighted aggregated association test for identification of rare variants involved in common diseases. Genetics. 2011 May; 188(1):181-8. Sul JH, Han B, He D, Eskin E. PMID: 21368279; PMCID: PMC3120154.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    170. Postassociation cleaning using linkage disequilibrium information. Genet Epidemiol. 2011 Jan; 35(1):1-10. Han B, Hackel BM, Eskin E. PMID: 21181893.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    171. Detection and reconstruction of tandemly organized de novo copy number variations. BMC Bioinformatics. 2010 Dec 14; 11 Suppl 11:S12. He D, Furlotte N, Eskin E. PMID: 21172047; PMCID: PMC3024866.
      View in: PubMed   Mentions: 4     Fields:    Translation:Animals
    172. Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population. Hum Mol Genet. 2011 Feb 15; 20(4):827-39. Kenny EE, Kim M, Gusev A, Lowe JK, Salit J, Smith JG, Kovvali S, Kang HM, Newton-Cheh C, Daly MJ, Stoffel M, Altshuler DM, Friedman JM, Eskin E, Breslow JL, Pe'er I. PMID: 21118897; PMCID: PMC3024042.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    173. In silico QTL mapping of basal liver iron levels in inbred mouse strains. Physiol Genomics. 2011 Feb 11; 43(3):136-47. McLachlan S, Lee SM, Steele TM, Hawthorne PL, Zapala MA, Eskin E, Schork NJ, Anderson GJ, Vulpe CD. PMID: 21062905; PMCID: PMC3055709.
      View in: PubMed   Mentions: 12     Fields:    Translation:Animals
    174. Imputation aware meta-analysis of genome-wide association studies. Genet Epidemiol. 2010 Sep; 34(6):537-42. Zaitlen N, Eskin E. PMID: 20717975; PMCID: PMC3102182.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    175. Multi-marker tagging single nucleotide polymorphism selection using estimation of distribution algorithms. Artif Intell Med. 2010 Nov; 50(3):193-201. Santana R, Mendiburu A, Zaitlen N, Eskin E, Lozano JA. PMID: 20650616.
      View in: PubMed   Mentions: 2     Fields:    
    176. Optimal algorithms for haplotype assembly from whole-genome sequence data. Bioinformatics. 2010 Jun 15; 26(12):i183-90. He D, Choi A, Pipatsrisawat K, Darwiche A, Eskin E. PMID: 20529904; PMCID: PMC2881399.
      View in: PubMed   Mentions: 46     Fields:    Translation:Cells
    177. Genome-wide case/control studies in hypertension: only the 'tip of the iceberg'. J Hypertens. 2010 Jun; 28(6):1115-23. Zhang K, Weder AB, Eskin E, O'Connor DT. PMID: 20216088; PMCID: PMC2873167.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    178. Fine mapping in 94 inbred mouse strains using a high-density haplotype resource. Genetics. 2010 Jul; 185(3):1081-95. Kirby A, Kang HM, Wade CM, Cotsapas C, Kostem E, Han B, Furlotte N, Kang EY, Rivas M, Bogue MA, Frazer KA, Johnson FM, Beilharz EJ, Cox DR, Eskin E, Daly MJ. PMID: 20439770; PMCID: PMC2907194.
      View in: PubMed   Mentions: 71     Fields:    Translation:HumansAnimals
    179. Variance component model to account for sample structure in genome-wide association studies. Nat Genet. 2010 Apr; 42(4):348-54. Kang HM, Sul JH, Service SK, Zaitlen NA, Kong SY, Freimer NB, Sabatti C, Eskin E. PMID: 20208533; PMCID: PMC3092069.
      View in: PubMed   Mentions: 1130     Fields:    Translation:Humans
    180. EMINIM: an adaptive and memory-efficient algorithm for genotype imputation. J Comput Biol. 2010 Mar; 17(3):547-60. Kang HM, Zaitlen NA, Eskin E. PMID: 20377463; PMCID: PMC3198882.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansAnimals
    181. Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease. Neuroimage. 2010 Jun; 51(2):542-54. Stein JL, Hua X, Morra JH, Lee S, Hibar DP, Ho AJ, Leow AD, Toga AW, Sul JH, Kang HM, Eskin E, Saykin AJ, Shen L, Foroud T, Pankratz N, Huentelman MJ, Craig DW, Gerber JD, Allen AN, Corneveaux JJ, Stephan DA, Webster J, DeChairo BM, Potkin SG, Jack CR, Weiner MW, Thompson PM, Alzheimer's Disease Neuroimaging Initiative. PMID: 20197096; PMCID: PMC2856746.
      View in: PubMed   Mentions: 94     Fields:    Translation:Humans
    182. Detecting the presence and absence of causal relationships between expression of yeast genes with very few samples. J Comput Biol. 2010 Mar; 17(3):533-46. Kang EY, Ye C, Shpitser I, Eskin E. PMID: 20377462; PMCID: PMC3198891.
      View in: PubMed   Mentions: 4     Fields:    Translation:Animals
    183. A high-resolution association mapping panel for the dissection of complex traits in mice. Genome Res. 2010 Feb; 20(2):281-90. Bennett BJ, Farber CR, Orozco L, Kang HM, Ghazalpour A, Siemers N, Neubauer M, Neuhaus I, Yordanova R, Guan B, Truong A, Yang WP, He A, Kayne P, Gargalovic P, Kirchgessner T, Pan C, Castellani LW, Kostem E, Furlotte N, Drake TA, Eskin E, Lusis AJ. PMID: 20054062; PMCID: PMC2813484.
      View in: PubMed   Mentions: 202     Fields:    Translation:Animals
    184. Identification of novel genes that mediate innate immunity using inbred mice. Genetics. 2009 Dec; 183(4):1535-44. Yang IV, Wade CM, Kang HM, Alper S, Rutledge H, Lackford B, Eskin E, Daly MJ, Schwartz DA. PMID: 19805818; PMCID: PMC2787437.
      View in: PubMed   Mentions: 37     Fields:    Translation:AnimalsCells
    185. Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairs. J Pharmacol Exp Ther. 2009 Nov; 331(2):419-28. Rana BK, Wessel J, Mahboubi V, Rao F, Haeller J, Gayen JR, Eskin E, Valle AM, Das M, Mahata SK, Taupenot L, Stridsberg M, Talley TT, Ziegler MG, Smith DW, Schork NJ, O'Connor DT, Taylor P. PMID: 19671882; PMCID: PMC2775266.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    186. Genome-wide association study of bipolar disorder in European American and African American individuals. Mol Psychiatry. 2009 Aug; 14(8):755-63. Smith EN, Bloss CS, Badner JA, Barrett T, Belmonte PL, Berrettini W, Byerley W, Coryell W, Craig D, Edenberg HJ, Eskin E, Foroud T, Gershon E, Greenwood TA, Hipolito M, Koller DL, Lawson WB, Liu C, Lohoff F, McInnis MG, McMahon FJ, Mirel DB, Murray SS, Nievergelt C, Nurnberger J, Nwulia EA, Paschall J, Potash JB, Rice J, Schulze TG, Scheftner W, Panganiban C, Zaitlen N, Zandi PP, Zöllner S, Schork NJ, Kelsoe JR. PMID: 19488044; PMCID: PMC3035981.
      View in: PubMed   Mentions: 189     Fields:    Translation:Humans
    187. Rapid and accurate multiple testing correction and power estimation for millions of correlated markers. PLoS Genet. 2009 Apr; 5(4):e1000456. Han B, Kang HM, Eskin E. PMID: 19381255; PMCID: PMC2663787.
      View in: PubMed   Mentions: 84     Fields:    Translation:Humans
    188. Linkage effects and analysis of finite sample errors in the HapMap. Hum Hered. 2009; 68(2):73-86. Zaitlen N, Kang HM, Eskin E. PMID: 19365134; PMCID: PMC2874737.
      View in: PubMed   Mentions: 4     Fields:    
    189. Using network component analysis to dissect regulatory networks mediated by transcription factors in yeast. PLoS Comput Biol. 2009 Mar; 5(3):e1000311. Ye C, Galbraith SJ, Liao JC, Eskin E. PMID: 19300475; PMCID: PMC2649002.
      View in: PubMed   Mentions: 21     Fields:    Translation:AnimalsCells
    190. Accurate discovery of expression quantitative trait loci under confounding from spurious and genuine regulatory hotspots. Genetics. 2008 Dec; 180(4):1909-25. Kang HM, Ye C, Eskin E. PMID: 18791227; PMCID: PMC2600931.
      View in: PubMed   Mentions: 80     Fields:    Translation:HumansAnimals
    191. Efficient association study design via power-optimized tag SNP selection. Ann Hum Genet. 2008 Nov; 72(Pt 6):834-47. Han B, Kang HM, Seo MS, Zaitlen N, Eskin E. PMID: 18702637; PMCID: PMC2574965.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    192. High-resolution mapping of gene expression using association in an outbred mouse stock. PLoS Genet. 2008 Aug 08; 4(8):e1000149. Ghazalpour A, Doss S, Kang H, Farber C, Wen PZ, Brozell A, Castellanos R, Eskin E, Smith DJ, Drake TA, Lusis AJ. PMID: 18688273; PMCID: PMC2483929.
      View in: PubMed   Mentions: 40     Fields:    Translation:AnimalsCells
    193. Increasing power in association studies by using linkage disequilibrium structure and molecular function as prior information. Genome Res. 2008 Apr; 18(4):653-60. Eskin E. PMID: 18353808; PMCID: PMC2279252.
      View in: PubMed   Mentions: 34     Fields:    Translation:Humans
    194. Efficient control of population structure in model organism association mapping. Genetics. 2008 Mar; 178(3):1709-23. Kang HM, Zaitlen NA, Wade CM, Kirby A, Heckerman D, Daly MJ, Eskin E. PMID: 18385116; PMCID: PMC2278096.
      View in: PubMed   Mentions: 756     Fields:    Translation:Animals
    195. Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping. BMC Genet. 2008 Feb 05; 9:14. Olshen AB, Gold B, Lohmueller KE, Struewing JP, Satagopan J, Stefanov SA, Eskin E, Kirchhoff T, Lautenberger JA, Klein RJ, Friedman E, Norton L, Ellis NA, Viale A, Lee CS, Borgen PI, Clark AG, Offit K, Boyd J. PMID: 18251999; PMCID: PMC2259380.
      View in: PubMed   Mentions: 24     Fields:    Translation:Humans
    196. Further evidence for association of GRK3 to bipolar disorder suggests a second disease mutation. Psychiatr Genet. 2007 Dec; 17(6):315-22. Barrett TB, Emberton JE, Nievergelt CM, Liang SG, Hauger RL, Eskin E, Schork NJ, Kelsoe JR. PMID: 18075471.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    197. A sequence-based variation map of 8.27 million SNPs in inbred mouse strains. Nature. 2007 Aug 30; 448(7157):1050-3. Frazer KA, Eskin E, Kang HM, Bogue MA, Hinds DA, Beilharz EJ, Gupta RV, Montgomery J, Morenzoni MM, Nilsen GB, Pethiyagoda CL, Stuve LL, Johnson FM, Daly MJ, Wade CM, Cox DR. PMID: 17660834.
      View in: PubMed   Mentions: 256     Fields:    Translation:AnimalsCells
    198. Incorporating homologues into sequence embeddings for protein analysis. J Bioinform Comput Biol. 2007 Jun; 5(3):717-38. Eskin E, Snir S. PMID: 17688313.
      View in: PubMed   Mentions: 2     Fields:    Translation:Cells
    199. Catecholamine release-inhibitory peptide catestatin (chromogranin A(352-372)): naturally occurring amino acid variant Gly364Ser causes profound changes in human autonomic activity and alters risk for hypertension. Circulation. 2007 May 01; 115(17):2271-81. Rao F, Wen G, Gayen JR, Das M, Vaingankar SM, Rana BK, Mahata M, Kennedy BP, Salem RM, Stridsberg M, Abel K, Smith DW, Eskin E, Schork NJ, Hamilton BA, Ziegler MG, Mahata SK, O'Connor DT. PMID: 17438154.
      View in: PubMed   Mentions: 53     Fields:    Translation:HumansCells
    200. Leveraging the HapMap correlation structure in association studies. Am J Hum Genet. 2007 Apr; 80(4):683-91. Zaitlen N, Kang HM, Eskin E, Halperin E. PMID: 17357074; PMCID: PMC1852710.
      View in: PubMed   Mentions: 33     Fields:    Translation:Humans
    201. Discovering tightly regulated and differentially expressed gene sets in whole genome expression data. Bioinformatics. 2007 Jan 15; 23(2):e84-90. Ye C, Eskin E. PMID: 17237110.
      View in: PubMed   Mentions: 8     Fields:    
    202. A note on phasing long genomic regions using local haplotype predictions. J Bioinform Comput Biol. 2006 Jun; 4(3):639-47. Eskin E, Sharan R, Halperin E. PMID: 16960967.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    203. Discrete profile comparison using information bottleneck. BMC Bioinformatics. 2006 Mar 20; 7 Suppl 1:S8. O'Rourke S, Chechik G, Friedman R, Eskin E. PMID: 16723011; PMCID: PMC1810319.
      View in: PubMed   Mentions:    Fields:    Translation:Cells
    204. Identification of additional variants within the human dopamine transporter gene provides further evidence for an association with bipolar disorder in two independent samples. Mol Psychiatry. 2006 Feb; 11(2):125-33, 115. Greenwood TA, Schork NJ, Eskin E, Kelsoe JR. PMID: 16261167.
      View in: PubMed   Mentions: 60     Fields:    Translation:HumansCellsCTClinical Trials
    205. A comparison of phasing algorithms for trios and unrelated individuals. Am J Hum Genet. 2006 Mar; 78(3):437-50. Marchini J, Cutler D, Patterson N, Stephens M, Eskin E, Halperin E, Lin S, Qin ZS, Munro HM, Abecasis GR, Donnelly P, International HapMap Consortium. PMID: 16465620; PMCID: PMC1380287.
      View in: PubMed   Mentions: 128     Fields:    Translation:Humans
    206. Polymorphisms and haplotypes of the regulator of G protein signaling-2 gene in normotensives and hypertensives. Hypertension. 2006 Mar; 47(3):415-20. Riddle EL, Rana BK, Murthy KK, Rao F, Eskin E, O'Connor DT, Insel PA. PMID: 16432041.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansCells
    207. Inference and analysis of haplotypes from combined genotyping studies deposited in dbSNP. Genome Res. 2005 Nov; 15(11):1594-600. Zaitlen NA, Kang HM, Feolo ML, Sherry ST, Halperin E, Eskin E. PMID: 16251470; PMCID: PMC1310648.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansAnimals
    208. Searching genomes for noncoding RNA using FastR. IEEE/ACM Trans Comput Biol Bioinform. 2005 Oct-Dec; 2(4):366-79. Zhang S, Haas B, Eskin E, Bafna V. PMID: 17044173.
      View in: PubMed   Mentions: 17     Fields:    Translation:AnimalsCells
    209. Whole-genome patterns of common DNA variation in three human populations. Science. 2005 Feb 18; 307(5712):1072-9. Hinds DA, Stuve LL, Nilsen GB, Halperin E, Eskin E, Ballinger DG, Frazer KA, Cox DR. PMID: 15718463.
      View in: PubMed   Mentions: 451     Fields:    Translation:Humans
    210. Assessing computational tools for the discovery of transcription factor binding sites. Nat Biotechnol. 2005 Jan; 23(1):137-44. Tompa M, Li N, Bailey TL, Church GM, De Moor B, Eskin E, Favorov AV, Frith MC, Fu Y, Kent WJ, Makeev VJ, Mironov AA, Noble WS, Pavesi G, Pesole G, Régnier M, Simonis N, Sinha S, Thijs G, van Helden J, Vandenbogaert M, Weng Z, Workman C, Ye C, Zhu Z. PMID: 15637633.
      View in: PubMed   Mentions: 440     Fields:    Translation:HumansAnimalsCells
    211. Whole-genome analysis of Alu repeat elements reveals complex evolutionary history. Genome Res. 2004 Nov; 14(11):2245-52. Price AL, Eskin E, Pevzner PA. PMID: 15520288; PMCID: PMC525682.
      View in: PubMed   Mentions: 98     Fields:    Translation:HumansCells
    212. Haplotype reconstruction from genotype data using Imperfect Phylogeny. Bioinformatics. 2004 Aug 12; 20(12):1842-9. Halperin E, Eskin E. PMID: 14988101.
      View in: PubMed   Mentions: 68     Fields:    
    213. Mismatch string kernels for discriminative protein classification. Bioinformatics. 2004 Mar 01; 20(4):467-76. Leslie CS, Eskin E, Cohen A, Weston J, Noble WS. PMID: 14990442.
      View in: PubMed   Mentions: 120     Fields:    Translation:Cells
    214. Combining text mining and sequence analysis to discover protein functional regions. Pac Symp Biocomput. 2004; 288-99. Eskin E, Agichtein E. PMID: 14992511.
      View in: PubMed   Mentions: 3     Fields:    
    215. Efficient reconstruction of haplotype structure via perfect phylogeny. J Bioinform Comput Biol. 2003 Apr; 1(1):1-20. Eskin E, Halperin E, Karp RM. PMID: 15290779.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    216. Protein family classification using sparse markov transducers. J Comput Biol. 2003; 10(2):187-213. Eskin E, Noble WS, Singer Y. PMID: 12804091.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansAnimals
    217. Genome-wide analysis of bacterial promoter regions. Pac Symp Biocomput. 2003; 29-40. Eskin E, Keich U, Gelfand MS, Pevzner PA. PMID: 12603015.
      View in: PubMed   Mentions: 10     Fields:    Translation:Cells
    218. The spectrum kernel: a string kernel for SVM protein classification. Pac Symp Biocomput. 2002; 564-75. Leslie C, Eskin E, Noble WS. PMID: 11928508.
      View in: PubMed   Mentions: 146     Fields:    
    219. Using substitution matrices to estimate probability distributions for biological sequences. J Comput Biol. 2002; 9(6):775-91. Eskin E, Noble WS, Singer Y. PMID: 12614546.
      View in: PubMed   Mentions: 1     Fields:    Translation:Cells
    220. Finding composite regulatory patterns in DNA sequences. Bioinformatics. 2002; 18 Suppl 1:S354-63. Eskin E, Pevzner PA. PMID: 12169566.
      View in: PubMed   Mentions: 70     Fields:    Translation:Cells
    221. Using mixtures of common ancestors for estimating the probabilities of discrete events in biological sequences. Bioinformatics. 2001; 17 Suppl 1:S65-73. Eskin E, Grundy WN, Singer Y. PMID: 11472994.
      View in: PubMed   Mentions:    Fields:    Translation:Cells
    222. Protein family classification using sparse Markov transducers. Proc Int Conf Intell Syst Mol Biol. 2000; 8:134-45. Eskin E, Grundy WN, Singer Y. PMID: 10977074.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimals
    223. Increasing accuracy in the diagnosis of acute appendicitis with modern diagnostic techniques. Am Surg. 1986 Apr; 52(4):222-5. Kniskern JH, Eskin EM, Fletcher HS. PMID: 3513683.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
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