Noah A Zaitlen

Title(s)Professor, Neurology
SchoolMedicine
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    Title(s)Professor, Human Genetics


    Collapse Research 
    Collapse research activities and funding
    Leveraging genetic variation to dissect gene regulatory networks of reprogramming to pluripotency
    NIH U01HG012079Sep 1, 2021 - May 31, 2026
    Role: Co-Principal Investigator
    Epigenomics of asthma risk factors and clinical subtypes in minority children
    NIH R01HL155024Jan 1, 2021 - Nov 30, 2024
    Role: Co-Principal Investigator
    Genomic Approaches to Population Health in Multi-Ethnic Hospital Systems
    NIH R01HG011345Sep 16, 2020 - Jul 31, 2024
    Role: Co-Principal Investigator
    Improved methods for inference of genotype-specific response to environmental toxins
    NIH R01ES029929Feb 1, 2019 - Jan 31, 2024
    Role: Co-Principal Investigator
    Epigenetics of Socio-Environmental Effects on Asthma in Minorities
    NIH R56MD013312Sep 25, 2018 - Sep 24, 2020
    Role: Principal Investigator
    (PQ3) A functional genomic approach to identification and interpretation of germline-tumor genetic interactions
    NIH R01CA227237Jun 8, 2018 - May 31, 2023
    Role: Co-Principal Investigator
    Leveraging Novel Multivariate Methods of Subphenotypes in Genetic Association Studies of Sjogren?s Syndrome
    NIH R03DE025665Sep 2, 2016 - Aug 31, 2018
    Role: Co-Principal Investigator
    Richer Models of Asthma Risk: Bridging the Environment-Genetics Divide
    NIH K25HL121295Aug 1, 2014 - Oct 31, 2019
    Role: Principal Investigator

    Collapse Bibliographic 
    Collapse selected 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. The Germline and Somatic Origins of Prostate Cancer Heterogeneity. Cancer Discov. 2025 May 02; 15(5):988-1017. Yamaguchi TN, Houlahan KE, Zhu H, Kurganovs N, Livingstone J, Fox NS, Yuan J, Sietsma Penington J, Jung CH, Schwarz T, Jaratlerdsiri W, van Riet J, Georgeson P, Mangiola S, Taraszka K, Lesurf R, Jiang J, Chow K, Heisler LE, Shiah YJ, Ramanand SG, Clarkson MJ, Nguyen A, Espiritu SMG, Stuchbery R, Jovelin R, Huang V, Bell C, O'Connor E, McCoy PJ, Lalansingh CM, Cmero M, Salcedo A, Chan EKF, Liu LY, Stricker PD, Bhandari V, Bornman RMS, Sendorek DHS, Lonie A, Prokopec SD, Fraser M, Peters JS, Foucal A, Mutambirwa SBA, Mcintosh L, Orain M, Wakefield M, Picard V, Park DJ, Hovington H, Kerger M, Bergeron A, Sabelnykova V, Seo JH, Pomerantz MM, Zaitlen N, Waszak SM, Gusev A, Lacombe L, Fradet Y, Ryan A, Kishan AU, Lolkema MP, Weischenfeldt J, Têtu B, Costello AJ, Hayes VM, Hung RJ, He HH, McPherson JD, Pasaniuc B, van der Kwast T, Papenfuss AT, Freedman ML, Pope BJ, Bristow RG, Mani RS, Corcoran NM, Reimand J, Hovens CM, Boutros PC. PMID: 39945744; PMCID: PMC12046336.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    2. Protocol to estimate the heritability of drug response with GxEMM and identify gene-drug interactions with TxEWAS. STAR Protoc. 2025 Apr 16; 6(2):103780. Sadowski M, Dahl AW, Zaitlen N. PMID: 40249708.
      View in: PubMed   Mentions:    Fields:    
    3. The impact of ambient contamination on demultiplexing methods for single-nucleus multiome experiments. Res Sq. 2025 Feb 10. Li T, Alvarez M, Liu C, Abuhanna K, Sun Y, Ernst J, Plath K, Balliu B, Luo C, Zaitlen N. PMID: 39989953; PMCID: PMC11844637.
      View in: PubMed   Mentions:
    4. The impact of ambient contamination on demultiplexing methods for single-nucleus multiome experiments. bioRxiv. 2025 Feb 08. Li T, Alvarez M, Liu C, Abuhanna K, Sun Y, Ernst J, Plath K, Balliu B, Luo C, Zaitlen N. PMID: 39975005; PMCID: PMC11839078.
      View in: PubMed   Mentions:
    5. Evaluation of a biomarker for amyotrophic lateral sclerosis derived from a hypomethylated DNA signature of human motor neurons. BMC Med Genomics. 2025 Jan 14; 18(1):10. Harvey C, Nowak A, Zhang S, Moll T, Weimer AK, Barcons AM, Souza CDS, Ferraiuolo L, Kenna K, Zaitlen N, Caggiano C, Shaw PJ, Snyder MP, Mill J, Hannon E, Cooper-Knock J. PMID: 39810183; PMCID: PMC11734586.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    6. Characterizing the genetic architecture of drug response using gene-context interaction methods. Cell Genom. 2024 Dec 11; 4(12):100722. Sadowski M, Thompson M, Mefford J, Haldar T, Oni-Orisan A, Border R, Pazokitoroudi A, Cai N, Ayroles JF, Sankararaman S, Dahl AW, Zaitlen N. PMID: 39637863.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    7. Evaluation of a biomarker for amyotrophic lateral sclerosis derived from a hypomethylated DNA signature of human motor neurons. Res Sq. 2024 Nov 26. Harvey C, Nowak A, Zhang S, Moll T, Weimer AK, Barcons AM, Dos Santos Souza C, Ferraiuolo L, Kenna K, Zaitlen N, Caggiano C, Shaw PJ, Snyder MP, Mill J, Hannon E, Cooper-Knock J. PMID: 39649175; PMCID: PMC11623773.
      View in: PubMed   Mentions:
    8. Hemochromatosis neural archetype reveals iron disruption in motor circuits. Sci Adv. 2024 Nov 22; 10(47):eadp4431. Loughnan R, Ahern J, Boyle M, Jernigan TL, Hagler DJ, Iversen JR, Frei O, Smith DM, Andreassen O, Zaitlen N, Sugrue L, Thompson WK, Dale A, Schork AJ, Fan CC. PMID: 39576859; PMCID: PMC11584016.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    9. Local genetic correlation via knockoffs reduces confounding due to cross-trait assortative mating. Am J Hum Genet. 2024 Dec 05; 111(12):2839-2848. Ma S, Wang F, Border R, Buxbaum J, Zaitlen N, Ionita-Laza I. PMID: 39547235; PMCID: PMC11639086.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    10. Genetic liability estimated from large-scale family data improves genetic prediction, risk score profiling, and gene mapping for major depression. Am J Hum Genet. 2024 Nov 07; 111(11):2494-2509. Dybdahl Krebs M, Georgii Hellberg KL, Lundberg M, Appadurai V, Ohlsson H, Pedersen E, Steinbach J, Matthews J, Border R, LaBianca S, Calle X, Meijsen JJ, iPSYCH Study Consortium, , Ingason A, Buil A, Vilhjálmsson BJ, Flint J, Bacanu SA, Cai N, Dahl A, Zaitlen N, Werge T, Kendler KS, Schork AJ. PMID: 39471805; PMCID: PMC11568754.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    11. Accurate prediction of disease-risk factors from volumetric medical scans by a deep vision model pre-trained with 2D scans. Nat Biomed Eng. 2025 Apr; 9(4):507-520. Avram O, Durmus B, Rakocz N, Corradetti G, An U, Nittala MG, Terway P, Rudas A, Chen ZJ, Wakatsuki Y, Hirabayashi K, Velaga S, Tiosano L, Corvi F, Verma A, Karamat A, Lindenberg S, Oncel D, Almidani L, Hull V, Fasih-Ahmad S, Esmaeilkhanian H, Cannesson M, Wykoff CC, Rahmani E, Arnold CW, Zhou B, Zaitlen N, Gronau I, Sankararaman S, Chiang JN, Sadda SR, Halperin E. PMID: 39354052.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    12. Assortative mating across nine psychiatric disorders is consistent and persistent over cultures and generations. medRxiv. 2024 Sep 22. Fan CC, Dehkordi SR, Border R, Shao L, Xu B, Loughnan R, Thompson WK, Hsu LY, Lin MC, Cheng CF, Lai RY, Su MH, Kao WY, Werge T, Wu CS, Schork AJ, Zaitlen N, Demur AB, Wang SH. PMID: 39371142; PMCID: PMC11451716.
      View in: PubMed   Mentions:
    13. Epigenetic patient stratification via contrastive machine learning refines hallmark biomarkers in minoritized children with asthma. Res Sq. 2024 Sep 13. Gorla A, Witonsky J, Elhawary JR, Chen ZJ, Mefford J, Perez-Garcia J, Huntsman S, Hu D, Eng C, Woodruff PG, Sankararaman S, Ziv E, Flint J, Zaitlen N, Burchard E, Rahmani E. PMID: 39315258; PMCID: PMC11419268.
      View in: PubMed   Mentions:
    14. Strong effect of demographic changes on Tuberculosis susceptibility in South Africa. PLOS Glob Public Health. 2024; 4(7):e0002643. Oyageshio OP, Myrick JW, Saayman J, van der Westhuizen L, Al-Hindi DR, Reynolds AW, Zaitlen N, Hoal EG, Uren C, Möller M, Henn BM. PMID: 39042651; PMCID: PMC11265723.
      View in: PubMed   Mentions: 1  
    15. Author Correction: Multi-ancestry polygenic mechanisms of type 2 diabetes. Nat Med. 2024 Jul; 30(7):2091. Smith K, Deutsch AJ, McGrail C, Kim H, Hsu S, Huerta-Chagoya A, Mandla R, Schroeder PH, Westerman KE, Szczerbinski L, Majarian TD, Kaur V, Williamson A, Zaitlen N, Claussnitzer M, Florez JC, Manning AK, Mercader JM, Gaulton KJ, Udler MS. PMID: 38760590.
      View in: PubMed   Mentions:    Fields:    
    16. Single-stranded pre-methylated 5mC adapters uncover the methylation profile of plasma ultrashort Single-stranded cell-free DNA. Nucleic Acids Res. 2024 Jun 24; 52(11):e50. Cheng JC, Swarup N, Morselli M, Huang WL, Aziz M, Caggiano C, Kordi M, Patel AA, Chia D, Kim Y, Li F, Wei F, Zaitlen N, Krysan K, Dubinett S, Pellegrini M, Wong DTW. PMID: 38797520; PMCID: PMC11194076.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    17. A scalable and robust variance components method reveals insights into the architecture of gene-environment interactions underlying complex traits. Am J Hum Genet. 2024 07 11; 111(7):1462-1480. Pazokitoroudi A, Liu Z, Dahl A, Zaitlen N, Rosset S, Sankararaman S. PMID: 38866020; PMCID: PMC11267529.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    18. MANOCCA: a robust and computationally efficient test of covariance in high-dimension multivariate omics data. Brief Bioinform. 2024 May 23; 25(4). Boetto C, Frouin A, Henches L, Auvergne A, Suzuki Y, Patin E, Bredon M, Chiu A, Consortium MI, Sankararaman S, Zaitlen N, Kennedy SP, Quintana-Murci L, Duffy D, Sokol H, Aschard H. PMID: 38856173; PMCID: PMC11163461.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    19. Brain cell-type shifts in Alzheimer's disease, autism, and schizophrenia interrogated using methylomics and genetics. Sci Adv. 2024 May 24; 10(21):eadn7655. Yap CX, Vo DD, Heffel MG, Bhattacharya A, Wen C, Yang Y, Kemper KE, Zeng J, Zheng Z, Zhu Z, Hannon E, Vellame DS, Franklin A, Caggiano C, Wamsley B, Geschwind DH, Zaitlen N, Gusev A, Pasaniuc B, Mill J, Luo C, Gandal MJ. PMID: 38781333; PMCID: PMC11114225.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    20. Electronic health record signatures identify undiagnosed patients with common variable immunodeficiency disease. Sci Transl Med. 2024 May; 16(745):eade4510. Johnson R, Stephens AV, Mester R, Knyazev S, Kohn LA, Freund MK, Bondhus L, Hill BL, Schwarz T, Zaitlen N, Arboleda VA, A Bastarache L, Pasaniuc B, Butte MJ. PMID: 38691621; PMCID: PMC11402387.
      View in: PubMed   Mentions: 3     Fields:    
    21. Investigating the sources of variable impact of pathogenic variants in monogenic metabolic conditions. medRxiv. 2024 May 01. Wei A, Border R, Fu B, Cullina S, Brandes N, Jang SK, Sankararaman S, Kenny E, Udler MS, Ntranos V, Zaitlen N, Arboleda V. PMID: 37745486; PMCID: PMC10516069.
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    22. Tissue informative cell-free DNA methylation sites in amyotrophic lateral sclerosis. medRxiv. 2024 Apr 10. Caggiano C, Morselli M, Qian X, Celona B, Thompson M, Wani S, Tosevska A, Taraszka K, Heuer G, Ngo S, Steyn F, Nestor P, Wallace L, McCombe P, Heggie S, Thorpe K, McElligott C, English G, Henders A, Henderson R, Lomen-Hoerth C, Wray N, McRae A, Pellegrini M, Garton F, Zaitlen N. PMID: 38645132; PMCID: PMC11030489.
      View in: PubMed   Mentions: 1  
    23. Multi-ancestry polygenic mechanisms of type 2 diabetes. Nat Med. 2024 Apr; 30(4):1065-1074. Smith K, Deutsch AJ, McGrail C, Kim H, Hsu S, Huerta-Chagoya A, Mandla R, Schroeder PH, Westerman KE, Szczerbinski L, Majarian TD, Kaur V, Williamson A, Zaitlen N, Claussnitzer M, Florez JC, Manning AK, Mercader JM, Gaulton KJ, Udler MS. PMID: 38443691; PMCID: PMC11175990.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    24. Cell-type deconvolution of bulk-blood RNA-seq reveals biological insights into neuropsychiatric disorders. Am J Hum Genet. 2024 02 01; 111(2):323-337. Boltz T, Schwarz T, Bot M, Hou K, Caggiano C, Lapinska S, Duan C, Boks MP, Kahn RS, Zaitlen N, Pasaniuc B, Ophoff R. PMID: 38306997; PMCID: PMC10870131.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    25. A comprehensive analysis of clinical and polygenic germline influences on somatic mutational burden. Am J Hum Genet. 2024 02 01; 111(2):242-258. Taraszka K, Groha S, King D, Tell R, White K, Ziv E, Zaitlen N, Gusev A. PMID: 38211585; PMCID: PMC10870141.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    26. A scalable and robust variance components method reveals insights into the architecture of gene-environment interactions underlying complex traits. bioRxiv. 2023 Dec 13. Pazokitoroudi A, Dahl A, Zaitlen N, Rosset S, Sankararaman S. PMID: 38168200; PMCID: PMC10760005.
      View in: PubMed   Mentions:
    27. GCLiPP: global crosslinking and protein purification method for constructing high-resolution occupancy maps for RNA binding proteins. Genome Biol. 2023 12 07; 24(1):281. Zhu WS, Litterman AJ, Sekhon HS, Kageyama R, Arce MM, Taylor KE, Zhao W, Criswell LA, Zaitlen N, Erle DJ, Ansel KM. PMID: 38062486; PMCID: PMC10701951.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansAnimalsCells
    28. Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder. Nat Genet. 2024 Feb; 56(2):234-244. LaBianca S, Brikell I, Helenius D, Loughnan R, Mefford J, Palmer CE, Walker R, Gådin JR, Krebs M, Appadurai V, Vaez M, Agerbo E, Pedersen MG, Børglum AD, Hougaard DM, Mors O, Nordentoft M, Mortensen PB, Kendler KS, Jernigan TL, Geschwind DH, Ingason A, Dahl AW, Zaitlen N, Dalsgaard S, Werge TM, Schork AJ. PMID: 38036780; PMCID: PMC11439085.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    29. SLIViT: a general AI framework for clinical-feature diagnosis from limited 3D biomedical-imaging data. Res Sq. 2023 Nov 21. Avram O, Durmus B, Rakocz N, Corradetti G, An U, Nitalla MG, Rudas A, Wakatsuki Y, Hirabayashi K, Velaga S, Tiosano L, Corvi F, Verma A, Karamat A, Lindenberg S, Oncel D, Almidani L, Hull V, Fasih-Ahmad S, Esmaeilkhanian H, Wykoff CC, Rahmani E, Arnold CW, Zhou B, Zaitlen N, Gronau I, Sankararaman S, Chiang JN, Sadda SR, Halperin E. PMID: 38045283; PMCID: PMC10690310.
      View in: PubMed   Mentions:
    30. Deep learning-based phenotype imputation on population-scale biobank data increases genetic discoveries. Nat Genet. 2023 Dec; 55(12):2269-2276. An U, Pazokitoroudi A, Alvarez M, Huang L, Bacanu S, Schork AJ, Kendler K, Pajukanta P, Flint J, Zaitlen N, Cai N, Dahl A, Sankararaman S. PMID: 37985819; PMCID: PMC10703681.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    31. Strong Effect of Demographic Changes on Tuberculosis Susceptibility in South Africa. medRxiv. 2023 Nov 03. Oyageshio OP, Myrick JW, Saayman J, van der Westhuizen L, Al-Hindi D, Reynolds AW, Zaitlen N, Uren C, Möller M, Henn BM. PMID: 37961495; PMCID: PMC10635255.
      View in: PubMed   Mentions:
    32. A biobank-scale test of marginal epistasis reveals genome-wide signals of polygenic epistasis. bioRxiv. 2023 Sep 12. Fu B, Pazokitoroudi A, Xue A, Anand A, Anand P, Zaitlen N, Sankararaman S. PMID: 37745394; PMCID: PMC10515811.
      View in: PubMed   Mentions:
    33. Genotype error due to low-coverage sequencing induces uncertainty in polygenic scoring. Am J Hum Genet. 2023 08 03; 110(8):1319-1329. Petter E, Ding Y, Hou K, Bhattacharya A, Gusev A, Zaitlen N, Pasaniuc B. PMID: 37490908; PMCID: PMC10432141.
      View in: PubMed   Mentions: 1     Fields:    
    34. Disease risk and healthcare utilization among ancestrally diverse groups in the Los Angeles region. Nat Med. 2023 07; 29(7):1845-1856. Caggiano C, Boudaie A, Shemirani R, Mefford J, Petter E, Chiu A, Ercelen D, He R, Tward D, Paul KC, Chang TS, Pasaniuc B, Kenny EE, Shortt JA, Gignoux CR, Balliu B, Arboleda VA, Belbin G, Zaitlen N. PMID: 37464048; PMCID: PMC11121511.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    35. Cell type deconvolution of bulk blood RNA-Seq to reveal biological insights of neuropsychiatric disorders. bioRxiv. 2023 May 25. Boltz T, Schwarz T, Bot M, Hou K, Caggiano C, Lapinska S, Duan C, Boks MP, Kahn RS, Zaitlen N, Pasaniuc B, Ophoff R. PMID: 37293101; PMCID: PMC10245943.
      View in: PubMed   Mentions:
    36. Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architecture. Nat Genet. 2023 06; 55(6):952-963. Kachuri L, Mak ACY, Hu D, Eng C, Huntsman S, Elhawary JR, Gupta N, Gabriel S, Xiao S, Keys KL, Oni-Orisan A, Rodríguez-Santana JR, LeNoir MA, Borrell LN, Zaitlen NA, Williams LK, Gignoux CR, Burchard EG, Ziv E. PMID: 37231098; PMCID: PMC10260401.
      View in: PubMed   Mentions: 28     Fields:    
    37. Effect of statins on the age of onset of age-related macular degeneration. Graefes Arch Clin Exp Ophthalmol. 2023 Aug; 261(8):2245-2255. Ganesh D, Chiang JN, Corradetti G, Zaitlen N, Halperin E, Sadda SR. PMID: 36917316.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    38. Multi-omic approach associates blood methylome with bronchodilator drug response in pediatric asthma. J Allergy Clin Immunol. 2023 06; 151(6):1503-1512. Perez-Garcia J, Herrera-Luis E, Li A, Mak ACY, Huntsman S, Oh SS, Elhawary JR, Eng C, Beckman KB, Hu D, Lorenzo-Diaz F, Lenoir MA, Rodriguez-Santana J, Zaitlen N, Villar J, Borrell LN, Burchard EG, Pino-Yanes M. PMID: 36796456.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    39. Phenotypic subtyping via contrastive learning. bioRxiv. 2023 Jan 06. Gorla A, Sankararaman S, Burchard E, Flint J, Zaitlen N, Rahmani E. PMID: 36711575; PMCID: PMC9881932.
      View in: PubMed   Mentions:
    40. Cross-trait assortative mating is widespread and inflates genetic correlation estimates. Science. 2022 11 18; 378(6621):754-761. Border R, Athanasiadis G, Buil A, Schork AJ, Cai N, Young AI, Werge T, Flint J, Kendler KS, Sankararaman S, Dahl AW, Zaitlen NA. PMID: 36395242; PMCID: PMC9901291.
      View in: PubMed   Mentions: 63     Fields:    
    41. Author Correction: Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Genome Med. 2022 Nov 16; 14(1):128. Johnson R, Ding Y, Venkateswaran V, Bhattacharya A, Boulier K, Chiu A, Knyazev S, Schwarz T, Freund M, Zhan L, Burch KS, Caggiano C, Hill B, Rakocz N, Balliu B, Denny CT, Sul JH, Zaitlen N, Arboleda VA, Halperin E, Sankararaman S, Butte MJ, UCLA Precision Health Data Discovery Repository Working Group, UCLA Precision Health ATLAS Working G, Lajonchere C, Geschwind DH, Pasaniuc B. PMID: 36384576; PMCID: PMC9670414.
      View in: PubMed   Mentions:    Fields:    
    42. Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations. PLoS Genet. 2022 11; 18(11):e1010447. Taraszka K, Zaitlen N, Eskin E. PMID: 36342933; PMCID: PMC9671458.
      View in: PubMed   Mentions: 3     Fields:    
    43. Author Correction: Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology. Nat Commun. 2022 Oct 03; 13(1):5806. Sajuthi SP, Everman JL, Jackson ND, Saef B, Rios CL, Moore CM, Mak ACY, Eng C, Fairbanks-Mahnke A, Salazar S, Elhawary J, Huntsman S, Medina V, Nickerson DA, Germer S, Zody MC, Abecasis G, Kang HM, Rice KM, Kumar R, Zaitlen NA, Oh S, NHLBI Trans–Omics for Precision Medicine (TOPMed) Consortium, Rodríguez-Santana J, Burchard EG, Seibold MA. PMID: 36192399; PMCID: PMC9530212.
      View in: PubMed   Mentions:    Fields:    
    44. Ancestry-driven recalibration of tumor mutational burden and disparate clinical outcomes in response to immune checkpoint inhibitors. Cancer Cell. 2022 10 10; 40(10):1161-1172.e5. Nassar AH, Adib E, Abou Alaiwi S, El Zarif T, Groha S, Akl EW, Nuzzo PV, Mouhieddine TH, Perea-Chamblee T, Taraszka K, El-Khoury H, Labban M, Fong C, Arora KS, Labaki C, Xu W, Sonpavde G, Haddad RI, Mouw KW, Giannakis M, Hodi FS, Zaitlen N, Schoenfeld AJ, Schultz N, Berger MF, MacConaill LE, Ananda G, Kwiatkowski DJ, Choueiri TK, Schrag D, Carrot-Zhang J, Gusev A. PMID: 36179682; PMCID: PMC9559771.
      View in: PubMed   Mentions: 48     Fields:    Translation:Humans
    45. Multi-context genetic modeling of transcriptional regulation resolves novel disease loci. Nat Commun. 2022 09 28; 13(1):5704. Thompson M, Gordon MG, Lu A, Tandon A, Halperin E, Gusev A, Ye CJ, Balliu B, Zaitlen N. PMID: 36171194; PMCID: PMC9519579.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCells
    46. Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Genome Med. 2022 Sep 09; 14(1):104. Johnson R, Ding Y, Venkateswaran V, Bhattacharya A, Boulier K, Chiu A, Knyazev S, Schwarz T, Freund M, Zhan L, Burch KS, Caggiano C, Hill B, Rakocz N, Balliu B, Denny CT, Sul JH, Zaitlen N, Arboleda VA, Halperin E, Sankararaman S, Butte MJ, UCLA Precision Health Data Discovery Repository Working Group, UCLA Precision Health ATLAS Working G, Lajonchere C, Geschwind DH, Pasaniuc B. PMID: 36085083; PMCID: PMC9461263.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansPHPublic Health
    47. Methylation risk scores are associated with a collection of phenotypes within electronic health record systems. NPJ Genom Med. 2022 Aug 25; 7(1):50. Thompson M, Hill BL, Rakocz N, Chiang JN, Geschwind D, Sankararaman S, Hofer I, Cannesson M, Zaitlen N, Halperin E. PMID: 36008412; PMCID: PMC9411568.
      View in: PubMed   Mentions: 28  
    48. Single-cell RNA-seq reveals cell type-specific molecular and genetic associations to lupus. Science. 2022 04 08; 376(6589):eabf1970. Perez RK, Gordon MG, Subramaniam M, Kim MC, Hartoularos GC, Targ S, Sun Y, Ogorodnikov A, Bueno R, Lu A, Thompson M, Rappoport N, Dahl A, Lanata CM, Matloubian M, Maliskova L, Kwek SS, Li T, Slyper M, Waldman J, Dionne D, Rozenblatt-Rosen O, Fong L, Dall'Era M, Balliu B, Regev A, Yazdany J, Criswell LA, Zaitlen N, Ye CJ. PMID: 35389781; PMCID: PMC9297655.
      View in: PubMed   Mentions: 157     Fields:    
    49. Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology. Nat Commun. 2022 03 28; 13(1):1632. Sajuthi SP, Everman JL, Jackson ND, Saef B, Rios CL, Moore CM, Mak ACY, Eng C, Fairbanks-Mahnke A, Salazar S, Elhawary J, Huntsman S, Medina V, Nickerson DA, Germer S, Zody MC, Abecasis G, Kang HM, Rice KM, Kumar R, Zaitlen NA, Oh S, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Rodríguez-Santana J, Burchard EG, Seibold MA. PMID: 35347136; PMCID: PMC8960819.
      View in: PubMed   Mentions: 18     Fields:    
    50. Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1. Genome Med. 2022 01 19; 14(1):7. Restuadi R, Steyn FJ, Kabashi E, Ngo ST, Cheng FF, Nabais MF, Thompson MJ, Qi T, Wu Y, Henders AK, Wallace L, Bye CR, Turner BJ, Ziser L, Mathers S, McCombe PA, Needham M, Schultz D, Kiernan MC, van Rheenen W, van den Berg LH, Veldink JH, Ophoff R, Gusev A, Zaitlen N, McRae AF, Henderson RD, Wray NR, Giacomotto J, Garton FC. PMID: 35042540; PMCID: PMC8767698.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansAnimals
    51. Massively parallel analysis of human 3' UTRs reveals that AU-rich element length and registration predict mRNA destabilization. G3 (Bethesda). 2022 01 04; 12(1). Siegel DA, Le Tonqueze O, Biton A, Zaitlen N, Erle DJ. PMID: 34849835; PMCID: PMC8728028.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansCells
    52. Constructing germline research cohorts from the discarded reads of clinical tumor sequences. Genome Med. 2021 11 08; 13(1):179. Gusev A, Groha S, Taraszka K, Semenov YR, Zaitlen N. PMID: 34749793; PMCID: PMC8576948.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansCells
    53. Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes. Nat Commun. 2021 06 09; 12(1):3505. Goodrich JK, Singer-Berk M, Son R, Sveden A, Wood J, England E, Cole JB, Weisburd B, Watts N, Caulkins L, Dornbos P, Koesterer R, Zappala Z, Zhang H, Maloney KA, Dahl A, Aguilar-Salinas CA, Atzmon G, Barajas-Olmos F, Barzilai N, Blangero J, Boerwinkle E, Bonnycastle LL, Bottinger E, Bowden DW, Centeno-Cruz F, Chambers JC, Chami N, Chan E, Chan J, Cheng CY, Cho YS, Contreras-Cubas C, Córdova E, Correa A, DeFronzo RA, Duggirala R, Dupuis J, Garay-Sevilla ME, García-Ortiz H, Gieger C, Glaser B, González-Villalpando C, Gonzalez ME, Grarup N, Groop L, Gross M, Haiman C, Han S, Hanis CL, Hansen T, Heard-Costa NL, Henderson BE, Hernandez JMM, Hwang MY, Islas-Andrade S, Jørgensen ME, Kang HM, Kim BJ, Kim YJ, Koistinen HA, Kooner JS, Kuusisto J, Kwak SH, Laakso M, Lange L, Lee JY, Lee J, Lehman DM, Linneberg A, Liu J, Loos RJF, Lyssenko V, Ma RCW, Martínez-Hernández A, Meigs JB, Meitinger T, Mendoza-Caamal E, Mohlke KL, Morris AD, Morrison AC, Ng MCY, Nilsson PM, O'Donnell CJ, Orozco L, Palmer CNA, Park KS, Post WS, Pedersen O, Preuss M, Psaty BM, Reiner AP, Revilla-Monsalve C, Rich SS, Rotter JI, Saleheen D, Schurmann C, Sim X, Sladek R, Small KS, So WY, Spector TD, Strauch K, Strom TM, Tai ES, Tam CHT, Teo YY, Thameem F, Tomlinson B, Tracy RP, Tuomi T, Tuomilehto J, Tusié-Luna T, van Dam RM, Vasan RS, Wilson JG, Witte DR, Wong TY, AMP-T2D-GENES Consortia, Burtt NP, Zaitlen N, McCarthy MI, Boehnke M, Pollin TI, Flannick J, Mercader JM, O'Donnell-Luria A, Baxter S, Florez JC, MacArthur DG, Udler MS. PMID: 34108472; PMCID: PMC8190084.
      View in: PubMed   Mentions: 36     Fields:    
    54. Admixed Populations Improve Power for Variant Discovery and Portability in Genome-Wide Association Studies. Front Genet. 2021; 12:673167. Lin M, Park DS, Zaitlen NA, Henn BM, Gignoux CR. PMID: 34108994; PMCID: PMC8181458.
      View in: PubMed   Mentions: 15  
    55. Comprehensive cell type decomposition of circulating cell-free DNA with CelFiE. Nat Commun. 2021 05 11; 12(1):2717. Caggiano C, Celona B, Garton F, Mefford J, Black BL, Henderson R, Lomen-Hoerth C, Dahl A, Zaitlen N. PMID: 33976150; PMCID: PMC8113516.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansCells
    56. Toward a fine-scale population health monitoring system. Cell. 2021 04 15; 184(8):2068-2083.e11. Belbin GM, Cullina S, Wenric S, Soper ER, Glicksberg BS, Torre D, Moscati A, Wojcik GL, Shemirani R, Beckmann ND, Cohain A, Sorokin EP, Park DS, Ambite JL, Ellis S, Auton A, CBIPM Genomics Team, Regeneron Genetics Center, Bottinger EP, Cho JH, Loos RJF, Abul-Husn NS, Zaitlen NA, Gignoux CR, Kenny EE. PMID: 33861964.
      View in: PubMed   Mentions: 65     Fields:    Translation:Humans
    57. A model and test for coordinated polygenic epistasis in complex traits. Proc Natl Acad Sci U S A. 2021 04 13; 118(15). Sheppard B, Rappoport N, Loh PR, Sanders SJ, Zaitlen N, Dahl A. PMID: 33833052; PMCID: PMC8053945.
      View in: PubMed   Mentions: 10     Fields:    
    58. Disentangling selection on genetically correlated polygenic traits via whole-genome genealogies. Am J Hum Genet. 2021 02 04; 108(2):219-239. Stern AJ, Speidel L, Zaitlen NA, Nielsen R. PMID: 33440170; PMCID: PMC7895848.
      View in: PubMed   Mentions: 30     Fields:    Translation:Humans
    59. Race and Genetic Ancestry in Medicine - A Time for Reckoning with Racism. N Engl J Med. 2021 Feb 04; 384(5):474-480. Borrell LN, Elhawary JR, Fuentes-Afflick E, Witonsky J, Bhakta N, Wu AHB, Bibbins-Domingo K, Rodríguez-Santana JR, Lenoir MA, Gavin JR, Kittles RA, Zaitlen NA, Wilkes DS, Powe NR, Ziv E, Burchard EG. PMID: 33406325; PMCID: PMC8979367.
      View in: PubMed   Mentions: 265     Fields:    Translation:Humans
    60. Author Correction: Multiplexed droplet single-cell RNA-sequencing using natural genetic variation. Nat Biotechnol. 2020 Nov; 38(11):1356. Kang HM, Subramaniam M, Targ S, Nguyen M, Maliskova L, McCarthy E, Wan E, Wong S, Byrnes L, Lanata CM, Gate RE, Mostafavi S, Marson A, Zaitlen N, Criswell LA, Ye CJ. PMID: 33057163.
      View in: PubMed   Mentions: 2     Fields:    
    61. Modeling epistasis in mice and yeast using the proportion of two or more distinct genetic backgrounds: Evidence for "polygenic epistasis". PLoS Genet. 2020 10; 16(10):e1009165. Rau CD, Gonzales NM, Bloom JS, Park D, Ayroles J, Palmer AA, Lusis AJ, Zaitlen N. PMID: 33104702; PMCID: PMC7644088.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimals
    62. 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: 1     Fields:    
    63. Genetic Influences on Disease Subtypes. Annu Rev Genomics Hum Genet. 2020 08 31; 21:413-435. Dahl A, Zaitlen N. PMID: 32873077.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    64. GBAT: a gene-based association test for robust detection of trans-gene regulation. Genome Biol. 2020 08 24; 21(1):211. Liu X, Mefford JA, Dahl A, He Y, Subramaniam M, Battle A, Price AL, Zaitlen N. PMID: 32831138; PMCID: PMC7444084.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    65. On the cross-population generalizability of gene expression prediction models. PLoS Genet. 2020 08; 16(8):e1008927. Keys KL, Mak ACY, White MJ, Eckalbar WL, Dahl AW, Mefford J, Mikhaylova AV, Contreras MG, Elhawary JR, Eng C, Hu D, Huntsman S, Oh SS, Salazar S, Lenoir MA, Ye JC, Thornton TA, Zaitlen N, Burchard EG, Gignoux CR. PMID: 32797036; PMCID: PMC7449671.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansCells
    66. 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: 33     Fields:    Translation:HumansCells
    67. Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex. Cell Rep. 2020 04 07; 31(1):107489. Werling DM, Pochareddy S, Choi J, An JY, Sheppard B, Peng M, Li Z, Dastmalchi C, Santpere G, Sousa AMM, Tebbenkamp ATN, Kaur N, Gulden FO, Breen MS, Liang L, Gilson MC, Zhao X, Dong S, Klei L, Cicek AE, Buxbaum JD, Adle-Biassette H, Thomas JL, Aldinger KA, O'Day DR, Glass IA, Zaitlen NA, Talkowski ME, Roeder K, State MW, Devlin B, Sanders SJ, Sestan N. PMID: 32268104; PMCID: PMC7295160.
      View in: PubMed   Mentions: 62     Fields:    Translation:HumansCells
    68. Efficient Estimation and Applications of Cross-Validated Genetic Predictions to Polygenic Risk Scores and Linear Mixed Models. J Comput Biol. 2020 04; 27(4):599-612. Mefford J, Park D, Zheng Z, Ko A, Ala-Korpela M, Laakso M, Pajukanta P, Yang J, Witte J, Zaitlen N. PMID: 32077750; PMCID: PMC7185352.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    69. A Robust Method Uncovers Significant Context-Specific Heritability in Diverse Complex Traits. Am J Hum Genet. 2020 01 02; 106(1):71-91. Dahl A, Nguyen K, Cai N, Gandal MJ, Flint J, Zaitlen N. PMID: 31901249; PMCID: PMC7042488.
      View in: PubMed   Mentions: 25     Fields:    Translation:HumansAnimals
    70. A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context. Nat Commun. 2019 10 21; 10(1):4788. Gallois A, Mefford J, Ko A, Vaysse A, Julienne H, Ala-Korpela M, Laakso M, Zaitlen N, Pajukanta P, Aschard H. PMID: 31636271; PMCID: PMC6803661.
      View in: PubMed   Mentions: 38     Fields:    Translation:Humans
    71. Ultrarare variants drive substantial cis heritability of human gene expression. Nat Genet. 2019 09; 51(9):1349-1355. Hernandez RD, Uricchio LH, Hartman K, Ye C, Dahl A, Zaitlen N. PMID: 31477931; PMCID: PMC6730564.
      View in: PubMed   Mentions: 51     Fields:    Translation:HumansCells
    72. Reverse GWAS: Using genetics to identify and model phenotypic subtypes. PLoS Genet. 2019 04; 15(4):e1008009. Dahl A, Cai N, Ko A, Laakso M, Pajukanta P, Flint J, Zaitlen N. PMID: 30951530; PMCID: PMC6469799.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    73. Genetic effects on the commensal microbiota in inflammatory bowel disease patients. PLoS Genet. 2019 03; 15(3):e1008018. Aschard H, Laville V, Tchetgen ET, Knights D, Imhann F, Seksik P, Zaitlen N, Silverberg MS, Cosnes J, Weersma RK, Xavier R, Beaugerie L, Skurnik D, Sokol H. PMID: 30849075; PMCID: PMC6426259.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansCells
    74. Genetic and environmental perturbations lead to regulatory decoherence. Elife. 2019 03 05; 8. Lea A, Subramaniam M, Ko A, Lehtimäki T, Raitoharju E, Kähönen M, Seppälä I, Mononen N, Raitakari OT, Ala-Korpela M, Pajukanta P, Zaitlen N, Ayroles JF. PMID: 30834892; PMCID: PMC6400502.
      View in: PubMed   Mentions: 29     Fields:    
    75. Tracing cellular heterogeneity in pooled genetic screens via multi-level barcoding. BMC Genomics. 2019 Feb 06; 20(1):107. Boettcher M, Covarrubias S, Biton A, Blau J, Wang H, Zaitlen N, McManus MT. PMID: 30727954; PMCID: PMC6364396.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    76. Adjusting for Principal Components of Molecular Phenotypes Induces Replicating False Positives. Genetics. 2019 04; 211(4):1179-1189. Dahl A, Guillemot V, Mefford J, Aschard H, Zaitlen N. PMID: 30692194; PMCID: PMC6456307.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansAnimals
    77. An evolutionary compass for detecting signals of polygenic selection and mutational bias. Evol Lett. 2019 Feb; 3(1):69-79. Uricchio LH, Kitano HC, Gusev A, Zaitlen NA. PMID: 30788143; PMCID: PMC6369964.
      View in: PubMed   Mentions: 14  
    78. Estimating cross-population genetic correlations of causal effect sizes. Genet Epidemiol. 2019 Mar; 43(2):180-188. Galinsky KJ, Reshef YA, Finucane HK, Loh PR, Zaitlen N, Patterson NJ, Brown BC, Price AL. PMID: 30474154; PMCID: PMC6375794.
      View in: PubMed   Mentions: 37     Fields:    
    79. Comparing Ethnicity-Specific Reference Intervals for Clinical Laboratory Tests from EHR Data. J Appl Lab Med. 2018 Nov 01; 3(3):366-377. Rappoport N, Paik H, Oskotsky B, Tor R, Ziv E, Zaitlen N, Butte AJ. PMID: 33636914; PMCID: PMC8404742.
      View in: PubMed   Mentions: 18     Fields:    
    80. Whole-Genome Sequencing of Pharmacogenetic Drug Response in Racially Diverse Children with Asthma. Am J Respir Crit Care Med. 2018 06 15; 197(12):1552-1564. Mak ACY, White MJ, Eckalbar WL, Szpiech ZA, Oh SS, Pino-Yanes M, Hu D, Goddard P, Huntsman S, Galanter J, Wu AC, Himes BE, Germer S, Vogel JM, Bunting KL, Eng C, Salazar S, Keys KL, Liberto J, Nuckton TJ, Nguyen TA, Torgerson DG, Kwok PY, Levin AM, Celedón JC, Forno E, Hakonarson H, Sleiman PM, Dahlin A, Tantisira KG, Weiss ST, Serebrisky D, Brigino-Buenaventura E, Farber HJ, Meade K, Lenoir MA, Avila PC, Sen S, Thyne SM, Rodriguez-Cintron W, Winkler CA, Moreno-Estrada A, Sandoval K, Rodriguez-Santana JR, Kumar R, Williams LK, Ahituv N, Ziv E, Seibold MA, Darnell RB, Zaitlen N, Hernandez RD, Burchard EG, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium. PMID: 29509491; PMCID: PMC6006403.
      View in: PubMed   Mentions: 50     Fields:    Translation:Humans
    81. 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: 1     Fields:    Translation:Humans
    82. Molecular Genetic Analysis Subdivided by Adversity Exposure Suggests Etiologic Heterogeneity in Major Depression. Am J Psychiatry. 2018 06 01; 175(6):545-554. Peterson RE, Cai N, Dahl AW, Bigdeli TB, Edwards AC, Webb BT, Bacanu SA, Zaitlen N, Flint J, Kendler KS. PMID: 29495898; PMCID: PMC5988935.
      View in: PubMed   Mentions: 29     Fields:    Translation:Humans
    83. 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: 26     Fields:    Translation:HumansCells
    84. Dual gene activation and knockout screen reveals directional dependencies in genetic networks. Nat Biotechnol. 2018 02; 36(2):170-178. Boettcher M, Tian R, Blau JA, Markegard E, Wagner RT, Wu D, Mo X, Biton A, Zaitlen N, Fu H, McCormick F, Kampmann M, McManus MT. PMID: 29334369; PMCID: PMC6072461.
      View in: PubMed   Mentions: 73     Fields:    Translation:HumansCells
    85. Multiplexed droplet single-cell RNA-sequencing using natural genetic variation. Nat Biotechnol. 2018 01; 36(1):89-94. Kang HM, Subramaniam M, Targ S, Nguyen M, Maliskova L, McCarthy E, Wan E, Wong S, Byrnes L, Lanata CM, Gate RE, Mostafavi S, Marson A, Zaitlen N, Criswell LA, Ye CJ. PMID: 29227470; PMCID: PMC5784859.
      View in: PubMed   Mentions: 421     Fields:    Translation:HumansCells
    86. 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: 10     Fields:    Translation:HumansCells
    87. Covariate selection for association screening in multiphenotype genetic studies. Nat Genet. 2017 Dec; 49(12):1789-1795. Aschard H, Guillemot V, Vilhjalmsson B, Patel CJ, Skurnik D, Ye CJ, Wolpin B, Kraft P, Zaitlen N. PMID: 29038595; PMCID: PMC5797835.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    88. CRISPR-Cas9-mediated functional dissection of 3'-UTRs. Nucleic Acids Res. 2017 Oct 13; 45(18):10800-10810. Zhao W, Siegel D, Biton A, Tonqueze OL, Zaitlen N, Ahituv N, Erle DJ. PMID: 28985357; PMCID: PMC5737544.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansCells
    89. Heritable natural variation of an anxiety-like behavior in larval zebrafish. J Neurogenet. 2017 09; 31(3):138-148. Wagle M, Nguyen J, Lee S, Zaitlen N, Guo S. PMID: 28678579; PMCID: PMC6051355.
      View in: PubMed   Mentions: 5     Fields:    Translation:Animals
    90. GLINT: a user-friendly toolset for the analysis of high-throughput DNA-methylation array data. Bioinformatics. 2017 Jun 15; 33(12):1870-1872. Rahmani E, Yedidim R, Shenhav L, Schweiger R, Weissbrod O, Zaitlen N, Halperin E. PMID: 28177067; PMCID: PMC5870777.
      View in: PubMed   Mentions: 32     Fields:    Translation:HumansCells
    91. Correction: Pleiotropic Mechanisms Indicated for Sex Differences in Autism. PLoS Genet. 2017 Jun; 13(6):e1006831. Mitra I, Tsang K, Ladd-Acosta C, Croen LA, Aldinger KA, Hendren RL, Traglia M, Lavillaureix A, Zaitlen N, Oldham MC, Levitt P, Nelson S, Amaral DG, Hertz-Picciotto I, Fallin MD, Weiss LA. PMID: 28591140; PMCID: PMC5462340.
      View in: PubMed   Mentions:    Fields:    
    92. Cis-eQTL-based trans-ethnic meta-analysis reveals novel genes associated with breast cancer risk. PLoS Genet. 2017 Mar; 13(3):e1006690. Hoffman JD, Graff RE, Emami NC, Tai CG, Passarelli MN, Hu D, Huntsman S, Hadley D, Leong L, Majumdar A, Zaitlen N, Ziv E, Witte JS. PMID: 28362817; PMCID: PMC5391966.
      View in: PubMed   Mentions: 35     Fields:    
    93. 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: 20     Fields:    Translation:HumansCells
    94. Differential methylation between ethnic sub-groups reflects the effect of genetic ancestry and environmental exposures. Elife. 2017 01 03; 6. Galanter JM, Gignoux CR, Oh SS, Torgerson D, Pino-Yanes M, Thakur N, Eng C, Hu D, Huntsman S, Farber HJ, Avila PC, Brigino-Buenaventura E, LeNoir MA, Meade K, Serebrisky D, Rodríguez-Cintrón W, Kumar R, Rodríguez-Santana JR, Seibold MA, Borrell LN, Burchard EG, Zaitlen N. PMID: 28044981; PMCID: PMC5207770.
      View in: PubMed   Mentions: 89     Fields:    Translation:HumansCellsPHPublic Health
    95. Genome-wide methylation data mirror ancestry information. Epigenetics Chromatin. 2017; 10:1. Rahmani E, Shenhav L, Schweiger R, Yousefi P, Huen K, Eskenazi B, Eng C, Huntsman S, Hu D, Galanter J, Oh SS, Waldenberger M, Strauch K, Grallert H, Meitinger T, Gieger C, Holland N, Burchard EG, Zaitlen N, Halperin E. PMID: 28149326; PMCID: PMC5267476.
      View in: PubMed   Mentions: 50     Fields:    Translation:HumansCells
    96. Mixed Model Association with Family-Biased Case-Control Ascertainment. Am J Hum Genet. 2017 Jan 05; 100(1):31-39. Hayeck TJ, Loh PR, Pollack S, Gusev A, Patterson N, Zaitlen NA, Price AL. PMID: 28017371; PMCID: PMC5223022.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    97. Genetic Mechanisms Leading to Sex Differences Across Common Diseases and Anthropometric Traits. Genetics. 2017 02; 205(2):979-992. Traglia M, Bseiso D, Gusev A, Adviento B, Park DS, Mefford JA, Zaitlen N, Weiss LA. PMID: 27974502; PMCID: PMC5289864.
      View in: PubMed   Mentions: 28     Fields:    
    98. The Effects of Migration and Assortative Mating on Admixture Linkage Disequilibrium. Genetics. 2017 01; 205(1):375-383. Zaitlen N, Huntsman S, Hu D, Spear M, Eng C, Oh SS, White MJ, Mak A, Davis A, Meade K, Brigino-Buenaventura E, LeNoir MA, Bibbins-Domingo K, Burchard EG, Halperin E. PMID: 27879348; PMCID: PMC5223515.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    99. Pleiotropic Mechanisms Indicated for Sex Differences in Autism. PLoS Genet. 2016 11; 12(11):e1006425. Mitra I, Tsang K, Ladd-Acosta C, Croen LA, Aldinger KA, Hendren RL, Traglia M, Lavillaureix A, Zaitlen N, Oldham MC, Levitt P, Nelson S, Amaral DG, Hertz-Picciotto I, Fallin MD, Weiss LA. PMID: 27846226; PMCID: PMC5147776.
      View in: PubMed   Mentions: 41     Fields:    Translation:HumansCells
    100. DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome. Am J Hum Genet. 2016 09 01; 99(3):555-566. Joshi RS, Garg P, Zaitlen N, Lappalainen T, Watson CT, Azam N, Ho D, Li X, Antonarakis SE, Brunner HG, Buiting K, Cheung SW, Coffee B, Eggermann T, Francis D, Geraedts JP, Gimelli G, Jacobson SG, Le Caignec C, de Leeuw N, Liehr T, Mackay DJ, Montgomery SB, Pagnamenta AT, Papenhausen P, Robinson DO, Ruivenkamp C, Schwartz C, Steiner B, Stevenson DA, Surti U, Wassink T, Sharp AJ. PMID: 27569549; PMCID: PMC5011056.
      View in: PubMed   Mentions: 44     Fields:    
    101. Transethnic Genetic-Correlation Estimates from Summary Statistics. Am J Hum Genet. 2016 07 07; 99(1):76-88. Brown BC, Asian Genetic Epidemiology Network Type 2 Diabetes Consortium, Ye CJ, Price AL, Zaitlen N. PMID: 27321947; PMCID: PMC5005434.
      View in: PubMed   Mentions: 119     Fields:    Translation:Humans
    102. Selection and explosive growth alter genetic architecture and hamper the detection of causal rare variants. Genome Res. 2016 07; 26(7):863-73. Uricchio LH, Zaitlen NA, Ye CJ, Witte JS, Hernandez RD. PMID: 27197206; PMCID: PMC4937562.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansCells
    103. Local Joint Testing Improves Power and Identifies Hidden Heritability in Association Studies. Genetics. 2016 07; 203(3):1105-16. Brown BC, Price AL, Patsopoulos NA, Zaitlen N. PMID: 27182951; PMCID: PMC4937483.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    104. 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: 126     Fields:    Translation:HumansCells
    105. Massively Parallel Identification of Regulatory Variants in Asthma. Ann Am Thorac Soc. 2016 Mar; 13 Suppl 1:S104. Biton A, Torgerson D, Letonqueze O, Zhao W, Zaitlen N, Erle DJ. PMID: 27027944; PMCID: PMC5015739.
      View in: PubMed   Mentions:    Fields:    
    106. A Novel Test for Detecting SNP-SNP Interactions in Case-Only Trio Studies. Genetics. 2016 Apr; 202(4):1289-97. Balliu B, Zaitlen N. PMID: 26865367; PMCID: PMC4905548.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    107. Genetic and socioeconomic study of mate choice in Latinos reveals novel assortment patterns. Proc Natl Acad Sci U S A. 2015 Nov 03; 112(44):13621-6. Zou JY, Park DS, Burchard EG, Torgerson DG, Pino-Yanes M, Song YS, Sankararaman S, Halperin E, Zaitlen N. PMID: 26483472; PMCID: PMC4640764.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    108. Multiple breast cancer risk variants are associated with differential transcript isoform expression in tumors. Hum Mol Genet. 2015 Dec 20; 24(25):7421-31. Caswell JL, Camarda R, Zhou AY, Huntsman S, Hu D, Brenner SE, Zaitlen N, Goga A, Ziv E. PMID: 26472073; PMCID: PMC4664170.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    109. Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores. Am J Hum Genet. 2015 Oct 01; 97(4):576-92. Vilhjálmsson BJ, Yang J, Finucane HK, Gusev A, Lindström S, Ripke S, Genovese G, Loh PR, Bhatia G, Do R, Hayeck T, Won HH, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Discovery, Biology, and Risk of , Kathiresan S, Pato M, Pato C, Tamimi R, Stahl E, Zaitlen N, Pasaniuc B, Belbin G, Kenny EE, Schierup MH, De Jager P, Patsopoulos NA, McCarroll S, Daly M, Purcell S, Chasman D, Neale B, Goddard M, Visscher PM, Kraft P, Patterson N, Price AL. PMID: 26430803; PMCID: PMC4596916.
      View in: PubMed   Mentions: 441     Fields:    
    110. Adapt-Mix: learning local genetic correlation structure improves summary statistics-based analyses. Bioinformatics. 2015 Jun 15; 31(12):i181-9. Park DS, Brown B, Eng C, Huntsman S, Hu D, Torgerson DG, Burchard EG, Zaitlen N. PMID: 26072481; PMCID: PMC4553832.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    111. The landscape of genomic imprinting across diverse adult human tissues. Genome Res. 2015 Jul; 25(7):927-36. Baran Y, Subramaniam M, Biton A, Tukiainen T, Tsang EK, Rivas MA, Pirinen M, Gutierrez-Arcelus M, Smith KS, Kukurba KR, Zhang R, Eng C, Torgerson DG, Urbanek C, GTEx Consortium, Li JB, Rodriguez-Santana JR, Burchard EG, Seibold MA, MacArthur DG, Montgomery SB, Zaitlen NA, Lappalainen T. PMID: 25953952; PMCID: PMC4484390.
      View in: PubMed   Mentions: 91     Fields:    
    112. COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis. Nat Genet. 2015 Jun; 47(6):654-60. Watkin LB, Jessen B, Wiszniewski W, Vece TJ, Jan M, Sha Y, Thamsen M, Santos-Cortez RL, Lee K, Gambin T, Forbes LR, Law CS, Stray-Pedersen A, Cheng MH, Mace EM, Anderson MS, Liu D, Tang LF, Nicholas SK, Nahmod K, Makedonas G, Canter DL, Kwok PY, Hicks J, Jones KD, Penney S, Jhangiani SN, Rosenblum MD, Dell SD, Waterfield MR, Papa FR, Muzny DM, Zaitlen N, Leal SM, Gonzaga-Jauregui C, Baylor-Hopkins Center for Mendelian Genomics, Boerwinkle E, Eissa NT, Gibbs RA, Lupski JR, Orange JS, Shum AK. PMID: 25894502; PMCID: PMC4513663.
      View in: PubMed   Mentions: 161     Fields:    Translation:HumansCells
    113. Mixed model with correction for case-control ascertainment increases association power. Am J Hum Genet. 2015 May 07; 96(5):720-30. Hayeck TJ, Zaitlen NA, Loh PR, Vilhjalmsson B, Pollack S, Gusev A, Yang J, Chen GB, Goddard ME, Visscher PM, Patterson N, Price AL. PMID: 25892111; PMCID: PMC4570278.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    114. Assessing allele-specific expression across multiple tissues from RNA-seq read data. Bioinformatics. 2015 Aug 01; 31(15):2497-504. Pirinen M, Lappalainen T, Zaitlen NA, GTEx Consortium, Dermitzakis ET, Donnelly P, McCarthy MI, Rivas MA. PMID: 25819081; PMCID: PMC4514921.
      View in: PubMed   Mentions: 33     Fields:    
    115. PIGS: improved estimates of identity-by-descent probabilities by probabilistic IBD graph sampling. BMC Bioinformatics. 2015; 16 Suppl 5:S9. Park DS, Baran Y, Hormozdiari F, Eng C, Torgerson DG, Burchard EG, Zaitlen N. PMID: 25860540; PMCID: PMC4402697.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    116. Variation in predictive ability of common genetic variants by established strata: the example of breast cancer and age. Epidemiology. 2015 Jan; 26(1):51-8. Aschard H, Zaitlen N, Lindström S, Kraft P. PMID: 25380502; PMCID: PMC5082110.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    117. Genetic and environmental components of family history in type 2 diabetes. Hum Genet. 2015 Feb; 134(2):259-67. Cornelis MC, Zaitlen N, Hu FB, Kraft P, Price AL. PMID: 25543539; PMCID: PMC4293229.
      View in: PubMed   Mentions: 28     Fields:    Translation:Humans
    118. Leveraging population admixture to characterize the heritability of complex traits. Nat Genet. 2014 Dec; 46(12):1356-62. Zaitlen N, Pasaniuc B, Sankararaman S, Bhatia G, Zhang J, Gusev A, Young T, Tandon A, Pollack S, Vilhjálmsson BJ, Assimes TL, Berndt SI, Blot WJ, Chanock S, Franceschini N, Goodman PG, He J, Hennis AJ, Hsing A, Ingles SA, Isaacs W, Kittles RA, Klein EA, Lange LA, Nemesure B, Patterson N, Reich D, Rybicki BA, Stanford JL, Stevens VL, Strom SS, Whitsel EA, Witte JS, Xu J, Haiman C, Wilson JG, Kooperberg C, Stram D, Reiner AP, Tang H, Price AL. PMID: 25383972; PMCID: PMC4244251.
      View in: PubMed   Mentions: 35     Fields:    Translation:Humans
    119. Intersection of population variation and autoimmunity genetics in human T cell activation. Science. 2014 Sep 12; 345(6202):1254665. Ye CJ, Feng T, Kwon HK, Raj T, Wilson MT, Asinovski N, McCabe C, Lee MH, Frohlich I, Paik HI, Zaitlen N, Hacohen N, Stranger B, De Jager P, Mathis D, Regev A, Benoist C. PMID: 25214635; PMCID: PMC4751028.
      View in: PubMed   Mentions: 117     Fields:    Translation:HumansCells
    120. Fast and accurate imputation of summary statistics enhances evidence of functional enrichment. Bioinformatics. 2014 Oct 15; 30(20):2906-14. Pasaniuc B, Zaitlen N, Shi H, Bhatia G, Gusev A, Pickrell J, Hirschhorn J, Strachan DP, Patterson N, Price AL. PMID: 24990607; PMCID: PMC4184260.
      View in: PubMed   Mentions: 93     Fields:    
    121. Massively parallel functional annotation of 3' untranslated regions. Nat Biotechnol. 2014 Apr; 32(4):387-91. Zhao W, Pollack JL, Blagev DP, Zaitlen N, McManus MT, Erle DJ. PMID: 24633241; PMCID: PMC3981918.
      View in: PubMed   Mentions: 67     Fields:    Translation:Humans
    122. Advantages and pitfalls in the application of mixed-model association methods. Nat Genet. 2014 Feb; 46(2):100-6. Yang J, Zaitlen NA, Goddard ME, Visscher PM, Price AL. PMID: 24473328; PMCID: PMC3989144.
      View in: PubMed   Mentions: 385     Fields:    Translation:Humans
    123. Quantifying missing heritability at known GWAS loci. PLoS Genet. 2013; 9(12):e1003993. Gusev A, Bhatia G, Zaitlen N, Vilhjalmsson BJ, Diogo D, Stahl EA, Gregersen PK, Worthington J, Klareskog L, Raychaudhuri S, Plenge RM, Pasaniuc B, Price AL. PMID: 24385918; PMCID: PMC3873246.
      View in: PubMed   Mentions: 48     Fields:    
    124. Genome-wide association study of ancestry-specific TB risk in the South African Coloured population. Hum Mol Genet. 2014 Feb 01; 23(3):796-809. Chimusa ER, Zaitlen N, Daya M, Möller M, van Helden PD, Mulder NJ, Price AL, Hoal EG. PMID: 24057671; PMCID: PMC3888262.
      View in: PubMed   Mentions: 76     Fields:    Translation:Humans
    125. Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits. PLoS Genet. 2013 May; 9(5):e1003520. Zaitlen N, Kraft P, Patterson N, Pasaniuc B, Bhatia G, Pollack S, Price AL. PMID: 23737753; PMCID: PMC3667752.
      View in: PubMed   Mentions: 140     Fields:    Translation:Humans
    126. Analysis of Latino populations from GALA and MEC studies reveals genomic loci with biased local ancestry estimation. Bioinformatics. 2013 Jun 01; 29(11):1407-15. Pasaniuc B, Sankararaman S, Torgerson DG, Gignoux C, Zaitlen N, Eng C, Rodriguez-Cintron W, Chapela R, Ford JG, Avila PC, Rodriguez-Santana J, Chen GK, Le Marchand L, Henderson B, Reich D, Haiman CA, Gonzàlez Burchard E, Halperin E. PMID: 23572411; PMCID: PMC3661056.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    127. A nonparametric test to detect quantitative trait loci where the phenotypic distribution differs by genotypes. Genet Epidemiol. 2013 May; 37(4):323-33. Aschard H, Zaitlen N, Tamimi RM, Lindström S, Kraft P. PMID: 23512279; PMCID: PMC4088942.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    128. Response to Sul and Eskin. Nat Rev Genet. 2013 Apr; 14(4):300. Price AL, Zaitlen NA, Reich D, Patterson N. PMID: 23438870; PMCID: PMC5586503.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    129. Informed conditioning on clinical covariates increases power in case-control association studies. PLoS Genet. 2012; 8(11):e1003032. Zaitlen N, Lindström S, Pasaniuc B, Cornelis M, Genovese G, Pollack S, Barton A, Bickeböller H, Bowden DW, Eyre S, Freedman BI, Friedman DJ, Field JK, Groop L, Haugen A, Heinrich J, Henderson BE, Hicks PJ, Hocking LJ, Kolonel LN, Landi MT, Langefeld CD, Le Marchand L, Meister M, Morgan AW, Raji OY, Risch A, Rosenberger A, Scherf D, Steer S, Walshaw M, Waters KM, Wilson AG, Wordsworth P, Zienolddiny S, Tchetgen ET, Haiman C, Hunter DJ, Plenge RM, Worthington J, Christiani DC, Schaumberg DA, Chasman DI, Altshuler D, Voight B, Kraft P, Patterson N, Price AL. PMID: 23144628; PMCID: PMC3493452.
      View in: PubMed   Mentions: 37     Fields:    
    130. Heritability in the genome-wide association era. Hum Genet. 2012 Oct; 131(10):1655-64. Zaitlen N, Kraft P. PMID: 22821350; PMCID: PMC3432754.
      View in: PubMed   Mentions: 66     Fields:    Translation:Humans
    131. Extremely low-coverage sequencing and imputation increases power for genome-wide association studies. Nat Genet. 2012 May 20; 44(6):631-5. Pasaniuc B, Rohland N, McLaren PJ, Garimella K, Zaitlen N, Li H, Gupta N, Neale BM, Daly MJ, Sklar P, Sullivan PF, Bergen S, Moran JL, Hultman CM, Lichtenstein P, Magnusson P, Purcell SM, Haas DW, Liang L, Sunyaev S, Patterson N, de Bakker PI, Reich D, Price AL. PMID: 22610117; PMCID: PMC3400344.
      View in: PubMed   Mentions: 113     Fields:    Translation:Humans
    132. Analysis of case-control association studies with known risk variants. Bioinformatics. 2012 Jul 01; 28(13):1729-37. Zaitlen N, Pasaniuc B, Patterson N, Pollack S, Voight B, Groop L, Altshuler D, Henderson BE, Kolonel LN, Le Marchand L, Waters K, Haiman CA, Stranger BE, Dermitzakis ET, Kraft P, Price AL. PMID: 22556366; PMCID: PMC3381970.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    133. Combining effects from rare and common genetic variants in an exome-wide association study of sequence data. BMC Proc. 2011 Nov 29; 5 Suppl 9:S44. Aschard H, Qiu W, Pasaniuc B, Zaitlen N, Cho MH, Carey V. PMID: 22373328; PMCID: PMC3287881.
      View in: PubMed   Mentions: 1  
    134. Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection. Am J Hum Genet. 2011 Sep 09; 89(3):368-81. Bhatia G, Patterson N, Pasaniuc B, Zaitlen N, Genovese G, Pollack S, Mallick S, Myers S, Tandon A, Spencer C, Palmer CD, Adeyemo AA, Akylbekova EL, Cupples LA, Divers J, Fornage M, Kao WH, Lange L, Li M, Musani S, Mychaleckyj JC, Ogunniyi A, Papanicolaou G, Rotimi CN, Rotter JI, Ruczinski I, Salako B, Siscovick DS, Tayo BO, Yang Q, McCarroll S, Sabeti P, Lettre G, De Jager P, Hirschhorn J, Zhu X, Cooper R, Reich D, Wilson JG, Price AL. PMID: 21907010; PMCID: PMC3169818.
      View in: PubMed   Mentions: 42     Fields:    
    135. 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: 3     Fields:    Translation:HumansCells
    136. Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium. PLoS Genet. 2011 Apr; 7(4):e1001371. Pasaniuc B, Zaitlen N, Lettre G, Chen GK, Tandon A, Kao WH, Ruczinski I, Fornage M, Siscovick DS, Zhu X, Larkin E, Lange LA, Cupples LA, Yang Q, Akylbekova EL, Musani SK, Divers J, Mychaleckyj J, Li M, Papanicolaou GJ, Millikan RC, Ambrosone CB, John EM, Bernstein L, Zheng W, Hu JJ, Ziegler RG, Nyante SJ, Bandera EV, Ingles SA, Press MF, Chanock SJ, Deming SL, Rodriguez-Gil JL, Palmer CD, Buxbaum S, Ekunwe L, Hirschhorn JN, Henderson BE, Myers S, Haiman CA, Reich D, Patterson N, Wilson JG, Price AL. PMID: 21541012; PMCID: PMC3080860.
      View in: PubMed   Mentions: 69     Fields:    
    137. Accurate estimation of expression levels of homologous genes in RNA-seq experiments. J Comput Biol. 2011 Mar; 18(3):459-68. Pasaniuc B, Zaitlen N, Halperin E. PMID: 21385047.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    138. 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: 11     Fields:    
    139. 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: 1     Fields:    
    140. New approaches to population stratification in genome-wide association studies. Nat Rev Genet. 2010 Jul; 11(7):459-63. Price AL, Zaitlen NA, Reich D, Patterson N. PMID: 20548291; PMCID: PMC2975875.
      View in: PubMed   Mentions: 514     Fields:    
    141. 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: 1275     Fields:    
    142. 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: 10     Fields:    
    143. Leveraging genetic variability across populations for the identification of causal variants. Am J Hum Genet. 2010 Jan; 86(1):23-33. Zaitlen N, Pasaniuc B, Gur T, Ziv E, Halperin E. PMID: 20085711; PMCID: PMC2801753.
      View in: PubMed   Mentions: 70     Fields:    Translation:Humans
    144. 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: 141     Fields:    
    145. 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: 3     Fields:    
    146. Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. Nat Genet. 2009 Jan; 41(1):35-46. Sabatti C, Service SK, Hartikainen AL, Pouta A, Ripatti S, Brodsky J, Jones CG, Zaitlen NA, Varilo T, Kaakinen M, Sovio U, Ruokonen A, Laitinen J, Jakkula E, Coin L, Hoggart C, Collins A, Turunen H, Gabriel S, Elliot P, McCarthy MI, Daly MJ, Järvelin MR, Freimer NB, Peltonen L. PMID: 19060910; PMCID: PMC2687077.
      View in: PubMed   Mentions: 276     Fields:    
    147. Shift-invariant adaptive double threading: learning MHC II-peptide binding. J Comput Biol. 2008 Sep; 15(7):927-42. Zaitlen N, Reyes-Gomez M, Heckerman D, Jojic N. PMID: 18771399.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    148. 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: 7     Fields:    
    149. 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: 763     Fields:    Translation:Animals
    150. 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: 19     Fields:    Translation:Humans
    151. 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: 10     Fields:    Translation:HumansAnimals
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