Jeanette Christine Papp

Title(s)Department Vice Chair, Human Genetics
SchoolMedicine
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    Other Positions
    Title(s)Adjunct Professor, Human Genetics


    Collapse Research 
    Collapse Research Activities and Funding
    Workshops on Genomics and Next Generation Computational Statistics for Big Data
    NIH R25HG011845Aug 16, 2021 - May 31, 2026
    Role: Co-Principal Investigator
    Bruins in Genomics: Dental, Oral & Craniofacial Research Training Program (BIG DOC)
    NIH R25DE030117Jan 15, 2021 - Dec 31, 2025
    Role: Co-Principal Investigator
    Clinical Trial Readiness for SCA1 and SCA3
    NIH/NINDS U01NS104326Jan 1, 2018 - Dec 31, 2022
    Role: Co-Principal Investigator
    NGS Data Analysis Skills for the Biosciences Pipeline
    NIH R25EB022364Sep 30, 2015 - Jun 30, 2019
    Role: Co-Principal Investigator
    Statistical Genomics and Systems Biology Workshop
    NIH R25GM103774May 1, 2013 - Apr 30, 2018
    Role: Principal Investigator
    BioMark MX/HX Genetic Analysis System
    NIH S10RR027143Nov 26, 2009 - Nov 25, 2010
    Role: Principal Investigator
    AB 3730XL, 96 Cap DNA Analyzer
    NIH S10RR022387Apr 15, 2006 - Apr 14, 2007
    Role: Principal Investigator
    ABI PRISM 7900HT Sequence Detection System
    NIH S10RR019420Apr 1, 2004 - Mar 31, 2005
    Role: Principal Investigator
    Training Grant in Genomic Analysis and Interpretation
    NIH T32HG002536Jul 1, 2002 - Jun 30, 2022
    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. Genetic variants of glucose metabolism and exposure to smoking in African American breast cancer. Endocr Relat Cancer. 2023 04 01; 30(4). Jung SY, Papp JC, Sobel EM, Pellegrini M, Yu H. PMID: 36705562; PMCID: PMC10095926.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    2. Unsupervised discovery of ancestry-informative markers and genetic admixture proportions in biobank-scale datasets. Am J Hum Genet. 2023 02 02; 110(2):314-325. Ko S, Chu BB, Peterson D, Okenwa C, Papp JC, Alexander DH, Sobel EM, Zhou H, Lange KL. PMID: 36610401; PMCID: PMC9943729.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    3. Towards a Genetic Linkage Map of the California Condor, an Endangered New World Vulture Species. Animals (Basel). 2022 Nov 24; 12(23). Romanov MN, Da Y, Chemnick LG, Thomas SM, Dandekar SS, Papp JC, Ryder OA. PMID: 36496789.
      View in: PubMed   Mentions:
    4. 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
    5. Corrigendum to: Facultative Parthenogenesis in California Condors. J Hered. 2022 May 16; 113(2):217. Ryder OA, Thomas S, Judson JM, Romanov MN, Dandekar S, Papp JC, Sidak-Loftis LC, Walker K, Stalis IH, Mace M, Steiner CC, Chemnick LG. PMID: 35575084; PMCID: PMC9113412.
      View in: PubMed   Mentions:    Fields:    
    6. Facultative Parthenogenesis in California Condors. J Hered. 2021 12 17; 112(7):569-574. Ryder OA, Thomas S, Judson JM, Romanov MN, Dandekar S, Papp JC, Sidak-Loftis LC, Walker K, Stalis IH, Mace M, Steiner CC, Chemnick LG. PMID: 34718632; PMCID: PMC8683835.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    7. Synergistic Effects of Genetic Variants of Glucose Homeostasis and Lifelong Exposures to Cigarette Smoking, Female Hormones, and Dietary Fat Intake on Primary Colorectal Cancer Development in African and Hispanic/Latino American Women. Front Oncol. 2021; 11:760243. Jung SY, Sobel EM, Pellegrini M, Yu H, Papp JC. PMID: 34692549; PMCID: PMC8529283.
      View in: PubMed   Mentions: 1  
    8. Molecular Biology Networks and Key Gene Regulators for Inflammatory Biomarkers Shared by Breast Cancer Development: Multi-Omics Systems Analysis. Biomolecules. 2021 09 18; 11(9). Jung SY, Papp JC, Pellegrini M, Yu H, Sobel EM. PMID: 34572592; PMCID: PMC8469138.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    9. Genetically determined elevated C-reactive protein associated with primary colorectal cancer risk: Mendelian randomization with lifestyle interactions. Am J Cancer Res. 2021; 11(4):1733-1753. Jung SY, Yu H, Pellegrini M, Papp JC, Sobel EM, Zhang ZF. PMID: 33948386; PMCID: PMC8085861.
      View in: PubMed   Mentions: 3  
    10. Genetically Predicted C-Reactive Protein Associated With Postmenopausal Breast Cancer Risk: Interrelation With Estrogen and Cancer Molecular Subtypes Using Mendelian Randomization. Front Oncol. 2020; 10:630994. Jung SY, Papp JC, Sobel EM, Pellegrini M, Yu H, Zhang ZF. PMID: 33614510; PMCID: PMC7888276.
      View in: PubMed   Mentions: 3  
    11. Pro-inflammatory cytokine polymorphisms and interactions with dietary alcohol and estrogen, risk factors for invasive breast cancer using a post genome-wide analysis for gene-gene and gene-lifestyle interaction. Sci Rep. 2021 01 13; 11(1):1058. Jung SY, Papp JC, Sobel EM, Pellegrini M, Yu H, Zhang ZF. PMID: 33441805; PMCID: PMC7807068.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    12. Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients. Sci Adv. 2020 12; 6(49). Bryant L, Li D, Cox SG, Marchione D, Joiner EF, Wilson K, Janssen K, Lee P, March ME, Nair D, Sherr E, Fregeau B, Wierenga KJ, Wadley A, Mancini GMS, Powell-Hamilton N, van de Kamp J, Grebe T, Dean J, Ross A, Crawford HP, Powis Z, Cho MT, Willing MC, Manwaring L, Schot R, Nava C, Afenjar A, Lessel D, Wagner M, Klopstock T, Winkelmann J, Catarino CB, Retterer K, Schuette JL, Innis JW, Pizzino A, Lüttgen S, Denecke J, Strom TM, Monaghan KG, DDD Study, Yuan ZF, Dubbs H, Bend R, Lee JA, Lyons MJ, Hoefele J, Günthner R, Reutter H, Keren B, Radtke K, Sherbini O, Mrokse C, Helbig KL, Odent S, Cogne B, Mercier S, Bezieau S, Besnard T, Kury S, Redon R, Reinson K, Wojcik MH, Õunap K, Ilves P, Innes AM, Kernohan KD, Care4Rare Canada Consortium, Costain G, Meyn MS, Chitayat D, Zackai E, Lehman A, Kitson H, CAUSES Study, Martin MG, Martinez-Agosto JA, Undiagnosed Diseases Network, Nelson SF, Palmer CGS, Papp JC, Parker NH, Sinsheimer JS, Vilain E, Wan J, Yoon AJ, Zheng A, Brimble E, Ferrero GB, Radio FC, Carli D, Barresi S, Brusco A, Tartaglia M, Thomas JM, Umana L, Weiss MM, Gotway G, Stuurman KE, Thompson ML, McWalter K, Stumpel CTRM, Stevens SJC, Stegmann APA, Tveten K, Vøllo A, Prescott T, Fagerberg C, Laulund LW, Larsen MJ, Byler M, Lebel RR, Hurst AC, Dean J, Schrier Vergano SA, Norman J, Mercimek-Andrews S, Neira J, Van Allen MI, Longo N, Sellars E, Louie RJ, Cathey SS, Brokamp E, Heron D, Snyder M, Vanderver A, Simon C, de la Cruz X, Padilla N, Crump JG, Chung W, Garcia B, Hakonarson HH, Bhoj EJ. PMID: 33268356; PMCID: PMC7821880.
      View in: PubMed   Mentions: 30     Fields:    Translation:HumansAnimals
    13. Genome-wide Association Analysis of Proinflammatory Cytokines and Gene-lifestyle Interaction for Invasive Breast Cancer Risk: The WHI dbGaP Study. Cancer Prev Res (Phila). 2021 01; 14(1):41-54. Jung SY, Scott PA, Papp JC, Sobel EM, Pellegrini M, Yu H, Han S, Zhang ZF. PMID: 32928877; PMCID: PMC7956151.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    14. Pro-inflammatory cytokine polymorphisms in ONECUT2 and HNF4A and primary colorectal carcinoma: a post genome-wide gene-lifestyle interaction study. Am J Cancer Res. 2020; 10(9):2955-2976. Jung SY, Papp JC, Sobel EM, Pellegrini M, Yu H, Zhang ZF. PMID: 33042629; PMCID: PMC7539781.
      View in: PubMed   Mentions: 3  
    15. Mendelian Randomization Study: The Association Between Metabolic Pathways and Colorectal Cancer Risk. Front Oncol. 2020; 10:1005. Jung SY, Papp JC, Sobel EM, Zhang ZF. PMID: 32850306; PMCID: PMC7396568.
      View in: PubMed   Mentions: 5  
    16. Diagnostic utility of transcriptome sequencing for rare Mendelian diseases. Genet Med. 2020 03; 22(3):490-499. Lee H, Huang AY, Wang LK, Yoon AJ, Renteria G, Eskin A, Signer RH, Dorrani N, Nieves-Rodriguez S, Wan J, Douine ED, Woods JD, Dell'Angelica EC, Fogel BL, Martin MG, Butte MJ, Parker NH, Wang RT, Shieh PB, Wong DA, Gallant N, Singh KE, Tavyev Asher YJ, Sinsheimer JS, Krakow D, Loo SK, Allard P, Papp JC, Undiagnosed Diseases Network, Palmer CGS, Martinez-Agosto JA, Nelson SF. PMID: 31607746; PMCID: PMC7405636.
      View in: PubMed   Mentions: 81     Fields:    Translation:HumansCells
    17. Post Genome-Wide Gene-Environment Interaction Study Using Random Survival Forest: Insulin Resistance, Lifestyle Factors, and Colorectal Cancer Risk. Cancer Prev Res (Phila). 2019 12; 12(12):877-890. Jung SY, Papp JC, Sobel EM, Zhang ZF. PMID: 31554631; PMCID: PMC6893139.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    18. Post genome-wide gene-environment interaction study: The effect of genetically driven insulin resistance on breast cancer risk using Mendelian randomization. PLoS One. 2019; 14(6):e0218917. Jung SY, Mancuso N, Papp J, Sobel E, Zhang ZF. PMID: 31246991; PMCID: PMC6597082.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    19. Breast Cancer Risk and Insulin Resistance: Post Genome-Wide Gene-Environment Interaction Study Using a Random Survival Forest. Cancer Res. 2019 05 15; 79(10):2784-2794. Jung SY, Papp JC, Sobel EM, Yu H, Zhang ZF. PMID: 30936085; PMCID: PMC6522308.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    20. OPENMENDEL: a cooperative programming project for statistical genetics. Hum Genet. 2020 Jan; 139(1):61-71. Zhou H, Sinsheimer JS, Bates DM, Chu BB, German CA, Ji SS, Keys KL, Kim J, Ko S, Mosher GD, Papp JC, Sobel EM, Zhai J, Zhou JJ, Lange K. PMID: 30915546; PMCID: PMC6763373.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    21. Genome-Wide Meta-analysis of Gene-Environmental Interaction for Insulin Resistance Phenotypes and Breast Cancer Risk in Postmenopausal Women. Cancer Prev Res (Phila). 2019 01; 12(1):31-42. Jung SY, Mancuso N, Yu H, Papp J, Sobel E, Zhang ZF. PMID: 30327367.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    22. Genetic Variants in Metabolic Signaling Pathways and Their Interaction with Lifestyle Factors on Breast Cancer Risk: A Random Survival Forest Analysis. Cancer Prev Res (Phila). 2018 01; 11(1):44-51. Jung SY, Papp JC, Sobel EM, Zhang ZF. PMID: 29074537; PMCID: PMC5754228.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    23. Interaction of insulin-like growth factor-I and insulin resistance-related genetic variants with lifestyle factors on postmenopausal breast cancer risk. Breast Cancer Res Treat. 2017 Jul; 164(2):475-495. Jung SY, Ho G, Rohan T, Strickler H, Bea J, Papp J, Sobel E, Zhang ZF, Crandall C. PMID: 28478612.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    24. Effect of genetic variants and traits related to glucose metabolism and their interaction with obesity on breast and colorectal cancer risk among postmenopausal women. BMC Cancer. 2017 04 26; 17(1):290. Jung SY, Sobel EM, Papp JC, Zhang ZF. PMID: 28446149; PMCID: PMC5405540.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    25. Genetics of Disorders of Sex Development: The DSD-TRN Experience. Endocrinol Metab Clin North Am. 2017 06; 46(2):519-537. Délot EC, Papp JC, DSD-TRN Genetics Workgroup, Sandberg DE, Vilain E. PMID: 28476235; PMCID: PMC5714504.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    26. Obesity and associated lifestyles modify the effect of glucose metabolism-related genetic variants on impaired glucose homeostasis among postmenopausal women. Genet Epidemiol. 2016 09; 40(6):520-30. Jung SY, Sobel EM, Papp JC, Crandall CJ, Fu AN, Zhang ZF. PMID: 27377425; PMCID: PMC5560051.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    27. Next Generation Statistical Genetics: Modeling, Penalization, and Optimization in High-Dimensional Data. Annu Rev Stat Appl. 2014 Jan 01; 1(1):279-300. Lange K, Papp JC, Sinsheimer JS, Sobel EM. PMID: 24955378; PMCID: PMC4062304.
      View in: PubMed   Mentions: 15  
    28. Tobacco smoking, NBS1 polymorphisms, and survival in lung and upper aerodigestive tract cancers with semi-Bayes adjustment for hazard ratio variation. Cancer Causes Control. 2014 Jan; 25(1):11-23. Yang T, Chang PY, Park SL, Bastani D, Chang SC, Morgenstern H, Tashkin DP, Mao JT, Papp JC, Rao JY, Cozen W, Mack TM, Greenland S, Zhang ZF. PMID: 24166361; PMCID: PMC3889468.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    29. The systems genetics resource: a web application to mine global data for complex disease traits. Front Genet. 2013; 4:84. van Nas A, Pan C, Ingram-Drake LA, Ghazalpour A, Drake TA, Sobel EM, Papp JC, Lusis AJ. PMID: 23730305; PMCID: PMC3657633.
      View in: PubMed   Mentions: 10  
    30. Mendel: the Swiss army knife of genetic analysis programs. Bioinformatics. 2013 Jun 15; 29(12):1568-70. Lange K, Papp JC, Sinsheimer JS, Sripracha R, Zhou H, Sobel EM. PMID: 23610370; PMCID: PMC3673222.
      View in: PubMed   Mentions: 66     Fields:    Translation:Humans
    31. Single nucleotide polymorphisms of 8 inflammation-related genes and their associations with smoking-related cancers. Int J Cancer. 2010 Nov 01; 127(9):2169-82. Oh SS, Chang SC, Cai L, Cordon-Cardo C, Ding BG, Greenland S, He N, Jiang Q, Kheifets L, Le A, Lee YC, Liu S, Lu ML, Mao JT, Morgenstern H, Mu LN, Pantuck A, Papp JC, Park SL, Rao JY, Reuter VE, Tashkin DP, Wang H, You NC, Yu SZ, Zhao JK, Belldegrun A, Zhang ZF. PMID: 20112337; PMCID: PMC2932751.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    32. Pathway analysis software: annotation errors and solutions. Mol Genet Metab. 2010 Oct-Nov; 101(2-3):134-40. Henderson-Maclennan NK, Papp JC, Talbot CC, McCabe ER, Presson AP. PMID: 20663702; PMCID: PMC2950253.
      View in: PubMed   Mentions: 5     Fields:    
    33. Associations between NBS1 polymorphisms, haplotypes and smoking-related cancers. Carcinogenesis. 2010 Jul; 31(7):1264-71. Park SL, Bastani D, Goldstein BY, Chang SC, Cozen W, Cai L, Cordon-Cardo C, Ding B, Greenland S, He N, Hussain SK, Jiang Q, Lee YC, Liu S, Lu ML, Mack TM, Mao JT, Morgenstern H, Mu LN, Oh SS, Pantuck A, Papp JC, Rao J, Reuter VE, Tashkin DP, Wang H, You NC, Yu SZ, Zhao JK, Zhang ZF. PMID: 20478923; PMCID: PMC2893801.
      View in: PubMed   Mentions: 23     Fields:    Translation:Humans
    34. A powerful score test to detect positive selection in genome-wide scans. Eur J Hum Genet. 2010 Oct; 18(10):1148-59. Zhong M, Lange K, Papp JC, Fan R. PMID: 20461112; PMCID: PMC2987455.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    35. Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC. Invest Ophthalmol Vis Sci. 2010 Aug; 51(8):4006-12. Aldave AJ, Rosenwasser GO, Yellore VS, Papp JC, Sobel EM, Pham MN, Chen MC, Dandekar S, Sripracha R, Rayner SA, Sassani JW, Gorin MB. PMID: 20357198; PMCID: PMC2910638.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    36. CCL3 genotype and current depression increase risk of HIV-associated dementia. Neurobehav HIV Med. 2009 Nov; 1:1-7. Levine AJ, Singer EJ, Sinsheimer JS, Hinkin CH, Papp J, Dandekar S, Giovanelli A, Shapshak P. PMID: 20725607; PMCID: PMC2923399.
      View in: PubMed   Mentions: 21  
    37. Genetic variation in immune regulation and DNA repair pathways and stomach cancer in China. Cancer Epidemiol Biomarkers Prev. 2009 Aug; 18(8):2304-9. Hussain SK, Mu LN, Cai L, Chang SC, Park SL, Oh SS, Wang Y, Goldstein BY, Ding BG, Jiang Q, Rao J, You NC, Yu SZ, Papp JC, Zhao JK, Wang H, Zhang ZF. PMID: 19661089; PMCID: PMC2725326.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansCells
    38. Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval. Cornea. 2009 Aug; 28(7):801-7. Aldave AJ, Yellore VS, Vo RC, Kamal KM, Rayner SA, Plaisier CL, Chen MC, Damani MR, Pham MN, Gorin MB, Sobel E, Papp J. PMID: 19574904; PMCID: PMC2714875.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    39. The value of avian genomics to the conservation of wildlife. BMC Genomics. 2009 Jul 14; 10 Suppl 2:S10. Romanov MN, Tuttle EM, Houck ML, Modi WS, Chemnick LG, Korody ML, Mork EM, Otten CA, Renner T, Jones KC, Dandekar S, Papp JC, Da Y, NISC Comparative Sequencing Program, Green ED, Magrini V, Hickenbotham MT, Glasscock J, McGrath S, Mardis ER, Ryder OA. PMID: 19607652; PMCID: PMC2966331.
      View in: PubMed   Mentions: 33     Fields:    Translation:AnimalsCells
    40. A heterozygote-homozygote test of Hardy-Weinberg equilibrium. Eur J Hum Genet. 2009 Nov; 17(11):1495-500. Zhou JJ, Lange K, Papp JC, Sinsheimer JS. PMID: 19367317; PMCID: PMC2986695.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    41. Associations between single nucleotide polymorphisms in double-stranded DNA repair pathway genes and familial breast cancer. Clin Cancer Res. 2009 Mar 15; 15(6):2192-203. Sehl ME, Langer LR, Papp JC, Kwan L, Seldon JL, Arellano G, Reiss J, Reed EF, Dandekar S, Korin Y, Sinsheimer JS, Zhang ZF, Ganz PA. PMID: 19276285; PMCID: PMC2778342.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    42. High-resolution functional profiling of a gammaherpesvirus RTA locus in the context of the viral genome. J Virol. 2009 Feb; 83(4):1811-22. Arumugaswami V, Sitapara R, Hwang S, Song MJ, Ho TN, Su NQ, Sue EY, Kanagavel V, Xing F, Zhang X, Zhao M, Deng H, Wu TT, Kanagavel S, Zhang L, Dandekar S, Papp J, Sun R. PMID: 19073723; PMCID: PMC2643748.
      View in: PubMed   Mentions: 5     Fields:    Translation:AnimalsCells
    43. Integrated weighted gene co-expression network analysis with an application to chronic fatigue syndrome. BMC Syst Biol. 2008 Nov 06; 2:95. Presson AP, Sobel EM, Papp JC, Suarez CJ, Whistler T, Rajeevan MS, Vernon SD, Horvath S. PMID: 18986552; PMCID: PMC2625353.
      View in: PubMed   Mentions: 97     Fields:    Translation:Humans
    44. Merging microsatellite data: enhanced methodology and software to combine genotype data for linkage and association analysis. BMC Bioinformatics. 2008 Jul 21; 9:317. Presson AP, Sobel EM, Pajukanta P, Plaisier C, Weeks DE, Aberg K, Papp JC. PMID: 18644149; PMCID: PMC2515855.
      View in: PubMed   Mentions: 2     Fields:    Translation:Cells
    45. A case-control study of the association of the polymorphisms and haplotypes of DNA ligase I with lung and upper-aerodigestive-tract cancers. Int J Cancer. 2008 Apr 01; 122(7):1630-8. Lee YC, Morgenstern H, Greenland S, Tashkin DP, Papp J, Sinsheimer J, Cao W, Hashibe M, You NC, Mao JT, Cozen W, Mack TM, Zhang ZF. PMID: 18059021; PMCID: PMC2676936.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    46. Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2. Ophthalmic Genet. 2007 Jun; 28(2):57-67. Aldave AJ, Sonmez B, Bourla N, Schultz G, Papp JC, Salem AK, Rayner SA, Yellore VS. PMID: 17558846.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    47. Replication and refinement of linkage of posterior polymorphous corneal dystrophy to the posterior polymorphous corneal dystrophy 1 locus on chromosome 20. Genet Med. 2007 Apr; 9(4):228-34. Yellore VS, Papp JC, Sobel E, Khan MA, Rayner SA, Farber DB, Aldave AJ. PMID: 17438387.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    48. Merging microsatellite data. J Comput Biol. 2006 Jul-Aug; 13(6):1131-47. Presson AP, Sobel E, Lange K, Papp JC. PMID: 16901233.
      View in: PubMed   Mentions: 7     Fields:    Translation:Cells
    49. Chromosome 19p13 loci in Finnish migraine with aura families. Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 05; 132B(1):85-9. Kaunisto MA, Tikka PJ, Kallela M, Leal SM, Papp JC, Korhonen A, Hämäläinen E, Harno H, Havanka H, Nissilä M, Säkö E, Ilmavirta M, Kaprio J, Färkkilä M, Ophoff RA, Palotie A, Wessman M. PMID: 15449251; PMCID: PMC6217809.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    50. Genome-wide mapping of human loci for essential hypertension. Lancet. 2003 Jun 21; 361(9375):2118-23. Caulfield M, Munroe P, Pembroke J, Samani N, Dominiczak A, Brown M, Benjamin N, Webster J, Ratcliffe P, O'Shea S, Papp J, Taylor E, Dobson R, Knight J, Newhouse S, Hooper J, Lee W, Brain N, Clayton D, Lathrop GM, Farrall M, Connell J, MRC British Genetics of Hypertension Study. PMID: 12826435.
      View in: PubMed   Mentions: 66     Fields:    Translation:Humans
    51. A susceptibility locus for migraine with aura, on chromosome 4q24. Am J Hum Genet. 2002 Mar; 70(3):652-62. Wessman M, Kallela M, Kaunisto MA, Marttila P, Sobel E, Hartiala J, Oswell G, Leal SM, Papp JC, Hämäläinen E, Broas P, Joslyn G, Hovatta I, Hiekkalinna T, Kaprio J, Ott J, Cantor RM, Zwart JA, Ilmavirta M, Havanka H, Färkkilä M, Peltonen L, Palotie A. PMID: 11836652; PMCID: PMC384944.
      View in: PubMed   Mentions: 46     Fields:    Translation:HumansCells
    52. Detection and integration of genotyping errors in statistical genetics. Am J Hum Genet. 2002 Feb; 70(2):496-508. Sobel E, Papp JC, Lange K. PMID: 11791215; PMCID: PMC384922.
      View in: PubMed   Mentions: 141     Fields:    Translation:Humans
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