Jeanette Papp, Ph.D.

Jeanette Papp portrait

Bioinformatics in Human Genetics Dr. Papp is the Director of the UCLA Genotyping and Sequencing Core (GenoSeq ), and a member of the UCLA Bioinformatics Core. She came to UCLA in 2000. Prior to that she worked at genome centers in Paris and Oxford. In addition to overseeing data generation and analysis in the Core, her research interests include developing novel bioinformatic solutions for the management and analysis of all types of genetic data within the Department of Human Genetics.

Publications

Zhong M, Lange K, Papp JC, and Ruzong Fan R. A Powerful Score Test to Detect Positive Selection in Genome-wide Scans. Eur J Hum Genet 2010; Epub ahead of print: .
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 YCA, 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,Wang YR, You NCY, Yu SZ, Zhao JK, Zhang ZF. Associations between NBS1 polymorphisms, haplotypes, and smoking-related cancers. Carcinogenesis 2010; 7: 1264-71.
Aldave AJ, Rosenwasser GOD, Yellore VS, Papp JC, Sobel EM, Pham MN, Chen MC, Dandekar S, Sripracha R, Rayner SA, Sassani JW, Gorin MB. 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; [Epub ahead of print]: .
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, Mu1 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. Single nucleotide polymorphisms of 8 inflammation-related genes and their associations with smoking-related cancers. Int J Cancer 2010; Epub ahead of print: .
Zhou JJ, Lange K, Papp JC, Sinsheimer JS A Heterozygote-Homozygote Test of Hardy-Weinberg Equilibrium. Eur J Hum Genet 2009; 17(11): 1495-1500.
Anderson SL, Chung WK, Frezzo J, Papp JC, Ekstein J, Dimauro S, Rubin BY. A novel mutation in NDUFS4 causes Leigh syndrome in an Ashkenazi Jewish family. J Inherit Metab Dis. 2009; [Epub ahead of print]: .
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. Associations between Single Nucleotide Polymorphisms in Double-Stranded DNA Repair Pathway Genes and Familial Breast Cancer. Clin Cancer Res 2009; 15: 2192-2203.
Levine AJ, Singer EJ, Sinsheimer JS, Hinkin CH, Papp J, Dandekar S, Giovanelli A, Shapshak P CCL3 genotype and current depression increase risk of HIV-associated dementia. Neurobehavioral HIV Medicine 2009; 1: 1-7.
Levine AJ, Singer EJ, Sinsheimer JS, Hinkin CH, Papp J, Dandekar S, Giovanelli A, Shapshak P CCL3 genotype and current depression increase risk of HIV-associated dementia. Neurobehavioral HIV Medicine 2009; 1: 1-7.
Aldave AJ, Yellore VS, Vo RC, Kamal KM, Rayner SA, Plaisier CL, Chen MC, Damani MR, Pham MN, Gorin MB, Sobel ES, Papp JC Exclusion of Positional Candidate Gene Coding Region Mutations in the Common Posterior Polymorphous Corneal Dystrophy 1 Candidate Gene Interval. Cornea 2009; 28(7): 801-807.
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 Genetic variation in immune regulation and DNA repair pathways and stomach cancer in China. Cancer Epidemiol Biomarkers Prev 2009; 18(8): 2304-2309.
Pluess AR, Sork VL, Dolan B, Davis FW, Grivet D, Merg K, Papp J, Smouse PE Short distance pollen movement in a wind-pollinated tree, Quercus lobata (Fagaceae). Forest Ecology and Management 2009; 258: 735-744.
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. 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; 122(7): 1630-1638.
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 T, Kanagavel S, Zhang L, Dandekar S, Papp J, Sun R. High-resolution Functional Profiling of a Gammaherpesvirus RTA Locus in the Context of the Viral Genome. J Virol. 2008; 83: 1811.
Presson AP, Sobel EM, Papp JC, Suarez CJ, Whistler T, Rajeevan MS, Vernon SD, Horvath S. Integrated weighted gene co-expression network analysis with an application to chronic fatigue syndrome. BMC Systems Biology 2008; 2: 95.
Presson AP, Sobel EM, Pajukanta P, Plaisier C, Weeks DE, Aberg K, Papp JC. Merging microsatellite data: enhanced methodology and software to combine genotype data for linkage and association analysis. BMC Bioinformatics 2008; 9: 317.
Aldave AJ, Sonmez B, Bourla N, Schultz G, Papp JC, Salem AK, Rayner SA, Yellore VS. Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2. Ophthalmic Genet 2007; 28: 57-67.
Yellore VS, Papp J, Sobel E, Khan MA, Rayner SA, Farber DB, Aldave AJ. Replication and Refinement of Linkage of Posterior Polymorphous Corneal Dystrophy to the PPCD1 Locus on Chromosome 20. Genetics in Medicine 2007; 9: 228-234.
Presson A, Sobel E, Lange, K. Papp JC. Merging Microsatellite Data. Journal of Computational Biology 2006; 13: 1131-1147.
Kaunisto MA, Tikka PJ, Kallela M, Leal SM, Papp JC, Korhonen A, Hamalainen E, Harno H, Havanka H, Nissila M, Sako E, Ilmavirta M, Kaprio J, Farkkila M, Ophoff RA, Palotie A, Wessman M. Chromosome 19p13 loci in Finnish migraine with aura families . Am J Med Genet B Neuropsychiatr Genet 2005; 132B(1): 85-89.
Novak U, Oppliger Leibundgut E, Hager J, Muhlematter D, Jotterand M, Besse C, Leupin N, Ratschiller D, Papp J, Kearsey G, Aebi S, Graber H, Jaggi R, Luthi JM, Meyer-Monard S, Lathrop M, Tobler A, Fey MF. A high-resolution allelotype of B-cell chronic lymphocytic leukemia (B-CLL). Blood. 2002; 100(5): 1787-94.
Wessman M, Kallela M, Kaunisto MA, Marttila P, Sobel E, Hartiala J, Oswell G, Leal SM, Papp JC, Hamalainen E, Broas P, Joslyn G, Hovatta I, Hiekkalinna T, Kaprio J, Ott J, Cantor RM, Zwart JA, Ilmavirta M, Havanka H, Farkkila M, Peltonen L, Palotie A. A susceptibility locus for migraine with aura, on chromosome 4q24. Am J Hum Genet. 2002; 70(3): 652-62.
Sobel E, Papp JC, Lange K Detection and integration of genotyping errors in statistical genetics. Am J Hum Genet. 2002; 70(2): 496-508.
Holm P, Senee V, Julier C, Kockum I, Blanc H, Papp J, Bartsocas C, Dahlquist G, Mato E, de Leiva A, Lathrop M, Luthman H, Nerup J, Pociot F, Ranningen K, Akesson K A genome-wide scan for type 1-diabetes susceptibility genes in Scandinavian families: Identification of new loci with evidence of interactions. Am J Hum Genet. 2001; 69: 1301-1313.
Gedde-Dahl T, Delpine M, Khallouf E, Van Maldergem L, Sobel E, Papp J, Meier M, Mégarbané A, Lathrop M, Capeau J, Magré J Congenital lipodystrophy Berardinelli-Seip reveals a new gene and a new protein. Journal of Investigative Dermatology 2001; 117: 1678.
Magre J, Delepine M, Khallouf E, Gedde-Dahl T Jr, Van Maldergem L, Sobel E, Papp J, Meier M, Megarbane A, Bachy A, Verloes A, d'Abronzo FH, Seemanova E, Assan R, Baudic N, Bourut C, Czernichow P, Huet F, Grigorescu F, de Kerdanet M, Lacombe D, Labrun. Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13. Nature Genetics. 2001; 28(4): 365 - 370.
Caulfield Mark, Munroe Patricia, Pembroke Janine, Samani Nilesh, Dominiczak Anna, Brown Morris, Benjamin Nigel, Webster John, Ratcliffe Peter, O'Shea Suzanne, Papp Jeanette, Taylor Elizabeth, Dobson Richard, Knight Joanne, Newhouse Stephen, Hooper Joel, Lee Wai, Brain Nick, Clayton David, Lathrop G Mark, Farrall Martin, Connell John, Connell John Genome-wide mapping of human loci for essential hypertension.. Lancet. 2003; 361(9375): 2118-23.

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