Jurg Ott - Publications

Rockefeller University, New York, NY, United States 

71 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Imai A, Nakaya A, Fahiminiya S, Tétreault M, Majewski J, Sakata Y, Takashima S, Lathrop M, Ott J. Beyond Homozygosity Mapping: Family-Control analysis based on Hamming distance for prioritizing variants in exome sequencing. Scientific Reports. 5: 12028. PMID 26143870 DOI: 10.1038/srep12028  0.52
2015 Levran O, Randesi M, da Rosa JC, Ott J, Rotrosen J, Adelson M, Kreek MJ. Overlapping dopaminergic pathway genetic susceptibility to heroin and cocaine addictions in African Americans. Annals of Human Genetics. 79: 188-98. PMID 25875614 DOI: 10.1111/ahg.12104  0.52
2014 Levran O, Peles E, Randesi M, Correa da Rosa J, Ott J, Rotrosen J, Adelson M, Kreek MJ. Dopaminergic pathway polymorphisms and heroin addiction: further support for association of CSNK1E variants. Pharmacogenomics. 15: 2001-9. PMID 25521358 DOI: 10.2217/pgs.14.145  0.44
2014 Zhang Y, Mayer-Blackwell B, Schlussman SD, Randesi M, Butelman ER, Ho A, Ott J, Kreek MJ. Extended access oxycodone self-administration and neurotransmitter receptor gene expression in the dorsal striatum of adult C57BL/6 J mice. Psychopharmacology. 231: 1277-87. PMID 24221825 DOI: 10.1007/s00213-013-3306-3  0.44
2013 Erdmann J, Stark K, Esslinger UB, Rumpf PM, Koesling D, de Wit C, Kaiser FJ, Braunholz D, Medack A, Fischer M, Zimmermann ME, Tennstedt S, Graf E, Eck S, Aherrahrou Z, ... ... Ott J, et al. Dysfunctional nitric oxide signalling increases risk of myocardial infarction. Nature. 504: 432-6. PMID 24213632 DOI: 10.1038/nature12722  0.44
2013 Levran O, Peles E, Randesi M, Shu X, Ott J, Shen PH, Adelson M, Kreek MJ. Association of genetic variation in pharmacodynamic factors with methadone dose required for effective treatment of opioid addiction. Pharmacogenomics. 14: 755-68. PMID 23651024 DOI: 10.2217/pgs.13.58  0.44
2013 Suo C, Toulopoulou T, Bramon E, Walshe M, Picchioni M, Murray R, Ott J. Analysis of multiple phenotypes in genome-wide genetic mapping studies. Bmc Bioinformatics. 14: 151. PMID 23639181 DOI: 10.1186/1471-2105-14-151  0.44
2013 Proudnikov D, Randesi M, Levran O, Yuferov V, Crystal H, Ho A, Ott J, Kreek MJ. Polymorphisms of the kappa opioid receptor and prodynorphin genes: HIV risk and HIV natural history. Journal of Acquired Immune Deficiency Syndromes (1999). 63: 17-26. PMID 23392455 DOI: 10.1097/QAI.0b013e318285cd0c  0.44
2013 Yuferov V, Ho A, Morgello S, Yang Y, Ott J, Kreek MJ. Expression of ephrin receptors and ligands in postmortem brains of HIV-infected subjects with and without cognitive impairment. Journal of Neuroimmune Pharmacology : the Official Journal of the Society On Neuroimmune Pharmacology. 8: 333-44. PMID 23314923 DOI: 10.1007/s11481-012-9429-1  0.44
2012 Shen Y, Liu Z, Ott J. Support Vector Machines with L1 penalty for detecting gene-gene interactions International Journal of Data Mining and Bioinformatics. 6: 463-470. PMID 23155775 DOI: 10.1504/IJDMB.2012.049300  0.44
2012 Ott J, Liu Z, Shen Y. Challenging false discovery rate: A partition test based on p values in human case-control association studies Human Heredity. 74: 45-50. PMID 23154528 DOI: 10.1159/000343752  0.44
2012 Ott J, Hoh J. Scan statistics in human gene mapping. American Journal of Human Genetics. 91: 970; author reply 97. PMID 23122592 DOI: 10.1016/j.ajhg.2012.07.026  0.52
2012 Proudnikov D, Randesi M, Levran O, Crystal H, Dorn M, Ott J, Ho A, Kreek MJ. Association of polymorphisms of the mu opioid receptor gene with the severity of HIV infection and response to HIV treatment. The Journal of Infectious Diseases. 205: 1745-56. PMID 22457278 DOI: 10.1093/infdis/jis264  0.44
2011 Schäffer AA, Lemire M, Ott J, Lathrop GM, Weeks DE. Coordinated conditional simulation with SLINK and SUP of many markers linked or associated to a trait in large pedigrees. Human Heredity. 71: 126-34. PMID 21734403 DOI: 10.1159/000324177  0.72
2011 Lee KT, Byun MJ, Kang KS, Park EW, Lee SH, Cho S, Kim H, Kim KW, Lee T, Park JE, Park W, Shin D, Park HS, Jeon JT, Choi BH, ... ... Ott J, et al. Neuronal genes for subcutaneous fat thickness in human and pig are identified by local genomic sequencing and combined SNP association study. Plos One. 6: e16356. PMID 21311593 DOI: 10.1371/journal.pone.0016356  0.52
2011 Kramer PL, Xu H, Woltjer RL, Westaway SK, Clark D, Erten-Lyons D, Kaye JA, Welsh-Bohmer KA, Troncoso JC, Markesbery WR, Petersen RC, Turner RS, Kukull WA, Bennett DA, Galasko D, ... ... Ott J, et al. Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study. Neurobiology of Aging. 32: 2113-22. PMID 20452100 DOI: 10.1016/j.neurobiolaging.2010.01.010  0.52
2010 Ott J, Macciardi F, Shen Y, Carta MG, Murru A, Triunfo R, Robledo R, Rinaldi A, Contu L, Siniscalco M. Pilot study on schizophrenia in Sardinia. Human Heredity. 70: 92-6. PMID 20558996 DOI: 10.1159/000313844  0.52
2010 Nielsen DA, Ji F, Yuferov V, Ho A, He C, Ott J, Kreek MJ. Genome-wide association study identifies genes that may contribute to risk for developing heroin addiction. Psychiatric Genetics. 20: 207-14. PMID 20520587 DOI: 10.1097/YPG.0b013e32833a2106  0.52
2010 Klein ML, Ferris FL, Francis PJ, Lindblad AS, Chew EY, Hamon SC, Ott J. Progression of geographic atrophy and genotype in age-related macular degeneration. Ophthalmology. 117: 1554-9, 1559.e1. PMID 20381870 DOI: 10.1016/j.ophtha.2009.12.012  0.52
2010 Nielsen DA, Hamon S, Yuferov V, Jackson C, Ho A, Ott J, Kreek MJ. Ethnic diversity of DNA methylation in the OPRM1 promoter region in lymphocytes of heroin addicts. Human Genetics. 127: 639-49. PMID 20237803 DOI: 10.1007/s00439-010-0807-6  0.52
2010 Briant JA, Nielsen DA, Proudnikov D, Londono D, Ho A, Ott J, Kreek MJ. Evidence for association of two variants of the nociceptin/orphanin FQ receptor gene OPRL1 with vulnerability to develop opiate addiction in Caucasians. Psychiatric Genetics. 20: 65-72. PMID 20032820 DOI: 10.1097/YPG.0b013e32833511f6  0.52
2009 Risch N, Herrell R, Lehner T, Liang KY, Eaves L, Hoh J, Griem A, Kovacs M, Ott J, Merikangas KR. Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: a meta-analysis. Jama. 301: 2462-71. PMID 19531786 DOI: 10.1001/jama.2009.878  0.52
2009 Yuferov V, Ji F, Nielsen DA, Levran O, Ho A, Morgello S, Shi R, Ott J, Kreek MJ. A functional haplotype implicated in vulnerability to develop cocaine dependence is associated with reduced PDYN expression in human brain. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 34: 1185-97. PMID 18923396 DOI: 10.1038/npp.2008.187  0.52
2009 Nielsen DA, Yuferov V, Hamon S, Jackson C, Ho A, Ott J, Kreek MJ. Increased OPRM1 DNA methylation in lymphocytes of methadone-maintained former heroin addicts. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 34: 867-73. PMID 18650805 DOI: 10.1038/npp.2008.108  0.52
2008 Kim IK, Ji F, Morrison MA, Adams S, Zhang Q, Lane AM, Capone A, Dryja TP, Ott J, Miller JW, DeAngelis MM. Comprehensive analysis of CRP, CFH Y402H and environmental risk factors on risk of neovascular age-related macular degeneration. Molecular Vision. 14: 1487-95. PMID 18704199  0.52
2008 Francis PJ, Appukuttan B, Simmons E, Landauer N, Stoddard J, Hamon S, Ott J, Ferguson B, Klein M, Stout JT, Neuringer M. Rhesus monkeys and humans share common susceptibility genes for age-related macular disease. Human Molecular Genetics. 17: 2673-80. PMID 18535016 DOI: 10.1093/hmg/ddn167  0.52
2008 Levran O, O'Hara K, Peles E, Li D, Barral S, Ray B, Borg L, Ott J, Adelson M, Kreek MJ. ABCB1 (MDR1) genetic variants are associated with methadone doses required for effective treatment of heroin dependence. Human Molecular Genetics. 17: 2219-27. PMID 18424454 DOI: 10.1093/hmg/ddn122  0.52
2008 Klein ML, Francis PJ, Rosner B, Reynolds R, Hamon SC, Schultz DW, Ott J, Seddon JM. CFH and LOC387715/ARMS2 genotypes and treatment with antioxidants and zinc for age-related macular degeneration. Ophthalmology. 115: 1019-25. PMID 18423869 DOI: 10.1016/j.ophtha.2008.01.036  0.52
2008 Bacolod MD, Schemmann GS, Wang S, Shattock R, Giardina SF, Zeng Z, Shia J, Stengel RF, Gerry N, Hoh J, Kirchhoff T, Gold B, Christman MF, Offit K, Gerald WL, ... ... Ott J, et al. The signatures of autozygosity among patients with colorectal cancer. Cancer Research. 68: 2610-21. PMID 18375840 DOI: 10.1158/0008-5472.CAN-07-5250  0.52
2008 Proudnikov D, Hamon S, Ott J, Kreek MJ. Association of polymorphisms in the melanocortin receptor type 2 (MC2R, ACTH receptor) gene with heroin addiction. Neuroscience Letters. 435: 234-9. PMID 18359160 DOI: 10.1016/j.neulet.2008.02.042  0.52
2008 Oosterhuis BE, LaForge KS, Proudnikov D, Ho A, Nielsen DA, Gianotti R, Barral S, Gordon D, Leal SM, Ott J, Kreek MJ. Catechol-O-methyltransferase (COMT) gene variants: possible association of the Val158Met variant with opiate addiction in Hispanic women. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 793-8. PMID 18270997 DOI: 10.1002/ajmg.b.30716  0.52
2008 Nielsen DA, Barral S, Proudnikov D, Kellogg S, Ho A, Ott J, Kreek MJ. TPH2 and TPH1: association of variants and interactions with heroin addiction. Behavior Genetics. 38: 133-50. PMID 18181017 DOI: 10.1007/s10519-007-9187-7  0.52
2008 Deangelis MM, Ji F, Adams S, Morrison MA, Harring AJ, Sweeney MO, Capone A, Miller JW, Dryja TP, Ott J, Kim IK. Alleles in the HtrA serine peptidase 1 gene alter the risk of neovascular age-related macular degeneration. Ophthalmology. 115: 1209-1215.e7. PMID 18164066 DOI: 10.1016/j.ophtha.2007.10.032  0.52
2007 Francis PJ, Schultz DW, Hamon S, Ott J, Weleber RG, Klein ML. Haplotypes in the complement factor H (CFH) gene: associations with drusen and advanced age-related macular degeneration. Plos One. 2: e1197. PMID 18043728 DOI: 10.1371/journal.pone.0001197  0.52
2007 Williams TJ, LaForge KS, Gordon D, Bart G, Kellogg S, Ott J, Kreek MJ. Prodynorphin gene promoter repeat associated with cocaine/alcohol codependence. Addiction Biology. 12: 496-502. PMID 17559549 DOI: 10.1111/j.1369-1600.2007.00069.x  0.52
2007 Francis PJ, George S, Schultz DW, Rosner B, Hamon S, Ott J, Weleber RG, Klein ML, Seddon JM. The LOC387715 gene, smoking, body mass index, environmental associations with advanced age-related macular degeneration. Human Heredity. 63: 212-8. PMID 17347568 DOI: 10.1159/000100046  0.52
2006 Barral S, Francis PJ, Schultz DW, Schain MB, Haynes C, Majewski J, Ott J, Acott T, Weleber RG, Klein ML. Expanded genome scan in extended families with age-related macular degeneration. Investigative Ophthalmology & Visual Science. 47: 5453-9. PMID 17122136 DOI: 10.1167/iovs.06-0655  0.52
2006 Cheung KM, Chan D, Karppinen J, Chen Y, Jim JJ, Yip SP, Ott J, Wong KK, Sham P, Luk KD, Cheah KS, Leong JC, Song YQ. Association of the Taq I allele in vitamin D receptor with degenerative disc disease and disc bulge in a Chinese population. Spine. 31: 1143-8. PMID 16648751 DOI: 10.1097/01.brs.0000216530.41838.d3  0.52
2006 Proudnikov D, LaForge KS, Hofflich H, Levenstien M, Gordon D, Barral S, Ott J, Kreek MJ. Association analysis of polymorphisms in serotonin 1B receptor (HTR1B) gene with heroin addiction: a comparison of molecular and statistically estimated haplotypes. Pharmacogenetics and Genomics. 16: 25-36. PMID 16344719  0.52
2005 Jim JJ, Noponen-Hietala N, Cheung KM, Ott J, Karppinen J, Sahraravand A, Luk KD, Yip SP, Sham PC, Song YQ, Leong JC, Cheah KS, Ala-Kokko L, Chan D. The TRP2 allele of COL9A2 is an age-dependent risk factor for the development and severity of intervertebral disc degeneration. Spine. 30: 2735-42. PMID 16371896 DOI: 10.1097/01.brs.0000190828.85331.ef  0.52
2005 Helms C, Saccone NL, Cao L, Daw JA, Cao K, Hsu TM, Taillon-Miller P, Duan S, Gordon D, Pierce B, Ott J, Rice J, Fernandez-Vina MA, Kwok PY, Menter A, et al. Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR. Human Genetics. 118: 466-76. PMID 16235096 DOI: 10.1007/s00439-005-0048-2  0.52
2005 Markovic D, Tang X, Guruju M, Levenstien MA, Hoh J, Kumar A, Ott J. Association of angiotensinogen gene polymorphisms with essential hypertension in African-Americans and Caucasians. Human Heredity. 60: 89-96. PMID 16210856 DOI: 10.1159/000088657  0.52
2005 Bleiber G, May M, Martinez R, Meylan P, Ott J, Beckmann JS, Telenti A. Use of a combined ex vivo/in vivo population approach for screening of human genes involved in the human immunodeficiency virus type 1 life cycle for variants influencing disease progression Journal of Virology. 79: 12674-12680. PMID 16188970 DOI: 10.1128/JVI.79.20.12674-12680.2005  0.52
2005 Levran O, Attwooll C, Henry RT, Milton KL, Neveling K, Rio P, Batish SD, Kalb R, Velleuer E, Barral S, Ott J, Petrini J, Schindler D, Hanenberg H, Auerbach AD. The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia. Nature Genetics. 37: 931-3. PMID 16116424 DOI: 10.1038/ng1624  0.52
2005 Zareparsi S, Branham KE, Li M, Shah S, Klein RJ, Ott J, Hoh J, Abecasis GR, Swaroop A. Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration. American Journal of Human Genetics. 77: 149-53. PMID 15895326 DOI: 10.1086/431426  0.52
2005 Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, Haynes C, Henning AK, SanGiovanni JP, Mane SM, Mayne ST, Bracken MB, Ferris FL, Ott J, Barnstable C, Hoh J. Complement factor H polymorphism in age-related macular degeneration. Science (New York, N.Y.). 308: 385-9. PMID 15761122 DOI: 10.1126/science.1109557  0.52
2005 Bart G, Kreek MJ, Ott J, LaForge KS, Proudnikov D, Pollak L, Heilig M. Increased attributable risk related to a functional mu-opioid receptor gene polymorphism in association with alcohol dependence in central Sweden. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 30: 417-22. PMID 15525999 DOI: 10.1038/sj.npp.1300598  0.52
2004 Yuferov V, Fussell D, LaForge KS, Nielsen DA, Gordon D, Ho A, Leal SM, Ott J, Kreek MJ. Redefinition of the human kappa opioid receptor gene (OPRK1) structure and association of haplotypes with opiate addiction. Pharmacogenetics. 14: 793-804. PMID 15608558 DOI: 10.1097/00008571-200412000-00002  0.52
2003 Wille A, Hoh J, Ott J. Sum statistics for the joint detection of multiple disease loci in case-control association studies with SNP markers. Genetic Epidemiology. 25: 350-9. PMID 14639704 DOI: 10.1002/gepi.10263  0.52
2001 Hoh J, Wille A, Ott J. Trimming, weighting, and grouping SNPs in human case-control association studies. Genome Research. 11: 2115-9. PMID 11731502 DOI: 10.1101/gr.204001  0.52
2001 Paassilta P, Lohiniva J, Göring HH, Perälä M, Räinä SS, Karppinen J, Hakala M, Palm T, Kröger H, Kaitila I, Vanharanta H, Ott J, Ala-Kokko L. Identification of a novel common genetic risk factor for lumbar disk disease. Jama. 285: 1843-9. PMID 11308397  0.52
2000 Hoh J, Wille A, Zee R, Cheng S, Reynolds R, Lindpaintner K, Ott J. Selecting SNPs in two-stage analysis of disease association data: a model-free approach. Annals of Human Genetics. 64: 413-7. PMID 11281279 DOI: 10.1017/S0003480000008290  0.52
1999 Schaid DJ, Buetow K, Weeks DE, Wijsman E, Guo SW, Ott J, Dahl C. Discovery of cancer susceptibility genes: study designs, analytic approaches, and trends in technology. Journal of the National Cancer Institute. Monographs. 1-16. PMID 10854480  0.72
1999 Le Saux O, Urban Z, Göring HH, Csiszar K, Pope FM, Richards A, Pasquali-Ronchetti I, Terry S, Bercovitch L, Lebwohl MG, Breuning M, van den Berg P, Kornet L, Doggett N, Ott J, et al. Pseudoxanthoma elasticum maps to an 820-kb region of the p13.1 region of chromosome 16. Genomics. 62: 1-10. PMID 10585762 DOI: 10.1006/geno.1999.5925  0.52
1998 Gieser L, Fujita R, Göring HHH, Ott J, Hoffman DR, Cideciyan AV, Birch DG, Jacobson SG, Swaroop A. A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27 American Journal of Human Genetics. 63: 1439-1447. PMID 9792872 DOI: 10.1086/302121  0.52
1995 Speer MC, Terwilliger JD, Ott J. Data simulation for GAW9 problems 1 and 2 Genetic Epidemiology. 12: 561-564. PMID 8787973 DOI: 10.1002/gepi.1370120606  0.44
1994 Weeks DE, Ott J, Lathrop GM. Detection of genetic interference: simulation studies and mouse data. Genetics. 136: 1217-26. PMID 8005426  0.72
1994 Tienari PJ, Terwilliger JD, Ott J, Palo J, Peltonen L. Two-locus linkage analysis in multiple sclerosis (MS). Genomics. 19: 320-5. PMID 7514567 DOI: 10.1006/geno.1994.1064  0.64
1993 Weeks DE, Lathrop GM, Ott J. Multipoint mapping under genetic interference. Human Heredity. 43: 86-97. PMID 8359820  0.72
1993 Terwilliger JD, Ott J. A novel polylocus method for linkage analysis using the lod-score or affected sib-pair method. Genetic Epidemiology. 10: 477-82. PMID 8314047 DOI: 10.1002/gepi.1370100625  0.64
1993 Terwilliger JD, Speer M, Ott J. Chromosome-based method for rapid computer simulation in human genetic linkage analysis. Genetic Epidemiology. 10: 217-24. PMID 8224802 DOI: 10.1002/gepi.1370100402  0.64
1993 Schork NJ, Boehnke M, Terwilliger JD, Ott J. Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits. American Journal of Human Genetics. 53: 1127-36. PMID 8213836  0.64
1992 Terwilliger JD, Ott J. A multisample bootstrap approach to the estimation of maximized-over-models lod score distributions. Cytogenetics and Cell Genetics. 59: 142-4. PMID 1737483  0.64
1992 Weeks DE, Lehner T, Ott J. Preliminary ranking procedures for multilocus ordering based on radiation hybrid data. Cytogenetics and Cell Genetics. 59: 125-7. PMID 1737477  0.72
1992 Terwilliger JD, Ding Y, Ott J. On the relative importance of marker heterozygosity and intermarker distance in gene mapping. Genomics. 13: 951-6. PMID 1505986  0.64
1992 Terwilliger JD, Ott J. A haplotype-based 'haplotype relative risk' approach to detecting allelic associations. Human Heredity. 42: 337-46. PMID 1493912  0.64
1991 Delisi LE, Crow TJ, Davies KE, Terwilliger JD, Ott J, Ram R, Flint T, Boccio A. No genetic linkage detected for schizophrenia to Xq27-q28. The British Journal of Psychiatry : the Journal of Mental Science. 158: 630-4. PMID 1677599  0.52
1990 Weeks DE, Lehner T, Squires-Wheeler E, Kaufmann C, Ott J. Measuring the inflation of the lod score due to its maximization over model parameter values in human linkage analysis. Genetic Epidemiology. 7: 237-43. PMID 2227370 DOI: 10.1002/gepi.1370070402  0.72
1990 Weeks DE, Brzustowicz L, Squires-Wheeler E, Cornblatt B, Lehner T, Stefanovich M, Bassett A, Gilliam TC, Ott J, Erlenmeyer-Kimling L. Report of a workshop on genetic linkage studies in schizophrenia. Schizophrenia Bulletin. 16: 673-86. PMID 2077644 DOI: 10.1093/schbul/16.4.673  0.44
1989 Weeks DE, Ott J. Risk calculations under heterogeneity. American Journal of Human Genetics. 45: 819-21. PMID 2816945  0.72
1989 Hsiao K, Baker HF, Crow TJ, Poulter M, Owen F, Terwilliger JD, Westaway D, Ott J, Prusiner SB. Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome. Nature. 338: 342-5. PMID 2564168 DOI: 10.1038/338342a0  0.64
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