Jurg Ott - Publications

Affiliations: 
Rockefeller University, New York, NY, United States 

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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
Low-probability matches
1997 Göring HH, Ott J. Relationship estimation in affected sib pair analysis of late-onset diseases. European Journal of Human Genetics : Ejhg. 5: 69-77. PMID 9195155  0.2
2007 Martinez-Mir A, Zlotogorski A, Gordon D, Petukhova L, Mo J, Gilliam TC, Londono D, Haynes C, Ott J, Hordinsky M, Nanova K, Norris D, Price V, Duvic M, Christiano AM. Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata. American Journal of Human Genetics. 80: 316-28. PMID 17236136 DOI: 10.1086/511442  0.16
2019 Levran O, Randesi M, Rotrosen J, Ott J, Adelson M, Kreek MJ. A 3' UTR SNP rs885863, a cis-eQTL for the circadian gene VIPR2 and lincRNA 689, is associated with opioid addiction. Plos One. 14: e0224399. PMID 31689297 DOI: 10.1371/journal.pone.0224399  0.01
2019 Butelman ER, Chen CY, Conybeare RA, Brown KG, Fry RS, Kimani R, Correa da Rosa J, Ott J, Kreek MJ. Are trait impulsivity and exposure to cannabis or alcohol associated with the age of trajectory of cocaine use? A gender-specific dimensional analysis in humans with cocaine dependence diagnosis. Experimental and Clinical Psychopharmacology. PMID 31424236 DOI: 10.1037/pha0000314  0.01
2019 Imai-Okazaki A, Li Y, Horpaopan S, Riazalhosseini Y, Garshasbi M, Mosse YP, Zhang D, Schrauwen I, Sharma A, Fann CSJ, Leal SM, Lathrop M, Ott J. Heterozygosity mapping for human dominant trait variants. Human Mutation. PMID 31018026 DOI: 10.1002/humu.23765  0.01
2019 Randesi M, van den Brink W, Levran O, Blanken P, van Ree JM, Ott J, Kreek MJ. VMAT2 gene (SLC18A2) variants associated with a greater risk for developing opioid dependence. Pharmacogenomics. PMID 30983500 DOI: 10.2217/pgs-2018-0137  0.01
2019 Yuferov V, Randesi M, Butelman ER, van den Brink W, Blanken P, van Ree JM, Ott J, Kreek MJ. Association of variants of prodynorphin promoter 68-bp repeats in caucasians with opioid dependence diagnosis: Effect on age trajectory of heroin use. Neuroscience Letters. 704: 100-105. PMID 30936032 DOI: 10.1016/j.neulet.2019.03.038  0.01
2019 Peles E, Levran O, Randesi M, Ott J, Kreek MJ, Adelson M. Genetic Variant in the CRH-binding Protein Gene (CRHBP) is Associated With Cessation of Cocaine Use in Methadone Maintenance Patients With Opioid Addiction. Journal of Addiction Medicine. PMID 30844877 DOI: 10.1097/ADM.0000000000000515  0.01
2018 Javanrouh N, Soltanian AR, Tapak L, Azizi F, Ott J, Daneshpour MS. A novel association of rs13334070 in the RPGRIP1L gene with adiposity factors discovered by joint linkage and linkage disequilibrium analysis in Iranian pedigrees: Tehran Cardiometabolic Genetic Study (TCGS). Genetic Epidemiology. PMID 30597647 DOI: 10.1002/gepi.22179  0.01
2018 Butelman ER, Chen CY, Fry RS, Kimani R, Levran O, Ott J, Correa da Rosa J, Kreek MJ. Re-evaluation of the KMSK scales, rapid dimensional measures of self-exposure to specific drugs: Gender-specific features. Drug and Alcohol Dependence. 190: 179-187. PMID 30041093 DOI: 10.1016/j.drugalcdep.2018.05.028  0.01
2018 Xu K, Liu X, Ott J, Jiang F, Zhang W, Wang L, Zhao J, Wang X. The combined effects of cardiovascular disease related SNPs on ischemic stroke. Journal of the Neurological Sciences. 388: 141-145. PMID 29627009 DOI: 10.1016/j.jns.2018.03.013  0.01
2018 Randesi M, van den Brink W, Levran O, Yuferov V, Blanken P, van Ree JM, Ott J, Kreek MJ. Dopamine gene variants in opioid addiction: comparison of dependent patients, nondependent users and healthy controls. Pharmacogenomics. 19: 95-104. PMID 29210332 DOI: 10.2217/pgs-2017-0134  0.01
2017 Imai A, Kohda M, Kobayashi K, Hirata T, Sakata Y, Murayama K, Ohtake A, Okazaki Y, Nakaya A, Ott J. HDR-del: A tool based on Hamming distance for prioritizing pathogenic chromosomal deletions in exome sequencing. Human Mutation. PMID 28722338 DOI: 10.1002/humu.23298  0.01
2017 Ott J. To aggregate or not, that is the question. A commentary on single-nucleotide variant proportion in genes: a new concept to explore major depression based on DNA sequencing data. Journal of Human Genetics. PMID 28148923 DOI: 10.1038/jhg.2017.7  0.01
2016 Randesi M, van den Brink W, Levran O, Blanken P, Butelman ER, Yuferov V, da Rosa JC, Ott J, van Ree JM, Kreek MJ. Variants of opioid system genes are associated with non-dependent opioid use and heroin dependence. Drug and Alcohol Dependence. 168: 164-169. PMID 27664554 DOI: 10.1016/j.drugalcdep.2016.08.634  0.01
2016 Imai A, Kohda M, Nakaya A, Sakata Y, Murayama K, Ohtake A, Lathrop M, Okazaki Y, Ott J. HDR: a statistical two-step approach successfully identifies disease genes in autosomal recessive families. Journal of Human Genetics. PMID 27357426 DOI: 10.1038/jhg.2016.85  0.01
2016 Levran O, Randesi M, Peles E, Correa da Rosa J, Ott J, Rotrosen J, Adelson M, Kreek MJ. African-specific variability in the acetylcholine muscarinic receptor M4: association with cocaine and heroin addiction. Pharmacogenomics. PMID 27269905 DOI: 10.2217/pgs-2016-0028  0.01
2016 Levran O, Peles E, Randesi M, Correa da Rosa J, Ott J, Rotrosen J, Adelson M, Kreek MJ. Glutamatergic and GABAergic susceptibility loci for heroin and cocaine addiction in subjects of African and European ancestry. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 64: 118-23. PMID 26277529 DOI: 10.1016/j.pnpbp.2015.08.003  0.01
2015 Ott J. Polygenic Models for Risk Prediction in Human Genetics. Human Heredity. 80: 162-4. PMID 27576755 DOI: 10.1159/000447593  0.01
2015 Levran O, Peles E, Randesi M, Correa da Rosa J, Ott J, Rotrosen J, Adelson M, Kreek MJ. Synaptic Plasticity and Signal Transduction Gene Polymorphisms and Vulnerability to Drug Addictions in Populations of European or African Ancestry. Cns Neuroscience & Therapeutics. 21: 898-904. PMID 26384852 DOI: 10.1111/cns.12450  0.01
2015 Levran O, Peles E, Randesi M, Correa da Rosa J, Ott J, Rotrosen J, Adelson M, Kreek MJ. Susceptibility loci for heroin and cocaine addiction in the serotonergic and adrenergic pathways in populations of different ancestry. Pharmacogenomics. 1-14. PMID 26227246 DOI: 10.2217/pgs.15.86  0.01
2015 Li Y, Cagirici HB, Horpaopan S, Ott J, Imai A, Majewski J, Lathrop M. Leveling the Playing Field in Homozygosity Mapping Using Map Distances. Annals of Human Genetics. PMID 26179257 DOI: 10.1111/ahg.12125  0.01
2015 Wang J, Tao Y, Song F, Sun Y, Ott J, Saffen D. Common Regulatory Variants of CYFIP1 Contribute to Susceptibility for Autism Spectrum Disorder (ASD) and Classical Autism. Annals of Human Genetics. PMID 26094621 DOI: 10.1111/ahg.12121  0.01
2015 Maass PG, Aydin A, Luft FC, Schächterle C, Weise A, Stricker S, Lindschau C, Vaegler M, Qadri F, Toka HR, Schulz H, Krawitz PM, Parkhomchuk D, Hecht J, Hollfinger I, ... ... Ott J, et al. PDE3A mutations cause autosomal dominant hypertension with brachydactyly. Nature Genetics. 47: 647-53. PMID 25961942 DOI: 10.1038/ng.3302  0.01
2015 Ott J, Wang J, Leal SM. Genetic linkage analysis in the age of whole-genome sequencing. Nature Reviews. Genetics. 16: 275-84. PMID 25824869 DOI: 10.1038/nrg3908  0.01
2015 Juyal G, Negi S, Sood A, Gupta A, Prasad P, Senapati S, Zaneveld J, Singh S, Midha V, van Sommeren S, Weersma RK, Ott J, Jain S, Juyal RC, Thelma BK. Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis. Gut. 64: 571-9. PMID 24837172 DOI: 10.1136/gutjnl-2013-306625  0.01
2014 Zhang Q, Long Q, Ott J. AprioriGWAS, a new pattern mining strategy for detecting genetic variants associated with disease through interaction effects. Plos Computational Biology. 10: e1003627. PMID 24901472 DOI: 10.1371/journal.pcbi.1003627  0.01
2014 Levran O, Randesi M, Li Y, Rotrosen J, Ott J, Adelson M, Kreek MJ. Drug addiction and stress-response genetic variability: association study in African Americans. Annals of Human Genetics. 78: 290-8. PMID 24766650 DOI: 10.1111/ahg.12064  0.01
2013 Li Y, Zhang K, Chen H, Sun F, Xu J, Wu Z, Li P, Zhang L, Du Y, Luan H, Li X, Wu L, Li H, Wu H, Li X, ... ... Ott J, et al. A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23. Nature Genetics. 45: 1361-5. PMID 24097066 DOI: 10.1038/ng.2779  0.01
2013 Negi S, Juyal G, Senapati S, Prasad P, Gupta A, Singh S, Kashyap S, Kumar A, Kumar U, Gupta R, Kaur S, Agrawal S, Aggarwal A, Ott J, Jain S, et al. A genome-wide association study reveals ARL15, a novel non-HLA susceptibility gene for rheumatoid arthritis in North Indians. Arthritis and Rheumatism. 65: 3026-35. PMID 23918589 DOI: 10.1002/art.38110  0.01
2013 Thomas BN, Thakur TJ, Yi L, Guindo A, Diallo DA, Ott J. Extensive ethnogenomic diversity of endothelial nitric oxide synthase (eNOS) polymorphisms. Gene Regulation and Systems Biology. 7: 1-10. PMID 23400313 DOI: 10.4137/GRSB.S10857  0.01
2012 Ott J, Sun D. Multilocus association analysis under polygenic models. International Journal of Data Mining and Bioinformatics. 6: 482-9. PMID 23155777  0.01
2012 Park T, Ott J. Data mining for high throughput data from genome-wide association studies. International Journal of Data Mining and Bioinformatics. 6: 461-2. PMID 23155774  0.01
2012 Guo L, Zhang W, Chang S, Zhang L, Ott J, Wang J. MK4MDD: a multi-level knowledge base and analysis platform for major depressive disorder. Plos One. 7: e46335. PMID 23071556 DOI: 10.1371/journal.pone.0046335  0.01
2012 Zhang L, Chang S, Li Z, Zhang K, Du Y, Ott J, Wang J. ADHDgene: a genetic database for attention deficit hyperactivity disorder. Nucleic Acids Research. 40: D1003-9. PMID 22080511 DOI: 10.1093/nar/gkr992  0.01
2011 Liu Z, Shen Y, Ott J. Multilocus association mapping using generalized ridge logistic regression. Bmc Bioinformatics. 12: 384. PMID 21958005 DOI: 10.1186/1471-2105-12-384  0.01
2011 Ott J, Wang J. Multiple phenotypes in genome-wide genetic mapping studies. Protein & Cell. 2: 519-22. PMID 21647556 DOI: 10.1007/s13238-011-1059-5  0.01
2011 Ott J, Kamatani Y, Lathrop M. Family-based designs for genome-wide association studies. Nature Reviews. Genetics. 12: 465-74. PMID 21629274 DOI: 10.1038/nrg2989  0.01
2011 Ott J. William Allan Award Address: On the role and soul of a statistical geneticist. American Journal of Human Genetics. 88: 264-8. PMID 21516615  0.01
2011 Ott J. Writings on genetic linkage in the annals. Annals of Human Genetics. 75: 344-7. PMID 21488851 DOI: 10.1111/j.1469-1809.2011.00645.x  0.01
2010 Korvala J, Hartikka H, Pihlajamäki H, Solovieva S, Ruohola JP, Sahi T, Barral S, Ott J, Ala-Kokko L, Männikkö M. Genetic predisposition for femoral neck stress fractures in military conscripts. Bmc Genetics. 11: 95. PMID 20961463 DOI: 10.1186/1471-2156-11-95  0.01
2010 Shen Y, Liu Z, Ott J. Systematic removal of outliers to reduce heterogeneity in case-control association studies. Human Heredity. 70: 227-31. PMID 20924194 DOI: 10.1159/000320422  0.01
2010 Wu L, Xi B, Zhang M, Shen Y, Zhao X, Cheng H, Hou D, Sun D, Ott J, Wang X, Mi J. Associations of six single nucleotide polymorphisms in obesity-related genes with BMI and risk of obesity in Chinese children. Diabetes. 59: 3085-9. PMID 20843981 DOI: 10.2337/db10-0273  0.01
2010 Cho S, Kim K, Kim YJ, Lee JK, Cho YS, Lee JY, Han BG, Kim H, Ott J, Park T. Joint identification of multiple genetic variants via elastic-net variable selection in a genome-wide association analysis. Annals of Human Genetics. 74: 416-28. PMID 20642809 DOI: 10.1111/j.1469-1809.2010.00597.x  0.01
2010 Wu C, Xu B, Yuan P, Ott J, Guan Y, Liu Y, Liu Z, Shen Y, Yu D, Lin D. Genome-wide examination of genetic variants associated with response to platinum-based chemotherapy in patients with small-cell lung cancer. Pharmacogenetics and Genomics. 20: 389-95. PMID 20463552 DOI: 10.1097/FPC.0b013e32833a6890  0.01
2010 Wang G, Yang Y, Ott J. Genome-wide conditional search for epistatic disease-predisposing variants in human association studies. Human Heredity. 70: 34-41. PMID 20413980 DOI: 10.1159/000293722  0.01
2010 Nash GM, Gimbel M, Cohen AM, Zeng ZS, Ndubuisi MI, Nathanson DR, Ott J, Barany F, Paty PB. KRAS mutation and microsatellite instability: two genetic markers of early tumor development that influence the prognosis of colorectal cancer. Annals of Surgical Oncology. 17: 416-24. PMID 19813061 DOI: 10.1245/s10434-009-0713-0  0.01
2009 Matthews AG, Li J, He C, Ott J, Andrade Md. Adjusting for HLA-DRbeta1 in a genome-wide association analysis of rheumatoid arthritis and related biomarkers. Bmc Proceedings. 3: S12. PMID 20017985  0.01
2009 Long Q, Zhang Q, Ott J. Detecting disease-associated genotype patterns. Bmc Bioinformatics. 10: S75. PMID 19208180 DOI: 10.1186/1471-2105-10-S1-S75  0.01
2009 Shaaban S, Matsuo T, Fujiwara H, Itoshima E, Furuse T, Hasebe S, Zhang Q, Ott J, Ohtsuki H. Chromosomes 4q28.3 and 7q31.2 as new susceptibility loci for comitant strabismus. Investigative Ophthalmology & Visual Science. 50: 654-61. PMID 18824738 DOI: 10.1167/iovs.08-2437  0.01
2009 Wang S, Haynes C, Barany F, Ott J. Genome-wide autozygosity mapping in human populations. Genetic Epidemiology. 33: 172-80. PMID 18814273 DOI: 10.1002/gepi.20344  0.01
2008 Cheng YW, Pincas H, Bacolod MD, Schemmann G, Giardina SF, Huang J, Barral S, Idrees K, Khan SA, Zeng Z, Rosenberg S, Notterman DA, Ott J, Paty P, Barany F. CpG island methylator phenotype associates with low-degree chromosomal abnormalities in colorectal cancer. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 14: 6005-13. PMID 18829479 DOI: 10.1158/1078-0432.CCR-08-0216  0.01
2008 Xu J, Yang Y, Ying Z, Ott J. Testing linkage disequilibrium from pooled DNA: a contingency table perspective. Statistics in Medicine. 27: 5801-15. PMID 18712782 DOI: 10.1002/sim.3407  0.01
2008 Matthews AG, Haynes C, Liu C, Ott J. Collapsing SNP genotypes in case-control genome-wide association studies increases the type I error rate and power. Statistical Applications in Genetics and Molecular Biology. 7: Article23. PMID 18673292 DOI: 10.2202/1544-6115.1325  0.01
2008 Zhang Q, Wang S, Ott J. Combining identity by descent and association in genetic case-control studies. Bmc Genetics. 9: 42. PMID 18601744 DOI: 10.1186/1471-2156-9-42  0.01
2008 Haider AS, Cohen J, Fei J, Zaba LC, Cardinale I, Toyoko K, Ott J, Krueger JG. Insights into gene modulation by therapeutic TNF and IFNgamma antibodies: TNF regulates IFNgamma production by T cells and TNF-regulated genes linked to psoriasis transcriptome. The Journal of Investigative Dermatology. 128: 655-66. PMID 17928893 DOI: 10.1038/sj.jid.5701064  0.01
2007 Virtanen IM, Karppinen J, Taimela S, Ott J, Barral S, Kaikkonen K, Heikkilä O, Mutanen P, Noponen N, Männikkö M, Tervonen O, Natri A, Ala-Kokko L. Occupational and genetic risk factors associated with intervertebral disc disease. Spine. 32: 1129-34. PMID 17471097 DOI: 10.1097/01.brs.0000261473.03274.5c  0.01
2007 Xu MQ, St Clair D, Ott J, Feng GY, He L. Brain-derived neurotrophic factor gene C-270T and Val66Met functional polymorphisms and risk of schizophrenia: a moderate-scale population-based study and meta-analysis. Schizophrenia Research. 91: 6-13. PMID 17289348 DOI: 10.1016/j.schres.2006.12.008  0.01
2007 Virtanen IM, Noponen N, Barral S, Karppinen J, Li H, Vuoristo M, Niinimäki J, Ott J, Ala-Kokko L, Männikkö M. Putative susceptibility locus on chromosome 21q for lumbar disc disease (LDD) in the Finnish population. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 22: 701-7. PMID 17266399 DOI: 10.1359/jbmr.070123  0.01
2007 DeAngelis MM, Ji F, Kim IK, Adams S, Capone A, Ott J, Miller JW, Dryja TP. Cigarette smoking, CFH, APOE, ELOVL4, and risk of neovascular age-related macular degeneration. Archives of Ophthalmology (Chicago, Ill. : 1960). 125: 49-54. PMID 17210851 DOI: 10.1001/archopht.125.1.49  0.01
2006 Ott J. Unknown parental phase--lod score versus information. A comment to Prof. Edwards' note. Annals of Human Genetics. 70: 974. PMID 17044873 DOI: 10.1111/j.1469-1809.2006.00292.x  0.01
2006 Levenstien MA, Ott J, Gordon D. Are molecular haplotypes worth the time and expense? A cost-effective method for applying molecular haplotypes. Plos Genetics. 2: e127. PMID 16933998 DOI: 10.1371/journal.pgen.0020127  0.01
2006 Tosic M, Ott J, Barral S, Bovet P, Deppen P, Gheorghita F, Matthey ML, Parnas J, Preisig M, Saraga M, Solida A, Timm S, Wang AG, Werge T, Cuénod M, et al. Schizophrenia and oxidative stress: glutamate cysteine ligase modifier as a susceptibility gene. American Journal of Human Genetics. 79: 586-92. PMID 16909399 DOI: 10.1086/507566  0.01
2006 Haider AS, Peters SB, Kaporis H, Cardinale I, Fei J, Ott J, Blumenberg M, Bowcock AM, Krueger JG, Carucci JA. Genomic analysis defines a cancer-specific gene expression signature for human squamous cell carcinoma and distinguishes malignant hyperproliferation from benign hyperplasia. The Journal of Investigative Dermatology. 126: 869-81. PMID 16470182 DOI: 10.1038/sj.jid.5700157  0.01
2005 Xu J, Yang Y, Ott J. Survival analysis of microarray expression data by transformation models. Computational Biology and Chemistry. 29: 91-4. PMID 15833436 DOI: 10.1016/j.compbiolchem.2005.02.001  0.01
2005 Noponen-Hietala N, Virtanen I, Karttunen R, Schwenke S, Jakkula E, Li H, Merikivi R, Barral S, Ott J, Karppinen J, Ala-Kokko L. Genetic variations in IL6 associate with intervertebral disc disease characterized by sciatica. Pain. 114: 186-94. PMID 15733644 DOI: 10.1016/j.pain.2004.12.015  0.01
2004 Ott J. Issues in association analysis: error control in case-control association studies for disease gene discovery. Human Heredity. 58: 171-4. PMID 15812174 DOI: 10.1159/000083544  0.01
2004 Dewan A, Ott J. Reanalysis of a genome scan for schizophrenia Loci using multigenic methods. Human Heredity. 57: 191-4. PMID 15583424 DOI: 10.1159/000081445  0.01
2004 Sherriff A, Ott J. Artificial neural networks as statistical tools in epidemiological studies: analysis of risk factors for early infant wheeze. Paediatric and Perinatal Epidemiology. 18: 456-63. PMID 15535822 DOI: 10.1111/j.1365-3016.2004.00592.x  0.01
2004 Ott J. Association of genetic loci: replication or not, that is the question. Neurology. 63: 955-8. PMID 15452283  0.01
1999 Annunen S, Paassilta P, Lohiniva J, Perälä M, Pihlajamaa T, Karppinen J, Tervonen O, Kröger H, Lähde S, Vanharanta H, Ryhänen L, Göring HH, Ott J, Prockop DJ, Ala-Kokko L. An allele of COL9A2 associated with intervertebral disc disease. Science (New York, N.Y.). 285: 409-12. PMID 10411504  0.01
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