| Year |
Citation |
Score |
| 2020 |
Randesi M, Levran O, den Brink WV, Blanken P, van Ree JM, Ott J, Kreek MJ. Further evidence for association of , and variants with opioid dependence. Pharmacogenomics. PMID 32757697 DOI: 10.2217/Pgs-2020-0045 |
0.341 |
|
| 2020 |
Horpaopan S, Fann CSJ, Lathrop M, Ott J. Shared genomic segment analysis with equivalence testing. Genetic Epidemiology. PMID 32677112 DOI: 10.1002/Gepi.22335 |
0.392 |
|
| 2020 |
Hsieh AR, Sie JJ, Chang CC, Ott J, Lian IB, Fann CSJ. Maximal Segmental Score Method for Localizing Recessive Disease Variants Based on Sequence Data. Frontiers in Genetics. 11: 555. PMID 32655614 DOI: 10.3389/Fgene.2020.00555 |
0.364 |
|
| 2020 |
Hsieh A, Sie JJ, Chang CC, Ott J, Lian I, Fann CSJ. Presentation_1_Maximal Segmental Score Method for Localizing Recessive Disease Variants Based on Sequence Data.zip Frontiers in Genetics. DOI: 10.3389/Fgene.2020.00555.S001 |
0.4 |
|
| 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 |
0.346 |
|
| 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 |
0.426 |
|
| 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 |
0.313 |
|
| 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 |
0.313 |
|
| 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 |
0.378 |
|
| 2018 |
Hwangbo S, Jang JY, Oh B, Okazaki AI, Ott J, Park T. Association test for rare variants using the hamming distance International Journal of Data Mining and Bioinformatics. 21: 301. DOI: 10.1504/Ijdmb.2018.10020341 |
0.353 |
|
| 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 |
0.34 |
|
| 2017 |
Randesi M, Levran O, Ott J, Blanken P, Brink Wvd, Ree JMv, Kreek MJ. Gene variants of the dopaminergic system are associated with non-dependent heroin use and heroin dependence Drug and Alcohol Dependence. 171. DOI: 10.1016/J.Drugalcdep.2016.08.476 |
0.308 |
|
| 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 |
0.376 |
|
| 2015 |
Taipale M, Jakkula E, Kämäräinen OP, Gao P, Skarp S, Barral S, Kiviranta I, Kröger H, Ott J, Wei GH, Ala-Kokko L, Männikkö M. Targeted re-sequencing of linkage region on 2q21 identifies a novel functional variant for hip and knee osteoarthritis. Osteoarthritis and Cartilage / Oars, Osteoarthritis Research Society. PMID 26603474 DOI: 10.1016/J.Joca.2015.10.019 |
0.31 |
|
| 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 |
0.377 |
|
| 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 |
0.374 |
|
| 2015 |
Guan X, Song Y, Ott J, Zhang Y, Li C, Xin T, Li Z, Gan Y, Li J, Zhou S, Zhou Y. The ADAMTS1 Gene Is Associated with Familial Mandibular Prognathism. Journal of Dental Research. PMID 26124221 DOI: 10.1177/0022034515589957 |
0.364 |
|
| 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 |
0.32 |
|
| 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 |
0.335 |
|
| 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 |
0.397 |
|
| 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 |
0.365 |
|
| 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 |
0.305 |
|
| 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 |
0.363 |
|
| 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 |
0.323 |
|
| 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 |
0.39 |
|
| 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 |
0.353 |
|
| 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 |
0.322 |
|
| 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 |
0.357 |
|
| 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 |
0.377 |
|
| 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 |
0.354 |
|
| 2012 |
Barral S, Bird T, Goate A, Farlow MR, Diaz-Arrastia R, Bennett DA, Graff-Radford N, Boeve BF, Sweet RA, Stern Y, Wilson RS, Foroud T, Ott J, Mayeux R. Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory. Neurology. 78: 1464-71. PMID 22539578 DOI: 10.1212/Wnl.0B013E3182553C48 |
0.346 |
|
| 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 |
0.406 |
|
| 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 |
0.62 |
|
| 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 |
0.394 |
|
| 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 |
0.408 |
|
| 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 |
0.366 |
|
| 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 |
0.341 |
|
| 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 |
0.385 |
|
| 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 |
0.37 |
|
| 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 |
0.378 |
|
| 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 |
0.34 |
|
| 2010 |
Proudnikov D, Kroslak T, Sipe JC, Randesi M, Li D, Hamon S, Ho A, Ott J, Kreek MJ. Association of polymorphisms of the cannabinoid receptor (CNR1) and fatty acid amide hydrolase (FAAH) genes with heroin addiction: impact of long repeats of CNR1. The Pharmacogenomics Journal. 10: 232-42. PMID 20010914 DOI: 10.1038/Tpj.2009.59 |
0.322 |
|
| 2010 |
Wu C, Xu B, Yuan P, Ott J, Guan Y, Liu Y, Shen Y, Liu Z, Yu D, Lin D. Abstract 2764: Genome-wide examination of genetic variants associated with response to platinum-based chemotherapy in patients with small-cell lung cancer Cancer Research. 70: 2764-2764. DOI: 10.1158/1538-7445.Am10-2764 |
0.336 |
|
| 2009 |
Levran O, Londono D, O'Hara K, Randesi M, Rotrosen J, Casadonte P, Linzy S, Ott J, Adelson M, Kreek MJ. Heroin addiction in African Americans: a hypothesis-driven association study. Genes, Brain, and Behavior. 8: 531-40. PMID 19500151 DOI: 10.1111/J.1601-183X.2009.00501.X |
0.357 |
|
| 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 |
0.386 |
|
| 2009 |
He G, Hamon S, Li D, Barral-Rodriguez S, Ott J. MHC fine mapping of human type 1 diabetes using the T1DGC data Diabetes, Obesity and Metabolism. 11: 53-59. PMID 19143815 DOI: 10.1111/J.1463-1326.2008.01003.X |
0.438 |
|
| 2009 |
Francis PJ, Hamon SC, Ott J, Weleber RG, Klein ML. Polymorphisms in C2, CFB and C3 are associated with progression to advanced age related macular degeneration associated with visual loss Journal of Medical Genetics. 46: 300-307. PMID 19015224 DOI: 10.1136/Jmg.2008.062737 |
0.356 |
|
| 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 |
0.349 |
|
| 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 |
0.358 |
|
| 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 |
0.327 |
|
| 2008 |
Yang Y, He C, Ott J. Testing association with interactions by partitioning chi-squares. Annals of Human Genetics. 73: 109-17. PMID 18798840 DOI: 10.1111/J.1469-1809.2008.00480.X |
0.327 |
|
| 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 |
0.345 |
|
| 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 |
0.393 |
|
| 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 |
0.341 |
|
| 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 |
0.35 |
|
| 2008 |
Levran O, Londono D, O'Hara K, Nielsen DA, Peles E, Rotrosen J, Casadonte P, Linzy S, Randesi M, Ott J, Adelson M, Kreek MJ. Genetic susceptibility to heroin addiction: a candidate gene association study. Genes, Brain, and Behavior. 7: 720-9. PMID 18518925 DOI: 10.1111/J.1601-183X.2008.00410.X |
0.362 |
|
| 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 |
0.306 |
|
| 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 |
0.315 |
|
| 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 |
0.309 |
|
| 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 |
0.342 |
|
| 2008 |
Nielsen DA, Ji F, Yuferov V, Ho A, Chen A, Levran O, Ott J, Kreek MJ. Genotype patterns that contribute to increased risk for or protection from developing heroin addiction. Molecular Psychiatry. 13: 417-28. PMID 18195715 DOI: 10.1038/Sj.Mp.4002147 |
0.377 |
|
| 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 |
0.344 |
|
| 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 |
0.393 |
|
| 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 |
0.306 |
|
| 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 |
0.339 |
|
| 2007 |
Kaňková K, Stejskalová A, Pácal L, Tschoplová S, Hertlová M, Krusová D, Izakovičová-Hollá L, Beránek M, Vašků A, Barral S, Ott J. Genetic risk factors for diabetic nephropathy on chromosomes 6p and 7q identified by the set-association approach. Diabetologia. 50: 990-999. PMID 17345061 DOI: 10.1007/S00125-007-0606-3 |
0.353 |
|
| 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 |
0.376 |
|
| 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 |
0.408 |
|
| 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 |
0.302 |
|
| 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 |
0.349 |
|
| 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 DOI: 10.1097/01.Fpc.0000182782.87932.D6 |
0.344 |
|
| 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 |
0.355 |
|
| 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 |
0.321 |
|
| 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 |
0.323 |
|
| 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 |
0.385 |
|
| 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 |
0.309 |
|
| 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 |
0.323 |
|
| 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 |
0.37 |
|
| 2004 |
Hoh J, Ott J. Genetic dissection of diseases: design and methods Current Opinion in Genetics & Development. 14: 229-232. PMID 15172663 DOI: 10.1016/J.Gde.2004.04.006 |
0.379 |
|
| 2004 |
Martinez-Mir A, Zlotogorski A, Ott J, Gordon D, Christiano AM. Genetic linkage studies in alopecia areata. The Journal of Investigative Dermatology. Symposium Proceedings. 8: 199-203. PMID 14582673 DOI: 10.1046/J.1087-0024.2003.00809.X |
0.393 |
|
| 2004 |
Ott J, Hoh J. Set association analysis of SNP case-control and microarray data. Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 10: 569-74. PMID 12935345 DOI: 10.1089/10665270360688192 |
0.437 |
|
| 2003 |
Noponen-Hietala N, Kyllönen E, Männikkö M, Ilkko E, Karppinen J, Ott J, Ala-Kokko L. Sequence variations in the collagen IX and XI genes are associated with degenerative lumbar spinal stenosis Annals of the Rheumatic Diseases. 62: 1208-1214. PMID 14644861 DOI: 10.1136/Ard.2003.008334 |
0.375 |
|
| 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 |
0.801 |
|
| 2003 |
Louie E, Ott J, Majewski J. Nucleotide frequency variation across human genes. Genome Research. 13: 2594-601. PMID 14613976 DOI: 10.1101/Gr.1317703 |
0.344 |
|
| 2003 |
Helms C, Cao L, Krueger JG, Wijsman EM, Chamian F, Gordon D, Heffernan M, Daw JA, Robarge J, Ott J, Kwok PY, Menter A, Bowcock AM. A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis. Nature Genetics. 35: 349-56. PMID 14608357 DOI: 10.1038/Ng1268 |
0.379 |
|
| 2003 |
Hoh J, Ott J. Mathematical multi-locus approaches to localizing complex human trait genes Nature Reviews Genetics. 4: 701-709. PMID 12951571 DOI: 10.1038/Nrg1155 |
0.361 |
|
| 2003 |
Majewski J, Schultz DW, Weleber RG, Schain MB, Edwards AO, Matise TC, Acott TS, Ott J, Klein ML. Age-related macular degeneration--a genome scan in extended families. American Journal of Human Genetics. 73: 540-50. PMID 12900797 DOI: 10.1086/377701 |
0.405 |
|
| 2003 |
Yang Y, Hoh J, Broger C, Neeb M, Edington J, Lindpaintner K, Ott J. Statistical methods for analyzing microarray feature data with replications. Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 10: 157-69. PMID 12804089 DOI: 10.1089/106652703321825946 |
0.301 |
|
| 2003 |
Yang Y, Zhang J, Hoh J, Matsuda F, Xu P, Lathrop M, Ott J. Efficiency of single-nucleotide polymorphism haplotype estimation from pooled DNA. Proceedings of the National Academy of Sciences of the United States of America. 100: 7225-30. PMID 12777616 DOI: 10.1073/Pnas.1237858100 |
0.308 |
|
| 2003 |
Schultz DW, Klein ML, Humpert A, Majewski J, Schain M, Weleber RG, Ott J, Acott TS. Lack of an association of apolipoprotein E gene polymorphisms with familial age-related macular degeneration. Archives of Ophthalmology (Chicago, Ill. : 1960). 121: 679-83. PMID 12742846 DOI: 10.1001/Archopht.121.5.679 |
0.378 |
|
| 2003 |
Hoh J, Matsuda F, Peng X, Markovic D, Lathrop MG, Ott J. SNP haplotype tagging from DNA pools of two individuals. Bmc Bioinformatics. 4: 14. PMID 12709267 DOI: 10.1186/1471-2105-4-14 |
0.324 |
|
| 2003 |
Gordon D, Corwin MB, Mellersh CS, Ostrander EA, Ott J. Establishing appropriate genome-wide significance levels for canine linkage analyses. The Journal of Heredity. 94: 1-7. PMID 12692155 DOI: 10.1093/Jhered/Esg009 |
0.337 |
|
| 2003 |
Liu J, Juo SH, Dewan A, Grunn A, Tong X, Brito M, Park N, Loth JE, Kanyas K, Lerer B, Endicott J, Penchaszadeh G, Knowles JA, Ott J, Gilliam TC, et al. Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12. Molecular Psychiatry. 8: 333-42. PMID 12660806 DOI: 10.1038/Sj.Mp.4001254 |
0.324 |
|
| 2003 |
Stib?rková B, Majewski J, Hodanová K, Ondrová L, Jerábková M, Zikánová M, Vylet'al P, Sebesta I, Marinaki A, Simmonds A, Matthijs G, Fryns JP, Torres R, Puig JG, Ott J, et al. Familial juvenile hyperuricaemic nephropathy (FJHN): linkage analysis in 15 families, physical and transcriptional characterisation of the FJHN critical region on chromosome 16p11.2 and the analysis of seven candidate genes. European Journal of Human Genetics : Ejhg. 11: 145-54. PMID 12634862 DOI: 10.1038/Sj.Ejhg.5200937 |
0.416 |
|
| 2003 |
Garcia-Barceló M, Sham MH, Lui VCH, Chen BLS, Ott J, Tam PKH. Association study of PHOX2B as a candidate gene for Hirschsprung’s disease Gut. 52: 563-567. PMID 12631670 DOI: 10.1136/Gut.52.4.563 |
0.374 |
|
| 2003 |
Yang Y, Ott J. Log-linear models for gene mapping with affected sib pair data. Human Heredity. 53: 227-36. PMID 12435886 DOI: 10.1159/000066196 |
0.405 |
|
| 2003 |
Zee RY, Hoh J, Cheng S, Reynolds R, Grow MA, Silbergleit A, Walker K, Steiner L, Zangenberg G, Fernandez-Ortiz A, Macaya C, Pintor E, Fernandez-Cruz A, Ott J, Lindpainter K. Multi-locus interactions predict risk for post-PTCA restenosis: an approach to the genetic analysis of common complex disease. The Pharmacogenomics Journal. 2: 197-201. PMID 12082592 DOI: 10.1038/Sj.Tpj.6500101 |
0.386 |
|
| 2002 |
Knappskog PM, Majewski J, Livneh A, Nilsen PT, Bringsli JS, Ott J, Boman H. Cold-induced sweating syndrome is caused by mutations in the CRLF1 gene. American Journal of Human Genetics. 72: 375-83. PMID 12509788 DOI: 10.1086/346120 |
0.353 |
|
| 2002 |
Gordon D, Finch SJ, Nothnagel M, Ott J. Power and sample size calculations for case-control genetic association tests when errors are present: application to single nucleotide polymorphisms. Human Heredity. 54: 22-33. PMID 12446984 DOI: 10.1159/000066696 |
0.337 |
|
| 2002 |
Acuña G, Foernzler D, Leong D, Rabbia M, Smit R, Dorflinger E, Gasser R, Hoh J, Ott J, Borroni E, To Z, Thompson A, Li J, Hashimoto L, Lindpaintner K. Pharmacogenetic analysis of adverse drug effect reveals genetic variant for susceptibility to liver toxicity. The Pharmacogenomics Journal. 2: 327-34. PMID 12439739 DOI: 10.1038/Sj.Tpj.6500123 |
0.354 |
|
| 2002 |
Anderson E, Berkovic S, Dulac O, Gardiner M, Jain S, Laue Friis M, Lindhout D, Noebels J, Ottman R, Scaramelli A, Serratosa J, Steinlein O, Avanzini G, Bailey-Wilson J, Cardon L, ... ... Ott J, et al. ILAE genetics commission conference report: molecular analysis of complex genetic epilepsies. Epilepsia. 43: 1262-7. PMID 12366744 DOI: 10.1046/J.1528-1157.2002.29502.X |
0.325 |
|
| 2002 |
Jain S, Tang X, Narayanan CS, Agarwal Y, Peterson SM, Brown CD, Ott J, Kumar A. Angiotensinogen gene polymorphism at -217 affects basal promoter activity and is associated with hypertension in African-Americans. The Journal of Biological Chemistry. 277: 36889-96. PMID 12145290 DOI: 10.1074/Jbc.M204732200 |
0.301 |
|
| 2002 |
Han Z, Heath SC, Shmulewitz D, Li W, Auerbach SB, Blundell ML, Lehner T, Ott J, Stoffel M, Friedman JM, Breslow JL. Candidate genes involved in cardiovascular risk factors by a family-based association study on the island of Kosrae, Federated States of Micronesia. American Journal of Medical Genetics. 110: 234-42. PMID 12116231 DOI: 10.1002/Ajmg.10445 |
0.3 |
|
| 2002 |
Martinez-Mir A, Gordon D, Horev L, Klapholz L, Ott J, Christiano AM, Zlotogorski A. Multiple cutaneous and uterine leiomyomas: refinement of the genetic locus for multiple cutaneous and uterine leiomyomas on chromosome 1q42.3-43. The Journal of Investigative Dermatology. 118: 876-80. PMID 11982768 DOI: 10.1046/J.1523-1747.2002.01741.X |
0.393 |
|
| 2002 |
Nothnagel M, Ott J. Statistical gene mapping of traits in humans--hypertension as a complex trait: is it amenable to genetic analysis? Seminars in Nephrology. 22: 105-14. PMID 11891504 DOI: 10.1053/Snep.2002.30209 |
0.365 |
|
| 2002 |
Emala CW, McQuitty CK, Eleff SM, Hopkins-Price P, Lawyer C, Hoh J, Ott J, Levine MA, Hirshman CA. Asthma, allergy, and airway hyperresponsiveness are not linked to the β2-adrenoceptor gene Chest. 121: 722-731. PMID 11888952 DOI: 10.1378/Chest.121.3.722 |
0.315 |
|
| 2002 |
Hoh J, Ott J. A train of thoughts on gene mapping. Theoretical Population Biology. 60: 149-53. PMID 11855949 DOI: 10.1006/Tpbi.2001.1536 |
0.383 |
|
| 2002 |
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, et al. A susceptibility locus for migraine with aura, on chromosome 4q24. American Journal of Human Genetics. 70: 652-62. PMID 11836652 DOI: 10.1086/339078 |
0.734 |
|
| 2001 |
Gordon D, Hoh J, Finch SJ, Levenstien MA, Edington J, Li W, Majewski J, Ott J. Two approaches for consolidating results from genome scans of complex traits: Selection methods and scan statistics Genetic Epidemiology. 21: S396-S402. PMID 11793706 DOI: 10.1002/Gepi.2001.21.S1.S396 |
0.405 |
|
| 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 |
0.793 |
|
| 2001 |
Majewski J, Li H, Ott J. The Ising model in physics and statistical genetics. American Journal of Human Genetics. 69: 853-62. PMID 11517425 DOI: 10.1086/323419 |
0.348 |
|
| 2001 |
Liu J, Nyholt DR, Magnussen P, Parano E, Pavone P, Geschwind D, Lord C, Iversen P, Hoh J, Ott J, Gilliam TC. A genomewide screen for autism susceptibility loci. American Journal of Human Genetics. 69: 327-40. PMID 11452361 DOI: 10.1086/321980 |
0.405 |
|
| 2001 |
Ott J. Neural networks and disease association studies. American Journal of Medical Genetics. 105: 60-1. PMID 11425001 DOI: 10.1002/1096-8628(20010108)105:1<60::Aid-Ajmg1062>3.0.Co;2-L |
0.309 |
|
| 2001 |
Lee MH, Gordon D, Ott J, Lu K, Ose L, Miettinen T, Gylling H, Stalenhoef AF, Pandya A, Hidaka H, Brewer B, Kojima H, Sakuma N, Pegoraro R, Salen G, et al. Fine mapping of a gene responsible for regulating dietary cholesterol absorption; founder effects underlie cases of phytosterolaemia in multiple communities European Journal of Human Genetics. 9: 375-384. PMID 11378826 DOI: 10.1038/Sj.Ejhg.5200628 |
0.407 |
|
| 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 DOI: 10.1001/Jama.285.14.1843 |
0.344 |
|
| 2001 |
Simonic I, Nyholt DR, Gericke GS, Gordon D, Matsumoto N, Ledbetter DH, Ott J, Weber JL. Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners. American Journal of Medical Genetics. 105: 163-7. PMID 11304830 DOI: 10.1002/Ajmg.1192 |
0.377 |
|
| 2001 |
Ott J, Hoh J. Statistical multilocus methods for disequilibrium analysis in complex traits. Human Mutation. 17: 285-8. PMID 11295826 DOI: 10.1002/Humu.25 |
0.413 |
|
| 2001 |
Sherriff A, Ott J. 20 Applications of neural networks for gene finding Advances in Genetics. 42: 287-297. PMID 11037328 DOI: 10.1016/S0065-2660(01)42029-3 |
0.36 |
|
| 2001 |
Ott J. Major strengths and weaknesses of the lod score method. Advances in Genetics. 42: 125-32. PMID 11037318 DOI: 10.1016/S0065-2660(01)42019-0 |
0.346 |
|
| 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: 10.1046/J.1469-1809.2000.6450413.X |
0.789 |
|
| 2000 |
Merette C, Brassard A, Potvin A, Bouvier H, Rousseau F, Edmond C, Bissonnette L, Roy MA, Maziade M, Ott J, Caron C. Significant linkage for tourette syndrome in a large French Canadian family American Journal of Human Genetics. 67: 1008-1013. PMID 10986045 DOI: 10.1086/303093 |
0.414 |
|
| 2000 |
Majewski J, Ott J. GT repeats are associated with recombination on human chromosome 22. Genome Research. 10: 1108-14. PMID 10958629 DOI: 10.1101/Gr.10.8.1108 |
0.319 |
|
| 2000 |
Hoh J, Ott J. Scan statistics to scan markers for susceptibility genes. Proceedings of the National Academy of Sciences of the United States of America. 97: 9615-7. PMID 10931953 DOI: 10.1073/Pnas.170179197 |
0.416 |
|
| 2000 |
Ott J, Hoh J. Statistical approaches to gene mapping. American Journal of Human Genetics. 67: 289-94. PMID 10884361 DOI: 10.1086/303031 |
0.438 |
|
| 2000 |
Gordon D, Simonic I, Ott J. Significant evidence for linkage disequilibrium over a 5-cM region among Afrikaners. Genomics. 66: 87-92. PMID 10843808 DOI: 10.1006/Geno.2000.6190 |
0.408 |
|
| 2000 |
Stibůrková B, Majewski J, Sebesta I, Zhang W, Ott J, Kmoch S. Familial juvenile hyperuricemic nephropathy: localization of the gene on chromosome 16p11.2-and evidence for genetic heterogeneity. American Journal of Human Genetics. 66: 1989-94. PMID 10780922 DOI: 10.1086/302936 |
0.412 |
|
| 2000 |
Leal SM, Ott J. Effects of stratification in the analysis of affected-sib-pair data: benefits and costs. American Journal of Human Genetics. 66: 567-75. PMID 10677317 DOI: 10.1086/302748 |
0.359 |
|
| 2000 |
Ott J. Predicting the range of linkage disequilibrium. Proceedings of the National Academy of Sciences of the United States of America. 97: 2-3. PMID 10618359 DOI: 10.1073/Pnas.97.1.2 |
0.432 |
|
| 2000 |
Hoh JJ, Ott J. Complex inheritance and localizing disease genes. Human Heredity. 50: 85-9. PMID 10545761 DOI: 10.1159/000022894 |
0.418 |
|
| 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 DOI: 10.1093/Oxfordjournals.Jncimonographs.A024219 |
0.556 |
|
| 1999 |
Ott J, Bhat A. Linkage analysis in heterogeneous and complex traits European Child and Adolescent Psychiatry. 8: 43-46. PMID 10638369 DOI: 10.1007/Pl00010693 |
0.388 |
|
| 1999 |
Bhat A, Lucek PR, Ott J. Analysis of complex traits using neural networks Genetic Epidemiology. 17. PMID 10597483 DOI: 10.1002/Gepi.1370170781 |
0.325 |
|
| 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 |
0.418 |
|
| 1999 |
Bhat A, Heath SC, Ott J. Heterogeneity for multiple disease loci in linkage analysis. Human Heredity. 49: 229-31. PMID 10436385 DOI: 10.1159/000022879 |
0.377 |
|
| 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 DOI: 10.1126/Science.285.5426.409 |
0.388 |
|
| 1999 |
Karayiorgou M, Sobin C, Blundell ML, Galke BL, Malinova L, Goldberg P, Ott J, Gogos JA. Family-based association studies support a sexually dimorphic effect of COMT and MAOA on genetic susceptibility to obsessive-compulsive disorder. Biological Psychiatry. 45: 1178-89. PMID 10331110 DOI: 10.1016/S0006-3223(98)00319-9 |
0.375 |
|
| 1999 |
Ott J, Rabinowitz D. A principal-components approach based on heritability for combining phenotype information. Human Heredity. 49: 106-11. PMID 10077732 DOI: 10.1159/000022854 |
0.307 |
|
| 1999 |
Gordon D, Heath SC, Ott J. True pedigree errors more frequent than apparent errors for single nucleotide polymorphisms. Human Heredity. 49: 65-70. PMID 10077724 DOI: 10.1159/000022846 |
0.319 |
|
| 1999 |
Ott J. Methods of analysis and resources available for genetic trait mapping. The Journal of Heredity. 90: 68-70. PMID 9987907 DOI: 10.1093/Jhered/90.1.68 |
0.358 |
|
| 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 |
0.417 |
|
| 1998 |
Devoto M, Shimoya K, Caminis J, Ott J, Tenenhouse A, Whyte MP, Sereda L, Hall S, Considine E, Williams CJ, Tromp G, Kuivaniemi H, Ala-Kokko L, Prockop DJ, Spotila LD. First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q. European Journal of Human Genetics : Ejhg. 6: 151-7. PMID 9781060 DOI: 10.1038/Sj.Ejhg.5200169 |
0.39 |
|
| 1998 |
Lucek P, Hanke J, Reich J, Solla SA, Ott J. Multi-locus nonparametric linkage analysis of complex trait loci with neural networks. Human Heredity. 48: 275-84. PMID 9748698 DOI: 10.1159/000022816 |
0.408 |
|
| 1998 |
Li W, Fann CS, Ott J. Low-order polynomial trends of female-to-male map distance ratios along human chromosomes. Human Heredity. 48: 266-70. PMID 9748696 DOI: 10.1159/000022814 |
0.301 |
|
| 1998 |
Simonic I, Gericke GS, Ott J, Weber JL. Identification of genetic markers associated with Gilles de la Tourette syndrome in an Afrikaner population. American Journal of Human Genetics. 63: 839-46. PMID 9718333 DOI: 10.1086/302002 |
0.415 |
|
| 1998 |
Klein ML, Schultz DW, Edwards A, Matise TC, Rust K, Berselli CB, Trzupek K, Weleber RG, Ott J, Wirtz MK, Acott TS. Age-related macular degeneration. Clinical features in a large family and linkage to chromosome 1q. Archives of Ophthalmology (Chicago, Ill. : 1960). 116: 1082-8. PMID 9715689 DOI: 10.1001/Archopht.116.8.1082 |
0.383 |
|
| 1998 |
Ahmad W, Brancolini V, Ul Haque MF, Lam H, Ul Haque S, Haider M, Maimon A, Aita VM, Owen J, Brown D, Zegarelli DJ, Ahmad M, Ott J, Christiano AM. A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1 [2] American Journal of Human Genetics. 62: 987-991. PMID 9529357 DOI: 10.1086/301799 |
0.306 |
|
| 1998 |
Knowles JA, Rao PA, Cox-Matise T, Loth JE, de Jesus GM, Levine L, Das K, Penchaszadeh GK, Alexander JR, Lerer B, Endicott J, Ott J, Gilliam TC, Baron M. No evidence for significant linkage between bipolar affective disorder and chromosome 18 pericentromeric markers in a large series of multiplex extended pedigrees. American Journal of Human Genetics. 62: 916-24. PMID 9529343 DOI: 10.1086/301785 |
0.39 |
|
| 1998 |
Banerjee P, Lewis CA, Kleyn PW, Shugart YY, Ross BM, Penchaszadeh GK, Ott J, Jacobson SG, Gilliam TC, Knowles JA. Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3. Genomics. 48: 171-7. PMID 9521870 DOI: 10.1006/Geno.1997.5174 |
0.394 |
|
| 1998 |
Plásilová M, Feráková E, Kádasi L, Poláková H, Gerinec A, Ott J, Ferák V. Linkage of autosomal recessive primary congenital glaucoma to the GLC3A locus in Roms (Gypsies) from Slovakia. Human Heredity. 48: 30-3. PMID 9463798 DOI: 10.1159/000022778 |
0.402 |
|
| 1998 |
Ahmad W, Ul Haque MF, Brancolini V, Tsou HC, Ul Haque S, Lam H, Aita VM, Owen J, DeBlaquiere M, Frank J, Cserhalmi-Friedman PB, Leask A, McGrath JA, Peacocke M, Ahmad M, ... Ott J, et al. Alopecia universalis associated with a mutation in the human hairless gene Science. 279: 720-724. PMID 9445480 DOI: 10.1126/Science.279.5351.720 |
0.351 |
|
| 1998 |
Leal SM, Ott J. Analysis of two-locus traits under heterogeneity for recessive versus dominant inheritance. Genetic Epidemiology. 14: 1097-100. PMID 9433630 DOI: 10.1002/(Sici)1098-2272(1997)14:6<1097::Aid-Gepi89>3.0.Co;2-C |
0.334 |
|
| 1998 |
Ahmad W, Brancolini V, ul Haque M, Lam H, ul Haque S, Haider M, Maimon A, Aita V, Ahmad M, Ott J, Christiano A. A locus for autosomal recessive hypodontia maps to chromosome 16q12.1 Journal of Dermatological Science. 16: S107. DOI: 10.1016/S0923-1811(98)83636-0 |
0.332 |
|
| 1997 |
McGee TL, Devoto M, Ott J, Berson EL, Dryja TP. Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele. American Journal of Human Genetics. 61: 1059-66. PMID 9345108 DOI: 10.1086/301614 |
0.383 |
|
| 1997 |
Ott J. Testing for interference in human genetic maps. Journal of Molecular Medicine. 75: 414-419. PMID 9231881 DOI: 10.1007/S001090050126 |
0.351 |
|
| 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 DOI: 10.1007/Bf03405880 |
0.342 |
|
| 1997 |
Karayiorgou M, Altemus M, Galke BL, Goldman D, Murphy DL, Ott J, Gogos JA. Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder. Proceedings of the National Academy of Sciences of the United States of America. 94: 4572-5. PMID 9114031 DOI: 10.1073/Pnas.94.9.4572 |
0.347 |
|
| 1997 |
Müller-Myhsok B, Heiland HJ, Müller CR, Meng G, Grimm T, Ott J. Mapping undetected mutations within a gene-evidence for two preferential regions in the DMD gene. Human Heredity. 47: 61-5. PMID 9097087 DOI: 10.1159/000154393 |
0.316 |
|
| 1997 |
Brzustowicz LM, Gardner JP, Hopp L, Jeanclos E, Ott J, Yang XY, Fekete Z, Aviv A. Linkage analysis using platelet-activating factor Ca2+ response in transformed lymphoblasts. Hypertension. 29: 158-64. PMID 9039096 DOI: 10.1161/01.Hyp.29.1.158 |
0.358 |
|
| 1997 |
Haghighi F, Ott J. Estimating recessive disease allele frequency based on genetic maps. European Journal of Human Genetics. 5: 203-205. DOI: 10.1007/Bf03405918 |
0.374 |
|
| 1996 |
Wildenauer DB, Schwab SG, Albus M, Hallmayer J, Lerer B, Maier W, Blackwood D, Muir W, Clair DS, Morris S, Moises HW, Yang L, Kristbjarnarson H, Helgason T, Wiese C, ... ... Ott J, et al. Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study American Journal of Medical Genetics. 67: 580-594. PMID 8950417 DOI: 10.1002/(Sici)1096-8628(19961122)67:6<580::Aid-Ajmg11>3.0.Co;2-P |
0.333 |
|
| 1996 |
DeLisi LE, Lofthouse R, Lehner T, Morganti C, Vita A, Shields G, Bass N, Ott J, Crow TJ. Failure to find a chromosome 18 pericentric linkage in families with schizophrenia. American Journal of Medical Genetics. 60: 532-4. PMID 8825890 DOI: 10.1002/Ajmg.1320600609 |
0.352 |
|
| 1996 |
Simonic I, Ott J. Novel etiological hypotheses imply new analysis methods for schizophrenia genetics Schizophrenia Research. 20: 235-237. PMID 8794515 DOI: 10.1016/0920-9964(96)00006-0 |
0.313 |
|
| 1996 |
Spotila LD, Caminis J, Devoto M, Shimoya K, Sereda L, Ott J, Whyte MP, Tenenhouse A, Prockop DJ. Osteopenia in 37 members of seven families: analysis based on a model of dominant inheritance. Molecular Medicine (Cambridge, Mass.). 2: 313-24. PMID 8784784 DOI: 10.1007/Bf03401629 |
0.362 |
|
| 1996 |
Ginns EI, Ott J, Egeland JA, Allen CR, Fann CS, Pauls DL, Weissenbachoff J, Carulli JP, Falls KM, Keith TP, Paul SM. A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish. Nature Genetics. 12: 431-5. PMID 8630500 DOI: 10.1038/Ng0496-431 |
0.353 |
|
| 1996 |
Ott J. Complex traits on the map Nature. 379: 772-773. PMID 8587599 DOI: 10.1038/379772A0 |
0.39 |
|
| 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 |
0.577 |
|
| 1995 |
Fann CS, Ott J. Parsimonious estimation of sex-specific map distances by stepwise maximum likelihood regression. Genomics. 29: 571-5. PMID 8575747 DOI: 10.1006/Geno.1995.9964 |
0.302 |
|
| 1995 |
Sasse G, Müller H, Chakraborty R, Ott J. Estimating the frequency of nonpaternity in Switzerland. Human Heredity. 44: 337-43. PMID 7860087 DOI: 10.1159/000154241 |
0.336 |
|
| 1995 |
Ott J, Donis-Keller H. Statistical methods in genetic mapping. Genomics. 22: 496-7. PMID 7806246 DOI: 10.1006/Geno.1994.1421 |
0.362 |
|
| 1995 |
Ott J. Linkage analysis with biological markers. Human Heredity. 45: 169-74. PMID 7615303 DOI: 10.1159/000154280 |
0.398 |
|
| 1995 |
Lazzarini A, Stenroos ES, Lehner T, McKoy V, Gold B, McCormack MK, Reid CS, Ott J, Johnson WG. Short tandem repeat polymorphism linkage studies in a new family with X-linked mental retardation (MRX20). American Journal of Medical Genetics. 57: 552-7. PMID 7573127 DOI: 10.1002/Ajmg.1320570407 |
0.345 |
|
| 1994 |
Mérette C, Lehner T, Ott J. Two new approaches toward linkage heterogeneity of FAD: two-locus models and age of onset as a discriminator. Genetic Epidemiology. 10: 455-9. PMID 8314043 DOI: 10.1002/Gepi.1370100621 |
0.357 |
|
| 1994 |
DeLisi LE, Devoto M, Lofthouse R, Poulter M, Smith A, Shields G, Bass N, Chen G, Vita A, Morganti C, Ott J, Crow TJ. Search for linkage to schizophrenia on the X and Y chromosomes. American Journal of Medical Genetics. 54: 113-121. PMID 8074161 DOI: 10.1002/Ajmg.1320540206 |
0.344 |
|
| 1994 |
Weeks DE, Ott J, Lathrop GM. Detection of genetic interference: simulation studies and mouse data. Genetics. 136: 1217-26. PMID 8005426 |
0.623 |
|
| 1994 |
Knowles JA, Shugart Y, Banerjee P, Gilliam TC, Lewis CA, Jacobson SG, Ott J. Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6p. Human Molecular Genetics. 3: 1401-3. PMID 7987322 DOI: 10.1093/Hmg/3.8.1401 |
0.381 |
|
| 1994 |
Chatkupt S, Speer MC, Ding Y, Thomas M, Stenroos ES, Dermody JJ, Koenigsberger MR, Ott J, Johnson WG. Linkage analysis of a candidate locus (HLA) in autosomal dominant sacral defect with anterior meningocele. American Journal of Medical Genetics. 52: 1-4. PMID 7977450 DOI: 10.1002/Ajmg.1320520102 |
0.358 |
|
| 1994 |
Gabizon R, Rosenman H, Meiner Z, Kahana I, Kahana E, Shugart Y, Ott J, Prusiner SB. Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 343: 385-90. PMID 7913755 DOI: 10.1098/Rstb.1994.0033 |
0.33 |
|
| 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 |
0.649 |
|
| 1993 |
Ott J. Detecting marker inconsistencies in human gene mapping. Human Heredity. 43: 25-30. PMID 8514322 DOI: 10.1159/000154109 |
0.355 |
|
| 1993 |
Petrukhin KE, Speer MC, Cayanis E, Bonaldo MdF, Tantravahi U, Soares MB, Fischer SG, Warburton D, Gilliam TC, Ott J. A Microsatellite Genetic Linkage Map of Human Chromosome 13 Genomics. 15: 76-85. PMID 8432553 DOI: 10.1006/Geno.1993.1012 |
0.386 |
|
| 1993 |
Bunge S, Wedemann H, David D, Terwilliger DJ, van den Born LI, Aulehla-Scholz C, Samanns C, Horn M, Ott J, Schwinger E. Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant retinitis pigmentosa. Genomics. 17: 230-3. PMID 8406457 DOI: 10.1006/Geno.1993.1309 |
0.339 |
|
| 1993 |
Weeks DE, Lathrop GM, Ott J. Multipoint mapping under genetic interference. Human Heredity. 43: 86-97. PMID 8359820 |
0.636 |
|
| 1993 |
Spence MA, Bishop DT, Boehnke M, Elston RC, Falk C, Hodge SE, Ott J, Rice J, Merikangas K, Kupfer D. Methodological issues in linkage analyses for psychiatric disorders: secular trends, assortative mating, bilineal pedigrees. Report of the MacArthur Foundation Network I Task Force on Methodological Issues. Human Heredity. 43: 166-72. PMID 8330880 DOI: 10.1159/000154173 |
0.311 |
|
| 1993 |
Hellsten E, Vesa J, Speer MC, Mäkelä TP, Järvelä I, Alitalo K, Ott J, Peltonen L. Refined Assignment of the Infantile Neuronal Ceroid Lipofuscinosis (INCL, CLN1) Locus at 1p32: Incorporation of Linkage Disequilibrium in Multipoint Analysis Genomics. 16: 720-725. PMID 8325646 DOI: 10.1006/Geno.1993.1253 |
0.366 |
|
| 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 |
0.619 |
|
| 1993 |
Leal SM, Ott J. A bootstrap approach to estimating power for linkage heterogeneity. Genetic Epidemiology. 10: 465-470. PMID 8314045 DOI: 10.1002/Gepi.1370100623 |
0.332 |
|
| 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 |
0.62 |
|
| 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 |
0.643 |
|
| 1993 |
Straub RE, Speer MC, Luo Y, Rojas K, Overhauser J, Ott J, Gilliam TC. A microsatellite genetic linkage map of human chromosome 18. Genomics. 15: 48-56. PMID 8094374 DOI: 10.1006/Geno.1993.1008 |
0.371 |
|
| 1992 |
Vieland V, Greenberg DA, Hodge SE, Ott J. Linkage analysis of two-locus diseases under single-locus and two-locus analysis models. Cytogenetics and Cell Genetics. 59: 145-6. PMID 1737484 DOI: 10.1159/000133229 |
0.372 |
|
| 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 DOI: 10.1159/000133228 |
0.549 |
|
| 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 DOI: 10.1159/000133222 |
0.469 |
|
| 1992 |
Arena JF, Schwartz C, Stevenson R, Lawrence L, Carpenter A, Duara R, Ledbetter D, Huang T, Lehner T, Ott J, Lubs HA. Spastic paraplegia with iron deposits in the basal ganglia: A new X-linked mental retardation syndrome American Journal of Medical Genetics. 43: 479-490. PMID 1605230 DOI: 10.1002/Ajmg.1320430172 |
0.308 |
|
| 1992 |
Brzustowicz LM, Kleyn PW, Boyce FM, Lien LL, Monaco AP, Penchaszadeh GK, Das K, Wang CH, Munsat TL, Ott J, Kunkel LM, Gilliam TC. Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6 Genomics. 13: 991-998. PMID 1505990 DOI: 10.1016/0888-7543(92)90012-H |
0.413 |
|
| 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 DOI: 10.1016/0888-7543(92)90006-E |
0.632 |
|
| 1992 |
Terwilliger JD, Ott J. A haplotype-based 'haplotype relative risk' approach to detecting allelic associations. Human Heredity. 42: 337-46. PMID 1493912 DOI: 10.1159/000154096 |
0.625 |
|
| 1992 |
Ott J. The future of multilocus linkage analysis. Annals of Medicine. 24: 401-3. PMID 1418926 DOI: 10.3109/07853899209147845 |
0.303 |
|
| 1992 |
Ott J. Introductory Remarks: Genetic Models and Statistical Approaches Annals of Medicine. 24: 375-377. PMID 1418921 DOI: 10.3109/07853899209147840 |
0.307 |
|
| 1992 |
Daniels RJ, Thomas NH, MacKinnon RN, Lehner T, Ott J, Flint TJ, Dubowitz V, Ignatius J, Donner M, Zerres K. Linkage analysis of spinal muscular atrophy. Genomics. 12: 335-9. PMID 1346777 DOI: 10.1016/0888-7543(92)90382-3 |
0.383 |
|
| 1992 |
Terwilliger JD, Ott J, Mamolini E, Beretta M, Cappellozza G, Moncinelli R, Scapoli C, Barale R, Barrai I, El-Hazmi MAF, Warsy AS, Saha N, Juneja RK, Gahne B, Tay JSH, et al. Subject Index, Vol. 42, 1992 Human Heredity. 42: 389-390. DOI: 10.1159/000154104 |
0.535 |
|
| 1992 |
Terwilliger JD, Ott J, Mamolini E, Beretta M, Cappellozza G, Moncinelli R, Scapoli C, Barale R, Barrai I, El-Hazmi MAF, Warsy AS, Saha N, Juneja RK, Gahne B, Tay JSH, et al. Contents, Vol. 42, 1992 Human Heredity. 42. DOI: 10.1159/000154094 |
0.526 |
|
| 1991 |
Baron M, Endicott J, Ott J. Genetic linkage in mental illness. Limitations and prospects. The British Journal of Psychiatry : the Journal of Mental Science. 157: 645-55. PMID 2279201 DOI: 10.1192/Bjp.157.5.645 |
0.347 |
|
| 1991 |
Ott J, Caesar J, Mächler M, Schinzel A, Schmid W. Presymptomatic exclusion of myotonic dystrophy in a one-generation pedigree of half-siblings. Human Heredity. 40: 305-7. PMID 2265856 DOI: 10.1159/000153950 |
0.342 |
|
| 1991 |
Baron M, Hamburger R, Sandkuyl LA, Risch N, Mandel B, Endicott J, Belmaker RH, Ott J. The impact of phenotypic variation on genetic analysis: application to X-linkage in manic-depressive illness. Acta Psychiatrica Scandinavica. 82: 196-203. PMID 2248044 DOI: 10.1111/J.1600-0447.1990.Tb03052.X |
0.361 |
|
| 1991 |
Passos-Bueno MR, Terwilliger J, Ott J, Vainzof M, Love DR, Davies KE, Zatz M. Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence. American Journal of Medical Genetics. 38: 140-6. PMID 2012126 DOI: 10.1002/Ajmg.1320380130 |
0.566 |
|
| 1991 |
Musarella MA, Anson-Cartwright L, Leal SM, Gilbert LD, Worton RG, Fishman GA, Ott J. Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa families. Genomics. 8: 286-96. PMID 1979051 DOI: 10.1016/0888-7543(90)90284-2 |
0.374 |
|
| 1991 |
Passos-Bueno MR, Byth B, Love D, Terwilliger J, Ott J, Rapaport D, Vainzof M, Zatz M, Davies KE. Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27. Journal of the Neurological Sciences. 102: 206-8. PMID 1883411 DOI: 10.1016/0022-510X(91)90070-N |
0.591 |
|
| 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 DOI: 10.1192/Bjp.158.5.630 |
0.616 |
|
| 1991 |
Kwan SP, Lehner T, Hagemann T, Lu B, Blaese M, Ochs H, Wedgwood R, Ott J, Craig IW, Rosen FS. Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22-Xp11.3. Genomics. 10: 29-33. PMID 1675197 DOI: 10.1016/0888-7543(91)90480-3 |
0.413 |
|
| 1990 |
Sankila EM, Lehner T, Eriksson AW, Forsius H, Kärnä J, Page D, Ott J, de la Chapelle A. Haplotype and multipoint linkage analysis in Finnish choroideremia families. Human Genetics. 84: 66-70. PMID 2575071 DOI: 10.1007/Bf00210674 |
0.399 |
|
| 1990 |
Brzustowicz LM, Lehner T, Castilla LH, Penchaszadeh GK, Wilhelmsen KC, Daniels R, Davies KE, Leppert M, Ziter F, Wood D, Dubowitz V, Zerres K, Hausmanowa-Petrusewicz I, Ott J, Munsat TL, et al. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2-13.3 Nature. 344: 540-541. PMID 2320125 DOI: 10.1038/344540A0 |
0.354 |
|
| 1990 |
Kwan SP, Terwilliger J, Parmley R, Raghu G, Sandkuyl LA, Ott J, Ochs H, Wedgwood R, Rosen F. Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus Genomics. 6: 238-242. PMID 2307467 DOI: 10.1016/0888-7543(90)90562-9 |
0.648 |
|
| 1990 |
Ott J, Bhattacharya S, Chen JD, Denton MJ, Donald J, Dubay C, Farrar GJ, Fishman GA, Frey D, Gal A. Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests. Proceedings of the National Academy of Sciences of the United States of America. 87: 701-4. PMID 2300556 DOI: 10.1073/Pnas.87.2.701 |
0.385 |
|
| 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 |
0.573 |
|
| 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 |
0.524 |
|
| 1990 |
Gilliam TC, Brzustowicz LM, Castilla LH, Lehner T, Penchaszadeh GK, Daniels RJ, Byth BC, Knowles J, Hislop JE, Shapira Y, Dubowitz V, Munsat TL, Ott J, Davies KE. Genetic homogeneity between acute and chronic forms of spinal muscular atrophy Nature. 345: 823-825. PMID 1972783 DOI: 10.1038/345823A0 |
0.353 |
|
| 1990 |
Ott J. Genetic linkage and complex diseases: A comment Genetic Epidemiology. 7: 35-36. DOI: 10.1002/Gepi.1370070109 |
0.33 |
|
| 1989 |
Kwan SP, Sandkuyl LA, Blaese M, Kunkel LM, Bruns G, Parmley R, Skarshaug S, Page DC, Ott J, Rosen FS. Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers. Genomics. 3: 39-43. PMID 2906042 DOI: 10.1016/0888-7543(88)90156-5 |
0.437 |
|
| 1989 |
Weeks DE, Ott J. Risk calculations under heterogeneity. American Journal of Human Genetics. 45: 819-21. PMID 2816945 |
0.382 |
|
| 1989 |
Sandkuyl LA, Ott J. Affective disorders: evaluation of a three-allele model accounting for clinical heterogeneity. Genetic Epidemiology. 6: 265-9. PMID 2731715 DOI: 10.1002/Gepi.1370060146 |
0.381 |
|
| 1989 |
Ott J. Statistical properties of the haplotype relative risk. Genetic Epidemiology. 6: 127-30. PMID 2731704 DOI: 10.1002/Gepi.1370060124 |
0.337 |
|
| 1989 |
Ott J. Computer-simulation methods in human linkage analysis. Proceedings of the National Academy of Sciences of the United States of America. 86: 4175-8. PMID 2726769 DOI: 10.1073/Pnas.86.11.4175 |
0.389 |
|
| 1989 |
Sandkuyl L, Ott J. Determining informativity of marker typing for genetic counseling in a pedigree. Human Genetics. 82: 159-162. PMID 2722192 DOI: 10.1007/Bf00284050 |
0.379 |
|
| 1989 |
Palotie A, Väisänen P, Ott J, Ryhänen L, Elima K, Vikkula M, Cheah K, Vuorio E, Peltonen L. Predisposition to familial osteoarthrosis linked to type II collagen gene. Lancet (London, England). 1: 924-7. PMID 2565419 DOI: 10.1016/S0140-6736(89)92507-5 |
0.37 |
|
| 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 |
0.581 |
|
| 1988 |
Zoghbi H, Sandkuyl L, Ott J, Daiger S, Pollack M, O'Brien W, Beaudet A. Assignment of autosomal dominant spinocerebellar ataxia centromeric to HLA using multilocus linkage analysis Human Immunology. 23: 161. DOI: 10.1016/0198-8859(88)90297-2 |
0.331 |
|
| 1987 |
Lathrop GM, Chotai J, Ott J, Lalouel JM. Tests of gene order from three-locus linkage data. Annals of Human Genetics. 51: 235-49. PMID 3688837 DOI: 10.1111/J.1469-1809.1987.Tb00876.X |
0.579 |
|
| 1987 |
Ott J, Lathrop GM. Goodness-of-fit tests for locus order in three-point mapping. Genetic Epidemiology. 4: 51-7. PMID 3569878 DOI: 10.1002/Gepi.1370040107 |
0.526 |
|
| 1987 |
Ott J, Mensink EJ, Thompson A, Schot JD, Schuurman RK. Heterogeneity in the map distance between X-linked agammaglobulinemia and a map of nine RFLP loci. Human Genetics. 74: 280-3. PMID 2877937 DOI: 10.1007/Bf00282549 |
0.349 |
|
| 1986 |
Gallmann M, Fràter-Schröder M, Scheffrahn W, Ott J, Schmid B, Bütler E, Biedermann V, Kierat L. Indication against genetic localisation of the human transcobalamin II gene (TC2) on chromosome 16. Clinical Genetics. 29: 349-53. PMID 3017611 DOI: 10.1111/J.1399-0004.1986.Tb00503.X |
0.354 |
|
| 1986 |
Ott J. Linkage probability and its approximate confidence interval under possible heterogeneity. Genetic Epidemiology. 1: 251-257. PMID 2952550 DOI: 10.1002/Gepi.1370030739 |
0.3 |
|
| 1985 |
Mensink EJ, Schot JD, Tippett P, Ott J, Schuurman RK. X-linked agammaglobulinemia and the red blood cell determinants Xg and 12E7 are not closely linked. Human Genetics. 68: 303-9. PMID 6595200 DOI: 10.1007/Bf00292589 |
0.321 |
|
| 1985 |
Ott J. A chi-square test to distinguish allelic association from other causes of phenotypic association between two loci. Genetic Epidemiology. 2: 79-84. PMID 4054594 DOI: 10.1002/Gepi.1370020108 |
0.381 |
|
| 1985 |
Ott J. Genetic analysis workshop III: Combining two‐point analyses under the constraints of a linear map and a constant female/male distance ratio Genetic Epidemiology. 2: 217-218. DOI: 10.1002/Gepi.1370020219 |
0.314 |
|
| 1984 |
Lathrop GM, Lalouel JM, Julier C, Ott J. Strategies for multilocus linkage analysis in humans. Proceedings of the National Academy of Sciences of the United States of America. 81: 3443-6. PMID 6587361 DOI: 10.1073/Pnas.81.11.3443 |
0.605 |
|
| 1983 |
Bird TD, Ott J, Giblett ER, Chance PF, Sumi SM, Kraft GH. Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I). Annals of Neurology. 14: 679-84. PMID 6651251 DOI: 10.1002/Ana.410140612 |
0.329 |
|
| 1983 |
Ott J. Linkage analysis and family classification under heterogeneity Annals of Human Genetics. 47: 311-320. PMID 6651220 DOI: 10.1111/J.1469-1809.1983.Tb01001.X |
0.325 |
|
| 1982 |
Ott J, Falk CT. Epistatic association and linkage analysis in human families. Human Genetics. 62: 296-300. PMID 7166304 DOI: 10.1007/Bf00304542 |
0.408 |
|
| 1980 |
Rossen RD, Brewer EJ, Sharp RM, Ott J, Templeton JW. Familial rheumatoid arthritis: linkage of HLA to disease susceptibility locus in four families where proband presented with juvenile rheumatoid arthritis. The Journal of Clinical Investigation. 65: 629-42. PMID 6766468 DOI: 10.1172/Jci109708 |
0.325 |
|
| 1980 |
Ott J. Detection of rare major genes in lipid levels. Human Genetics. 51: 79-91. PMID 500096 DOI: 10.1007/Bf00278296 |
0.339 |
|
| 1979 |
Ott J. Human gene mapping by postreduction and recombination frequencies under complete interference. Clinical Genetics. 15: 11-6. PMID 759051 DOI: 10.1111/J.1399-0004.1979.Tb02023.X |
0.388 |
|
| 1977 |
Ott J. Linkage analysis with misclassification at one locus. Clinical Genetics. 12: 119-24. PMID 891013 DOI: 10.1111/J.1399-0004.1977.Tb00913.X |
0.328 |
|
| 1976 |
Ott J, Linder D, McCaw BK, Lovrien EW, Hecht F. Estimating distances from the centromere by means of benign ovarian teratomas in man Annals of Human Genetics. 40: 191-196. PMID 1015813 DOI: 10.1111/J.1469-1809.1976.Tb00179.X |
0.305 |
|
| 1976 |
Ott J. Note on the prior probability of autosomal linkage. Annals of Human Genetics. 39: 433-4. PMID 952484 DOI: 10.1111/J.1469-1809.1976.Tb00148.X |
0.332 |
|
| 1976 |
Ott J, Hecht F, Linder D, Lovrien EW, McCaw BK. Human centromere mapping using teratoma data Birth Defects: Original Article Series. 12: 396-398. PMID 799523 DOI: 10.1159/000130641 |
0.301 |
|
| 1975 |
Bremner WJ, Ott J, Moore DJ, Paulsen CA. Reifenstein's syndrome: investigation of linkage to X-chromosomal loci. Clinical Genetics. 6: 216-20. PMID 4547688 DOI: 10.1111/J.1399-0004.1974.Tb00654.X |
0.341 |
|
| 1975 |
Ott J, Goldstein JL, Harrod MJ. Linkage investigation of a large family with Reifenstein's syndrome Clinical Genetics. 7: 342-344. PMID 236106 DOI: 10.1111/J.1399-0004.1975.Tb00339.X |
0.339 |
|
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