Year |
Citation |
Score |
2015 |
Single RM, Strayer N, Thomson G, Paunic V, Albrecht M, Maiers M. Asymmetric linkage disequilibrium: Tools for assessing multiallelic LD. Human Immunology. PMID 26359129 DOI: 10.1016/J.Humimm.2015.09.001 |
0.469 |
|
2014 |
Thomson G, Single RM. Conditional asymmetric linkage disequilibrium (ALD): extending the biallelic r2 measure. Genetics. 198: 321-31. PMID 25023400 DOI: 10.1534/Genetics.114.165266 |
0.462 |
|
2014 |
Lancaster AK, Meyer D, Nelson M, Mack SJ, Single RM, Hollenbach JA, Thomson G. Preliminary population genetic analyses of data from the IHWG anthropology/human genetic diversity component F1000research. 5. DOI: 10.7490/F1000Research.1096260.1 |
0.772 |
|
2013 |
Wissemann WT, Hill-Burns EM, Zabetian CP, Factor SA, Patsopoulos N, Hoglund B, Holcomb C, Donahue RJ, Thomson G, Erlich H, Payami H. Association of Parkinson disease with structural and regulatory variants in the HLA region. American Journal of Human Genetics. 93: 984-93. PMID 24183452 DOI: 10.1016/J.Ajhg.2013.10.009 |
0.473 |
|
2012 |
Fernandez Vina MA, Hollenbach JA, Lyke KE, Sztein MB, Maiers M, Klitz W, Cano P, Mack S, Single R, Brautbar C, Israel S, Raimondi E, Khoriaty E, Inati A, Andreani M, ... ... Thomson G, et al. Tracking human migrations by the analysis of the distribution of HLA alleles, lineages and haplotypes in closed and open populations. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 367: 820-9. PMID 22312049 DOI: 10.1098/Rstb.2011.0320 |
0.557 |
|
2011 |
Hill-Burns EM, Factor SA, Zabetian CP, Thomson G, Payami H. Evidence for more than one Parkinson's disease-associated variant within the HLA region. Plos One. 6: e27109. PMID 22096524 DOI: 10.1371/Journal.Pone.0027109 |
0.398 |
|
2011 |
Hollenbach JA, Mack SJ, Gourraud PA, Single RM, Maiers M, Middleton D, Thomson G, Marsh SGE, Varney MD. A community standard for immunogenomic data reporting and analysis: Proposal for a STrengthening the REporting of Immunogenomic Studies statement Tissue Antigens. 78: 333-344. PMID 21988720 DOI: 10.1111/J.1399-0039.2011.01777.X |
0.484 |
|
2011 |
Mack SJ, Guidry PA, Marthandan N, Smith T, Campbell J, Dunn P, Karp DR, Single RM, Thomson G, Wiser J, Scheuermann RH, Erlich HA. The Immport Ambiguity Resolution Tool: A Frequency-Based Approach To Resolving Allelic And Genotypic Ambiguity In Hla Genotype Data Human Immunology. 72. DOI: 10.1016/J.Humimm.2011.07.225 |
0.458 |
|
2010 |
Hollenbach JA, Thompson SD, Bugawan TL, Ryan M, Sudman M, Marion M, Langefeld CD, Thomson G, Erlich HA, Glass DN. Juvenile idiopathic arthritis and HLA class I and class II interactions and age-at-onset effects. Arthritis and Rheumatism. 62: 1781-91. PMID 20191588 DOI: 10.1002/Art.27424 |
0.496 |
|
2010 |
Bronson PG, Komorowski LK, Ramsay PP, May SL, Noble J, Lane JA, Thomson G, Claas FH, Seldin MF, Kelly JA, Harley JB, Moser KL, Gaffney PM, Behrens T, Criswell LA, et al. Analysis of maternal-offspring HLA compatibility, parent-of-origin effects, and noninherited maternal antigen effects for HLA-DRB1 in systemic lupus erythematosus. Arthritis and Rheumatism. 62: 1712-7. PMID 20191587 DOI: 10.1002/Art.27426 |
0.788 |
|
2010 |
Valdes AM, Thomson G, Barcellos LF. Genetic variation within the HLA class III influences T1D susceptibility conferred by high-risk HLA haplotypes Genes and Immunity. 11: 209-218. PMID 20054343 DOI: 10.1038/Gene.2009.104 |
0.681 |
|
2010 |
Karp DR, Marthandan N, Marsh SG, Ahn C, Arnett FC, Deluca DS, Diehl AD, Dunivin R, Eilbeck K, Feolo M, Guidry PA, Helmberg W, Lewis S, Mayes MD, Mungall C, ... ... Thomson G, et al. Novel sequence feature variant type analysis of the HLA genetic association in systemic sclerosis. Human Molecular Genetics. 19: 707-19. PMID 19933168 DOI: 10.1093/Hmg/Ddp521 |
0.485 |
|
2010 |
Thomson G, Marthandan N, Hollenbach JA, Mack SJ, Erlich HA, Single RM, Waller MJ, Marsh SG, Guidry PA, Karp DR, Scheuermann RH, Thompson SD, Glass DN, Helmberg W. Sequence feature variant type (SFVT) analysis of the HLA genetic association in juvenile idiopathic arthritis. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 359-70. PMID 19908388 |
0.397 |
|
2010 |
Lancaster AK, Single RM, Solberg OD, Nelson MP, Thomson G. Lightning talk: PyPop – a software pipeline for large-scale multilocus population genomics Nature Precedings. DOI: 10.1038/Npre.2010.4700.1 |
0.682 |
|
2010 |
Hollenbach JA, Meller J, Thompson S, Langefeld C, Bugawan T, Sudman M, Thomson G, Ryan M, Erlich H, Glass D. 45-OR: Fine-Mapping of MHC Region Variants in Juvenile Idiopathic Arthritis (JIA) Reveals Evidence of Additional Predisposing Sites Telomeric to Class I Human Immunology. 71: S141. DOI: 10.1016/J.Humimm.2010.06.259 |
0.35 |
|
2009 |
Barcellos LF, May SL, Ramsay PP, Quach HL, Lane JA, Nititham J, Noble JA, Taylor KE, Quach DL, Chung SA, Kelly JA, Moser KL, Behrens TW, Seldin MF, Thomson G, et al. High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions. Plos Genetics. 5: e1000696. PMID 19851445 DOI: 10.1371/Journal.Pgen.1000696 |
0.651 |
|
2009 |
Bronson PG, Ramsay PP, Thomson G, Barcellos LF. Analysis of maternal-offspring HLA compatibility, parent-of-origin and non-inherited maternal effects for the classical HLA loci in type 1 diabetes. Diabetes, Obesity & Metabolism. 11: 74-83. PMID 19143818 DOI: 10.1111/J.1463-1326.2008.01006.X |
0.817 |
|
2009 |
Valdes AM, Thomson G. Several loci in the HLA class III region are associated with T1D risk after adjusting for DRB1-DQB1 Diabetes, Obesity and Metabolism. 11: 46-52. PMID 19143814 DOI: 10.1111/J.1463-1326.2008.01002.X |
0.498 |
|
2009 |
Thomson G, Karp DR, Marthandan N, Guidry PA, Mack SJ, Single RM, Scheuermann RH, Helmberg W. 249-P: Sequence feature variant type (SFVT) analysis of HLA DR-DQ amino acids in type 1 diabetes Human Immunology. 70. DOI: 10.1016/J.Humimm.2009.09.282 |
0.334 |
|
2009 |
Hollenbach J, Bugawan T, Sudman M, Thomson G, Thompson S, Ryan M, Langefeld C, Erlich H, Glass D. 220-P: Examination of HLA class II amino acid variation in juvenile idiopathic arthritis (JIA) implicates P4 with position 86 Human Immunology. 70. DOI: 10.1016/J.Humimm.2009.09.253 |
0.36 |
|
2009 |
Mack SJ, Erlich HA, Feolo M, Fernandez-Vina M, Gourrauud P-, Helmberg W, Kanga U, Kupatawintu P, Lancaster A, Maiers M, Maldonado-Torres H, Marsh SGE, Meyer D, Middleton D, Mueller CR, ... ... Thomson G, et al. 150-P: IDAWG - the Immunogenomic Data-Analysis Working Group Human Immunology. 70. DOI: 10.1016/J.Humimm.2009.09.183 |
0.714 |
|
2008 |
Solberg OD, Mack SJ, Lancaster AK, Single RM, Tsai Y, Sanchez-Mazas A, Thomson G. Balancing selection and heterogeneity across the classical human leukocyte antigen loci: a meta-analytic review of 497 population studies. Human Immunology. 69: 443-64. PMID 18638659 DOI: 10.1016/J.Humimm.2008.05.001 |
0.799 |
|
2008 |
Thomson G, Barcellos LF, Valdes AM. Searching for additional disease loci in a genomic region. Advances in Genetics. 60: 253-92. PMID 18358324 DOI: 10.1016/S0065-2660(07)00411-7 |
0.619 |
|
2008 |
Thomson G. Investigation of the mode of inheritance of the HLA associated diseases by the method of antigen genotype frequencies among diseased individuals. Tissue Antigens. 21: 81-104. PMID 6405504 DOI: 10.1111/J.1399-0039.1983.Tb00377.X |
0.434 |
|
2008 |
Thomson G. The mode of inheritance of the HLA-linked gene predisposing to narcolepsy. Tissue Antigens. 26: 201-203. PMID 3876617 DOI: 10.1111/J.1399-0039.1985.Tb00958.X |
0.312 |
|
2008 |
Payami H, Thomson G, Khan MA, Grennan DM, Sanders P, Dyer P, Dostal C. Genetics of rheumatoid arthritis. Tissue Antigens. 27: 57-63. PMID 3705054 DOI: 10.1111/J.1399-0039.1986.Tb01499.X |
0.369 |
|
2008 |
Hollenbach J, Bugawan T, Sudman M, Thomson G, Thompson S, Ryan M, Langefeld C, Erlich H, Glass D. 177-P: Association of HLA-DR-DQ haplotypes with juvenile idiopathic arthritis (JIA) Human Immunology. 69. DOI: 10.1016/J.Humimm.2008.08.196 |
0.437 |
|
2008 |
Solberg OD, Mack SJ, Single RM, Lancaster AK, Thomson G, Sanchez-Mazas A. 6-OR: Global patterns of polymorphism and selection at the classical HLA loci: A meta-analysis of 497 population studies Human Immunology. 69. DOI: 10.1016/J.Humimm.2008.08.007 |
0.773 |
|
2007 |
Thomson G, Valdes AM. Conditional genotype analysis: detecting secondary disease loci in linkage disequilibrium with a primary disease locus. Bmc Proceedings. 1: S163. PMID 18466509 DOI: 10.1186/1753-6561-1-S1-S163 |
0.494 |
|
2007 |
Dupuis J, Albers K, Allen-Brady K, Cho K, Elston RC, Kappen HJ, Tang H, Thomas A, Thomson G, Tsung E, Yang Q, Zhang W, Zhao K, Zheng G, Ziegler JT. Effect of linkage disequilibrium between markers in linkage and association analyses. Genetic Epidemiology. 31: S139-48. PMID 18046770 DOI: 10.1002/Gepi.20291 |
0.375 |
|
2007 |
Thomson G, Valdes AM, Noble JA, Kockum I, Grote MN, Najman J, Erlich HA, Cucca F, Pugliese A, Steenkiste A, Dorman JS, Caillat-Zucman S, Hermann R, Ilonen J, Lambert AP, et al. Relative predispositional effects of HLA class II DRB1-DQB1 haplotypes and genotypes on type 1 diabetes: a meta-analysis. Tissue Antigens. 70: 110-27. PMID 17610416 DOI: 10.1111/J.1399-0039.2007.00867.X |
0.531 |
|
2007 |
Steenkiste A, Valdes AM, Feolo M, Hoffman D, Concannon P, Noble J, Schoch G, Hansen J, Helmberg W, Dorman JS, Thomson G, Pugliese A. 14th International HLA and Immunogenetics Workshop: Report on the HLA component of type 1 diabetes Tissue Antigens. 69: 214-225. PMID 17445204 DOI: 10.1111/J.1399-0039.2006.00772.X |
0.498 |
|
2007 |
Lancaster AK, Single RM, Solberg OD, Nelson MP, Thomson G. PyPop update--a software pipeline for large-scale multilocus population genomics. Tissue Antigens. 69: 192-7. PMID 17445199 DOI: 10.1111/J.1399-0039.2006.00769.X |
0.758 |
|
2007 |
Mack SJ, Sanchez-Mazas A, Single RM, Meyer D, Hill J, Dron HA, Jani AJ, Thomson G, Erlich HA. Population samples and genotyping technology. Tissue Antigens. 69: 188-91. PMID 17445198 DOI: 10.1111/J.1399-0039.2006.00768.X |
0.658 |
|
2007 |
Single RM, Meyer D, Mack SJ, Lancaster A, Erlich HA, Thomson G. 14th International HLA and Immunogenetics Workshop: report of progress in methodology, data collection, and analyses. Tissue Antigens. 69: 185-7. PMID 17445197 DOI: 10.1111/J.1399-0039.2006.00767.X |
0.801 |
|
2007 |
Tu B, MacK SJ, Lazaro A, Lancaster A, Thomson G, Cao K, Chen M, Ling G, Hartzman R, Ng J, Hurley CK. HLA-A, -B, -C, -DRB1 allele and haplotype frequencies in an African American population Tissue Antigens. 69: 73-85. PMID 17212710 DOI: 10.1111/J.1399-0039.2006.00728.X |
0.783 |
|
2006 |
Barcellos LF, Sawcer S, Ramsay PP, Baranzini SE, Thomson G, Briggs F, Cree BC, Begovich AB, Villoslada P, Montalban X, Uccelli A, Savettieri G, Lincoln RR, DeLoa C, Haines JL, et al. Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis. Human Molecular Genetics. 15: 2813-24. PMID 16905561 DOI: 10.1093/Hmg/Ddl223 |
0.758 |
|
2006 |
Meyer D, Single RM, Mack SJ, Erlich HA, Thomson G. Signatures of demographic history and natural selection in the human major histocompatibility complex Loci. Genetics. 173: 2121-42. PMID 16702436 DOI: 10.1534/Genetics.105.052837 |
0.705 |
|
2005 |
Valdes AM, Thomson G, Graham J, Zarghami M, McNeney B, Kockum I, Smith A, Lathrop M, Steenkiste AR, Dorman JS, Noble JA, Hansen JA, Pugliese A, Lernmark A. D6S265*15 marks a DRB1*15, DQB1*0602 haplotype associated with attenuated protection from type 1 diabetes mellitus Diabetologia. 48: 2540-2543. PMID 16320082 DOI: 10.1007/S00125-005-0011-8 |
0.499 |
|
2005 |
Carlton VE, Hu X, Chokkalingam AP, Schrodi SJ, Brandon R, Alexander HC, Chang M, Catanese JJ, Leong DU, Ardlie KG, Kastner DL, Seldin MF, Criswell LA, Gregersen PK, Beasley E, ... Thomson G, et al. PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis. American Journal of Human Genetics. 77: 567-81. PMID 16175503 DOI: 10.1086/468189 |
0.413 |
|
2005 |
Malkki M, Single R, Carrington M, Thomson G, Petersdorf E. MHC microsatellite diversity and linkage disequilibrium among common HLA-A, HLA-B, DRB1 haplotypes: Implications for unrelated donor hematopoietic transplantation and disease association studies Tissue Antigens. 66: 114-124. PMID 16029431 DOI: 10.1111/J.1399-0039.2005.00453.X |
0.473 |
|
2005 |
Chen JJ, Duan T, Single R, Mather K, Thomson G. Hardy-Weinberg testing of a single homozygous genotype. Genetics. 170: 1439-42. PMID 15911570 DOI: 10.1534/Genetics.105.043190 |
0.552 |
|
2005 |
Valdes AM, Wapelhorst B, Concannon P, Erlich HA, Thomson G, Noble JA. Extended DR3-D6S273-HLA-B haplotypes are associated with increased susceptibility to type 1 diabetes in US Caucasians Tissue Antigens. 65: 115-119. PMID 15663750 DOI: 10.1111/J.1399-0039.2005.00348.X |
0.537 |
|
2005 |
Thomson G, Single RM, Lancaster A, Solberg O, Meyer D, Mack SJ, Erlich H. Population genetic analyses of the 13th IHW anthropology data Human Immunology. 66: 66. DOI: 10.1016/J.Humimm.2005.08.125 |
0.763 |
|
2005 |
Thomson G, Valdes AM, Dorman JS, Steenkiste A, Noble JA, Concannon P, Smith AG, John H, Lernmark A, Pugliese A. The HLA component of type 1 diabetes Human Immunology. 66: 64. DOI: 10.1016/J.Humimm.2005.08.122 |
0.334 |
|
2004 |
Lambert AP, Gillespie KM, Thomson G, Cordell HJ, Todd JA, Gale EA, Bingley PJ. Absolute risk of childhood-onset type 1 diabetes defined by human leukocyte antigen class II genotype: a population-based study in the United Kingdom. The Journal of Clinical Endocrinology and Metabolism. 89: 4037-43. PMID 15292346 DOI: 10.1210/Jc.2003-032084 |
0.449 |
|
2004 |
Cao K, Moormann AM, Lyke KE, Masaberg C, Sumba OP, Doumbo OK, Koech D, Lancaster A, Nelson M, Meyer D, Single R, Hartzman RJ, Plowe CV, Kazura J, Mann DL, ... ... Thomson G, et al. Differentiation between African populations is evidenced by the diversity of alleles and haplotypes of HLA class I loci. Tissue Antigens. 63: 293-325. PMID 15009803 DOI: 10.1111/J.0001-2815.2004.00192.X |
0.814 |
|
2004 |
Gorman JD, Lum RF, Chen JJ, Suarez-Almazor ME, Thomson G, Criswell LA. Impact of shared epitope genotype and ethnicity on erosive disease: a meta-analysis of 3,240 rheumatoid arthritis patients. Arthritis and Rheumatism. 50: 400-12. PMID 14872482 DOI: 10.1002/Art.20006 |
0.5 |
|
2004 |
Williams F, Meenagh A, Single R, McNally M, Kelly P, Nelson MP, Meyer D, Lancaster A, Thomson G, Middleton D. High resolution HLA-DRB1 identification of a Caucasian population. Human Immunology. 65: 66-77. PMID 14700598 DOI: 10.1016/J.Humimm.2003.10.004 |
0.814 |
|
2004 |
Oksenberg JR, Barcellos LF, Cree BA, Baranzini SE, Bugawan TL, Khan O, Lincoln RR, Swerdlin A, Mignot E, Lin L, Goodin D, Erlich HA, Schmidt S, Thomson G, Reich DE, et al. Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans. American Journal of Human Genetics. 74: 160-7. PMID 14669136 DOI: 10.1086/380997 |
0.681 |
|
2003 |
Barcellos LF, Thomson G. Genetic analysis of multiple sclerosis in Europeans. Journal of Neuroimmunology. 143: 1-6. PMID 14575906 DOI: 10.1016/J.Jneuroim.2003.08.004 |
0.588 |
|
2003 |
Walsh EC, Mather KA, Schaffner SF, Farwell L, Daly MJ, Patterson N, Cullen M, Carrington M, Bugawan TL, Erlich H, Campbell J, Barrett J, Miller K, Thomson G, Lander ES, et al. An integrated haplotype map of the human major histocompatibility complex. American Journal of Human Genetics. 73: 580-90. PMID 12920676 DOI: 10.1086/378101 |
0.69 |
|
2003 |
Lancaster A, Nelson MP, Meyer D, Single RM, Thomson G. PyPop: a software framework for population genomics: analyzing large-scale multi-locus genotype data. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 514-25. PMID 12603054 |
0.774 |
|
2002 |
Kotb M, Norrby-Teglund A, McGeer A, El-Sherbini H, Dorak MT, Khurshid A, Green K, Peeples J, Wade J, Thomson G, Schwartz B, Low DE. An immunogenetic and molecular basis for differences in outcomes of invasive group A streptococcal infections. Nature Medicine. 8: 1398-404. PMID 12436116 DOI: 10.1038/Nm1202-800 |
0.373 |
|
2002 |
Guo SW, Amos C, Deng HW, Thomson G. Detecting genetic differences [8] (multiple letters) Fertility and Sterility. 78: 441-444. PMID 12137901 DOI: 10.1016/S0015-0282(02)03262-4 |
0.344 |
|
2002 |
Noble JA, Valdes AM, Bugawan TL, Apple RJ, Thomson G, Erlich HA. The HLA class I A locus affects susceptibility to type 1 diabetes. Human Immunology. 63: 657-64. PMID 12121673 DOI: 10.1016/S0198-8859(02)00421-4 |
0.522 |
|
2002 |
Single RM, Meyer D, Hollenbach JA, Nelson MP, Noble JA, Erlich HA, Thomson G. Haplotype frequency estimation in patient populations: the effect of departures from Hardy-Weinberg proportions and collapsing over a locus in the HLA region. Genetic Epidemiology. 22: 186-95. PMID 11788963 DOI: 10.1002/Gepi.0163 |
0.597 |
|
2001 |
Valdes AM, Noble JA, Gnin E, Clerget-Darpoux F, Erlich HA, Thomson G. Modeling of HLA class II susceptibility to type I diabetes reveals an effect associated with DPB1 Genetic Epidemiology. 21: 212-223. PMID 11668578 DOI: 10.1002/Gepi.1030 |
0.572 |
|
2001 |
Thomson G. An overview of the genetic analysis of complex diseases, with reference to type I diabetes Best Practice and Research: Clinical Endocrinology and Metabolism. 15: 265-277. PMID 11554770 DOI: 10.1053/Beem.2001.0145 |
0.399 |
|
2001 |
Meyer D, Thomson G. How selection shapes variation of the human major histocompatibility complex: a review. Annals of Human Genetics. 65: 1-26. PMID 11415519 DOI: 10.1046/J.1469-1809.2001.6510001.X |
0.628 |
|
2001 |
Hollenbach JA, Thomson G, Cao K, Fernandez-Vina M, Erlich HA, Bugawan TL, Winkler C, Winter M, Klitz W. HLA diversity, differentiation, and haplotype evolution in mesoamerican natives Human Immunology. 62: 378-390. PMID 11295471 DOI: 10.1016/S0198-8859(01)00212-9 |
0.577 |
|
2001 |
Thomson G. 28 Significance levels in genome scans Advances in Genetics. 42: 475-486. PMID 11037336 DOI: 10.1016/S0065-2660(01)42037-2 |
0.392 |
|
2000 |
Adams EJ, Cooper S, Thomson G, Parham P. Common chimpanzee have greater diversity than humans at two of the three highly polymorphic MHC class I genes Immunogenetics. 51: 410-424. PMID 10866107 DOI: 10.1007/s002510050639 |
0.407 |
|
2000 |
Génin E, Ober C, Weitkamp L, Thomson G. A robust test for assortative mating. European Journal of Human Genetics : Ejhg. 8: 119-24. PMID 10757643 DOI: 10.1038/Sj.Ejhg.5200430 |
0.486 |
|
2000 |
Noble JA, Valdes AM, Thomson G, Erlich HA. The HLA class II locus DPB1 can influence susceptibility to type 1 diabetes Diabetes. 49: 121-125. PMID 10615959 DOI: 10.2337/Diabetes.49.1.121 |
0.513 |
|
1999 |
Valdes AM, McWeeney SK, Meyer D, Nelson MP, Thomson G. Locus and population specific evolution in HLA class II genes. Annals of Human Genetics. 63: 27-43. PMID 10738519 DOI: 10.1046/J.1469-1809.1999.6310027.X |
0.749 |
|
1999 |
Chen JJ, Hollenbach JA, Trachtenberg EA, Just JJ, Carrington M, Rønningen KS, Begovich A, King MC, McWeeney S, Mack SJ, Erlich HA, Thomson G. Hardy-Weinberg testing for HLA class II (DRB1, DQA1, DQB1, AND DPB1) loci in 26 human ethnic groups Tissue Antigens. 54: 533-542. PMID 10674966 DOI: 10.1034/J.1399-0039.1999.540601.X |
0.662 |
|
1999 |
Valdes AM, McWeeney SK, Thomson G. Evidence for linkage and association to alcohol dependence on chromosome 19. Genetic Epidemiology. 17: S367-72. PMID 10597464 DOI: 10.1002/Gepi.1370170762 |
0.581 |
|
1999 |
Adams EJ, Thomson G, Parham P. Evidence for an HLA-C-like locus in the orangutan Pongo pygmaeus Immunogenetics. 49: 865-871. PMID 10436180 DOI: 10.1007/S002510050566 |
0.401 |
|
1999 |
Valdes AM, Thomson G, Erlich HA, Noble JA. Association between type 1 diabetes age of onset and HLA among sibling pairs Diabetes. 48: 1658-1661. PMID 10426387 DOI: 10.2337/Diabetes.48.8.1658 |
0.406 |
|
1999 |
Guédez Y, Kotby A, El-Demellawy M, Galal A, Thomson G, Zaher S, Kassem S, Kotb M. HLA class II associations with rheumatic heart disease are more evident and consistent among clinically homogeneous patients. Circulation. 99: 2784-90. PMID 10351973 DOI: 10.1161/01.Cir.99.21.2784 |
0.458 |
|
1999 |
Salamon H, Klitz W, Easteal S, Gao X, Erlich HA, Fernandez-Viña M, Trachtenberg EA, McWeeney SK, Nelson MP, Thomson G. Evolution of HLA class II molecules: Allelic and amino acid site variability across populations. Genetics. 152: 393-400. PMID 10224269 |
0.587 |
|
1999 |
Mu H, Chen JJ, Jiang Y, King MC, Thomson G, Criswell LA. Tumor necrosis factor a microsatellite polymorphism is associated with rheumatoid arthritis severity through an interaction with the HLA-DRB1 shared epitope Arthritis and Rheumatism. 42: 438-442. PMID 10088765 DOI: 10.1002/1529-0131(199904)42:3<438::Aid-Anr7>3.0.Co;2-F |
0.372 |
|
1999 |
Genin E, Ober C, Thomson G. Tell me your HLA, I will tell you whom to marry Annals of Human Genetics. 63: 358-358. DOI: 10.1111/J.1469-1809.1999.Ahg634_0351_9.X |
0.462 |
|
1998 |
Grote MN, Klitz W, Thomson G. Constrained disequilibrium values and hitchhiking in a three-locus system Genetics. 150: 1295-1307. PMID 9799280 |
0.361 |
|
1998 |
Rigby AS, MacGregor AJ, Thomson G. HLA haplotype sharing in rheumatoid arthritis sibships: Risk estimates subdivided by proband genotype Genetic Epidemiology. 15: 403-418. PMID 9671989 DOI: 10.1002/(Sici)1098-2272(1998)15:4<403::Aid-Gepi6>3.0.Co;2-2 |
0.402 |
|
1997 |
Barcellos LF, Thomson G, Carrington M, Schafer J, Begovich AB, Lin P, Xu XH, Min BQ, Marti D, Klitz W. Chromosome 19 single-locus and multilocus haplotype associations with multiple sclerosis: Evidence of a new susceptibility locus in caucasian and chinese patients Journal of the American Medical Association. 278: 1256-1261. PMID 9333267 |
0.584 |
|
1997 |
Barcellos LF, Klitz W, Field LL, Tobias R, Bowcock AM, Wilson R, Nelson MP, Nagatomi J, Thomson G. Association mapping of disease loci, by use of a pooled DNA genomic screen American Journal of Human Genetics. 61: 734-747. PMID 9326338 DOI: 10.1086/515512 |
0.537 |
|
1997 |
Just JJ, King MC, Thomson G, Klitz W. African-American HLA class II allele and haplotype diversity Tissue Antigens. 49: 547-555. PMID 9174158 DOI: 10.1111/j.1399-0039.1997.tb02801.x |
0.411 |
|
1997 |
Valdes AM, McWeeney S, Thomson G. HLA class II DR-DQ amino acids and insulin-dependent diabetes mellitus: Application of the haplotype method American Journal of Human Genetics. 60: 717-728. PMID 9042932 |
0.37 |
|
1997 |
Valdes AM, Thomson G. Detecting disease-predisposing variants: The haplotype method American Journal of Human Genetics. 60: 703-716. PMID 9042931 |
0.379 |
|
1997 |
Just JJ, King MC, Thomson G, Klitz W. African-American HLA class II allele and haplotype diversity. Tissue Antigens. 48: 636-44. PMID 9008305 DOI: 10.1111/J.1399-0039.1996.Tb02686.X |
0.507 |
|
1996 |
Noble JA, Valdes AM, Cook M, Klitz W, Thomson G, Erlich HA. The role of HLA class II genes in insulin-dependent diabetes mellitus: Molecular analysis of 180 Caucasian, multiplex families American Journal of Human Genetics. 59: 1134-1148. PMID 8900244 |
0.434 |
|
1996 |
Salamon H, Tarhio J, Rønningen K, Thomson G. On Distinguishing Unique Combinations in Biological Sequences Journal of Computational Biology. 3: 407-423. PMID 8891958 DOI: 10.1089/Cmb.1996.3.407 |
0.376 |
|
1996 |
Luo DF, Buzzetti R, Rotter JI, Maclaren NK, Raffel LJ, Nisticò L, Giovannini C, Pozzilli P, Thomson G, She JX. Confirmation of three susceptibility genes to insulin-dependent diabetes mellitus: IDDM4, IDDM5 and IDDM8 Human Molecular Genetics. 5: 693-698. PMID 8733139 DOI: 10.1093/Hmg/5.5.693 |
0.316 |
|
1996 |
Field LL, Tobias R, Thomson G, Plon S. Susceptibility to insulin-dependent diabetes mellitus maps to a locus (IDDM11) on human chromosome 14q24.3-q31 Genomics. 33: 1-8. PMID 8617492 DOI: 10.1006/Geno.1996.0153 |
0.419 |
|
1996 |
Thomson G, Barcellos L, Klitz W, Field L, Tobias R, Bowcock A, Wilson R, Gilbert S. Association mapping with a pooled DNA genomic screen of the non-HLA genes in IDDM, RA and MS Human Immunology. 47: 152. DOI: 10.1016/0198-8859(96)85525-X |
0.555 |
|
1996 |
Hollenbach J, Barcellos L, Thomson G, Winkler C, Winter M, Klitz W. HLA differentiation among Mesoamerican natives Human Immunology. 47: 62. DOI: 10.1016/0198-8859(96)85024-5 |
0.611 |
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1996 |
Calandro L, Grote M, Roth M, Barcellos L, Baer D, Sensabaugh G, Thomson G, Klitz W. Hemochromatosis and HLA: New evidence and methods Human Immunology. 47: 40. DOI: 10.1016/0198-8859(96)84897-X |
0.597 |
|
1996 |
Barcellos L, Lin P, Schafer J, Thomson G, Klitz W. Gene partnerships with HLA in multiple sclerosis: DR2 and APOE Human Immunology. 47: 30. DOI: 10.1016/0198-8859(96)84837-3 |
0.609 |
|
1996 |
Reichstetter S, Martinez-Gamboa L, Klitz W, Hollenbach J, Kalden J, Thomson G, Wassmuth R. P55 - DQB1 exon2 and promoter allele frequencies and haplotypes in native American Indians and a GermanCcaucasoid Population Human Immunology. 47: 14. DOI: 10.1016/0198-8859(96)84750-1 |
0.437 |
|
1995 |
Thomson G. HLA Disease Associations: Models for the Study of Complex Human Genetic Disorders Critical Reviews in Clinical Laboratory Sciences. 32: 183-219. PMID 7598790 DOI: 10.3109/10408369509084684 |
0.483 |
|
1995 |
Jin K, Speed TP, Thomson G. Tests of random mating for a highly polymorphic locus: Application to HLA data Biometrics. 51: 1064-1076. PMID 7548691 DOI: 10.2307/2533005 |
0.369 |
|
1994 |
Zheng C, Thomson G, Peng Y. Allelic instability in mitosis can explain "genome imprinting" and other genetic phenomena in psoriasis. American Journal of Medical Genetics. 51: 163-164. PMID 8092195 DOI: 10.1002/Ajmg.1320510218 |
0.424 |
|
1994 |
She JX, Bui MM, Tian XH, Muir A, Wakeland EK, Zorovich B, Zhang LP, Liu MC, Thomson G, Maclaren NK. Additive susceptibility to insulin-dependent diabetes conferred by HLA-DQB1 and insulin genes. Autoimmunity. 18: 195-203. PMID 7858104 DOI: 10.3109/08916939409007996 |
0.407 |
|
1994 |
Thomson G, Motro U. Affected sib pair identity by state analyses. Genetic Epidemiology. 11: 353-364. PMID 7813897 DOI: 10.1002/Gepi.1370110405 |
0.394 |
|
1993 |
Thomson G. AGFAP Method: Applicability under different ascertainment schemes and a parental contributions test Genetic Epidemiology. 10: 289-310. PMID 8224808 DOI: 10.1002/Gepi.1370100503 |
0.454 |
|
1991 |
Motro U, Thomson G. Affected kin-pair IBD methods: genetic models. Genetic Epidemiology. 8: 317-327. PMID 1761204 DOI: 10.1002/Gepi.1370080504 |
0.397 |
|
1989 |
Robinson WP, Linden SMVD, Khan MA, Rentsch H-, Cats A, Russell A, Thomson G. HLA–Bw60 increases susceptibility to ankylosing spondylitis in HLA–B27+ patients Arthritis & Rheumatism. 32: 1135-1141. PMID 2789045 DOI: 10.1002/Anr.1780320912 |
0.435 |
|
1989 |
Motro U, Thomson G, Kuhner MK, Robinson WP. Affected sib pair IBS methods: detection of linkage and genetic models. Progress in Clinical and Biological Research. 329: 105-10. PMID 2622936 |
0.671 |
|
1989 |
Thomson G, Robinson WP, Kuhner MK, Joe S, Klitz W. HLA and insulin gene associations with IDDM. Genetic Epidemiology. 6: 155-60. PMID 2567257 DOI: 10.1002/Gepi.1370060129 |
0.768 |
|
1989 |
Klitz W, Kuhner MK, Robinson W, Esposito M, Thomson G. Clues to IDDM pathogenesis from genetic and serological traits in multiply affected families. Genetic Epidemiology. 6: 117-22. PMID 2567254 DOI: 10.1002/Gepi.1370060122 |
0.797 |
|
1989 |
Payami H, Joe S, Thomson G. Autoimmune thyroid disease in type I diabetic families. Genetic Epidemiology. 6: 137-141. PMID 2499500 DOI: 10.1002/Gepi.1370060126 |
0.506 |
|
1988 |
Thomson G. HLA DISEASE ASSOCIATIONS: Models for Insulin Dependent Diabetes Mellitus and the Study of Complex Human Genetic Disorders Annual Review of Genetics. 22: 31-50. PMID 3071252 DOI: 10.1146/Annurev.Ge.22.120188.000335 |
0.451 |
|
1988 |
Thomson G, Robinson WP, Kuhner MK, Joe S, MacDonald MJ, Gottschall JL, Barbosa J, Rich SS, Bertrams J, Baur MP. Genetic heterogeneity, modes of inheritance, and risk estimates for a joint study of Caucasians with insulin-dependent diabetes mellitus. American Journal of Human Genetics. 43: 799-816. PMID 3057885 |
0.732 |
|
1988 |
Klitz W, Borot N, Thomson G. A population analysis of C4 typing Human Immunology. 23: 114. DOI: 10.1016/0198-8859(88)90184-X |
0.311 |
|
1987 |
Klitz W, Lo SK, Neugebauer M, Baur MP, Albert ED, Thomson G. A comprehensive search for segregation distortion in HLA. Human Immunology. 18: 163-180. PMID 3558014 DOI: 10.1016/0198-8859(87)90013-9 |
0.49 |
|
1987 |
Louis EJ, Payami H, Thomson G. The affected sib method. V. Testing the assumptions. Annals of Human Genetics. 51: 75-92. PMID 3314668 DOI: 10.1111/J.1469-1809.1987.Tb00867.X |
0.707 |
|
1987 |
Hedrick PW, Thomson G, Klitz W. Evolutionary genetics and HLA: another classic example Biological Journal of the Linnean Society. 31: 311-331. DOI: 10.1111/J.1095-8312.1987.Tb01996.X |
0.476 |
|
1986 |
Louis EJ, Payami H, Klitz W, Lo SK, Thomson G. A synergistic three allele model for the HLA-linked components of coeliac disease predisposition. Genetic Epidemiology. Supplement. 1: 277-82. PMID 3569858 DOI: 10.1002/Gepi.1370030743 |
0.682 |
|
1986 |
Louis EJ, Thomson G. Three-allele synergistic mixed model for insulin-dependent diabetes mellitus. Diabetes. 35: 958-63. PMID 3488932 DOI: 10.2337/Diab.35.9.958 |
0.7 |
|
1986 |
Payami H, Louis EJ, Klitz W, Lo SK, Thomson G. Family and population analysis of multiple sclerosis. Genetic Epidemiology. Supplement. 1: 381-6. PMID 3471670 DOI: 10.1002/Gepi.1370030758 |
0.598 |
|
1986 |
Thomson G, Klitz W, Louis EJ, Lo SK, Bertrams J, Baur M, Neugebauer M. HLA and IDDM predisposition: new aspects. Genetic Epidemiology. Supplement. 1: 363-8. PMID 3471669 DOI: 10.1002/Gepi.1370030756 |
0.656 |
|
1985 |
Thomson G, Nicholas FW, Bodmer WF, O'Neill ME, Hedrick PW, Hudes E. Analysis of negative and multiple HLA antigen disease associations. Tissue Antigens. 26: 293-306. PMID 3867175 DOI: 10.1111/J.1399-0039.1985.Tb02227.X |
0.503 |
|
1985 |
Payami H, Thomson G, Motro U, Louis EJ, Hudes E. The affected sib method. IV. Sib trios. Annals of Human Genetics. 49: 303-14. PMID 3865624 DOI: 10.1111/J.1469-1809.1985.Tb01706.X |
0.713 |
|
1984 |
Payami H, Thomson G, Louis EJ. The affected sib method. III. Selection and recombination. American Journal of Human Genetics. 36: 352-62. PMID 6711560 |
0.615 |
|
1984 |
Thomson G, Baur MP. Third order linkage disequilibrium Tissue Antigens. 24: 250-255. PMID 6515638 DOI: 10.1111/J.1399-0039.1984.Tb02134.X |
0.343 |
|
1983 |
Thomson G, Motro U, Selvin S. Statistical aspects of measuring the strength of associations between HLA antigens and diseases Tissue Antigens. 21: 320-328. PMID 6857627 DOI: 10.1111/J.1399-0039.1983.Tb00178.X |
0.459 |
|
1983 |
Louis EJ, Thomson G, Payami H. The affected sib method. II. The intermediate model. Annals of Human Genetics. 47: 225-43. PMID 6688509 DOI: 10.1111/J.1469-1809.1983.Tb00991.X |
0.672 |
|
1983 |
Thomson G. The human histocompatibility system: anthropological considerations. American Journal of Physical Anthropology. 62: 81-89. PMID 6624903 DOI: 10.1002/Ajpa.1330620112 |
0.537 |
|
1982 |
Motro U, Thomson G. ON HETEROZYGOSITY AND THE EFFECTIVE SIZE OF POPULATIONS SUBJECT TO SIZE CHANGES. Evolution; International Journal of Organic Evolution. 36: 1059-1066. PMID 28567820 DOI: 10.1111/J.1558-5646.1982.Tb05474.X |
0.335 |
|
1981 |
Bengtsson BO, Thomson G. Measuring the strength of associations between HLA antigens and diseases. Tissue Antigens. 18: 356-363. PMID 7344182 DOI: 10.1111/J.1399-0039.1981.Tb01404.X |
0.47 |
|
1981 |
Thomson G. A review of theoretical aspects of HLA and disease associations Theoretical Population Biology. 20: 168-208. PMID 7342351 DOI: 10.1016/0040-5809(81)90009-5 |
0.428 |
|
1980 |
Thomson G. A two locus model for juvenile diabetes Annals of Human Genetics. 43: 383-398. PMID 7396412 DOI: 10.1111/J.1469-1809.1980.Tb01572.X |
0.35 |
|
1976 |
Thomson GJ, Feldman MW. Population genetics of modifiers of meiotic drive. III. Equilibrium analysis of a general model for the genetic control of segregation distortion. Theoretical Population Biology. 10: 10-25. PMID 973199 DOI: 10.1016/0040-5809(76)90003-4 |
0.506 |
|
1975 |
Thomson GJ, Feldman MW. Population genetics of modifiers of meiotic drive: IV. On the evolution of sex-ratio distortion. Theoretical Population Biology. 8: 202-11. PMID 1198352 DOI: 10.1016/0040-5809(75)90032-5 |
0.408 |
|
1974 |
Feldman MW, Franklin I, Thomson GJ. Selection in complex genetic systems. I. The symmetric equilibria of the three-locus symmetric viability model. Genetics. 76: 135-62. PMID 4818262 |
0.473 |
|
1974 |
Thomson GJ, Feldman MW. Population genetics of modifiers of meiotic drive. II. Linkage modification in the segregation distortion system. Theoretical Population Biology. 5: 155-62. PMID 4207693 DOI: 10.1016/0040-5809(74)90038-0 |
0.477 |
|
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