| Year |
Citation |
Score |
| 2020 |
Chen J, Bacelis J, Sole-Navais P, Srivastava A, Juodakis J, Rouse A, Hallman M, Teramo K, Melbye M, Feenstra B, Freathy RM, Smith GD, Lawlor DA, Murray JC, Williams SM, et al. Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype-based genetic score analysis in 10,734 mother-infant pairs. Plos Medicine. 17: e1003305. PMID 32841251 DOI: 10.1371/Journal.Pmed.1003305 |
0.339 |
|
| 2020 |
Hunt SC, Hansen MEB, Verhulst S, McQuillan MA, Beggs W, Lai TP, Mokone GG, Mpoloka SW, Meskel DW, Belay G, Nyambo TB, Abnet CC, Yeager M, Chanock SJ, Province MA, ... Williams SM, et al. Genetics and Geography of Leukocyte Telomere Length in Sub-Saharan Africans. Human Molecular Genetics. PMID 32821950 DOI: 10.1093/Hmg/Ddaa187 |
0.383 |
|
| 2020 |
Miller AK, Azhibekov T, O'Toole JF, Sedor JR, Williams SM, Redline RW, Bruggeman LA. Association of preeclampsia with infant APOL1 genotype in African Americans. Bmc Medical Genetics. 21: 110. PMID 32434471 DOI: 10.1186/S12881-020-01048-4 |
0.372 |
|
| 2020 |
McHenry ML, Bartlett J, Igo RP, Wampande EM, Benchek P, Mayanja-Kizza H, Fluegge K, Hall NB, Gagneux S, Tishkoff SA, Wejse C, Sirugo G, Boom WH, Joloba M, Williams SM, et al. Interaction between host genes and Mycobacterium tuberculosis lineage can affect tuberculosis severity: evidence for coevolution? Plos Genetics. 16: e1008728. PMID 32352966 DOI: 10.1371/Journal.Pgen.1008728 |
0.334 |
|
| 2020 |
Musanabaganwa C, Mihigo B, Tumusime R, Uwanyirigira M, da Rocha J, Hayat M, Govender M, Buto P, Nyunga T, Ramesar RS, Rotimi C, Souopgui J, Wonkam A, Williams SM, Jansen S, et al. Building Skills and Resources for Genomics, Epigenetics, and Bioinformatics Research for Africa: Report of the Joint 11th Conference of the African Society of Human Genetics and 12th H3Africa Consortium, 2018. The American Journal of Tropical Medicine and Hygiene. PMID 32207403 DOI: 10.4269/Ajtmh.19-0837 |
0.357 |
|
| 2020 |
El-Kamah GY, Mohamed AM, Gad YZ, Abdelhak S, Hennig BJ, Ramesar RS, Landouré G, Gaye A, Newport MJ, Williams SM, Ramsay M. Developing a Road Map to Spread Genomic Knowledge in Africa: Meeting Report: 10th Conference of the African Society of Human Genetics, Cairo, Egypt. The American Journal of Tropical Medicine and Hygiene. PMID 32124726 DOI: 10.4269/Ajtmh.19-0408 |
0.326 |
|
| 2020 |
McHenry ML, Williams SM, Stein CM. Genetics and evolution of tuberculosis pathogenesis: New perspectives and approaches. Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases. 104204. PMID 31981609 DOI: 10.1016/J.Meegid.2020.104204 |
0.316 |
|
| 2020 |
McHenry ML, Bartlett J, Igo RP, Wampande EM, Benchek P, Mayanja-Kizza H, Fluegge K, Hall NB, Gagneux S, Tishkoff SA, Wejse C, Sirugo G, Boom WH, Joloba M, Williams SM, et al. Association between IFN- γ levels and rs3212227 genotype using available data combined cohorts. Plos Genetics. DOI: 10.1371/Journal.Pgen.1008728.S003 |
0.31 |
|
| 2020 |
Miller A, Chen A, Buchner D, Williams S. Abstract P455: Epistatic Regulation of Hematological-related Traits and Gene Expression in Mice Reveals Additional Heritability Missed by Standard GWAS-type Analyses Circulation. 141. DOI: 10.1161/Circ.141.Suppl_1.P455 |
0.403 |
|
| 2019 |
Manduchi E, Hemerich D, van Setten J, Tragante V, Harakalova M, Pei J, Williams SM, van der Harst P, Asselbergs FW, Moore JH. A comparison of two workflows for regulome and transcriptome-based prioritization of genetic variants associated with myocardial mass. Genetic Epidemiology. PMID 31145509 DOI: 10.1002/Gepi.22215 |
0.37 |
|
| 2019 |
Sirugo G, Williams SM, Tishkoff SA. The Missing Diversity in Human Genetic Studies. Cell. 177: 26-31. PMID 30901543 DOI: 10.1016/J.Cell.2019.02.048 |
0.376 |
|
| 2019 |
Amosco MD, Tavera GR, Villar VAM, Naniong JMA, David-Bustamante LMG, Williams SM, Jose PA, Palmes-Saloma CP. Non-additive effects of ACVR2A in preeclampsia in a Philippine population. Bmc Pregnancy and Childbirth. 19: 11. PMID 30621627 DOI: 10.1186/S12884-018-2152-Z |
0.38 |
|
| 2019 |
Williams S. Genetic diversity matters New Scientist. 241: 22-23. DOI: 10.1016/S0262-4079(19)30552-4 |
0.305 |
|
| 2018 |
Huusko JM, Karjalainen MK, Graham BE, Zhang G, Farrow EG, Miller NA, Jacobsson B, Eidem HR, Murray JC, Bedell B, Breheny P, Brown NW, Bødker FL, Litterman NK, Jiang PP, ... ... Williams SM, et al. Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth. Plos Genetics. 14: e1007673. PMID 30212495 DOI: 10.1371/Journal.Pgen.1007673 |
0.301 |
|
| 2018 |
Huusko JM, Karjalainen MK, Graham BE, Zhang G, Farrow EG, Miller NA, Jacobsson B, Eidem HR, Murray JC, Bedell B, Breheny P, Brown NW, Bødker FL, Litterman NK, Jiang PP, ... ... Williams SM, et al. Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth. Plos Genetics. 14: e1007394. PMID 30001343 DOI: 10.1371/Journal.Pgen.1007394 |
0.377 |
|
| 2018 |
Manduchi E, Williams SM, Chesi A, Johnson ME, Wells AD, Grant SFA, Moore JH. Leveraging epigenomics and contactomics data to investigate SNP pairs in GWAS. Human Genetics. PMID 29797095 DOI: 10.1007/S00439-018-1893-0 |
0.383 |
|
| 2018 |
Marrs C, Chesmore K, Menon R, Williams S. Maternal human telomerase reverse transcriptase variants are associated with preterm labor and preterm premature rupture of membranes. Plos One. 13: e0195963. PMID 29771920 DOI: 10.1371/Journal.Pone.0195963 |
0.317 |
|
| 2018 |
Hellwege JN, Russell SB, Williams SM, Edwards TL, Velez Edwards DR. Gene-based evaluation of low-frequency variation and genetically-predicted gene expression impacting risk of keloid formation. Annals of Human Genetics. PMID 29484647 DOI: 10.1111/Ahg.12245 |
0.389 |
|
| 2017 |
Stein CM, Sausville L, Wejse C, Sobota RS, Zetola NM, Hill PC, Boom WH, Scott WK, Sirugo G, Williams SM. Genomics of human pulmonary tuberculosis: from genes to pathways. Current Genetic Medicine Reports. 5: 149-166. PMID 29805915 DOI: 10.1007/S40142-017-0130-9 |
0.321 |
|
| 2017 |
Chesmore K, Bartlett J, Williams SM. The ubiquity of pleiotropy in human disease. Human Genetics. PMID 29164333 DOI: 10.1007/S00439-017-1854-Z |
0.368 |
|
| 2017 |
Li X, Redline S, Zhang X, Williams S, Zhu X. Height associated variants demonstrate assortative mating in human populations. Scientific Reports. 7: 15689. PMID 29146993 DOI: 10.1038/S41598-017-15864-X |
0.393 |
|
| 2017 |
Chen A, Liu Y, Williams SM, Morris N, Buchner DA. Widespread epistasis regulates glucose homeostasis and gene expression. Plos Genetics. 13: e1007025. PMID 28961251 DOI: 10.1371/Journal.Pgen.1007025 |
0.339 |
|
| 2017 |
Graham BE, Darabos C, Huang M, Muglia LJ, Moore JH, Williams SM. Evolutionarily derived networks to inform disease pathways. Genetic Epidemiology. PMID 28944497 DOI: 10.1002/Gepi.22078 |
0.343 |
|
| 2017 |
Sausville LN, Jones CC, Aldrich MC, Blot WJ, Pozzi A, Williams SM. Genetic variation in the eicosanoid pathway is associated with non-small-cell lung cancer (NSCLC) survival. Plos One. 12: e0180471. PMID 28704416 DOI: 10.1371/Journal.Pone.0180471 |
0.335 |
|
| 2017 |
Sobota RS, Stein CM, Kodaman N, Maro I, Wieland-Alter W, Igo RP, Magohe A, Malone LL, Chervenak K, Hall NB, Matee M, Mayanja-Kizza H, Joloba M, Moore JH, Scott WK, ... ... Williams SM, et al. A chromosome 5q31.1 locus associates with tuberculin skin test reactivity in HIV-positive individuals from tuberculosis hyper-endemic regions in east Africa. Plos Genetics. 13: e1006710. PMID 28628665 DOI: 10.1371/Journal.Pgen.1006710 |
0.321 |
|
| 2017 |
Manuck TA, Huang M, Muglia L, Williams SM. Evolutionary Triangulation to Refine Genetic Association Studies of Spontaneous Preterm Birth. American Journal of Perinatology. PMID 28561145 DOI: 10.1055/S-0037-1603508 |
0.396 |
|
| 2017 |
Kodaman N, Sobota RS, Asselbergs FW, Oetjens MT, Moore JH, Brown NJ, Aldrich MC, Williams SM. Genetic Effects on the Correlation Structure of CVD Risk Factors: Exome-Wide Data From a Ghanaian Population. Global Heart. PMID 28408189 DOI: 10.1016/J.Gheart.2017.01.013 |
0.343 |
|
| 2017 |
Marrs C, Chesmore K, Saade G, Menon R, Williams S. 18: Maternal gene variants in human telomerase reverse transcriptase are associated with preterm labor and preterm premature rupture of membranes American Journal of Obstetrics and Gynecology. 216: S12-S13. DOI: 10.1016/J.Ajog.2016.11.908 |
0.312 |
|
| 2017 |
Manuck TA, Huang M, Muglia L, Williams SM. 11: Use of evolutionary triangulation to refine genetic association studies of spontaneous preterm birth (SPTB) American Journal of Obstetrics and Gynecology. 216: S9. DOI: 10.1016/J.Ajog.2016.11.901 |
0.359 |
|
| 2016 |
Jacobson DR, Alexander AA, Tagoe C, Garvey WT, Williams SM, Tishkoff S, Modiano D, Sirima SB, Kalidi I, Toure A, Buxbaum JN. The prevalence and distribution of the amyloidogenic transthyretin (TTR) V122I allele in Africa. Molecular Genetics & Genomic Medicine. 4: 548-56. PMID 27652282 DOI: 10.1002/Mgg3.231 |
0.331 |
|
| 2016 |
Frost HR, Shen L, Saykin AJ, Williams SM, Moore JH. Identifying significant gene-environment interactions using a combination of screening testing and hierarchical false discovery rate control. Genetic Epidemiology. PMID 27578615 DOI: 10.1002/Gepi.21997 |
0.312 |
|
| 2016 |
Sobota RS, Kodaman N, Mera R, Piazuelo MB, Bravo LE, Pazos A, Zabaleta J, Delgado AG, El-Rifai W, Morgan DR, Wilson KT, Correa P, Williams SM, Schneider BG. Erratum to: Epigenetic and genetic variation in GATA5 is associated with gastric disease risk. Human Genetics. PMID 27417435 DOI: 10.1007/S00439-016-1708-0 |
0.322 |
|
| 2016 |
Baharian S, Barakatt M, Gignoux CR, Shringarpure S, Errington J, Blot WJ, Bustamante CD, Kenny EE, Williams SM, Aldrich MC, Gravel S. The Great Migration and African-American Genomic Diversity. Plos Genetics. 12: e1006059. PMID 27232753 DOI: 10.1371/Journal.Pgen.1006059 |
0.311 |
|
| 2016 |
Sobota RS, Kodaman N, Mera R, Piazuelo MB, Bravo LE, Pazos A, Zabaleta J, Delgado AG, El-Rifai W, Morgan DR, Wilson KT, Correa P, Williams SM, Schneider BG. Epigenetic and genetic variation in GATA5 is associated with gastric disease risk. Human Genetics. PMID 27225266 DOI: 10.1007/S00439-016-1687-1 |
0.342 |
|
| 2016 |
Huang M, Graham BE, Zhang G, Harder R, Kodaman N, Moore JH, Muglia L, Williams SM. Evolutionary triangulation: informing genetic association studies with evolutionary evidence. Biodata Mining. 9: 12. PMID 27042214 DOI: 10.1186/S13040-016-0091-7 |
0.376 |
|
| 2016 |
Shi SQ, White MJ, Borsetti HM, Pendergast JS, Hida A, Ciarleglio CM, de Verteuil PA, Cadar AG, Cala C, McMahon DG, Shelton RC, Williams SM, Johnson CH. Molecular analyses of circadian gene variants reveal sex-dependent links between depression and clocks. Translational Psychiatry. 6: e748. PMID 26926884 DOI: 10.1038/Tp.2016.9 |
0.348 |
|
| 2015 |
Barsh GS, Cooper GM, Copenhaver GP, Gibson G, McCarthy MI, Tang H, Williams SM. PLOS Genetics Data Sharing Policy: In Pursuit of Functional Utility. Plos Genetics. 11: e1005716. PMID 26655768 DOI: 10.1371/Journal.Pgen.1005716 |
0.305 |
|
| 2015 |
Kim M, Cooper BA, Venkat R, Phillips JB, Eidem HR, Hirbo J, Nutakki S, Williams SM, Muglia LJ, Capra JA, Petren K, Abbot P, Rokas A, McGary KL. GEneSTATION 1.0: a synthetic resource of diverse evolutionary and functional genomic data for studying the evolution of pregnancy-associated tissues and phenotypes. Nucleic Acids Research. PMID 26567549 DOI: 10.1093/Nar/Gkv1137 |
0.335 |
|
| 2015 |
Russell SB, Smith JC, Huang M, Trupin JS, Williams SM. Pleiotropic Effects of Immune Responses Explain Variation in the Prevalence of Fibroproliferative Diseases. Plos Genetics. 11: e1005568. PMID 26540410 DOI: 10.1371/Journal.Pgen.1005568 |
0.34 |
|
| 2015 |
White MJ, Kodaman NM, Harder RH, Asselbergs FW, Vaughan DE, Brown NJ, Moore JH, Williams SM. Genetics of Plasminogen Activator Inhibitor-1 (PAI-1) in a Ghanaian Population. Plos One. 10: e0136379. PMID 26322636 DOI: 10.1371/Journal.Pone.0136379 |
0.417 |
|
| 2015 |
Christiaens I, Ang QW, Gordon LN, Fang X, Williams SM, Pennell CE, Olson DM. Two novel genetic variants in the mineralocorticoid receptor gene associated with spontaneous preterm birth. Bmc Medical Genetics. 16: 59. PMID 26260058 DOI: 10.1186/S12881-015-0205-Y |
0.368 |
|
| 2015 |
Villegas R, Delahanty R, Williams S, Li H, O'Brian R, Shi J, Cai Q, Xiang YB, Shu XO. Genetic Variation and Insulin Resistance in Middle-Aged Chinese Men. Annals of Human Genetics. PMID 26252243 DOI: 10.1111/Ahg.12124 |
0.314 |
|
| 2015 |
White MJ, Eren F, A??rba?l? D, Chen J, Hu T, Moore JH, Williams SM, A??rba?l? M. A systems genetics approach to dyslipidemia in children and adolescents. Omics : a Journal of Integrative Biology. 19: 248-59. PMID 25671407 DOI: 10.1089/Omi.2014.0140 |
0.365 |
|
| 2015 |
Sobota RS, Shriner D, Kodaman N, Goodloe R, Zheng W, Gao YT, Edwards TL, Amos CI, Williams SM. Addressing population-specific multiple testing burdens in genetic association studies. Annals of Human Genetics. 79: 136-47. PMID 25644736 DOI: 10.1111/Ahg.12095 |
0.369 |
|
| 2015 |
Williams SM. Epistasis in the risk of human neuropsychiatric disease. Methods in Molecular Biology (Clifton, N.J.). 1253: 71-93. PMID 25403528 DOI: 10.1007/978-1-4939-2155-3_5 |
0.33 |
|
| 2014 |
Velez Edwards DR, Tsosie KS, Williams SM, Edwards TL, Russell SB. Admixture mapping identifies a locus at 15q21.2-22.3 associated with keloid formation in African Americans. Human Genetics. 133: 1513-23. PMID 25280642 DOI: 10.1007/S00439-014-1490-9 |
0.405 |
|
| 2014 |
Wang YJ, Tayo BO, Bandyopadhyay A, Wang H, Feng T, Franceschini N, Tang H, Gao J, Sung YJ, Elston RC, Williams SM, Cooper RS, Mu TW, Zhu X. The association of the vanin-1 N131S variant with blood pressure is mediated by endoplasmic reticulum-associated degradation and loss of function. Plos Genetics. 10: e1004641. PMID 25233454 DOI: 10.1371/Journal.Pgen.1004641 |
0.379 |
|
| 2014 |
Kodaman N, Sobota RS, Mera R, Schneider BG, Williams SM. Disrupted human-pathogen co-evolution: a model for disease. Frontiers in Genetics. 5: 290. PMID 25202324 DOI: 10.3389/Fgene.2014.00290 |
0.326 |
|
| 2014 |
Ciesielski TH, Pendergrass SA, White MJ, Kodaman N, Sobota RS, Huang M, Bartlett J, Li J, Pan Q, Gui J, Selleck SB, Amos CI, Ritchie MD, Moore JH, Williams SM. Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factors. Biodata Mining. 7: 10. PMID 25071867 DOI: 10.1186/1756-0381-7-10 |
0.339 |
|
| 2014 |
White MJ, Tacconelli A, Chen JS, Wejse C, Hill PC, Gomes VF, Velez-Edwards DR, Østergaard LJ, Hu T, Moore JH, Novelli G, Scott WK, Williams SM, Sirugo G. Epiregulin (EREG) and human V-ATPase (TCIRG1): genetic variation, ethnicity and pulmonary tuberculosis susceptibility in Guinea-Bissau and The Gambia. Genes and Immunity. 15: 370-7. PMID 24898387 DOI: 10.1038/Gene.2014.28 |
0.398 |
|
| 2014 |
Giglia JL, White MJ, Hart AJ, Toro JJ, Freytes CO, Holt CC, Cai Y, Williams SM, Brandt SJ. A single nucleotide polymorphism in SLC7A5 is associated with gastrointestinal toxicity after high-dose melphalan and autologous stem cell transplantation for multiple myeloma. Biology of Blood and Marrow Transplantation : Journal of the American Society For Blood and Marrow Transplantation. 20: 1014-20. PMID 24704384 DOI: 10.1016/J.Bbmt.2014.03.022 |
0.347 |
|
| 2014 |
Huang J, Huffman JE, Yamakuchi M, Yamkauchi M, Trompet S, Asselbergs FW, Sabater-Lleal M, Trégouët DA, Chen WM, Smith NL, Kleber ME, Shin SY, Becker DM, Tang W, Dehghan A, ... ... Williams SM, et al. Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2. Arteriosclerosis, Thrombosis, and Vascular Biology. 34: 1093-101. PMID 24578379 DOI: 10.1161/Atvbaha.113.302088 |
0.345 |
|
| 2014 |
Darabos C, White MJ, Graham BE, Leung DN, Williams SM, Moore JH. The multiscale backbone of the human phenotype network based on biological pathways. Biodata Mining. 7: 1. PMID 24460644 DOI: 10.1186/1756-0381-7-1 |
0.318 |
|
| 2014 |
Villegas R, Williams SM, Gao YT, Long J, Shi J, Cai H, Li H, Chen CC, Tai ES, Hu F, Cai Q, Zheng W, Shu XO. Genetic variation in the peroxisome proliferator-activated receptor (PPAR) and peroxisome proliferator-activated receptor gamma co-activator 1 (PGC1) gene families and type 2 diabetes. Annals of Human Genetics. 78: 23-32. PMID 24359475 DOI: 10.1111/Ahg.12044 |
0.361 |
|
| 2013 |
Zhang G, Muglia LJ, Chakraborty R, Akey JM, Williams SM. Signatures of natural selection on genetic variants affecting complex human traits. Applied & Translational Genomics. 2: 78-94. PMID 27896059 DOI: 10.1016/J.Atg.2013.10.002 |
0.365 |
|
| 2013 |
Williams SM. Identifying population differences in genes that affect body mass index. Genome Medicine. 5: 102. PMID 24286457 DOI: 10.1186/Gm506 |
0.369 |
|
| 2013 |
Labuda D, Yotova V, Lefebvre JF, Moreau C, Utermann G, Williams SM. X-linked MTMR8 diversity and evolutionary history of sub-Saharan populations. Plos One. 8: e80710. PMID 24282552 DOI: 10.1371/Journal.Pone.0080710 |
0.339 |
|
| 2013 |
Agirbasli M, Eren F, Agirbasli D, White MJ, Williams SM. Multi-locus candidate gene analyses of lipid levels in a pediatric Turkish cohort: lessons learned on LPL, CETP, LIPC, ABCA1, and SHBG. Omics : a Journal of Integrative Biology. 17: 636-45. PMID 23988150 DOI: 10.1089/Omi.2013.0066 |
0.326 |
|
| 2013 |
Franceschini N, Fox E, Zhang Z, Edwards TL, Nalls MA, Sung YJ, Tayo BO, Sun YV, Gottesman O, Adeyemo A, Johnson AD, Young JH, Rice K, Duan Q, Chen F, ... ... Williams SM, et al. Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. American Journal of Human Genetics. 93: 545-54. PMID 23972371 DOI: 10.1016/J.Ajhg.2013.07.010 |
0.366 |
|
| 2013 |
Gui J, Moore JH, Williams SM, Andrews P, Hillege HL, van der Harst P, Navis G, Van Gilst WH, Asselbergs FW, Gilbert-Diamond D. A Simple and Computationally Efficient Approach to Multifactor Dimensionality Reduction Analysis of Gene-Gene Interactions for Quantitative Traits. Plos One. 8: e66545. PMID 23805232 DOI: 10.1371/Journal.Pone.0066545 |
0.323 |
|
| 2013 |
Predazzi IM, Rokas A, Deinard A, Schnetz-Boutaud N, Williams ND, Bush WS, Tacconelli A, Friedrich K, Fazio S, Novelli G, Haines JL, Sirugo G, Williams SM. Putting pleiotropy and selection into context defines a new paradigm for interpreting genetic data. Circulation. Cardiovascular Genetics. 6: 299-307. PMID 23616601 DOI: 10.1161/Circgenetics.113.000126 |
0.362 |
|
| 2013 |
Monda KL, Chen GK, Taylor KC, Palmer C, Edwards TL, Lange LA, Ng MC, Adeyemo AA, Allison MA, Bielak LF, Chen G, Graff M, Irvin MR, Rhie SK, Li G, ... ... Williams SM, et al. A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry. Nature Genetics. 45: 690-6. PMID 23583978 DOI: 10.1038/Ng.2608 |
0.355 |
|
| 2013 |
Molineros JE, Maiti AK, Sun C, Looger LL, Han S, Kim-Howard X, Glenn S, Adler A, Kelly JA, Niewold TB, Gilkeson GS, Brown EE, Alarcón GS, Edberg JC, Petri M, ... ... Williams SM, et al. Admixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody production. Plos Genetics. 9: e1003222. PMID 23441136 DOI: 10.1371/Journal.Pgen.1003222 |
0.39 |
|
| 2013 |
Collins RL, Hu T, Wejse C, Sirugo G, Williams SM, Moore JH. Multifactor dimensionality reduction reveals a three-locus epistatic interaction associated with susceptibility to pulmonary tuberculosis. Biodata Mining. 6: 4. PMID 23418869 DOI: 10.1186/1756-0381-6-4 |
0.334 |
|
| 2013 |
Hu T, Chen Y, Kiralis JW, Collins RL, Wejse C, Sirugo G, Williams SM, Moore JH. An information-gain approach to detecting three-way epistatic interactions in genetic association studies. Journal of the American Medical Informatics Association : Jamia. 20: 630-6. PMID 23396514 DOI: 10.1136/Amiajnl-2012-001525 |
0.382 |
|
| 2013 |
Kodaman N, Aldrich MC, Smith JR, Signorello LB, Bradley K, Breyer J, Cohen SS, Long J, Cai Q, Giles J, Bush WS, Blot WJ, Matthews CE, Williams SM. A small number of candidate gene SNPs reveal continental ancestry in African Americans. Annals of Human Genetics. 77: 56-66. PMID 23278390 DOI: 10.1111/J.1469-1809.2012.00738.X |
0.344 |
|
| 2012 |
Villegas R, Delahanty R, Gao YT, Long J, Williams SM, Xiang YB, Cai H, Li HL, Hu F, Cai Q, Zheng W, Shu XO. Joint effect of genetic and lifestyle risk factors on type 2 diabetes risk among Chinese men and women. Plos One. 7: e49464. PMID 23185337 DOI: 10.1371/Journal.Pone.0049464 |
0.345 |
|
| 2012 |
Huang J, Sabater-Lleal M, Asselbergs FW, Tregouet D, Shin SY, Ding J, Baumert J, Oudot-Mellakh T, Folkersen L, Johnson AD, Smith NL, Williams SM, Ikram MA, Kleber ME, Becker DM, et al. Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation. Blood. 120: 4873-81. PMID 22990020 DOI: 10.1182/Blood-2012-06-436188 |
0.357 |
|
| 2012 |
Carey RM, Schoeffel CD, Gildea JJ, Jones JE, McGrath HE, Gordon LN, Park MJ, Sobota RS, Underwood PC, Williams J, Sun B, Raby B, Lasky-Su J, Hopkins PN, Adler GK, ... Williams SM, et al. Salt sensitivity of blood pressure is associated with polymorphisms in the sodium-bicarbonate cotransporter. Hypertension. 60: 1359-66. PMID 22987918 DOI: 10.1161/Hypertensionaha.112.196071 |
0.344 |
|
| 2012 |
Kim NC, Andrews PC, Asselbergs FW, Frost HR, Williams SM, Harris BT, Read C, Askland KD, Moore JH. Gene ontology analysis of pairwise genetic associations in two genome-wide studies of sporadic ALS. Biodata Mining. 5: 9. PMID 22839596 DOI: 10.1186/1756-0381-5-9 |
0.39 |
|
| 2012 |
Sirugo G, Edwards DR, Ryckman KK, Bisseye C, White MJ, Kebbeh B, Morris GA, Adegbola RA, Tacconelli A, Predazzi IM, Novelli G, Vannberg FO, Odunsi K, Page GP, Williams SM. PTX3 genetic variation and dizygotic twinning in the Gambia: could pleiotropy with innate immunity explain common dizygotic twinning in Africa? Annals of Human Genetics. 76: 454-63. PMID 22834944 DOI: 10.1111/J.1469-1809.2012.00723.X |
0.389 |
|
| 2012 |
Barsh GS, Copenhaver GP, Gibson G, Williams SM. Guidelines for genome-wide association studies. Plos Genetics. 8: e1002812. PMID 22792080 DOI: 10.1371/Journal.Pgen.1002812 |
0.389 |
|
| 2012 |
Griswold AJ, Ma D, Cukier HN, Nations LD, Schmidt MA, Chung RH, Jaworski JM, Salyakina D, Konidari I, Whitehead PL, Wright HH, Abramson RK, Williams SM, Menon R, Martin ER, et al. Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways. Human Molecular Genetics. 21: 3513-23. PMID 22543975 DOI: 10.1093/Hmg/Dds164 |
0.351 |
|
| 2012 |
Walther M, De Caul A, Aka P, Njie M, Amambua-Ngwa A, Walther B, Predazzi IM, Cunnington A, Deininger S, Takem EN, Ebonyi A, Weis S, Walton R, Rowland-Jones S, Sirugo G, ... Williams SM, et al. HMOX1 gene promoter alleles and high HO-1 levels are associated with severe malaria in Gambian children. Plos Pathogens. 8: e1002579. PMID 22438807 DOI: 10.1371/Journal.Ppat.1002579 |
0.317 |
|
| 2012 |
Velez Edwards DR, Tacconelli A, Wejse C, Hill PC, Morris GA, Edwards TL, Gilbert JR, Myers JL, Park YS, Stryjewski ME, Abbate E, Estevan R, Rabna P, Novelli G, Hamilton CD, ... ... Williams SM, et al. MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphisms. Plos One. 7: e32275. PMID 22384203 DOI: 10.1371/Journal.Pone.0032275 |
0.364 |
|
| 2012 |
Edwards TL, Velez Edwards DR, Villegas R, Cohen SS, Buchowski MS, Fowke JH, Schlundt D, Long J, Long JR, Cai Q, Zheng W, Shu XO, Hargreaves MK, Smith J, Jeffrey S, ... Williams SM, et al. HTR1B, ADIPOR1, PPARGC1A, and CYP19A1 and obesity in a cohort of Caucasians and African Americans: an evaluation of gene-environment interactions and candidate genes. American Journal of Epidemiology. 175: 11-21. PMID 22106445 DOI: 10.1093/Aje/Kwr272 |
0.364 |
|
| 2012 |
Pennell C, Ang Q, Merialdi M, Katz M, Olsen J, Murray J, Olson D, Jacobsson B, Williams S, Menon R. O541 TWO NOVEL GENETIC VARIANTS ASSOCIATE WITH EARLY SPONTANEOUS PRETERM BIRTH IN CAUCASIAN POPULATIONS International Journal of Gynecology & Obstetrics. 119: S451-S452. DOI: 10.1016/S0020-7292(12)60971-0 |
0.35 |
|
| 2011 |
Myking S, Myhre R, Gjessing HK, Morken NH, Sengpiel V, Williams SM, Ryckman KK, Magnus P, Jacobsson B. Candidate gene analysis of spontaneous preterm delivery: new insights from re-analysis of a case-control study using case-parent triads and control-mother dyads. Bmc Medical Genetics. 12: 174. PMID 22208904 DOI: 10.1186/1471-2350-12-174 |
0.301 |
|
| 2011 |
Signorello LB, Shi J, Cai Q, Zheng W, Williams SM, Long J, Cohen SS, Li G, Hollis BW, Smith JR, Blot WJ. Common variation in vitamin D pathway genes predicts circulating 25-hydroxyvitamin D Levels among African Americans. Plos One. 6: e28623. PMID 22205958 DOI: 10.1371/Journal.Pone.0028623 |
0.311 |
|
| 2011 |
Salyakina D, Cukier HN, Lee JM, Sacharow S, Nations LD, Ma D, Jaworski JM, Konidari I, Whitehead PL, Wright HH, Abramson RK, Williams SM, Menon R, Haines JL, Gilbert JR, et al. Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk. Plos One. 6: e26049. PMID 22016809 DOI: 10.1371/Journal.Pone.0026049 |
0.328 |
|
| 2011 |
Villegas R, Williams S, Gao Y, Cai Q, Li H, Elasy T, Cai H, Edwards T, Xiang YB, Zheng W, Long J, Ou Shu X. Peroxisome Proliferator-Activated Receptor Delta (PPARD) Genetic Variation and Type 2 Diabetes in Middle-Aged Chinese Women Annals of Human Genetics. 75: 621-629. PMID 21834910 DOI: 10.1111/J.1469-1809.2011.00669.X |
0.365 |
|
| 2011 |
Williams SM, Tishkoff SA. Exploring genomic studies in Africa. Genome Medicine. 3: 45. PMID 21745422 DOI: 10.1186/Gm261 |
0.335 |
|
| 2011 |
Ryckman KK, Williams SM, Krohn MA, Simhan HN. Interaction between interleukin-1 receptor 2 and Toll-like receptor 4, and cervical cytokines. Journal of Reproductive Immunology. 90: 220-6. PMID 21704385 DOI: 10.1016/J.Jri.2011.03.007 |
0.327 |
|
| 2011 |
Williams SM, Haines JL. Correcting away the hidden heritability. Annals of Human Genetics. 75: 348-50. PMID 21488852 DOI: 10.1111/J.1469-1809.2011.00640.X |
0.323 |
|
| 2011 |
Agirbasli M, Guney AI, Ozturhan HS, Agirbasli D, Ulucan K, Sevinc D, Kirac D, Ryckman KK, Williams SM. Multifactor dimensionality reduction analysis of MTHFR, PAI-1, ACE, PON1, and eNOS gene polymorphisms in patients with early onset coronary artery disease. European Journal of Cardiovascular Prevention and Rehabilitation : Official Journal of the European Society of Cardiology, Working Groups On Epidemiology & Prevention and Cardiac Rehabilitation and Exercise Physiology. 18: 803-9. PMID 21450592 DOI: 10.1177/1741826711398806 |
0.364 |
|
| 2011 |
Epplein M, Signorello LB, Zheng W, Peek RM, Michel A, Williams SM, Pawlita M, Correa P, Cai Q, Blot WJ. Race, African ancestry, and Helicobacter pylori infection in a low-income United States population. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 20: 826-34. PMID 21357376 DOI: 10.1158/1055-9965.Epi-10-1258 |
0.308 |
|
| 2011 |
Morris GA, Edwards DR, Hill PC, Wejse C, Bisseye C, Olesen R, Edwards TL, Gilbert JR, Myers JL, Stryjewski ME, Abbate E, Estevan R, Hamilton CD, Tacconelli A, Novelli G, ... ... Williams SM, et al. Interleukin 12B (IL12B) genetic variation and pulmonary tuberculosis: a study of cohorts from The Gambia, Guinea-Bissau, United States and Argentina. Plos One. 6: e16656. PMID 21339808 DOI: 10.1371/Journal.Pone.0016656 |
0.396 |
|
| 2011 |
Penrod NM, Poku KA, Vaughan DE, Vaughn DE, Asselbergs FW, Brown NJ, Moore JH, Williams SM. Epistatic interactions in genetic regulation of t-PA and PAI-1 levels in a Ghanaian population. Plos One. 6: e16639. PMID 21304999 DOI: 10.1371/Journal.Pone.0016639 |
0.341 |
|
| 2011 |
Cohen SS, Gammon MD, North KE, Millikan RC, Lange EM, Williams SM, Zheng W, Cai Q, Long J, Smith JR, Signorello LB, Blot WJ, Matthews CE. ADIPOQ, ADIPOR1, and ADIPOR2 polymorphisms in relation to serum adiponectin levels and BMI in black and white women. Obesity (Silver Spring, Md.). 19: 2053-62. PMID 21273992 DOI: 10.1038/Oby.2010.346 |
0.35 |
|
| 2011 |
Lee CR, Pretorius M, Schuck RN, Burch LH, Bartlett J, Williams SM, Zeldin DC, Brown NJ. Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with forearm vasodilator responses in humans. Hypertension. 57: 116-22. PMID 21098312 DOI: 10.1161/Hypertensionaha.110.161695 |
0.336 |
|
| 2011 |
Edwards DR, Romero R, Kusanovic JP, Hassan SS, Mazaki-Tovi S, Vaisbuch E, Kim CJ, Erez O, Chaiworapongsa T, Pearce BD, Bartlett J, Friel LA, Salisbury BA, Anant MK, Vovis GF, ... ... Williams SM, et al. Polymorphisms in maternal and fetal genes encoding for proteins involved in extracellular matrix metabolism alter the risk for small-for-gestational-age. The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 24: 362-80. PMID 20617897 DOI: 10.3109/14767058.2010.497572 |
0.337 |
|
| 2010 |
Ryckman KK, Fielding K, Hill AV, Mendy M, Rayco-Solon P, Sirugo G, van der Sande MA, Waight P, Whittle HC, Hall AJ, Williams SM, Hennig BJ. Host genetic factors and vaccine-induced immunity to HBV infection: haplotype analysis. Plos One. 5: e12273. PMID 20806065 DOI: 10.1371/Journal.Pone.0012273 |
0.324 |
|
| 2010 |
Sirugo G, Williams SM, Royal CD, Newport MJ, Hennig BJ, Mariani-Costantini R, Buonaguro FM, Velez Edwards DR, Ibrahim M, Soodyall H, Wonkam A, Ramesar R, Rotimi CN. Report on the 6th African Society of Human Genetics (AfSHG) Meeting, March 12-15, 2009, Yaounde, Cameroon. The American Journal of Tropical Medicine and Hygiene. 83: 226-9. PMID 20682860 DOI: 10.4269/Ajtmh.2010.10-0208 |
0.312 |
|
| 2010 |
Sirugo G, Williams SM. HbS and HbC associate with malaria transmission: human genetics links to vaccinology? Vaccine. 28: 6403. PMID 20674877 DOI: 10.1016/J.Vaccine.2010.07.044 |
0.323 |
|
| 2010 |
Romero R, Friel LA, Velez Edwards DR, Kusanovic JP, Hassan SS, Mazaki-Tovi S, Vaisbuch E, Kim CJ, Erez O, Chaiworapongsa T, Pearce BD, Bartlett J, Salisbury BA, Anant MK, Vovis GF, ... ... Williams SM, et al. A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM). American Journal of Obstetrics and Gynecology. 203: 361.e1-361.e30. PMID 20673868 DOI: 10.1016/J.Ajog.2010.05.026 |
0.357 |
|
| 2010 |
Peprah EK, Allen EG, Williams SM, Woodard LM, Sherman SL. Genetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African population. Annals of Human Genetics. 74: 316-25. PMID 20597902 DOI: 10.1111/J.1469-1809.2010.00582.X |
0.359 |
|
| 2010 |
Romero R, Velez Edwards DR, Kusanovic JP, Hassan SS, Mazaki-Tovi S, Vaisbuch E, Kim CJ, Chaiworapongsa T, Pearce BD, Friel LA, Bartlett J, Anant MK, Salisbury BA, Vovis GF, Lee MS, ... ... Williams SM, et al. Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes. American Journal of Obstetrics and Gynecology. 202: 431.e1-34. PMID 20452482 DOI: 10.1016/J.Ajog.2010.03.026 |
0.345 |
|
| 2010 |
Menon R, Fortunato SJ, Edwards DR, Williams SM. Association of genetic variants, ethnicity and preterm birth with amniotic fluid cytokine concentrations. Annals of Human Genetics. 74: 165-83. PMID 20369436 DOI: 10.1111/J.1469-1809.2010.00562.X |
0.344 |
|
| 2010 |
Ryckman KK, Morken NH, White MJ, Velez DR, Menon R, Fortunato SJ, Magnus P, Williams SM, Jacobsson B. Maternal and fetal genetic associations of PTGER3 and PON1 with preterm birth. Plos One. 5: e9040. PMID 20140262 DOI: 10.1371/Journal.Pone.0009040 |
0.41 |
|
| 2010 |
Bryc K, Auton A, Nelson MR, Oksenberg JR, Hauser SL, Williams S, Froment A, Bodo JM, Wambebe C, Tishkoff SA, Bustamante CD. Genome-wide patterns of population structure and admixture in West Africans and African Americans. Proceedings of the National Academy of Sciences of the United States of America. 107: 786-91. PMID 20080753 DOI: 10.1073/Pnas.0909559107 |
0.337 |
|
| 2010 |
Moore JH, Asselbergs FW, Williams SM. Bioinformatics challenges for genome-wide association studies. Bioinformatics (Oxford, England). 26: 445-55. PMID 20053841 DOI: 10.1093/Bioinformatics/Btp713 |
0.369 |
|
| 2010 |
Muszkat M, Kurnik D, Sofowora GG, Solus J, Xie HG, Harris PA, Williams SM, Wood AJ, Stein CM. Desensitization of vascular response in vivo: contribution of genetic variation in the [alpha]2B-adrenergic receptor subtype. Journal of Hypertension. 28: 278-84. PMID 20051907 DOI: 10.1097/Hjh.0B013E328333D212 |
0.32 |
|
| 2010 |
Williams SM, Velez DR, Menon R. Geographic ancestry and markers of preterm birth. Expert Review of Molecular Diagnostics. 10: 27-32. PMID 20014920 DOI: 10.1586/Erm.09.70 |
0.303 |
|
| 2009 |
Sloan CD, Andrew AD, Duell EJ, Williams SM, Karagas MR, Moore JH. Genetic population structure analysis in New Hampshire reveals Eastern European ancestry. Plos One. 4: e6928. PMID 19738909 DOI: 10.1371/Journal.Pone.0006928 |
0.377 |
|
| 2009 |
Moore JH, Williams SM. Epistasis and its implications for personal genetics. American Journal of Human Genetics. 85: 309-20. PMID 19733727 DOI: 10.1016/J.Ajhg.2009.08.006 |
0.383 |
|
| 2009 |
Ryckman KK, Williams SM, Krohn MA, Simhan HN. Genetic association of Toll-like receptor 4 with cervical cytokine concentrations during pregnancy. Genes and Immunity. 10: 636-40. PMID 19554026 DOI: 10.1038/Gene.2009.47 |
0.307 |
|
| 2009 |
Menon R, Pearce B, Velez DR, Merialdi M, Williams SM, Fortunato SJ, Thorsen P. Racial disparity in pathophysiologic pathways of preterm birth based on genetic variants. Reproductive Biology and Endocrinology : Rb&E. 7: 62. PMID 19527514 DOI: 10.1186/1477-7827-7-62 |
0.363 |
|
| 2009 |
Moore PE, Ryckman KK, Williams SM, Patel N, Summar ML, Sheller JR. Genetic variants of GSNOR and ADRB2 influence response to albuterol in African-American children with severe asthma. Pediatric Pulmonology. 44: 649-54. PMID 19514054 DOI: 10.1002/Ppul.21033 |
0.303 |
|
| 2009 |
Greene CS, Penrod NM, Williams SM, Moore JH. Failure to replicate a genetic association may provide important clues about genetic architecture. Plos One. 4: e5639. PMID 19503614 DOI: 10.1371/Journal.Pone.0005639 |
0.403 |
|
| 2009 |
Tishkoff SA, Reed FA, Friedlaender FR, Ehret C, Ranciaro A, Froment A, Hirbo JB, Awomoyi AA, Bodo JM, Doumbo O, Ibrahim M, Juma AT, Kotze MJ, Lema G, Moore JH, ... ... Williams SM, et al. The genetic structure and history of Africans and African Americans. Science (New York, N.Y.). 324: 1035-44. PMID 19407144 DOI: 10.1126/Science.1172257 |
0.669 |
|
| 2009 |
Sile S, Velez DR, Gillani NB, Narsia T, Moore JH, George AL, Vanoye CG, Williams SM. CLCNKB-T481S and essential hypertension in a Ghanaian population. Journal of Hypertension. 27: 298-304. PMID 19226700 DOI: 10.1097/Hjh.0B013E3283140C9E |
0.315 |
|
| 2009 |
Tyler AL, Asselbergs FW, Williams SM, Moore JH. Shadows of complexity: what biological networks reveal about epistasis and pleiotropy. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 31: 220-7. PMID 19204994 DOI: 10.1002/Bies.200800022 |
0.341 |
|
| 2009 |
Ryckman KK, Simhan HN, Krohn MA, Williams SM. Predicting risk of bacterial vaginosis: the role of race, smoking and corticotropin-releasing hormone-related genes. Molecular Human Reproduction. 15: 131-7. PMID 19131402 DOI: 10.1093/Molehr/Gan081 |
0.338 |
|
| 2009 |
Sloan CD, Duell EJ, Shi X, Irwin R, Andrew AS, Williams SM, Moore JH. Ecogeographic genetic epidemiology. Genetic Epidemiology. 33: 281-9. PMID 19025788 DOI: 10.1002/Gepi.20386 |
0.337 |
|
| 2009 |
Velez DR, Fortunato S, Thorsen P, Lombardi SJ, Williams SM, Menon R. Spontaneous preterm birth in African Americans is associated with infection and inflammatory response gene variants. American Journal of Obstetrics and Gynecology. 200: 209.e1-27. PMID 19019335 DOI: 10.1016/J.Ajog.2008.08.051 |
0.374 |
|
| 2008 |
Moore PE, Williams SM, Gebretsadik T, Jiang L, Minton PL, Shintani A, Phillips Iii JA, Dawson EP, Hartert TV. beta(2)-adrenergic receptor promoter haplotype influences spirometric response during an acute asthma exacerbation. Clinical and Translational Science. 1: 155-61. PMID 20443840 DOI: 10.1111/J.1752-8062.2008.00036.X |
0.326 |
|
| 2008 |
Schoenhard JA, Asselbergs FW, Poku KA, Stocki SA, Gordon S, Vaughan DE, Brown NJ, Moore JH, Williams SM. Male-female differences in the genetic regulation of t-PA and PAI-1 levels in a Ghanaian population. Human Genetics. 124: 479-88. PMID 18953568 DOI: 10.1007/S00439-008-0573-X |
0.335 |
|
| 2008 |
Velez DR, Fortunato SJ, Thorsen P, Lombardi SJ, Williams SM, Menon R. Preterm birth in Caucasians is associated with coagulation and inflammation pathway gene variants. Plos One. 3: e3283. PMID 18818748 DOI: 10.1371/Journal.Pone.0003283 |
0.403 |
|
| 2008 |
Menon R, Velez DR, Morgan N, Lombardi SJ, Fortunato SJ, Williams SM. Genetic regulation of amniotic fluid TNF-alpha and soluble TNF receptor concentrations affected by race and preterm birth. Human Genetics. 124: 243-53. PMID 18807256 DOI: 10.1007/S00439-008-0547-Z |
0.369 |
|
| 2008 |
Roth SM, Williams SM, Jiang L, Menon KS, Jeka JJ. Susceptibility genes for gentamicin-induced vestibular dysfunction. Journal of Vestibular Research : Equilibrium & Orientation. 18: 59-68. PMID 18776599 DOI: 10.1096/Fasebj.21.5.A415-A |
0.334 |
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| 2008 |
Ciarleglio CM, Ryckman KK, Servick SV, Hida A, Robbins S, Wells N, Hicks J, Larson SA, Wiedermann JP, Carver K, Hamilton N, Kidd KK, Kidd JR, Smith JR, Friedlaender J, ... ... Williams SM, et al. Genetic differences in human circadian clock genes among worldwide populations. Journal of Biological Rhythms. 23: 330-40. PMID 18663240 DOI: 10.1177/0748730408320284 |
0.374 |
|
| 2008 |
Fortunato SJ, Menon R, Velez DR, Thorsen P, Williams SM. Racial disparity in maternal-fetal genetic epistasis in spontaneous preterm birth. American Journal of Obstetrics and Gynecology. 198: 666.e1-9; discussion. PMID 18538149 DOI: 10.1016/J.Ajog.2008.02.003 |
0.334 |
|
| 2008 |
Sirugo G, Hennig BJ, Adeyemo AA, Matimba A, Newport MJ, Ibrahim ME, Ryckman KK, Tacconelli A, Mariani-Costantini R, Novelli G, Soodyall H, Rotimi CN, Ramesar RS, Tishkoff SA, Williams SM. Genetic studies of African populations: an overview on disease susceptibility and response to vaccines and therapeutics. Human Genetics. 123: 557-98. PMID 18512079 DOI: 10.1007/S00439-008-0511-Y |
0.369 |
|
| 2008 |
Ryckman KK, Jiang L, Li C, Bartlett J, Haines JL, Williams SM. A prevalence-based association test for case-control studies. Genetic Epidemiology. 32: 600-5. PMID 18473366 DOI: 10.1002/Gepi.20342 |
0.354 |
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| 2008 |
Ryckman K, Williams SM. Calculation and use of the Hardy-Weinberg model in association studies. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit 1.18. PMID 18428419 DOI: 10.1002/0471142905.Hg0118S57 |
0.374 |
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| 2008 |
Velez DR, Fortunato SJ, Williams SM, Menon R. Interleukin-6 (IL-6) and receptor (IL6-R) gene haplotypes associate with amniotic fluid protein concentrations in preterm birth. Human Molecular Genetics. 17: 1619-30. PMID 18276608 DOI: 10.1093/Hmg/Ddn049 |
0.311 |
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| 2008 |
Velez DR, Menon R, Simhan H, Fortunato S, Canter JA, Williams SM. Mitochondrial DNA variant A4917G, smoking and spontaneous preterm birth. Mitochondrion. 8: 130-5. PMID 18082471 DOI: 10.1016/J.Mito.2007.10.007 |
0.343 |
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| 2008 |
Sile S, Velez DR, Gillani NB, Alexander CA, Alexander CR, George AL, Williams SM. Haplotype diversity in four genes (CLCNKA, CLCNKB, BSND, NEDD4L) involved in renal salt reabsorption. Human Heredity. 65: 33-46. PMID 17652939 DOI: 10.1159/000106060 |
0.326 |
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| 2008 |
Zabaleta J, Schneider BG, Ryckman K, Hooper PF, Camargo MC, Piazuelo MB, Sierra RA, Fontham ET, Correa P, Williams SM, Ochoa AC. Ethnic differences in cytokine gene polymorphisms: potential implications for cancer development. Cancer Immunology, Immunotherapy : Cii. 57: 107-14. PMID 17618436 DOI: 10.1007/S00262-007-0358-4 |
0.34 |
|
| 2008 |
Pratap S, Williams SM, Levy SE. Evaluation of pooled allelotyping versus individual genotyping for genome-wide association analysis of complex disease Bmc Bioinformatics. 9: 11. DOI: 10.1186/1471-2105-9-S7-P11 |
0.362 |
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| 2008 |
Jacobsson B, Ryckman K, Morken N, Magnus P, Williams S. 29: Maternal and fetal genetic associations with preterm delivery American Journal of Obstetrics and Gynecology. 199. DOI: 10.1016/J.Ajog.2008.09.883 |
0.333 |
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| 2008 |
Fortunato S, WIlliams S, Velez DR, Menon R. 28: Significant interaction between genetic variants in preterm birth associate with amniotic fluid protein concentrations and racial disparity American Journal of Obstetrics and Gynecology. 199. DOI: 10.1016/J.Ajog.2008.09.882 |
0.341 |
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| 2007 |
Sile S, Gillani NB, Velez DR, Vanoye CG, Yu C, Byrne LM, Gainer JV, Brown NJ, Williams SM, George AL. Functional BSND variants in essential hypertension. American Journal of Hypertension. 20: 1176-1182. PMID 17954364 DOI: 10.1016/J.Amjhyper.2007.07.003 |
0.359 |
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| 2007 |
Yotova V, Lefebvre JF, Kohany O, Jurka J, Michalski R, Modiano D, Utermann G, Williams SM, Labuda D. Tracing genetic history of modern humans using X-chromosome lineages. Human Genetics. 122: 431-43. PMID 17680273 DOI: 10.1007/S00439-007-0413-4 |
0.358 |
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| 2007 |
Olesen R, Wejse C, Velez DR, Bisseye C, Sodemann M, Aaby P, Rabna P, Worwui A, Chapman H, Diatta M, Adegbola RA, Hill PC, Østergaard L, Williams SM, Sirugo G. DC-SIGN (CD209), pentraxin 3 and vitamin D receptor gene variants associate with pulmonary tuberculosis risk in West Africans. Genes and Immunity. 8: 456-67. PMID 17611589 DOI: 10.1038/Sj.Gene.6364410 |
0.327 |
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| 2007 |
Asselbergs FW, Williams SM, Hebert PR, Coffey CS, Hillege HL, Snieder H, Navis G, Vaughan DE, van Gilst WH, Moore JH. The effects of polymorphisms in genes from the renin-angiotensin, bradykinin, and fibrinolytic systems on plasma t-PA and PAI-1 levels are dependent on environmental context. Human Genetics. 122: 275-81. PMID 17593394 DOI: 10.1007/S00439-007-0400-9 |
0.345 |
|
| 2007 |
Velez DR, Menon R, Thorsen P, Jiang L, Simhan H, Morgan N, Fortunato SJ, Williams SM. Ethnic differences in interleukin 6 (IL-6) and IL6 receptor genes in spontaneous preterm birth and effects on amniotic fluid protein levels. Annals of Human Genetics. 71: 586-600. PMID 17346257 DOI: 10.1111/J.1469-1809.2007.00352.X |
0.344 |
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| 2007 |
Cauci S, Di Santolo M, Casabellata G, Ryckman K, Williams SM, Guaschino S. Association of interleukin-1beta and interleukin-1 receptor antagonist polymorphisms with bacterial vaginosis in non-pregnant Italian women. Molecular Human Reproduction. 13: 243-50. PMID 17314118 DOI: 10.1093/Molehr/Gam002 |
0.317 |
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| 2007 |
Pennell CE, Jacobsson B, Williams SM, Buus RM, Muglia LJ, Dolan SM, Morken NH, Ozcelik H, Lye SJ, Relton C. Genetic epidemiologic studies of preterm birth: guidelines for research. American Journal of Obstetrics and Gynecology. 196: 107-18. PMID 17306646 DOI: 10.1016/J.Ajog.2006.03.109 |
0.351 |
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| 2007 |
Velez DR, Guruju M, Vinukonda G, Prater A, Kumar A, Williams SM. Angiotensinogen promoter sequence variants in essential hypertension. American Journal of Hypertension. 19: 1278-85. PMID 17161775 DOI: 10.1016/J.Amjhyper.2006.05.020 |
0.327 |
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| 2007 |
Lind JM, Hutcheson-Dilks HB, Williams SM, Moore JH, Essex M, Ruiz-Pesini E, Wallace DC, Tishkoff SA, O'Brien SJ, Smith MW. Elevated male European and female African contributions to the genomes of African American individuals. Human Genetics. 120: 713-22. PMID 17006671 DOI: 10.1007/S00439-006-0261-7 |
0.314 |
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| 2006 |
Menon R, Fortunato SJ, Thorsen P, Williams S. Genetic associations in preterm birth: a primer of marker selection, study design, and data analysis. Journal of the Society For Gynecologic Investigation. 13: 531-541. PMID 17088082 DOI: 10.1016/J.Jsgi.2006.09.006 |
0.414 |
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| 2006 |
Agirbasli D, Agirbasli M, Williams SM, Phillips JA. Interaction among 5,10 methylenetetrahydrofolate reductase, plasminogen activator inhibitor and endothelial nitric oxide synthase gene polymorphisms predicts the severity of coronary artery disease in Turkish patients. Coronary Artery Disease. 17: 413-417. PMID 16845248 DOI: 10.1097/00019501-200608000-00003 |
0.3 |
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| 2006 |
Menon R, Velez DR, Simhan H, Ryckman K, Jiang L, Thorsen P, Vogel I, Jacobsson B, Merialdi M, Williams SM, Fortunato SJ. Multilocus interactions at maternal tumor necrosis factor-alpha, tumor necrosis factor receptors, interleukin-6 and interleukin-6 receptor genes predict spontaneous preterm labor in European-American women. American Journal of Obstetrics and Gynecology. 194: 1616-24. PMID 16731080 DOI: 10.1016/J.Ajog.2006.03.059 |
0.315 |
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| 2006 |
Kurnik D, Muszkat M, Li C, Sofowora GG, Solus J, Xie H, Harris PA, Jiang L, McMunn C, Ihrie P, Dawson EP, Williams SM, Wood AJJ, Stein CM. Variations in the α2A‐adrenergic receptor gene and their functional effects Clinical Pharmacology & Therapeutics. 79: 173-185. PMID 16513442 DOI: 10.1016/J.Clpt.2005.10.006 |
0.368 |
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| 2006 |
Lohmueller KE, Wong LJC, Mauney MM, Jiang L, Felder RA, Jose PA, Williams SM. Patterns of genetic variation in the hypertension candidate gene GRK4: Ethnic variation and haplotype structure Annals of Human Genetics. 70: 27-41. PMID 16441255 DOI: 10.1111/J.1529-8817.2005.00197.X |
0.415 |
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| 2006 |
Sanada H, Yatabe J, Midorikawa S, Hashimoto S, Watanabe T, Moore JH, Ritchie MD, Williams SM, Pezzullo JC, Sasaki M, Eisner GM, Jose PA, Felder RA. Single-nucleotide polymorphisms for diagnosis of salt-sensitive hypertension. Clinical Chemistry. 52: 352-60. PMID 16439609 DOI: 10.1373/Clinchem.2005.059139 |
0.302 |
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| 2006 |
Zhu K, Hunter S, Payne-Wilks K, Sutcliffe C, Bentley C, Roland CL, Williams SM. Potential differences in breast cancer risk factors based on CYP1A1 MspI and African-American-specific genotypes. Ethnicity & Disease. 16: 207. DOI: 10.13016/N1Oi-Iala |
0.315 |
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| 2006 |
Pennell CE, Jacobsson B, Williams SM, Buus RM, Muglia LJ, Dolan SM, Morken N, Ozcelik H, Lye SJ, Relton C. WITHDRAWN: Genetic epidemiological studies of preterm birth: Guidelines for research American Journal of Obstetrics and Gynecology. DOI: 10.1016/J.Ajog.2006.03.055 |
0.324 |
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| 2005 |
Garland EM, Winker R, Williams SM, Jiang L, Stanton K, Byrne DW, Biaggioni I, Cascorbi I, Phillips JA, Harris PA, Rüdiger H, Robertson D. Endothelial NO synthase polymorphisms and postural tachycardia syndrome. Hypertension. 46: 1103-10. PMID 16203873 DOI: 10.1161/01.Hyp.0000185462.08685.Da |
0.334 |
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| 2005 |
Muszkat M, Kurnik D, Solus J, Sofowora GG, Xie H, Jiang L, Mcmunn C, Ihrie P, Harris JR, Dawson EP, Williams SM, Wood AJJ, Stein CM. Variation in the alpha2B-adrenergic receptor gene (ADRA2B) and its relationship to vascular response in vivo. Pharmacogenetics and Genomics. 15: 407-414. PMID 15900214 DOI: 10.1097/01213011-200506000-00006 |
0.349 |
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| 2005 |
Moore JH, Williams SM. Traversing the conceptual divide between biological and statistical epistasis: Systems biology and a more modern synthesis Bioessays. 27: 637-646. PMID 15892116 DOI: 10.1002/Bies.20236 |
0.364 |
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| 2005 |
Soares ML, Coelho T, Sousa A, Batalov S, Conceição I, Sales-LuÃs ML, Ritchie MD, Williams SM, Nievergelt CM, Schork NJ, Saraiva MJ, Buxbaum JN. Susceptibility and modifier genes in Portuguese transthyretin V30M amyloid polyneuropathy: complexity in a single-gene disease. Human Molecular Genetics. 14: 543-53. PMID 15649951 DOI: 10.1093/Hmg/Ddi051 |
0.368 |
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| 2005 |
MUSZKAT M, SOFOWORA G, KURNIK D, SOLUS J, JIANG L, WILLIAMS S, DAWSON E, WOOD A, STEIN C. Sequence analysis of the ?-ADRENERGIC receptor (ADRA2B) gene and in-vivo functional effects of novel variants Clinical Pharmacology & Therapeutics. 77: P25-P25. DOI: 10.1016/J.Clpt.2004.11.095 |
0.345 |
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| 2004 |
Williams SM, Ritchie MD, Phillips JA, Dawson E, Prince M, Dzhura E, Willis A, Semenya A, Summar M, White BC, Addy JH, Kpodonu J, Wong LJ, Felder RA, Jose PA, et al. Multilocus analysis of hypertension: a hierarchical approach. Human Heredity. 57: 28-38. PMID 15133310 DOI: 10.1159/000077387 |
0.377 |
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| 2004 |
Smith MW, Patterson N, Lautenberger JA, Truelove AL, McDonald GJ, Waliszewska A, Kessing BD, Malasky MJ, Scafe C, Le E, De Jager PL, Mignault AA, Yi Z, De The G, Essex M, ... ... Williams SM, et al. A high-density admixture map for disease gene discovery in african americans. American Journal of Human Genetics. 74: 1001-13. PMID 15088270 DOI: 10.1086/420856 |
0.303 |
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| 2004 |
Williams SM, Haines JL, Moore JH. The use of animal models in the study of complex disease: all else is never equal or why do so many human studies fail to replicate animal findings? Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 26: 170-9. PMID 14745835 DOI: 10.1002/Bies.10401 |
0.357 |
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| 2004 |
Velez DR, Menon R, Fortunato S, Williams S. Polymorphisms on TNFR2 loci: Racial disparity in genotypic and allelic frequencies American Journal of Obstetrics and Gynecology. 191. DOI: 10.1016/J.Ajog.2004.10.250 |
0.324 |
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| 2004 |
Menon R, Velez DR, Williams S, Fortunato S. Documentation of genotypic and allelic frequency variations in TNF receptor 1 Loci between ethnic groups American Journal of Obstetrics and Gynecology. 191. DOI: 10.1016/J.Ajog.2004.10.049 |
0.311 |
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| 2003 |
Willis AS, Freeman ML, Summar SR, Barr FE, Williams SM, Dawson E, Summar ML. Ethnic diversity in a critical gene responsible for glutathione synthesis. Free Radical Biology & Medicine. 34: 72-6. PMID 12498981 DOI: 10.1016/S0891-5849(02)01178-4 |
0.347 |
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| 2002 |
Tishkoff SA, Williams SM. Genetic analysis of African populations: human evolution and complex disease. Nature Reviews. Genetics. 3: 611-21. PMID 12154384 DOI: 10.1038/Nrg865 |
0.362 |
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| 2002 |
Moore JH, Williams SM. New strategies for identifying gene-gene interactions in hypertension Annals of Medicine. 34: 88-95. PMID 12108579 DOI: 10.1080/07853890252953473 |
0.357 |
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| 2002 |
Engert JC, Vohl MC, Williams SM, Lepage P, Loredo-Osti JC, Faith J, Doré C, Renaud Y, Burtt NP, Villeneuve A, Hirschhorn JN, Altshuler D, Groop LC, Després JP, Gaudet D, et al. 5' flanking variants of resistin are associated with obesity. Diabetes. 51: 1629-34. PMID 11978666 DOI: 10.2337/Diabetes.51.5.1629 |
0.329 |
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| 2002 |
Bengra C, Mifflin TE, Khripin Y, Manunta P, Williams SM, Jose PA, Felder RA. Genotyping of essential hypertension single-nucleotide polymorphisms by a homogeneous PCR method with universal energy transfer primers. Clinical Chemistry. 48: 2131-2140. DOI: 10.1093/Clinchem/48.12.2131 |
0.363 |
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| 2001 |
Tishkoff SA, Varkonyi R, Cahinhinan N, Abbes S, Argyropoulos G, Destro-Bisol G, Drousiotou A, Dangerfield B, Lefranc G, Loiselet J, Piro A, Stoneking M, Tagarelli A, Tagarelli G, Touma EH, ... Williams SM, et al. Haplotype diversity and linkage disequilibrium at human G6PD: recent origin of alleles that confer malarial resistance. Science (New York, N.Y.). 293: 455-62. PMID 11423617 DOI: 10.1126/Science.1061573 |
0.335 |
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| 2000 |
Tarumi T, Martincic D, Whitlock JA, Addy JH, Williams SM, Gailani D. Conserved worldwide linkage disequilibrium in the human factor XI gene Genomics. 70: 269-272. PMID 11112356 DOI: 10.1006/Geno.2000.6393 |
0.388 |
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| 2000 |
Williams SM, Addy JH, Phillips JA, Dai M, Kpodonu J, Afful J, Jackson H, Joseph K, Eason F, Murray MM, Epperson P, Aduonum A, Wong LJ, Jose PA, Felder RA. Combinations of variations in multiple genes are associated with hypertension. Hypertension. 36: 2-6. PMID 10904004 DOI: 10.1161/01.Hyp.36.1.2 |
0.406 |
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| 1994 |
Kozol AJ, Traniello JFA, Williams SM. Genetic variation in the endangered burying beetle Nicrophorus americanus (Coleoptera: Silphidae) Annals of the Entomological Society of America. 87: 928-935. DOI: 10.1093/Aesa/87.6.928 |
0.337 |
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| 1990 |
Williams SM, Robbins LG, Cluster PD, Allard RW, Strobeck C. Superstructure of the Drosophila ribosomal gene family. Proceedings of the National Academy of Sciences of the United States of America. 87: 3156-60. PMID 2109326 DOI: 10.1073/Pnas.87.8.3156 |
0.309 |
|
| 1987 |
Williams SM. Differences in life history traits between alcohol dehydrogenase genotypes of Drosophila mercatorum: background and maternal genotype effects Genetica. 74: 149-153. PMID 3506533 DOI: 10.1007/Bf00055227 |
0.303 |
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