Scott M. Williams - Publications


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

Year Citation  Score
2021 Graff M, Justice AE, Young KL, Marouli E, Zhang X, Fine RS, Lim E, Buchanan V, Rand K, Feitosa MF, Wojczynski MK, Yanek LR, Shao Y, Rohde R, Adeyemo AA, ... ... Williams SM, et al. Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. American Journal of Human Genetics. PMID 33713608 DOI: 10.1016/j.ajhg.2021.02.011  0.52
2021 Stein CM, Benchek P, Bartlett J, Igo RP, Sobota RS, Chervenak K, Mayanja-Kizza H, von Reyn CF, Lahey T, Bush WS, Boom WH, Scott WK, Marsit C, Sirugo G, Williams SM. Methylome-wide analysis reveals epigenetic marks associated with resistance to tuberculosis in HIV-infected individuals from East Africa. The Journal of Infectious Diseases. PMID 33400784 DOI: 10.1093/infdis/jiaa785  0.48
2020 Olvany JM, Sausville LN, White MJ, Tacconelli A, Tavera G, Sobota RS, Ciccacci C, Bohlbro AS, Wejse C, Williams SM, Sirugo G. CLEC4E (Mincle) genetic variation associates with pulmonary tuberculosis in Guinea-Bissau (West Africa). Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases. 104560. PMID 32971250 DOI: 10.1016/j.meegid.2020.104560  0.48
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  0.52
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  0.92
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  0.92
2019 Barsh GS, Cooper GM, Copenhaver GP, Sirugo G, Tang H, Williams SM. Evaluating the strength of genetic results: Risks and responsibilities. Plos Genetics. 15: e1008437. PMID 31603891 DOI: 10.1371/journal.pgen.1008437  0.48
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  0.52
2019 Sirugo G, Williams SM, Tishkoff SA. The Missing Diversity in Human Genetic Studies. Cell. 177: 1080. PMID 31051100 DOI: 10.1016/j.cell.2019.04.032  0.92
2019 Sirugo G, Williams SM, Tishkoff SA, Cordell HJ, Marchini J, Barsh GS, Copenhaver GP. The Plight of Muntaser Ibrahim. Plos Genetics. 15: e1008100. PMID 30908486 DOI: 10.1371/journal.pgen.1008100  0.92
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  0.92
2019 Moore JH, Mackay TFC, Williams SM. Testing the assumptions of parametric linear models: the need for biological data mining in disciplines such as human genetics. Biodata Mining. 12: 6. PMID 30792817 DOI: 10.1186/s13040-019-0194-z  0.52
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  0.52
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  0.52
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  0.52
2018 Chernikova DA, Madan JC, Housman ML, Zain-Ul-Abideen M, Lundgren SN, Morrison HG, Sogin ML, Williams SM, Moore JH, Karagas MR, Hoen AG. The premature infant gut microbiome during the first 6 weeks of life differs based on gestational maturity at birth. Pediatric Research. PMID 29795209 DOI: 10.1038/s41390-018-0022-z  0.52
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  0.48
2017 Mechanic LE, Lindström S, Daily KM, Sieberts SK, Amos CI, Chen HS, Cox NJ, Dathe M, Feuer EJ, Guertin MJ, Hoffman J, Liu Y, Moore JH, Myers CL, Ritchie MD, ... ... Williams SM, et al. Up For A Challenge (U4C): Stimulating innovation in breast cancer genetic epidemiology. Plos Genetics. 13: e1006945. PMID 28957327 DOI: 10.1371/journal.pgen.1006945  0.52
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  0.52
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  0.52
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  0.52
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  0.52
2016 Kodaman N, Aldrich MC, Sobota R, Asselbergs FW, Poku KA, Brown NJ, Moore JH, Williams SM. Cardiovascular Disease Risk Factors in Ghana during the Rural-to-Urban Transition: A Cross-Sectional Study. Plos One. 11: e0162753. PMID 27732601 DOI: 10.1371/journal.pone.0162753  0.52
2016 Kodaman N, Aldrich MC, Sobota R, Asselbergs FW, Brown NJ, Moore JH, Williams SM. Plasminogen Activator Inhibitor-1 and Diagnosis of the Metabolic Syndrome in a West African Population. Journal of the American Heart Association. 5. PMID 27697752 DOI: 10.1161/JAHA.116.003867  0.52
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  1
2016 Modongo C, Pasipanodya JG, Magazi BT, Srivastava S, Zetola NM, Williams SM, Sirugo G, Gumbo T. Artificial intelligence and amikacin exposures predictive of outcome in multidrug-resistant tuberculosis patients. Antimicrobial Agents and Chemotherapy. PMID 27458224 DOI: 10.1128/AAC.00962-16  0.48
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  1
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  1
2016 Bartlett J, Predazzi IM, Williams SM, Bush WS, Kim Y, Havas S, Toth PP, Fazio S, Miller M. Is Isolated Low High-Density Lipoprotein Cholesterol a Cardiovascular Disease Risk Factor? New Insights From the Framingham Offspring Study. Circulation. Cardiovascular Quality and Outcomes. PMID 27166203 DOI: 10.1161/CIRCOUTCOMES.115.002436  1
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  1
2016 Sobota RS, Dara A, Manning JE, Niangaly A, Bailey JA, Kone AK, Thera MA, Djimdé AA, Vernet G, Leissner P, Williams SM, Plowe CV, Doumbo OK. Expression of complement and toll-like receptor pathway genes is associated with malaria severity in Mali: a pilot case control study. Malaria Journal. 15: 150. PMID 26961973 DOI: 10.1186/s12936-016-1189-6  1
2016 Sobota RS, Stein CM, Kodaman N, Scheinfeldt LB, Maro I, Wieland-Alter W, Igo RP, Magohe A, Malone LL, Chervenak K, Hall NB, Modongo C, Zetola N, Matee M, Joloba M, ... ... Williams SM, et al. A Locus at 5q33.3 Confers Resistance to Tuberculosis in Highly Susceptible Individuals. American Journal of Human Genetics. 98: 514-524. PMID 26942285 DOI: 10.1016/j.ajhg.2016.01.015  1
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  1
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  1
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  1
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  1
2015 Siwo GH, Williams SM, Moore JH. Erratum to: The future of genomic medicine education in Africa. Genome Medicine. 7: 70. PMID 26321605 DOI: 10.1186/s13073-015-0193-8  0.52
2015 Ciesielski TH, Marsit CJ, Williams SM. Maternal psychiatric disease and epigenetic evidence suggest a common biology for poor fetal growth. Bmc Pregnancy and Childbirth. 15: 192. PMID 26303856 DOI: 10.1186/s12884-015-0627-8  1
2015 Modongo C, Pasipanodya JG, Zetola NM, Williams SM, Sirugo G, Gumbo T. Amikacin Concentrations Predictive of Ototoxicity in Multidrug-Resistant Tuberculosis Patients. Antimicrobial Agents and Chemotherapy. 59: 6337-43. PMID 26248372 DOI: 10.1128/AAC.01050-15  1
2015 Siwo GH, Williams SM, Moore JH. The future of genomic medicine education in Africa. Genome Medicine. 7: 47. PMID 26246857 DOI: 10.1186/s13073-015-0175-x  0.52
2015 Williams SM, Moore JH. Lumping versus splitting: the need for biological data mining in precision medicine. Biodata Mining. 8: 16. PMID 26085842 DOI: 10.1186/s13040-015-0049-1  1
2015 Dahal K, Sharma SP, Fung E, Lee J, Moore JH, Unterborn JN, Williams SM. Meta-analysis of Randomized Controlled Trials of Genotype-guided versus Standard Dosing of Warfarin. Chest. PMID 25811981 DOI: 10.1378/chest.14-2947  1
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  1
2015 White MJ, Eren F, Agirbasli D, Williams SM, Agirbasli M. SHBG gene polymorphism (rs1799941) associates with metabolic syndrome in children and adolescents. Plos One. 10: e0116915. PMID 25647406 DOI: 10.1371/journal.pone.0116915  1
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  1
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  1
2014 Modongo C, Sobota RS, Kesenogile B, Ncube R, Sirugo G, Williams SM, Zetola NM. Successful MDR-TB treatment regimens including amikacin are associated with high rates of hearing loss. Bmc Infectious Diseases. 14: 542. PMID 25300708 DOI: 10.1186/1471-2334-14-542  1
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  1
2014 Sanada H, Yokokawa H, Yatabe J, Williams SM, Felder RA, Jose PA, Takenosita S. Association between lifestyle-related disorders and visceral fat mass in Japanese males: a hospital based cross-sectional study. Environmental Health and Preventive Medicine. 19: 429-35. PMID 25248615 DOI: 10.1007/s12199-014-0411-9  1
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  1
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  1
2014 Davis MA, Gilbert-Diamond D, Karagas MR, Li Z, Moore JH, Williams SM, Frost HR. A dietary-wide association study (DWAS) of environmental metal exposure in US children and adults. Plos One. 9: e104768. PMID 25198543 DOI: 10.1371/journal.pone.0104768  1
2014 Sobota RS, Ramogola-Masire D, Williams SM, Zetola NM. Co-infection with HPV types from the same species provides natural cross-protection from progression to cervical cancer. Infectious Agents and Cancer. 9: 26. PMID 25152769 DOI: 10.1186/1750-9378-9-26  1
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  1
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  1
2014 Sirugo G, Predazzi IM, Bartlett J, Tacconelli A, Walther M, Williams SM. G6PD A- deficiency and severe malaria in The Gambia: heterozygote advantage and possible homozygote disadvantage. The American Journal of Tropical Medicine and Hygiene. 90: 856-9. PMID 24615128 DOI: 10.4269/ajtmh.13-0622  1
2014 Kodaman N, Pazos A, Schneider BG, Piazuelo MB, Mera R, Sobota RS, Sicinschi LA, Shaffer CL, Romero-Gallo J, de Sablet T, Harder RH, Bravo LE, Peek RM, Wilson KT, Cover TL, ... Williams SM, et al. Human and Helicobacter pylori coevolution shapes the risk of gastric disease. Proceedings of the National Academy of Sciences of the United States of America. 111: 1455-60. PMID 24474772 DOI: 10.1073/pnas.1318093111  1
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  1
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  1
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  0.52
2013 Williams SM, Moore JH. Big Data analysis on autopilot? Biodata Mining. 6: 22. PMID 24314297 DOI: 10.1186/1756-0381-6-22  1
2013 Williams SM. Identifying population differences in genes that affect body mass index. Genome Medicine. 5: 102. PMID 24286457 DOI: 10.1186/gm506  1
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  1
2013 Samuels DC, Li C, Li B, Song Z, Torstenson E, Boyd Clay H, Rokas A, Thornton-Wells TA, Moore JH, Hughes TM, Hoffman RD, Haines JL, Murdock DG, Mortlock DP, Williams SM. Recurrent tissue-specific mtDNA mutations are common in humans. Plos Genetics. 9: e1003929. PMID 24244193 DOI: 10.1371/journal.pgen.1003929  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2013 Felder RA, White MJ, Williams SM, Jose PA. Diagnostic tools for hypertension and salt sensitivity testing. Current Opinion in Nephrology and Hypertension. 22: 65-76. PMID 23197156 DOI: 10.1097/MNH.0b013e32835b3693  1
2013 Hadjixenofontos A, Schmidt MA, Whitehead PL, Konidari I, Hedges DJ, Wright HH, Abramson RK, Menon R, Williams SM, Cuccaro ML, Haines JL, Gilbert JR, Pericak-Vance MA, Martin ER, McCauley JL. Evaluating mitochondrial DNA variation in autism spectrum disorders. Annals of Human Genetics. 77: 9-21. PMID 23130936 DOI: 10.1111/j.1469-1809.2012.00736.x  1
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  1
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  1
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  1
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  1
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  1
2012 Sanada H, Yokokawa H, Yoneda M, Yatabe J, Sasaki Yatabe M, Williams SM, Felder RA, Jose PA. High body mass index is an important risk factor for the development of type 2 diabetes. Internal Medicine (Tokyo, Japan). 51: 1821-6. PMID 22821094 DOI: DN/JST.JSTAGE/internalmedicine/51.7410  1
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  1
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  1
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  1
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  1
2012 Myatt L, Eschenbach DA, Lye SJ, Mesiano S, Murtha AP, Williams SM, Pennell CE. A standardized template for clinical studies in preterm birth. Reproductive Sciences (Thousand Oaks, Calif.). 19: 474-82. PMID 22344727 DOI: 10.1177/1933719111426602  1
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  1
2012 Curia MC, De Iure S, De Lellis L, Veschi S, Mammarella S, White MJ, Bartlett J, Di Iorio A, Amatetti C, Lombardo M, Di Gregorio P, Battista P, Mariani-Costantini R, Williams SM, Cama A. Increased variance in germline allele-specific expression of APC associates with colorectal cancer. Gastroenterology. 142: 71-77.e1. PMID 21995949 DOI: 10.1053/j.gastro.2011.09.048  1
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  1
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  1
2011 Williams SM, Tishkoff SA. Exploring genomic studies in Africa. Genome Medicine. 3: 45. PMID 21745422 DOI: 10.1186/gm261  0.92
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  1
2011 Cukier HN, Salyakina D, Blankstein SF, Robinson JL, Sacharow S, Ma D, Wright HH, Abramson RK, Menon R, Williams SM, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 493-501. PMID 21480499 DOI: 10.1002/ajmg.b.31188  1
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  1
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  1
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  1
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  0.4
2011 Hennig BJ, Velez-Edwards DR, Schim van der Loeff MF, Bisseye C, Edwards TL, Tacconelli A, Novelli G, Aaby P, Kaye S, Scott WK, Jaye A, Whittle HC, Williams SM, Hill AV, Sirugo G. CD4 intragenic SNPs associate with HIV-2 plasma viral load and CD4 count in a community-based study from Guinea-Bissau, West Africa. Journal of Acquired Immune Deficiency Syndromes (1999). 56: 1-8. PMID 20924289 DOI: 10.1097/QAI.0b013e3181f638ed  1
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  1
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  1
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  1
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  1
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  1
2010 Williams SM. Endophenotypes, heritability, and underlying complexity in hypertension. American Journal of Hypertension. 23: 819. PMID 20644531 DOI: 10.1038/ajh.2010.101  1
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  1
2010 Russell SB, Russell JD, Trupin KM, Gayden AE, Opalenik SR, Nanney LB, Broquist AH, Raju L, Williams SM. Epigenetically altered wound healing in keloid fibroblasts. The Journal of Investigative Dermatology. 130: 2489-96. PMID 20555348 DOI: 10.1038/jid.2010.162  1
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  1
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  1
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