| Year |
Citation |
Score |
| 2023 |
Armstrong ND, Srinivasasainagendra V, Ammous F, Assimes TL, Beitelshees AL, Brody J, Cade BE, Ida Chen YD, Chen H, de Vries PS, Floyd JS, Franceschini N, Guo X, Hellwege JN, House JS, ... ... Edwards TL, et al. Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program. Frontiers in Genetics. 14: 1278215. PMID 38162683 DOI: 10.3389/fgene.2023.1278215 |
0.552 |
|
| 2023 |
Wang A, Shen J, Rodriguez AA, Saunders EJ, Chen F, Janivara R, Darst BF, Sheng X, Xu Y, Chou AJ, Benlloch S, Dadaev T, Brook MN, Plym A, Sahimi A, ... ... Edwards TL, et al. Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants. Nature Genetics. PMID 37945903 DOI: 10.1038/s41588-023-01534-4 |
0.549 |
|
| 2023 |
Roychowdhury T, Klarin D, Levin MG, Spin JM, Rhee YH, Deng A, Headley CA, Tsao NL, Gellatly C, Zuber V, Shen F, Hornsby WE, Laursen IH, Verma SS, Locke AE, ... ... Edwards TL, et al. Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target. Nature Genetics. PMID 37845353 DOI: 10.1038/s41588-023-01510-y |
0.671 |
|
| 2023 |
Chen F, Madduri RK, Rodriguez AA, Darst BF, Chou A, Sheng X, Wang A, Shen J, Saunders EJ, Rhie SK, Bensen JT, Ingles SA, Kittles RA, Strom SS, Rybicki BA, ... ... Edwards TL, et al. Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry. European Urology. PMID 36872133 DOI: 10.1016/j.eururo.2023.01.022 |
0.513 |
|
| 2023 |
Jasper EA, Hellwege JN, Breeyear JH, Xiao B, Jarvik GP, Stanaway IB, Leppig KA, Chittoor G, Hayes MG, Dikilitas O, Kullo IJ, Holm IA, Verma SS, Edwards TL, Velez Edwards DR. Genetic Predictors of Blood Pressure Traits are Associated with Preeclampsia. Medrxiv : the Preprint Server For Health Sciences. PMID 36824881 DOI: 10.1101/2023.02.09.23285734 |
0.573 |
|
| 2023 |
Pike MM, Schildcrout J, Baldwin S, Edwards T, Lipworth L, Robinson-Cohen C. Genetic Variants Associated With Systolic Blood Pressure in Children and Adolescents. Journal of the American Heart Association. 12: e027993. PMID 36718908 DOI: 10.1161/JAHA.122.027993 |
0.318 |
|
| 2022 |
Vujkovic M, Ramdas S, Lorenz KM, Guo X, Darlay R, Cordell HJ, He J, Gindin Y, Chung C, Myers RP, Schneider CV, Park J, Lee KM, Serper M, Carr RM, ... ... Edwards TL, et al. A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation. Nature Genetics. PMID 35654975 DOI: 10.1038/s41588-022-01078-z |
0.587 |
|
| 2022 |
Piekos JA, Hellwege JN, Zhang Y, Torstenson ES, Jarvik GP, Dikilitas O, Kullo IJ, Schaid DJ, Crosslin DR, Pendergrass SA, Lee MTM, Roden D, Denny JC, Edwards TL, Velez Edwards DR. Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid. Human Genetics. PMID 35226188 DOI: 10.1007/s00439-022-02442-z |
0.616 |
|
| 2021 |
Park J, Lucas AM, Zhang X, Chaudhary K, Cho JH, Nadkarni G, Dobbyn A, Chittoor G, Josyula NS, Katz N, Breeyear JH, Ahmadmehrabi S, Drivas TG, Chavali VRM, Fasolino M, ... ... Edwards TL, et al. Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations. Nature Medicine. PMID 33432171 DOI: 10.1038/s41591-020-1133-8 |
0.718 |
|
| 2020 |
Surendran P, Feofanova EV, Lahrouchi N, Ntalla I, Karthikeyan S, Cook J, Chen L, Mifsud B, Yao C, Kraja AT, Cartwright JH, Hellwege JN, Giri A, Tragante V, Thorleifsson G, ... ... Edwards TL, et al. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Nature Genetics. PMID 33230300 DOI: 10.1038/s41588-020-00713-x |
0.306 |
|
| 2020 |
Klarin D, Verma SS, Judy R, Dikilitas O, Wolford BN, Paranjpe I, Levin MG, Pan C, Tcheandjieu C, Spin JM, Lynch J, Assimes TL, Nyrønning LÅ, Mattsson E, Edwards TL, et al. Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program. Circulation. PMID 32981348 DOI: 10.1161/CIRCULATIONAHA.120.047544 |
0.608 |
|
| 2020 |
Vujkovic M, Keaton JM, Lynch JA, Miller DR, Zhou J, Tcheandjieu C, Huffman JE, Assimes TL, Lorenz K, Zhu X, Hilliard AT, Judy RL, Huang J, Lee KM, Klarin D, ... ... Edwards TL, et al. Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis. Nature Genetics. PMID 32541925 DOI: 10.1038/S41588-020-0637-Y |
0.349 |
|
| 2019 |
Tin A, Marten J, Halperin Kuhns VL, Li Y, Wuttke M, Kirsten H, Sieber KB, Qiu C, Gorski M, Yu Z, Giri A, Sveinbjornsson G, Li M, Chu AY, Hoppmann A, ... ... Edwards TL, et al. Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. Nature Genetics. PMID 31578528 DOI: 10.1038/S41588-019-0504-X |
0.618 |
|
| 2019 |
Teumer A, Li Y, Ghasemi S, Prins BP, Wuttke M, Hermle T, Giri A, Sieber KB, Qiu C, Kirsten H, Tin A, Chu AY, Bansal N, Feitosa MF, Wang L, ... ... Edwards TL, et al. Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. Nature Communications. 10: 4130. PMID 31511532 DOI: 10.1038/S41467-019-11576-0 |
0.634 |
|
| 2019 |
Bick AG, Akwo E, Robinson-Cohen C, Lee K, Lynch J, Assimes TL, DuVall S, Edwards T, Fang H, Freiberg SM, Giri A, Huffman JE, Huang J, Hull L, Kember RL, et al. Association of APOL1 Risk Alleles with Cardiovascular Disease in African Americans in the Million Veteran Program. Circulation. PMID 31337231 DOI: 10.1161/Circulationaha.118.036589 |
0.338 |
|
| 2019 |
Edwards TL, Giri A, Hellwege JN, Hartmann KE, Stewart EA, Jeff JM, Bray MJ, Pendergrass SA, Torstenson ES, Keaton JM, Jones SH, Gogoi RP, Kuivaniemi H, Jackson KL, Kho AN, et al. A -Ethnic Genome-Wide Association Study of Uterine Fibroids. Frontiers in Genetics. 10: 511. PMID 31249589 DOI: 10.3389/Fgene.2019.00511 |
0.629 |
|
| 2019 |
Wuttke M, Li Y, Li M, Sieber KB, Feitosa MF, Gorski M, Tin A, Wang L, Chu AY, Hoppmann A, Kirsten H, Giri A, Chai JF, Sveinbjornsson G, Tayo BO, ... ... Edwards TL, et al. A catalog of genetic loci associated with kidney function from analyses of a million individuals. Nature Genetics. 51: 957-972. PMID 31152163 DOI: 10.1038/s41588-019-0407-x |
0.608 |
|
| 2019 |
Hellwege JN, Stallings S, Torstenson ES, Carroll R, Borthwick KM, Brilliant MH, Crosslin D, Gordon A, Hripcsak G, Jarvik GP, Linneman JG, Devi P, Peissig PL, Sleiman PAM, Hakonarson H, ... ... Edwards TL, et al. Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network. Scientific Reports. 9: 6077. PMID 30988330 DOI: 10.1038/S41598-019-42427-Z |
0.7 |
|
| 2018 |
Takeuchi F, Akiyama M, Matoba N, Katsuya T, Nakatochi M, Tabara Y, Narita A, Saw WY, Moon S, Spracklen CN, Chai JF, Kim YJ, Zhang L, Wang C, Li H, ... ... Edwards TL, et al. Interethnic analyses of blood pressure loci in populations of East Asian and European descent. Nature Communications. 9: 5052. PMID 30487518 DOI: 10.1038/S41467-018-07345-0 |
0.327 |
|
| 2018 |
Wang H, Nandakumar P, Tekola-Ayele F, Tayo BO, Ware EB, Gu CC, Lu Y, Yao J, Zhao W, Smith JA, Hellwege JN, Guo X, Edwards TL, Loos RJF, Arnett DK, et al. Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31. European Journal of Human Genetics : Ejhg. PMID 30262922 DOI: 10.1038/S41431-018-0277-1 |
0.312 |
|
| 2018 |
Mosley JD, Feng Q, Wells QS, Van Driest SL, Shaffer CM, Edwards TL, Bastarache L, Wei WQ, Davis LK, McCarty CA, Thompson W, Chute CG, Jarvik GP, Gordon AS, Palmer MR, et al. A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers. Nature Communications. 9: 3522. PMID 30166544 DOI: 10.1038/S41467-018-05624-4 |
0.668 |
|
| 2018 |
Barbeira AN, Dickinson SP, Bonazzola R, Zheng J, Wheeler HE, Torres JM, Torstenson ES, Shah KP, Garcia T, Edwards TL, Stahl EA, Huckins LM, Nicolae DL, Cox NJ, et al. Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. Nature Communications. 9: 1825. PMID 29739930 DOI: 10.1038/S41467-018-03621-1 |
0.323 |
|
| 2018 |
Wei WQ, Li X, Feng Q, Kubo M, Kullo IJ, Peissig PL, Karlson EW, Jarvik GP, Lee MTM, Shang N, Larson EA, Edwards T, Shaffer C, Mosley JD, Maeda S, et al. Variants are Associated with Residual Cardiovascular Risk in Patients Receiving Statins. Circulation. PMID 29703846 DOI: 10.1161/Circulationaha.117.031356 |
0.544 |
|
| 2018 |
Bastarache L, Hughey JJ, Hebbring S, Marlo J, Zhao W, Ho WT, Van Driest SL, McGregor TL, Mosley JD, Wells QS, Temple M, Ramirez AH, Carroll R, Osterman T, Edwards T, et al. Phenotype risk scores identify patients with unrecognized Mendelian disease patterns. Science (New York, N.Y.). 359: 1233-1239. PMID 29590070 DOI: 10.1126/Science.Aal4043 |
0.423 |
|
| 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 |
0.332 |
|
| 2017 |
Sapkota Y, Vivo I, Steinthorsdottir V, Fassbender A, Bowdler L, Buring JE, Edwards TL, Jones S, O D, Peterse D, Rexrode KM, Ridker PM, Schork AJ, Thorleifsson G, Wallace LM, et al. Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry. Scientific Reports. 7: 11380. PMID 28900119 DOI: 10.1038/s41598-017-10440-9 |
0.359 |
|
| 2017 |
Hellwege JN, Jeff JM, Wise LA, Gallagher CS, Wellons M, Hartmann KE, Jones SF, Torstenson ES, Dickinson S, Ruiz-Narváez EA, Rohland N, Allen A, Reich D, Tandon A, Pasaniuc B, ... ... Edwards TL, et al. A multi-stage genome-wide association study of uterine fibroids in African Americans. Human Genetics. PMID 28836065 DOI: 10.1007/S00439-017-1836-1 |
0.303 |
|
| 2017 |
Sapkota Y, Steinthorsdottir V, Morris AP, Fassbender A, Rahmioglu N, De Vivo I, Buring JE, Zhang F, Edwards TL, Jones S, O D, Peterse D, Rexrode KM, Ridker PM, Schork AJ, et al. Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism. Nature Communications. 8: 15539. PMID 28537267 DOI: 10.1038/Ncomms15539 |
0.348 |
|
| 2017 |
Liang J, Le TH, Edwards DRV, Tayo BO, Gaulton KJ, Smith JA, Lu Y, Jensen RA, Chen G, Yanek LR, Schwander K, Tajuddin SM, Sofer T, Kim W, Kayima J, ... ... Edwards TL, et al. Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. Plos Genetics. 13: e1006728. PMID 28498854 DOI: 10.1371/Journal.Pgen.1006728 |
0.301 |
|
| 2016 |
Liu C, Kraja AT, Smith JA, Brody JA, Franceschini N, Bis JC, Rice K, Morrison AC, Lu Y, Weiss S, Guo X, Palmas W, Martin LW, Chen YI, Surendran P, ... ... Edwards TL, et al. Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. Nature Genetics. PMID 27618448 DOI: 10.1038/Ng.3660 |
0.316 |
|
| 2016 |
Chami N, Chen MH, Slater AJ, Eicher JD, Evangelou E, Tajuddin SM, Love-Gregory L, Kacprowski T, Schick UM, Nomura A, Giri A, Lessard S, Brody JA, Schurmann C, Pankratz N, ... ... Edwards TL, et al. Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits. American Journal of Human Genetics. PMID 27346685 DOI: 10.1016/J.Ajhg.2016.05.007 |
0.328 |
|
| 2016 |
Lessard S, Manning AK, Low-Kam C, Auer PL, Giri A, Graff M, Schurmann C, Yaghootkar H, Luan J, Esko T, Karaderi T, ... ... Edwards TL, et al. Testing the Role of Predicted Gene Knockouts in Human Anthropometric Trait Variation. Human Molecular Genetics. PMID 26908616 DOI: 10.1093/Hmg/Ddw055 |
0.301 |
|
| 2015 |
Giri A, Wu JM, Ward RM, Hartmann KE, Park AJ, North KE, Graff M, Wallace RB, Bareh G, Qi L, O'Sullivan MJ, Reiner AP, Edwards TL, Velez Edwards DR. Genetic Determinants of Pelvic Organ Prolapse among African American and Hispanic Women in the Women's Health Initiative. Plos One. 10: e0141647. PMID 26545240 DOI: 10.1371/Journal.Pone.0141647 |
0.305 |
|
| 2015 |
Shoemaker MB, Bollmann A, Lubitz SA, Ueberham L, Saini H, Montgomery J, Edwards T, Yoneda Z, Sinner MF, Arya A, Sommer P, Delaney J, Goyal SK, Saavedra P, Kanagasundram A, et al. Common genetic variants and response to atrial fibrillation ablation. Circulation. Arrhythmia and Electrophysiology. 8: 296-302. PMID 25684755 DOI: 10.1161/Circep.114.001909 |
0.334 |
|
| 2015 |
Zhu X, Feng T, Tayo BO, Liang J, Young JH, Franceschini N, Smith JA, Yanek LR, Sun YV, Edwards TL, Chen W, Nalls M, Fox E, Sale M, Bottinger E, et al. Meta-analysis of correlated traits via summary statistics from GWASs with an application in hypertension. American Journal of Human Genetics. 96: 21-36. PMID 25500260 DOI: 10.1016/J.Ajhg.2014.11.011 |
0.335 |
|
| 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 |
0.366 |
|
| 2014 |
Cronin RM, Field JR, Bradford Y, Shaffer CM, Carroll RJ, Mosley JD, Bastarache L, Edwards TL, Hebbring SJ, Lin S, Hindorff LA, Crane PK, Pendergrass SA, Ritchie MD, Crawford DC, et al. Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index. Frontiers in Genetics. 5: 250. PMID 25177340 DOI: 10.3389/Fgene.2014.00250 |
0.677 |
|
| 2014 |
Ward RM, Velez Edwards DR, Edwards T, Giri A, Jerome RN, Wu JM. Genetic epidemiology of pelvic organ prolapse: a systematic review. American Journal of Obstetrics and Gynecology. 211: 326-35. PMID 24721264 DOI: 10.1016/J.Ajog.2014.04.006 |
0.421 |
|
| 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, 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 |
0.477 |
|
| 2013 |
Edwards TL, Michels KA, Hartmann KE, Velez Edwards DR. BET1L and TNRC6B associate with uterine fibroid risk among European Americans. Human Genetics. 132: 943-53. PMID 23604678 DOI: 10.1007/S00439-013-1306-3 |
0.343 |
|
| 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, 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 |
0.475 |
|
| 2013 |
Peters U, Jiao S, Schumacher FR, Hutter CM, Aragaki AK, Baron JA, Berndt SI, Bézieau S, Brenner H, Butterbach K, Caan BJ, Campbell PT, Carlson CS, Casey G, Chan AT, ... ... Edwards T, et al. Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. Gastroenterology. 144: 799-807.e24. PMID 23266556 DOI: 10.1053/J.Gastro.2012.12.020 |
0.408 |
|
| 2012 |
Long J, Edwards T, Signorello LB, Cai Q, Zheng W, Shu XO, Blot WJ. Evaluation of genome-wide association study-identified type 2 diabetes loci in African Americans. American Journal of Epidemiology. 176: 995-1001. PMID 23144361 DOI: 10.1093/Aje/Kws176 |
0.422 |
|
| 2012 |
Zhang B, Shrubsole MJ, Li G, Cai Q, Edwards T, Smalley WE, Ness RM, Zheng W. Association of genetic variants for colorectal cancer differs by subtypes of polyps in the colorectum. Carcinogenesis. 33: 2417-23. PMID 23027627 DOI: 10.1093/Carcin/Bgs308 |
0.415 |
|
| 2012 |
Jia P, Wang L, Fanous AH, Pato CN, Edwards TL, Zhao Z. Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia. Plos Computational Biology. 8: e1002587. PMID 22792057 DOI: 10.1371/Journal.Pcbi.1002587 |
0.306 |
|
| 2012 |
Edwards TL, Shrubsole MJ, Cai Q, Li G, Dai Q, Rex DK, Ulbright TM, Fu Z, Murff HJ, Smalley W, Ness R, Zheng W. A study of prostaglandin pathway genes and interactions with current nonsteroidal anti-inflammatory drug use in colorectal adenoma. Cancer Prevention Research (Philadelphia, Pa.). 5: 855-63. PMID 22551900 DOI: 10.1158/1940-6207.Capr-11-0459 |
0.364 |
|
| 2012 |
Zhu X, Shrubsole MJ, Ness RM, Cai Q, Long J, Chen Z, Deng X, Smalley WE, Edwards T, Zheng W, Dai Q. Abstract 1674: Two phase study of KCNJ1 polymorphisms, calcium, magnesium and colorectal adenoma risk, results from the Tennessee Colorectal Polyp Study Cancer Research. 72: 1674-1674. DOI: 10.1158/1538-7445.Am2012-1674 |
0.368 |
|
| 2012 |
Edwards T, Giri A, Motley S, Duong W, Fowke JH. Abstract 45: Examining genetic markers of obesity and metabolism against prostate cancer risk using Metabochip. Cancer Epidemiology Biomarkers & Prevention. 21: 45-45. DOI: 10.1158/1055-9965.Gwas-45 |
0.428 |
|
| 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 |
0.399 |
|
| 2011 |
Deng X, Shrubsole MJ, Ness RM, Cai Q, Edwards T, Long J, Chen Z, Su Y, Zhu X, Sun P, Luo J, Smalley WE, Zheng W, Dai Q. Abstract LB-452: Genetic polymorphisms in the TRPM7 gene and colorectal adenoma risk Cancer Research. 71. DOI: 10.1158/1538-7445.Am2011-Lb-452 |
0.395 |
|
| 2011 |
Sun P, Shrubsole MJ, Ness RM, Cai Q, Long J, Edwards T, Chen Z, Zhu X, Deng X, Luo J, Smalley WE, Zheng W, Dai Q. Abstract 3763: Calcium intake, CABP1 polymorphisms, and the risk of colorectal adenoma: Results from Tennessee Colorectal Polyp Study Cancer Research. 71: 3763-3763. DOI: 10.1158/1538-7445.Am2011-3763 |
0.374 |
|
| 2010 |
Cattaert T, Urrea V, Naj AC, De Lobel L, De Wit V, Fu M, Mahachie John JM, Shen H, Calle ML, Ritchie MD, Edwards TL, Van Steen K. FAM-MDR: a flexible family-based multifactor dimensionality reduction technique to detect epistasis using related individuals. Plos One. 5: e10304. PMID 20421984 DOI: 10.1371/Journal.Pone.0010304 |
0.474 |
|
| 2010 |
Edwards TL, Turner SD, Torstenson ES, Dudek SM, Martin ER, Ritchie MD. A general framework for formal tests of interaction after exhaustive search methods with applications to MDR and MDR-PDT. Plos One. 5: e9363. PMID 20186329 DOI: 10.1371/Journal.Pone.0009363 |
0.597 |
|
| 2010 |
Edwards TL, Scott WK, Almonte C, Burt A, Powell EH, Beecham GW, Wang L, Züchner S, Konidari I, Wang G, Singer C, Nahab F, Scott B, Stajich JM, Pericak-Vance M, et al. Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. Annals of Human Genetics. 74: 97-109. PMID 20070850 DOI: 10.1111/J.1469-1809.2009.00560.X |
0.303 |
|
| 2010 |
Edwards TL, Torstensen E, Dudek S, Martin ER, Ritchie MD. A cross-validation procedure for general pedigrees and matched odds ratio fitness metric implemented for the multifactor dimensionality reduction pedigree disequilibrium test. Genetic Epidemiology. 34: 194-9. PMID 19697353 DOI: 10.1002/Gepi.20447 |
0.467 |
|
| 2009 |
Edwards TL, Pericak-Vance M, Gilbert JR, Haines JL, Martin ER, Ritchie MD. An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 721-35. PMID 19105203 DOI: 10.1002/Ajmg.B.30899 |
0.484 |
|
| 2009 |
Edwards TL, Lewis K, Velez DR, Dudek S, Ritchie MD. Exploring the performance of Multifactor Dimensionality Reduction in large scale SNP studies and in the presence of genetic heterogeneity among epistatic disease models. Human Heredity. 67: 183-92. PMID 19077437 DOI: 10.1159/000181157 |
0.472 |
|
| 2008 |
Edwards TL, Wang X, Chen Q, Wormly B, Riley B, O'Neill FA, Walsh D, Ritchie MD, Kendler KS, Chen X. Interaction between interleukin 3 and dystrobrevin-binding protein 1 in schizophrenia. Schizophrenia Research. 106: 208-17. PMID 18804346 DOI: 10.1016/J.Schres.2008.07.022 |
0.473 |
|
| 2008 |
Bush WS, Edwards TL, Dudek SM, McKinney BA, Ritchie MD. Alternative contingency table measures improve the power and detection of multifactor dimensionality reduction. Bmc Bioinformatics. 9: 238. PMID 18485205 DOI: 10.1186/1471-2105-9-238 |
0.602 |
|
| 2008 |
Edwards TL, Bush WS, Turner SD, Dudek SM, Torstenson ES, Schmidt M, Martin E, Ritchie MD. Generating linkage disequilibrium patterns in data simulations using genomeSIMLA Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 4973: 24-35. DOI: 10.1007/978-3-540-78757-0_3 |
0.602 |
|
| 2007 |
Ritchie MD, Bartlett J, Bush WS, Edwards TL, Motsinger AA, Torstenson ES. Exploring epistasis in candidate genes for rheumatoid arthritis. Bmc Proceedings. 1: S70. PMID 18466572 DOI: 10.1186/1753-6561-1-S1-S70 |
0.643 |
|
| 2007 |
Bartlett CW, Vieland VJ, Bartlett J, Bell JT, Bhattacharjee S, Clerget-Darpoux F, Bush WS, Edwards TL, Gao G, Halder I, Huang Y, Kotti S, Larkin EK, Li H, Motsinger AA, et al. Discussing gene-gene interaction: warning--translating equations to English may result in jabberwocky. Genetic Epidemiology. 31: S61-7. PMID 18046759 DOI: 10.1002/gepi.20281 |
0.604 |
|
| 2007 |
Ritchie MD, Edwards TL, Fanelli TJ, Motsinger AA. Genetic heterogeneity is not as threatening as you might think. Genetic Epidemiology. 31: 797-800. PMID 17654613 DOI: 10.1002/Gepi.20256 |
0.434 |
|
| 2006 |
Martin E, Thornton-Wells T, Edwards T, Hahn L, Bronson P, Gilbert J, Haines J, Pericak-Vance M, Ritchie M. P1-355: Joint analysis of candidate genes in AD through data reduction Alzheimer's & Dementia. 2: S201-S202. DOI: 10.1016/J.Jalz.2006.05.733 |
0.481 |
|
| Show low-probability matches. |