| Year |
Citation |
Score |
| 2020 |
Dershem R, Gorvin CM, Metpally RPR, Krishnamurthy S, Smelser DT, Hannan FM, Carey DJ, Thakker RV, Breitwieser GE. Familial Hypocalciuric Hypercalcemia Type 1 and Autosomal-Dominant Hypocalcemia Type 1: Prevalence in a Large Healthcare Population. American Journal of Human Genetics. PMID 32386559 DOI: 10.1016/J.Ajhg.2020.04.006 |
0.404 |
|
| 2020 |
Shah S, Henry A, Roselli C, Lin H, Sveinbjörnsson G, Fatemifar G, Hedman ÅK, Wilk JB, Morley MP, Chaffin MD, Helgadottir A, Verweij N, Dehghan A, Almgren P, Andersson C, ... ... Smelser DT, et al. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure. Nature Communications. 11: 163. PMID 31919418 DOI: 10.1038/S41467-019-13690-5 |
0.366 |
|
| 2019 |
Dershem R, Metpally RPR, Jeffreys K, Krishnamurthy S, Smelser DT, Hershfinkel M, Carey DJ, Robishaw JD, Breitwieser GE. Rare-variant pathogenicity triage and inclusion of synonymous variants improves analysis of disease associations of orphan G protein-coupled receptors. The Journal of Biological Chemistry. PMID 31628190 DOI: 10.1074/Jbc.Ra119.009253 |
0.377 |
|
| 2019 |
Haggerty CM, Damrauer SM, Levin MG, Birtwell D, Carey DJ, Golden AM, Hartzel DN, Hu Y, Judy R, Kelly MA, Kember RL, Kirchner HL, Leader JB, Liang L, McDermott-Roe C, ... ... Smelser DT, et al. Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants. Circulation. PMID 31216868 DOI: 10.1161/Circulationaha.119.039573 |
0.349 |
|
| 2018 |
Choi SH, Weng LC, Roselli C, Lin H, Haggerty CM, Shoemaker MB, Barnard J, Arking DE, Chasman DI, Albert CM, Chaffin M, Tucker NR, Smith JD, Gupta N, Gabriel S, ... ... Smelser DT, et al. Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation. Jama. 320: 2354-2364. PMID 30535219 DOI: 10.1001/Jama.2018.18179 |
0.334 |
|
| 2017 |
Shan Y, Tromp G, Kuivaniemi H, Smelser DT, Verma SS, Ritchie MD, Elmore JR, Carey DJ, Conley YP, Gorin MB, Weeks DE. Genetic risk models: Influence of model size on risk estimates and precision. Genetic Epidemiology. PMID 28198095 DOI: 10.1002/Gepi.22035 |
0.338 |
|
| 2016 |
Jones GT, Tromp G, Kuivaniemi H, Gretarsdottir S, Baas AF, Giusti B, Strauss E, van 't Hof FN, Webb T, Erdman R, Ritchie MD, Elmore JR, Verma A, Pendergrass S, Kullo IJ, ... ... Smelser DT, et al. Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci. Circulation Research. PMID 27899403 DOI: 10.1161/Circresaha.116.308765 |
0.388 |
|
| 2016 |
Carey DJ, Fetterolf SN, Davis FD, Faucett WA, Kirchner HL, Mirshahi U, Murray MF, Smelser DT, Gerhard GS, Ledbetter DH. The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 26866580 DOI: 10.1038/Gim.2015.187 |
0.304 |
|
| 2016 |
Agrawal V, Smelser DT, Carey DJ, Vadakara JJ, Khan SS. Effect of the CEP72 Genotype and CYP3A5-Mediated Metabolism in Predicting Vincristine-Associated Peripheral Neuropathy Blood. 128: 5963-5963. DOI: 10.1182/Blood.V128.22.5963.5963 |
0.395 |
|
| 2014 |
Schrodi SJ, Mukherjee S, Shan Y, Tromp G, Sninsky JJ, Callear AP, Carter TC, Ye Z, Haines JL, Brilliant MH, Crane PK, Smelser DT, Elston RC, Weeks DE. Genetic-based prediction of disease traits: prediction is very difficult, especially about the future. Frontiers in Genetics. 5: 162. PMID 24917882 DOI: 10.3389/Fgene.2014.00162 |
0.366 |
|
| 2013 |
Yan XS, Barnholtz-Sloan J, Chu X, Li L, Colonie R, Webster J, Smelser D, Patel N, Prichard J, Stark A. Adiposity, inflammation, genetic variants and risk of post-menopausal breast cancer findings from a prospective-specimen-collection, retrospective-blinded-evaluation (PRoBE) design approach. Springerplus. 2: 638. PMID 24340245 DOI: 10.1186/2193-1801-2-638 |
0.378 |
|
| 2012 |
Ned RM, Yesupriya A, Imperatore G, Smelser DT, Moonesinghe R, Chang MH, Dowling NF. The ACE I/D polymorphism in US adults: limited evidence of association with hypertension-related traits and sex-specific effects by race/ethnicity. American Journal of Hypertension. 25: 209-15. PMID 21993364 DOI: 10.1038/Ajh.2011.182 |
0.36 |
|
| 2011 |
Yan X(, Patel N, Smelser D, Gerhard G, Stark A. PS2-41: The FTO Gene, Its Variants and Post-menopausal Breast Cancer Clinical Medicine & Research. 9: 143-143. DOI: 10.3121/Cmr.2011.1020.Ps2-41 |
0.365 |
|
| 2010 |
Ned RM, Yesupriya A, Imperatore G, Smelser DT, Moonesinghe R, Chang MH, Dowling NF. Inflammation gene variants and susceptibility to albuminuria in the U.S. population: analysis in the Third National Health and Nutrition Examination Survey (NHANES III), 1991-1994. Bmc Medical Genetics. 11: 155. PMID 21054877 DOI: 10.1186/1471-2350-11-155 |
0.358 |
|
| 2010 |
Smelser DT, Golden A, Masker K, Elmore JR, Carey DJ. C-B3-03: Association of Epidemiologic and Genetic Factors With Abdominal Aortic Aneurysm (AAA) Clinical Medicine & Research. 8: 50-50. DOI: 10.3121/Cmr.8.1.50-A |
0.446 |
|
| 2010 |
Smelser DT, Gerhard GS, Patel N, Golden A, Stark A. Abstract A82: TheFTOobesity gene and the risk of postmenopausal breast cancer among the medically underserved population in rural Pennsylvania Cancer Epidemiology, Biomarkers & Prevention. 19. DOI: 10.1158/1055-9965.Disp-10-A82 |
0.408 |
|
| 2009 |
Aberg K, Dai F, Sun G, Keighley ED, Indugula SR, Roberts ST, Zhang Q, Smelser D, Viali S, Tuitele J, Jin L, Deka R, Weeks DE, McGarvey ST. Susceptibility loci for adiposity phenotypes on 8p, 9p, and 16q in American Samoa and Samoa. Obesity (Silver Spring, Md.). 17: 518-24. PMID 19238140 DOI: 10.1038/Oby.2008.558 |
0.578 |
|
| 2008 |
Aberg K, Sun G, Smelser D, Indugula SR, Tsai HJ, Steele MS, Tuitele J, Deka R, McGarvey ST, Weeks DE. Applying novel genome-wide linkage strategies to search for loci influencing type 2 diabetes and adult height in American Samoa. Human Biology. 80: 99-123. PMID 18720898 DOI: 10.3378/1534-6617(2008)80[99:Anglst]2.0.Co;2 |
0.586 |
|
| 2008 |
Dai F, Sun G, Åberg K, Keighley ED, Indugula SR, Roberts ST, Smelser D, Viali S, Jin L, Deka R, Weeks DE, McGarvey ST. A whole genome linkage scan identifies multiple chromosomal regions influencing adiposity-related traits among Samoans. Annals of Human Genetics. 72: 780-792. PMID 18616661 DOI: 10.1111/J.1469-1809.2008.00462.X |
0.592 |
|
| 2007 |
Dai F, Keighley ED, Sun G, Indugula SR, Roberts ST, Aberg K, Smelser D, Tuitele J, Jin L, Deka R, Weeks DE, McGarvey ST. Genome-wide scan for adiposity-related phenotypes in adults from American Samoa International Journal of Obesity. 31: 1832-1842. PMID 17621312 DOI: 10.1038/Sj.Ijo.0803675 |
0.565 |
|
| 2005 |
Sun G, Kaushal R, Pal P, Wolujewicz M, Smelser D, Cheng H, Lu M, Chakraborty R, Jin L, Deka R. Whole-genome amplification: relative efficiencies of the current methods. Legal Medicine (Tokyo, Japan). 7: 279-86. PMID 15990351 DOI: 10.1016/J.Legalmed.2005.05.001 |
0.545 |
|
| 2004 |
Tsai HJ, Sun G, Smelser D, Viali S, Tufa J, Jin L, Weeks DE, McGarvey ST, Deka R. Distribution of genome-wide linkage disequilibrium based on microsatellite loci in the Samoan population. Human Genomics. 1: 327-34. PMID 15588493 DOI: 10.1186/1479-7364-1-5-327 |
0.58 |
|
| 2002 |
McGarvey S, Forrest W, Weeks D, Sun G, Smelser D, Tufa J, Viali S, Deka R. Human leptin locus (LEP) alleles and BMI in Samoans. International Journal of Obesity. 26: 783-788. PMID 12037648 DOI: 10.1038/Sj.Ijo.0801996 |
0.573 |
|
| 1999 |
Deka R, Guangyun S, Smelser D, Zhong Y, Kimmel M, Chakraborty R. Rate and directionality of mutations and effects of allele size constraints at anonymous, gene-associated, and disease-causing trinucleotide loci. Molecular Biology and Evolution. 16: 1166-77. PMID 10486972 DOI: 10.1093/Oxfordjournals.Molbev.A026207 |
0.591 |
|
| 1999 |
Deka R, Guangyun S, Wiest J, Smelser D, Chunhua S, Zhong Y, Chakraborty R. Patterns of Instability of Expanded CAG Repeats at the ERDA1 Locus in General Populations American Journal of Human Genetics. 65: 192-198. PMID 10364532 DOI: 10.1086/302453 |
0.562 |
|
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