Sharon R. Kardia - Publications

Affiliations: 
University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
Epidemiology

15 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
2020 Ni X, Zhou M, Wang H, He KY, Broeckel U, Hanis C, Kardia S, Redline S, Cooper RS, Tang H, Zhu X. Detecting fitness epistasis in recently admixed populations with genome-wide data. Bmc Genomics. 21: 476. PMID 32652930 DOI: 10.1186/S12864-020-06874-7  0.342
2018 Chen H, Huffman JE, Brody JA, Wang C, Lee S, Li Z, Gogarten SM, Sofer T, Bielak LF, Bis JC, Blangero J, Bowler RP, Cade BE, Cho MH, Correa A, ... ... Kardia S, et al. Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies. American Journal of Human Genetics. PMID 30639324 DOI: 10.1016/J.Ajhg.2018.12.012  0.33
2017 Nandakumar P, Lee D, Richard MA, Tekola-Ayele F, Tayo BO, Ware E, Sung YJ, Salako B, Ogunniyi A, Gu CC, Grove ML, Fornage M, Kardia S, Rotima C, Cooper RS, et al. Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestry. Journal of Hypertension. PMID 28234671 DOI: 10.1097/Hjh.0000000000001319  0.368
2016 Wang H, Choi Y, Tayo B, Wang X, Morris N, Zhang X, Broeckel U, Hanis C, Kardia S, Redline S, Cooper RS, Tang H, Zhu X. Genome-wide survey in African Americans demonstrates potential epistasis of fitness in the human genome. Genetic Epidemiology. PMID 27917522 DOI: 10.1002/Gepi.22026  0.356
2016 Sung YJ, Winkler TW, Manning AK, Aschard H, Gudnason V, Harris TB, Smith AV, Boerwinkle E, Brown MR, Morrison AC, Fornage M, Lin LA, Richard M, Bartz TM, Psaty BM, ... ... Kardia S, et al. An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group. Genetic Epidemiology. PMID 27230302 DOI: 10.1002/Gepi.21978  0.367
2011 Zhu X, Young JH, Fox E, Keating BJ, Franceschini N, Kang S, Tayo B, Adeyemo A, Sun YV, Li Y, Morrison A, Newton-Cheh C, Liu K, Ganesh SK, Kutlar A, ... ... Kardia S, et al. Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium. Human Molecular Genetics. 20: 2285-95. PMID 21422096 DOI: 10.1093/Hmg/Ddr113  0.424
2011 Simino J, Shi G, Kume R, Schwander K, Province MA, Gu CC, Kardia S, Chakravarti A, Ehret G, Olshen RA, Turner ST, Ho LT, Zhu X, Jaquish C, Paltoo D, et al. Five blood pressure loci identified by an updated genome-wide linkage scan: meta-analysis of the Family Blood Pressure Program. American Journal of Hypertension. 24: 347-54. PMID 21151011 DOI: 10.1038/Ajh.2010.238  0.405
2009 Basu A, Tang H, Arnett D, Gu CC, Mosley T, Kardia S, Luke A, Tayo B, Cooper R, Zhu X, Risch N. Admixture mapping of quantitative trait loci for BMI in African Americans: evidence for loci on chromosomes 3q, 5q, and 15q. Obesity (Silver Spring, Md.). 17: 1226-31. PMID 19584881 DOI: 10.1038/Oby.2009.24  0.389
2009 Sammalisto S, Hiekkalinna T, Schwander K, Kardia S, Weder AB, Rodriguez BL, Doria A, Kelly JA, Bruner GR, Harley JB, Redline S, Larkin EK, Patel SR, Ewan AJ, Weber JL, et al. Genome-wide linkage screen for stature and body mass index in 3.032 families: evidence for sex- and population-specific genetic effects. European Journal of Human Genetics : Ejhg. 17: 258-66. PMID 18781184 DOI: 10.1038/Ejhg.2008.152  0.377
2007 Gu CC, Hunt SC, Kardia S, Turner ST, Chakravarti A, Schork N, Olshen R, Curb D, Jaquish C, Boerwinkle E, Rao DC. An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP). Human Genetics. 121: 577-90. PMID 17372766 DOI: 10.1007/S00439-007-0349-8  0.415
2007 Greenwood TA, Libiger O, Kardia S, Hanis C, Morrison AC, Gu CC, Rice T, Miller M, Turner ST, Myers RH, Grove J, Hsiao CF, Weder AB, Schork NJ. Comprehensive linkage and linkage heterogeneity analysis of 4344 sibling pairs affected with hypertension from the Family Blood Pressure Program. Genetic Epidemiology. 31: 195-210. PMID 17266112 DOI: 10.1002/Gepi.20202  0.411
2005 Jorgenson E, Tang H, Gadde M, Province M, Leppert M, Kardia S, Schork N, Cooper R, Rao DC, Boerwinkle E, Risch N. Ethnicity and human genetic linkage maps. American Journal of Human Genetics. 76: 276-90. PMID 15627237 DOI: 10.1086/427926  0.369
2002 Stengård JH, Clark AG, Weiss KM, Kardia S, Nickerson DA, Salomaa V, Ehnholm C, Boerwinkle E, Sing CF. Contributions of 18 additional DNA sequence variations in the gene encoding apolipoprotein E to explaining variation in quantitative measures of lipid metabolism. American Journal of Human Genetics. 71: 501-17. PMID 12165926 DOI: 10.1086/342217  0.319
2002 Boerwinkle E, Brown CA, Carrejo M, Ferrell R, Hanis C, Hutchinson R, Kardia S, Sing C, Turner S, Weder A, Chakravarti A, Cooper R, Jacob H, NS, Hunt S, et al. Multi-center genetic study of hypertension: The Family blood pressure program (FBPP) Hypertension. 39: 3-9. PMID 11799070 DOI: 10.1161/Hy1201.100415  0.372
2000 Bray MS, Krushkal J, Li L, Ferrell R, Kardia S, Sing CF, Turner ST, Boerwinkle E. Positional genomic analysis identifies the β2-adrenergic receptor gene as a susceptibility locus for human hypertension Circulation. 101: 2877-2882. PMID 10869257 DOI: 10.1161/01.Cir.101.25.2877  0.361
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