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Items: 1 to 20 of 93

1.

A Genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction.

Taylor JY, Schwander K, Kardia SL, Arnett D, Liang J, Hunt SC, Rao DC, Sun YV.

Sci Rep. 2016 Jan 11;6:18812. doi: 10.1038/srep18812.

2.

Resequencing of the CETP gene in American whites and African blacks: Association of rare and common variants with HDL-cholesterol levels.

Pirim D, Wang X, Niemsiri V, Radwan ZH, Bunker CH, Hokanson JE, Hamman RF, Barmada MM, Demirci FY, Kamboh MI.

Metabolism. 2016 Jan;65(1):36-47. doi: 10.1016/j.metabol.2015.09.020. Epub 2015 Sep 30.

PMID:
26683795
3.

Dietary fat and carbohydrate modulate the effect of the ATP-binding cassette A1 (ABCA1) R230C variant on metabolic risk parameters in premenopausal women from the Genetics of Atherosclerotic Disease (GEA) Study.

Jacobo-Albavera L, Posadas-Romero C, Vargas-Alarcón G, Romero-Hidalgo S, Posadas-Sánchez R, González-Salazar Mdel C, Carnevale A, Canizales-Quinteros S, Medina-Urrutia A, Antúnez-Argüelles E, Villarreal-Molina T.

Nutr Metab (Lond). 2015 Nov 16;12:45. doi: 10.1186/s12986-015-0040-3. eCollection 2015.

4.

Two-Variance-Component Model Improves Genetic Prediction in Family Datasets.

Tucker G, Loh PR, MacLeod IM, Hayes BJ, Goddard ME, Berger B, Price AL.

Am J Hum Genet. 2015 Nov 5;97(5):677-90. doi: 10.1016/j.ajhg.2015.10.002.

PMID:
26544803
5.

Mapping asthma-associated variants in admixed populations.

Mersha TB.

Front Genet. 2015 Sep 29;6:292. doi: 10.3389/fgene.2015.00292. eCollection 2015. Review.

6.

Measurement by a Novel LC-MS/MS Methodology Reveals Similar Serum Concentrations of Vitamin D-Binding Protein in Blacks and Whites.

Henderson CM, Lutsey PL, Misialek JR, Laha TJ, Selvin E, Eckfeldt JH, Hoofnagle AN.

Clin Chem. 2016 Jan;62(1):179-87. doi: 10.1373/clinchem.2015.244541. Epub 2015 Oct 9.

PMID:
26453697
7.

Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.

Danjou F, Zoledziewska M, Sidore C, Steri M, Busonero F, Maschio A, Mulas A, Perseu L, Barella S, Porcu E, Pistis G, Pitzalis M, Pala M, Menzel S, Metrustry S, Spector TD, Leoni L, Angius A, Uda M, Moi P, Thein SL, Galanello R, Abecasis GR, Schlessinger D, Sanna S, Cucca F.

Nat Genet. 2015 Nov;47(11):1264-71. doi: 10.1038/ng.3307. Epub 2015 Sep 14.

PMID:
26366553
8.

Potential Signals of Natural Selection in the Top Risk Loci for Coronary Artery Disease: 9p21 and 10q11.

Zanetti D, Carreras-Torres R, Esteban E, Via M, Moral P.

PLoS One. 2015 Aug 7;10(8):e0134840. doi: 10.1371/journal.pone.0134840. eCollection 2015.

9.

Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration.

Lanktree MB, Elbers CC, Li Y, Zhang G, Duan Q, Karczewski KJ, Guo Y, Tragante V, North KE, Cushman M, Asselbergs FW, Wilson JG, Lange LA, Drenos F, Reiner AP, Barnes MR, Keating BJ.

J Lipid Res. 2015 Sep;56(9):1781-6. doi: 10.1194/jlr.P059477. Epub 2015 Jul 21.

PMID:
26199122
10.

Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans.

Carty CL, Keene KL, Cheng YC, Meschia JF, Chen WM, Nalls M, Bis JC, Kittner SJ, Rich SS, Tajuddin S, Zonderman AB, Evans MK, Langefeld CD, Gottesman R, Mosley TH, Shahar E, Woo D, Yaffe K, Liu Y, Sale MM, Dichgans M, Malik R, Longstreth WT Jr, Mitchell BD, Psaty BM, Kooperberg C, Reiner A, Worrall BB, Fornage M; COMPASS and METASTROKE Consortia.

Stroke. 2015 Aug;46(8):2063-8. doi: 10.1161/STROKEAHA.115.009044. Epub 2015 Jun 18.

PMID:
26089329
11.

Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols.

Moore CB, Verma A, Pendergrass S, Verma SS, Johnson DH, Daar ES, Gulick RM, Haubrich R, Robbins GK, Ritchie MD, Haas DW.

Open Forum Infect Dis. 2015 Jan 9;2(1):ofu113. doi: 10.1093/ofid/ofu113. eCollection 2015 Jan.

12.

Uncovering physiological mechanisms for health disparities in type 2 diabetes.

Staiano AE, Harrington DM, Johannsen NM, Newton RL Jr, Sarzynski MA, Swift DL, Katzmarzyk PT.

Ethn Dis. 2015 Winter;25(1):31-7. Review.

13.

Association of a 62 Variants Type 2 Diabetes Genetic Risk Score With Markers of Subclinical Atherosclerosis: A Transethnic, Multicenter Study.

Dauriz M, Porneala BC, Guo X, Bielak LF, Peyser PA, Durant NH, Carnethon MR, Bonadonna RC, Bonora E, Bowden DW, Florez JC, Fornage M, Hivert MF, Jacobs DR Jr, Kabagambe EK, Lewis CE, Murabito JM, Rasmussen-Torvik LJ, Rich SS, Vassy JL, Yao J, Carr JJ, Kardia SL, Siscovick D, O'Donnell CJ, Rotter JI, Dupuis J, Meigs JB.

Circ Cardiovasc Genet. 2015 Jun;8(3):507-15. doi: 10.1161/CIRCGENETICS.114.000740. Epub 2015 Mar 24.

PMID:
25805414
14.

Genome-wide significant loci: how important are they? Systems genetics to understand heritability of coronary artery disease and other common complex disorders.

Björkegren JL, Kovacic JC, Dudley JT, Schadt EE.

J Am Coll Cardiol. 2015 Mar 3;65(8):830-45. doi: 10.1016/j.jacc.2014.12.033. Review.

15.

Resequencing of LPL in African Blacks and associations with lipoprotein-lipid levels.

Pirim D, Wang X, Radwan ZH, Niemsiri V, Bunker CH, Barmada MM, Kamboh MI, Demirci FY.

Eur J Hum Genet. 2015 Sep;23(9):1244-53. doi: 10.1038/ejhg.2014.268. Epub 2015 Jan 28.

16.

Genetic overlap between diagnostic subtypes of ischemic stroke.

Holliday EG, Traylor M, Malik R, Bevan S, Falcone G, Hopewell JC, Cheng YC, Cotlarciuc I, Bis JC, Boerwinkle E, Boncoraglio GB, Clarke R, Cole JW, Fornage M, Furie KL, Ikram MA, Jannes J, Kittner SJ, Lincz LF, Maguire JM, Meschia JF, Mosley TH, Nalls MA, Oldmeadow C, Parati EA, Psaty BM, Rothwell PM, Seshadri S, Scott RJ, Sharma P, Sudlow C, Wiggins KL, Worrall BB, Rosand J, Mitchell BD, Dichgans M, Markus HS, Levi C, Attia J, Wray NR; Australian Stroke Genetics Collaborative; Wellcome Trust Case Control Consortium 2; International Stroke Genetics Consortium.

Stroke. 2015 Mar;46(3):615-9. doi: 10.1161/STROKEAHA.114.007930. Epub 2015 Jan 22.

PMID:
25613305
17.

Insight in genome-wide association of metabolite quantitative traits by exome sequence analyses.

Demirkan A, Henneman P, Verhoeven A, Dharuri H, Amin N, van Klinken JB, Karssen LC, de Vries B, Meissner A, Göraler S, van den Maagdenberg AM, Deelder AM, C 't Hoen PA, van Duijn CM, van Dijk KW.

PLoS Genet. 2015 Jan 8;11(1):e1004835. doi: 10.1371/journal.pgen.1004835. eCollection 2015 Jan.

18.

Variants for HDL-C, LDL-C, and triglycerides identified from admixture mapping and fine-mapping analysis in African American families.

Shetty PB, Tang H, Feng T, Tayo B, Morrison AC, Kardia SL, Hanis CL, Arnett DK, Hunt SC, Boerwinkle E; Candidate Gene Association Resource (CARe) Consortium, Rao DC, Cooper RS, Risch N, Zhu X.

Circ Cardiovasc Genet. 2015 Feb;8(1):106-13. doi: 10.1161/CIRCGENETICS.114.000481. Epub 2014 Dec 31.

19.

Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE study.

Franceschini N, Hu Y, Reiner AP, Buyske S, Nalls M, Yanek LR, Li Y, Hindorff LA, Cole SA, Howard BV, Stafford JM, Carty CL, Sethupathy P, Martin LW, Lin DY, Johnson KC, Becker LC, North KE, Dehghan A, Bis JC, Liu Y, Greenland P, Manson JE, Maeda N, Garcia M, Harris TB, Becker DM, O'Donnell C, Heiss G, Kooperberg C, Boerwinkle E.

PLoS One. 2014 Dec 26;9(12):e113203. doi: 10.1371/journal.pone.0113203. eCollection 2014.

20.

Chromosome 16q22 variants in a region associated with cardiovascular phenotypes correlate with ZFHX3 expression in a transcript-specific manner.

Martin RI, Owens WA, Cunnington MS, Mayosi BM, Koref MS, Keavney BD.

BMC Genet. 2014 Dec 24;15:136. doi: 10.1186/s12863-014-0136-1.

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