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Items: 1 to 20 of 68

1.

Cohort studies and the genetics of complex disease.

Manolio TA.

Nat Genet. 2009 Jan;41(1):5-6. doi: 10.1038/ng0109-5. No abstract available.

PMID:
19112455
2.

Genome-wide linkage analysis of lipids in nondiabetic Chinese and Japanese from the SAPPHIRe family study.

Hsiao CF, Chiu YF, Chiang FT, Ho LT, Lee WJ, Hung YJ, Chen YD, Donlon TA, Jorgenson E, Curb D, Risch N, Hsiung CA; SAPPHIRe Study Group.

Am J Hypertens. 2006 Dec;19(12):1270-7.

PMID:
17161774
3.

Human genetics: pleiotropic mutations.

Stower H.

Nat Rev Genet. 2011 Dec 6;13(1):5. doi: 10.1038/nrg3132. No abstract available.

PMID:
22143242
4.

Spotlight on HDL biology: new insights in metabolism, function, and translation.

Rader DJ.

Cardiovasc Res. 2014 Aug 1;103(3):337-40. doi: 10.1093/cvr/cvu164. Epub 2014 Jul 14. No abstract available.

PMID:
25028388
5.

Recent developments in genome and exome-wide analyses of plasma lipids.

Lange LA, Willer CJ, Rich SS.

Curr Opin Lipidol. 2015 Apr;26(2):96-102. doi: 10.1097/MOL.0000000000000159. Review.

PMID:
25692345
6.

Genome-wide association studies for blood lipids. A great start but a long way to go.

Tai ES, Ordovas JM.

Curr Opin Lipidol. 2010 Apr;21(2):101-3. doi: 10.1097/MOL.0b013e32833851d0. No abstract available.

PMID:
20216311
7.

Quantitative genetics: heritability is not always missing.

Brookfield JF.

Curr Biol. 2013 Apr 8;23(7):R276-8. doi: 10.1016/j.cub.2013.02.040.

8.

Genome scan for loci regulating HDL cholesterol levels in Finnish extended pedigrees with early coronary heart disease.

Kangas-Kontio T, Kakko S, Tamminen M, von Rohr P, Hoeschele I, Juvonen T, Kere J, Savolainen MJ.

Eur J Hum Genet. 2010 May;18(5):604-13. doi: 10.1038/ejhg.2009.202. Epub 2009 Nov 25.

9.

A mixed-model approach for genome-wide association studies of correlated traits in structured populations.

Korte A, Vilhjálmsson BJ, Segura V, Platt A, Long Q, Nordborg M.

Nat Genet. 2012 Sep;44(9):1066-71. doi: 10.1038/ng.2376. Epub 2012 Aug 19.

10.

Heritability, weak effects, and rare variants in genomewide association studies.

Cambien F.

Clin Chem. 2011 Sep;57(9):1263-6. doi: 10.1373/clinchem.2010.155655. No abstract available.

11.

Mapping rare and common causal alleles for complex human diseases.

Raychaudhuri S.

Cell. 2011 Sep 30;147(1):57-69. doi: 10.1016/j.cell.2011.09.011.

12.

Genetics: Alzheimer disease and dyslipidaemia.

Duarte JH.

Nat Rev Cardiol. 2015 Jun;12(6):318. doi: 10.1038/nrcardio.2015.67. Epub 2015 Apr 28. No abstract available.

PMID:
25917149
13.

The genetics of status epilepticus.

Schauwecker PE.

Epilepsia. 2009 Dec;50 Suppl 12:22-4. doi: 10.1111/j.1528-1167.2009.02372.x. No abstract available.

14.

Genomic medicine for improved prediction and primordial prevention of cardiovascular disease.

Thanassoulis G, Peloso GM, O'Donnell CJ.

Arterioscler Thromb Vasc Biol. 2013 Sep;33(9):2049-50. doi: 10.1161/ATVBAHA.113.301814. No abstract available. Erratum in: Arterioscler Thromb Vasc Biol. 2013 Nov;33(11):e131.

15.

[News in cardiovascular genetics open for new therapeutic possibilities].

Nilsson PM, Orho-Melander M, Melander O.

Lakartidningen. 2011 Mar 9-15;108(10):540-3. Review. Swedish. No abstract available.

PMID:
21744555
16.

Association of known loci with lipid levels among children and prediction of dyslipidemia in adults.

Tikkanen E, Tuovinen T, Widén E, Lehtimäki T, Viikari J, Kähönen M, Peltonen L, Raitakari OT, Ripatti S.

Circ Cardiovasc Genet. 2011 Dec;4(6):673-80. doi: 10.1161/CIRCGENETICS.111.960369. Epub 2011 Oct 7.

17.

Common and rare variants in alcohol dependence.

Edenberg HJ.

Biol Psychiatry. 2011 Sep 15;70(6):498-9. doi: 10.1016/j.biopsych.2011.07.007. No abstract available.

PMID:
21864733
18.

Identification of novel genetic susceptibility loci for Behçet's disease using a genome-wide association study.

Fei Y, Webb R, Cobb BL, Direskeneli H, Saruhan-Direskeneli G, Sawalha AH.

Arthritis Res Ther. 2009;11(3):R66. doi: 10.1186/ar2695. Epub 2009 May 14.

19.

Sex-Specific Parental Effects on Offspring Lipid Levels.

Predazzi IM, Sobota RS, Sanna S, Bush WS, Bartlett J, Lilley JS, Linton MF, Schlessinger D, Cucca F, Fazio S, Williams SM.

J Am Heart Assoc. 2015 Jun 30;4(7). pii: e001951. doi: 10.1161/JAHA.115.001951.

20.

[The status for genetics of coronary artery disease].

Ozaki K, Tanaka T.

Nihon Rinsho. 2011 Nov;69 Suppl 9:217-21. Japanese. No abstract available.

PMID:
22724204

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