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Items: 1 to 20 of 140

1.

Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study.

Ehret GB, O'Connor AA, Weder A, Cooper RS, Chakravarti A.

Eur J Hum Genet. 2009 Dec;17(12):1650-7. doi: 10.1038/ejhg.2009.94. Epub 2009 Jun 17.

2.

Variants on chromosome 6p22.3 associated with blood pressure in the HyperGEN study: follow-up of FBPP quantitative trait loci.

Simino J, Shi G, Arnett D, Broeckel U, Hunt SC, Rao DC.

Am J Hypertens. 2011 Nov;24(11):1227-33. doi: 10.1038/ajh.2011.140. Epub 2011 Aug 18.

3.

Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies.

Nguyen KD, Pihur V, Ganesh SK, Rakha A, Cooper RS, Hunt SC, Freedman BI, Coresh J, Kao WH, Morrison AC, Boerwinkle E, Ehret GB, Chakravarti A.

Circ Res. 2013 Jan 18;112(2):318-26. doi: 10.1161/CIRCRESAHA.112.276725. Epub 2012 Nov 12.

4.

Autosomal linkage scan for loci predisposing to comorbid dependence on multiple substances.

Yang BZ, Han S, Kranzler HR, Farrer LA, Elston RC, Gelernter J.

Am J Med Genet B Neuropsychiatr Genet. 2012 Jun;159B(4):361-9. doi: 10.1002/ajmg.b.32037. Epub 2012 Feb 21.

5.

Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31.

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, Fornage M, Rotimi C, Kardia SLR, Cooper RS, Rao DC, Ehret G, Chakravarti A, Zhu X.

Eur J Hum Genet. 2019 Feb;27(2):269-277. doi: 10.1038/s41431-018-0277-1. Epub 2018 Sep 27.

PMID:
30262922
6.

Genome-wide linkage and regional association study of blood pressure response to the cold pressor test in Han Chinese: the genetic epidemiology network of salt sensitivity study.

Yang X, Gu D, He J, Hixson JE, Rao DC, Lu F, Mu J, Jaquish CE, Chen J, Huang J, Shimmin LC, Rice TK, Chen J, Wu X, Liu D, Kelly TN.

Circ Cardiovasc Genet. 2014 Aug;7(4):521-8. doi: 10.1161/CIRCGENETICS.113.000332. Epub 2014 Jul 15.

7.

A genome-wide search for linkage of estimated glomerular filtration rate (eGFR) in the Family Investigation of Nephropathy and Diabetes (FIND).

Thameem F, Igo RP Jr, Freedman BI, Langefeld C, Hanson RL, Schelling JR, Elston RC, Duggirala R, Nicholas SB, Goddard KA, Divers J, Guo X, Ipp E, Kimmel PL, Meoni LA, Shah VO, Smith MW, Winkler CA, Zager PG, Knowler WC, Nelson RG, Pahl MV, Parekh RS, Kao WH, Rasooly RS, Adler SG, Abboud HE, Iyengar SK, Sedor JR; Family Investigation of Nephropathy and Diabetes Research Group.

PLoS One. 2013 Dec 17;8(12):e81888. doi: 10.1371/journal.pone.0081888. eCollection 2013.

8.

Genome-wide linkage scan for nicotine dependence in European Americans and its converging results with African Americans in the Mid-South Tobacco Family sample.

Li MD, Ma JZ, Payne TJ, Lou XY, Zhang D, Dupont RT, Elston RC.

Mol Psychiatry. 2008 Apr;13(4):407-16. Epub 2007 Jun 19.

PMID:
17579606
9.

Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study.

Fox ER, Young JH, Li Y, Dreisbach AW, Keating BJ, Musani SK, Liu K, Morrison AC, Ganesh S, Kutlar A, Ramachandran VS, Polak JF, Fabsitz RR, Dries DL, Farlow DN, Redline S, Adeyemo A, Hirschorn JN, Sun YV, Wyatt SB, Penman AD, Palmas W, Rotter JI, Townsend RR, Doumatey AP, Tayo BO, Mosley TH Jr, Lyon HN, Kang SJ, Rotimi CN, Cooper RS, Franceschini N, Curb JD, Martin LW, Eaton CB, Kardia SL, Taylor HA, Caulfield MJ, Ehret GB, Johnson T; International Consortium for Blood Pressure Genome-wide Association Studies (ICBP-GWAS), Chakravarti A, Zhu X, Levy D.

Hum Mol Genet. 2011 Jun 1;20(11):2273-84. doi: 10.1093/hmg/ddr092. Epub 2011 Mar 4.

10.

Admixture mapping of quantitative trait loci for BMI in African Americans: evidence for loci on chromosomes 3q, 5q, and 15q.

Basu A, Tang H, Arnett D, Gu CC, Mosley T, Kardia S, Luke A, Tayo B, Cooper R, Zhu X, Risch N.

Obesity (Silver Spring). 2009 Jun;17(6):1226-31. doi: 10.1038/oby.2009.24. Epub 2009 Feb 19.

11.

Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q.

Zuo L, Gelernter J, Zhang CK, Zhao H, Lu L, Kranzler HR, Malison RT, Li CS, Wang F, Zhang XY, Deng HW, Krystal JH, Zhang F, Luo X.

Neuropsychopharmacology. 2012 Jan;37(2):557-66. doi: 10.1038/npp.2011.229. Epub 2011 Sep 28. Erratum in: Neuropsychopharmacology. 2012 Jan;37(2):581-2.

12.

Evaluating the context-dependent effect of family history of stroke in a genome scan for hypertension.

Morrison AC, Brown A, Kardia SL, Turner ST, Boerwinkle E; Genetic Epidemiology Network of Arteriopathy (GENOA) Study.

Stroke. 2003 May;34(5):1170-5. Epub 2003 Apr 24.

PMID:
12714704
13.

Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.

Suarez BK, Duan J, Sanders AR, Hinrichs AL, Jin CH, Hou C, Buccola NG, Hale N, Weilbaecher AN, Nertney DA, Olincy A, Green S, Schaffer AW, Smith CJ, Hannah DE, Rice JP, Cox NJ, Martinez M, Mowry BJ, Amin F, Silverman JM, Black DW, Byerley WF, Crowe RR, Freedman R, Cloninger CR, Levinson DF, Gejman PV.

Am J Hum Genet. 2006 Feb;78(2):315-33. Epub 2006 Jan 3.

14.

Confirmation and generalization of an alcohol-dependence locus on chromosome 10q.

Panhuysen CI, Kranzler HR, Yu Y, Weiss RD, Brady K, Poling J, Farrer LA, Gelernter J.

Neuropsychopharmacology. 2010 May;35(6):1325-32. doi: 10.1038/npp.2010.1. Epub 2010 Feb 10.

15.

A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease.

Mathias RA, Kim Y, Sung H, Yanek LR, Mantese VJ, Hererra-Galeano JE, Ruczinski I, Wilson AF, Faraday N, Becker LC, Becker DM.

BMC Med Genomics. 2010 Jun 7;3:22. doi: 10.1186/1755-8794-3-22.

16.

Multiple genes for essential-hypertension susceptibility on chromosome 1q.

Chang YP, Liu X, Kim JD, Ikeda MA, Layton MR, Weder AB, Cooper RS, Kardia SL, Rao DC, Hunt SC, Luke A, Boerwinkle E, Chakravarti A.

Am J Hum Genet. 2007 Feb;80(2):253-64. Epub 2006 Dec 20.

17.

An international collaborative family-based whole-genome linkage scan for high-grade myopia.

Li YJ, Guggenheim JA, Bulusu A, Metlapally R, Abbott D, Malecaze F, Calvas P, Rosenberg T, Paget S, Creer RC, Kirov G, Owen MJ, Zhao B, White T, Mackey DA, Young TL.

Invest Ophthalmol Vis Sci. 2009 Jul;50(7):3116-27. doi: 10.1167/iovs.08-2781. Epub 2009 Mar 25.

18.

Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations.

North KE, Franceschini N, Avery CL, Baird L, Graff M, Leppert M, Chung JH, Zhang J, Hanis C, Boerwinkle E, Volcik KA, Grove ML, Mosley TH, Gu C, Heiss G, Pankow JS, Couper DJ, Ballantyne CM, Linda Kao WH, Weder AB, Cooper RS, Ehret GB, O'Connor AA, Chakravarti A, Hunt SC.

Acta Diabetol. 2010 Dec;47 Suppl 1:199-207. doi: 10.1007/s00592-009-0162-z. Epub 2009 Oct 24.

19.
20.

A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits.

Guo Y, Tomlinson B, Chu T, Fang YJ, Gui H, Tang CS, Yip BH, Cherny SS, Hur YM, Sham PC, Lam TH, Thomas NG.

PLoS One. 2012;7(2):e31489. doi: 10.1371/journal.pone.0031489. Epub 2012 Feb 24. Erratum in: PLoS One. 2012;7(6). doi:10.1371/annotation/4415f88f-ab10-44dd-8ba9-1a57ade740c1.

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