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1 - 25 of 38 results for author:"Munroe P.B." in Literature citations

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Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmia.

Jamshidi Y., Nolte I.M., Dalageorgou C., Zheng D., Johnson T., Bastiaenen R., Ruddy S., Talbott D., Norris K.J., Snieder H. et al.

J. Am. Coll. Cardiol. 60:841-850(2012) · Mapped (1)

Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase.

Salvi E., Kutalik Z., Glorioso N., Benaglio P., Frau F., Kuznetsova T., Arima H., Hoggart C., Tichet J., Nikitin Y.P. et al.

Hypertension 59:248-255(2012) · Mapped (7)

Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in Europeans.

Putku M., Kepp K., Org E., Sober S., Comas D., Viigimaa M., Veldre G., Juhanson P., Hallast P., Tonisson N. et al.

Hum. Mutat. 32:806-814(2011) · Mapped (7)

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.

Sotoodehnia N., Isaacs A., de Bakker P.I., Dorr M., Newton-Cheh C., Nolte I.M., van der Harst P., Muller M., Eijgelsheim M., Alonso A. et al.

Nat. Genet. 42:1068-1076(2010) · Mapped (1)

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.

Procardis Consortium
Speliotes E.K., Willer C.J., Berndt S.I., Monda K.L., Thorleifsson G., Jackson A.U., Lango Allen H., Lindgren C.M., Luan J., Magi R. et al.

Nat. Genet. 42:937-948(2010) · Mapped (6)

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.

Heid I.M., Jackson A.U., Randall J.C., Winkler T.W., Qi L., Steinthorsdottir V., Thorleifsson G., Zillikens M.C., Speliotes E.K., Magi R. et al.

Nat. Genet. 42:949-960(2010) · Mapped (60)

Biological, clinical and population relevance of 95 loci for blood lipids.

Teslovich T.M., Musunuru K., Smith A.V., Edmondson A.C., Stylianou I.M., Koseki M., Pirruccello J.P., Ripatti S., Chasman D.I., Willer C.J. et al.

Nature 466:707-713(2010) · UniProtKB (2) · Mapped (18)

Meta-analysis and imputation refines the association of 15q25 with smoking quantity.

Wellcome Trust Case Control Consortium
Liu J.Z., Tozzi F., Waterworth D.M., Pillai S.G., Muglia P., Middleton L., Berrettini W., Knouff C.W., Yuan X., Waeber G. et al.

Nat. Genet. 42:436-440(2010) · Mapped (10)

Genetic loci influencing kidney function and chronic kidney disease.

Chambers J.C., Zhang W., Lord G.M., van der Harst P., Lawlor D.A., Sehmi J.S., Gale D.P., Wass M.N., Ahmadi K.R., Bakker S.J. et al.

Nat. Genet. 42:373-375(2010) · Mapped (3)

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.

Wellcome Trust Case Control Consortium
Craddock N., Hurles M.E., Cardin N., Pearson R.D., Plagnol V., Robson S., Vukcevic D., Barnes C., Conrad D.F., Giannoulatou E. et al.

Nature 464:713-720(2010) · Mapped (3)

Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.

BRIGHT Consortium
Talmud P.J., Drenos F., Shah S., Shah T., Palmen J., Verzilli C., Gaunt T.R., Pallas J., Lovering R., Li K. et al.

Am. J. Hum. Genet. 85:628-642(2009) · Mapped (10,092)

Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.

Wellcome Trust Case Control Consortium
Nolte I.M., Wallace C., Newhouse S.J., Waggott D., Fu J., Soranzo N., Gwilliam R., Deloukas P., Savelieva I., Zheng D. et al.

PLoS ONE 4:e6138-e6138(2009) · Mapped (14)

Genome-wide association study identifies eight loci associated with blood pressure.

Wellcome Trust Case Control Consortium
Newton-Cheh C., Johnson T., Gateva V., Tobin M.D., Bochud M., Coin L., Najjar S.S., Zhao J.H., Heath S.C., Eyheramendy S. et al.

Nat. Genet. 41:666-676(2009) · Mapped (91)

Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion.

Newhouse S., Farrall M., Wallace C., Hoti M., Burke B., Howard P., Onipinla A., Lee K., Shaw-Hawkins S., Dobson R. et al.

PLoS ONE 4:e5003-e5003(2009) · Mapped (7)

Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations.

Org E., Eyheramendy S., Juhanson P., Gieger C., Lichtner P., Klopp N., Veldre G., Doring A., Viigimaa M., Sober S. et al.

Hum. Mol. Genet. 18:2288-2296(2009) · Mapped (7)

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.

Wellcome Trust Case Control Consortium
Willer C.J., Speliotes E.K., Loos R.J., Li S., Lindgren C.M., Heid I.M., Berndt S.I., Elliott A.L., Jackson A.U., Lamina C. et al.

Nat. Genet. 41:25-34(2009) · Mapped (30)

SLC2A9 is a high-capacity urate transporter in humans.

Caulfield M.J., Munroe P.B., O'Neill D., Witkowska K., Charchar F.J., Doblado M., Evans S., Eyheramendy S., Onipinla A., Howard P. et al.

PLoS Med. 5:e197-e197(2008) · Mapped (1)

Glutathione S-transferase variants and hypertension.

Delles C., Padmanabhan S., Lee W.K., Miller W.H., McBride M.W., McClure J.D., Brain N.J., Wallace C., Marcano A.C., Schmieder R.E. et al.

J. Hypertens. 26:1343-1352(2008) · Mapped (15)

Common variants near MC4R are associated with fat mass, weight and risk of obesity.

Wellcome Trust Case Control Consortium
Loos R.J., Lindgren C.M., Li S., Wheeler E., Zhao J.H., Prokopenko I., Inouye M., Freathy R.M., Attwood A.P., Beckmann J.S. et al.

Nat. Genet. 40:768-775(2008) · Mapped (5)

Genome-wide association analysis identifies 20 loci that influence adult height.

Wellcome Trust Case Control Consortium
Weedon M.N., Lango H., Lindgren C.M., Wallace C., Evans D.M., Mangino M., Freathy R.M., Perry J.R., Stevens S., Hall A.S. et al.

Nat. Genet. 40:575-583(2008) · Mapped (77)

Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.

Wallace C., Newhouse S.J., Braund P., Zhang F., Tobin M., Falchi M., Ahmadi K., Dobson R.J., Marcano A.C., Hajat C. et al.

Am. J. Hum. Genet. 82:139-149(2008) · Mapped (31)

Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension.

Braga Marcano A.C., Burke B., Gungadoo J., Wallace C., Kaisaki P.J., Woon P.Y., Farrall M., Clayton D., Brown M., Dominiczak A. et al.

J. Med. Genet. 44:603-605(2007) · UniProtKB (1)

Polymorphic variation in the 11beta-hydroxylase gene associates with reduced 11-hydroxylase efficiency.

Barr M., MacKenzie S.M., Friel E.C., Holloway C.D., Wilkinson D.M., Brain N.J., Ingram M.C., Fraser R., Brown M., Samani N.J. et al.

Hypertension 49:113-119(2007) · Mapped (11)

Association of WNK1 gene polymorphisms and haplotypes with ambulatory blood pressure in the general population.

Tobin M.D., Raleigh S.M., Newhouse S., Braund P., Bodycote C., Ogleby J., Cross D., Gracey J., Hayes S., Smith T. et al.

Circulation 112:3423-3429(2005) · Mapped (9)

Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study.

Newhouse S.J., Wallace C., Dobson R., Mein C., Pembroke J., Farrall M., Clayton D., Brown M., Samani N., Dominiczak A. et al.

Hum. Mol. Genet. 14:1805-1814(2005) · Mapped (7)

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