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Results 1 to 25 of 47

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Genetic epidemiological studies of coronary heart diseaseKEAVNEY, Bernard.International journal of epidemiology. 2002, Vol 31, Num 4, pp 730-736, issn 0300-5771Article

Angiotensin converting enzyme insertion or deletion polymorphism and coronary restenosis: meta-analysis of 16 studiesBONNICI, Francois; KEAVNEY, Bernard; COLLINS, Rory et al.BMJ. British medical journal (International ed.). 2002, Vol 325, Num 7363, pp 517-519, issn 0959-8146Article

Plasma potassium level is associated with common genetic variation in the β-subunit of the epithelial sodium channelGAUKRODGER, Nicole; AVERY, Peter J; KEAVNEY, Bernard et al.American journal of physiology. Regulatory, integrative and comparative physiology. 2008, Vol 63, Num 3, issn 0363-6119, R1068-R1072Article

Measured haplotype analysis of the aldosterone synthase gene and heart sizeMAYOSI, Bongani M; KEAVNEY, Bernard; WATKINS, Hugh et al.European journal of human genetics. 2003, Vol 11, Num 5, pp 395-401, issn 1018-4813, 7 p.Article

Left ventricular torsion, energetics, and diastolic function in normal human agingHOLLINGSWORTH, Kieren G; BLAMIRE, Andrew M; KEAVNEY, Bernard D et al.American journal of physiology. Heart and circulatory physiology. 2012, Vol 71, Num 2, issn 0363-6135, H885-H892Article

Toll-like receptor 4 gene polymorphisms and myocardial infarction : no association in a Caucasian population. CommentaryKEAVNEY, Bernard; KOCH, Werner; HOPPMANN, Petra et al.European heart journal. 2006, Vol 27, Num 21, issn 0195-668X, 2489-2490,2524-2529 [8 p.]Article

Four paraoxonase gene polymorphisms in 11 212 cases of coronary heart disease and 12 786 controls: meta-analysis of 43 studiesWHEELER, Jeremy G; KEAVNEY, Bernard D; WATKINS, Hugh et al.Lancet (British edition). 2004, Vol 363, Num 9410, pp 689-695, issn 0140-6736, 7 p.Article

Recommendations for national and local regulatory authorities concerning research in aenetic markers of disease : Genetics of coronary heart disease: Current understanding and future prospectsGRANGER, Christopher B; KEAVNEY, Bernard; FRANCOMANO, Clair et al.The American heart journal. 2000, Vol 140, Num 4, pp S3-S5, issn 0002-8703Article

A New Phenotype of Brain Iron Accumulation with Dystonia, Optic Atrophy, and Peripheral NeuropathyHORVATH, Rita; HOLINSKI-FEDER, Elke; NURNBERG, Peter et al.Movement disorders. 2012, Vol 27, Num 6, pp 789-793, issn 0885-3185, 5 p.Article

Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variantsGRIFFIN, Helen R; TÖPF, Ana; SCAMBLER, Peter et al.Heart (London 1996). 2010, Vol 96, Num 20, pp 1651-1655, issn 1355-6037, 5 p.Article

Genotype at a promoter polymorphism of the interleukin-6 gene is associated with baseline levels of plasma C-reactive proteinVICKERS, Mark A; GREEN, Fiona R; TERRY, Catherine et al.Cardiovascular research. 2002, Vol 53, Num 4, pp 1029-1034, issn 0008-6363Article

Genetics of coronary heart disease: Current knowledge and research principles : Genetics of coronary heart disease: Current understanding and future prospectsWINKELMANN, Bernhard R; HAGER, Joerg; KRAUS, William E et al.The American heart journal. 2000, Vol 140, Num 4, pp S11-S26, issn 0002-8703Article

Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertensionMAYOSI, Bongani M; AVERY, Peter J; FARRALL, Martin et al.European heart journal. 2008, Vol 29, Num 4, pp 525-530, issn 0195-668X, 6 p.Article

Common Variation at the 11-β Hydroxysteroid Dehydrogenase Type 1 Gene Is Associated With Left Ventricular MassRAHMAN, Thahira J; MAYOSI, Bongani M; HALL, Darroch et al.Circulation. Cardiovascular genetics (Print). 2011, Vol 4, Num 2, pp 156-162, issn 1942-325X, 7 p.Article

Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiencyDICKINSON, Rachel Emma; GRIFFIN, Helen; PAGAN, Sarah et al.Blood. 2011, Vol 118, Num 10, pp 2656-2658, issn 0006-4971, 3 p.Article

Mutations in the Sarcomere Gene MYH7 in Ebstein AnomalyPOSTMA, Alex V; VAN ENGELEN, Klaartje; MOORMAN, Antoon F. M et al.Circulation. Cardiovascular genetics (Print). 2011, Vol 4, Num 1, pp 43-50, issn 1942-325X, 8 p.Article

Ambulatory Blood Pressure Is Associated With Polymorphic Variation in P2X Receptor GenesPALOMINO-DOZA, Julian; RAHMAN, Thahira J; AVERY, Peter J et al.Hypertension (Dallas, Tex. 1979). 2008, Vol 52, Num 5, pp 980-985, issn 0194-911X, 6 p.Article

Common variation in the CD36 (fatty acid translocase) gene is associated with left-ventricular massHALL, Darroch; MAYOSI, Bongani M; RAHMAN, Thahira J et al.Journal of hypertension. 2011, Vol 29, Num 4, pp 690-695, issn 0263-6352, 6 p.Article

Association of apolipoprotein E genotypes with lipid levels and coronary riskBENNET, Anna M; DI ANGELANTONIO, Emanuele; DANESH, John et al.JAMA, the journal of the American Medical Association. 2007, Vol 298, Num 11, pp 1300-1311, issn 0098-7484, 12 p.Article

Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution : A family studyBAKER, Michelle; GAUKRODGER, Nicole; MAYOSI, Bongani M et al.Diabetes (New York, NY). 2005, Vol 54, Num 8, pp 2492-2496, issn 0012-1797, 5 p.Article

Genotype at the - 174G/C polymorphism of the interleukin-6 gene is associated with common carotid artery intimal-medial thickness : Family study and meta-analysisMAYOSI, Bongani M; AVERY, Peter J; BAKER, Michelle et al.Stroke (1970). 2005, Vol 36, Num 10, pp 2215-2219, issn 0039-2499, 5 p.Article

Apolipoprotein E isoforms, serum cholesterol, and cancer. CommentariesKATAN, M. B; KEAVNEY, Bernard; THOMPSON, John R et al.International journal of epidemiology. 2004, Vol 33, Num 1, pp 9-42, issn 0300-5771, 34 p.Article

Trans-ethnic fine mapping of a quantitative trait locus for circulating angiotensin I-converting enzyme (ACE)MCKENZIE, Colin A; ABECASIS, Goncalo R; CARDON, Lon R et al.Human molecular genetics (Print). 2001, Vol 10, Num 10, pp 1077-1084, issn 0964-6906Article

Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous ThromboembolismHELGADOTTIR, Anna; GRETARSDOTTIR, Solveig; TREGOUET, David-Alexandre et al.Journal of the American College of Cardiology. 2012, Vol 60, Num 8, pp 722-729, issn 0735-1097, 8 p.Article

Coronary Artery Disease-Related Genetic Variant on Chromosome 10q11 Is Associated With Carotid Intima-Media Thickness and AtherosclerosisKIECHL, Stefan; LAXTON, Ross C; WATKINS, Hugh et al.Arteriosclerosis, thrombosis, and vascular biology. 2010, Vol 30, Num 12, pp 2678-2683, issn 1079-5642, 6 p.Article

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