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Shapour Jalilzadeh
Shapour Jalilzadeh
Head of Validation
在 populationbio.com 的电子邮件经过验证
标题
引用次数
引用次数
年份
A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
Nature genetics 47 (10), 1121-1130, 2015
25842015
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
J Winkelmann, B Schormair, P Lichtner, S Ripke, L Xiong, S Jalilzadeh, ...
Nature genetics 39 (8), 1000-1006, 2007
7962007
A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
Statistical genetics and bioinformatics Goel Anuj 1 2 Ongen Halit 1 2 ...
Nature genetics 43 (4), 339-344, 2011
7062011
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
DE Arking, A Pfeufer, W Post, WHL Kao, C Newton-Cheh, M Ikeda, K West, ...
Nature genetics 38 (6), 644-651, 2006
6302006
The influence of age and sex on genetic associations with adult body size and shape: a large-scale genome-wide interaction study
TW Winkler, AE Justice, M Graff, L Barata, MF Feitosa, S Chu, ...
PLoS genetics 11 (10), e1005378, 2015
4542015
Interactions between vascular wall and perivascular adipose tissue reveal novel roles for adiponectin in the regulation of endothelial nitric oxide synthase function in human …
M Margaritis, AS Antonopoulos, J Digby, R Lee, S Reilly, P Coutinho, ...
Circulation 127 (22), 2209-2221, 2013
3602013
Evidence From Human Myectomy Samples That MYBPC3 Mutations Cause Hypertrophic Cardiomyopathy Through Haploinsufficiency
S Marston, ON Copeland, A Jacques, K Livesey, V Tsang, WJ McKenna, ...
Circulation research 105 (3), 219-222, 2009
2922009
Apolipoprotein (a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism
A Helgadottir, S Gretarsdottir, G Thorleifsson, H Holm, RS Patel, ...
Journal of the American College of Cardiology 60 (8), 722-729, 2012
2292012
Common variants in myocardial ion channel genes modify the QT interval in the general population: results from the KORA study
A Pfeufer, S Jalilzadeh, S Perz, JC Mueller, M Hinterseer, T Illig, M Akyol, ...
Circulation research 96 (6), 693-701, 2005
2002005
Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection
D Adlam, TM Olson, N Combaret, JC Kovacic, SE Iismaa, A Al-Hussaini, ...
Journal of the American College of Cardiology 73 (1), 58-66, 2019
1972019
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape
JS Ried, J Jeff M, AY Chu, JL Bragg-Gresham, J Van Dongen, JE Huffman, ...
Nature communications 7 (1), 1-11, 2016
952016
Normal passive viscoelasticity but abnormal myofibrillar force generation in human hypertrophic cardiomyopathy
AC Hoskins, A Jacques, SC Bardswell, WJ McKenna, V Tsang, ...
Journal of molecular and cellular cardiology 49 (5), 737-745, 2010
832010
The molecular phenotype of human cardiac myosin associated with hypertrophic obstructive cardiomyopathy
AM Jacques, N Briceno, AE Messer, CE Gallon, S Jalilzadeh, E Garcia, ...
Cardiovascular research 79 (3), 481-491, 2008
592008
Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity
P Yang, TT Koopmann, A Pfeufer, S Jalilzadeh, E Schulze-Bahr, S Kääb, ...
European journal of human genetics 16 (3), 350-357, 2008
432008
The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA …
M Akyol, S Jalilzadeh, MF Sinner, S Perz, BM Beckmann, C Gieger, T Illig, ...
European heart journal 28 (3), 305-309, 2007
342007
Correction: the influence of age and sex on genetic associations with adult body size and shape: a large-scale genome-wide interaction study
TW Winkler, AE Justice, M Graff, L Barata, MF Feitosa, S Chu, ...
PLoS genetics 12 (6), e1006166, 2016
152016
Progressive multifocal leukoencephalopathy genetic risk variants for pharmacovigilance of immunosuppressant therapies
E Hatchwell, EB Smith III, S Jalilzadeh, CD Bruno, Y Taoufik, ...
Frontiers in Neurology 13, 1016377, 2022
142022
Common gene variants associated with drug induced long Qt syndrome
S Kääb, A Pfeufer, M Hinterseer, M Näbauer, S Jalilzadeh, A George, ...
32005
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (vol 11, e1005378, 2015)
TW Winkler, AE Justice, M Graff, L Barata, MF Feitosa, S Chu, ...
PLOS GENETICS, 2016
12016
The common E298D-variant of the endothelial nitric oxide synthase is associated with atrial fibrillation in a large linkage-disequilibrium based approach
MF Sinner, A Pfeufer, M Akyol, A Wacker, S Jalilzadeh, BM Beckmann, ...
Circulation 114 (suppl_18), II_723-II_723, 2006
12006
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