Yalda Jamshidi
Yalda Jamshidi
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Meta-analysis of genome-wide association studies in> 80 000 subjects identifies multiple loci for C-reactive protein levels
A Dehghan, J Dupuis, M Barbalic, JC Bis, G Eiriksdottir, C Lu, N Pellikka, ...
Circulation 123 (7), 731-738, 2011
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
N Sotoodehnia, A Isaacs, PIW De Bakker, M Dörr, C Newton-Cheh, ...
Nature genetics 42 (12), 1068, 2010
Elite swimmers and the D allele of the ACE I/D polymorphism
D Woods, M Hickman, Y Jamshidi, D Brull, V Vassiliou, A Jones, ...
Human genetics 108 (3), 230-232, 2001
Variation in the PPARα gene is associated with altered function in vitro and plasma lipid concentrations in Type II diabetic subjects
DM Flavell, IP Torra, Y Jamshidi, D Evans, JR Diamond, RS Elkeles, ...
Diabetologia 43 (5), 673-680, 2000
Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders
M Den Hoed, M Eijgelsheim, T Esko, BJJM Brundel, DS Peal, DM Evans, ...
Nature genetics 45 (6), 621, 2013
Peroxisome proliferator–activated receptor α gene regulates left ventricular growth in response to exercise and hypertension
Y Jamshidi, HE Montgomery, HW Hense, SG Myerson, IP Torra, B Staels, ...
Circulation 105 (8), 950-955, 2002
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
J Huang, B Howie, S McCarthy, Y Memari, K Walter, JL Min, P Danecek, ...
Nature communications 6 (1), 1-9, 2015
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
DE Arking, SL Pulit, L Crotti, P Van Der Harst, PB Munroe, TT Koopmann, ...
Nature genetics 46 (8), 826-836, 2014
Characterization of the human PPARα promoter: identification of a functional nuclear receptor response element
I Pineda Torra, Y Jamshidi, DM Flavell, JC Fruchart, B Staels
Molecular endocrinology 16 (5), 1013-1028, 2002
Peroxisome proliferator-activated receptor α gene variants influence progression of coronary atherosclerosis and risk of coronary artery disease
DM Flavell, Y Jamshidi, E Hawe, I Pineda Torra, MR Taskinen, MH Frick, ...
Circulation 105 (12), 1440-1445, 2002
Genome-wide association analysis identifies multiple loci related to resting heart rate
M Eijgelsheim, C Newton-Cheh, N Sotoodehnia, PIW de Bakker, M Müller, ...
Human molecular genetics 19 (19), 3885-3894, 2010
A Large Candidate Gene Survey Identifies the KCNE1 D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes
S Kääb, DC Crawford, MF Sinner, ER Behr, PJ Kannankeril, AAM Wilde, ...
Circulation: Cardiovascular Genetics 5 (1), 91-99, 2012
Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height
MB Lanktree, Y Guo, M Murtaza, JT Glessner, SD Bailey, ...
The American Journal of Human Genetics 88 (1), 6-18, 2011
Insertion/deletion polymorphism of the angiotensin I-converting enzyme gene and arterial oxygen saturation at high altitude
DR Woods, AJ Pollard, DJ Collier, Y Jamshidi, V Vassiliou, E Hawe, ...
American journal of respiratory and critical care medicine 166 (3), 362-366, 2002
Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmia
Y Jamshidi, IM Nolte, C Dalageorgou, D Zheng, T Johnson, R Bastiaenen, ...
Journal of the American College of Cardiology 60 (9), 841-850, 2012
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study
ER Behr, E Savio-Galimberti, J Barc, AG Holst, E Petropoulou, BP Prins, ...
Cardiovascular research 106 (3), 520-529, 2015
Investigating the causal relationship of C-reactive protein with 32 complex somatic and psychiatric outcomes: a large-scale cross-consortium Mendelian randomization study
BP Prins, A Abbasi, A Wong, A Vaez, I Nolte, N Franceschini, PE Stuart, ...
PLoS medicine 13 (6), 2016
Whole-genome sequence-based analysis of thyroid function
PN Taylor, E Porcu, S Chew, PJ Campbell, M Traglia, SJ Brown, ...
Nature communications 6 (1), 1-11, 2015
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
NJ Timpson, K Walter, JL Min, I Tachmazidou, G Malerba, SY Shin, ...
Nature communications 5, 4871, 2014
Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies
IM Nolte, C Wallace, SJ Newhouse, D Waggott, J Fu, N Soranzo, ...
PloS one 4 (7), e6138, 2009
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