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Dr. Ghazaleh Fatemifar
Dr. Ghazaleh Fatemifar
Institute of Health Informatics, University College London
Verified email at ucl.ac.uk
Title
Cited by
Cited by
Year
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
A Okbay, BML Baselmans, JE De Neve, P Turley, MG Nivard, MA Fontana, ...
Nature genetics 48 (6), 624-633, 2016
8132016
Causal associations of adiposity and body fat distribution with coronary heart disease, stroke subtypes, and type 2 diabetes mellitus: a Mendelian randomization analysis
CE Dale, G Fatemifar, TM Palmer, J White, D Prieto-Merino, D Zabaneh, ...
Circulation 135 (24), 2373-2388, 2017
2592017
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Y Lu, FR Day, S Gustafsson, ML Buchkovich, J Na, V Bataille, ...
Nature communications 7 (1), 1-15, 2016
2322016
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
S Shah, A Henry, C Roselli, H Lin, G Sveinbj÷rnsson, G Fatemifar, ...
Nature communications 11 (1), 1-12, 2020
1952020
Metabolomic profiling of statin use and genetic inhibition of HMG-CoA reductase
P WŘrtz, Q Wang, P Soininen, AJ Kangas, G Fatemifar, T Tynkkynen, ...
Journal of the American college of cardiology 67 (10), 1200-1210, 2016
1542016
UK phenomics platform for developing and validating electronic health record phenotypes: CALIBER
S Denaxas, A Gonzalez-Izquierdo, K Direk, NK Fitzpatrick, G Fatemifar, ...
Journal of the American Medical Informatics Association 26 (12), 1545-1559, 2019
982019
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
952015
Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances
G Fatemifar, CJ Hoggart, L Paternoster, JP Kemp, I Prokopenko, ...
Human Molecular Genetics 22 (18), 3807-3817, 2013
792013
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 (1), 1-11, 2014
752014
Postnatal Growth and DNA Methylation Are Associated With Differential Gene Expression of the TACSTD2 Gene and Childhood Fat Mass
A Groom, C Potter, DC Swan, G Fatemifar, DM Evans, SM Ring, V Turcot, ...
Diabetes 61 (2), 391-400, 2012
602012
Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations
BP Prins, KB Kuchenbaecker, Y Bao, M Smart, D Zabaneh, G Fatemifar, ...
Scientific reports 7 (1), 1-9, 2017
572017
Strong association of common variants in the CDKN2A/CDKN2B region with type 2 diabetes in French Europids
K Duesing, G Fatemifar, G Charpentier, M Marre, J Tichet, S Hercberg, ...
Diabetologia 51 (5), 821-826, 2008
542008
Associations between measures of sarcopenic obesity and risk of cardiovascular disease and mortality: a cohort study and Mendelian randomization analysis using the UK Biobank
RE Farmer, R Mathur, AF Schmidt, K Bhaskaran, G Fatemifar, ...
Journal of the American Heart Association 8 (13), e011638, 2019
482019
TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport
M Schmidts, Y Hou, CR CortÚs, DA Mans, C Huber, K Boldt, M Patel, ...
Nature communications 6 (1), 1-14, 2015
462015
The relationship between sleep duration, cognition and dementia: a Mendelian randomization study
A Henry, M Katsoulis, S Masi, G Fatemifar, S Denaxas, D Acosta, ...
International journal of epidemiology 48 (3), 849-860, 2019
392019
Evaluation of the association of IGF2BP2 variants with type 2 diabetes in French Caucasians
K Duesing, G Fatemifar, G Charpentier, M Marre, J Tichet, S Hercberg, ...
Diabetes 57 (7), 1992-1996, 2008
382008
Genome-wide association study identifies four loci associated with eruption of permanent teeth
F Geller, B Feenstra, H Zhang, JR Shaffer, T Hansen, AL Esserlind, ...
PLoS genetics 7 (9), e1002275, 2011
362011
Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesia
KM Gorman, E Meyer, D Grozeva, E Spinelli, A McTague, A Sanchis-Juan, ...
The American Journal of Human Genetics 104 (5), 948-956, 2019
242019
Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9
AF Schmidt, MV Holmes, D Preiss, DI Swerdlow, S Denaxas, G Fatemifar, ...
BMC cardiovascular disorders 19 (1), 1-10, 2019
172019
The association between primary tooth emergence and anthropometric measures in young adults: findings from a large prospective cohort study
G Fatemifar, DM Evans, JH Tobias
PloS one 9 (5), e96355, 2014
162014
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