| 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 | 1029 | 2016 |
| Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure S Shah, A Henry, C Roselli, H Lin, G Sveinbjörnsson, G Fatemifar, ... Nature communications 11 (1), 163, 2020 | 524 | 2020 |
| 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 | 371 | 2017 |
| 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), 10495, 2016 | 296 | 2016 |
| Metabolomic profiling of statin use and genetic inhibition of HMG-CoA reductase P Würtz, Q Wang, P Soininen, AJ Kangas, G Fatemifar, T Tynkkynen, ... Journal of the American college of cardiology 67 (10), 1200-1210, 2016 | 200 | 2016 |
| 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 | 172 | 2019 |
| Whole-genome sequence-based analysis of thyroid function PN Taylor, E Porcu, S Chew, PJ Campbell, M Traglia, SJ Brown, ... Nature communications 6 (1), 5681, 2015 | 112 | 2015 |
| 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), 11008, 2017 | 101 | 2017 |
| 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 | 96 | 2013 |
| 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 | 90 | 2019 |
| 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 | 89 | 2019 |
| 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), 4871, 2014 | 79 | 2014 |
| 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 | 62 | 2012 |
| 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 | 58 | 2019 |
| TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport M Schmidts, Y Hou, CR Cortés, DA Mans, C Huber, K Boldt, M Patel, ... Nature communications 6 (1), 7074, 2015 | 53 | 2015 |
| 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, 821-826, 2008 | 53 | 2008 |
| 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 | 49 | 2011 |
| Machine learning for subtype definition and risk prediction in heart failure, acute coronary syndromes and atrial fibrillation: systematic review of validity and clinical utility A Banerjee, S Chen, G Fatemifar, M Zeina, RT Lumbers, J Mielke, S Gill, ... BMC medicine 19, 1-14, 2021 | 46 | 2021 |
| 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 | 39 | 2008 |
| 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, 1-10, 2019 | 30 | 2019 |
