| Large-scale association analysis identifies new risk loci for coronary artery disease CARDIoGRAMplusC4D Consortium, P Deloukas, S Kanoni, C Willenborg, ... Nature genetics 45 (1), 25-33, 2013 | 1728 | 2013 |
| 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 | 683 | 2011 |
| A genome-wide scan for human obesity genes reveals a major susceptibility locus on chromosome 10 J Hager, C Dina, S Francke, S Dubois, M Houari, V Vatin, E Vaillant, ... Nature genetics 20 (3), 304-308, 1998 | 496 | 1998 |
| Rationale and design of the LURIC study-a resource for functional genomics, pharmacogenomics and long-term prognosis of cardiovascular disease BR Winkelmann, W März, BO Boehm, R Zotz, J Hager, P Hellstern, ... Pharmacogenomics 2 (sup1), S1-S73, 2001 | 399 | 2001 |
| Indication for linkage of the human OB gene region with extreme obesity K Clement, C Garner, J Hager, A Philippi, C LeDuc, A Carey, TJR Harris, ... Diabetes 45 (5), 687-690, 1996 | 268 | 1996 |
| Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1 L Palmieri, V Papaleo, V Porcelli, P Scarcia, L Gaita, R Sacco, J Hager, ... Molecular psychiatry 15 (1), 38-52, 2010 | 239 | 2010 |
| A missense mutation in the glucagon receptor gene is associated with non–insulin–dependent diabetes mellitus J Hager, L Hansen, C Vaisse, N Vionnet, A Philippi, W Poller, G Velho, ... Nature genetics 9 (3), 299-304, 1995 | 235 | 1995 |
| A polymorphism in the 5′ untranslated region of the human ob gene is associated with low leptin levels J Hager, K Clement, S Francke, C Dina, J Raison, N Lahlou, N Rich, ... International journal of obesity 22 (3), 200-205, 1998 | 183 | 1998 |
| Genome-wide population-based association study of extremely overweight young adults–the GOYA study L Paternoster, DM Evans, E Aagaard Nohr, C Holst, V Gaborieau, ... PloS one 6 (9), e24303, 2011 | 152 | 2011 |
| Analysis of 1508 Plasma Samples by Capillary-Flow Data-Independent Acquisition Profiles Proteomics of Weight Loss and Maintenance'[S] R Bruderer, J Muntel, S Müller, OM Bernhardt, T Gandhi, O Cominetti, ... Molecular & Cellular Proteomics 18 (6), 1242-1254, 2019 | 150 | 2019 |
| Genetic studies of the sulfonylurea receptor gene locus in NIDDM and in morbid obesity among French Caucasians EH Hani, K Clément, G Velho, N Vionnet, J Hager, A Philippi, C Dina, ... Diabetes 46 (4), 688-694, 1997 | 142 | 1997 |
| Mutation discovery in mice by whole exome sequencing H Fairfield, GJ Gilbert, M Barter, RR Corrigan, M Curtain, Y Ding, ... Genome biology 12, 1-12, 2011 | 130 | 2011 |
| Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism A Philippi, E Roschmann, F Tores, P Lindenbaum, A Benajou, ... Molecular psychiatry 10 (10), 950-960, 2005 | 111 | 2005 |
| Genetics of coronary heart disease: current knowledge and research principles BR Winkelmann, J Hager, WE Kraus, P Merlini, B Keavney, PJ Grant, ... American heart journal 140 (4), S11-S26, 2000 | 103 | 2000 |
| Large scale association analysis identifies three susceptibility loci for coronary artery disease S Saade, JB Cazier, M Ghassibe-Sabbagh, S Youhanna, DA Badro, ... PloS one 6 (12), e29427, 2011 | 98 | 2011 |
| Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models TD Andrews, B Whittle, MA Field, B Balakishnan, Y Zhang, Y Shao, V Cho, ... Open biology 2 (5), 120061, 2012 | 96 | 2012 |
| Proteomic biomarker discovery in 1000 human plasma samples with mass spectrometry O Cominetti, A Núñez Galindo, J Corthésy, S Oller Moreno, I Irincheeva, ... Journal of proteome research 15 (2), 389-399, 2016 | 95 | 2016 |
| Genetic and environmental influences on total plasma homocysteine and its role in coronary artery disease risk M Ghassibe-Sabbagh, DE Platt, S Youhanna, AB Abchee, K Stewart, ... Atherosclerosis 222 (1), 180-186, 2012 | 95 | 2012 |
| Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism G Maussion, J Carayol, AM Lepagnol-Bestel, F Tores, Y Loe-Mie, ... Human molecular genetics 17 (16), 2541-2551, 2008 | 92 | 2008 |
| Genetic variation in coronary heart disease and myocardial infarction: methodological overview and clinical evidence BR Winkelmann, J Hager Pharmacogenomics 1 (1), 73-94, 2000 | 86 | 2000 |
