| Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility A Franke, T Balschun, TH Karlsen, J Sventoraityte, S Nikolaus, G Mayr, ... Nature genetics 40 (11), 1319-1323, 2008 | 725 | 2008 |
| 15q13. 3 microdeletions increase risk of idiopathic generalized epilepsy I Helbig, HC Mefford, AJ Sharp, M Guipponi, M Fichera, A Franke, ... Nature genetics 41 (2), 160-162, 2009 | 647 | 2009 |
| Correlation between genetic and geographic structure in Europe O Lao, TT Lu, M Nothnagel, O Junge, S Freitag-Wolf, A Caliebe, ... Current Biology 18 (16), 1241-1248, 2008 | 598 | 2008 |
| A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis S Buch, F Stickel, E Trepo, M Way, A Herrmann, HD Nischalke, M Brosch, ... Nature genetics 47 (12), 1443-1448, 2015 | 458 | 2015 |
| Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes JR Lemke, D Lal, EM Reinthaler, I Steiner, M Nothnagel, M Alber, ... Nature genetics 45 (9), 1067-1072, 2013 | 447 | 2013 |
| Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes JR Lemke, D Lal, EM Reinthaler, I Steiner, M Nothnagel, M Alber, ... Nature genetics 45 (9), 1067-1072, 2013 | 447 | 2013 |
| Genome-wide association analysis in primary sclerosing cholangitis TH Karlsen, A Franke, E Melum, A Kaser, JR Hov, T Balschun, BA Lie, ... Gastroenterology 138 (3), 1102-1111, 2010 | 373 | 2010 |
| Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci D Ellinghaus, E Ellinghaus, RP Nair, PE Stuart, T Esko, A Metspalu, ... The American Journal of Human Genetics 90 (4), 636-647, 2012 | 352 | 2012 |
| Power and sample size calculations for case-control genetic association tests when errors are present: application to single nucleotide polymorphisms D Gordon, SJ Finch, M Nothnagel, J Ott Human heredity 54 (1), 22-33, 2002 | 338 | 2002 |
| Identification of a shared genetic susceptibility locus for coronary heart disease and periodontitis AS Schaefer, GM Richter, B Groessner-Schreiber, B Noack, M Nothnagel, ... PLoS genetics 5 (2), e1000378, 2009 | 288 | 2009 |
| Wnt signaling and Dupuytren's disease GH Dolmans, PM Werker, HC Hennies, D Furniss, EA Festen, L Franke, ... New England Journal of Medicine 365 (4), 307-317, 2011 | 282 | 2011 |
| Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis S Hofmann, A Franke, A Fischer, G Jacobs, M Nothnagel, KI Gaede, ... Nature genetics 40 (9), 1103-1106, 2008 | 281 | 2008 |
| A global analysis of Y-chromosomal haplotype diversity for 23 STR loci J Purps, S Siegert, S Willuweit, M Nagy, C Alves, R Salazar, ... Forensic Science International: Genetics 12, 12-23, 2014 | 269 | 2014 |
| De novo loss-or gain-of-function mutations in KCNA2 cause epileptic encephalopathy S Syrbe, U Hedrich, E Riesch, T Djémié, S Müller, RS Møller, B Maher, ... Nature genetics 47 (4), 393-399, 2015 | 249 | 2015 |
| Genome-wide search for novel human uORFs and N-terminal protein extensions using ribosomal footprinting C Fritsch, A Herrmann, M Nothnagel, K Szafranski, K Huse, F Schumann, ... Genome research 22 (11), 2208-2218, 2012 | 231 | 2012 |
| A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individuals A Nebel, R Kleindorp, A Caliebe, M Nothnagel, H Blanche, O Junge, ... Mechanisms of ageing and development 132 (6-7), 324-330, 2011 | 218 | 2011 |
| A genome-wide association study identifies GLT6D1 as a susceptibility locus for periodontitis AS Schaefer, GM Richter, M Nothnagel, T Manke, H Dommisch, G Jacobs, ... Human molecular genetics 19 (3), 553-562, 2010 | 205 | 2010 |
| A comprehensive evaluation of SNP genotype imputation M Nothnagel, D Ellinghaus, S Schreiber, M Krawczak, A Franke Human genetics 125, 163-171, 2009 | 196 | 2009 |
| Genomic and geographic distribution of SNP-defined runs of homozygosity in Europeans M Nothnagel, TT Lu, M Kayser, M Krawczak Human molecular genetics 19 (15), 2927-2935, 2010 | 171 | 2010 |
| Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation E Gardella, F Becker, RS Møller, J Schubert, JR Lemke, LHG Larsen, ... Annals of neurology 79 (3), 428-436, 2016 | 167 | 2016 |
