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New genetic loci link adipose and insulin biology to body fat distribution D Shungin, TW Winkler, DC Croteau-Chonka, T Ferreira, AE Locke, ... Nature 518 (7538), 187-196, 2015 | 1625 | 2015 |
Identification of seven loci affecting mean telomere length and their association with disease V Codd, CP Nelson, E Albrecht, M Mangino, J Deelen, JL Buxton, ... Nature genetics 45 (4), 422-427, 2013 | 983 | 2013 |
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma JC Chambers, W Zhang, J Sehmi, X Li, MN Wass, P Van der Harst, ... Nature genetics 43 (11), 1131-1138, 2011 | 620 | 2011 |
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals Z Dastani, MF Hivert, N Timpson, JRB Perry, X Yuan, RA Scott, ... PLoS genetics 8 (3), e1002607, 2012 | 565 | 2012 |
A genome-wide association study identifies five loci influencing facial morphology in Europeans F Liu, F Van Der Lijn, C Schurmann, G Zhu, MM Chakravarty, PG Hysi, ... PLoS Genetics 8 (9), e1002932, 2012 | 399 | 2012 |
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age J Deelen, M Beekman, HW Uh, L Broer, KL Ayers, Q Tan, Y Kamatani, ... Human molecular genetics 23 (16), 4420-4432, 2014 | 284 | 2014 |
Oculo-auriculo-vertebral spectrum (OAVS): clinical evaluation and severity scoring of 53 patients and proposal for a new classification C Tasse, S Böhringer, S Fischer, HJ Lüdecke, B Albrecht, D Horn, ... European journal of medical genetics 48 (4), 397-411, 2005 | 263 | 2005 |
A Meta-Analysis of Thyroid-Related Traits Reveals Novel Loci and Gender-Specific Differences in the Regulation of Thyroid Function E Porcu, M Medici, G Pistis, CB Volpato, SG Wilson, AR Cappola, SD Bos, ... PLoS genetics 9 (2), e1003266, 2013 | 258 | 2013 |
A comprehensive molecular study on Coffin–Siris and Nicolaides–Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling D Wieczorek, N Bögershausen, F Beleggia, S Steiner-Haldenstätt, E Pohl, ... Human molecular genetics 22 (25), 5121-5135, 2013 | 242 | 2013 |
Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels HHM Draisma, R Pool, M Kobl, R Jansen, AK Petersen, AAM Vaarhorst, ... Nature communications 6 (1), 7208, 2015 | 207 | 2015 |
Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation Ö Altug Teber, G Gillessen-Kaesbach, S Fischer, S Böhringer, B Albrecht, ... European Journal of Human Genetics 12 (11), 879-890, 2004 | 204 | 2004 |
A 12-gene pharmacogenetic panel to prevent adverse drug reactions: an open-label, multicentre, controlled, cluster-randomised crossover implementation study JJ Swen, CH van der Wouden, LEN Manson, H Abdullah-Koolmees, ... The Lancet 401 (10374), 347-356, 2023 | 199 | 2023 |
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels TO Kilpeläinen, JFM Carli, AA Skowronski, Q Sun, J Kriebel, MF Feitosa, ... Nature communications 7 (1), 10494, 2016 | 185 | 2016 |
A novel real-time PCR assay for quantitative analysis of methylated alleles (QAMA): analysis of the retinoblastoma locus M Zeschnigk, S Böhringer, EA Price, Z Onadim, L Maßhöfer, DR Lohmann Nucleic acids research 32 (16), e125-e125, 2004 | 156 | 2004 |
Gene set analysis of GWAS data for human longevity highlights the relevance of the insulin/IGF-1 signaling and telomere maintenance pathways J Deelen, HW Uh, R Monajemi, D van Heemst, PE Thijssen, S Böhringer, ... Age 35, 235-249, 2013 | 152 | 2013 |
Genetic determination of human facial morphology: links between cleft-lips and normal variation S Boehringer, F van der Lijn, F Liu, M Günther, S Sinigerova, S Nowak, ... European Journal of Human Genetics 19 (11), 1192-1197, 2011 | 145 | 2011 |
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A family with autosomal dominant oculo-auriculo-vertebral spectrum C Tasse, F Majewski, S Böhringer, S Fischer, HJ Lüdecke, ... Clinical dysmorphology 16 (1), 1-7, 2007 | 114 | 2007 |
Validation of genetic modifiers for Duchenne muscular dystrophy: a multicentre study assessing SPP1 and LTBP4 variants JC van den Bergen, M Hiller, S Böhringer, L Vijfhuizen, HB Ginjaar, ... Journal of Neurology, Neurosurgery & Psychiatry 86 (10), 1060-1065, 2015 | 112 | 2015 |