| A reference panel of 64,976 haplotypes for genotype imputation S McCarthy, S Das, W Kretzschmar, O Delaneau, AR Wood, A Teumer, ... Nature Genetics 8 (10), 1279–1283, 2016 | 869 | 2016 |
| Next-generation genotype imputation service and methods S Das, L Forer, S Schönherr, C Sidore, AE Locke, A Kwong, SI Vrieze, ... Nature genetics 48 (10), 1284-1287, 2016 | 638 | 2016 |
| Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11. 2 locus S Jacquemont, A Reymond, F Zufferey, L Harewood, RG Walters, ... Nature 478 (7367), 97-102, 2011 | 361 | 2011 |
| Reference-based phasing using the Haplotype Reference Consortium panel PR Loh, P Danecek, PF Palamara, C Fuchsberger, YA Reshef, ... Nature genetics 48 (11), 1443, 2016 | 304 | 2016 |
| HaploGrep 2: mitochondrial haplogroup classification in the era of high-throughput sequencing H Weissensteiner, D Pacher, A Kloss-Brandstätter, L Forer, G Specht, ... Nucleic acids research 44 (W1), W58-W63, 2016 | 205 | 2016 |
| Disease burden and risk profile in referred patients with moderate chronic kidney disease: composition of the German Chronic Kidney Disease (GCKD) cohort S Titze, M Schmid, A Köttgen, M Busch, J Floege, C Wanner, ... Nephrology Dialysis Transplantation 30 (3), 441-451, 2015 | 77 | 2015 |
| mtDNA-Server: next-generation sequencing data analysis of human mitochondrial DNA in the cloud H Weissensteiner, L Forer, C Fuchsberger, B Schöpf, A Kloss-Brandstätter, ... Nucleic acids research 44 (W1), W64-W69, 2016 | 55 | 2016 |
| Prevalence and correlates of gout in a large cohort of patients with chronic kidney disease: the German Chronic Kidney Disease (GCKD) study J Jing, JT Kielstein, UT Schultheiss, T Sitter, SI Titze, ES Schaeffner, ... Nephrology Dialysis Transplantation 30 (4), 613-621, 2015 | 53 | 2015 |
| Cloudgene: A graphical execution platform for MapReduce programs on private and public clouds S Schönherr, L Forer, H Weißensteiner, F Kronenberg, G Specht, ... BMC bioinformatics 13 (1), 200, 2012 | 48 | 2012 |
| Experiences with workflows for automating data-intensive bioinformatics O Spjuth, E Bongcam-Rudloff, GC Hernández, L Forer, M Giovacchini, ... Biology direct 10 (1), 43, 2015 | 46 | 2015 |
| Genetic risk variants for membranous nephropathy: extension of and association with other chronic kidney disease aetiologies P Sekula, Y Li, HC Stanescu, M Wuttke, AB Ekici, D Bockenhauer, G Walz, ... Nephrology Dialysis Transplantation 32 (2), 325-332, 2017 | 40 | 2017 |
| Large-scale mitochondrial DNA analysis in Southeast Asia reveals evolutionary effects of cultural isolation in the multi-ethnic population of Myanmar M Summerer, J Horst, G Erhart, H Weißensteiner, S Schönherr, D Pacher, ... BMC evolutionary biology 14 (1), 17, 2014 | 40 | 2014 |
| Sensory phenotype and risk factors for painful diabetic neuropathy: a cross-sectional observational study J Raputova, I Srotova, E Vlckova, C Sommer, N Üçeyler, F Birklein, ... Pain 158 (12), 2340, 2017 | 39 | 2017 |
| A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms S Mack, S Coassin, R Rueedi, NA Yousri, I Seppälä, C Gieger, ... Journal of lipid research 58 (9), 1834-1844, 2017 | 35 | 2017 |
| CONAN: copy number variation analysis software for genome-wide association studies L Forer, S Schönherr, H Weissensteiner, F Haider, T Kluckner, C Gieger, ... BMC bioinformatics 11 (1), 318, 2010 | 24 | 2010 |
| Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ... BioRxiv, 563866, 2019 | 23 | 2019 |
| A novel but frequent variant in LPA KIV-2 is associated with a pronounced Lp(a) and cardiovascular risk reduction S Coassin, G Erhart, H Weissensteiner, M Eca Guimarães de Araújo, ... European heart journal 38 (23), 1823-1831, 2017 | 23 | 2017 |
| Association of relative telomere length with cardiovascular disease in a large chronic kidney disease cohort: the GCKD study J Raschenberger, B Kollerits, S Titze, A Köttgen, B Bärthlein, AB Ekici, ... Atherosclerosis 242 (2), 529-534, 2015 | 23 | 2015 |
| Validation of next-generation sequencing of entire mitochondrial genomes and the diversity of mitochondrial DNA mutations in oral squamous cell carcinoma A Kloss-Brandstätter, H Weissensteiner, G Erhart, G Schäfer, L Forer, ... PLoS One 10 (8), 2015 | 22 | 2015 |
| Evaluation of gene–obesity interaction effects on cholesterol levels: A genetic predisposition score on HDL-cholesterol is modified by obesity C Lamina, L Forer, S Schönherr, B Kollerits, JS Ried, C Gieger, A Peters, ... Atherosclerosis 225 (2), 363-369, 2012 | 20 | 2012 |
Sebastian SchoenherrMedical University of InnsbruckBestätigte E-Mail-Adresse bei i-med.ac.at
