| 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 | 3755 | 2016 |
| A reference panel of 64,976 haplotypes for genotype imputation Nature genetics 48 (10), 1279-1283, 2016 | 3162 | 2016 |
| Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps A Mahajan, D Taliun, M Thurner, NR Robertson, JM Torres, NW Rayner, ... Nature genetics 50 (11), 1505-1513, 2018 | 1776 | 2018 |
| Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ... Nature 590 (7845), 290-299, 2021 | 1769 | 2021 |
| Reference-based phasing using the Haplotype Reference Consortium panel PR Loh, P Danecek, PF Palamara, C Fuchsberger, Y A Reshef, ... Nature genetics 48 (11), 1443-1448, 2016 | 1742 | 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 | 938 | 2016 |
| HaploGrep: a fast and reliable algorithm for automatic classification of mitochondrial DNA haplogroups A Kloss‐Brandstätter, D Pacher, S Schönherr, H Weissensteiner, R Binna, ... Human mutation 32 (1), 25-32, 2011 | 611 | 2011 |
| Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation A Mahajan, CN Spracklen, W Zhang, MCY Ng, LE Petty, H Kitajima, ... Nature genetics 54 (5), 560-572, 2022 | 475 | 2022 |
| Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes A Mahajan, J Wessel, SM Willems, W Zhao, NR Robertson, AY Chu, ... Nature genetics 50 (4), 559-571, 2018 | 455 | 2018 |
| The GenomeAsia 100K Project enables genetic discoveries across Asia Nature 576 (7785), 106-111, 2019 | 375 | 2019 |
| 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 | 210 | 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 | 197 | 2016 |
| 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 | 164 | 2017 |
| 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 | 147 | 2015 |
| Genetic drivers of heterogeneity in type 2 diabetes pathophysiology K Suzuki, K Hatzikotoulas, L Southam, HJ Taylor, X Yin, KM Lorenz, ... Nature 627 (8003), 347-357, 2024 | 134 | 2024 |
| A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response Y Luo, M Kanai, W Choi, X Li, S Sakaue, K Yamamoto, K Ogawa, ... Nature Genetics 53 (10), 1504-1516, 2021 | 124 | 2021 |
| Discontinuation versus continuation of renin-angiotensin-system inhibitors in COVID-19 (ACEI-COVID): a prospective, parallel group, randomised, controlled, open-label trial A Bauer, M Schreinlechner, N Sappler, T Dolejsi, H Tilg, BA Aulinger, ... The Lancet Respiratory Medicine 9 (8), 863-872, 2021 | 107 | 2021 |
| 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 | 95 | 2017 |
| Experiences with workflows for automating data-intensive bioinformatics O Spjuth, E Bongcam-Rudloff, GC Hernández, L Forer, M Giovacchini, ... Biology direct 10, 1-12, 2015 | 89 | 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 | 85 | 2017 |
Lukas ForerMedical University InnsbruckGeverifieerd e-mailadres voor i-med.ac.at
