| 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 | 2456 | 2016 |
| A reference panel of 64,976 haplotypes for genotype imputation Nature genetics 48 (10), 1279-1283, 2016 | 2380 | 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 | 1215 | 2018 |
| 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 | 1199 | 2016 |
| 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 | 859 | 2021 |
| 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 | 672 | 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 | 565 | 2011 |
| 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 | 326 | 2018 |
| The GenomeAsia 100K Project enables genetic discoveries across Asia Nature 576 (7785), 106-111, 2019 | 207 | 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 | 149 | 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 | 137 | 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 | 115 | 2015 |
| A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms [S] S Mack, S Coassin, R Rueedi, NA Yousri, I Seppälä, C Gieger, ... Journal of lipid research 58 (9), 1834-1844, 2017 | 106 | 2017 |
| Experiences with workflows for automating data-intensive bioinformatics O Spjuth, E Bongcam-Rudloff, GC Hernández, L Forer, M Giovacchini, ... Biology direct 10 (1), 1-12, 2015 | 74 | 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 | 71 | 2017 |
| 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 | 70 | 2021 |
| 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, 1-12, 2014 | 70 | 2014 |
| 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 | 65 | 2017 |
| 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, 1-9, 2012 | 60 | 2012 |
| 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 | 55 | 2022 |
Lukas ForerMedical University InnsbruckVerified email at i-med.ac.at
