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Sebastian Schoenherr
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A reference panel of 64,976 haplotypes for genotype imputation
S McCarthy, S Das, W Kretzschmar, O Delaneau, AR Wood, A Teumer, ...
Nature genetics 48 (10), 1279, 2016
19652016
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
19192016
Reference-based phasing using the Haplotype Reference Consortium panel
PR Loh, P Danecek, PF Palamara, C Fuchsberger, YA Reshef, ...
Nature genetics 48 (11), 1443-1448, 2016
9422016
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
9382018
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
5672016
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
5292011
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
4962021
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
2702018
The GenomeAsia 100K Project enables genetic discoveries across Asia
GenomeAsia100K Consortium
Nature 576 (7785), 106, 2019
1372019
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
1342015
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
1232016
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
962015
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
902017
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
682017
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
682015
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), 1-12, 2014
662014
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), 1-9, 2012
602012
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
512017
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), e0135643, 2015
472015
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
342021
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