Sebastian Schoenherr
Sebastian Schoenherr
Bestätigte E-Mail-Adresse bei i-med.ac.at - Startseite
Titel
Zitiert von
Zitiert von
Jahr
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
18212016
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
16912016
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
8362016
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
8062018
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
5132016
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
5092011
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
3542021
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
2402018
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
1222015
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
1122016
The GenomeAsia 100K Project enables genetic discoveries across Asia
GenomeAsia100K Consortium
Nature 576 (7785), 106, 2019
1072019
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
802017
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
652017
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
632015
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
622014
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
592012
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
462015
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
442017
Mitochondrial DNA copy number is associated with mortality and infections in a large cohort of patients with chronic kidney disease
F Fazzini, C Lamina, L Fendt, UT Schultheiss, F Kotsis, AA Hicks, ...
Kidney international 96 (2), 480-488, 2019
282019
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