Sebastian Schoenherr
Sebastian Schoenherr
Bestätigte E-Mail-Adresse bei i-med.ac.at - Startseite
TitelZitiert vonJahr
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
7022016
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, 2016
4802016
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
3772011
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
2372016
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
1682016
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, 2018
872018
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, 2014
672014
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, 2018
602018
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
472012
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
452016
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, 2014
442014
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
402014
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
362015
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, 2016
322016
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
262017
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
252010
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
192015
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
192015
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
192012
eCOMPAGT integrates mtDNA: import, validation and export of mitochondrial DNA profiles for population genetics, tumour dynamics and genotype-phenotype association studies
H Weißensteiner, S Schönherr, G Specht, F Kronenberg, A Brandstätter
BMC bioinformatics 11 (1), 122, 2010
152010
Das System kann den Vorgang jetzt nicht ausführen. Versuchen Sie es später erneut.
Artikel 1–20