Lukas Forer
Title
Cited by
Cited by
Year
A reference panel of 64,976 haplotypes for genotype imputation
S McCarthy, S Das, W Kretzschmar, O Delaneau, AR Wood, A Teumer, ...
Nature Genetics 8 (10), 1279–1283, 2016
12262016
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
10122016
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
5212016
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11. 2 locus
S Jacquemont, A Reymond, F Zufferey, L Harewood, RG Walters, ...
Nature 478 (7367), 97-102, 2011
4052011
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
3292016
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
902015
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ...
BioRxiv, 563866, 2019
792019
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
782016
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
702015
Sensory phenotype and risk factors for painful diabetic neuropathy: a cross-sectional observational study
J Raputova, I Srotova, E Vlckova, C Sommer, N Üçeyler, F Birklein, ...
Pain 158 (12), 2340, 2017
602017
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
552015
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
532017
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
522012
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
492017
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
472014
The GenomeAsia 100K Project enables genetic discoveries across Asia
GenomeAsia100K Consortium
Nature 576 (7785), 106, 2019
392019
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
322015
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
302017
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
242015
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
242010
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Articles 1–20