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European Journal of Human Genetics : EJHG|May 17, 2020
The exhaustive genomic scan approach, with an application to rare-variant association analysisGeorge Kanoungi, Michael Nothnagel, Tim Becker, et al.Bioinformatics (Oxford, England)|September 26, 2014
METAINTER: meta-analysis of multiple regression models in genome-wide association studiesTatsiana Vaitsiakhovich, Dmitriy Drichel, Christine Herold, et al.BMC Proceedings|December 19, 2014
Analysis of the progression of systolic blood pressure using imputation of missing phenotype valuesTatsiana Vaitsiakhovich, Dmitriy Drichel, Marina Angisch, et al.Human Heredity|March 9, 2012
Integrated genome-wide pathway association analysis with INTERSNPChristine Herold, Manuel Mattheisen, André Lacour, et al.BMC Bioinformatics|September 14, 2012
Quick, "imputation-free" meta-analysis with proxy-SNPsChristian Meesters, Markus Leber, Christine Herold, et al.Plos One|November 9, 2013
A one-degree-of-freedom test for supra-multiplicativity of SNP effectsChristine Herold, Alfredo Ramirez, Dmitriy Drichel, et al.Human Heredity|December 16, 2014
Rare variant testing of imputed data: an analysis pipeline typifiedDmitriy Drichel, Christine Herold, André Lacour, et al.BMC Bioinformatics|April 17, 2015
Novel genetic matching methods for handling population stratification in genome-wide association studiesAndré Lacour, Vitalia Schüller, Dmitriy Drichel, et al.Nature Communications|January 3, 2024
A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren's diseaseSophie A Riesmeijer, Zoha Kamali, Michael Ng, et al.Hereditary Cancer in Clinical Practice|December 8, 2017
Exome sequencing characterizes the somatic mutation spectrum of early serrated lesions in a patient with serrated polyposis syndrome (SPS)Sukanya Horpaopan, Jutta Kirfel, Sophia Peters, et al.Pageof 3