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André Lacour

Showing results (1-10 of 13) with videos related to

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Bioinformatics (Oxford, England)|May 7, 2016
Haplotype synthesis analysis reveals functional variants underlying known genome-wide associated susceptibility lociAndré Lacour, David Ellinghaus, Stefan Schreiber, 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.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 28, 2016
Alzheimer's disease risk variants modulate endophenotypes in mild cognitive impairmentEva Louwersheimer, Steffen Wolfsgruber, Ana Espinosa, et al.
Human Molecular Genetics|July 17, 2014
SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's diseaseAlfredo Ramirez, Wiesje M van der Flier, Christine Herold, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|May 7, 2016
Haplotype synthesis analysis reveals functional variants underlying known genome-wide associated susceptibility lociAndré Lacour, David Ellinghaus, Stefan Schreiber, 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.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 28, 2016
Alzheimer's disease risk variants modulate endophenotypes in mild cognitive impairmentEva Louwersheimer, Steffen Wolfsgruber, Ana Espinosa, et al.
Human Molecular Genetics|July 17, 2014
SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's diseaseAlfredo Ramirez, Wiesje M van der Flier, Christine Herold, et al.
Pageof 2