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Verneri Anttila

Showing results (21-30 of 53) with videos related to

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Plos One|October 21, 2016
Genome-Wide Meta-Analysis of Sciatica in Finnish PopulationSusanna Lemmelä, Svetlana Solovieva, Rahman Shiri, et al.
American Journal of Human Genetics|April 22, 2008
Consistently replicating locus linked to migraine on 10q22-q23Verneri Anttila, Dale R Nyholt, Mikko Kallela, et al.
Plos One|September 29, 2017
Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variantsBendik S Winsvold, Francesco Bettella, Aree Witoelar, et al.
Bioinformatics (Oxford, England)|September 25, 2016
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysisJie Zheng, A Mesut Erzurumluoglu, Benjamin L Elsworth, et al.
Nature Genetics|April 11, 2018
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell typesHilary K Finucane, Yakir A Reshef, Verneri Anttila, et al.
Nature Genetics|September 29, 2015
Partitioning heritability by functional annotation using genome-wide association summary statisticsHilary K Finucane, Brendan Bulik-Sullivan, Alexander Gusev, et al.
Nature Genetics|June 14, 2011
Genome-wide association study reveals three susceptibility loci for common migraine in the general populationDaniel I Chasman, Markus Schürks, Verneri Anttila, et al.
Nature Genetics|March 22, 2016
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general populationElise B Robinson, Beate St Pourcain, Verneri Anttila, et al.
Human Molecular Genetics|December 18, 2009
European lactase persistence genotype shows evidence of association with increase in body mass indexJohannes Kettunen, Kaisa Silander, Olli Saarela, et al.
Journal of Medical Genetics|July 31, 2017
Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsiesEduardo Pérez-Palma, Ingo Helbig, Karl Martin Klein, et al.
Pageof 6

Showing results (21-30 of 53) with videos related to

Sort By:
Pageof 6
Plos One|October 21, 2016
Genome-Wide Meta-Analysis of Sciatica in Finnish PopulationSusanna Lemmelä, Svetlana Solovieva, Rahman Shiri, et al.
American Journal of Human Genetics|April 22, 2008
Consistently replicating locus linked to migraine on 10q22-q23Verneri Anttila, Dale R Nyholt, Mikko Kallela, et al.
Plos One|September 29, 2017
Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variantsBendik S Winsvold, Francesco Bettella, Aree Witoelar, et al.
Bioinformatics (Oxford, England)|September 25, 2016
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysisJie Zheng, A Mesut Erzurumluoglu, Benjamin L Elsworth, et al.
Nature Genetics|April 11, 2018
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell typesHilary K Finucane, Yakir A Reshef, Verneri Anttila, et al.
Nature Genetics|September 29, 2015
Partitioning heritability by functional annotation using genome-wide association summary statisticsHilary K Finucane, Brendan Bulik-Sullivan, Alexander Gusev, et al.
Nature Genetics|June 14, 2011
Genome-wide association study reveals three susceptibility loci for common migraine in the general populationDaniel I Chasman, Markus Schürks, Verneri Anttila, et al.
Nature Genetics|March 22, 2016
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general populationElise B Robinson, Beate St Pourcain, Verneri Anttila, et al.
Human Molecular Genetics|December 18, 2009
European lactase persistence genotype shows evidence of association with increase in body mass indexJohannes Kettunen, Kaisa Silander, Olli Saarela, et al.
Journal of Medical Genetics|July 31, 2017
Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsiesEduardo Pérez-Palma, Ingo Helbig, Karl Martin Klein, et al.
Pageof 6