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Showing results (801-810 of 819) with videos related to

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Human Genetics|February 23, 2016
Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain AtlasElse Eising, Sjoerd M H Huisman, Ahmed Mahfouz, et al.
European Journal of Human Genetics : EJHG|March 31, 2011
Meta-analysis of genome-wide association for migraine in six population-based European cohortsLannie Ligthart, Boukje de Vries, Albert V Smith, et al.
Cephalalgia : an International Journal of Headache|September 3, 2014
Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studiesDale R Nyholt, , Verneri Anttila, et al.
Human Molecular Genetics|August 5, 2008
A high-density association screen of 155 ion transport genes for involvement with common migraineDale R Nyholt, K Steven LaForge, Mikko Kallela, et al.
Cephalalgia : an International Journal of Headache|December 15, 2015
Gene-based pleiotropy across migraine with aura and migraine without aura patient groupsHuiying Zhao, Else Eising, Boukje de Vries, et al.
Nature Genetics|July 31, 2007
C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophyAnna Richards, Arn M J M van den Maagdenberg, Joanna C Jen, et al.
Nature Genetics|June 12, 2012
Genome-wide association analysis identifies susceptibility loci for migraine without auraTobias Freilinger, Verneri Anttila, Boukje de Vries, et al.
Neurology|April 5, 2019
Large-scale plasma metabolome analysis reveals alterations in HDL metabolism in migraineGerrit L J Onderwater, Lannie Ligthart, Mariska Bot, et al.
Nature Genetics|July 31, 2012
De novo mutations in ATP1A3 cause alternating hemiplegia of childhoodErin L Heinzen, Kathryn J Swoboda, Yuki Hitomi, et al.
Brain : a Journal of Neurology|September 9, 2016
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestationsAnine H Stam, Parul H Kothari, Aisha Shaikh, et al.
Pageof 82

Showing results (801-810 of 819) with videos related to

Sort By:
Pageof 82
Human Genetics|February 23, 2016
Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain AtlasElse Eising, Sjoerd M H Huisman, Ahmed Mahfouz, et al.
European Journal of Human Genetics : EJHG|March 31, 2011
Meta-analysis of genome-wide association for migraine in six population-based European cohortsLannie Ligthart, Boukje de Vries, Albert V Smith, et al.
Cephalalgia : an International Journal of Headache|September 3, 2014
Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studiesDale R Nyholt, , Verneri Anttila, et al.
Human Molecular Genetics|August 5, 2008
A high-density association screen of 155 ion transport genes for involvement with common migraineDale R Nyholt, K Steven LaForge, Mikko Kallela, et al.
Cephalalgia : an International Journal of Headache|December 15, 2015
Gene-based pleiotropy across migraine with aura and migraine without aura patient groupsHuiying Zhao, Else Eising, Boukje de Vries, et al.
Nature Genetics|July 31, 2007
C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophyAnna Richards, Arn M J M van den Maagdenberg, Joanna C Jen, et al.
Nature Genetics|June 12, 2012
Genome-wide association analysis identifies susceptibility loci for migraine without auraTobias Freilinger, Verneri Anttila, Boukje de Vries, et al.
Neurology|April 5, 2019
Large-scale plasma metabolome analysis reveals alterations in HDL metabolism in migraineGerrit L J Onderwater, Lannie Ligthart, Mariska Bot, et al.
Nature Genetics|July 31, 2012
De novo mutations in ATP1A3 cause alternating hemiplegia of childhoodErin L Heinzen, Kathryn J Swoboda, Yuki Hitomi, et al.
Brain : a Journal of Neurology|September 9, 2016
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestationsAnine H Stam, Parul H Kothari, Aisha Shaikh, et al.
Pageof 82