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Showing results (51-60 of 56) with videos related to

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European Journal of Human Genetics : EJHG|December 14, 2023
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative geneEleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, et al.
American Journal of Human Genetics|March 26, 2019
De Novo Missense Substitutions in the Gene Encoding CDK8, a Regulator of the Mediator Complex, Cause a Syndromic Developmental DisorderEduardo Calpena, Alexia Hervieu, Teresa Kaserer, et al.
Annals of Neurology|June 29, 2021
Genome-Wide Association Study Identifies Risk Loci for Cluster HeadacheEmer O'Connor, Carmen Fourier, Caroline Ran, et al.
Nature Genetics|February 4, 2022
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk allelesHeidi Hautakangas, Bendik S Winsvold, Sanni E Ruotsalainen, et al.
Annals of Neurology|July 24, 2023
Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk FactorBendik S Winsvold, Aster V E Harder, Caroline Ran, et al.
Brain : a Journal of Neurology|August 25, 2021
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implicationsKatrine M Johannesen, Yuanyuan Liu, Mahmoud Koko, et al.
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Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
European Journal of Human Genetics : EJHG|December 14, 2023
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative geneEleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, et al.
American Journal of Human Genetics|March 26, 2019
De Novo Missense Substitutions in the Gene Encoding CDK8, a Regulator of the Mediator Complex, Cause a Syndromic Developmental DisorderEduardo Calpena, Alexia Hervieu, Teresa Kaserer, et al.
Annals of Neurology|June 29, 2021
Genome-Wide Association Study Identifies Risk Loci for Cluster HeadacheEmer O'Connor, Carmen Fourier, Caroline Ran, et al.
Nature Genetics|February 4, 2022
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk allelesHeidi Hautakangas, Bendik S Winsvold, Sanni E Ruotsalainen, et al.
Annals of Neurology|July 24, 2023
Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk FactorBendik S Winsvold, Aster V E Harder, Caroline Ran, et al.
Brain : a Journal of Neurology|August 25, 2021
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implicationsKatrine M Johannesen, Yuanyuan Liu, Mahmoud Koko, et al.
Pageof 6