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Showing results (771-780 of 778) with videos related to

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Nature Genetics|December 6, 2016
Identification of context-dependent expression quantitative trait loci in whole bloodDaria V Zhernakova, Patrick Deelen, Martijn Vermaat, et al.
Nature Genetics|July 23, 2013
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac deathConnie R Bezzina, Julien Barc, Yuka Mizusawa, et al.
Nature Genetics|December 6, 2016
Disease variants alter transcription factor levels and methylation of their binding sitesMarc Jan Bonder, René Luijk, Daria V Zhernakova, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in <i>POPDC2</i> cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
American Journal of Human Genetics|May 23, 2025
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
Scientific Data|September 2, 2025
The Indo-European Cognate Relationships datasetCormac Anderson, Matthew Scarborough, Lechosław Jocz, et al.
Nature Genetics|February 12, 2013
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopiaVirginie J M Verhoeven, Pirro G Hysi, Robert Wojciechowski, et al.
Nature Genetics|February 25, 2022
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibilityJulien Barc, Rafik Tadros, Charlotte Glinge, et al.
Pageof 78

Showing results (771-780 of 778) with videos related to

Sort By:
Pageof 78
You have reached the last page of results.This site can display upto 778 results.
Nature Genetics|December 6, 2016
Identification of context-dependent expression quantitative trait loci in whole bloodDaria V Zhernakova, Patrick Deelen, Martijn Vermaat, et al.
Nature Genetics|July 23, 2013
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac deathConnie R Bezzina, Julien Barc, Yuka Mizusawa, et al.
Nature Genetics|December 6, 2016
Disease variants alter transcription factor levels and methylation of their binding sitesMarc Jan Bonder, René Luijk, Daria V Zhernakova, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Biallelic variants in <i>POPDC2</i> cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
American Journal of Human Genetics|May 23, 2025
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathyMichele Nicastro, Alexa M C Vermeer, Pieter G Postema, et al.
Scientific Data|September 2, 2025
The Indo-European Cognate Relationships datasetCormac Anderson, Matthew Scarborough, Lechosław Jocz, et al.
Nature Genetics|February 12, 2013
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopiaVirginie J M Verhoeven, Pirro G Hysi, Robert Wojciechowski, et al.
Nature Genetics|February 25, 2022
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibilityJulien Barc, Rafik Tadros, Charlotte Glinge, et al.
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