Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Peter Heutink

Showing results (81-90 of 240) with videos related to

Pageof 24
Sort By:
Neurobiology of Aging|November 3, 2015
Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variantsCornelis Blauwendraat, Carlo Wilke, Iris E Jansen, et al.
Genome Biology and Evolution|November 13, 2015
Reassessing the Evolutionary History of the 17q21 Inversion PolymorphismJoao M Alves, Ana C Lima, Isa A Pais, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 1, 2008
Genotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's diseaseMaria G Macedo, Dagmar Verbaan, Yue Fang, et al.
Annals of Neurology|March 17, 2015
Polygenic risk of Parkinson disease is correlated with disease age at onsetValentina Escott-Price, , Mike A Nalls, et al.
Plos One|July 5, 2013
FADS2 Genetic Variance in Combination with Fatty Acid Intake Might Alter Composition of the Fatty Acids in BrainThais S Rizzi, Sophie van der Sluis, Catherine Derom, et al.
Genome Medicine|June 12, 2016
Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobeCornelis Blauwendraat, Margherita Francescatto, J Raphael Gibbs, et al.
Cell Death & Disease|November 14, 2025
Chr:17q21.31 locus risk haplotype H1 susceptibility to ferroptosis is mediated by endolysosomal pathwayEldem Sadikoglou, Daniel Domingo-Fernández, Natalia Savytska, et al.
Psychiatric Genetics|March 20, 2008
Screening of the epsilon sarcoglycan gene in Tourette syndrome and obsessive compulsive disorderHilga Katerberg, Danielle C Cath, Marina A J Tijssen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2017
The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjectsCornelis Blauwendraat, Carlo Wilke, Javier Simón-Sánchez, et al.
Annals of Neurology|January 6, 2004
Chromosomal translocation t(18;21)(q23;q22.1) indicates novel susceptibility loci for frontotemporal dementia with ALSJohannes Prudlo, Burkhard Alber, Vera M Kalscheuer, et al.
Pageof 24

Showing results (81-90 of 240) with videos related to

Sort By:
Pageof 24
Neurobiology of Aging|November 3, 2015
Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variantsCornelis Blauwendraat, Carlo Wilke, Iris E Jansen, et al.
Genome Biology and Evolution|November 13, 2015
Reassessing the Evolutionary History of the 17q21 Inversion PolymorphismJoao M Alves, Ana C Lima, Isa A Pais, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 1, 2008
Genotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's diseaseMaria G Macedo, Dagmar Verbaan, Yue Fang, et al.
Annals of Neurology|March 17, 2015
Polygenic risk of Parkinson disease is correlated with disease age at onsetValentina Escott-Price, , Mike A Nalls, et al.
Plos One|July 5, 2013
FADS2 Genetic Variance in Combination with Fatty Acid Intake Might Alter Composition of the Fatty Acids in BrainThais S Rizzi, Sophie van der Sluis, Catherine Derom, et al.
Genome Medicine|June 12, 2016
Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobeCornelis Blauwendraat, Margherita Francescatto, J Raphael Gibbs, et al.
Cell Death & Disease|November 14, 2025
Chr:17q21.31 locus risk haplotype H1 susceptibility to ferroptosis is mediated by endolysosomal pathwayEldem Sadikoglou, Daniel Domingo-Fernández, Natalia Savytska, et al.
Psychiatric Genetics|March 20, 2008
Screening of the epsilon sarcoglycan gene in Tourette syndrome and obsessive compulsive disorderHilga Katerberg, Danielle C Cath, Marina A J Tijssen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2017
The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjectsCornelis Blauwendraat, Carlo Wilke, Javier Simón-Sánchez, et al.
Annals of Neurology|January 6, 2004
Chromosomal translocation t(18;21)(q23;q22.1) indicates novel susceptibility loci for frontotemporal dementia with ALSJohannes Prudlo, Burkhard Alber, Vera M Kalscheuer, et al.
Pageof 24