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 Holmans

Showing results (71-80 of 173) with videos related to

Pageof 18
Sort By:
Biological Psychiatry|March 28, 2008
Linkage disequilibrium mapping of a chromosome 15q25-26 major depression linkage region and sequencing of NTRK3Ranjana Verma, Peter Holmans, James A Knowles, et al.
Neurobiology of Aging|May 16, 2026
Predicted brain-regional gene expression patterns in individuals living with Alzheimer's diseaseAli Razavi, Jiahui Hou, Shu-Ju Lin, et al.
Human Molecular Genetics|July 25, 2014
De novo CNVs in bipolar affective disorder and schizophreniaLyudmila Georgieva, Elliott Rees, Jennifer L Moran, et al.
JAMA Psychiatry|March 27, 2024
Genetic and Phenotypic Features of Schizophrenia in the UK BiobankSophie E Legge, Antonio F Pardiñas, Grace Woolway, et al.
Human Molecular Genetics|April 27, 2026
Combining polygenic risk scores to understand genetic liability to physical-mental health multimorbidity in UK BiobankDaniel Stow, Ruby S M Tsang, Ioanna K Katzourou, et al.
Human Molecular Genetics|September 22, 2017
A modifier of Huntington's disease onset at the MLH1 locusJong-Min Lee, Michael J Chao, Denise Harold, et al.
Neuron|June 8, 2015
Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in SchizophreniaAndrew J Pocklington, Elliott Rees, James T R Walters, et al.
Medrxiv : the Preprint Server for Health Sciences|March 10, 2025
A Novel Method to Disentangle Tightly Linked Risk and Resilience Genes for Brain Disorders: Application to Alzheimer's DiseaseEric J Barnett, Jonathan L Hess, Jiahui Hou, et al.
Lancet (London, England)|October 5, 2010
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysisNigel M Williams, Irina Zaharieva, Andrew Martin, et al.
Nature Communications|September 10, 2021
Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutationsElliott Rees, Hugo D J Creeth, Hai-Gwo Hwu, et al.
Pageof 18

Showing results (71-80 of 173) with videos related to

Sort By:
Pageof 18
Biological Psychiatry|March 28, 2008
Linkage disequilibrium mapping of a chromosome 15q25-26 major depression linkage region and sequencing of NTRK3Ranjana Verma, Peter Holmans, James A Knowles, et al.
Neurobiology of Aging|May 16, 2026
Predicted brain-regional gene expression patterns in individuals living with Alzheimer's diseaseAli Razavi, Jiahui Hou, Shu-Ju Lin, et al.
Human Molecular Genetics|July 25, 2014
De novo CNVs in bipolar affective disorder and schizophreniaLyudmila Georgieva, Elliott Rees, Jennifer L Moran, et al.
JAMA Psychiatry|March 27, 2024
Genetic and Phenotypic Features of Schizophrenia in the UK BiobankSophie E Legge, Antonio F Pardiñas, Grace Woolway, et al.
Human Molecular Genetics|April 27, 2026
Combining polygenic risk scores to understand genetic liability to physical-mental health multimorbidity in UK BiobankDaniel Stow, Ruby S M Tsang, Ioanna K Katzourou, et al.
Human Molecular Genetics|September 22, 2017
A modifier of Huntington's disease onset at the MLH1 locusJong-Min Lee, Michael J Chao, Denise Harold, et al.
Neuron|June 8, 2015
Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in SchizophreniaAndrew J Pocklington, Elliott Rees, James T R Walters, et al.
Medrxiv : the Preprint Server for Health Sciences|March 10, 2025
A Novel Method to Disentangle Tightly Linked Risk and Resilience Genes for Brain Disorders: Application to Alzheimer's DiseaseEric J Barnett, Jonathan L Hess, Jiahui Hou, et al.
Lancet (London, England)|October 5, 2010
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysisNigel M Williams, Irina Zaharieva, Andrew Martin, et al.
Nature Communications|September 10, 2021
Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutationsElliott Rees, Hugo D J Creeth, Hai-Gwo Hwu, et al.
Pageof 18