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 (51-60 of 173) with videos related to

Pageof 18
Sort By:
The Lancet. Neurology|June 24, 2017
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association studyDavina J Hensman Moss, Antonio F Pardiñas, Douglas Langbehn, et al.
European Journal of Human Genetics : EJHG|November 6, 2014
No evidence for rare recessive and compound heterozygous disruptive variants in schizophreniaDouglas M Ruderfer, Elaine T Lim, Giulio Genovese, et al.
Brain Communications|September 25, 2023
Pathway-specific polygenic scores for Alzheimer's disease are associated with changes in brain structure in younger and older adultsJudith R Harrison, Sonya F Foley, Emily Baker, et al.
Human Molecular Genetics|May 13, 2016
RNA-Seq of Huntington's disease patient myeloid cells reveals innate transcriptional dysregulation associated with proinflammatory pathway activationJames R C Miller, Kitty K Lo, Ralph Andre, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 6, 2018
Predictive modeling of schizophrenia from genomic data: Comparison of polygenic risk score with kernel support vector machines approachTimothy Vivian-Griffiths, Emily Baker, Karl M Schmidt, et al.
Nature Communications|August 2, 2025
Whole-exome sequencing analysis identifies risk genes for schizophreniaSophie L Chick, Peter Holmans, Darren Cameron, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 19, 2007
Investigating the role of p11 (S100A10) sequence variation in susceptibility to major depressionRanjana Verma, David J Cutler, Peter Holmans, et al.
Schizophrenia Bulletin|April 10, 2021
Risk Factors, Clinical Features, and Polygenic Risk Scores in Schizophrenia and Schizoaffective Disorder Depressive-TypeCharlotte A Dennison, Sophie E Legge, Leon Hubbard, et al.
Neurobiology of Aging|November 8, 2015
A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterinYuetiva Deming, Jian Xia, Yefei Cai, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|June 24, 2014
Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variantsJoanna Martin, Miriam Cooper, Marian L Hamshere, et al.
Pageof 18

Showing results (51-60 of 173) with videos related to

Sort By:
Pageof 18
The Lancet. Neurology|June 24, 2017
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association studyDavina J Hensman Moss, Antonio F Pardiñas, Douglas Langbehn, et al.
European Journal of Human Genetics : EJHG|November 6, 2014
No evidence for rare recessive and compound heterozygous disruptive variants in schizophreniaDouglas M Ruderfer, Elaine T Lim, Giulio Genovese, et al.
Brain Communications|September 25, 2023
Pathway-specific polygenic scores for Alzheimer's disease are associated with changes in brain structure in younger and older adultsJudith R Harrison, Sonya F Foley, Emily Baker, et al.
Human Molecular Genetics|May 13, 2016
RNA-Seq of Huntington's disease patient myeloid cells reveals innate transcriptional dysregulation associated with proinflammatory pathway activationJames R C Miller, Kitty K Lo, Ralph Andre, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 6, 2018
Predictive modeling of schizophrenia from genomic data: Comparison of polygenic risk score with kernel support vector machines approachTimothy Vivian-Griffiths, Emily Baker, Karl M Schmidt, et al.
Nature Communications|August 2, 2025
Whole-exome sequencing analysis identifies risk genes for schizophreniaSophie L Chick, Peter Holmans, Darren Cameron, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 19, 2007
Investigating the role of p11 (S100A10) sequence variation in susceptibility to major depressionRanjana Verma, David J Cutler, Peter Holmans, et al.
Schizophrenia Bulletin|April 10, 2021
Risk Factors, Clinical Features, and Polygenic Risk Scores in Schizophrenia and Schizoaffective Disorder Depressive-TypeCharlotte A Dennison, Sophie E Legge, Leon Hubbard, et al.
Neurobiology of Aging|November 8, 2015
A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterinYuetiva Deming, Jian Xia, Yefei Cai, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|June 24, 2014
Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variantsJoanna Martin, Miriam Cooper, Marian L Hamshere, et al.
Pageof 18