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

Maria Niarchou

Showing results (11-20 of 49) with videos related to

Pageof 5
Sort By:
The American Journal of Psychiatry|May 2, 2013
Defective processing speed and nonclinical psychotic experiences in children: longitudinal analyses in a large birth cohortMaria Niarchou, Stanley Zammit, James Walters, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 16, 2022
A phenome-wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record dataMaria Niarchou, Julia M Sealock, Peter Straub, et al.
Annals of the New York Academy of Sciences|February 28, 2023
Confronting ethical and social issues related to the genetics of musicalityReyna L Gordon, Daphne O Martschenko, Srishti Nayak, et al.
Journal of Psychiatric Research|November 21, 2018
The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion SyndromeSamuel J R A Chawner, Maria Niarchou, Joanne L Doherty, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 23, 2021
Linking the genomic signatures of human beat synchronization and learned song in birdsReyna L Gordon, Andrea Ravignani, Julia Hyland Bruno, et al.
The British Journal of Psychiatry : the Journal of Mental Science|October 12, 2013
Psychopathology and cognition in children with 22q11.2 deletion syndromeMaria Niarchou, Stanley Zammit, Stephanie H M van Goozen, et al.
Journal of Medical Genetics|November 29, 2022
Psychopathology in mothers of children with pathogenic Copy Number VariantsMaria Niarchou, Adam C Cunningham, Samuel J R A Chawner, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
Rare coding variation in OCD implicates shared genes with other psychiatric disordersSeulgi Jung, Matthew W Halvorson, Nancy Pedersen, et al.
The British Journal of Psychiatry : the Journal of Mental Science|September 9, 2017
Childhood cognitive development in 22q11.2 deletion syndrome: case-control studySamuel J R A Chawner, Joanne L Doherty, Hayley Moss, et al.
Schizophrenia Research|February 19, 2014
Further evidence for high rates of schizophrenia in 22q11.2 deletion syndromeStephen Monks, Maria Niarchou, Aimée R Davies, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
The American Journal of Psychiatry|May 2, 2013
Defective processing speed and nonclinical psychotic experiences in children: longitudinal analyses in a large birth cohortMaria Niarchou, Stanley Zammit, James Walters, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 16, 2022
A phenome-wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record dataMaria Niarchou, Julia M Sealock, Peter Straub, et al.
Annals of the New York Academy of Sciences|February 28, 2023
Confronting ethical and social issues related to the genetics of musicalityReyna L Gordon, Daphne O Martschenko, Srishti Nayak, et al.
Journal of Psychiatric Research|November 21, 2018
The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion SyndromeSamuel J R A Chawner, Maria Niarchou, Joanne L Doherty, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 23, 2021
Linking the genomic signatures of human beat synchronization and learned song in birdsReyna L Gordon, Andrea Ravignani, Julia Hyland Bruno, et al.
The British Journal of Psychiatry : the Journal of Mental Science|October 12, 2013
Psychopathology and cognition in children with 22q11.2 deletion syndromeMaria Niarchou, Stanley Zammit, Stephanie H M van Goozen, et al.
Journal of Medical Genetics|November 29, 2022
Psychopathology in mothers of children with pathogenic Copy Number VariantsMaria Niarchou, Adam C Cunningham, Samuel J R A Chawner, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
Rare coding variation in OCD implicates shared genes with other psychiatric disordersSeulgi Jung, Matthew W Halvorson, Nancy Pedersen, et al.
The British Journal of Psychiatry : the Journal of Mental Science|September 9, 2017
Childhood cognitive development in 22q11.2 deletion syndrome: case-control studySamuel J R A Chawner, Joanne L Doherty, Hayley Moss, et al.
Schizophrenia Research|February 19, 2014
Further evidence for high rates of schizophrenia in 22q11.2 deletion syndromeStephen Monks, Maria Niarchou, Aimée R Davies, et al.
Pageof 5