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

Bru Cormand

Showing results (121-130 of 138) with videos related to

Pageof 14
Sort By:
Biological Psychiatry|September 8, 2009
Case-control study of six genes asymmetrically expressed in the two cerebral hemispheres: association of BAIAP2 with attention-deficit/hyperactivity disorderMarta Ribasés, Rosa Bosch, Amaia Hervás, et al.
Psychological Medicine|February 3, 2021
Polygenic association between attention-deficit/hyperactivity disorder liability and cognitive impairmentsIsabella Vainieri, Joanna Martin, Anna-Sophie Rommel, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 20, 2011
Exploring DRD4 and its interaction with SLC6A3 as possible risk factors for adult ADHD: a meta-analysis in four European populationsCristina Sánchez-Mora, Marta Ribasés, Miquel Casas, et al.
Molecular Psychiatry|August 18, 2018
Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencingJordi Corominas, Marieke Klein, Tetyana Zayats, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|August 3, 2016
Meta-analysis of the DRD5 VNTR in persistent ADHDMarieke Klein, Stefanie Berger, Martine Hoogman, et al.
Nature Genetics|September 26, 2022
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroupsManuel Mattheisen, Jakob Grove, Thomas D Als, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|October 7, 2014
Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorderCristina Sánchez-Mora, Josep A Ramos-Quiroga, Rosa Bosch, et al.
Translational Psychiatry|January 31, 2019
ADGRL3 (LPHN3) variants predict substance use disorderMauricio Arcos-Burgos, Jorge I Vélez, Ariel F Martinez, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|November 6, 2009
Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHDBarbara Franke, Alejandro Arias Vasquez, Stefan Johansson, et al.
Science (New York, N.Y.)|April 21, 2018
Paternally inherited cis-regulatory structural variants are associated with autismWilliam M Brandler, Danny Antaki, Madhusudan Gujral, et al.
Pageof 14

Showing results (121-130 of 138) with videos related to

Sort By:
Pageof 14
Biological Psychiatry|September 8, 2009
Case-control study of six genes asymmetrically expressed in the two cerebral hemispheres: association of BAIAP2 with attention-deficit/hyperactivity disorderMarta Ribasés, Rosa Bosch, Amaia Hervás, et al.
Psychological Medicine|February 3, 2021
Polygenic association between attention-deficit/hyperactivity disorder liability and cognitive impairmentsIsabella Vainieri, Joanna Martin, Anna-Sophie Rommel, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 20, 2011
Exploring DRD4 and its interaction with SLC6A3 as possible risk factors for adult ADHD: a meta-analysis in four European populationsCristina Sánchez-Mora, Marta Ribasés, Miquel Casas, et al.
Molecular Psychiatry|August 18, 2018
Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencingJordi Corominas, Marieke Klein, Tetyana Zayats, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|August 3, 2016
Meta-analysis of the DRD5 VNTR in persistent ADHDMarieke Klein, Stefanie Berger, Martine Hoogman, et al.
Nature Genetics|September 26, 2022
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroupsManuel Mattheisen, Jakob Grove, Thomas D Als, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|October 7, 2014
Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorderCristina Sánchez-Mora, Josep A Ramos-Quiroga, Rosa Bosch, et al.
Translational Psychiatry|January 31, 2019
ADGRL3 (LPHN3) variants predict substance use disorderMauricio Arcos-Burgos, Jorge I Vélez, Ariel F Martinez, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|November 6, 2009
Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHDBarbara Franke, Alejandro Arias Vasquez, Stefan Johansson, et al.
Science (New York, N.Y.)|April 21, 2018
Paternally inherited cis-regulatory structural variants are associated with autismWilliam M Brandler, Danny Antaki, Madhusudan Gujral, et al.
Pageof 14