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

Marieke Klein

Showing results (31-40 of 61) with videos related to

Pageof 7
Sort By:
Nature Genetics|June 2, 2022
A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sexDanny Antaki, James Guevara, Adam X Maihofer, et al.
The American Journal of Psychiatry|March 2, 2019
Genetic Markers of ADHD-Related Variations in Intracranial VolumeMarieke Klein, Raymond K Walters, Ditte Demontis, 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.
The American Journal of Psychiatry|March 3, 2022
Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and PsychopathologySébastien Jacquemont, Guillaume Huguet, Marieke Klein, 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|November 12, 2025
Rare genetic variants confer a high risk of ADHD and implicate neuronal biologyDitte Demontis, Jinjie Duan, Yu-Han H Hsu, 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.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|October 27, 2025
Cell type-specific methylome-wide association studies of childhood ADHD symptomsMandy Meijer, Marieke Klein, Doretta Caramaschi, et al.
Medrxiv : the Preprint Server for Health Sciences|May 5, 2025
Cell type-specific methylome-wide association studies of childhood ADHD symptomsMandy Meijer, Marieke Klein, Doretta Caramaschi, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Combinatorial effects of gene dosage, polygenic background and environment on complex traitsMolly F Sacks, Marieke Klein, Tim B Bigdeli, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Nature Genetics|June 2, 2022
A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sexDanny Antaki, James Guevara, Adam X Maihofer, et al.
The American Journal of Psychiatry|March 2, 2019
Genetic Markers of ADHD-Related Variations in Intracranial VolumeMarieke Klein, Raymond K Walters, Ditte Demontis, 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.
The American Journal of Psychiatry|March 3, 2022
Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and PsychopathologySébastien Jacquemont, Guillaume Huguet, Marieke Klein, 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|November 12, 2025
Rare genetic variants confer a high risk of ADHD and implicate neuronal biologyDitte Demontis, Jinjie Duan, Yu-Han H Hsu, 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.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|October 27, 2025
Cell type-specific methylome-wide association studies of childhood ADHD symptomsMandy Meijer, Marieke Klein, Doretta Caramaschi, et al.
Medrxiv : the Preprint Server for Health Sciences|May 5, 2025
Cell type-specific methylome-wide association studies of childhood ADHD symptomsMandy Meijer, Marieke Klein, Doretta Caramaschi, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Combinatorial effects of gene dosage, polygenic background and environment on complex traitsMolly F Sacks, Marieke Klein, Tim B Bigdeli, et al.
Pageof 7