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Showing 1–20 of 20 results

Advanced filters: Author: Jeremy Veenstra-VanderWeele Clear advanced filters

Genome-wide analyses identify 30 loci associated with obsessive–compulsive disorder

Genome-wide analyses identify 30 independent loci associated with obsessive–compulsive disorder, highlighting genetic overlap with other psychiatric disorders and implicating putative effector genes and cell types contributing to its etiology.

Nora I. Strom
Zachary F. Gerring
Manuel Mattheisen
ResearchOpen Access13 May 2025
Nature Genetics

Volume: 57, P: 1389-1401
Impact of Maternal Serotonin Transporter Genotype on Placental Serotonin, Fetal Forebrain Serotonin, and Neurodevelopment

Christopher L Muller
Allison MJ Anacker
Jeremy Veenstra-VanderWeele
Research23 Aug 2016
Neuropsychopharmacology

Volume: 42, P: 427-436
Essential Contributions of Serotonin Transporter Inhibition to the Acute and Chronic Actions of Fluoxetine and Citalopram in the SERT Met172 Mouse

Alex G Nackenoff
Alexandra B Moussa-Tooks
Randy D Blakely
Research30 Oct 2015
Neuropsychopharmacology

Volume: 41, P: 1733-1741
A non-canonical striatopallidal Go pathway that supports motor control

The basal ganglia direct and indirect pathways are classically described as anatomically segregated and functionally opposing. Here the authors describe a non-canonical direct pathway made of axon collaterals to the globus pallidus that promotes motor action.

Marie A. Labouesse
Arturo Torres-Herraez
Christoph Kellendonk
ResearchOpen Access23 Oct 2023
Nature Communications

Volume: 14, P: 1-20
Developmental impact of glutamate transporter overexpression on dopaminergic neuron activity and stereotypic behavior

Muhammad O. Chohan
Jared M. Kopelman
Susanne E. Ahmari
Research20 Jan 2022
Molecular Psychiatry

Volume: 27, P: 1515-1526
Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin

Lauren A Weiss
Jeremy Veenstra-VanderWeele
Mark Abney
Research04 Aug 2004
European Journal of Human Genetics

Volume: 12, P: 949-954
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes

An integrated analysis of de novo and inherited coding variants in 42,607 individuals with autism spectrum disorder identifies 60 risk genes of which five have not previously been associated with neurodevelopmental disorders.

Xueya Zhou
Pamela Feliciano
Wendy K. Chung
ResearchOpen Access18 Aug 2022
Nature Genetics

Volume: 54, P: 1305-1319
Intervention in the Context of Development: Pathways Toward New Treatments

Jeremy Veenstra-VanderWeele
Zachary Warren
Reviews03 Sept 2014
Neuropsychopharmacology

Volume: 40, P: 225-237
Networking in Autism: Leveraging Genetic, Biomarker and Model System Findings in the Search for New Treatments

Jeremy Veenstra-VanderWeele
Randy D Blakely
Reviews21 Sept 2011
Neuropsychopharmacology

Volume: 37, P: 196-212
Autism spectrum disorder

Autism spectrum disorder — or autism — is a neurodevelopmental disorder that typically manifests in young children. This Primer by Lord and colleagues reviews the epidemiology, mechanisms, clinical detection and treatment of autism.

Catherine Lord
Traolach S. Brugha
Jeremy Veenstra-VanderWeele
Reviews16 Jan 2020
Nature Reviews Disease Primers

Volume: 6, P: 1-23
Predictors of placebo response in three large clinical trials of the V1a receptor antagonist balovaptan in autism spectrum disorder

Russell Tobe
Yajing Zhu
Eric Hollander
ResearchOpen Access12 Apr 2023
Neuropsychopharmacology

Volume: 48, P: 1201-1216
Revealing the complex genetic architecture of obsessive–compulsive disorder using meta-analysis

Paul D Arnold
Kathleen D Askland
Gwyneth Zai
Research01 Aug 2017
Molecular Psychiatry

Volume: 23, P: 1181-1188
Research and training in autism spectrum disorder to catalyze the next genomic and neuroscience revolutions

Sergiu P. Paşca
Jeremy Veenstra-VanderWeele
James C. McPartland
News29 Jun 2020
Molecular Psychiatry

Volume: 26, P: 1429-1431
Impaired macroautophagy confers substantial risk for intellectual disability in children with autism spectrum disorders

Ahrom Ham
Audrey Yuen Chang
Guomei Tang
News06 Sept 2024
Molecular Psychiatry

Volume: 30, P: 810-824
Arbaclofen in Children and Adolescents with Autism Spectrum Disorder: A Randomized, Controlled, Phase 2 Trial

Jeremy Veenstra-VanderWeele
Edwin H Cook
Randall L Carpenter
Research17 Oct 2016
Neuropsychopharmacology

Volume: 42, P: 1390-1398
Association between the Casein Kinase 1 Epsilon Gene Region and Subjective Response to D-Amphetamine

Jeremy Veenstra-VanderWeele
Asfia Qaadir
Harriet de Wit
Research12 Oct 2005
Neuropsychopharmacology

Volume: 31, P: 1056-1063
Molecular Genetics of the Platelet Serotonin System in First-Degree Relatives of Patients with Autism

Sarah Cross
Soo-Jeong Kim
Jeremy Veenstra-VanderWeele
Research04 Apr 2007
Neuropsychopharmacology

Volume: 33, P: 353-360
Integrin β3 Haploinsufficiency Modulates Serotonin Transport and Antidepressant-Sensitive Behavior in Mice

Matthew Mazalouskas
Tammy Jessen
Ana M D Carneiro
Research16 Feb 2015
Neuropsychopharmacology

Volume: 40, P: 2015-2024
Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder

Christie L. Burton
Mathieu Lemire
Paul D. Arnold
ResearchOpen Access02 Feb 2021
Translational Psychiatry

Volume: 11, P: 1-10
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes

Pamela Feliciano
Xueya Zhou
Wendy K. Chung
ResearchOpen Access23 Aug 2019
npj Genomic Medicine

Volume: 4, P: 1-14