Joseph D Buxbaum
Icahn School of Medicine at Mount Sinai
H-index: 144
North America-United States
Top articles of Joseph D Buxbaum
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Brief Report: Assessment of a Caregiver-Implemented Intervention for Improving Social Communication Skills in Toddlers and Young Children with Autism | Journal of Autism and Developmental Disorders | Audrey A Rouhandeh Christine Honsberger Nathaniel A Shanok Erin Brooker Lozott Tess Levy | 2024/2 |
Transient peripheral blood transcriptomic response to ketamine treatment in children with ADNP syndrome | medRxiv | Ariela S Buxbaum Grice Laura Sloofman Tess Levy Hannah Walker Gauri Ganesh | 2024/1/31 |
An evolutionary perspective on complex neuropsychiatric disease | Jon M McClellan Anthony W Zoghbi Joseph D Buxbaum Carolina Cappi James J Crowley | 2024/1/3 | |
Identification of moderate effect size genes in autism spectrum disorder through a novel gene pairing approach | medRxiv | Madison Caballero F Kyle Satterstrom Joseph Buxbaum Behrang Mahjani | 2024 |
Genome-wide association study identifies 30 obsessive-compulsive disorder associated loci | medRxiv | Nora I Strom Zachary F Gerring Marco Galimberti Dongmei Yu Matthew W Halvorsen | 2024 |
Blended Genome Exome (BGE) as a Cost Efficient Alternative to Deep Whole Genomes or Arrays | bioRxiv | Matthew DeFelice Jonna L Grimsby Daniel Howrigan Kai Yuan Sinead B Chapman | 2024/4/4 |
Missense variants in RPH3A cause defects in excitatory synaptic function and are associated with a clinically variable neurodevelopmental disorder | Genetics in Medicine | Lisa Pavinato Jennifer Stanic Marta Barzasi Antonia Gurgone Giuseppe Chiantia | 2023/11/1 |
CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASD | Brain | Lisa Pavinato Andrea Delle Vedove Diana Carli Marta Ferrero Silvia Carestiato | 2023/2/1 |
A consensus protocol for functional connectivity analysis in the rat brain | Nature neuroscience | Joanes Grandjean Gabriel Desrosiers-Gregoire Cynthia Anckaerts Diego Angeles-Valdez Fadi Ayad | 2023/4 |
Direct additive genetics and maternal effect contribute to the risk of Tourette disorder | Journal of Neurology, Neurosurgery & Psychiatry | Behrang Mahjani Lambertus Klei Ariela S Buxbaum Grice Henrik Larsson Christina M Hultman | 2023/8/1 |
T63. CROSS-DISORDER ANALYSIS OF AUTISM AND ADHD USING RARE VARIANTS: INSIGHTS FROM DANISH IPSYCH EXOMES | European Neuropsychopharmacology | Jinjie Duan Jakob Grove Ditte Demontis F Kyle Satterstrom Jack Fu | 2023/10/1 |
Latin American Trans‐ancestry INitiative for OCD genomics (LATINO): Study protocol | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | James J Crowley Carolina Cappi Marcos E Ochoa‐Panaifo Renee M Frederick Minjee Kook | 2023/11/9 |
Large 22q13. 3 deletions perturb peripheral transcriptomic and metabolomic profiles in Phelan-McDermid syndrome | Human Genetics and Genomics Advances | Michael S Breen Xuanjia Fan Tess Levy Rebecca M Pollak Brett Collins | 2023/1/12 |
Postsynaptic Protein Shank3a Deficiency Synergizes with Alzheimer's Disease Neuropathology to Impair Cognitive Performance in the 3xTg-AD Murine Model | Journal of Neuroscience | Olivier Landry Arnaud François Méryl-Farelle Oye Mintsa Mi-Mba Marie-Therese Traversy Cyntia Tremblay | 2023/6/28 |
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations | Nature genetics | Dongjing Liu Dara Meyer Brian Fennessy Claudia Feng Esther Cheng | 2023/3 |
Associations of sex, race, and apolipoprotein e alleles with multiple domains of cognition among older adults | JAMA neurology | Skylar Walters Alex G Contreras Jaclyn M Eissman Shubhabrata Mukherjee Michael L Lee | 2023/9/1 |
Acetate supplementation rescues social deficits and alters transcriptional regulation in prefrontal cortex of Shank3 deficient mice | Brain, Behavior, and Immunity | Aya Osman Nicholas L Mervosh Ana N Strat Tanner J Euston Gillian Zipursky | 2023/11/1 |
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies LRRC4C, LHX5-AS1 and nominates ancestry-specific loci PTPRK, GRB14, and KIAA0825 as novel risk loci … | medRxiv | Farid Rajabli Penelope Benchek Giuseppe Tosto Nicholas Kushch Jin Sha | 2023 |
Comorbidities in autism spectrum disorder and their etiologies | Translational Psychiatry | Vahe Khachadourian Behrang Mahjani Sven Sandin Alexander Kolevzon Joseph D Buxbaum | 2023/2/25 |
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder | The American Journal of Human Genetics | Dmitrijs Rots Taryn E Jakub Crystal Keung Adam Jackson Siddharth Banka | 2023/6/1 |
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