Multiple rare variants in the etiology of autism spectrum disorders

por Buxbaum, Joseph D.
Publicado 2009

SHANK3 haploinsufficiency: a “common” but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders

por Betancur, Catalina, Buxbaum, Joseph D
Publicado 2013

Molecular Autism: accelerating and integrating research into neurodevelopmental conditions

por Buxbaum, Joseph D, Baron-Cohen, Simon
Publicado 2010

DSM-5: the debate continues

por Buxbaum, Joseph D, Baron-Cohen, Simon
Publicado 2013

Capping four years of growth of Molecular Autism: impact factor coming in 2014

por Buxbaum, Joseph D, Baron-Cohen, Simon
Publicado 2013

Insulin-like growth factor-1 rescues synaptic and motor deficits in a mouse model of autism and developmental delay

por Bozdagi, Ozlem, Tavassoli, Teresa, Buxbaum, Joseph D
Publicado 2013

Genetics in psychiatry: common variant association studies

por Buxbaum, Joseph D, Baron-Cohen, Simon, Devlin, Bernie
Publicado 2010

Understanding autism in the light of sex/gender

por Lai, Meng-Chuan, Baron-Cohen, Simon, Buxbaum, Joseph D
Publicado 2015

A SPECTRAL APPROACH INTEGRATING FUNCTIONAL GENOMIC ANNOTATIONS FOR CODING AND NONCODING VARIANTS

por IONITA-LAZA, IULIANA, MCCALLUM, KENNETH, XU, BIN, BUXBAUM, JOSEPH
Publicado 2016

Behavioral Phenotyping of an Improved Mouse Model of Phelan–McDermid Syndrome with a Complete Deletion of the Shank3 Gene

por Drapeau, Elodie, Riad, Mohammed, Kajiwara, Yuji, Buxbaum, Joseph D.
Publicado 2018

A genome-wide scan statistic framework for whole-genome sequence data analysis

por He, Zihuai, Xu, Bin, Buxbaum, Joseph, Ionita-Laza, Iuliana
Publicado 2019

Did Hans Asperger actively assist the Nazi euthanasia program?

por Baron-Cohen, Simon, Klin, Ami, Silberman, Steve, Buxbaum, Joseph D.
Publicado 2018

The Alzheimer Amyloid Precursor Protein (APP) and Fe65, an APP-Binding Protein, Regulate Cell Movement

por Sabo, Shasta L., Ikin, Annat F., Buxbaum, Joseph D., Greengard, Paul
Publicado 2001

A New Testing Strategy to Identify Rare Variants with Either Risk or Protective Effect on Disease

por Ionita-Laza, Iuliana, Buxbaum, Joseph D., Laird, Nan M., Lange, Christoph
Publicado 2011

Absence of strong strain effects in behavioral analyses of Shank3-deficient mice

por Drapeau, Elodie, Dorr, Nate P., Elder, Gregory A., Buxbaum, Joseph D.
Publicado 2014

Neuropsychiatric decompensation in adolescents and adults with Phelan-McDermid syndrome: a systematic review of the literature

por Kolevzon, Alexander, Delaby, Elsa, Berry-Kravis, Elizabeth, Buxbaum, Joseph D., Betancur, Catalina
Publicado 2019

Haploinsufficiency of Cyfip1 Produces Fragile X-Like Phenotypes in Mice

por Bozdagi, Ozlem, Sakurai, Takeshi, Dorr, Nathan, Pilorge, Marion, Takahashi, Nagahide, Buxbaum, Joseph D.
Publicado 2012

Linking White and Grey Matter in Schizophrenia: Oligodendrocyte and Neuron Pathology in the Prefrontal Cortex

por Höistad, Malin, Segal, Devorah, Takahashi, Nagahide, Sakurai, Takeshi, Buxbaum, Joseph D., Hof, Patrick R.
Publicado 2009

Identification of Rare Causal Variants in Sequence-Based Studies: Methods and Applications to VPS13B, a Gene Involved in Cohen Syndrome and Autism

por Ionita-Laza, Iuliana, Capanu, Marinela, De Rubeis, Silvia, McCallum, Kenneth, Buxbaum, Joseph D.
Publicado 2014

Comorbidities in autism spectrum disorder and their etiologies

por Khachadourian, Vahe, Mahjani, Behrang, Sandin, Sven, Kolevzon, Alexander, Buxbaum, Joseph D., Reichenberg, Abraham, Janecka, Magdalena
Publicado 2023