Multiple rare variants in the etiology of autism spectrum disorders

Tekijä Buxbaum, Joseph D.
Julkaistu 2009

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

Tekijä Betancur, Catalina, Buxbaum, Joseph D
Julkaistu 2013

<it>Molecular Autism</it>: accelerating and integrating research into neurodevelopmental conditions

Tekijä Buxbaum Joseph D, Baron-Cohen Simon
Julkaistu 2010-02-01

Molecular Autism: accelerating and integrating research into neurodevelopmental conditions

Tekijä Buxbaum, Joseph D, Baron-Cohen, Simon
Julkaistu 2010

Response to Ott and Hoh

Tekijä Ionita-Laza, Iuliana, Buxbaum, Joseph D.
Julkaistu 2012

DSM-5: the debate continues

Tekijä Buxbaum, Joseph D, Baron-Cohen, Simon
Julkaistu 2013

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

Tekijä Buxbaum, Joseph D, Baron-Cohen, Simon
Julkaistu 2013

Genetics and genomics of autism spectrum disorder: embracing complexity

Tekijä De Rubeis, Silvia, Buxbaum, Joseph D.
Julkaisussa Hum Mol Genet (2015)

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

Tekijä Bozdagi, Ozlem, Tavassoli, Teresa, Buxbaum, Joseph D
Julkaistu 2013

Genetics in psychiatry: common variant association studies

Tekijä Buxbaum, Joseph D, Baron-Cohen, Simon, Devlin, Bernie
Julkaistu 2010

Scan-Statistic Approach Identifies Clusters of Rare Disease Variants in LRP2, a Gene Linked and Associated with Autism Spectrum Disorders, in Three Datasets

Tekijä Ionita-Laza, Iuliana, Makarov, Vlad, Buxbaum, Joseph D.
Julkaistu 2012

Understanding autism in the light of sex/gender

Tekijä Lai, Meng-Chuan, Baron-Cohen, Simon, Buxbaum, Joseph D
Julkaisussa Mol Autism (2015)

Phelan McDermid syndrome: from genetic discoveries to animal models and treatments

Tekijä Harony-Nicolas, Hala, De Rubeis, Silvia, Buxbaum, Joseph D.
Julkaisussa J Child Neurol (2015)

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

Tekijä Drapeau, Elodie, Riad, Mohammed, Kajiwara, Yuji, Buxbaum, Joseph D.
Julkaisussa eNeuro (2018)

Linking oligodendrocyte and myelin dysfunction to neurocircuitry abnormalities in schizophrenia

Tekijä Takahashi, Nagahide, Sakurai, Takeshi, Davis, Kenneth L., Buxbaum, Joseph D.
Julkaistu 2010

Disrupted circuits in mouse models of autism spectrum disorder and intellectual disability

Tekijä Golden, Carla E.M., Buxbaum, Joseph D., De Rubeis, Silvia
Julkaisussa Curr Opin Neurobiol (2017)

Did Hans Asperger actively assist the Nazi euthanasia program?

Tekijä Baron-Cohen, Simon, Klin, Ami, Silberman, Steve, Buxbaum, Joseph D.
Julkaisussa Mol Autism (2018)

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

Tekijä Sabo, Shasta L., Ikin, Annat F., Buxbaum, Joseph D., Greengard, Paul
Julkaistu 2001

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

Tekijä Ionita-Laza, Iuliana, Buxbaum, Joseph D., Laird, Nan M., Lange, Christoph
Julkaistu 2011

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

Tekijä Drapeau, Elodie, Dorr, Nate P., Elder, Gregory A., Buxbaum, Joseph D.
Julkaistu 2014