Joseph D. Buxbaum

发表

Computational challenges in modeling maternal effects in psychiatric disorders

Behrang Mahjani, Yudi Pawitan, Lambertus Klei, 2016 .

AnnTools: a comprehensive and versatile annotation toolkit for genomic variants

Vladimir Makarov, Seungtai Yoon, Joseph D. Buxbaum, 2012, Bioinform..

FUN-LDA: A LATENT DIRICHLET ALLOCATION MODEL FOR PREDICTING TISSUE-SPECIFIC FUNCTIONAL EFFECTS OF NONCODING VARIATION

Iuliana Ionita-Laza, Krzysztof Kiryluk, Valentina Boeva, 2016, bioRxiv.

Strong synaptic transmission impact by copy number variations in schizophrenia

Raquel E. Gur, Mark Weiser, Muredach P. Reilly, 2010, Proceedings of the National Academy of Sciences.

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Robert T. Schultz, Margaret A. Pericak-Vance, Takeshi Sakurai, 2009, Nature.

Copy Number Variations in Alternative Splicing Gene Networks Impact Lifespan

Vilmundur Gudnason, Lenore J. Launer, Tamara B. Harris, 2013, PloS one.

Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls

Kathryn Roeder, Stephan Ripke, Shannon Gross, 2013, PLoS genetics.

Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, American journal of human genetics.

Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis

Robert C. Green, Andrew J. Saykin, Liana G. Apostolova, 2012, Nature Genetics.

Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study

Robert C. Green, Andrew J. Saykin, Liana G. Apostolova, 2020, Nature Communications.

Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias

Margaret A. Pericak-Vance, Matthew P. Frosch, M. Ilyas Kamboh, 2014, PLoS genetics.

Rare Complete Knockouts in Humans: Population Distribution and Significant Role in Autism Spectrum Disorders

Kathryn Roeder, Stephan Ripke, Shannon Gross, 2013, Neuron.

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

Takeshi Sakurai, Patrick R. Hof, Joseph D. Buxbaum, 2009, Front. Neuroanat..

The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders

Takeshi Sakurai, Joseph D. Buxbaum, J. Buxbaum, 2009, Trends in Neurosciences.

Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

John A. Sweeney, Geraldine Dawson, Daniel H. Geschwind, 2009, PLoS genetics.

Common risk variants identified in autism spectrum disorder

Jakob Grove, Esben Agerbo, Anders D. Børglum, 2017, bioRxiv.

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

Alexander Kolevzon, Joseph D. Buxbaum, A. Kolevzon, 2019, Molecular Autism.

Gene Expression Patterns Associated with Posttraumatic Stress Disorder Following Exposure to the World Trade Center Attacks

Florian Holsboer, Casey Sarapas, Bertram Müller-Myhsok, 2009, Biological Psychiatry.

Molecular and Cellular Evidence for an Oligodendrocyte Abnormality in Schizophrenia

Patrick R. Hof, Joseph D. Buxbaum, Vahram Haroutunian, 2002, Neurochemical Research.

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

Yuji Kajiwara, Joseph D. Buxbaum, J. Buxbaum, 2018, eNeuro.

A large‐scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders

Takeshi Sakurai, Joseph D. Buxbaum, Malek Faham, 2008, Autism research : official journal of the International Society for Autism Research.

TISSUE-SPECIFIC FUNCTIONAL EFFECT PREDICTION OF GENETIC VARIATION AND APPLICATIONS TO COMPLEX TRAIT GENETICS

Iuliana Ionita-Laza, Krzysztof Kiryluk, Joseph D. Buxbaum, 2016 .

Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes

Kathryn Roeder, Xin He, Richard A. Gibbs, 2013, PLoS genetics.

New translational perspectives for blood-based biomarkers of PTSD: From glucocorticoid to immune mediators of stress susceptibility

Scott J. Russo, Nikolaos P. Daskalakis, Joseph D. Buxbaum, 2016, Experimental Neurology.

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

Thomas Bourgeron, Ellen M. Wijsman, Gillian Baird, 2014, Nature Communications.

Multiple rare variants in the etiology of autism spectrum disorders

Joseph D. Buxbaum, J. Buxbaum, 2009, Dialogues in clinical neuroscience.

Network Topologies and Convergent Aetiologies Arising from Deletions and Duplications Observed in Individuals with Autism

Caleb Webber, Chris P. Ponting, Christian R. Marshall, 2013, PLoS genetics.

A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism

Bekim Sadikovic, Roger E. Stevenson, Daniel H. Geschwind, 2012, Proceedings of the National Academy of Sciences.

In vivo 1H-magnetic resonance spectroscopy study of the attentional networks in autism

Silvia Bernardi, Jin Fan, Patrick R. Hof, 2011, Brain Research.

Evidence That Tumor Necrosis Factor α Converting Enzyme Is Involved in Regulated α-Secretase Cleavage of the Alzheimer Amyloid Protein Precursor*

Joseph D. Buxbaum, Jacques J. Peschon, J. Buxbaum, 1998, The Journal of Biological Chemistry.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

Rapid and Objective Assessment of Neural Function in Autism Spectrum Disorder Using Transient Visual Evoked Potentials

James Gordon, Teresa Tavassoli, Alexander Kolevzon, 2016, PloS one.

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

Iuliana Ionita-Laza, Christoph Lange, Nan M. Laird, 2011, PLoS genetics.

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Robert T. Schultz, Takeshi Sakurai, Joseph Piven, 2009, Nature.

Individual common variants exert weak effects on the risk for autism spectrum disorders

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2012, Human molecular genetics.

HDAC2 regulates atypical antipsychotic responses through the modulation of mGlu2 promoter activity

Scott J. Russo, Mitra Heshmati, Javier González-Maeso, 2012, Nature Neuroscience.

A genome-wide scan for common alleles affecting risk for autism

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2010, Human molecular genetics.