Related references
Note: Only part of the references are listed.Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group
L. Schmaal et al.
MOLECULAR PSYCHIATRY (2017)
First-in-man study with a novel PEGylated recombinant human insulin-like growth factor-I
H. Kletzl et al.
GROWTH HORMONE & IGF RESEARCH (2017)
Animal Models of Speech and Vocal Communication Deficits Associated With Psychiatric Disorders
Genevieve Konopka et al.
BIOLOGICAL PSYCHIATRY (2016)
Essential Roles for ARID1B in Dendritic Arborization and Spine Morphology of Developing Pyramidal Neurons
Minhan Ka et al.
JOURNAL OF NEUROSCIENCE (2016)
CHD8 haploinsufficiency results in autistic-like phenotypes in mice
Yuta Katayama et al.
NATURE (2016)
De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature
Yongguo Yu et al.
BMC GENOMICS (2015)
FoxP1 orchestration of ASD-relevant signaling pathways in the striatum
Daniel J. Araujo et al.
GENES & DEVELOPMENT (2015)
Dentate gyrus volume and memory performance in major depressive disorder
Scott Travis et al.
JOURNAL OF AFFECTIVE DISORDERS (2015)
HISAT: a fast spliced aligner with low memory requirements
Daehwan Kim et al.
NATURE METHODS (2015)
Mammalian SWI/SNF chromatin remodeling complexes and cancer: Mechanistic insights gained from human genomics
Cigall Kadoch et al.
SCIENCE ADVANCES (2015)
The P7C3 class of neuroprotective compounds exerts antidepressant efficacy in mice by increasing hippocampal neurogenesis
A. K. Walker et al.
MOLECULAR PSYCHIATRY (2015)
Large-scale discovery of novel genetic causes of developmental disorders
T. W. Fitzgerald et al.
NATURE (2015)
ARID1B-mediated disorders: Mutations and possible mechanisms
Joe C. H. Sim et al.
INTRACTABLE & RARE DISEASES RESEARCH (2015)
The ARID1B Phenotype: What We Have Learned so Far
Gijs W. E. Santen et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2014)
featureCounts: an efficient general purpose program for assigning sequence reads to genomic features
Yang Liao et al.
BIOINFORMATICS (2014)
Tissue-specific SMARCA4 binding at active and repressed regulatory elements during embryogenesis
Catia Attanasio et al.
GENOME RESEARCH (2014)
Decreased hippocampal volume and increased anxiety in a transgenic mouse model expressing the human CYP2C19 gene
A. Persson et al.
MOLECULAR PSYCHIATRY (2014)
Functional recovery with recombinant human IGF1 treatment in a mouse model of Rett Syndrome
Jorge Castro et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
56Fe particle exposure results in a long-lasting increase in a cellular index of genomic instability and transiently suppresses adult hippocampal neurogenesis in vivo
Nathan A. DeCarolis et al.
LIFE SCIENCES IN SPACE RESEARCH (2014)
Autism-related behavioral abnormalities in synapsin knockout mice
Barbara Greco et al.
BEHAVIOURAL BRAIN RESEARCH (2013)
A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling
Dagmar Wieczorek et al.
HUMAN MOLECULAR GENETICS (2013)
Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients
Gijs W. E. Santen et al.
HUMAN MUTATION (2013)
From neural development to cognition: unexpected roles for chromatin
Jehnna L. Ronan et al.
NATURE REVIEWS GENETICS (2013)
Hippocampal Granule Neuron Number and Dentate Gyrus Volume in Antidepressant-Treated and Untreated Major Depression
Maura Boldrini et al.
NEUROPSYCHOPHARMACOLOGY (2013)
Haploinsufficiency of ARID1B, a Member of the SWI/SNF-A Chromatin-Remodeling Complex, Is a Frequent Cause of Intellectual Disability
Juliane Hoyer et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B
C. Halgren et al.
CLINICAL GENETICS (2012)
GENCODE: The reference human genome annotation for The ENCODE Project
Jennifer Harrow et al.
GENOME RESEARCH (2012)
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome
Gijs W. E. Santen et al.
NATURE GENETICS (2012)
Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome
Yoshinori Tsurusaki et al.
NATURE GENETICS (2012)
Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders
Brian J. O'Roak et al.
SCIENCE (2012)
Abnormal speech spectrum and increased pitch variability in young autistic children
Yoram S. Bonneh et al.
FRONTIERS IN HUMAN NEUROSCIENCE (2011)
edgeR: a Bioconductor package for differential expression analysis of digital gene expression data
Mark D. Robinson et al.
BIOINFORMATICS (2010)
Chromatin remodelling during development
Lena Ho et al.
NATURE (2010)
Behavioural phenotyping assays for mouse models of autism
Jill L. Silverman et al.
NATURE REVIEWS NEUROSCIENCE (2010)
Is this the Coffin-Siris Syndrome or the BOD Syndrome?
Ariel Brautbar et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2009)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
AutDB: a gene reference resource for autism research
Saumyendra N. Basu et al.
NUCLEIC ACIDS RESEARCH (2009)
Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice
Daniela Tropea et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Genome-wide atlas of gene expression in the adult mouse brain
Ed S. Lein et al.
NATURE (2007)
Dandy-Walker variant in Coffin-Siris syndrome
T Imai et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2001)