Related references
Note: Only part of the references are listed.Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease
Galen E. B. Wright et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2019)
Excitation-inhibition balance as a framework for investigating mechanisms in neuropsychiatric disorders
Vikaas S. Sohal et al.
MOLECULAR PSYCHIATRY (2019)
Abnormal brain development in child and adolescent carriers of mutant huntingtin
Ellen van der Plas et al.
NEUROLOGY (2019)
CAG Repeat Not Polyglutamine Length Determines Timing of Huntington's Disease Onset
Jong-Min Lee et al.
CELL (2019)
HTT haplogroups in Finnish patients with Huntington disease
Susanna Ylonen et al.
NEUROLOGY-GENETICS (2019)
Repetitive behaviors in autism are linked to imbalance of corticostriatal connectivity: a functional connectivity MRI study
Angela E. Abbott et al.
SOCIAL COGNITIVE AND AFFECTIVE NEUROSCIENCE (2018)
Effect of early embryonic deletion of huntingtin from pyramidal neurons on the development and long-term survival of neurons in cerebral cortex and striatum
I. Dragatsis et al.
NEUROBIOLOGY OF DISEASE (2018)
Effect of Trinucleotide Repeats in the Huntington's Gene on Intelligence
Jessica K. Lee et al.
EBIOMEDICINE (2018)
Intracellular calcium dysregulation in autism spectrum disorder: An analysis of converging organelle signaling pathways
Rachel L. Nguyen et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2018)
Activation of autophagy rescues synaptic and cognitive deficits in fragile X mice
Jingqi Yan et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2018)
Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years - Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2014
Jon Baio et al.
MMWR SURVEILLANCE SUMMARIES (2018)
Sex-Specific Effects of the Huntington Gene on Normal Neurodevelopment
Jessica K. Lee et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2017)
What Is the Male-to-Female Ratio in Autism Spectrum Disorder? A Systematic Review and Meta-Analysis
Rachel Loomes et al.
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY (2017)
A de novo dominant mutation in KIF1A associated with axonal neuropathy, spasticity and autism spectrum disorder
Pedro J. Tomaselli et al.
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM (2017)
Elimination of huntingtin in the adult mouse leads to progressive behavioral deficits, bilateral thalamic calcification, and altered brain iron homeostasis
Paula Dietrich et al.
PLOS GENETICS (2017)
Linguistic camouflage in girls with autism spectrum disorder
Julia Parish-Morris et al.
MOLECULAR AUTISM (2017)
Huntingtin gene repeat size variations affect risk of lifetime depression
Sarah L. Gardiner et al.
TRANSLATIONAL PSYCHIATRY (2017)
Postnatal and adult consequences of loss of huntingtin during development: Implications for Huntington's disease
Eduardo E. Arteaga-Bracho et al.
NEUROBIOLOGY OF DISEASE (2016)
Huntington disease reduced penetrance alleles occur at high frequency in the general population
Chris Kay et al.
NEUROLOGY (2016)
Selective expression of mutant huntingtin during development recapitulates characteristic features of Huntington's disease
Aldrin E. Molero et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2016)
The role of sex-differential biology in risk for autism spectrum disorder
Donna M. Werling
BIOLOGY OF SEX DIFFERENCES (2016)
Prevalence of Huntington's disease gene CAG trinucleotide repeat alleles in patients with bipolar disorder
Eliana Marisa Ramos et al.
BIPOLAR DISORDERS (2015)
Autism: reduced connectivity between cortical areas involved in face expression, theory of mind, and the sense of self
Wei Cheng et al.
BRAIN (2015)
Huntingtin functions as a scaffold for selective macroautophagy
Yan-Ning Rui et al.
NATURE CELL BIOLOGY (2015)
Mutant Huntingtin Affects Cortical Progenitor Cell Division and Development of the Mouse Neocortex
Maria Molina-Calavita et al.
JOURNAL OF NEUROSCIENCE (2014)
Huntingtin Is Required for Normal Excitatory Synapse Development in Cortical and Striatal Circuits
Spencer U. McKinstry et al.
JOURNAL OF NEUROSCIENCE (2014)
Loss of mTOR-Dependent Macroautophagy Causes Autistic-like Synaptic Pruning Deficits
Guomei Tang et al.
NEURON (2014)
The genetic relationship between handedness and neurodevelopmental disorders
William M. Brandler et al.
TRENDS IN MOLECULAR MEDICINE (2014)
High Frequency of Intermediate Alleles on Huntington Disease-Associated Haplotypes in British Columbia's General Population
Alicia Semaka et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2013)
Autism genetics
Antonio M. Persico et al.
BEHAVIOURAL BRAIN RESEARCH (2013)
Characterization of the Huntington intermediate CAG repeat expansion phenotype in PHAROS
Annie Killoran et al.
NEUROLOGY (2013)
Faster Perceptual Learning through Excitotoxic Neurodegeneration
Christian Beste et al.
CURRENT BIOLOGY (2012)
Origin and evolution of genes and genomes. Crucial role of triplet expansions
Zakharia M. Frenkel et al.
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS (2012)
An evolutionary recent neuroepithelial cell adhesion function of huntingtin implicates ADAM10-Ncadherin
Valentina Lo Sardo et al.
NATURE NEUROSCIENCE (2012)
Variation within the Huntington's Disease Gene Influences Normal Brain Structure
Mark Muehlau et al.
PLOS ONE (2012)
An Overview of the Genetic Structure within the Italian Population from Genome-Wide Data
Cornelia Di Gaetano et al.
PLOS ONE (2012)
Smaller intracranial volume in prodromal Huntington's disease: evidence for abnormal neurodevelopment
Peggy C. Nopoulos et al.
BRAIN (2011)
Ciliogenesis is regulated by a huntingtin-HAP1-PCM1 pathway and is altered in Huntington disease
Guy Keryer et al.
JOURNAL OF CLINICAL INVESTIGATION (2011)
Spatial and Temporal Requirements for huntingtin (Htt) in Neuronal Migration and Survival during Brain Development
Yiai Tong et al.
JOURNAL OF NEUROSCIENCE (2011)
A Behavioral Comparison of Male and Female Adults with High Functioning Autism Spectrum Conditions
Meng-Chuan Lai et al.
PLOS ONE (2011)
Prevalence of Incompletely Penetrant Huntington's Disease Alleles Among Individuals With Major Depressive Disorder
Roy H. Perlis et al.
AMERICAN JOURNAL OF PSYCHIATRY (2010)
Principal Pathogenetic Components and Biological Endophenotypes in Autism Spectrum Disorders
Roberto Sacco et al.
AUTISM RESEARCH (2010)
AUTISM IN THALIDOMIDE EMBRYOPATHY: A POPULATION STUDY
K. Strömland et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2010)
Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1
L. Palmieri et al.
MOLECULAR PSYCHIATRY (2010)
Huntingtin Is Required for Mitotic Spindle Orientation and Mammalian Neurogenesis
Juliette D. Godin et al.
NEURON (2010)
Tandem repeat polymorphisms: modulators of disease susceptibility and candidates for 'missing heritability'
Anthony J. Hannan
TRENDS IN GENETICS (2010)
CAG Expansion in the Huntington Disease Gene Is Associated with a Specific and Targetable Predisposing Haplogroup
Simon C. Warby et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Thalidomide and Misoprostol: Ophthalmologic Manifestations and Associations Both Expected and Unexpected
Marilyn T. Miller et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2009)
Simple sequence repeats: genetic modulators of brain function and behavior
John W. Fondon et al.
TRENDS IN NEUROSCIENCES (2008)
Hyperconnectivity of local neocortical microcircuitry induced by prenatal exposure to valproic acid
Tania Rinaldi et al.
CEREBRAL CORTEX (2008)
Clinical, morphological, and biochemical correlates of head circumference in autism
Roberto Sacco et al.
BIOLOGICAL PSYCHIATRY (2007)
Huntingtin facilitates dynein/dynactin-mediated vesicle transport
Juliane P. Caviston et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Molecular mechanisms of autism:: a possible role for Ca2+ signaling
Jocelyn F. Krey et al.
CURRENT OPINION IN NEUROBIOLOGY (2007)
Autism spectrum disorders: developmental disconnection syndromes
Daniel H. Geschwind et al.
CURRENT OPINION IN NEUROBIOLOGY (2007)
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
Christelle M. Durand et al.
NATURE GENETICS (2007)
Neuroanatomic observations of the brain in autism: a review and future directions
ML Bauman et al.
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE (2005)
Why the frontal cortex in autism might be talking only to itself: local over-connectivity but long-distance disconnection
E Courchesne et al.
CURRENT OPINION IN NEUROBIOLOGY (2005)
Implementing false discovery rate control: increasing your power
KJF Verhoeven et al.
OIKOS (2005)
Mutant huntingtin impairs axonal trafficking in mammalian neurons in vivo and in vitro
E Trushina et al.
MOLECULAR AND CELLULAR BIOLOGY (2004)
Huntingtin controls neurotrophic support and survival of neurons by enhancing BDNF vesicular transport along microtubules
LR Gauthier et al.
CELL (2004)
Effect of population stratification on case-control association studies - I. Elevation in false positive rates and comparison to confounding risk ratios (a simulation study)
GA Heiman et al.
HUMAN HEREDITY (2004)
Effect of population stratification on case-control association studies - II. False-positive rates and their limiting behavior as number of subpopulations increases
P Gorroochurn et al.
HUMAN HEREDITY (2004)
Model of autism: increased ratio of excitation/inhibition in key neural systems
JLR Rubenstein et al.
GENES BRAIN AND BEHAVIOR (2003)
Autism and Mobius sequence - An exploratory study of children in northeastern Brazil
JM Bandim et al.
ARQUIVOS DE NEURO-PSIQUIATRIA (2003)
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
S Jamain et al.
NATURE GENETICS (2003)
Neurons lacking huntingtin differentially colonize brain and survive in chimeric mice
A Reiner et al.
JOURNAL OF NEUROSCIENCE (2001)
Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease
C Zuccato et al.
SCIENCE (2001)
Huntingtin's neuroprotective activity occurs via inhibition of procaspase-9 processing
D Rigamonti et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Inactivation of Hdh in the brain and testis results in progressive neurodegeneration and sterility in mice
I Dragatsis et al.
NATURE GENETICS (2000)
Prenatal exposure of rats to valproic acid reproduces the cerebellar anomalies associated with autism
JL Ingram et al.
NEUROTOXICOLOGY AND TERATOLOGY (2000)
Share Paper
