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Copy-number variations associated with neuropsychiatric conditions

Nature (London), 2008-10, Vol.455 (7215), p.919-923

2008

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A framework for the interpretation of de novo mutation in human disease

Nature genetics, 2014-09, Vol.46 (9), p.944-950

2014

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Expression of microRNAs and other small RNAs in prefrontal cortex in schizophrenia, bipolar disorder and depressed subjects

PloS one, 2014-01, Vol.9 (1), p.e86469-e86469

2014

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Between a ROC and a hard place: decision making and making decisions about using the SCQ

Journal of child psychology and psychiatry, 2007-09, Vol.48 (9), p.932-940

2007

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Combining Information From Multiple Sources in the Diagnosis of Autism Spectrum Disorders

Journal of the American Academy of Child and Adolescent Psychiatry, 2006-09, Vol.45 (9), p.1094-1103

2006

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Feedforward and feedback motor control abnormalities implicate cerebellar dysfunctions in autism spectrum disorder

The Journal of neuroscience, 2015-02, Vol.35 (5), p.2015-2025

2015

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A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?

Biological psychiatry (1969), 2015-05, Vol.77 (9), p.775-784

2015

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A Quantitative Electrophysiological Biomarker of Duplication 15q11.2-q13.1 Syndrome

PloS one, 2016-12, Vol.11 (12), p.e0167179-e0167179

2016

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Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder

Biological psychiatry (1969), 2008-06, Vol.63 (12), p.1111-1117

2008

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A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism

American journal of human genetics, 2008-01, Vol.82 (1), p.160-164

2008

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

Neuron (Cambridge, Mass.), 2013-01, Vol.77 (2), p.235-242

2013

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Environmental and state-level regulatory factors affect the incidence of autism and intellectual disability

PLoS computational biology, 2014-03, Vol.10 (3), p.e1003518

2014

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Saccadic eye movement abnormalities in autism spectrum disorder indicate dysfunctions in cerebellum and brainstem

Molecular autism, 2014-09, Vol.5 (1), p.47-47, Article 47

2014

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Intellectual Disability Is Associated with Increased Runs of Homozygosity in Simplex Autism

American journal of human genetics, 2013-07, Vol.93 (1), p.103-109

2013

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Association of the oxytocin receptor gene ( OXTR) in Caucasian children and adolescents with autism

Neuroscience letters, 2007-04, Vol.417 (1), p.6-9

2007

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Recurrent 16p11.2 microdeletions in autism

Human molecular genetics, 2008-02, Vol.17 (4), p.628-638

2008

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A survey of seizures and current treatments in 15q duplication syndrome

Epilepsia (Copenhagen), 2014-03, Vol.55 (3), p.396-402

2014

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Using the Autism Diagnostic Interview—Revised to Increase Phenotypic Homogeneity in Genetic Studies of Autism

Biological psychiatry (1969), 2007-02, Vol.61 (4), p.438-448

2007

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Successful Electroconvulsive Therapy in a Patient With Catatonia and Maternal Duplication 15q11-13 Syndrome

The journal of ECT, 2024-07

2024

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Autism as a paradigmatic complex genetic disorder

Annual review of genomics and human genetics, 2004-01, Vol.5 (1), p.379-405

2004

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The Autism Diagnostic Observation Schedule-Generic: A Standard Measure of Social and Communication Deficits Associated with the Spectrum of Autism

Journal of autism and developmental disorders, 2000-06, Vol.30 (3), p.205-223

2000

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Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE

Human molecular genetics, 2011-11, Vol.20 (22), p.4360-4370

2011

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A functional common polymorphism in a Sp1 recognition site of the epidermal growth factor receptor gene promoter

Cancer research (Chicago, Ill.), 2005, Vol.65 (1), p.46-53

2005

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Maternal Serotonin Levels Are Associated With Cognitive Ability and Core Symptoms in Autism Spectrum Disorder

Journal of the American Academy of Child and Adolescent Psychiatry, 2018-11, Vol.57 (11), p.867-875

2018

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Copy-number variations associated with neuropsychiatric conditions

A framework for the interpretation of de novo mutation in human disease

Expression of microRNAs and other small RNAs in prefrontal cortex in schizophrenia, bipolar disorder and depressed subjects

Between a ROC and a hard place: decision making and making decisions about using the SCQ

Combining Information From Multiple Sources in the Diagnosis of Autism Spectrum Disorders

Feedforward and feedback motor control abnormalities implicate cerebellar dysfunctions in autism spectrum disorder

A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?

A Quantitative Electrophysiological Biomarker of Duplication 15q11.2-q13.1 Syndrome

Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder

A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism

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

Environmental and state-level regulatory factors affect the incidence of autism and intellectual disability

Saccadic eye movement abnormalities in autism spectrum disorder indicate dysfunctions in cerebellum and brainstem

Intellectual Disability Is Associated with Increased Runs of Homozygosity in Simplex Autism

Association of the oxytocin receptor gene ( OXTR) in Caucasian children and adolescents with autism

Recurrent 16p11.2 microdeletions in autism

Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls

A survey of seizures and current treatments in 15q duplication syndrome

Using the Autism Diagnostic Interview—Revised to Increase Phenotypic Homogeneity in Genetic Studies of Autism

Successful Electroconvulsive Therapy in a Patient With Catatonia and Maternal Duplication 15q11-13 Syndrome

Autism as a paradigmatic complex genetic disorder

The Autism Diagnostic Observation Schedule-Generic: A Standard Measure of Social and Communication Deficits Associated with the Spectrum of Autism

Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE

A functional common polymorphism in a Sp1 recognition site of the epidermal growth factor receptor gene promoter

Maternal Serotonin Levels Are Associated With Cognitive Ability and Core Symptoms in Autism Spectrum Disorder

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