4.5 Article

Support for calcium channel gene defects in autism spectrum disorders

Related references

Note: Only part of the references are listed.
Article Genetics & Heredity

Rare Deletions at the Neurexin 3 Locus in Autism Spectrum Disorder

Andrea K. Vaags et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2012)

Article Multidisciplinary Sciences

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Benjamin M. Neale et al.

NATURE (2012)

Article Multidisciplinary Sciences

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

Stephan J. Sanders et al.

NATURE (2012)

Article Multidisciplinary Sciences

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

Brian J. O'Roak et al.

NATURE (2012)

Review Genetics & Heredity

The continuing value of twin studies in the omics era

Jenny van Dongen et al.

NATURE REVIEWS GENETICS (2012)

Article Neurosciences

De Novo Gene Disruptions in Children on the Autistic Spectrum

Ivan Iossifov et al.

NEURON (2012)

Article Psychiatry

Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism

Joachim Hallmayer et al.

ARCHIVES OF GENERAL PSYCHIATRY (2011)

Article Multidisciplinary Sciences

Spatio-temporal transcriptome of the human brain

Hyo Jung Kang et al.

NATURE (2011)

Article Biochemistry & Molecular Biology

Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome

Sergiu P. Pasca et al.

NATURE MEDICINE (2011)

Article Multidisciplinary Sciences

Mouse model of Timothy syndrome recapitulates triad of autistic traits

Patrick L. Bader et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)

Article Biochemistry & Molecular Biology

A User's Guide to the Encyclopedia of DNA Elements (ENCODE)

Richard M. Myers et al.

PLOS BIOLOGY (2011)

Article Clinical Neurology

Contributions of the environment and environmentally vulnerable physiology to autism spectrum disorders

Martha R. Herbert

CURRENT OPINION IN NEUROLOGY (2010)

Article Genetics & Heredity

MaCH: Using Sequence and Genotype Data to Estimate Haplotypes and Unobserved Genotypes

Yun Li et al.

GENETIC EPIDEMIOLOGY (2010)

Article Genetics & Heredity

Common SNPs explain a large proportion of the heritability for human height

Jian Yang et al.

NATURE GENETICS (2010)

Review Genetics & Heredity

Genotype imputation for genome-wide association studies

Jonathan Marchini et al.

NATURE REVIEWS GENETICS (2010)

Article Genetics & Heredity

The 1000 Genomes Project: new opportunities for research and social challenges

Marc Via et al.

GENOME MEDICINE (2010)

Article Multidisciplinary Sciences

Genetic Calcium Signaling Abnormalities in the Central Nervous System: Seizures, Migraine, and Autism

J. Jay Gargus

YEAR IN HUMAN AND MEDICAL GENETICS 2009 (2009)

Review Multidisciplinary Sciences

Finding the missing heritability of complex diseases

Teri A. Manolio et al.

NATURE (2009)

Review Genetics & Heredity

Genetic overlap between autism, schizophrenia and bipolar disorder

Liam S. Carroll et al.

GENOME MEDICINE (2009)

Article Biochemistry & Molecular Biology

Whole-genome association study of bipolar disorder

P. Sklar et al.

MOLECULAR PSYCHIATRY (2008)

Article Multidisciplinary Sciences

A second generation human haplotype map of over 3.1 million SNPs

Kelly A. Frazer et al.

NATURE (2007)

Article Genetics & Heredity

A new multipoint method for genome-wide association studies by imputation of genotypes

Jonathan Marchini et al.

NATURE GENETICS (2007)

Article Genetics & Heredity

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Peter Szatmari et al.

NATURE GENETICS (2007)

Article Biochemistry & Molecular Biology

Voltage-gated calcium channels in genetic diseases

Isabelle Bidaud et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2006)

Article Psychology, Developmental

Combining information from multiple sources in the diagnosis of autism spectrum disorders

Susan Risi et al.

JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY (2006)

Article Biochemistry & Molecular Biology

CACNA1H mutations in autism spectrum disorders

Igor Splawski et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2006)

Article Genetics & Heredity

Replication of autism linkage:: Fine-mapping peak at 17q21

RM Cantor et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2005)

Article Genetics & Heredity

Evidence for sex-specific risk alleles in autism spectrum disorder

JL Stone et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2004)

Review Pharmacology & Pharmacy

Ca2+ channels as integrators of G protein-mediated signaling in neurons

J Strock et al.

MOLECULAR PHARMACOLOGY (2004)

Review Neurosciences

Brain anatomy and development in autism: review of structural MRI studies

P Brambilla et al.

BRAIN RESEARCH BULLETIN (2003)

Letter Genetics & Heredity

The Autism Genetic Resource Exchange: A resource for the study of autism and related neuropsychiatric conditions

DH Geschwind et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2001)

Article Multidisciplinary Sciences

Targeted mutation of the murine arylhydrocarbon receptor nuclear translocator 2 (Arnt2) gene reveals partial redundancy with Arnt

B Keith et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)

Article Genetics & Heredity

Family-based tests of association in the presence of linkage

SL Lake et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2000)

Article Genetics & Heredity

The transmission/disequilibrium test and parental-genotype reconstruction for X-chromosomal markers

S Horvath et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2000)