4.5 Article

Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder

Related references

Note: Only part of the references are listed.
Review Clinical Neurology

Sex differences in autism spectrum disorders

Donna M. Werling et al.

CURRENT OPINION IN NEUROLOGY (2013)

Article Multidisciplinary Sciences

Examining and interpreting the female protective effect against autistic behavior

Elise B. Robinson et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)

Article Genetics & Heredity

SHANK1 Deletions in Males with Autism Spectrum Disorder

Daisuke Sato 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)

Article Neurosciences

De Novo Gene Disruptions in Children on the Autistic Spectrum

Ivan Iossifov et al.

NEURON (2012)

Review Biotechnology & Applied Microbiology

Autism genetics: searching for specificity and convergence

Jamee M. Berg et al.

GENOME BIOLOGY (2012)

Article Genetics & Heredity

Common genetic variants, acting additively, are a major source of risk for autism

Lambertus Klei et al.

MOLECULAR AUTISM (2012)

Article Psychiatry

Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism

Joachim Hallmayer et al.

ARCHIVES OF GENERAL PSYCHIATRY (2011)

Editorial Material Genetics & Heredity

Where's the Evidence?

Veronica J. Vieland

HUMAN HEREDITY (2011)

Article Multidisciplinary Sciences

A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

Satoru Yokoyama et al.

NATURE (2011)

Article Genetics & Heredity

Next-Generation Sequencing of a 40 Mb Linkage Interval Reveals TSPAN12 Mutations in Patients with Familial Exudative Vitreoretinopathy

Konstantinos Nikopoulos et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2010)

Article Psychiatry

Sibling Recurrence and the Genetic Epidemiology of Autism

John N. Constantino et al.

AMERICAN JOURNAL OF PSYCHIATRY (2010)

Article Biochemistry & Molecular Biology

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

Richard Anney et al.

HUMAN MOLECULAR GENETICS (2010)

Article Biochemistry & Molecular Biology

Massively parallel sequencing and rare disease

Sarah B. Ng et al.

HUMAN MOLECULAR GENETICS (2010)

Article Multidisciplinary Sciences

Functional impact of global rare copy number variation in autism spectrum disorders

Dalila Pinto et al.

NATURE (2010)

Article Multidisciplinary Sciences

A map of human genome variation from population-scale sequencing

David Altshuler et al.

NATURE (2010)

Review Genetics & Heredity

Genotype imputation for genome-wide association studies

Jonathan Marchini et al.

NATURE REVIEWS GENETICS (2010)

Article Genetics & Heredity

IFRD1 Is a Candidate Gene for SMNA on Chromosome 7q22-q23

Zoran Brkanac et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2009)

Article Multidisciplinary Sciences

A genome-wide linkage and association scan reveals novel loci for autism

Lauren A. Weiss et al.

NATURE (2009)

Article Multidisciplinary Sciences

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

Kai Wang et al.

NATURE (2009)

Article Multidisciplinary Sciences

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

Joseph T. Glessner et al.

NATURE (2009)

Article Medicine, General & Internal

Isolated Familial Hypogonadotropic Hypogonadism and a GNRH1 Mutation

Jerome Bouligand et al.

NEW ENGLAND JOURNAL OF MEDICINE (2009)

Review Pediatrics

Epidemiology of Pervasive Developmental Disorders

Eric Fombonne

PEDIATRIC RESEARCH (2009)

Article Genetics & Heredity

Structural variation of chromosomes in autism spectrum disorder

Christian R. Marshall et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2008)

Review Genetics & Heredity

Advances in autism genetics: on the threshold of a new neurobiology

Brett S. Abrahams et al.

NATURE REVIEWS GENETICS (2008)

Article Biochemistry & Molecular Biology

A second-generation combined linkage-physical map of the human genome

Tara C. Matise et al.

GENOME RESEARCH (2007)

Article Genetics & Heredity

PLINK: A tool set for whole-genome association and population-based linkage analyses

Shaun Purcell et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2007)

Article Multidisciplinary Sciences

Strong association of de novo copy number mutations with autism

Jonathan Sebat et al.

SCIENCE (2007)

Article Genetics & Heredity

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Peter Szatmari et al.

NATURE GENETICS (2007)

Article Genetics & Heredity

Thermometers: Something for statistical geneticists to think about

Veronica J. Vieland

HUMAN HEREDITY (2006)

Article Biochemistry & Molecular Biology

HSulf-1 and HSulf-2 are potent inhibitors of myeloma tumor growth in vivo

YM Dai et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2005)

Article Cell Biology

EBF2 regulates osteoblast-dependent differentiation of osteoclasts

M Kieslinger et al.

DEVELOPMENTAL CELL (2005)

Article Genetics & Heredity

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

RM Cantor et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2005)

Article Neurosciences

Intergenerational transmission of subthreshold autistic traits in the general population

JN Constantino et al.

BIOLOGICAL PSYCHIATRY (2005)

Article Genetics & Heredity

Evidence for sex-specific risk alleles in autism spectrum disorder

JL Stone et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2004)

Article Genetics & Heredity

A combined linkage-physical map of the human genome

X Kong et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2004)

Article Biochemistry & Molecular Biology

Human tribbles, a protein family controlling mitogen-activated protein kinase cascades

E Kiss-Toth et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2004)

Article Medicine, General & Internal

Unique lipoprotein phenotype and genotype associated with exceptional longevity

N Barzilai et al.

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2003)

Article Genetics & Heredity

A genomewide screen of 345 families for autism-susceptibility loci

AL Yonan et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2003)

Article Genetics & Heredity

Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

H Stefansson et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2003)

Article Multidisciplinary Sciences

A role for casein kinase 2α in the Drosophila circadian clock

JM Lin et al.

NATURE (2002)

Article Biochemistry & Molecular Biology

Charcot-Marie-Tooth disease neurofilament mutations disrupt neurofilament assembly and axonal transport

J Brownlees et al.

HUMAN MOLECULAR GENETICS (2002)

Article Genetics & Heredity

Neuregulin 1 and susceptibility to schizophrenia

H Stefansson et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2002)

Article Genetics & Heredity

Merlin-rapid analysis of dense genetic maps using sparse gene flow trees

GR Abecasis et al.

NATURE GENETICS (2002)

Article Genetics & Heredity

A genomewide screen for autism susceptibility loci

JJ Liu et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2001)

Article Genetics & Heredity

Power comparison of parametric and nonparametric linkage tests in small pedigrees

PC Sham et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2000)