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

Molecular autism, 2012-10, Vol.3 (1), p.9-9, Article 9

2012

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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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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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The contribution of de novo coding mutations to autism spectrum disorder

Nature (London), 2014-11, Vol.515 (7526), p.216-221

2014

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Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Neuron (Cambridge, Mass.), 2011-06, Vol.70 (5), p.863-885

2011

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Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

Nature genetics, 2008-08, Vol.40 (8), p.955-962

2008

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Adjusting Head Circumference for Covariates in Autism: Clinical Correlates of a Highly Heritable Continuous Trait

Biological psychiatry (1969), 2013-10, Vol.74 (8), p.576-584

2013

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Gene expression analysis by transcript profiling coupled to a gene database query

Nature biotechnology, 1999-08, Vol.17 (8), p.798-803

1999

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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

Neuron (Cambridge, Mass.), 2015-09, Vol.87 (6), p.1215-1233

2015

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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Nature genetics, 2017-07, Vol.49 (7), p.978-985

2017

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Expansion of the Hox Gene Family and the Evolution of Chordates

Proceedings of the National Academy of Sciences - PNAS, 1993-07, Vol.90 (13), p.6300-6304

1993

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Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

Molecular autism, 2017-05, Vol.8 (1), p.21-21, Article 21

2017

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Gene loss and gain in the evolution of the vertebrates

Development (Cambridge), 1994, Vol.1994 (Supplement), p.155-161

1994

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Expression Pattern of a Murine Homeobox Gene, Dbx, Displays Extreme Spatial Restriction in Embryonic Forebrain and Spinal Cord

Proceedings of the National Academy of Sciences - PNAS, 1992-09, Vol.89 (17), p.8053-8057

1992

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Common variants at five new loci associated with early-onset inflammatory bowel disease

Nature genetics, 2009-12, Vol.41 (12), p.1335-1340

2009

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No evidence for association of Autism with rare heterozygous point mutations in contactin-associated protein-like 2

PLoS genetics, 2015-01, Vol.11 (1)

2015

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A genomewide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?

Biological psychiatry (1969), 2014-09, Vol.77 (9), p.775-784

2014

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Evolution of Hox Genes

Annual review of genetics, 1994-01, Vol.28 (1), p.423-442

1994

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Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism

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

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

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

No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins

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

The contribution of de novo coding mutations to autism spectrum disorder

Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15q11.2, Specifically Breakpoints 1 to 2

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

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

Adjusting Head Circumference for Covariates in Autism: Clinical Correlates of a Highly Heritable Continuous Trait

Gene expression analysis by transcript profiling coupled to a gene database query

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Expansion of the Hox Gene Family and the Evolution of Chordates

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

Gene loss and gain in the evolution of the vertebrates

Expression Pattern of a Murine Homeobox Gene, Dbx, Displays Extreme Spatial Restriction in Embryonic Forebrain and Spinal Cord

Common variants at five new loci associated with early-onset inflammatory bowel disease

No Evidence for Association of Autism with Rare Heterozygous Point Mutations in Contactin-Associated Protein-Like 2 ( CNTNAP2 ), or in Other Contactin-Associated Proteins or Contactins: e1004852

No evidence for association of Autism with rare heterozygous point mutations in contactin-associated protein-like 2

A genomewide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?

Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15 q 11.2, Specifically Breakpoints 1 to 2

Evolution of Hox Genes

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