Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism

Association statistics under the PPL framework

(2010) Yungui Huang et al.   GENETIC EPIDEMIOLOGY

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

(2010) R. Anney et al.   HUMAN MOLECULAR GENETICS

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

(2010) A. T. Pagnamenta et al.   JOURNAL OF MEDICAL GENETICS

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

(2010) Dalila Pinto et al.   NATURE

Identification of a Schizophrenia-Associated Functional Noncoding Variant inNOS1AP

(2009) Naomi S. Wratten et al.   AMERICAN JOURNAL OF PSYCHIATRY

Recurrent Rearrangements in Synaptic and Neurodevelopmental Genes and Shared Biologic Pathways in Schizophrenia, Autism, and Mental Retardation

(2009) Audrey Guilmatre et al.   ARCHIVES OF GENERAL PSYCHIATRY

Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals

(2009) E.K. Bijlsma et al.   European Journal of Medical Genetics

A Multilocus Model of the Genetic Architecture of Autoimmune Thyroid Disorder, with Clinical Implications

(2008) Veronica J. Vieland et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Structural Variation of Chromosomes in Autism Spectrum Disorder

(2008) Christian R. Marshall et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genome-wide Linkage Analyses of Quantitative and Categorical Autism Subphenotypes

(2008) Xiao-Qing Liu et al.   BIOLOGICAL PSYCHIATRY

Epilepsy in Autism is Associated with Intellectual Disability and Gender: Evidence from a Meta-Analysis

(2008) Claire Amiet et al.   BIOLOGICAL PSYCHIATRY

Using disease symptoms to improve detection of linkage under genetic heterogeneity

(2008) Alexandre Bureau et al.   GENETIC EPIDEMIOLOGY

Practical Considerations for Dividing Data into Subsets Prior to PPL Analysis

(2008) M. Govil et al.   HUMAN HEREDITY

Decomposing the autism phenotype into familial dimensions

(2007) Peter Szatmari et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS