A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Regulation of Synapse Structure and Function by Distinct Myosin II Motors

(2011) M. D. Rubio et al.   JOURNAL OF NEUROSCIENCE

Identification d’une voie synaptique associée à l’autisme

(2011) Christelle M. Durand et al.   M S-MEDECINE SCIENCES

SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles

(2010) Dries Castermans et al.   HUMAN MOLECULAR GENETICS

Genomic and geographic distribution of SNP-defined runs of homozygosity in Europeans

(2010) Michael Nothnagel et al.   HUMAN MOLECULAR GENETICS

Runs of Homozygosity Identify a Recessive Locus 12q21.31 for Human Adult Height

(2010) Tie-Lin Yang et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

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

(2010) Dalila Pinto et al.   NATURE

Smoking in adult attention-deficit/hyperactivity disorder: Interaction between 15q13 nicotinic genes and Temperament Character Inventory scores

(2010) Mirko Manchia et al.   WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY

The Role of DNA Copy Number Variation in Schizophrenia

(2009) Gloria W.C. Tam et al.   BIOLOGICAL PSYCHIATRY

A 2-base pair deletion polymorphism in the partial duplication of the α7 nicotinic acetylcholine gene (CHRFAM7A) on chromosome 15q14 is associated with schizophrenia

(2009) Melissa L. Sinkus et al.   BRAIN RESEARCH

Understanding and Determining the Etiology of Autism

(2009) Salvatore A. Currenti   CELLULAR AND MOLECULAR NEUROBIOLOGY

Association between a Genetic Variant of the Alpha-7 Nicotinic Acetylcholine Receptor Subunit and Four Types of Dementia

(2009) Ágnes Fehér et al.   DEMENTIA AND GERIATRIC COGNITIVE DISORDERS

Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence

(2009) Sabina Benko et al.   NATURE GENETICS

Fgf10 Regulates Transition Period of Cortical Stem Cell Differentiation to Radial Glia Controlling Generation of Neurons and Basal Progenitors

(2009) Setsuko Sahara et al.   NEURON

Mutations inSYNGAP1in Autosomal Nonsyndromic Mental Retardation

(2009) Fadi F. Hamdan et al.   NEW ENGLAND JOURNAL OF MEDICINE

No evidence for excess runs of homozygosity in bipolar disorder

(2009) Anna E. Vine et al.   PSYCHIATRIC GENETICS

The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders

(2009) Catalina Betancur et al.   TRENDS IN NEUROSCIENCES

A Systematic Approach to Mapping Recessive Disease Genes in Individuals from Outbred Populations

(2009) Friedhelm Hildebrandt et al.   PLoS Genetics

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

(2008) Dan E. Arking et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Disruption of Neurexin 1 Associated with Autism Spectrum Disorder

(2008) Hyung-Goo Kim 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

Expression and adhesion profiles of SynCAM molecules indicate distinct neuronal functions

(2008) Lisa A. Thomas et al.   JOURNAL OF COMPARATIVE NEUROLOGY

Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies

(2008) Klaus-Peter Lesch et al.   JOURNAL OF NEURAL TRANSMISSION

Neuroligins and neurexins link synaptic function to cognitive disease

(2008) Thomas C. Südhof   NATURE

Xenobiotic metabolizing enzymes in the central nervous system: Contribution of cytochrome P450 enzymes in normal and pathological human brain

(2007) Fabien Dutheil et al.   BIOCHIMIE