Association and gene-gene interactions study of reelin signaling pathway related genes with autism in the Han Chinese population

Common genetic variants on 1p13.2 associate with risk of autism

(2013) K Xia et al.   MOLECULAR PSYCHIATRY

ApoER2 and VLDLr Are Required for Mediating Reelin Signalling Pathway for Normal Migration and Positioning of Mesencephalic Dopaminergic Neurons

(2013) Ahmed Sharaf et al.   PLoS One

Association study between genes in Reelin signaling pathway and autism identifies DAB1 as a susceptibility gene in a Chinese Han population

(2013) Jun Li et al.   PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY

Prevalence of autism in mainland China, Hong Kong and Taiwan: a systematic review and meta-analysis

(2013) Xiang Sun et al.   Molecular Autism

Reelin and its complex involvement in brain development and function

(2012) Silvia Lakatosova et al.   INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY

The involvement of Reelin in neurodevelopmental disorders

(2012) Timothy D. Folsom et al.   NEUROPHARMACOLOGY

The choice of null distributions for detecting gene-gene interactions in genome-wide association studies

(2011) Can Yang et al.   BMC BIOINFORMATICS

No association of polymorphisms in the CDK5, NDEL1, and LIS1 with autism in Chinese Han population

(2011) Lifang Wang et al.   PSYCHIATRY RESEARCH

Linkage and candidate gene studies of autism spectrum disorders in European populations

(2010) Richard Holt et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

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

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

Polymorphisms of candidate genes in Slovak autistic patients

(2010) Silvia Kelemenova et al.   PSYCHIATRIC GENETICS

No significant association between RELN polymorphism and autism in case-control and family-based association study in Chinese Han population

(2010) Yiqun He et al.   PSYCHIATRY RESEARCH

Histological study in the brain of the reelin/Dab1-compound mutant mouse

(2009) Tatsuro Yamamoto et al.   ANATOMICAL SCIENCE INTERNATIONAL

Detecting purely epistatic multi-locus interactions by an omnibus permutation test on ensembles of two-locus analyses

(2009) Waranyu Wongseree et al.   BMC BIOINFORMATICS

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

(2009) Lauren A. Weiss et al.   NATURE

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

(2009) Kai Wang et al.   NATURE

Detecting gene–gene interactions that underlie human diseases

(2009) Heather J Cordell   NATURE REVIEWS GENETICS

The association analysis of RELN and GRM8 genes with autistic spectrum disorder in chinese han population

(2007) Hui Li et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS