Ras-like without CAAX 2 (RIT2): a susceptibility gene for autism spectrum disorder

FOXP3 gene variations and susceptibility to autism: A case–control study

(2017) Mohammad Reza Safari et al.   GENE

Glutamate receptor, metabotropic 7 (GRM7) gene variations and susceptibility to autism: A case-control study

(2016) Rezvan Noroozi et al.   Autism Research

Synaptosome-Associated Protein 25 (SNAP25) Gene Association Analysis Revealed Risk Variants for ASD, in Iranian Population

(2016) Mohammad reza Safari et al.   JOURNAL OF MOLECULAR NEUROSCIENCE

Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations

(2015) Xiaoxi Liu et al.   Autism Research

Assessment of RIT2 rs12456492 association with Parkinson's disease in Mainland China

(2015) Zhen-hua Liu et al.   NEUROBIOLOGY OF AGING

RIT2 polymorphism is associated with Parkinson's disease in a Han Chinese population

(2015) Kun Nie et al.   NEUROBIOLOGY OF AGING

RIT2 rs12456492 polymorphism and the risk of Parkinson’s disease: A meta-analysis

(2015) Xiaona Zhang et al.   NEUROSCIENCE LETTERS

The RIT2 and STX1B polymorphisms are associated with Parkinson's disease

(2015) Jian-Yong Wang et al.   PARKINSONISM & RELATED DISORDERS

Genetic association of RIT2 rs12456492 polymorphism and Parkinson’s disease susceptibility in Asian populations: a meta-analysis

(2015) Yanjun Lu et al.   Scientific Reports

The role of de novo mutations in the genetics of autism spectrum disorders

(2014) Michael Ronemus et al.   NATURE REVIEWS GENETICS

A de novo convergence of autism genetics and molecular neuroscience

(2014) Niklas Krumm et al.   TRENDS IN NEUROSCIENCES

RIT2 variant is not associated with Parkinson's disease in a Taiwanese population

(2013) Chin-Hsien Lin et al.   NEUROBIOLOGY OF AGING

Correction: Transcriptome Analysis of Medicinal Plant Salvia miltiorrhiza and Identification of Genes Related to Tanshinone Biosynthesis

(2013) Lei Yang et al.   PLoS One

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC

(2012) M L Hamshere et al.   MOLECULAR PSYCHIATRY

Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2

(2011) Nathan Pankratz et al.   ANNALS OF NEUROLOGY

The Plasma Membrane-Associated GTPase Rin Interacts with the Dopamine Transporter and Is Required for Protein Kinase C-Regulated Dopamine Transporter Trafficking

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

HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants

(2011) L. D. Ward et al.   NUCLEIC ACIDS RESEARCH

Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson's Disease

(2011) Chuong B. Do et al.   PLoS Genetics

Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders

(2010) Jill A Rosenfeld et al.   GENETICS IN MEDICINE

Contact in the genetics of autism and schizophrenia

(2009) J. Peter H. Burbach et al.   TRENDS IN NEUROSCIENCES

Structural Variation of Chromosomes in Autism Spectrum Disorder

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

Analysis of Gene Expression in Parkinson's Disease: Possible Involvement of Neurotrophic Support and Axon Guidance in Dopaminergic Cell Death

(2008) Koen Bossers et al.   BRAIN PATHOLOGY

Autism: Many Genes, Common Pathways?

(2008) Daniel H. Geschwind   CELL

Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network

(2008) I. Iossifov et al.   GENOME RESEARCH