Yanyan Ruan

Beijing, 100191, China

Last Updated: 09/26/2026

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Found 22 publications

Replication of previous GWAS hits suggests the association between rs4307059 near MSNP1AS and autism in a Chinese Han population.

Replication of previous GWAS hits suggests the association between rs4307059 near MSNP1AS and autism in a Chinese Han population.

Journal: Progress in neuro-psychopharmacology & biological psychiatry

Published: September 25, 2018

Association study and mutation sequencing of genes on chromosome 15q11-q13 identified GABRG3 as a susceptibility gene for autism in Chinese Han population.

Association study and mutation sequencing of genes on chromosome 15q11-q13 identified GABRG3 as a susceptibility gene for autism in Chinese Han population.

Journal: Translational psychiatry

Published: March 10, 2018

Genetic variants in the transcription regulatory region of MEGF10 are associated with autism in Chinese Han population.

Genetic variants in the transcription regulatory region of MEGF10 are associated with autism in Chinese Han population.

Journal: Scientific reports

Published: January 18, 2017

Association of oligodendrocytes differentiation regulator gene DUSP15 with autism.

Association of oligodendrocytes differentiation regulator gene DUSP15 with autism.

Journal: The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry

Published: May 26, 2016

Genome-Wide Association Study Suggested the PTPRD Polymorphisms Were Associated With Weight Gain Effects of Atypical Antipsychotic Medications.

Genome-Wide Association Study Suggested the PTPRD Polymorphisms Were Associated With Weight Gain Effects of Atypical Antipsychotic Medications.

Journal: Schizophrenia bulletin

Published: December 15, 2015

The Human MSI2 Gene is Associated with Schizophrenia in the Chinese Han Population.

The Human MSI2 Gene is Associated with Schizophrenia in the Chinese Han Population.

Journal: Neuroscience bulletin

Published: November 29, 2015

RAB18, a protein associated with Warburg Micro syndrome, controls neuronal migration in the developing cerebral cortex.

RAB18, a protein associated with Warburg Micro syndrome, controls neuronal migration in the developing cerebral cortex.

Journal: Molecular brain

Published: October 23, 2015

Chromatin remodeling gene EZH2 involved in the genetic etiology of autism in Chinese Han population.

Chromatin remodeling gene EZH2 involved in the genetic etiology of autism in Chinese Han population.

Journal: Neuroscience letters

Published: July 17, 2015

Genetic Evidence for Possible Involvement of the Calcium Channel Gene CACNA1A in Autism Pathogenesis in Chinese Han Population.

Genetic Evidence for Possible Involvement of the Calcium Channel Gene CACNA1A in Autism Pathogenesis in Chinese Han Population.

Journal: PloS one

Published: July 05, 2015

Schizophrenia Related Variants in CACNA1C also Confer Risk of Autism.

Schizophrenia Related Variants in CACNA1C also Confer Risk of Autism.

Journal: PloS one

Published: April 26, 2015

Ezh2 is involved in radial neuronal migration through regulating Reelin expression in cerebral cortex.

Ezh2 is involved in radial neuronal migration through regulating Reelin expression in cerebral cortex.

Journal: Scientific reports

Published: March 17, 2015

A2BP1 gene polymorphisms association with olanzapine-induced weight gain.

A2BP1 gene polymorphisms association with olanzapine-induced weight gain.

Journal: Pharmacological research

Published: January 12, 2015

Showing 1-12 of 22

Last Updated: 09/26/2026