> "Vitamin D-related genes are subjected to significant de novo mutation burdens in autism spectrum disorder" was online published in American journal of medical genetics.
April 13, 2017
> "Enhanced tumor growth inhibition by mesenchymal stem cells derived from iPSCs with targeted integration of interleukin24 into rDNA loci" was online published in Oncotarget.
March 28, 2017
> "Characterization of chromosomal abnormalities in pregnancy losses reveals critical genes and loci for human early development." was online published in Human Mutation.
February 28, 2017
> "A Novel Alzheimer-Associated SNP in Tmp21 Increases Amyloidogenesis." was online published in Molecular neurobiology.
February 23, 2017
> "Ubiquitin-related network underlain by (CAG)n loci modulate age at onset in Machado-Joseph disease." was online published in Brain.
February 15, 2017
> "De novo genic mutations among a Chinese autism spectrum disorder cohort." was online published in Nature Communications.
November 8, 2016
> "Altered Expression of EPO Might Underlie Hepatic Hemangiomas in LRRK2 Knockout Mice." was online published in BioMed Research International.
October 31, 2016
> "WDR73 missense mutation causes infantile onset intellectual disability and cerebellar hypoplasia in a consanguineous family." was online published in ScienceDirect.
October 28, 2016
> "Risperidone-induced topological alterations of anatomical brain network in first-episode drug-naive schizophrenia patients: a longitudinal diffusion tensor imaging study." was online published in Psychological Medicine.
June 24, 2016
> "mtDNA Heteroplasmy in Monozygotic Twins Discordant for Schizophrenia." was online published in Mol Neurobiol.
June 24, 2016
> "Analyses MAPT, GRN, and C9orf72 mutations in Chinese patients with frontotemporal dementia." was online published in Neurobiology Of Aging.
May 20, 2016
> "AKAP2 identified as a novel gene mutated in a Chinese family with adolescent idiopathic scoliosis." was online published in Journal of Medical Genetics.
March 17, 2016
> "Identification of RELN variation p.Thr3192Ser in a Chinese family with schizophrenia." was online published in Scientific Reports.
April 13, 2016
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