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MirSNP, a database of polymorphisms altering miRNA target sites, identifies miRNA-related SNPs in GWAS SNPs and eQTLs
BackgroundNumerous single nucleotide polymorphisms (SNPs) associated with complex diseases have been identified by genome-wide association studies (GWAS) and expression quantitative trait lociExpand
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Anterior cingulum abnormalities in male patients with schizophrenia determined through diffusion tensor imaging.
OBJECTIVE This study used diffusion tensor imaging to examine fractional anisotropy in the anterior cingulum and posterior cingulum bundles in patients with schizophrenia. METHOD Twenty-one maleExpand
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Genome-wide association study identifies a susceptibility locus for schizophrenia in Han Chinese at 11p11.2
To identify susceptibility loci for schizophrenia, we performed a two-stage genome-wide association study (GWAS) of schizophrenia in the Han Chinese population (GWAS: 746 individuals withExpand
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Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia
We conducted a genome-wide association study (GWAS) with replication in 36,180 Chinese individuals and performed further transancestry meta-analyses with data from the Psychiatry Genomics ConsortiumExpand
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Abnormal anterior cingulum in patients with schizophrenia: a diffusion tensor imaging study
Diffusion tensor imaging (DTI) can non-invasively examine the molecular diffusion of water in vivo and directly reflects the anatomical integrity of neural fibers in white matter. FractionalExpand
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Copy-number mutations on chromosome 17q24.2-q24.3 in congenital generalized hypertrichosis terminalis with or without gingival hyperplasia.
  • M. Sun, N. Li, +24 authors X. Zhang
  • Biology, Medicine
  • American journal of human genetics
  • 12 June 2009
Congenital generalized hypertrichosis terminalis (CGHT) is a rare condition characterized by universal excessive growth of pigmented terminal hairs and often accompanied with gingival hyperplasia. InExpand
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Association between the FOXP2 gene and autistic disorder in Chinese population
Several genomewide screens indicated that chromosome 7q was linked to autistic disorder. FOXP2, located on 7q31, is a putative transcription factor containing a polyglutamine tract and a forkhead DNAExpand
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Association of the ENGRAILED 2 (EN2) gene with autism in Chinese Han population
  • L. Wang, M. Jia, +11 authors D. Zhang
  • Biology, Medicine
  • American journal of medical genetics. Part B…
  • 5 June 2008
Human ENGRAILED 2 (EN2) gene is localized to 7q36, an autism susceptibility locus. En2 knockout mice display hypoplasia of cerebellum and a decrease in the number of Purkinje cell, which are similarExpand
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Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis
Cross-ethnic genetic studies can leverage power from differences in disease epidemiology and population-specific genetic architecture. In particular, the differences in linkage disequilibrium andExpand
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Positive association of the Disrupted‐in‐Schizophrenia‐1 gene (DISC1) with schizophrenia in the Chinese han population
  • M. Qu, F. Tang, +8 authors D. Zhang
  • Biology, Medicine
  • American journal of medical genetics. Part B…
  • 5 April 2007
Disrupted‐in‐Schizophrenia‐1 (DISC1) is located on 1q42.1, one of the most promising susceptibility loci in schizophrenia linkage studies. A non‐synonymous genetic variation rs821616 (Ser704Cys) inExpand
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