Search Results - "Feng, Guoyin"
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Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia
Published in Nature genetics (01-11-2017)“…A genome-wide association analysis using data from Chinese individuals combined with a transethnic meta-analysis of Psychiatry Genomics Consortium data…”
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Sclerostin Mediates Bone Response to Mechanical Unloading Through Antagonizing Wnt/β‐Catenin Signaling
Published in Journal of bone and mineral research (01-10-2009)“…Reduced mechanical stress leads to bone loss, as evidenced by disuse osteoporosis in bedridden patients and astronauts. Osteocytes have been identified as…”
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CACNA1C, schizophrenia and major depressive disorder in the Han Chinese population
Published in British journal of psychiatry (01-01-2014)“…Common psychiatric disorders are highly heritable, indicating that genetic factors play an important role in their aetiology. The CACNA1C gene, which codes for…”
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Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese
Published in Biological psychiatry (1969) (15-08-2016)“…Abstract Background Compelling evidence suggested the role of copy number variations (CNVs) in schizophrenia susceptibility. Most of the evidence was from…”
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Metabolomic Profiling to Identify Potential Serum Biomarkers for Schizophrenia and Risperidone Action
Published in Journal of proteome research (02-12-2011)“…Despite recent advances in understanding the pathophysiology of schizophrenia and the mechanisms of antipsychotic drug action, the development of biomarkers…”
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Common variants on 8p12 and 1q24.2 confer risk of schizophrenia
Published in Nature genetics (01-12-2011)“…Yongyong Shi, Lin He and colleagues report a genome-wide association study for schizophrenia in the Han Chinese population. They identify two new…”
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Rates of Adult Schizophrenia Following Prenatal Exposure to the Chinese Famine of 1959-1961
Published in JAMA : the journal of the American Medical Association (03-08-2005)“…CONTEXT Schizophrenia is a common major mental disorder. Intrauterine nutritional deficiency may increase the risk of schizophrenia. The main evidence comes…”
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Exploring off-targets and off-systems for adverse drug reactions via chemical-protein interactome--clozapine-induced agranulocytosis as a case study
Published in PLoS computational biology (01-03-2011)“…In the era of personalized medical practice, understanding the genetic basis of patient-specific adverse drug reaction (ADR) is a major challenge. Clozapine…”
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Wls is expressed in the epidermis and regulates embryonic hair follicle induction in mice
Published in PloS one (24-09-2012)“…Wnt proteins are secreted molecules that play multiple roles during hair follicle development and postnatal hair cycling. Wntless (Wls) is a cargo protein…”
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A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population
Published in Human molecular genetics (15-07-2011)“…High-grade myopia (HM) is highly heritable, and has a high prevalence in the Han Chinese population. We carried out a genome-wide association study involving…”
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Rare CNVs and Tag SNPs at 15q11.2 Are Associated With Schizophrenia in the Han Chinese Population
Published in Schizophrenia bulletin (01-05-2013)“…Rare copy number variations (CNVs) were involved in the etiology of neuropsychiatric disorders, and some of them appeared to be shared risk factors for several…”
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Common Variants in Major Histocompatibility Complex Region and TCF4 Gene Are Significantly Associated with Schizophrenia in Han Chinese
Published in Biological psychiatry (1969) (01-10-2010)“…Background Schizophrenia is a complex major psychiatric disorder affecting ∼1% of the world population. Recently, in a genome-wide association study and a…”
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CNTNAP2 is significantly associated with schizophrenia and major depression in the Han Chinese population
Published in Psychiatry research (30-05-2013)“…Abstract CNTNAP2 , located on 7q35–36.1, encodes a single-pass transmembrane protein mediating cell–cell interactions in the nervous system. CNTNAP2 has been…”
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Indian hedgehog mutations causing brachydactyly type A1 impair Hedgehog signal transduction at multiple levels
Published in Cell research (01-09-2011)“…Brachydactyly type A1 (BDAI), the first recorded Mendelian autosomal dominant disorder in humans, is characterized by a shortening or absence of the middle…”
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Altered Levels of Acute Phase Proteins in the Plasma of Patients with Schizophrenia
Published in Analytical chemistry (Washington) (01-06-2006)“…Schizophrenia is a relatively common psychiatric syndrome that affects virtually all brain functions. We investigated the plasma proteome of 22 schizophrenia…”
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The PstI/RsaI and DraI polymorphisms of CYP2E1 and head and neck cancer risk: a meta-analysis based on 21 case-control studies
Published in BMC cancer (22-10-2010)“…CYP2E1 encodes a member of the cytochrome P450 superfamily of enzymes which play a central role in activating and detoxifying many carcinogens and endogenous…”
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Common SNPs in myelin transcription factor 1-like (MYT1L): association with major depressive disorder in the Chinese Han population
Published in PloS one (27-10-2010)“…Myelin transcription factor 1-like (MYT1L) is a member of the myelin transcription factor 1 (MYT1) gene family, and the neural specific,…”
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ITIH family genes confer risk to schizophrenia and major depressive disorder in the Han Chinese population
Published in Progress in neuro-psychopharmacology & biological psychiatry (03-06-2014)“…As a major extracellular matrix component, ITIHs played an important role in inflammation and carcinogenesis. Several genome-wide association studies have…”
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A systematic genetic polymorphism analysis of the CYP2C9 gene in four different geographical Han populations in mainland China
Published in Genomics (San Diego, Calif.) (01-05-2011)“…While many studies have been focused on CYP2C9*2 and *3 there was a lack of large full gene sequencing on CYP2C9, and this study was designed to fill this gap…”
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Systematic functional characterization of cytochrome P450 2E1 promoter variants in the Chinese Han population
Published in PloS one (17-07-2012)“…CYP2E1 promoter polymorphisms can lead to significant interindividual differences in expression of CYP2E1. Using a database of CYP2E1 gene polymorphisms…”
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