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Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ‐glutamyltransferase cholestasis

Hepatology (Baltimore, Md.), 2017-05, Vol.65 (5), p.1655-1669

2017

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Association of novel TMEM67 variants with mild phenotypes of high gamma‐glutamyl transpeptidase cholestasis and congenital hepatic fibrosis

Journal of cellular physiology, 2022-06, Vol.237 (6), p.2713-2723

2022

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TJP2 hepatobiliary disorders: Novel variants and clinical diversity

Human mutation, 2020-02, Vol.41 (2), p.502-511

2020

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Splicing Analysis of MYO5B Noncanonical Variants in Patients with Low Gamma-Glutamyltransferase Cholestasis

Human mutation, 2023-07, Vol.2023, p.1-12

2023

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MYO5B‐associated diseases: Novel liver‐related variants and genotype‐phenotype correlation

Liver international, 2022-02, Vol.42 (2), p.402-411

2022

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Biallelic loss-of-function ZFYVE19 mutations are associated with congenital hepatic fibrosis, sclerosing cholangiopathy and high-GGT cholestasis

Journal of medical genetics, 2021-08, Vol.58 (8), p.514-525

2021

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HLA‐A02:07 Allele Associates with Clarithromycin‐Induced Cutaneous Adverse Drug Reactions in Chinese Patients

Basic & clinical pharmacology & toxicology, 2018-09, Vol.123 (3), p.308-313

2018

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Association between HLA-B∗46:01 and cutaneous adverse drug reactions in Han Chinese

Journal of bio-X research, 2018-09, Vol.1 (2), p.73-78

2018

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Transcript selection for the genetic diagnosis of KIF12-associated progressive familial intrahepatic cholestasis

Gastroenterology report, 2024, Vol.12, p.goad073-goad073

2024

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HLA-B58:01 allele is associated with augmented risk for both mild and severe cutaneous adverse reactions induced by allopurinol in Han Chinese

Pharmacogenomics, 2012-07, Vol.13 (10), p.1193-1201

2012

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Association of AKT1 gene polymorphisms with risk of schizophrenia and with response to antipsychotics in the Chinese population

The journal of clinical psychiatry, 2007-09, Vol.68 (9), p.1358-1367

2007

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Serum prolactin levels, plasma risperidone levels, polymorphism of cytochrome P450 2D6 and clinical response in patients with schizophrenia

Journal of psychopharmacology (Oxford), 2007-11, Vol.21 (8), p.837-842

2007

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Response of risperidone treatment may be associated with polymorphisms of HTT gene in Chinese schizophrenia patients

Neuroscience letters, 2007-02, Vol.414 (1), p.1-4

2007

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A Gene Locus Responsible for Dyschromatosis Symmetrica Hereditaria (DSH) Maps to Chromosome 6q24.2-q25.2

American journal of human genetics, 2003-08, Vol.73 (2), p.377-382

2003

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Association of DRD2 polymorphisms and chlorpromazine-induced extrapyramidal syndrome in Chinese schizophrenic patients

Acta pharmacologica Sinica, 2006-08, Vol.27 (8), p.966

2006

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Association analysis of polymorphisms in the upstream region of the human dopamine D4 receptor gene in schizophrenia

Schizophrenia research, 2003-12, Vol.65 (1), p.9-14

2003

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Recurrent AKR1D1 c.580-13T>A Variant

The Journal of molecular diagnostics : JMD, 2023-04, Vol.25 (4), p.227-233

2023

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Association of DRD2 polymorphisms and chlorpromazine‐induced extrapyramidal syndrome in Chinese schizophrenic patients1

Acta pharmacologica Sinica, 2006-08, Vol.27 (8), p.966-970

2006

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Recurrent AKR1D1 c.580-13T>A Variant: A Cause of Δ4-3-Oxosteroid-5β-Reductase Deficiency

The Journal of molecular diagnostics : JMD, 2023-04, Vol.25 (4), p.227-233

2023

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Recurrent AKR1D1 c.580-13T>A Variant: A Cause of Δ 4 -3-Oxosteroid-5β-Reductase Deficiency

The Journal of molecular diagnostics : JMD, 2023-04, Vol.25 (4), p.227

2023

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Defects in myosin VB are associated with a spectrum of previously undiagnosed low [gamma]-glutamyltransferase cholestasis

Hepatology (Baltimore, Md.), 2017-05, Vol.65 (5), p.1655

2017

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Preparation and properties of W–Cu–Zn alloy with low W–W contiguity

Rare metals, 2016-03, Vol.35 (3), p.242-248

2016

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New Early Cretaceous Pterosaur-Bird Track Assemblage from Xinjiang,China： Palaeoethology and Palaeoenvironment

Acta geologica Sinica (Beijing), 2013-12, Vol.87 (6), p.1477-1485

English ed., 2013

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A high-throughput-compatible assay to measure the degradation of endogenous Huntingtin proteins

Acta pharmacologica Sinica, 2016-09, Vol.37 (10), p.1307-1314

2016

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Association study between NPY and YWHAH gene polymorphisms and schizophrenia

Yíchuán xuébào, 2005-12, Vol.32 (12), p.1235-1240

2005

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Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ‐glutamyltransferase cholestasis

Association of novel TMEM67 variants with mild phenotypes of high gamma‐glutamyl transpeptidase cholestasis and congenital hepatic fibrosis

TJP2 hepatobiliary disorders: Novel variants and clinical diversity

Splicing Analysis of MYO5B Noncanonical Variants in Patients with Low Gamma-Glutamyltransferase Cholestasis

MYO5B‐associated diseases: Novel liver‐related variants and genotype‐phenotype correlation

Biallelic loss-of-function ZFYVE19 mutations are associated with congenital hepatic fibrosis, sclerosing cholangiopathy and high-GGT cholestasis

HLA‐A02:07 Allele Associates with Clarithromycin‐Induced Cutaneous Adverse Drug Reactions in Chinese Patients

Association between HLA-B∗46:01 and cutaneous adverse drug reactions in Han Chinese

Transcript selection for the genetic diagnosis of KIF12-associated progressive familial intrahepatic cholestasis

HLA-B58:01 allele is associated with augmented risk for both mild and severe cutaneous adverse reactions induced by allopurinol in Han Chinese

Association of AKT1 gene polymorphisms with risk of schizophrenia and with response to antipsychotics in the Chinese population

Serum prolactin levels, plasma risperidone levels, polymorphism of cytochrome P450 2D6 and clinical response in patients with schizophrenia

Response of risperidone treatment may be associated with polymorphisms of HTT gene in Chinese schizophrenia patients

A Gene Locus Responsible for Dyschromatosis Symmetrica Hereditaria (DSH) Maps to Chromosome 6q24.2-q25.2

Association of DRD2 polymorphisms and chlorpromazine-induced extrapyramidal syndrome in Chinese schizophrenic patients

Association analysis of polymorphisms in the upstream region of the human dopamine D4 receptor gene in schizophrenia

Recurrent AKR1D1 c.580-13T>A Variant

Association of DRD2 polymorphisms and chlorpromazine‐induced extrapyramidal syndrome in Chinese schizophrenic patients1

Recurrent AKR1D1 c.580-13T>A Variant: A Cause of Δ4-3-Oxosteroid-5β-Reductase Deficiency

Recurrent AKR1D1 c.580-13T>A Variant: A Cause of Δ 4 -3-Oxosteroid-5β-Reductase Deficiency

Defects in myosin VB are associated with a spectrum of previously undiagnosed low [gamma]-glutamyltransferase cholestasis

Preparation and properties of W–Cu–Zn alloy with low W–W contiguity

New Early Cretaceous Pterosaur-Bird Track Assemblage from Xinjiang,China： Palaeoethology and Palaeoenvironment

A high-throughput-compatible assay to measure the degradation of endogenous Huntingtin proteins

Association study between NPY and YWHAH gene polymorphisms and schizophrenia

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