Dr. Fann, Cathy S.-J.
范盛娟 博士
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Methods for identifying differentially methylated regions for sequence- and array-based data.
Brief Funct Genomics., Nov 01, 2016
DNA methylation is one of the most important epigenetic mechanisms, and participates in the pathogenic processes of many diseases. Different ......
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Susceptible genes of restless legs syndrome in migraine
CEPHALALGIA, Oct 01, 2016
Objective:Several genetic variants have been found to increase the risk of restless legs syndrome (RLS). The aim of the present study was to ......
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Using propensity score adjustment method in genetic association studies.
Comput Biol Chem., Jun 01, 2016
The statistical tests for single locus disease association are mostly under-powered. If a disease associated causal single nucleotide polymo ......
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Haplotypes of the D-Amino Acid Oxidase Gene Are Significantly Associated with Schizophrenia and Its Neurocognitive Deficits.
PLoS One., Mar 17, 2016
D-amino acid oxidase (DAO) has been reported to be associated with schizophrenia. This study aimed to search for genetic variants associated ......
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A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples.
MOLECULAR PSYCHIATRY, Sep 08, 2015
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List of Highlights
文件紀錄
Genome-wide analyses identify novel risk loci for cluster headache in Han Chinese residing in Taiwan
Journal of Headache and Pain Nov 21, 2022
Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes
Communications Biology Nov 03, 2022
Genome-wide analysis identified novel susceptible genes of restless legs syndrome in migraineurs
The Journal of Headache and Pain Mar 29, 2022
Genome-wide association study reveals susceptibility loci for self-reported headache in a large community-based Asian population
Cephalalgia Aug 18, 2021
Accelerated cardiovascular risk after viral clearance in hepatitis C patients with the NAMPT-rs61330082 TT genotype: An 8-year prospective cohort study
Virulence Jan 15, 2021
Differentiation of remitting neuromyelitis optica spectrum disorders from multiple sclerosis by integrating parameters from serum proteins and lymphocyte subsets.
J Neuroimmunol. May 15, 2018
Genome-wide association study identifies novel susceptibility loci for migraine in Han Chinese resided in Taiwan.
Cephalalgia. Mar 01, 2018
Comprehensive human leukocyte antigen genotyping of patients with type 1 diabetes mellitus in Taiwan.
Pediatr Diabetes. Jan 31, 2018
A non-threshold region-specific method for detecting rare variants in complex diseases.
PLoS One Nov 30, 2017
Effects of sex and generation on hepatitis B viral load in families with hepatocellular carcinoma.
World J Gastroenterol. Feb 07, 2017
Methods for identifying differentially methylated regions for sequence- and array-based data.
Brief Funct Genomics. Nov 01, 2016
Susceptible genes of restless legs syndrome in migraine
CEPHALALGIA Oct 01, 2016
Using propensity score adjustment method in genetic association studies.
Comput Biol Chem. Jun 01, 2016
Haplotypes of the D-Amino Acid Oxidase Gene Are Significantly Associated with Schizophrenia and Its Neurocognitive Deficits.
PLoS One. Mar 17, 2016
A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples.
MOLECULAR PSYCHIATRY Sep 08, 2015
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study
Nature Communications Jul 07, 2015
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study.
Nat Commun. Jul 07, 2015
Genetic polymorphisms and tissue expression of interleukin-22 associated with risk and therapeutic response of gastric mucosa-associated lymphoid tissue lymphoma.
BLOOD CANCER JOURNAL Oct 10, 2014
A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease.
TRANSLATIONAL RESEARCH Jun 01, 2013
Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations
NATURE GENETICS Jul 15, 2012
Meta-analysis identifies common variants associated with body mass index in east Asians
NATURE GENETICS Feb 19, 2012
ANXA7, PPP3CB, DNAJC9, and ZMYND17 genes at chromosome 10q22 associated with the subgroup of schizophrenia with deficits in attention and executive function.
BIOLOGICAL PSYCHIATRY Jul 01, 2011
Genome-wide association study of bipolar I disorder in the Han Chinese population
MOLECULAR PSYCHIATRY Apr 13, 2010
A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese.
PLoS genetics Feb 19, 2010
Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling.
Hum Mutat. May 09, 2008
A genome-wide study of preferential amplification/hybridization in microarray-based pooled DNA experiments.
Nucleic Acids Research. Aug 23, 2006
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