Chi‐fan Yang

发表

Involvement of tonB-exbBD1D2 operon in infection of Xanthomonas campestris phage phi L7.

Y. Tseng, C. Hung, Chiou-Ying Yang, 2003, Biochemical and biophysical research communications.

Insertion/deletion mutations of type I oculocutaneous albinism in Chinese patients from Taiwan

Chang-Hai Tsai, Jer-Yuarn Wu, Shuan-Pei Lin, 1999, Human mutation.

Germline breast cancer susceptibility gene mutations and breast cancer outcomes

A. Yang, Hung-Pin Peng, J. Jian, 2018, BMC Cancer.

Filamin B Loss‐of‐Function Mutation in Dimerization Domain Causes Autosomal‐Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies

F. Tsai, Yuan-Tsong Chen, Jer-Yuarn Wu, 2017, Human mutation.

A Genome-Wide Association Study Identifies Susceptibility Variants for Type 2 Diabetes in Han Chinese

Fuu-Jen Tsai, Lee-Ming Chuang, Yuan-Tsong Chen, 2010, PLoS genetics.

Towards a reference genome that captures global genetic diversity

David I. K. Martin, P. Kwok, M. Xiao, 2020, Nature Communications.

Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients

F. Tsai, Chang-Hai Tsai, Jer-Yuarn Wu, 2001, Pediatrics international : official journal of the Japan Pediatric Society.

PSORS2 is due to mutations in CARD14.

A. Bowcock, W. Hwu, Cailin E. Joyce, 2012, American Journal of Human Genetics.

A siRNA targets and inhibits a broad range of SARS‐CoV‐2 infections including Delta variant

Pan‐Chyr Yang, Ya-Min Tsai, Sui‐Yuan Chang, 2022, EMBO molecular medicine.

Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.

Yuan-Tsong Chen, Jer-Yuarn Wu, Yu-Hung Wu, 2018, American journal of human genetics.

Homozygosity Mapping and Whole-Genome Sequencing Links a Missense Mutation in POMGNT1 to Autosomal Recessive Retinitis Pigmentosa.

Shih-Jen Chen, Yuan-Tsong Chen, Chien-Hsiun Chen, 2016, Investigative ophthalmology & visual science.

Pharmacogenetics of dipeptidyl peptidase 4 inhibitors in a Taiwanese population with type 2 diabetes

W. Sheu, I. Lee, F. Tsai, 2017, Oncotarget.

A novel mutation (Q239R) identified in a Taiwan Chinese patient with type VI mucopolysaccharidosis (Maroteaux‐Lamy syndrome)

F. Tsai, Jer-Yuarn Wu, J. Chang, 2000, Human mutation.

Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association

F. Tsai, Chang-Hai Tsai, Jer-Yuarn Wu, 2000, Journal of Human Genetics.

Mutation analysis of Wilson disease in Taiwan and description of six new mutations

F. Tsai, Y. Jong, Chang-Hai Tsai, 1998, Human mutation.

Identification of a polymorphism (G83S) in the TWIST gene in Taiwanese

Jer-Yuarn Wu, Cheng-Chun Lee, Chi‐fan Yang, 2000 .

GENOME-WIDE ASSOCIATION STUDY META-ANALYSIS REVEALS TRANS-ETHNIC REPLICATION OF MEAN ARTERIAL AND PULSE PRESSURE LOCI

Cai, Y. J. Kim, Y. Teo, 2022 .

Three novel beta-galactosidase gene mutations in Han Chinese patients with GM1 gangliosidosis are correlated with disease severity

F. Tsai, Jer-Yuarn Wu, Chi-fan Yang, 2010, Journal of Biomedical Science.

A promoter sequence variant of ZNF750 is linked with familial psoriasis.

Y. Chien, W. Hwu, Yuan-Tsong Chen, 2008, The Journal of investigative dermatology.

Germline breast cancer susceptibility gene mutations and breast cancer outcomes

A. Yang, Hung-Pin Peng, J. Jian, 2018, BMC Cancer.

Genome-Wide Association Study Meta-Analysis Reveals Transethnic Replication of Mean Arterial and Pulse Pressure Loci

Cai, Y. J. Kim, Korea, 2013, Hypertension.

Genome-Wide Association Study Meta-Analysis Reveals Transethnic Replication of Mean Arterial and Pulse Pressure Loci

Cai, Y. J. Kim, Japan., 2013, Hypertension.

Mucopolysaccharidosis type VI: Report of two Taiwanese patients and identification of one novel mutation.

F. Tsai, Jer-Yuarn Wu, S. P. Lin, 2001, Journal of the Formosan Medical Association = Taiwan yi zhi.

PSORS2 is due to mutations in CARD14.

A. Bowcock, W. Hwu, Cailin E. Joyce, 2012, American journal of human genetics.

A novel in‐frame deletion mutation (c106‐111del) identified in a Taiwan Chinese patient with type IVA mucopolysaccharidosis

Jer-Yuarn Wu, Shuan-Pei Lin, Cheng-Chun Lee, 2001, Human mutation.