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Triphalangeal thumb–polysyndactyly syndrome and syndactyly type IV are caused by genomic duplications involving the long range, limb-specific SHH enhancer

Journal of medical genetics, 2008-09, Vol.45 (9), p.589-595

2008

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Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia

British journal of dermatology (1951), 2008-03, Vol.158 (3), p.614-617

2008

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Two novel mutations and evidence for haploinsufficiency of the ADAR gene in dyschromatosis symmetrica hereditaria

British journal of dermatology (1951), 2006-04, Vol.154 (4), p.636-642

2006

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Polymorphic microsatellites and Wilson disease (WD)

American journal of human genetics, 1993-10, Vol.53 (4), p.864-873

1993

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Lean techniques for the improvement of patients’ flow in emergency department

World journal of emergency medicine, 2014-01, Vol.5 (1), p.24-28

2014

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Samaritan donor interchange in living donor liver transplantation

Hepatobiliary & pancreatic diseases international, 2014-02, Vol.13 (1), p.105-109

2014

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Modulation of graft vascular inflow guided by flowmetry and manometry in liver transplantation

Hepatobiliary & pancreatic diseases international, 2011-12, Vol.10 (6), p.649-656

2011

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Another pedigree with pure autosomal dominant spastic paraplegia (AD-FSP) from Tibet mapping to 14q11.2-q24.3

Human genetics, 1997-10, Vol.100 (5-6), p.620-623

1997

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Founder Effect of a Prevalent Phenylketonuria Mutation in the Oriental Population

Proceedings of the National Academy of Sciences - PNAS, 1991-03, Vol.88 (6), p.2146-2150

1991

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Missense mutations prevalent in orientals with phenylketonuria: Molecular characterization and clinical implications

Genomics (San Diego, Calif.), 1991-06, Vol.10 (2), p.449-456

1991

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Molecular genetics of phenylketonuria in Orientals: linkage disequilibrium between a termination mutation and haplotype 4 of the phenylalanine hydroxylase gene

American journal of human genetics, 1989-11, Vol.45 (5), p.675-680

1989

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The Spectrum of β-Thalassemia Genes in China and Southeast Asia

Blood, 1986-10, Vol.68 (4), p.964-966

1986

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The same TATA box β-thalassemia mutation in Chinese and US blacks: another example of independent origins of mutation

Human genetics, 1986-10, Vol.74 (2), p.162-164

1986

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Review of Silicon Photonics Technology and Platform Development

Journal of lightwave technology, 2021-07, Vol.39 (13), p.4374-4389

2021

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Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU)

American journal of human genetics, 1989-08, Vol.45 (2), p.319-324

1989

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Real-world COVID-19 vaccine effectiveness against the Omicron BA.2 variant in a SARS-CoV-2 infection-naive population

Nature medicine, 2023-02, Vol.29 (2), p.348-357

2023

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Cloning and Sequencing of a β-Thalassemia Gene from South China

Hemoglobin, 1988, Vol.12 (5-6), p.615-619

1988

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β-Thalassemia in China: a Systematic Molecular Characterization of β-Thalassemia Mutations

Hemoglobin, 1988, Vol.12 (5-6), p.621-628

1988

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Identification of three novel PKU mutations among Chinese: Evidence for recombination or recurrent mutation at the PAH locus

Genomics (San Diego, Calif.), 1992, Vol.13 (1), p.230-231

1992

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Identification of three novel missense PKU mutations among Chinese

Genomics (San Diego, Calif.), 1992-07, Vol.13 (3), p.894-895

1992

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A randomized controlled trial on the psychophysiological effects of physical exercise and Tai-chi in patients with chronic schizophrenia

Schizophrenia research, 2016-03, Vol.171 (1), p.42-49

2016

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Identification of a novel phyenylketonuria (PKU) mutation in the Chinese : further evidence for multiple origins of PKU in Asia

American journal of human genetics, 1991, Vol.48 (3), p.628-630

1991

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Revealing the role of SPP1 + macrophages in glioma prognosis and therapeutic targeting by investigating tumor-associated macrophage landscape in grade 2 and 3 gliomas

Cell & bioscience, 2024-03, Vol.14 (1), p.37-37, Article 37

2024

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Modeling biogas production from organic fraction of MSW co-digested with MSWI ashes in anaerobic bioreactors

Bioresource technology, 2010-08, Vol.101 (16), p.6329-6335

2010

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Non‐invasive prenatal testing for fetal chromosomal abnormalities by low‐coverage whole‐genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center

Ultrasound in obstetrics & gynecology, 2014-03, Vol.43 (3), p.254-264

2014

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Triphalangeal thumb–polysyndactyly syndrome and syndactyly type IV are caused by genomic duplications involving the long range, limb-specific SHH enhancer

Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia

Two novel mutations and evidence for haploinsufficiency of the ADAR gene in dyschromatosis symmetrica hereditaria

Polymorphic microsatellites and Wilson disease (WD)

Lean techniques for the improvement of patients’ flow in emergency department

Samaritan donor interchange in living donor liver transplantation

Modulation of graft vascular inflow guided by flowmetry and manometry in liver transplantation

Another pedigree with pure autosomal dominant spastic paraplegia (AD-FSP) from Tibet mapping to 14q11.2-q24.3

Founder Effect of a Prevalent Phenylketonuria Mutation in the Oriental Population

Missense mutations prevalent in orientals with phenylketonuria: Molecular characterization and clinical implications

Molecular genetics of phenylketonuria in Orientals: linkage disequilibrium between a termination mutation and haplotype 4 of the phenylalanine hydroxylase gene

The Spectrum of β-Thalassemia Genes in China and Southeast Asia

The same TATA box β-thalassemia mutation in Chinese and US blacks: another example of independent origins of mutation

Review of Silicon Photonics Technology and Platform Development

Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU)

Real-world COVID-19 vaccine effectiveness against the Omicron BA.2 variant in a SARS-CoV-2 infection-naive population

Cloning and Sequencing of a β-Thalassemia Gene from South China

β-Thalassemia in China: a Systematic Molecular Characterization of β-Thalassemia Mutations

Identification of three novel PKU mutations among Chinese: Evidence for recombination or recurrent mutation at the PAH locus

Identification of three novel missense PKU mutations among Chinese

A randomized controlled trial on the psychophysiological effects of physical exercise and Tai-chi in patients with chronic schizophrenia

Identification of a novel phyenylketonuria (PKU) mutation in the Chinese : further evidence for multiple origins of PKU in Asia

Revealing the role of SPP1 + macrophages in glioma prognosis and therapeutic targeting by investigating tumor-associated macrophage landscape in grade 2 and 3 gliomas

Modeling biogas production from organic fraction of MSW co-digested with MSWI ashes in anaerobic bioreactors

Non‐invasive prenatal testing for fetal chromosomal abnormalities by low‐coverage whole‐genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center

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