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Application of a flipped classroom teaching model based on micro-videos in the standardized training of dermatological residents in China

Frontiers in medicine, 2023-10, Vol.10, p.1250168-1250168

2023

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Validation of Susceptibility Loci for Vitiligo Identified by GWAS in the Chinese Han Population

Frontiers in genetics, 2020-12, Vol.11, p.542275-542275

2020

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E-selectin rs5361 and FCGR2A rs1801274 variants were associated with increased risk of gastric cancer in a Chinese population

Molecular carcinogenesis, 2012-08, Vol.51 (8), p.597-607

2012

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Association analysis of single nucleotide polymorphisms at five loci: comparison between atopic dermatitis and asthma in the Chinese Han population

PloS one, 2012-04, Vol.7 (4), p.e35334-e35334

2012

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Genome-wide association study identifies two new susceptibility loci for atopic dermatitis in the Chinese Han population

Nature genetics, 2011-07, Vol.43 (7), p.690-694

2011

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Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21

Nature genetics, 2009-02, Vol.41 (2), p.205-210

2009

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Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC

Nature genetics, 2010-07, Vol.42 (7), p.614-618

2010

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Association analyses identifying two common susceptibility loci shared by psoriasis and systemic lupus erythematosus in the Chinese Han population

Journal of medical genetics, 2013-12, Vol.50 (12), p.812-818

2013

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One Mutation of the ED1 Gene in a Chinese Han Family with X-Linked Hypohidrotic Ectodermal Dysplasia

Annals of Dermatology, 2014, 26(1), , pp.111-113

2014

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Identification of a Missense Variant in LNPEP that Confers Psoriasis Risk

Journal of investigative dermatology, 2014-02, Vol.134 (2), p.359-365

2014

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Association Analyses Identify Three Susceptibility Loci for Vitiligo in the Chinese Han Population

Journal of investigative dermatology, 2013-02, Vol.133 (2), p.403-410

2013

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Association analyses confirm five susceptibility loci for systemic lupus erythematosus in the Han Chinese population

Arthritis research & therapy, 2015-03, Vol.17 (1), p.85-85, Article 85

2015

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Variants in TNFSF4, TNFAIP3, TNIP1, BLK, SLC15A4 and UBE2L3 interact to confer risk of systemic lupus erythematosus in Chinese population

Rheumatology international, 2014-04, Vol.34 (4), p.459-464

2014

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Exome sequencing identifies a COL14A1 mutation in a large Chinese pedigree with punctate palmoplantar keratoderma

Journal of medical genetics, 2012-09, Vol.49 (9), p.563-568

2012

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Association analyses identify two susceptibility loci 5q31 and 5q22.1 for atopic dermatitis in Chinese Han population

Asian Pacific journal of allergy and immunology, 2017-12, Vol.35 (4), p.196-202

2017

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Exome sequencing identified a missense mutation of EPS8L3 in Marie Unna hereditary hypotrichosis

Journal of medical genetics, 2012-12, Vol.49 (12), p.727-730

2012

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Association of the chromosome 11p13.5 variant and atopic dermatitis with a family history of atopy in the Chinese Han population

Asian Pacific journal of allergy and immunology, 2016-06, Vol.34 (2), p.109-114

2016

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A novel missense mutation of keratin 17 gene in a chinese family with steatocystoma multiplex

Annals of Dermatology, 2013, 25(4), , pp.508-510

2013

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A simple oligonucleotide biochip capable of rapidly detecting known mitochondrial DNA mutations in Chinese patients with Leber's hereditary optic neuropathy (LHON)

Disease markers, 2011-01, Vol.30 (4), p.181-190

2011

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Agricultural GMO safety administration in China

Journal of Integrative Agriculture, 2015-11, Vol.14 (11), p.2157-2165

2015

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Development of a DNA biochip for detection of known mtDNA mutations associated with MELAS and MERRF syndromes.

Yíchuán, 2008-10, Vol.30 (10), p.1279

2008

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Exome sequencing identifies MVK mutations in disseminated superficial actinic porokeratosis

Nature genetics, 2012-10, Vol.44 (10), p.1156-1160

2012

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LETTER TO THE EDITOR : One Mutation of the ED1 Gene in a Chinese Han Family with X-Linked Hypohidrotic Ectodermal Dysplasia

Annals of dermatology, 2014-02, Vol.26 (1), p.111

2014

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One Mutation of the ED1 Gene in a Chinese Han Family with X-Linked Hypohidrotic Ectodermal Dysplasia

Annals of dermatology, 2014-02, p.111-113

2014

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A Novel Missense Mutation of Keratin 17 Gene in a Chinese Family with Steatocystoma Multiplex

Annals of dermatology, 2013-11, Vol.25 (4), p.508-510

2013

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Application of a flipped classroom teaching model based on micro-videos in the standardized training of dermatological residents in China

Validation of Susceptibility Loci for Vitiligo Identified by GWAS in the Chinese Han Population

E-selectin rs5361 and FCGR2A rs1801274 variants were associated with increased risk of gastric cancer in a Chinese population

Association analysis of single nucleotide polymorphisms at five loci: comparison between atopic dermatitis and asthma in the Chinese Han population

Genome-wide association study identifies two new susceptibility loci for atopic dermatitis in the Chinese Han population

Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21

Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC

Association analyses identifying two common susceptibility loci shared by psoriasis and systemic lupus erythematosus in the Chinese Han population

One Mutation of the ED1 Gene in a Chinese Han Family with X-Linked Hypohidrotic Ectodermal Dysplasia

Identification of a Missense Variant in LNPEP that Confers Psoriasis Risk

Association Analyses Identify Three Susceptibility Loci for Vitiligo in the Chinese Han Population

Association analyses confirm five susceptibility loci for systemic lupus erythematosus in the Han Chinese population

Variants in TNFSF4, TNFAIP3, TNIP1, BLK, SLC15A4 and UBE2L3 interact to confer risk of systemic lupus erythematosus in Chinese population

Exome sequencing identifies a COL14A1 mutation in a large Chinese pedigree with punctate palmoplantar keratoderma

Association analyses identify two susceptibility loci 5q31 and 5q22.1 for atopic dermatitis in Chinese Han population

Exome sequencing identified a missense mutation of EPS8L3 in Marie Unna hereditary hypotrichosis

Association of the chromosome 11p13.5 variant and atopic dermatitis with a family history of atopy in the Chinese Han population

A novel missense mutation of keratin 17 gene in a chinese family with steatocystoma multiplex

A simple oligonucleotide biochip capable of rapidly detecting known mitochondrial DNA mutations in Chinese patients with Leber's hereditary optic neuropathy (LHON)

Agricultural GMO safety administration in China

Development of a DNA biochip for detection of known mtDNA mutations associated with MELAS and MERRF syndromes.

Exome sequencing identifies MVK mutations in disseminated superficial actinic porokeratosis

LETTER TO THE EDITOR : One Mutation of the ED1 Gene in a Chinese Han Family with X-Linked Hypohidrotic Ectodermal Dysplasia

One Mutation of the ED1 Gene in a Chinese Han Family with X-Linked Hypohidrotic Ectodermal Dysplasia

A Novel Missense Mutation of Keratin 17 Gene in a Chinese Family with Steatocystoma Multiplex

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