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Predictive factors for central lymph node and lateral cervical lymph node metastases in papillary thyroid carcinoma

Clinical & translational oncology, 2019-11, Vol.21 (11), p.1482-1491

2019

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Gene-gene interactions between HLA-C, ERAP1, TNFAIP3 and TRAF3IP2 and the risk of psoriasis in the Chinese Han population

British journal of dermatology (1951), 2013-10, Vol.169 (4), p.941-943

2013

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Association of UBASH3A gene polymorphism and atopic dermatitis in the Chinese Han population

Genes and immunity, 2017-09, Vol.18 (3), p.158-162

2017

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TNIP1, SLC15A4, ETS1, RasGRP3 and IKZF1 are associated with clinical features of systemic lupus erythematosus in a Chinese Han population

Lupus, 2010-09, Vol.19 (10), p.1181-1186

2010

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Multiple variants in 5q31.1 are associated with systemic lupus erythematosus susceptibility and subphenotypes in the Han Chinese population

British journal of dermatology (1951), 2017-09, Vol.177 (3), p.801-808

2017

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Progressive symmetrical erythrokeratoderma: report of two Chinese families and evaluation for mutations in the loricrin, connexin 30.3 and connexin 31 genes

Clinical and experimental dermatology, 2013-12, Vol.38 (8), p.925-927

2013

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Genetic variants of the genes encoding zinc finger protein 313 and interleukin-13 confer a risk for psoriasis in a Chinese Uygur population

Clinical and experimental dermatology, 2013-10, Vol.38 (7), p.768-774

2013

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Childhood psoriasis: a study of 277 patients from China

Journal of the European Academy of Dermatology and Venereology, 2007-07, Vol.21 (6), p.762-765

2007

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A novel frameshift mutation of the EDA1 gene in a Chinese Han family with X-linked hypohidrotic ectodermal dysplasia

Clinical and experimental dermatology, 2009-01, Vol.34 (1), p.74-76

2009

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Utility of the neutrophil/lymphocyte ratio for predicting malignancy risk and prognosis in patients with dermatomyositis

Clinical and experimental dermatology, 2020-06, Vol.45 (4), p.471-473

2020

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Two novel CYLD gene mutations in Chinese families with trichoepithelioma and a literature review of 16 families with trichoepithelioma reported in China

British journal of dermatology (1951), 2005-12, Vol.153 (6), p.1213-1215

2005

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A missense mutation in the GJB3 gene responsible for erythrokeratodermia variabilis in a Chinese family

Clinical and experimental dermatology, 2012-12, Vol.37 (8), p.919-921

2012

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Follow-up analysis of 180 Chinese Han families: identification of a novel locus for psoriasis at 2p22.3-11.2

British journal of dermatology (1951), 2008-03, Vol.158 (3), p.512-517

2008

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Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1

Journal of dermatological science, 2010-12, Vol.60 (3), p.193-196

2010

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Requirement for Hippocampal CA3 NMDA Receptors in Associative Memory Recall

Science (American Association for the Advancement of Science), 2002-07, Vol.297 (5579), p.211-218

2002

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The familial risk of acne vulgaris in Chinese Hans - a case-control study

Journal of the European Academy of Dermatology and Venereology, 2007-05, Vol.21 (5), p.602-605

2007

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Novel missense mutation of keratin in Chinese family with steatocystoma multiplex

Journal of the European Academy of Dermatology and Venereology, 2009-06, Vol.23 (6), p.723-724

2009

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Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3

British journal of dermatology (1951), 2004-05, Vol.150 (5), p.837-842

2004

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Formation of Temporal Memory Requires NMDA Receptors within CA1 Pyramidal Neurons

Neuron (Cambridge, Mass.), 2000-02, Vol.25 (2), p.473-480

2000

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A novel deletion mutation in the LPAR6 gene underlies autosomal recessive woolly hair with hypotrichosis

Clinical and experimental dermatology, 2013-10, Vol.38 (7), p.796-798

2013

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Comparison of clinical features of HLA-Cw0602-positive and -negative psoriasis patients in a han chinese population

Acta dermato-venereologica, 2007, Vol.87 (4), p.335-340

2007

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A single-nucleotide polymorphism rs4639966 in 11q23.3 is associated with clinical features of systemic lupus erythematosus in the Chinese population

Lupus, 2012-12, Vol.21 (14), p.1538-1542

2012

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Genetic variant rs4982958 at 14q11.2 is associated with allergic rhinitis in a Chinese Han population running title: 14q11.2 is a susceptibility locus for allergic rhinitis

Journal of investigational allergology & clinical immunology, 2012, Vol.22 (1), p.55-62

2012

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Genetic polymorphisms of superoxide dismutases, catalase, and glutathione peroxidase in age-related cataract

Molecular vision, 2011, Vol.17, p.2325-2332

2011

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Association of HLA-DRB1 alleles with keloids in Chinese Han individuals

Tissue antigens, 2010-10, Vol.76 (4), p.276-281

2010

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Predictive factors for central lymph node and lateral cervical lymph node metastases in papillary thyroid carcinoma

Gene-gene interactions between HLA-C, ERAP1, TNFAIP3 and TRAF3IP2 and the risk of psoriasis in the Chinese Han population

Association of UBASH3A gene polymorphism and atopic dermatitis in the Chinese Han population

TNIP1, SLC15A4, ETS1, RasGRP3 and IKZF1 are associated with clinical features of systemic lupus erythematosus in a Chinese Han population

Multiple variants in 5q31.1 are associated with systemic lupus erythematosus susceptibility and subphenotypes in the Han Chinese population

Progressive symmetrical erythrokeratoderma: report of two Chinese families and evaluation for mutations in the loricrin, connexin 30.3 and connexin 31 genes

Genetic variants of the genes encoding zinc finger protein 313 and interleukin-13 confer a risk for psoriasis in a Chinese Uygur population

Childhood psoriasis: a study of 277 patients from China

A novel frameshift mutation of the EDA1 gene in a Chinese Han family with X-linked hypohidrotic ectodermal dysplasia

Utility of the neutrophil/lymphocyte ratio for predicting malignancy risk and prognosis in patients with dermatomyositis

Two novel CYLD gene mutations in Chinese families with trichoepithelioma and a literature review of 16 families with trichoepithelioma reported in China

A missense mutation in the GJB3 gene responsible for erythrokeratodermia variabilis in a Chinese family

Follow-up analysis of 180 Chinese Han families: identification of a novel locus for psoriasis at 2p22.3-11.2

Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1

Requirement for Hippocampal CA3 NMDA Receptors in Associative Memory Recall

The familial risk of acne vulgaris in Chinese Hans - a case-control study

Novel missense mutation of keratin in Chinese family with steatocystoma multiplex

Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3

Formation of Temporal Memory Requires NMDA Receptors within CA1 Pyramidal Neurons

A novel deletion mutation in the LPAR6 gene underlies autosomal recessive woolly hair with hypotrichosis

Comparison of clinical features of HLA-Cw0602-positive and -negative psoriasis patients in a han chinese population

A single-nucleotide polymorphism rs4639966 in 11q23.3 is associated with clinical features of systemic lupus erythematosus in the Chinese population

Genetic variant rs4982958 at 14q11.2 is associated with allergic rhinitis in a Chinese Han population running title: 14q11.2 is a susceptibility locus for allergic rhinitis

Genetic polymorphisms of superoxide dismutases, catalase, and glutathione peroxidase in age-related cataract

Association of HLA-DRB1 alleles with keloids in Chinese Han individuals

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