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Academic Journal

Identification of Coding Variants in 10q22.1 Associated with Vitiligo in the Chinese Han Population.

  • Authors : Tang X; Department of Dermatology and Institute of Dermatology at No. 1 Hospital, Anhui Medical University, Hefei, China.; Key Laboratory of Dermatology, Ministry of Education, Hefei, China.

Subjects: Vitiligo*/Vitiligo*/Vitiligo*/genetics; Humans ; Genome-Wide Association Study

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2024 Mar; Vol. 28 (3), pp. 123-130.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Genetic Association Study Between the COL11A1 and COL18A1 Genes and High Myopia in a Han Chinese Population.

  • Authors : Wu H; 1 Sichuan Provincial Key Laboratory for Human Disease Gene Study, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China , Chengdu, China .; 2 Department of Laboratory Medicine, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital , Chengdu, China .

Subjects: Genome-Wide Association Study*; Asian People/Asian People/Asian People/*genetics ; Collagen Type VIII/Collagen Type VIII/Collagen Type VIII/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2018 Jun; Vol. 22 (6), pp. 359-365. Date of Electronic Publication: 2018 May 21.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

A Common Variant at 11q23.3 Is Associated with Susceptibility to Atopic Dermatitis in the Han Chinese Population.

  • Authors : Li Y; Department of Dermatology, First Affiliated Hospital, Anhui Medical University, Hefei, China.; Key Laboratory of Dermatology (Anhui Medical University), Ministry of Education, Hefei, China.

Subjects: Genetic Loci* ; Genetic Predisposition to Disease*; Chromosomes, Human, Pair 11/Chromosomes, Human, Pair 11/Chromosomes, Human, Pair 11/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2021 Oct; Vol. 25 (10), pp. 638-645. Date of Electronic Publication: 2021 Oct Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Association Analysis Between Common Variants of the TRPM1 Gene and Three Mental Disorders in the Han Chinese Population.

  • Authors : Ma C; Department of Biology, School of Life Science, Anhui Medical University, Hefei, China.; Li X

Subjects: Mental Disorders/Mental Disorders/Mental Disorders/*genetics ; TRPM Cation Channels/TRPM Cation Channels/TRPM Cation Channels/*genetics; Adult

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2020 Oct; Vol. 24 (10), pp. 649-657. Date of Electronic Publication: 2020 Oct Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Copy Number Variation in MUC5AC and Susceptibility to Allergic Rhinitis: A Low-Coverage Whole-Genome Sequencing and Validation Cohort Study.

  • Authors : Wang Y; Department of Otolaryngology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.; Li L

Subjects: Mucin 5AC/Mucin 5AC/Mucin 5AC/*genetics ; Rhinitis, Allergic/Rhinitis, Allergic/Rhinitis, Allergic/*genetics; Adult

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2020 Apr; Vol. 24 (4), pp. 173-180. Date of Electronic Publication: 2020 Mar 25.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Association of EPHA3 Gene Polymorphisms with Nonsyndromic Cleft Lip With or Without Cleft Palate.

  • Authors : Chen R; 1 Department of Oral and Maxillofacial Plastic and Traumatic Surgery, Beijing Stomatological Hospital, Capital Medical University , Beijing, China .; Guo S

Subjects: Brain/Brain/Brain/*abnormalities ; Cleft Lip/Cleft Lip/Cleft Lip/*genetics ; Cleft Palate/Cleft Palate/Cleft Palate/*genetics Orofacial Cleft 1

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2018 Jul; Vol. 22 (7), pp. 420-424. Date of Electronic Publication: 2018 Jun 22.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Common Variants in ALPL Gene Contribute to the Risk of Kidney Stones in the Han Chinese Population.

  • Authors : Li X; 1 Department of Emergency Surgery, Shaanxi Provincial People's Hospital , Xi'an, Shaanxi, China .; Dang X

Subjects: Genetic Predisposition to Disease* ; Polymorphism, Single Nucleotide*; Alkaline Phosphatase/Alkaline Phosphatase/Alkaline Phosphatase/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2018 Mar; Vol. 22 (3), pp. 187-192. Date of Electronic Publication: 2018 Feb 28.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Association Analysis of Single Nucleotide Polymorphisms in C1QTNF6, RAC2, and an Intergenic Region at 14q32.2 with Graves' Disease in Chinese Han Population.

  • Authors : Zhang XH; 1 Ruijin Hospital, Shanghai Jiao Tong University School of Medicine , Shanghai, China .; 2 Shanghai-Ministry of Science and Technology (MOST) Key Laboratory of Health and Disease Genomics, Department of Genetics, Chinese National Human Genome Center and Shanghai Industrial Technology Institute (SITI) , Shanghai, China .

Subjects: Collagen/Collagen/Collagen/*genetics ; Graves Disease/Graves Disease/Graves Disease/*genetics ; rac GTP-Binding Proteins/rac GTP-Binding Proteins/rac GTP-Binding Proteins/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2017 Aug; Vol. 21 (8), pp. 479-484. Date of Electronic Publication: 2017 Jun 30.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

The KSR2-rs7973260 Polymorphism is Associated with Metabolic Phenotypes, but Not Psychological Phenotypes, in Chinese Elders.

  • Authors : Wang Y; 1 Rugao People's Hospital , Rugao, China .; Ma T

Subjects: Depression/Depression/Depression/*genetics ; Protein Serine-Threonine Kinases/Protein Serine-Threonine Kinases/Protein Serine-Threonine Kinases/*genetics; Aged

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2017 Jul; Vol. 21 (7), pp. 416-421. Date of Electronic Publication: 2017 May 24.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Association Between Three SNPs and Thromboangiitis Obliterans in Xinjiang Uyghur Population.

  • Authors : Shi ZF; 1 Xinjiang Medical University , Xinjiang, China .; 2 Department of Vascular Surgery, People's Hospital of Xinjiang Uygur Autonomous Region , Urumqi, Xinjiang, China .

Subjects: Asian People*/Asian People*/Asian People*/ethnology ; Asian People*/Asian People*/Asian People*/genetics ; Genetic Predisposition to Disease*

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2016 Feb; Vol. 20 (2), pp. 55-62. Date of Electronic Publication: 2016 Feb 01.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic Cited Medium: Internet

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  • 1-10 of  11 results for ""Genome-Wide Association Study""