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Academic Journal

Association study of six candidate genes with major depressive disorder in the North-Western population of Pakistan.

  • Authors : Alam N; School of Basic Medical Sciences, Health Science Center, Xi'an Jiaotong University, Xi'an, Shaanxi, China.; Department of Biotechnology and Genetic Engineering, Hazara University, Mansehra, Pakistan.

Subjects: Depressive Disorder, Major/Depressive Disorder, Major/Depressive Disorder, Major/*genetics ; Genes/Genes/Genes/*genetics ; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics

  • Source: PloS one [PLoS One] 2021 Aug 19; Vol. 16 (8), pp. e0248454. Date of Electronic Publication: 2021 Aug 19 (Print Publication: 2021).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

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Academic Journal

Association of IL16 polymorphisms with periodontitis in Brazilians: A case- control study.

  • Authors : Souza VH; Post-Graduation Program in Biosciences and Physiopathology, Department of Clinical Analysis and Biomedicine, and Laboratory of Immunogenetics, State University of Maringá, Maringá, Paraná, Brazil.; Department of Basic Health Sciences, State University of Maringá, Maringá, Paraná, Brazil.

Subjects: Genetic Predisposition to Disease*; Interleukin-16/Interleukin-16/Interleukin-16/*genetics ; Periodontitis/Periodontitis/Periodontitis/*genetics

  • Source: PloS one [PLoS One] 2020 Sep 11; Vol. 15 (9), pp. e0239101. Date of Electronic Publication: 2020 Sep 11 (Print Publication: 2020).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

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Academic Journal

Association of NOD2 and IFNG single nucleotide polymorphisms with leprosy in the Amazon ethnic admixed population.

  • Authors : Leturiondo AL; Programa de Pós-Graduação em Medicina Tropical, Universidade do Estado do Amazonas, Manaus, Brazil.; Laboratório de Biologia Molecular, Fundação Alfredo da Matta, Manaus, Brazil.

Subjects: Genetic Predisposition to Disease* ; Polymorphism, Single Nucleotide*; Interferon-gamma/Interferon-gamma/Interferon-gamma/*genetics

  • Source: PLoS neglected tropical diseases [PLoS Negl Trop Dis] 2020 May 20; Vol. 14 (5), pp. e0008247. Date of Electronic Publication: 2020 May 20 (Print Publication: 2020).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101291488 Publication Model: eCollection

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Academic Journal

A TNFSF13B functional variant is not involved in systemic sclerosis and giant cell arteritis susceptibility.

Subjects: Genetic Predisposition to Disease*; B-Cell Activating Factor/B-Cell Activating Factor/B-Cell Activating Factor/*genetics ; Giant Cell Arteritis/Giant Cell Arteritis/Giant Cell Arteritis/*genetics

  • Source: PloS one [PLoS One] 2018 Dec 26; Vol. 13 (12), pp. e0209343. Date of Electronic Publication: 2018 Dec 26 (Print Publication: 2018).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

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Academic Journal

A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1.

  • Authors : Chen Y; Genomics and Computational Biology Graduate Group, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.; Division of Human Genetics, Department of Pediatrics, at The Children's Hospital of Philadelphia, and The Perelman School of Medicine at The University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.

Subjects: Genetic Predisposition to Disease* ; Genome-Wide Association Study*; Biliary Atresia/Biliary Atresia/Biliary Atresia/*diagnosis

  • Source: PLoS genetics [PLoS Genet] 2018 Aug 13; Vol. 14 (8), pp. e1007532. Date of Electronic Publication: 2018 Aug 13 (Print Publication: 2018).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection

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Academic Journal

Malaria severity: Possible influence of the E670G PCSK9 polymorphism: A preliminary case-control study in Malian children.

  • Authors : Arama C; Malaria Research and Training Center, International Centers for Excellence in Research, Université des Sciences, des Techniques et des Technologies de Bamako, Bamako, Mali.; Diarra I

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

  • Source: PloS one [PLoS One] 2018 Feb 15; Vol. 13 (2), pp. e0192850. Date of Electronic Publication: 2018 Feb 15 (Print Publication: 2018).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

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Academic Journal

Genotype combination contributes to psoriasis: An exhaustive algorithm perspective.

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

Subjects: Algorithms* ; Genetic Predisposition to Disease*; Psoriasis/Psoriasis/Psoriasis/*genetics

  • Source: PloS one [PLoS One] 2017 Oct 11; Vol. 12 (10), pp. e0186067. Date of Electronic Publication: 2017 Oct 11 (Print Publication: 2017).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

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Academic Journal

Genetic analysis of indel markers in three loci associated with Parkinson's disease.

  • Authors : Huo Z; Department of Forensic Genetics and Biology, China Medical University, Shenyang North New Area, Shenyang, P.R., China.; Luo X

Subjects: Genetic Loci* ; Genetic Predisposition to Disease*; Carrier Proteins/Carrier Proteins/Carrier Proteins/*genetics

  • Source: PloS one [PLoS One] 2017 Sep 05; Vol. 12 (9), pp. e0184269. Date of Electronic Publication: 2017 Sep 05 (Print Publication: 2017).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

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Academic Journal

Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study.

  • Authors : Leo PJ; Institute of Health and Biomedical Innovation, Queensland University of Technology, Translational Research Institute, Princess Alexandra Hospital, Woolloongabba, Australia.; Madeleine MM

Subjects: Genetic Predisposition to Disease* ; Genome-Wide Association Study*; HLA-B Antigens/HLA-B Antigens/HLA-B Antigens/*genetics

  • Source: PLoS genetics [PLoS Genet] 2017 Aug 14; Vol. 13 (8), pp. e1006866. Date of Electronic Publication: 2017 Aug 14 (Print Publication: 2017).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection

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Academic Journal

The role of a FADS1 polymorphism in the association of fatty acid blood levels, BMI and blood pressure in young children-Analyses based on path models.

Subjects: Body Mass Index* ; Genetic Predisposition to Disease* ; Polymorphism, Single Nucleotide*

  • Source: PloS one [PLoS One] 2017 Jul 21; Vol. 12 (7), pp. e0181485. Date of Electronic Publication: 2017 Jul 21 (Print Publication: 2017).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection

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