المؤلفون: Phani NM; Department of Biotechnology, School of Life Sciences, Manipal University, Planetarium Complex, Manipal, 576104, Karnataka, India., Vohra M; Department of Biotechnology, School of Life Sciences, Manipal University, Planetarium Complex, Manipal, 576104, Karnataka, India., Rajesh S; Department of Biotechnology, School of Life Sciences, Manipal University, Planetarium Complex, Manipal, 576104, Karnataka, India., Adhikari P; Department of Medicine, Kasturba Medical College, Manipal University, Mangalore, 575001, Karnataka, India., Nagri SK; Department of Medicine, Kasturba Medical College, Manipal University, Manipal, 576104, Karnataka, India., D'Souza SC; Department of Medicine, Kasturba Medical College, Manipal University, Mangalore, 575001, Karnataka, India., Satyamoorthy K; Department of Biotechnology, School of Life Sciences, Manipal University, Planetarium Complex, Manipal, 576104, Karnataka, India., Rai PS; Department of Biotechnology, School of Life Sciences, Manipal University, Planetarium Complex, Manipal, 576104, Karnataka, India. padmalatha.rai@manipal.edu.

المصدر: Molecular genetics and genomics : MGG [Mol Genet Genomics] 2016 Feb; Vol. 291 (1), pp. 193-204. Date of Electronic Publication: 2015 Aug 05.

نوع المنشور: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't; Systematic Review

بيانات الدورية: Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 101093320 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1617-4623 (Electronic) Linking ISSN: 16174623 NLM ISO Abbreviation: Mol Genet Genomics Subsets: MEDLINE

مواضيع طبية MeSH: Adiponectin/*genetics , Asian People/*genetics , Diabetes Mellitus, Type 2/*genetics , Genetic Predisposition to Disease/*genetics , Obesity/*genetics , PPAR gamma/*genetics , Polymorphism, Single Nucleotide/*genetics , Proteins/*genetics, Adiposity/genetics ; Alpha-Ketoglutarate-Dependent Dioxygenase FTO ; Case-Control Studies ; Female ; Humans ; India ; Male ; Middle Aged

المؤلفون: Fernandes RC; Department of Biotechnology, School of Life Sciences, Planetarium Complex, Manipal University, Manipal, Karnataka, 576104, India., Hasan M, Gupta H, Geetha K, Rai PS, Hande MH, D'Souza SC, Adhikari P, Brand A, Satyamoorthy K

المصدر: Molecular genetics and genomics : MGG [Mol Genet Genomics] 2015 Jun; Vol. 290 (3), pp. 1155-68. Date of Electronic Publication: 2015 Jan 09.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 101093320 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1617-4623 (Electronic) Linking ISSN: 16174623 NLM ISO Abbreviation: Mol Genet Genomics Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Variation*, Asian People/*genetics , Catalase/*genetics , Glutathione Transferase/*genetics , Malaria/*genetics , Superoxide Dismutase/*genetics, Adult ; Antioxidants/metabolism ; Case-Control Studies ; Female ; Genetic Predisposition to Disease ; Genotype ; Glutathione S-Transferase pi/genetics ; Humans ; India ; Malaria/enzymology ; Male ; Middle Aged ; Polymorphism, Restriction Fragment Length ; Polymorphism, Single Nucleotide/genetics ; Risk Factors ; Young Adult

المؤلفون: Kotambail A; aDepartment of Biotechnology, School of Life Sciences bDepartment of Psychiatry, Kasturba Medical College, Manipal University, Manipal, Karnataka, India., Mathur A, Bhat SM, Rai PS, Sharma PS, Satyamoorthy K

المصدر: Psychiatric genetics [Psychiatr Genet] 2015 Feb; Vol. 25 (1), pp. 39-40.

نوع المنشور: Letter; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9106748 Publication Model: Print Cited Medium: Internet ISSN: 1473-5873 (Electronic) Linking ISSN: 09558829 NLM ISO Abbreviation: Psychiatr Genet Subsets: MEDLINE

مواضيع طبية MeSH: Antipsychotic Agents/*therapeutic use , Asian People/*genetics , Bipolar Disorder/*drug therapy , Bipolar Disorder/*genetics , Carboxy-Lyases/*genetics , Lithium Compounds/*therapeutic use, Case-Control Studies ; Genetic Association Studies ; Genotype ; Humans ; India ; Polymorphism, Single Nucleotide

المؤلفون: Phani NM; Division of Biotechnology, School of Life Sciences, Manipal University, Manipal, Karnataka, India., Guddattu V; Department of Statistics, Manipal University, Manipal, Karnataka, India., Bellampalli R; Division of Biotechnology, School of Life Sciences, Manipal University, Manipal, Karnataka, India., Seenappa V; Division of Biotechnology, School of Life Sciences, Manipal University, Manipal, Karnataka, India., Adhikari P; Department of Medicine, Kasturba Medical College, Manipal University, Mangalore, Karnataka, India., Nagri SK; Department of Medicine, Kasturba Medical College, Manipal University, Manipal, Karnataka, India., D Souza SC; Department of Medicine, Kasturba Medical College, Manipal University, Mangalore, Karnataka, India., Mundyat GP; Division of Biotechnology, School of Life Sciences, Manipal University, Manipal, Karnataka, India., Satyamoorthy K; Division of Biotechnology, School of Life Sciences, Manipal University, Manipal, Karnataka, India., Rai PS; Division of Biotechnology, School of Life Sciences, Manipal University, Manipal, Karnataka, India.

المصدر: PloS one [PLoS One] 2014 Sep 23; Vol. 9 (9), pp. e107021. Date of Electronic Publication: 2014 Sep 23 (Print Publication: 2014).

نوع المنشور: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't; Review; Systematic Review

بيانات الدورية: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE

مواضيع طبية MeSH: Asian People/*genetics , Diabetes Mellitus, Type 2/*ethnology , Diabetes Mellitus, Type 2/*genetics , Potassium Channels, Inwardly Rectifying/*genetics , White People/*genetics, Adult ; Aged ; Case-Control Studies ; DNA Copy Number Variations ; Genetic Association Studies ; Genetic Predisposition to Disease ; Genetic Variation ; Humans ; India ; Middle Aged ; Polymorphism, Single Nucleotide