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Whole genome expression and biochemical correlates of extreme constitutional types defined in AyurvedaEGLN1 involvement in high-altitude adaptation revealed through genetic analysis of extreme constitution types defined in Ayurveda.Complex patterns of genomic admixture within southern AfricaCombined genetic effects of EGLN1 and VWF modulate thrombotic outcome in hypoxia revealed by Ayurgenomics approachFootprints of genetic susceptibility to pulmonary tuberculosis: cytokine gene variants in north IndiansThe Indian Genome Variation database (IGVdb): a project overview.Polymorphisms of TNF-enhancer and gene for FcgammaRIIa correlate with the severity of falciparum malaria in the ethnically diverse Indian population.Variations in host genes encoding adhesion molecules and susceptibility to falciparum malaria in India.Diverse facets of COMT: from a plausible predictive marker to a potential drug target for schizophrenia.Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma.LIG1 polymorphisms: the Indian scenario.Polymorphisms in host genes encoding NOSII, C-reactive protein, and adhesion molecules thrombospondin and E-selectin are risk factors for Plasmodium falciparum malaria in India.Extensive copy number variations in admixed Indian population of African ancestry: potential involvement in adaptation.IGVBrowser--a genomic variation resource from diverse Indian populations.Genetic profile of patients with epilepsy on first-line antiepileptic drugs and potential directions for personalized treatment.Single nucleotide polymorphisms in homocysteine metabolism pathway genes: association of CHDH A119C and MTHFR C677T with hyperhomocysteinemia.Utilizing linkage disequilibrium information from Indian Genome Variation Database for mapping mutations: SCA12 case study.Allelic heterogeneity of molecular events in human coagulation factor IX in Asian Indians. Mutation in brief #965. Online.Evaluation of genetic markers linked to hemophilia A locus: an Indian experience.Spectrum of large copy number variations in 26 diverse Indian populations: potential involvement in phenotypic diversity.Deletion of the APOBEC3B gene strongly impacts susceptibility to falciparum malaria.Presence of strong association of the major histocompatibility complex (MHC) class I allele HLA-A*26:01 with idiopathic hypoparathyroidism.Genetic differentiation of populations residing in areas of high malaria endemicity in India.Molecular diagnosis of Wilson disease using prevalent mutations and informative single-nucleotide polymorphism markers.Population diversity and adaptive evolution in keratinization genes: impact of environment in shaping skin phenotypes.Genetic contribution of CYP1A1 variant on treatment outcome in epilepsy patients: a functional and interethnic perspective.Differential serum cytokine levels are associated with cytokine gene polymorphisms in north Indians with active pulmonary tuberculosis.Evaluation of PINK1 variants in Indian Parkinson's disease patients.HLA Alleles and Amino-Acid Signatures of the Peptide-Binding Pockets of HLA Molecules in VitiligoMolecular and Functional Studies of Tyrosinase Variants Among Indian Oculocutaneous Albinism Type 1 PatientsAnalysis of single nucleotide polymorphisms of PRNP gene in twenty-four ethnic groups of IndiaParkin polymorphisms: risk for Parkinson’s disease in Indian population
P50
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P50
name
Indian Genome Variation Consortium
@en
type
label
Indian Genome Variation Consortium
@en
prefLabel
Indian Genome Variation Consortium
@en