Rajat Hegde

Dharwad, KA, India

Last Updated: 09/26/2026

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Found 13 publications

G>A transition at 376 position of the glucose-6-phosphate dehydrogenase (G6PD) gene plays a key role in causing G6PD deficiency in the Siddi population of Karnataka.

G>A transition at 376 position of the glucose-6-phosphate dehydrogenase (G6PD) gene plays a key role in causing G6PD deficiency in the Siddi population of Karnataka.

Journal: The National medical journal of India

Published: October 24, 2024

Variation in Exon 29 of the NOS1 Gene Does Not Contribute to Parkinson's Disease in the North Karnataka Population.

Variation in Exon 29 of the NOS1 Gene Does Not Contribute to Parkinson's Disease in the North Karnataka Population.

Journal: Cureus

Published: September 16, 2023

WITHDRAWN: Mutational analysis of the F8 gene and phenotypic characterization of Hemophilia A.

WITHDRAWN: Mutational analysis of the F8 gene and phenotypic characterization of Hemophilia A.

Journal: Blood research

Published: June 09, 2023

Novel and PCR ready rapid DNA isolation from Drosophila.

Novel and PCR ready rapid DNA isolation from Drosophila.

Journal: Nucleosides, nucleotides & nucleic acids

Published: July 25, 2022

Rapid and inexpensive method of PCR ready DNA isolation from human peripheral blood and saliva.

Rapid and inexpensive method of PCR ready DNA isolation from human peripheral blood and saliva.

Journal: Analytical biochemistry

Published: April 22, 2022

Total Reflection X-ray Fluorescence Analysis of Plasma Elements in Autistic Children from India.

Total Reflection X-ray Fluorescence Analysis of Plasma Elements in Autistic Children from India.

Journal: Biological trace element research

Published: February 01, 2022

Interplay of Oxidative Stress and Nitric Oxide Synthase Gene Expression on Cardiovascular Responses in Preeclampsia.

Interplay of Oxidative Stress and Nitric Oxide Synthase Gene Expression on Cardiovascular Responses in Preeclampsia.

Journal: Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia

Published: January 31, 2022

Analysis of Genetic Variations in Connexin 26 ( GJB2 ) Gene among Nonsyndromic Hearing Impairment: Familial Study.

Analysis of Genetic Variations in Connexin 26 ( GJB2 ) Gene among Nonsyndromic Hearing Impairment: Familial Study.

Journal: Global medical genetics

Published: December 21, 2021

Clinical profile of hemophilia B patients from Karnataka.

Clinical profile of hemophilia B patients from Karnataka.

Journal: Journal of family medicine and primary care

Published: September 04, 2021

Genetic Analysis of Neuroligin 4Y Gene in Autism Population of India.

Genetic Analysis of Neuroligin 4Y Gene in Autism Population of India.

Journal: Global medical genetics

Published: June 30, 2021

Genetic analysis of the postsynaptic transmembrane X-linked neuroligin 3 gene in autism.

Genetic analysis of the postsynaptic transmembrane X-linked neuroligin 3 gene in autism.

Journal: Genomics & informatics

Published: April 21, 2021

Molecular alteration in the Gap Junction Beta 2 (GJB2) gene associated with non-syndromic sensorineural hearing impairment.

Molecular alteration in the Gap Junction Beta 2 (GJB2) gene associated with non-syndromic sensorineural hearing impairment.

Journal: Intractable & rare diseases research

Published: February 22, 2021

Showing 1-12 of 13

Last Updated: 09/26/2026