Periyasamy Govindaraj

Hosur Road
Bengaluru, KA 560029, India

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 69 publications

TTC19 and FMNL2 gene variants in a pediatric case of mitochondrial disorder with renal tubular acidosis.

TTC19 and FMNL2 gene variants in a pediatric case of mitochondrial disorder with renal tubular acidosis.

Journal: Mitochondrion

Published: February 11, 2026

Placental mitochondrial DNA variants, copy number and telomere length alterations in relation to antenatal depressive symptoms.

Placental mitochondrial DNA variants, copy number and telomere length alterations in relation to antenatal depressive symptoms.

Journal: Psychiatry research

Published: January 19, 2026

Expanding the Phenotype of STAMBP-Related Microcephaly-Capillary Malformation Syndrome.

Expanding the Phenotype of STAMBP-Related Microcephaly-Capillary Malformation Syndrome.

Journal: American journal of medical genetics. Part A

Published: December 01, 2025

Novel MC1R variants cause red hair and lighter skin color.

Novel MC1R variants cause red hair and lighter skin color.

Journal: HGG advances

Published: June 07, 2025

Lead exposure during development alters synaptic organization and protein expression in rat hippocampus.

Lead exposure during development alters synaptic organization and protein expression in rat hippocampus.

Journal: Journal of hazardous materials

Published: June 06, 2025

Establishment of human induced pluripotent stem cell line, NIMHi020-A from fibroblasts of a patient with IBA57 variant (p.Tyr113Cys).

Establishment of human induced pluripotent stem cell line, NIMHi020-A from fibroblasts of a patient with IBA57 variant (p.Tyr113Cys).

Journal: Stem cell research

Published: May 24, 2025

Mechanisms and routes of G-protein coupled receptor-mediated Tau degradation in Alzheimer's disease.

Mechanisms and routes of G-protein coupled receptor-mediated Tau degradation in Alzheimer's disease.

Journal: Cytokine & growth factor reviews

Published: March 12, 2025

Prevalence of Low EPHX1 Activity-Associated Genotypes in Himalayan Populations of India.

Prevalence of Low EPHX1 Activity-Associated Genotypes in Himalayan Populations of India.

Journal: American journal of human biology : the official journal of the Human Biology Council

Published: December 23, 2024

A human induced pluripotent stem cell line, NIMHi016-A, established from fibroblasts of a neuromuscular disease patient carrying PGK1/p. Asn5Lys variant.

A human induced pluripotent stem cell line, NIMHi016-A, established from fibroblasts of a neuromuscular disease patient carrying PGK1/p. Asn5Lys variant.

Journal: Stem cell research

Published: October 25, 2024

Association of early pregnancy telomere length and mitochondrial copy number with gestational diabetes mellitus and depressive symptoms.

Association of early pregnancy telomere length and mitochondrial copy number with gestational diabetes mellitus and depressive symptoms.

Journal: Psychoneuroendocrinology

Published: October 01, 2024

Adult-Onset Neuronal Ceroid Lipofuscinosis: CLN5 Variant Presenting as Focal Dystonia.

Adult-Onset Neuronal Ceroid Lipofuscinosis: CLN5 Variant Presenting as Focal Dystonia.

Journal: Tremor and other hyperkinetic movements (New York, N.Y.)

Published: August 04, 2024

Exploring the evidence for mitochondrial dysfunction and genetic abnormalities in the etiopathogenesis of tropical ataxic neuropathy.

Exploring the evidence for mitochondrial dysfunction and genetic abnormalities in the etiopathogenesis of tropical ataxic neuropathy.

Journal: Journal of neurogenetics

Published: July 08, 2024

Showing 1-12 of 69

Last Updated: 09/26/2026