Vadlamudi R. Rao

Banjara Hills
Hyderabad, TG, India

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 18 publications

Midfacial toddler excoriation syndrome (MiTES): case series, diagnostic criteria and evidence for a pathogenic mechanism.

Midfacial toddler excoriation syndrome (MiTES): case series, diagnostic criteria and evidence for a pathogenic mechanism.

Journal: The British journal of dermatology

Published: November 15, 2023

Novel Stop-Gain TSC2 Gene Mutation in an Indian Child of Tuberous Sclerosis Complex.

Novel Stop-Gain TSC2 Gene Mutation in an Indian Child of Tuberous Sclerosis Complex.

Journal: Indian dermatology online journal

Published: June 17, 2023

Identification and Development of a High-Risk District Model in the Prevention of β-Thalassemia in Telangana State, India.

Identification and Development of a High-Risk District Model in the Prevention of β-Thalassemia in Telangana State, India.

Journal: Hemoglobin

Published: October 02, 2020

Re-testing reported significant SNPs related to suicide in a historical high -risk isolated population from north east India.

Re-testing reported significant SNPs related to suicide in a historical high -risk isolated population from north east India.

Journal: Hereditas

Published: February 02, 2020

PARK2 and PARK7 Gene Polymorphisms as Risk Factors Associated with Serum Element Concentrations and Clinical Symptoms of Parkinson's Disease.

PARK2 and PARK7 Gene Polymorphisms as Risk Factors Associated with Serum Element Concentrations and Clinical Symptoms of Parkinson's Disease.

Journal: Cellular and molecular neurobiology

Published: May 15, 2019

Loss of function mutation in the P2X7, a ligand-gated ion channel gene associated with hypertrophic cardiomyopathy.

Loss of function mutation in the P2X7, a ligand-gated ion channel gene associated with hypertrophic cardiomyopathy.

Journal: Purinergic signalling

Published: December 16, 2018

An Uncommon Variant Hemoglobin: Hb Ty Gard Detected from Gujarat, India.

An Uncommon Variant Hemoglobin: Hb Ty Gard Detected from Gujarat, India.

Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Published: October 15, 2018

Explaining suicide attempt with personality traits of aggression and impulsivity in a high risk tribal population of India.

Explaining suicide attempt with personality traits of aggression and impulsivity in a high risk tribal population of India.

Journal: PloS one

Published: April 28, 2017

Metallomic Biomarkers in Cerebrospinal fluid and Serum in patients with Parkinson's disease in Indian population.

Metallomic Biomarkers in Cerebrospinal fluid and Serum in patients with Parkinson's disease in Indian population.

Journal: Scientific reports

Published: March 07, 2016

Burden among Parkinson's disease care givers for a community based study from India.

Burden among Parkinson's disease care givers for a community based study from India.

Journal: Journal of the neurological sciences

Published: August 31, 2015

Evaluation of PARKIN gene variants in West Bengal Parkinson's disease patients.

Evaluation of PARKIN gene variants in West Bengal Parkinson's disease patients.

Journal: Journal of human genetics

Published: November 30, 2014

Genetic Affinity of the Bhil, Kol and Gond Mentioned in Epic Ramayana.

Genetic Affinity of the Bhil, Kol and Gond Mentioned in Epic Ramayana.

Journal: PloS one

Published: September 07, 2014

Showing 1-12 of 18

Last Updated: 09/26/2026