Sumantra K. Sarkar

244, AJC Bose Road
Kolkata, WB, India

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 62 publications

Rare and novel variant load threshold for KIF7, GJA1 and PDE1C genes elevates the risk of severity of congenital heart defects in Down syndrome.

Rare and novel variant load threshold for KIF7, GJA1 and PDE1C genes elevates the risk of severity of congenital heart defects in Down syndrome.

Journal: PloS one

Published: November 15, 2024

Prevalence of HIV, hepatitis B and hepatitis C infections among patients with thalassemia attending a tertiary care (rural) hospital.

Prevalence of HIV, hepatitis B and hepatitis C infections among patients with thalassemia attending a tertiary care (rural) hospital.

Journal: Journal of family medicine and primary care

Published: October 29, 2023

Magnetic Resonance Imaging Evaluation of Common Spinal Intramedullary Tumours: Ependymoma and Astrocytoma.

Magnetic Resonance Imaging Evaluation of Common Spinal Intramedullary Tumours: Ependymoma and Astrocytoma.

Journal: Mymensingh medical journal : MMJ

Published: July 01, 2023

Diagnostic Accuracy of Magnetic Resonance Imaging in Evaluation of Anterior Cruciate Ligament Tear.

Diagnostic Accuracy of Magnetic Resonance Imaging in Evaluation of Anterior Cruciate Ligament Tear.

Journal: Mymensingh medical journal : MMJ

Published: January 03, 2023

Genetic aetiology of Down syndrome birth: novel variants of maternal DNMT3B and RFC1 genes increase risk of meiosis II nondisjunction in the oocyte.

Genetic aetiology of Down syndrome birth: novel variants of maternal DNMT3B and RFC1 genes increase risk of meiosis II nondisjunction in the oocyte.

Journal: Molecular genetics and genomics : MGG

Published: June 30, 2022

Measurement of Bone Mineral Density in the Transfusion Dependent Thalassemic Patients.

Measurement of Bone Mineral Density in the Transfusion Dependent Thalassemic Patients.

Journal: Mymensingh medical journal : MMJ

Published: April 06, 2022

Genetic and acquired blistering disorders of pediatric age group: An experience from Eastern India.

Genetic and acquired blistering disorders of pediatric age group: An experience from Eastern India.

Journal: Indian journal of pathology & microbiology

Published: August 03, 2021

Understanding etiology of chromosome 21 nondisjunction from gene × environment models.

Understanding etiology of chromosome 21 nondisjunction from gene × environment models.

Journal: Scientific reports

Published: July 27, 2021

Evaluation of vitamin D profile in juvenile idiopathic arthritis.

Evaluation of vitamin D profile in juvenile idiopathic arthritis.

Journal: Modern rheumatology

Published: April 20, 2021

Immunogenicity and safety of the first indigenously developed Indian tetravalent influenza vaccine (split virion) in healthy children (6 months to 17 years of age): a randomized, multicenter, phase III clinical trial.

Immunogenicity and safety of the first indigenously developed Indian tetravalent influenza vaccine (split virion) in healthy children (6 months to 17 years of age): a randomized, multicenter, phase III clinical trial.

Journal: Human vaccines & immunotherapeutics

Published: August 27, 2020

Jaundice at the Onset: A Rare Event in Kawasaki Disease.

Jaundice at the Onset: A Rare Event in Kawasaki Disease.

Journal: Indian journal of pediatrics

Published: April 29, 2020

The etiology of Down syndrome: Maternal MCM9 polymorphisms increase risk of reduced recombination and nondisjunction of chromosome 21 during meiosis I within oocyte.

The etiology of Down syndrome: Maternal MCM9 polymorphisms increase risk of reduced recombination and nondisjunction of chromosome 21 during meiosis I within oocyte.

Journal: PLoS genetics

Published: January 18, 2020

Showing 1-12 of 62

Last Updated: 09/26/2026