Merin George
Mumbai, MH 400012, India
Last Updated: 09/26/2026
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Found 11 publications
A Rare Variant in RPS26 Gene Causing Variable Phenotype of Diamond-Blackfan Anemia Type 10 (DBA10) in an Indian Family.
Journal: Indian journal of pediatrics
Published: September 24, 2025
DNA methylation signatures from peripheral blood revealed epigenetic alterations in Fanconi anemia.
Journal: Human genetics
Published: July 14, 2025
Analysis of BRCA1, BRCA2 and PALB2 related Fanconi anemia identifies scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes.
Journal: medRxiv : the preprint server for health sciences
Published: June 26, 2025
BRCA1-, BRCA2-, and PALB2-related Fanconi anemia: Scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes.
Journal: American journal of human genetics
Published: May 15, 2025
Phenotype puzzle: the role of novel LMBRD1 gene variant in Cbl deficiency causing Dyskeratosis Congenita-like clinical manifestations.
Journal: Journal of human genetics
Published: November 29, 2024
A Clinical Conundrum with Diagnostic and Therapeutic Challenge: a Tale of Two Disorders in One Case.
A Clinical Conundrum with Diagnostic and Therapeutic Challenge: a Tale of Two Disorders in One Case.
Journal: Journal of clinical immunology
Published: March 04, 2023
A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects.
Journal: Human mutation
Published: March 18, 2021
Nitric oxide synthase-2 (NOS2) gene polymorphism c.1832C>T (Ser608Leu) associated with nitrosative stress in Fanconi anaemia.
Journal: Molecular biology reports
Published: December 14, 2020
Severe telomere shortening in Fanconi anemia complementation group L.
Journal: Molecular biology reports
Published: October 06, 2020
Showing 1-11 of 11
Last Updated: 09/26/2026