Rekha Athiyarath

Vellore, TN, India

Last Updated: 09/26/2026

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Found 13 publications

Targeted Filaggrin Gene (FLG) Sequencing: A Pilot Study among Indian Children with Atopic Dermatitis.

Targeted Filaggrin Gene (FLG) Sequencing: A Pilot Study among Indian Children with Atopic Dermatitis.

Journal: Indian dermatology online journal

Published: April 04, 2024

Restrictive Dermopathy Due to ZMPSTE24 Mutation: A Case Report with a Novel Finding of Corpus Callosum Agenesis.

Restrictive Dermopathy Due to ZMPSTE24 Mutation: A Case Report with a Novel Finding of Corpus Callosum Agenesis.

Journal: Indian journal of dermatology

Published: April 04, 2024

Blended Phenotypes From a SERPINA 11 Pathogenic Variant Over Underlying Immune Fetal Hydrops: A Rare Case Report and Literature Review.

Blended Phenotypes From a SERPINA 11 Pathogenic Variant Over Underlying Immune Fetal Hydrops: A Rare Case Report and Literature Review.

Journal: Maternal-fetal medicine (Wolters Kluwer Health, Inc.)

Published: February 05, 2024

Exploring the clinical utility of exome sequencing/Mono, Duo, Trio in prenatal testing: a retrospective study in a tertiary care centre in South India.

Exploring the clinical utility of exome sequencing/Mono, Duo, Trio in prenatal testing: a retrospective study in a tertiary care centre in South India.

Journal: Journal of perinatal medicine

Published: November 17, 2023

Corrigendum to "Impact of maternal iron deficiency anemia on fetal iron status and placental iron transporters in human pregnancy" [Blood Cells Mol. Dis. 99 (2023) 102727].

Corrigendum to "Impact of maternal iron deficiency anemia on fetal iron status and placental iron transporters in human pregnancy" [Blood Cells Mol. Dis. 99 (2023) 102727].

Journal: Blood cells, molecules & diseases

Published: April 24, 2023

Impact of maternal iron deficiency anemia on fetal iron status and placental iron transporters in human pregnancy.

Impact of maternal iron deficiency anemia on fetal iron status and placental iron transporters in human pregnancy.

Journal: Blood cells, molecules & diseases

Published: July 06, 2022

Meconium Ileus due to GUCY2C gene mutations in three unrelated South Indian families.

Meconium Ileus due to GUCY2C gene mutations in three unrelated South Indian families.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: November 18, 2020

Novel frameshift variant (c.409dupG) in SLC25A38 is a common cause of congenital sideroblastic anaemia in the Indian subcontinent.

Novel frameshift variant (c.409dupG) in SLC25A38 is a common cause of congenital sideroblastic anaemia in the Indian subcontinent.

Journal: Journal of clinical pathology

Published: April 11, 2020

Association of genetic variants with response to iron supplements in pregnancy.

Association of genetic variants with response to iron supplements in pregnancy.

Journal: Genes & nutrition

Published: January 02, 2015

Genetic modifiers of secondary iron overload in beta thalassemia major.

Genetic modifiers of secondary iron overload in beta thalassemia major.

Journal: Blood cells, molecules & diseases

Published: December 12, 2014

Association of growth differentiation factor 15 (GDF15) polymorphisms with serum GDF15 and ferritin levels in β-thalassemia.

Association of growth differentiation factor 15 (GDF15) polymorphisms with serum GDF15 and ferritin levels in β-thalassemia.

Journal: Annals of hematology

Published: August 31, 2013

Two novel missense mutations in iron transport protein transferrin causing hypochromic microcytic anaemia and haemosiderosis: molecular characterization and structural implications.

Two novel missense mutations in iron transport protein transferrin causing hypochromic microcytic anaemia and haemosiderosis: molecular characterization and structural implications.

Journal: British journal of haematology

Published: July 30, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026