Ekta Jajodia

Hemoglobin P-Nilotic in an Indian Male: Expanding the Geographic Distribution of a Rare Hemoglobin Variant.

Journal: Hemoglobin

Published: August 19, 2026

Novel ABCG8 Mutation in Pediatric Sitosterolemia: A Case Report of Siblings with Hemolytic Anemia.

Journal: Hematology, transfusion and cell therapy

Published: July 25, 2025

Heterozygous Beta Thalassemia with Segmental Duplication of chr16p13.3 Leading to Thalassemia Intermedia Phenotype: A Report of 2 Cases with Review of Literature.

Journal: Hemoglobin

Published: April 25, 2025

A novel case of autosomal-dominant cutis laxa caused by a de novo likely pathogenic variant in ALDH18A1: case report and literature review.

Journal: Journal of human genetics

Published: February 28, 2025

Kissing Triangles: A Peculiar Pattern of Hemoglobin Camden in Capillary Zone Electrophoresis.

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

Published: October 13, 2024

Isolated Hemolytic Anemia in Phosphoglycerate Kinase 1 Deficiency Associated with a Novel PGK1:c.746 A > G;p.(Asn249Ser) Variant.

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

Published: September 04, 2024

Detection Discrepancy: Capillary Zone Electrophoresis Misses Hemoglobin Malmo Identified by Cation Exchange-High Performance Liquid Chromatography.

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

Published: August 08, 2024

Hb Koya Dora: An Under-recognized Variant of Alpha Thalassemia in India.

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

Published: August 06, 2024

Identification of a novel cryptic variant chromosomal rearrangement involving 9q34, 22q11.2, and 5q22 resulting in ins(9;22) and t(5;22) in chronic myeloid leukemia: a case report.

Journal: Annals of hematology

Published: July 26, 2024

Hemoglobin P-Nilotic in an Indian Male: Expanding the Geographic Distribution of a Rare Hemoglobin Variant.

Hemoglobin P-Nilotic in an Indian Male: Expanding the Geographic Distribution of a Rare Hemoglobin Variant.

Novel ABCG8 Mutation in Pediatric Sitosterolemia: A Case Report of Siblings with Hemolytic Anemia.

Novel ABCG8 Mutation in Pediatric Sitosterolemia: A Case Report of Siblings with Hemolytic Anemia.

Heterozygous Beta Thalassemia with Segmental Duplication of chr16p13.3 Leading to Thalassemia Intermedia Phenotype: A Report of 2 Cases with Review of Literature.

Heterozygous Beta Thalassemia with Segmental Duplication of chr16p13.3 Leading to Thalassemia Intermedia Phenotype: A Report of 2 Cases with Review of Literature.

A novel case of autosomal-dominant cutis laxa caused by a de novo likely pathogenic variant in ALDH18A1: case report and literature review.

A novel case of autosomal-dominant cutis laxa caused by a de novo likely pathogenic variant in ALDH18A1: case report and literature review.

Kissing Triangles: A Peculiar Pattern of Hemoglobin Camden in Capillary Zone Electrophoresis.

Kissing Triangles: A Peculiar Pattern of Hemoglobin Camden in Capillary Zone Electrophoresis.

Isolated Hemolytic Anemia in Phosphoglycerate Kinase 1 Deficiency Associated with a Novel PGK1:c.746 A > G;p.(Asn249Ser) Variant.

Isolated Hemolytic Anemia in Phosphoglycerate Kinase 1 Deficiency Associated with a Novel PGK1:c.746 A > G;p.(Asn249Ser) Variant.

Detection Discrepancy: Capillary Zone Electrophoresis Misses Hemoglobin Malmo Identified by Cation Exchange-High Performance Liquid Chromatography.

Detection Discrepancy: Capillary Zone Electrophoresis Misses Hemoglobin Malmo Identified by Cation Exchange-High Performance Liquid Chromatography.

Hb Koya Dora: An Under-recognized Variant of Alpha Thalassemia in India.

Hb Koya Dora: An Under-recognized Variant of Alpha Thalassemia in India.

Identification of a novel cryptic variant chromosomal rearrangement involving 9q34, 22q11.2, and 5q22 resulting in ins(9;22) and t(5;22) in chronic myeloid leukemia: a case report.

Identification of a novel cryptic variant chromosomal rearrangement involving 9q34, 22q11.2, and 5q22 resulting in ins(9;22) and t(5;22) in chronic myeloid leukemia: a case report.

De-novo ATR-16 syndrome associated with inherited hemoglobin Evanston causing HbH phenotype: a rare occurrence.

De-novo ATR-16 syndrome associated with inherited hemoglobin Evanston causing HbH phenotype: a rare occurrence.

Significance of Somatic Mutation Profiling in CML Beyond BCR-ABL: A Retrospective Study of the Indian Population.

Significance of Somatic Mutation Profiling in CML Beyond BCR-ABL: A Retrospective Study of the Indian Population.

Validation of a novel NGS based BCR::ABL1 kinase domain mutation detection assay in Indian cohort.

Validation of a novel NGS based BCR::ABL1 kinase domain mutation detection assay in Indian cohort.