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Congenital dyserythropoietic anemia type IV with high fetal hemoglobin caused by heterozygous KLF1 p.Glu325Lys: first report in an Indian infant

Annals of hematology, 2021, Vol.100 (1), p.281-283

2021

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Hemolytic erythrocytosis: an amalgamated phenotype from coinherited Chuvash polycythemia and G6PD Kerala-Kalyan with acquired transient stomatocytosis

Annals of hematology, 2021-08, Vol.100 (8), p.2107-2109

2021

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Plasminogen Activator Inhibitor-1 4G/5G Promoter Polymorphism in Indian Patients with Deep Vein Thrombosis

Indian journal of hematology & blood transfusion, 2024-04, Vol.40 (2), p.331-334

2024

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Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII Deficiency

Indian journal of hematology & blood transfusion, 2023-04, Vol.39 (2), p.276-283

2023

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Correction to: Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII Deficiency

Indian journal of hematology & blood transfusion, 2023-07, Vol.39 (3), p.519-521

2023

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Women in Selected Communities of Punjab, India Have a High Prevalence of Iron, Zinc, Vitamin B12, and Folate Deficiencies: Implications for a Multiply-Fortified Salt Intervention

Nutrients, 2023-07, Vol.15 (13), p.3024

2023

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Next-Generation Sequencing Based Approach to Identify Underlying Genetic Defects of Glanzmann Thrombasthenia

Indian journal of hematology & blood transfusion, 2021-07, Vol.37 (3), p.414-421

2021

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Correction to “High Drug Loading Nanoparticles Stabilized with Autologous Serum Proteins Passively Inhibits Tumor Growth”

Biomacromolecules, 2024-08

2024

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High Drug Loading Nanoparticles Stabilized with Autologous Serum Proteins Passively Inhibits Tumor Growth

Biomacromolecules, 2022-12, Vol.23 (12), p.5065-5073

2022

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Quintuply-fortified salt for the improvement of micronutrient status among women of reproductive age and preschool-aged children in Punjab, India: protocol for a randomized, controlled, community-based trial

BMC nutrition, 2022-09, Vol.8 (1), p.1-98, Article 98

2022

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Autosomal dominant familial periodic fever patient with a missense variant c.215GA (p.Cys72Tyr) in TNFRSF1A gene presenting as neutrophilia

European journal of medical genetics, 2021-05, Vol.64 (5)

2021

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Laboratory Approach to Hemolytic Anemia

Indian journal of pediatrics, 2020, Vol.87 (1), p.66-74

2020

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Next-generation sequencing-based molecular diagnosis of chronic non-spherocytic hemolysis in erythrocytic enzymopathies

Canadian Journal of Biotechnology, 2017-10, Vol.1 (Special Issue), p.83-83

2017

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A homozygous KLF1 gene mutation presenting as mild Thalassemia Intermedia unraveled by targeted Next Generation Sequencing

Canadian Journal of Biotechnology, 2017-10, Vol.1 (Special Issue), p.85-85

2017

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Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next‐generation sequencing: First South Asian study

British journal of haematology, 2020-03, Vol.188 (5), p.784-795

2020

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Genetic Spectrum of Inherited/Congenital Hemolytic Anemias in Indian Patients

Blood, 2021-11, Vol.138 (Supplement 1), p.4151-4151

2021

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A nonsense variant in the Hexokinase 1 gene (HK1) causing severe non‐spherocytic haemolytic anaemia: genetic analysis exemplifies ambiguity due to multiple Isoforms

British journal of haematology, 2019-09, Vol.186 (5), p.e142-e145

2019

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Imatinib responsive erythrocytosis in a patient with FIP1L1::PDGFRA rearranged myeloid neoplasm with hypereosinophilia – Another manifestation of a stem cell neoplasm

Leukemia research, 2022-10, Vol.121, p.106922-106922, Article 106922

2022

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Non-deletional haemoglobin H (Hb H) disease morphologically masquerading as congenital dyserythropoietic anaemia type II: a diagnostic pitfall

Journal of clinical pathology, 2024-04, Vol.77 (4), p.257

2024

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Autosomal dominant familial periodic fever patient with a missense variant c.215G>A (p.Cys72Tyr) in TNFRSF1A gene presenting as neutrophilia

European journal of medical genetics, 2021-05, Vol.64 (5), p.104191, Article 104191

2021

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Hemoglobin Andrew‐Minneapolis‐Bijnor HBB:c.[413T>C;435G>C] in a complex genotype with β‐thalassemia trait: A diagnostic and management conundrum

International journal of laboratory hematology, 2022-08, Vol.44 (4), p.e164-e167

2022

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Next-Generation Sequencing–Based Diagnosis of Unexplained Inherited Hemolytic Anemias Reveals Wide Genetic and Phenotypic Heterogeneity

The Journal of molecular diagnostics : JMD, 2020-04, Vol.22 (4), p.579-590

2020

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Unearthing the genotype‐inhibitor phenotype association in severe haemophilia A: A north Indian cohort study

Haemophilia : the official journal of the World Federation of Hemophilia, 2024-03, Vol.30 (2), p.410-418

2024

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Dehydrated hereditary stomatocytosis masquerading as primary haemochromatosis: a diagnostic challenge

Pathology, 2023-10, Vol.55 (6), p.876-879

2023

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Hemoglobin Beth Israel [HBB:c.308A>G (p.Asn103Ser)]: an ultra-rare, low oxygen-affinity, non-methemoglobinemic hemoglobin diagnosed on targeted resequencing as cause of dominantly inherited benign cyanosis

Annals of hematology, 2022-12, Vol.101 (12), p.2799-2801

2022

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Congenital dyserythropoietic anemia type IV with high fetal hemoglobin caused by heterozygous KLF1 p.Glu325Lys: first report in an Indian infant

Hemolytic erythrocytosis: an amalgamated phenotype from coinherited Chuvash polycythemia and G6PD Kerala-Kalyan with acquired transient stomatocytosis

Plasminogen Activator Inhibitor-1 4G/5G Promoter Polymorphism in Indian Patients with Deep Vein Thrombosis

Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII Deficiency

Correction to: Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII Deficiency

Women in Selected Communities of Punjab, India Have a High Prevalence of Iron, Zinc, Vitamin B12, and Folate Deficiencies: Implications for a Multiply-Fortified Salt Intervention

Next-Generation Sequencing Based Approach to Identify Underlying Genetic Defects of Glanzmann Thrombasthenia

Correction to “High Drug Loading Nanoparticles Stabilized with Autologous Serum Proteins Passively Inhibits Tumor Growth”

High Drug Loading Nanoparticles Stabilized with Autologous Serum Proteins Passively Inhibits Tumor Growth

Quintuply-fortified salt for the improvement of micronutrient status among women of reproductive age and preschool-aged children in Punjab, India: protocol for a randomized, controlled, community-based trial

Autosomal dominant familial periodic fever patient with a missense variant c.215GA (p.Cys72Tyr) in TNFRSF1A gene presenting as neutrophilia

Laboratory Approach to Hemolytic Anemia

Next-generation sequencing-based molecular diagnosis of chronic non-spherocytic hemolysis in erythrocytic enzymopathies

A homozygous KLF1 gene mutation presenting as mild Thalassemia Intermedia unraveled by targeted Next Generation Sequencing

Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next‐generation sequencing: First South Asian study

Genetic Spectrum of Inherited/Congenital Hemolytic Anemias in Indian Patients

A nonsense variant in the Hexokinase 1 gene (HK1) causing severe non‐spherocytic haemolytic anaemia: genetic analysis exemplifies ambiguity due to multiple Isoforms

Imatinib responsive erythrocytosis in a patient with FIP1L1::PDGFRA rearranged myeloid neoplasm with hypereosinophilia – Another manifestation of a stem cell neoplasm

Non-deletional haemoglobin H (Hb H) disease morphologically masquerading as congenital dyserythropoietic anaemia type II: a diagnostic pitfall

Autosomal dominant familial periodic fever patient with a missense variant c.215G>A (p.Cys72Tyr) in TNFRSF1A gene presenting as neutrophilia

Hemoglobin Andrew‐Minneapolis‐Bijnor HBB:c.[413T>C;435G>C] in a complex genotype with β‐thalassemia trait: A diagnostic and management conundrum

Next-Generation Sequencing–Based Diagnosis of Unexplained Inherited Hemolytic Anemias Reveals Wide Genetic and Phenotypic Heterogeneity

Unearthing the genotype‐inhibitor phenotype association in severe haemophilia A: A north Indian cohort study

Dehydrated hereditary stomatocytosis masquerading as primary haemochromatosis: a diagnostic challenge

Hemoglobin Beth Israel [HBB:c.308A>G (p.Asn103Ser)]: an ultra-rare, low oxygen-affinity, non-methemoglobinemic hemoglobin diagnosed on targeted resequencing as cause of dominantly inherited benign cyanosis

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