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List of works by Reena Das

A high frequency of Gilbert syndrome (UGT1A1*28/*28) and associated hyperbilirubinemia but not cholelithiasis in adolescent and adult north Indian patients with transfusion-dependent β-thalassemia

scientific article published on 16 July 2020

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

scientific article published on 23 May 2019

A novel germline RUNX1 mutation with co-occurrence of somatic alterations in a case of myeloid neoplasm with familial thrombocytopenia: first report from India

scientific article published on 16 April 2019

A rare association of giant adrenal myelolipoma in a young female double heterozygous for HbD Punjab and β-thalassemia trait ⬇️

scientific article published on July 1, 2011

Arthritic presentation of childhood malignancy: beware of normal blood counts

scientific article published on August 5, 2010

Coagulation F13A1 V34L, fibrinogen and homocysteine versus conventional risk factors in the pathogenesis of MI in young persons.

scientific article published on 5 October 2017

DNA staining in agarose and polyacrylamide gels by methyl green

scientific article published on 26 September 2018

De novo haemoglobin sabine masquerading as double heterozygosity for HbQ-India and β-thalassemia trait: first report from South Asia

scientific article published on 07 February 2020

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

scientific article published on 10 October 2019

Effect of deletions in the α-globin gene on the phenotype severity of β-thalassemia

scientific article published in 2022

Gaucher's Disease with Cardiac Valve Calcification and Stenosis: A Rare Presentation due to Homozygous p.D409H Mutation in a North Indian Family.

scientific article published on 18 February 2016

Genetic basis of unexplained erythrocytosis in Indian patients

scientific article published on 13 June 2019

HbH disease due to compound heterozygosity for hemoglobins Zürich-Albisrieden and Sallanches

scientific article published on 13 January 2020

Hematological Evaluation of Primary Extra Nodal Versus Nodal NHL: A Study from North India ⬇️

scientific article published on May 8, 2011

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

scientific article published on 08 October 2020

Horizontal gaze palsy with progressive myoclonic epilepsy: Rare presentation of Gaucher′s disease

scientific article published on March 1, 2013

Laboratory Approach to Hemolytic Anemia

scientific article published on 10 December 2019

Laboratory screening of thrombophilia testing requisitions for adequacy/appropriateness and reduced abnormal results ⬇️

scientific article published on June 18, 2012

Mesenteric vessel thrombosis and hypercoagulable states ⬇️

scientific article published on April 1, 2011

Micro mapping the frequencies of beta thalassemia and sickle cell anemia in India: A way forward to plan control strategies ⬇️

scientific article published on May 1, 2012

Missing Hb Q-India Peak in a Triple-Heterozygous Patient with Hb D-Punjab/Hb Q-India/β-Thalassemia Trait

scientific article published on 25 May 2020

Overhydrated stomatocytosis associated with a complex RHAG genotype including a novel de novo mutation.

scientific article published on 20 March 2018

Pediatric patients with bicytopenia/pancytopenia: Review of etiologies and clinico-hematological profile at a tertiary center ⬇️

scientific article published on January 1, 2011

Profiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes ⬇️

scientific article published on February 10, 2010

Prothrombin G20210A is not prevalent in North India ⬇️

scientific article published on 01 October 2003

Sickle-β+ thalassemia with splenic calcification and bone marrow infarction: a case report ⬇️

scientific article published on May 1, 2008

The utility of fluorescence in situ hybridization testing in patients clinically suspected of myelodysplastic syndrome or myelodysplastic syndrome/myeloproliferative neoplasm overlap is limited in the absence of significant morphological dysplasia

scientific article published on 27 August 2020

Ultra-rare Hb Regina (<i>HBB</i>:c.289C&gt;G) with coinherited β-thalassaemia trait: solving the puzzle for extreme erythrocytosis

scientific article published in 2022

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