R. Das

J. Ahluwalia, R. Kumar, R. Das, 2013, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Indian patients with nonalcoholic fatty liver disease presenting with raised transaminases are different at presentation.

Y. Chawla, R. Dhiman, N. Kalra, 2007, World journal of gastroenterology.

Conventional risk factors of coronary artery disease in a tertiary care hospital of Chandigarh in Northern part of India

J. Thakur, M. Rohit, R. Das, 2011 .

Thrombophilic risk factors are laterally associated with Apolipoprotein E gene polymorphisms in deep vein thrombosis patients: An Indian study

J. Ahluwalia, N. Varma, R. Das, 2018, Phlebology.

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

M. Bellgard, A. Bittles, M. Black, 2009, The HUGO Journal.

A decision support scheme for beta thalassemia and HbE carrier screening

Soumendra Nath Sanyal, S. Saha, Kartick Dey, 2020, Journal of advanced research.

Misdiagnosis of double heterozygous εGγ(Aγδβ)0-thalassemia/β++ thalassemia as homozygous β-thalassemia: A pitfall for molecular diagnostic laboratories.

A. Khadwal, R. Das, Prashant Sharma, 2019, Blood cells, molecules & diseases.

Iron status, inflammation and hepcidin in ESRD patients: The confounding role of intravenous iron therapy

H. Kohli, V. Jha, K. Gupta, 2010, Indian journal of nephrology.

A descriptive profile of β-thalassaemia mutations in India, Pakistan and Sri Lanka

M. Bellgard, A. Bittles, M. Black, 2010, Journal of Community Genetics.

Chronic eosinophilic leukemia with recurrent STAT5B N642H mutation-An entity with features of myelodysplastic syndrome/ myeloproliferative neoplasm overlap.

J. Ahluwalia, Anand Balakrishnan, P. Malhotra, 2021, Leukemia research.

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

N. Krebs, N. Dahiya, K. Brown, 2022, BMC Nutrition.

Arthritic presentation of acute leukemia in children: experience from a tertiary care centre in North India

J. Ahluwalia, D. Gupta, N. Varma, 2010, Rheumatology International.

Arthritic presentation of childhood malignancy: beware of normal blood counts

J. Ahluwalia, N. Varma, Surjit Singh, 2011, Rheumatology International.

Randomized controlled trial of twice-daily versus alternate-day oral iron therapy in the treatment of iron-deficiency anemia

D. Lad, N. Jindal, P. Malhotra, 2019, Annals of Hematology.

Frequency of primary iron overload and HFE gene mutations (C282Y, H63D and S65C) in chronic liver disease patients in north India.

Y. Chawla, A. Duseja, G. Garewal, 2007, World journal of gastroenterology.

Plasminogen Activator Inhibitor-1 4G/5G Promoter Polymorphism in Adults with Splanchnic Vein Thrombosis: A Case–Control Study

S. Rana, J. Ahluwalia, N. Varma, 2021, Indian Journal of Hematology and Blood Transfusion.

AUTOMATED RETICULOCYTE RESPONSE IS A GOOD PREDICTOR OF BONE-MARROW RECOVERY IN PEDIATRIC MALIGNANCIES

R. Marwaha, G. Garewal, Ajay Rawal, 2006, Pediatric hematology and oncology.

Outcome of adult acute lymphoblastic leukemia with BFM protocol in a resource-constrained setting

Sanjay Jain, Suresh C. Sharma, J. Ahluwalia, 2007, Leukemia & lymphoma.

Splenectomy in a case of splenic vein thrombosis unmasks essential thrombocythemia.

U. Kaur, G. Garewal, R. Das, 2002, Clinical and laboratory haematology.

A novel ATRX splice variant causing acquired HbH disease in myelodysplastic syndrome with excess blasts-1.

P. Malhotra, R. Das, Nabhajit Mallik, 2021, Cancer genetics.

Clinico-hematological, immunophenotyping, and molecular transcript profile of BCR–ABL-positive B cell acute lymphoblastic leukemias

R. Marwaha, A. Trehan, D. Bansal, 2013, Journal of Hematopathology.

Heterogeneous distribution of factor V Leiden in patients from north India with venous thromboembolism

Y. Chawla, G. Garewal, R. Das, 2003, Journal of thrombosis and haemostasis : JTH.

Factor V Leiden: prevalence in the indigenous population and cases of thrombosis in North India.

G. Garewal, R. Das, U. Trehan, 1997, British journal of haematology.

Inherited thrombophilia profile in patients with recurrent miscarriages: Experience from a tertiary care center in north India

M. Rohilla, J. Ahluwalia, N. Varma, 2015, Obstetrics & gynecology science.

Mesenteric vessel thrombosis and hypercoagulable states.

J. Ahluwalia, N. Varma, R. Das, 2011, Indian journal of pathology & microbiology.

Genetic and Nongenetic Determinants of Variable Warfarin Dose Requirements: A Report from North India

N. Shafiq, S. Malhotra, J. Ahluwalia, 2021, Public Health Genomics.

Thromboembolic complications in childhood nephrotic syndrome: a clinical profile

A. Rawat, K. Sodhi, J. Ahluwalia, 2014, Clinical and Experimental Nephrology.

Paratrabecular myelofibrosis and occult mastocytosis are strong morphological clues to suspect FIP1L1-PDGFRA translocation in hypereosinophilia

S. Naseem, J. Ahluwalia, P. Malhotra, 2019, Indian Journal of Hematology and Blood Transfusion.

Obscure pathogenesis of primary iron overload in Indians warrants more focused research

G. Chandak, R. Das, 2011, Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology.

Prevalence of the H63D mutation of the HFE in north India: its presence does not cause iron overload in beta thalassemia trait

G. Garewal, J. Ahluwalia, R. Das, 2005, European journal of haematology.

Effect of Placental Transfusion on Iron Stores in Moderately Preterm Neonates of 30–33 weeks Gestation

Praveen Kumar, V. Sundaram, R. Das, 2018, The Indian Journal of Pediatrics.

Prevalence of obesity, diabetes mellitus and hyperlipidaemia in patients with cryptogenic liver cirrhosis.

Y. Chawla, A. Duseja, A. Bhansali, 2004, Tropical gastroenterology : official journal of the Digestive Diseases Foundation.

Indian Society of Hematology and Blood Transfusion (ISHBT) Consensus Document on Hematological Practice During COVID-19 Pandemic

S. Shetty, A. Srivastava, H. Pati, 2021, Indian Journal of Hematology and Blood Transfusion.

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

P. Malhotra, R. Das, Prashant Sharma, 2022, International journal of laboratory hematology.

Coagulation factor VIII, IX and XI levels in north Indian patients with venous thromboembolism: first study from India

J. Ahluwalia, P. Malhotra, R. Das, 2016, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

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

R. Das, Prashant Sharma, M. Jamwal, 2022, Annals of Hematology.

Identification of rare and novel deletions that cause (δβ)0‐thalassaemia and hereditary persistence of foetal haemoglobin in Indian population

M. Chandy, A. Srivastava, R. Das, 2014, European journal of haematology.

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

R. Marwaha, J. Ahluwalia, A. Trehan, 2011, Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion.

HEMATOLOGICAL DISORDERS IN DOWN SYNDROME: Ten-Year Experience at a Tertiary Care Centre in North India

R. Marwaha, G. Garewal, J. Ahluwalia, 2005, Pediatric hematology and oncology.

First report of Mediterranean stomatocytosis/macrothrombocytopenia in an Indian family: a diagnostic dilemma.

B. Thapa, A. Maitra, A. Trehan, 2017, Pathology.

H63D mutation in HFE gene is common in Indians and is associated with the European haplotype

R. Das, B. Dhillon, S. Prakash, 2012, Journal of Genetics.

Serum Ferritin in Thalassemia Intermedia

R. Marwaha, A. Trehan, R. Das, 2014, Indian Journal of Hematology and Blood Transfusion.

Hematological Practice in India.

J. Ahluwalia, R. Das, M. Sachdeva, 2016, Hematology/oncology clinics of North America.

A rare occurrence of haemophilia A in a female due to compound heterozygosity of a de novo missense variant (presenting as pseudohomozygous) in F8 gene with Xq28 deletion inherited from mother

J. Ahluwalia, A. Trehan, D. Bansal, 2022, International journal of laboratory hematology.

Effect of Sepsis on Iron Parameters in a Population with High Prevalence of Malnutrition and Iron Deficiency: A Cross-Sectional Case–Control Pilot Study

P. Kumar-M, P. Bhatia, R. Rameshkumar, 2021, Indian Journal of Hematology and Blood Transfusion.

DNA staining in agarose and polyacrylamide gels by methyl green

N. Varma, R. Das, M. Sachdeva, 2018, Biotechnic & histochemistry : official publication of the Biological Stain Commission.

Clericuzio‐type poikiloderma with neutropenia in a patient from India

V. Scaria, U. Saikia, A. Bishnoi, 2020, American journal of medical genetics. Part A.

Profile of hematological abnormalities of Indian HIV infected individuals

R. K. Sachdeva, Aman Sharma, A. Wanchu, 2009, BMC blood disorders.

Fine‐needle aspiration biopsy in fungal infections

P. Dey, A. Chakrabarti, R. Das, 1997, Diagnostic cytopathology.

Peripheral smear discloses histoplasmosis.

R. Das, M. Updesh, S. Sachdeva, 2010, Blood.

Serum iron indices in COVID‐19‐associated mucormycosis: A case–control study

S. Rudramurthy, A. Chakrabarti, N. Panda, 2021, Mycoses.

Pediatric disorders of sex development

R. Marwaha, I. Panigrahi, K. Kulkarni, 2009, Indian journal of pediatrics.

A Phase 2 Randomized Controlled Trial of Single-Agent Hydroxyurea Versus Thalidomide Among Adult Transfusion Dependent β Thalassemia Patients

D. Lad, N. Shafiq, P. Malhotra, 2023, Indian Journal of Hematology and Blood Transfusion.

Bone marrow erythroblastic dysplasia on morphology correlates significantly with flow cytometric apoptosis and peripheral blood eryptosis

A. Khadwal, R. Das, Prashant Sharma, 2023, Journal of Microscopy and Ultrastructure.

Guidelines for screening, diagnosis and management of hemoglobinopathies

D. Mohanty, R. Saxena, K. Ghosh, 2014, Indian journal of human genetics.

Xmn1‐Gγ polymorphism and clinical predictors of severity of disease in β‐thalassemia intermedia

R. Marwaha, S. Oberoi, J. Kaur, 2011, Pediatric blood & cancer.

A Flow Cytometric Cell-cycle Assay Using Methyl Green.

N. Varma, R. Das, Prashant Sharma, 2020, Analytical Biochemistry.

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

R. Chatterjee, K. Nayek, R. Das, 2022, Hemoglobin.

Anemia in malignancies: Pathogenetic and diagnostic considerations

R. Das, Prashant Sharma, B. Gaspar, 2015, Hematology.

Osseous sarcoid with lytic lesions in skull

N. Khandelwal, P. Malhotra, R. Das, 2014, Rheumatology International.

ThalInd, a β‐thalassemia and hemoglobinopathies database for India: defining a model country‐specific and disease‐centric bioinformatics resource

Matthew Bellgard, M. Bellgard, M. Black, 2011, Human mutation.

Molecular Pathology of Thalassemia and Triplicated Locus in North Indian Population; Interaction with Heterozygous Thalassemia

D. Kaul, G. Garewal, R. Das, 2001, Hematology.

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

J. Ahluwalia, A. Saxena, R. Das, 2008, Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion.

Extreme Genotype/Phenotype Heterogeneity of Double Heterozygous Sickle β-Thalassemia in a Family: Implications in Antenatal Diagnosis

A. Trehan, R. Das, Prashant Sharma, 2021, Indian Journal of Hematology and Blood Transfusion.

Evaluation of the genetic basis of phenotypic heterogeneity in north Indian patients with Thalassemia major

Nidhi Sharma, J. Ahluwalia, A. Trehan, 2010, European journal of haematology.

Alpha globin gene deletions in amelioration of clinical severity in beta haemoglobinopathy subjects with the Î²0/Î²+ genotype

R. Chatterjee, K. Nayek, R. Das, 2020, medRxiv.

HbSD-Punjab: Clinical and Hematological Profile of a Rare Hemoglobinopathy

R. Marwaha, J. Ahluwalia, A. Trehan, 2014, Journal of pediatric hematology/oncology.

β-Thalassemia Intermedia Caused by Compound Heterozygosity for Hb Lepore-Hollandia and β-Thalassemia is Rare in the Indian Population

D. Bansal, R. Das, Prashant Sharma, 2015, Hemoglobin.

Performance analysis of machine learning algorithms and screening formulae for β-thalassemia trait screening of Indian antenatal women

I. Nielsen, Kartick Dey, R. Das, 2022, Int. J. Medical Informatics.

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

D. Bansal, R. Das, Prashant Sharma, 2020, Annals of Hematology.

Nucleotide −88 (C‐T) promoter mutation is a common β‐thalassemia mutation in the Jat Sikhs of Punjab, India

R. Marwaha, G. Garewal, J. Ahluwalia, 2005, American journal of hematology.

Wide Spectrum of Molecular and Clinical Heterogeneity in HbH Disease in North Indian Patients

D. Weatherall, C. Fisher, A. Trehan, 2014 .

Spectrum of β-Thalassemia Mutations in Punjabis

G. Garewal, R. Das, 2003 .

The clinical significance of the spectrum of interactions of CAP+1 (A→C), a silent β‐globin gene mutation, with other β‐thalassemia mutations and globin gene modifiers in north Indians

G. Garewal, J. Ahluwalia, R. Das, 2007, European journal of haematology.

Bone Marrow Involvement in Neuroblastoma: A Study of Hemato-morphological Features

R. Marwaha, S. Naseem, J. Ahluwalia, 2015, Indian Journal of Hematology and Blood Transfusion.

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

J. Ahluwalia, A. Trehan, D. Bansal, 2020, Indian Journal of Hematology and Blood Transfusion.

PARVOVIRUS B19-ASSOCIATED TRANSIENT RED CELL APLASIA IN CHILDREN: The Role of Bone Marrow Examination in Unusual Presentations

G. Garewal, J. Ahluwalia, R. Das, 2004, Pediatric hematology and oncology.

Genetic polymorphisms, Biochemical Factors, and Conventional Risk Factors in Young and Elderly North Indian Patients With Acute Myocardial Infarction

J. Ahluwalia, R. Kumar, R. Das, 2016, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Bone marrow examination of HIV-infected children in HAART era reveals a spectrum of abnormalities: a study from single tertiary care center of North India

R. K. Sachdeva, S. Naseem, J. Ahluwalia, 2021, Journal of Hematopathology.

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

R. Marwaha, S. Naseem, J. Ahluwalia, 2011, Indian journal of pathology & microbiology.

Transfusion-Associated Graft-Versus-Host Disease with a Non-fatal Course

S. Naseem, R. Das, M. Sachdeva, 2016, Indian Journal of Hematology and Blood Transfusion.

Growth failure in hereditary spherocytosis and the effect of splenectomy

A. Trehan, D. Bansal, R. Das, 2017, Indian Pediatrics.

Hereditary spherocytosis in children: Profile and post-splenectomy outcome

R. Marwaha, A. Trehan, D. Bansal, 2014, Indian Pediatrics.

UGT1A1 Gene Polymorphisms in North Indian Neonates Presenting with Unconjugated Hyperbilirubinemia

R. Prasad, S. Agrawal, Praveen Kumar, 2009, Pediatric Research.

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

J. Ahluwalia, M. Rohit, R. Das, 2018, Acta cardiologica.

North Indian Patients With Acute Myocardial Infarction Genetic polymorphisms , Biochemical Factors , and Conventional Risk Factors in Young and Elderly

J. Ahluwalia, R. Kumar, R. Das, 2014 .

Prothrombotic gene polymorphisms and plasma factors in young north Indian survivors of acute myocardial infarction

J. Ahluwalia, R. Kumar, R. Das, 2012, Journal of Thrombosis and Thrombolysis.

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

J. Ahluwalia, R. Das, P. Sharma, 2012, International Journal of Laboratory Hematology.

Erdheim–Chester disease with unusual clinicopathological features complicated by DRESS syndrome, disseminated Cytomegalovirus infection and hemophagocytic lymphohistiocytosis

A. Bhalla, R. Das, R. Vasishta, 2017, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.

Availability of technology to evaluate for pulmonary embolism in academic emergency departments in the United States

G. Garewal, J. Ahluwalia, R. Das, 2003, Journal of thrombosis and haemostasis : JTH.

Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians.

Y. Chawla, A. Duseja, G. Garewal, 2018, Blood cells, molecules & diseases.

Post-transplant cyclophosphamide pharmacokinetics and haploidentical hematopoietic cell transplantation outcomes: an exploratory study

D. Lad, S. Malhotra, Amol N. Patil, 2022, Leukemia & lymphoma.

A Case of Autosplenectomy in Sickle Cell Trait Following an Exposure to High Altitude.

U. Yanamandra, P. Malhotra, R. Das, 2018, Wilderness & environmental medicine.

The first case report of a patient with coexisting hemophilia B and Down syndrome

J. Ahluwalia, I. Panigrahi, R. Das, 2017, Blood research.

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

D. Lad, R. Das, M. Jamwal, 2021, European journal of medical genetics.

Hepatic and Cardiac Iron-load in Children on Long-term Chelation with Deferiprone for Thalassemia Major

N. Khandelwal, A. Bhatia, K. Sodhi, 2018, Indian Pediatrics.

Clinicoinvestigational and Demographic Profile of Children with Thalassemia Major

R. Marwaha, A. Trehan, D. Bansal, 2015, Indian Journal of Hematology and Blood Transfusion.

Genetic basis of unexplained erythrocytosis in Indian patients

S. Naseem, J. Ahluwalia, P. Malhotra, 2019, European journal of haematology.

Late Emergence of Polycythemia in a Case of Hb Chandigarh [β94(FG1)Asp→Gly]

R. Das, S. Dash, 2004, Hemoglobin.

Molecular Genetics of Inherited Red Cell Membrane Disorders

R. Das, A. Aggarwal, M. Jamwal, 2019, Hematopathology.

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

A. Maitra, P. Malhotra, R. Das, 2018, Journal of Clinical Pathology.

Severe hemophagocytic lymphohistiocytosis in adults-experience from an intensive care unit from North India

Navneet Singh, R. Agarwal, D. Gupta, 2012, Indian journal of critical care medicine : peer-reviewed, official publication of Indian Society of Critical Care Medicine.

End-stage Renal Disease in Griscelli Syndrome

V. Mahajan, R. Das, Shivanjali Sood, 2022, Indian Journal of Nephrology.

Rapidly fatal reactive hemophagocytosis syndrome associated with visceral leishmaniasis

D. Dayal, R. Das, L. Tiwari, 2011, Journal of Pediatric Infectious Diseases.

Factors affecting efficacy of packed red blood cell transfusion in neonates

N. Marwaha, Praveen Kumar, S. Dutta, 2016, European Journal of Pediatrics.

A comparative evaluation of Eosin‐5′‐maleimide flow cytometry reveals a high diagnostic efficacy for hereditary spherocytosis

D. Bansal, P. Malhotra, R. Das, 2016, International journal of laboratory hematology.

T-cell/Natural killer-cell neoplasms presenting as leukemia- Case series from single tertiary care center

S. Naseem, J. Ahluwalia, N. Varma, 2016, International journal of hematology-oncology and stem cell research.

Primary bone marrow lymphoma is a rare neoplasm with poor outcome: case series from single tertiary care centre and review of literature

S. Naseem, J. Ahluwalia, P. Malhotra, 2016, Hematological oncology.

Role of blood and bone marrow examination in the diagnosis of mature lymphoid neoplasms in patients presenting with isolated splenomegaly

S. Naseem, J. Ahluwalia, P. Malhotra, 2015, Hematology.

Thrombocytopenia as a presenting feature of Kawasaki disease: a case series from North India

J. Ahluwalia, D. Gupta, R. Kumar, 2009, Rheumatology International.

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

D. Lad, R. Das, H. Virk, 2022, Leukemia research.

Severe epidermolysis bullosa/Kindler syndrome‐like phenotype of an autoinflammatory syndrome in a child

A. Kubba, A. Bishnoi, B. Radotra, 2021, Clinical and experimental dermatology.

Spectrum of diseases diagnosed on bone marrow examination of 285 infants in a single tertiary care center

R. Marwaha, S. Naseem, J. Ahluwalia, 2015, Hematology.

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

P. Malhotra, N. Varma, R. Das, 2019, Leukemia & lymphoma.

Plasma cell leukemia in North India: retrospective analysis of a distinct clinicohematological entity from a tertiary care center and review of literature

R. Srinivasan, S. Naseem, J. Ahluwalia, 2016, Blood research.

Detection of c.755T>C; p.L265P/c.751C>T;p.264R/* compound heterozygous MYD88 mutation in a case of Waldenstrom macroglobulinemia

D. Lad, A. Bal, R. Das, 2021, Indian Journal of Hematology and Blood Transfusion.

Evaluation of a flow cytometric test for G6PD‐deficient erythrocytes

A. Bal, N. Varma, A. Khadwal, 2021, Tropical medicine & international health : TM & IH.

Hyperfibrotic myelodysplastic syndrome: a report of three cases from north India.

P. Das, D. Jain, R. Das, 2009, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Cervical esophageal web and celiac disease

S. Sinha, Kartar Singh, K. K. Prasad, 2008, Journal of gastroenterology and hepatology.

The utility of bone marrow examination in renal transplantation: nine years of experience from north India.

V. Sakhuja, G. Garewal, J. Ahluwalia, 2006, Transplantation.

Iron Deficiency and Iron Deficiency Anemia in 3–5 months-old, Breastfed Healthy Infants

Sudarsan Krishnaswamy, D. Bansal, P. Bhatia, 2017, The Indian Journal of Pediatrics.

Parvovirus B19 infection-associated red-cell aplasia in renal-transplant recipients: clues from the bone marrow.

V. Sakhuja, G. Garewal, J. Ahluwalia, 2004, Transplantation.

Budd‐Chiari syndrome associated with homozygous factor V Leiden mutation

Y. Chawla, R. Dhiman, G. Garewal, 1999, British journal of haematology.

Macrophage activation syndrome in children with systemic onset juvenile idiopathic arthritis: clinical experience from northwest India

A. Rawat, J. Ahluwalia, N. Varma, 2012, Rheumatology International.

MYD88, CARD11, and CD79B Oncogenic Mutations are Rare Events in the Indian Cohort of De Novo Nodal Diffuse Large B-Cell Lymphoma

R. Srinivasan, A. Bal, P. Malhotra, 2019, Applied immunohistochemistry & molecular morphology : AIMM.

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

R. Das, 2012, Indian journal of human genetics.

Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three cases.

D. Bansal, P. Malhotra, R. Das, 2016, Clinica chimica acta; international journal of clinical chemistry.

Outcomes of splenectomy versus cladribine for hairy cell leukemia in resource limited settings

D. Lad, Sanjay Jain, P. Malhotra, 2014, Leukemia & lymphoma.

Methylenetetrahydrofolate reductase gene polymorphisms: association with risk for pediatric acute lymphoblastic leukemia in north Indians

R. Marwaha, J. Ahluwalia, A. Trehan, 2010, Leukemia & lymphoma.

An Autopsy Case of β-Thalassemia Major Illuminating the Pathological Spectrum of the Disease

D. Bansal, R. Sood, R. Das, 2021, Hemoglobin.

Serum transferrin receptor-ferritin index shows concomitant iron deficiency anemia and anemia of chronic disease is common in patients with rheumatoid arthritis in north India.

G. Garewal, R. Das, P. Bambery, 2008, Indian journal of pathology & microbiology.

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

N. Kalra, R. Das, K. Gupta, 2011, Indian journal of pathology & microbiology.

Role of FAB classification of acute leukemias in era of immunophenotyping.

J. Ahluwalia, N. Varma, R. Das, 2006, Indian journal of pathology & microbiology.

Acute leukemia/myelodysplastic syndrome as a sequelae of carcinoma breast: a report of five cases from north India.

G. Garewal, J. Ahluwalia, P. Malhotra, 2009, Indian journal of pathology & microbiology.

Prothrombotic Profile in Children With Peripheral Gangrene

S. Naseem, J. Ahluwalia, N. Varma, 2011, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Long‐term real‐world outcomes of patients with acute promyelocytic leukaemia treated with arsenic trioxide and all‐trans retinoic acid without chemotherapy—a retrospective, single‐centre study

D. Lad, S. Naseem, U. Yanamandra, 2022, British Journal of Haematology.

Assessment of Right Ventricular Function in Post Operative Patients of Tetralogy of Fallots and Its Predictive Factors

R. Kumar, R. Kalra, R. Das, 2014 .

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

Sandeep Rao, J. Kaur, P. Malhotra, 2016, The Indian Journal of Pediatrics.

Effect of antiretroviral therapy on hemoglobin A2 values can have implications in antenatal beta-thalassemia screening programs

Aman Sharma, R. Das, Prashant Sharma, 2016, Infectious Diseases.

Comparative study of myelodysplastic syndromes and normal bone marrow biopsies with conventional staining and immunocytochemistry.

P. Dey, G. Garewal, R. Das, 2005, Analytical and quantitative cytology and histology.

Is it safe to use intravenous iron sucrose during pregnancy? A randomized controlled trial -

V. Suri, R. Das, Sunita Dubey, 2013 .

Hemophagocytic syndrome as the presenting manifestation of visceral leishmaniasis.

U. Dutta, R. Das, K. Singh, 2002, The Journal of the Association of Physicians of India.

Haematological profile of 21 patients with hairy cell leukaemia in a tertiary care centre of north India

S. Naseem, J. Ahluwalia, P. Malhotra, 2015, The Indian journal of medical research.

Automated alkaline-pH electrophoresis followed by densitometry does not correlate with cation-exchange (CE)-HPLC in quantification of HbA2 and variant hemoglobins

R. Das, Prashant Sharma, S. Sreedharanunni, 2015, Clinical chemistry and laboratory medicine.

Hematological and genetic profiles of persons with co‐inherited heterozygous β‐thalassemia and supernumerary α‐globin genes

A. Trehan, P. Malhotra, A. Khadwal, 2023, European Journal of Haematology.

CE-HPLC Derived P2 and P3-Peaks in Health and in Hb D-Punjab and HbE States

R. Das, Prashant Sharma, S. Chhabra, 2020, Indian Journal of Hematology and Blood Transfusion.

Achondroplasia-First Report from India of a Rare FGFR3 Gene Variant.

P. Srivastava, J. Kaur, I. Panigrahi, 2021, Laboratory medicine.

Homozygosity mapping reveals founder SEC23B‐Y462C mutations in Indian congenital dyserythropoietic anemia type II

U. Saikia, S. Naseem, B. Singleton, 2015, Clinical Genetics.

Familial genotypic and phenotypic heterogeneity and its implications on genetic counseling exemplified in two cases of hereditary pyropoikilocytosis/erythrocytic spectrin‐linked hemolytic anemia masquerading as congenital dyserythropoietic anemia

A. Maitra, S. Naseem, A. Trehan, 2021, Pediatric blood & cancer.

Marburg I Polymorphism (G511E) in Adults with Deep Vein Thrombosis

J. Ahluwalia, P. Malhotra, N. Varma, 2019, Indian Journal of Hematology and Blood Transfusion.

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

S. Naseem, J. Ahluwalia, P. Malhotra, 2020, International journal of laboratory hematology.

Seckel syndrome with chromosomal 18 deletion

R. Marwaha, I. Panigrahi, K. Kulkarni, 2009, Indian journal of pediatrics.

Next-generation sequencing unravels homozygous mutation in glucose-6-phosphate isomerase, GPIc.1040G>A (p.Arg347His) causing hemolysis in an Indian infant.

A. Maitra, D. Bansal, R. Das, 2017, Clinica chimica acta; international journal of clinical chemistry.

Correlating clinical and laboratory diagnostic modalities in the diagnosis of epidermolysis bullosa in a resource‐poor setting

A. Bishnoi, R. Das, D. Chatterjee, 2022, Journal of cutaneous pathology.

Autologous Stem Cell Transplantation for Multiple Myeloma: Single Centre Experience from North India

D. Lad, U. Yanamandra, P. Malhotra, 2018, Indian Journal of Hematology and Blood Transfusion.

Developmental profile in children with iron deficiency anemia and its changes after therapeutic iron supplementation

D. Bansal, P. Malhi, R. Das, 2010, Indian journal of pediatrics.

Next-generation sequencing-based diagnosis of unexplained inherited hemolytic anemias reveals wide genetic and phenotypic heterogeneity.

A. Maitra, A. Trehan, D. Bansal, 2020, The Journal of molecular diagnostics : JMD.

Retinopathy of Prematurity and Glucose-6-Phosphate Dehydrogenase Activity: A Case-Control Study.

S. Dutta, D. Katoch, R. Das, 2023, Indian Journal of Pediatrics.

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

A. Khadwal, R. Das, Prashant Sharma, 2020, Pediatric blood & cancer.

Preclinical safety assessment of photoluminescent metal quantum clusters stabilized with autologous serum proteins for host specific theranostics

Pranjali Yadav, A. Shanavas, R. Das, 2023, Nanotheranostics.

High Risk Apml Treated Successfully with Four Cycles of ATO and ATRA Combination in Resource Constrained Settings

S. Naseem, U. Yanamandra, P. Malhotra, 2015 .

Spectrum of pure red cell aplasia in adult population of north-west India

Sanjay Jain, J. Ahluwalia, P. Malhotra, 2008, Hematology.

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

A. Trehan, D. Bansal, R. Das, 2022, Journal of Clinical Pathology.

Investigation of persistent hypochromic microcytosis unmasks hemoglobin Evanston [α 14 (A12) Try → Arg] in a patient of cyclic thrombocytopenia preceding Takayasu's disease

G. Garewal, J. Ahluwalia, R. Das, 2005, Hematology.

A well curated cost-effective next generation sequencing panel identifies a diverse landscape of pathogenic and novel germline variants in bone marrow failure cohort in a resource constraint setting.

Minu Singh, A. Trehan, D. Bansal, 2023, The Journal of molecular diagnostics : JMD.

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

N. Krebs, N. Dahiya, K. Brown, 2023, Nutrients.

Vortex‐dislodged cells from bone marrow trephine biopsy yield satisfactory results for flow cytometric immunophenotyping

S. Naseem, J. Ahluwalia, N. Varma, 2016, International journal of laboratory hematology.

Optimal Reference Gene Selection for Expression Studies in Human Reticulocytes.

Prashant Sharma, Pankaj Malhotra, D. Bansal, 2018, The Journal of molecular diagnostics : JMD.

Homozygous KLF1 mutation c.901C>T (p.Arg301Cys) resulting in mild thalassemia intermedia in an Indian: A next-generation sequencing diagnosis.

A. Maitra, J. Kaur, P. Malhotra, 2018, Blood Cells, Molecules & Diseases.

Molecular spectrum of inherited FVII deficiency in North India revealed a recurrent variant with a founder effect

J. Ahluwalia, A. Trehan, D. Bansal, 2022, Haemophilia : the official journal of the World Federation of Hemophilia.

Compound Heterozygous Hemoglobin SD Disease Presenting As Sickle Cell Crisis in Pregnancy

Rakhi, P. Malhotra, R. Das, 2016 .

Pulmonary and hematological alterations in idiopathic ulcerative colitis.

M. Gulati, S. Sinha, Kartar Singh, 2003, Indian Journal of Gastroenterology.

First report of homocystinuria-megaloblastic anaemia, cobalamin E complementation type, in an Indian child.

A. Maitra, A. Trehan, D. Bansal, 2019, Pathology (Sydney).

Assessment of insulin resistance and effect of metformin in nonalcoholic steatohepatitis--a preliminary report.

Y. Chawla, A. Duseja, R. Das, 2004, Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology.

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

A. Maitra, D. Bansal, R. Das, 2019, British journal of haematology.

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

J. Ahluwalia, A. Trehan, D. Bansal, 2022, Indian Journal of Hematology and Blood Transfusion.

Prenatal diagnosis for hemophilia A (intron 22 inversion) reveals a rare association with Klinefelter syndrome with diagnostic difficulties in molecular interpretation.

J. Ahluwalia, J. Kaur, R. Das, 2022, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

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

A. Shanavas, R. Das, M. Jamwal, 2022, Biomacromolecules.

Preclinical safety assessment of photoluminescent metal quantum clusters stabilized with autologous serum proteins for host specific theranostics

Pranjali Yadav, A. Shanavas, R. Das, 2023, Nanotheranostics.

Phenotypic and genetic heterogeneity arising from a novel substitution at amino acid position Val205 in GATA1 related X-linked thrombocytopenia with dyserythropoietic anemia.

A. Maitra, D. Bansal, R. Das, 2019, Blood cells, molecules & diseases.

Identification of peripheral blood CD26+ leukemic stem cells has a potential role in the rapid diagnosis of chronic myeloid leukemia

S. Naseem, P. Malhotra, N. Varma, 2022, International journal of laboratory hematology.

Genomics of iron refractory iron deficiency anemia phenotype reveals a spectrum of novel pathogenic biallelic and monoallelic TMPRSS6 variants and rare overlapping disorders.

A. Trehan, P. Bhatia, R. Das, 2023, Gene.

Anemia in malignancies: Pathogenetic and diagnostic considerations

R. Das, Prashant Sharma, B. Gaspar, 2015, Hematology.

CASE REPORT: Mesenteric Venous Thrombosis Causing Jejunal Stricture: Secondary to Hypercoagulable States and Primary Portal Hypertension

K. Vaiphei, Kartar Singh, U. Dutta, 2002, Digestive Diseases and Sciences.

Myxomatous stromal changes and necrosis of bone marrow--a retrospective study of 3 years.

J. Ahluwalia, Vijay Kumar, N. Varma, 2004, Indian journal of pathology & microbiology.

A Screening Approach for Inherited Erythrocytosis due to the VHL:c.598C > T Mutation (Chuvash Polycythemia)

D. Bansal, P. Malhotra, Anuradha Singh, 2023, Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion.

Pyruvate kinase deficiency: A rare cause of hemolytic anemia: A case report from North-Eastern India

R. Das, T. Dolai, Ankita Sen, 2022, Journal of Hematology and Allied Sciences.