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Indian Journal of Pediatrics|December 12, 2019
Laboratory Approach to Hemolytic AnemiaManu Jamwal, Prashant Sharma, Reena Das
Acta Cardiologica|October 6, 2017
Coagulation F13A1 V34L, fibrinogen and homocysteine versus conventional risk factors in the pathogenesis of MI in young personsVikarn Vishwajeet, Manu Jamwal, Prashant Sharma, et al.
British Journal of Haematology|October 12, 2019
Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next-generation sequencing: First South Asian studyAnu Aggarwal, Manu Jamwal, Prashant Sharma, et al.
Journal of Clinical Pathology|March 22, 2018
Overhydrated stomatocytosis associated with a complex <i>RHAG</i> genotype including a novel <i>de novo</i> mutationManu Jamwal, Anu Aggarwal, Man Updesh Singh Sachdeva, et al.
Biomacromolecules|October 11, 2022
High Drug Loading Nanoparticles Stabilized with Autologous Serum Proteins Passively Inhibits Tumor GrowthMimansa, Manu Jamwal, Reena Das, et al.
Cancer Genetics|July 31, 2021
A novel ATRX splice variant causing acquired HbH disease in myelodysplastic syndrome with excess blasts-1Nabhajit Mallik, Namrata Singh, Manu Jamwal, et al.
European Journal of Medical Genetics|March 23, 2021
Autosomal dominant familial periodic fever patient with a missense variant c.215G>A (p.Cys72Tyr) in TNFRSF1A gene presenting as neutrophiliaSweta Rajpal, Manu Jamwal, Deepesh Lad, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 23, 2017
Next-generation sequencing unravels homozygous mutation in glucose-6-phosphate isomerase, GPIc.1040G>A (p.Arg347His) causing hemolysis in an Indian infantManu Jamwal, Anu Aggarwal, Anirban Das, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 25, 2016
Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three casesManu Jamwal, Anu Aggarwal, Verinder Kumar, et al.
The Journal of Molecular Diagnostics : JMD|February 10, 2020
Next-Generation Sequencing-Based Diagnosis of Unexplained Inherited Hemolytic Anemias Reveals Wide Genetic and Phenotypic HeterogeneityManu Jamwal, Anu Aggarwal, Arindam Palodhi, et al.
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