Manu Jamwal

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 14

Top Topics

Dna Methylation

Iron Deficiency

Top Venues

Journal of clinical pathology

Haemophilia : the official journal of the World Federation of Hemophilia

This page only lists publications with an associated author ORCID identifier.

Publications

Debadrita Ray, Ritika Sharma, Narender Kumar, Chander Hans, Harikishan Senee, Manu Jamwal, Jasmina Ahluwalia, Reena Das, Deepak Bansal, Arihant Jain
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)
Manu Jamwal, Sreejesh Sreedharanunni, Ravina Taak, Namrata Singh, Sanjeev Chhabra, Jasbir Kaur, Shilpa Amatya, Prashant Sharma, Amita Trehan, Reena Das
Non-deletional haemoglobin H (Hb H) disease morphologically masquerading as congenital dyserythropoietic anaemia type II: a diagnostic pitfall. Journal of clinical pathology 77 (4) (2024)
Debadrita Ray, Ritika Sharma, Narender Kumar, Chander Hans, Harikishan Senee, Manu Jamwal, Jasmina Ahluwalia, Reena Das, Deepak Bansal, Arihant Jain
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 30 (2) (2024)
Anoop Kumar, Manu Jamwal, Smriti Gupta, Ritika Sharma, Namrata Singh, Laveena Kaushal, Sahil Kumar, Vinod Kumar, Biswanath Behera, Dipankar De, Sanjeev Handa, Uma Nahar, Debajyoti Chatterjee, Reena Das, Rahul Mahajan
Molecular profiling of an Indian EB cohort - a single centre experience. Clinical and experimental dermatology (2024)
Debadrita Ray, Ritika Sharma, Narender Kumar, Chander Hans, Harikishan Senee, Manu Jamwal, Jasmina Ahluwalia, Reena Das, Deepak Bansal, Arihant Jain
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 30 (2) (2024)
Manu Jamwal, Sreejesh Sreedharanunni, Ravina Taak, Namrata Singh, Sanjeev Chhabra, Jasbir Kaur, Shilpa Amatya, Prashant Sharma, Amita Trehan, Reena Das
Non-deletional haemoglobin H (Hb H) disease morphologically masquerading as congenital dyserythropoietic anaemia type II: a diagnostic pitfall. Journal of clinical pathology 77 (4) (2024)
Manu Jamwal, Sreejesh Sreedharanunni, Ravina Taak, Namrata Singh, Sanjeev Chhabra, Jasbir Kaur, Shilpa Amatya, Prashant Sharma, Amita Trehan, Reena Das
Non-deletional haemoglobin H (Hb H) disease morphologically masquerading as congenital dyserythropoietic anaemia type II: a diagnostic pitfall. Journal of clinical pathology (2023)
Yvonne E Goh, Mari S Manger, Mona Duggal, Reena Das, Shipra Saklani, Surbhi Agarwal, Deepmala Budhija, Manu Jamwal, Bidhi L Singh, Neha Dahiya, Hanqi Luo, Julie M Long, Jamie Westcott, Nancy F Krebs, Rosalind S Gibson, Kenneth H Brown, Christine M McDonald
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 15 (13) (2023)
Namrata Singh, Prateek Bhatia, Manu Jamwal, Alka Rani Khadwal, Sanjeev Chhabra, Jasbir Kaur Hira, Reena Das, Prashant Sharma
First reported co-occurrence of "GATA1-mutated X-linked thrombocytopenia with thalassemia (XLTT)" with heterozygous β-thalassemia. International journal of laboratory hematology (2023)
Diksha D Yadav, Manu Jamwal, Namrata Singh, Ritika Sharma, Reena Das, Amita Trehan, Deepak Bansal, Sanjeev Chhabra, Prashant Sharma
Hb Mizuho ( HBB : c.206T>C): Pitfalls of Screening Tests in an Unstable Hemoglobin Variant Diagnosed after Targeted Next-Generation Sequencing. Hemoglobin 45 (5) (2022)
Rahul Mahajan, Seema Manjunath, Manoj Gopal Madakshira, Debajyoti Chatterjee, Anuradha Bishnoi, Dipankar De, Sanjeev Handa, Bishan Dass Radotra, Manu Jamwal, Reena Das
Correlating clinical and laboratory diagnostic modalities in the diagnosis of epidermolysis bullosa in a resource-poor setting. Journal of cutaneous pathology 49 (5) (2022)
Nabhajit Mallik, Manu Jamwal, Ritika Sharma, Namrata Singh, Prashant Sharma, Deepak Bansal, Amita Trehan, Sanjeev Chhabra, Reena Das
Ultra-rare Hb Regina ( HBB :c.289C>G) with coinherited β-thalassaemia trait: solving the puzzle for extreme erythrocytosis. Journal of clinical pathology 75 (11) (2022)
Manu Jamwal, Anu Aggarwal, Prashant Sharma, Deepak Bansal, Amita Trehan, Man Updesh Singh Sachdeva, Shano Naseem, Arindam Maitra, Reena Das
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. Pediatric blood & cancer 68 (10) (2021)
Anu Aggarwal, Manu Jamwal, Prashant Sharma, Man Updesh Singh Sachdeva, Deepak Bansal, Pankaj Malhotra, Reena Das
Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next-generation sequencing: First South Asian study. British journal of haematology 188 (5) (2019)