1. A nonsense variant in the Hexokinase 1 gene (HK1) causing severe non‐spherocytic haemolytic anaemia: genetic analysis exemplifies ambiguity due to multiple Isoforms. (23rd May 2019) Authors: Jamwal, Manu; Aggarwal, Anu; Palodi, Arindam; Sharma, Prashant; Bansal, Deepak; Maitra, Arindam; Das, Reena Journal: British journal of haematology Issue: Volume 186:Number 5(2019) Page Start: e142 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel germline RUNX1 mutation with co-occurrence of somatic alterations in a case of myeloid neoplasm with familial thrombocytopenia: first report from India. Issue 10 (24th August 2019) Authors: Rajpal, Sweta; Jain, Arihant; Jamwal, Manu; Jain, Nidhi; Sachdeva, Man U. S.; Malhotra, Pankaj; Varma, Neelam; Das, Reena Journal: Leukemia & lymphoma Issue: Volume 60:Issue 10(2019) Page Start: 2568 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Chronic eosinophilic leukemia with recurrent STAT5B N642H mutation—An entity with features of myelodysplastic syndrome/ myeloproliferative neoplasm overlap. (January 2022) Authors: Sreedharanunni, Sreejesh; Jamwal, Manu; Balakrishnan, Anand; Aravindan, Arun Vijayalakshmi; Sharma, Ritika; Singh, Namrata; Rajpal, Sweta; Singla, Shelly; Khadwal, Alka Rani; Ahluwalia, Jasmina; Malhotra, Pankaj; Das, Reena Journal: Leukemia research Issue: Volume 112(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Clericuzio‐type poikiloderma with neutropenia in a patient from India. Issue 1 (27th October 2020) Authors: Bishnoi, Anuradha; Jamwal, Manu; Das, Reena; Scaria, Vinod; Vishwajeet, Vikarn; De, Dipankar; Saikia, Uma Nahar; Mahajan, Rahul Journal: American journal of medical genetics Issue: Volume 185:Issue 1(2021) Page Start: 278 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Coagulation F13A1 V34L, fibrinogen and homocysteine versus conventional risk factors in the pathogenesis of MI in young persons. Issue 4 (4th July 2018) Authors: Vishwajeet, Vikarn; Jamwal, Manu; Sharma, Prashant; Das, Reena; Ahluwalia, Jasmina; Dogra, Rupinder Kaur; Rohit, Manoj Kumar Journal: Acta cardiologica Issue: Volume 73:Issue 4(2018) Page Start: 328 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Comparison of Methods for Estimating Discretionary Salt Intake in Field Settings. (14th June 2022) Authors: Goh, Yvonne; Manger, Mari; Saklani, Shipra; Agarwal, Surbhi; Budhija, Deepmala; Jamwal, Manu; Chauhan, Anshul; Singh, Bidhi; Dahiya, Neha; Duggal, Mona; Das, Reena; Long, Julie; Westcott, Jamie; Krebs, Nancy; Gibson, Rosalind; Brown, Kenneth; McDonald, Christine Journal: Current developments in nutrition Issue: Volume 6(2022)Supplement 1 Page Start: 571 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Correlating clinical and laboratory diagnostic modalities in the diagnosis of epidermolysis bullosa in a resource‐poor setting. (15th February 2022) Authors: Mahajan, Rahul; Manjunath, Seema; Madakshira, Manoj Gopal; Chatterjee, Debajyoti; Bishnoi, Anuradha; De, Dipankar; Handa, Sanjeev; Dass Radotra, Bishan; Jamwal, Manu; Das, Reena Journal: Journal of cutaneous pathology Issue: Volume 49:Number 5(2022) Page Start: 454 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. De novo haemoglobin sabine masquerading as double heterozygosity for HbQ-India and β-thalassemia trait: first report from South Asia. Issue 4 (7th February 2020) Authors: Jamwal, Manu; Kaur, Jasbir; Chhabra, Sanjeev; Trehan, Amita; Sharma, Prashant; Das, Reena Journal: Journal of clinical pathology Issue: Volume 73:Issue 4(2020) Page Start: 236 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next‐generation sequencing: First South Asian study. (10th October 2019) Authors: Aggarwal, Anu; Jamwal, Manu; Sharma, Prashant; Sachdeva, Man Updesh Singh; Bansal, Deepak; Malhotra, Pankaj; Das, Reena Journal: British journal of haematology Issue: Volume 188:Number 5(2020) Page Start: 784 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. 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. Issue 10 (12th June 2021) Authors: Jamwal, Manu; Aggarwal, Anu; Sharma, Prashant; Bansal, Deepak; Trehan, Amita; Sachdeva, Man Updesh Singh; Naseem, Shano; Maitra, Arindam; Das, Reena Journal: Pediatric blood & cancer Issue: Volume 68:Issue 10(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗