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ICMR-National Institute of Immunohaematology

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2021-Till Date

2016-2020

2011-2015

2006-2010

Publications 2021-Till Date
Year
1 Kulkarni S, Mishra G, Maru H, Parchure D, Gupta D, Bajaj AK, Sindhwani SP, Chaphekar A, Shah R, Frec C, Madkaikar M, Fichou Y. Molecular characterization of rare D--/D-- variants in individuals of Indian origin
BloodTransfus. 2022 Jan;20(1):59-65.(IF:3.443)
2 Kulkarni BP, Ghargi K, Shanmukhaiah C and Shetty SD. Rare Occurrence of Inhibitors in Von Willebrand Disease: A Case Report
Front. Med. 2022 Jan 11;8:807664. doi: 10.3389/fmed.2021.807664. (IF:5.091)
3 Dhangar S, Panchal P, Ghatanatti J, Suralkar J, Shah A, Vundinti BR. disability associated with chromosomal copy number variations.
BMC Med Genomics. 2022 Jan 3;15(1):2..Erratum in: BMC Med Genomics. 2022 Jan 18;15(1):11.(IF:2.931)
4 Madathil Govindaraj G, Jain A, Edavazhippurath A, Bhoyar RC, Dhanasooraj D, Mishra A, Gupta V, Nair M, Shiny PM, Uppuluri R, Kumar A, Kashyap A, Ajith Kumar VT, Shankaran G, Senthivel V, Imran M, Kumar Divakar M, Sawant S, Dalvi A, Madkaikar M, Raj R, Sivasubbu S, Scaria V. Clinical, immunological and genomic characteristics of children with X-linked gammaglobulinemia from Kerala, South India.
Hum Immunol. 2022 Jan 21:S0198-8859(22)00005-2. (IF: 2.85)
5 Sampagar A, Gosavi M, Kedar P, Patel T, Dongerdiye R, Mahantashetti N. Clinical, laboratory, and mutational profile of children with glucose phosphate isomerase deficiency: a single centre report.Int
J Hematol. 2022 Feb;115(2):255-262. (IF:2.49)
6 Thaker P, Colah RB, Patel J, Raicha B, Mistry A, Mehta V, Italia Y, Desai S, Dave K, Shanmugam R, Ghosh K and Mukherjee MB Newborn Screening for Sickle Cell Disease Among Tribal Populations in the States of Gujarat and Madhya Pradesh in India: Evaluation and Outcome Over 6 Years.
Front Med (Lausanne)2022 Feb 15;8:731884. (IF :5.091)
7 Shanmukhaiah C, Jijina F, Kannan S, Pai NG, Kulkarni B, Khuba SV, Shaikh M, Joshi A, Phatale R, Apte S. Efficacy of emicizumab in von Willebrand disease (VWD) patients with and without alloantibodies to von Willebrand factor (VWF): Report of two cases and review of literature.
Haemophilia. 2022 Mar;28(2):286-291. (IF: 4.287)
8 Deorukhkar A, Kulkarni A, Kedar P. Three novel mutations in CYB5R3 gene causing NADH-cytochrome b5 reductase enzyme deficiency leads to recessive congenital methaemoglobinemia.
Mol Biol Rep. 2022 Mar;49(3):2141-2147 (IF: 2.316 )
9 9)Lashkari HP, Madkaikar M, Dalvi A, Gupta M, Bustamante J, Sharma M, Rawat A, Bhatia P, Bhat KG, Rao S, Kamath N, Moideen F, Latour S, Winter S, Bhavani GS, Girisha KM. Clinical and Genetic Spectrum of Inborn Errors of Immunity in a Tertiary Care Center in Southern India.
Indian J Pediatr. 2022 Mar;89(3):233-242 (IF:1.967)
10 11)Madathil Govindaraj G, Jain A, Edavazhippurath A, Bhoyar RC, Dhanasooraj D, Mishra A, Gupta V, Nair M, Shiny PM, Uppuluri R, Kumar A, Kashyap A, Ajith Kumar VT, Shankaran G, Senthivel V, Imran M, Kumar Divakar M, Sawant S, Dalvi A, Madkaikar M, Raj R, Sivasubbu S, Scaria V. Clinical, immunological and genomic characteristics of children with X-linked agammaglobulinemia from Kerala, South India
Hum Immunol. 2022 Apr;83(4):335-345. doi: 10.1016/j.humimm.2022.01.003. Epub 2022 Jan 21 (IF:2.85)
11 Iyengar VV, Gowri V, Taur P; COE consortium, Desai MM Vanishing Lymphocytes in a Case of Vanishing Bone Disease
J Clin Immunol. 2022 Apr 42(3): 706-708. (IF:8.317)
12 Maurya N, Mohanty P, Dhangar S, Panchal P, Jijina F, Mathan SLP, Shanmukhaiah C, Madkaikar M, Vundinti BR Comprehensive analysis of genetic factors predicting overall survival in Myelodysplastic syndromes
Sci Rep. 2022 Apr 8;12(1):5925. doi: 10.1038/s41598-022-09864-9. (IF 4.379)
13 Gowri V, Taur P, Chougule A; COE consortia, Desai M STAT 3 GOF with Polycythemia: a Twist to the Tale-First Case Report from India.
J Clin Immunol. 2022 May;42(4):866-868 (IF:8.317)
14 Madkaikar M, Desai MM. Iyengar VV, Chougule A, Gowri V, Taur P, Prabhu S, Bodhanwala M, Bargir UA, Scand J XMEN saved by magnesium.
Immunol. 2022 May;95(5):e13154. doi: 10.1111/sji.13154. Epub 2022 Mar 9. (IF:3.487)
15 Kawankar N, Shetty S, Kulkarni B. Novel RASGRP2 variants in platelet function defects: Indian study
Br J Haematol. 2022 May;197(3):377-380 (IF 6.998)
16 Parchure D, Madkaikar M, Kulkarni S. Algorithm development and diagnostic accuracy testing for non-invasive foetal RHD genotyping: an Indian experience.
Blood Transfus. 2022 May;20(3):235-244. doi: 10.2450/2021.0022-21. Epub 2021 Mar 31. (IF: 3.443)
17 Gorivale M, Hariharan P, Kargutkar N, Mehta P, Sawant P, Nadkarni A. Diagnostic challenges posed by a rare unstable hemoglobin variant Hb Southampton HBB c.320T C with pyrimidine 5 nucleotidase deficiency and the response to HU therapy
Blood Cells Mol Dis. 2022 May 7;96:102667. doi:10.1016/j.bcmd.2022.102667. Online ahead of print (IF :3.039)
18 Taur P, Madkaikar M, Desai M.Hiwarkar P, Bargir U, Pandrowala A, Bodhanwala M, Thakker N SLGT2 Inhibitor Rescues Myelopoiesis in G6PC3 Deficiency
J Clin Immunol. 2022 Jul 15. doi: 10.1007/s10875-022-01323-4. Online ahead of print. (IF 8.317)
19 Gupta A, Jain M, Sheety T, Salunkhe L, Gorivale M, Nadkarni A Hemoglobin Reims- a rare alphga globin chain varinay and its interaction with beta thalassemia
Journal of Hematopathology. Received: 21 June 2022 / Accepted: 31 August 2022 doi.org/10.1007/s12308-022-00512-9 (IF :0.196)
20 Pankaj Kumar, Amit Bugalia Pallavi Thaker, Manju Gorivale, Nighat Hussai,Anita Nadkarni ,Nabhajit Mallik, Co- inheritance of Hb Ottawa and HbS: a rare interaction leading to an interesting diagnostic challenge
Journal of Hematopathology. https://doi.org/10.1007/s12308-022-00514-7. Received: 15 July 2022 / Accepted: 6 September 2022 (IF:0.196)
21 Kedar P, Dongerdiye R, Chandrakala S, Bargir UA, Madkaikar M. Targeted next-generation sequencing revealed a novel homozygous mutation in the LRBA gene causes severe haemolysis associated with Inborn Errors of Immunity in an Indian family
Hematology. 2022 Dec;27(1):441-448. doi: 10.1080/16078454.2022.2058736. (IF :2.269)
22 Fujii J, Homma T, Kobayashi S, Warang P, Madkaikar M, Mukherjee MB. Erythrocytes as a preferential target of oxidative stress in blood.
Free Radic Res. 2021 Jan 17:1-19. (IF:2.839).
23 Seema A Korgaonkar, Durga Chougule, Uday Khopkar, Vidya Kharkar, Vikram Lahoria, Prasad Khadilkar, Manisha Madkaikar, Vandana Pradhan. Quantitative estimation of Antidesmoglein Autoantibodies by ELISA in Pemphigus patients and its correlation with disease activity.
Indian J Dermatol 2021 Jan; 66(1);98-9.
24 Yadav RM, Bargir UA, Ganapule A, Dalvi A, Gupta M,Madkaikar M. HLA-DR covers Bare Lymphocyte Syndrome.
Scand J Immunol. 2021 Feb;93(2):e12968. doi: 10.1111/sji.12968.(IF:2.717)
25 Bargir UA,Madkaikar M. Chalazia, A Late Manifestation of Primary Immunodeficiency Disorders.
Ocul Immunol Inflamm.2021 Feb 17;29(2):264. (IF:2.112)
26 Saikia B, Rawat A, Minz RW, Suri D, Pandiarajan V, Jindal A, Sahu S, Karim A, Desai M, Taur PD, Pandrowala A, Gowri V, Madkaikar M, Dalvi A, Yadav RM, Lashkari HP, Raj R, Uppuluri R, Swaminathan VV, Bhattad S, Cyril G, Kumar H, Shukla A, Kalra M, Govindar Clinical Profile of Hyper-IgE Syndrome in India.
Front Immunol. 2021 Feb 26;12:626593. doi: 10.3389/fimmu.2021.626593. (IF:6.429)
27 Taur PD, Gowri V, Pandrowala AA, Iyengar VV, Chougule A, Golwala Z, Chandak S, Agarwal R, Keni P, Dighe N, Bodhanwala M, Prabhu S, George B, Fouzia NA, Edison ES, Arunachalam AK, Madkaikar MR, Dalvi AD, Yadav RM, Bargir UA, Kambli PM, Rawat A, Das J, Josh Clinical and Molecular Findings in Mendelian Susceptibility to Mycobacterial Diseases: Experience From India.
Front Immunol. 2021 Feb 25;12:631298. doi: 10.3389/fimmu.2021.631298.(IF:6.429)
28 Rawat A, Vignesh P, Sudhakar M, Sharma M, Suri D, Jindal A, Gupta A, Shandilya JK, Loganathan SK, Kaur G, Chawla S, Patra PK, Khadwal A, Saikia B, Minz RW, Aggarwal V, Taur P, Pandrowala A, Gowri V, Desai M, Kulkarni M, Hule G, Bargir U, Kambli P, Madkaik Clinical, Immunological, and Molecular Profile of Chronic Granulomatous Disease: A Multi-Centric Study of 236 Patients From India.
Front Immunol. 2021 Feb 25;12:625320. doi: 10.3389/fimmu.2021.625320.(IF:6.429)
29 More TA,Kedar PS. Genotypic analysis of SLC4A1 A858D mutation in Indian population associated with distal renal tubular Acidosis (dRTA) coupled with hemolytic anemia.
Gene. 2021 Feb 15;769:145241. doi: 10.1016/j.gene.2020.145241.
30 Vignesh P, Rawat A, Kumrah R, Singh A, Gummadi A, Sharma M, Kaur A, Nameirakpam J, Jindal A, Suri D, Gupta A, Khadwal A, Saikia B, Minz RW, Sharma K, Desai M, Taur P, Gowri V, Pandrowala A, Dalvi A, Jodhawat N, Kambli P, Madkaikar MR, Bhattad S, Ramprakas Clinical, Immunological, and Molecular Features of Severe Combined Immune Deficiency: A Multi-Institutional Experience From India.
Front Immunol. 2021 Feb 8;11:619146. doi: 10.3389/fimmu.2020.619146. (IF:6.429)
31 Shah A, George M, Dhangar S, Rajendran A, Mohan S,Vundinti BR. Severetelomereshorteningin Fanconi anemia complementation group L.
Mol Biol Rep. 2021 Jan;48(1):585-593.(IF:1.402)
32 Rawat A, Jindal AK, Suri D, Vignesh P, Gupta A, Saikia B, Minz RW, Banday AZ, Tyagi R, Arora K, Joshi V, Mondal S, Shandilya JK, Sharma M, Desai M, Taur P, Pandrowala A, Gowri V, Sawant-Desai S, Gupta M, Dalvi AD, Madkaikar M, Aggarwal A, Raj R, Uppuluri Clinical and Genetic Profile of X-Linked Agammaglobulinemia: A Multicenter Experience From India.
Front Immunol. 2021 Jan 15;11:612323. doi: 10.3389/fimmu. (IF:6.429)
33 Bhave A , Iyer L, Kazi N , Gorivale M , Nadkarni A. Hemoglobin Olympia [ ? codon 20 (B2) G ?A, Val?Met]: a silent Hemoglobin variant
J Clin Diag Res. 2021 Mar; 15(3): EC19-EC21(IF:0.754)
34 Madkaikar M, Gupta N, Yadav RM, Bargir UA. India's crusade against COVID-19.
Nat Immunol. 2021 Mar;22(3):258-259. doi: 10.1038/s41590-021-00876-7.(IF:20.4)
35 Shabrish S, Kelkar M, Yadav RM, Bargir UA, Gupta M, Dalvi A, Aluri J, Kulkarni M, Shinde S, Sawant-Desai S, Kambli P, Hule G, Setia P, Jodhawat N, Gaikwad P, Dhawale A, Nambiar N, Gowri V, Pandrowala A, Taur P, Raj R, Uppuluri R, Sharma R, Kini P, Sivasan The Spectrum of Clinical, Immunological, and Molecular Findings in Familial Hemophagocytic Lymphohistiocytosis: Experience From India.
Front Immunol. 2021 Mar 5;12:612583. doi: 10.3389/fimmu.2021.612583. (IF:6.429)
36 Hariharan P, Nadkarni A Insight of fetal to adult hemoglobin switch: Genetic modulators and therapeutic targets.
Blood Reviews 2021 Mar 6:100823. doi: 10.1016/j.blre.2021.100823.(IF: 6.6)
37 Zian Z, Berry SPD, Bahmaie N, Ghotbi D, Kashif A, Madkaikar M, Bargir UA, Abdullahi H, Khan H, Azizi G. The clinical efficacy of Rituximab administration in autoimmunity disorders, primary immunodeficiency diseases and malignancies.
Int Immunopharmacol. 2021 Mar 24;95:107565. doi:10.1016/j.intimp.2021.107565.(IF:3.9)
38 George M, Solanki A, Mohanty P, Dhangar S, Rajendran A, Mohan S, Vundinti BR. Nitric oxide synthase-2 (NOS2) gene polymorphism c.1832C>T (Ser608Leu) associated with nitrosative stress in Fanconi anaemia.
Mol Biol Rep. 2021 Mar 28. doi: 10.1007/s11033-021-06293-1.(IF:1.402)
39 Suri D, Rikhi R, Jindal AK, Rawat A, Sudhakar M, Vignesh P, Gupta A, Kaur A, Sharma J, Ahluwalia J, Bhatia P, Khadwal A, Raj R, Uppuluri R, Desai M, Taur P, Pandrowala AA, Gowri V,Madkaikar MR, Lashkari HP, Bhattad S, Kumar H, Verma S, Imai K, Nonoyama S Wiskott Aldrich Syndrome: A Multi-Institutional Experience From India.
Front Immunol. 2021 Apr 16;12:627651.eCollection 2021. (IF : 7.561)
40 Pradhan VD, Khadilkar PV, Nadkar MY, Kini SH, Roumenina LT, Rajadhyaksha AG, Khan TA, Chougule D, Ghosh K, Bayry J, Kaveri S Impact of Autoantibodies to Complement Components on the Disease Activity in SLE.
J Assoc Physicians India. 2021 Apr;69(4):11-12. (IF : 0.313)
41 John R, Dalal B,Shankarkumar A, Devarajan PV Innovative BetulinNanosuspension exhibits enhanced anticancer activity in a Triple Negative Breast Cancer Cell line and Zebrafish angiogenesis model.
Int J Pharm. 2021 May 1;600:120511.(IF : 5.875)
42 Yadav RM, Dalvi A, Gupta M, Bargir UA, Shabrish S, Aluri J, Kulkarni M, Hule G, Kambli P, Setia P, Jodhawat N, Taur P, Desai M,Madkaikar MR. Spectrum of Inborn errors of immunity in a cohort of 90 patients presenting with complications to BCG vaccination in India.
Scand J Immunol. 2021 May;93(5):e13010.(IF : 3.487)
43 Fujii J, Homma T, Kobayashi S, Warang P,Madkaikar M, Mukherjee MB. Erythrocytes as a preferential target of oxidative stress in blood.
Free Radic Res. 2021 May;55(5):562-580. (IF : 4.148)
44 Sane M, Dighe V,Patil R, Hassan PA, Gawali S, Patravale V. Bivalirudin and sirolimus co-eluting coronary stent: Potential strategy for the prevention of stent thrombosis and restenosis.
Int J Pharm. 2021 May 1;600:120403. doi: 10.1016/j.ijpharm.2021.120403. Epub 2021 Mar 10. (IF : 5.875)
45 Yadav RM,Madkaikar MR. Interpreting the impact of hydroxychloroquine prophylaxis on SARS-CoV-2 infection.
Indian J Med Res. 2021 May&Jun;153(5&6):564-565. (IF : 2.375)
46 Thakar M, Saxena V, Janakiram N, Ravi V, Desai A, Singh S, Shivanna N, Minz RY, Singh A, Chatterjee M,Madkaikar M, Bembalkar S, Mukherjee A, Mahesh V. Reference Ranges of Different Lymphocyte Subsets in Indian Children: A Multi-Centric Study.
Indian Pediatr. 2021 May 15;58(5):424-429. (IF : 1.411)
47 Afroz T, Mishra G, Saleh AJM,Madkaikar M, Kulkarni S Molecular characterization of a rare Rh phenotype Dc-from the Indian subcontinent.
TransfusApher Sci. 2021 Jun;60(3):103109. (IF: 1.285)doi: 10.1016/j.transci.2021.103109. Epub 2021 Mar 8. (IF : 1.764)
48 Zian Z, Berry SPD, Bahmaie N, Ghotbi D, Kashif A, Madkaikar M, Bargir UA, Abdullahi H, Khan H, Azizi G. The clinical efficacy of Rituximab administration in autoimmunity disorders, primary immunodeficiency diseases and malignancies.
Int Immunopharmacol. 2021 Jun;95:107565. (IF:4.932)
49 Jain A, Govindaraj GM, Edavazhippurath A, Faisal N, Bhoyar RC, Gupta V, Uppuluri R, Manakkad SP, Kashyap A, Kumar A, Divakar MK, Imran M, Sawant S, Dalvi A, Chakyar K,Madkaikar M, Raj R, Sivasubbu S, Scaria V. Whole genome sequencing identifies novel structural variant in a large Indian family affected with X-linked agammaglobulinemia.
PLoS One. 2021 Jul 12;16(7):e0254407. doi: 10.1371/journal.pone.0254407. eCollection 2021.(IF : 3.240)
50 Roos D, van Leeuwen K, Hsu AP, Priel DL, Begtrup A, Brandon R, Rawat A, Vignesh P,Madkaikar M, Stasia MJ, Bakri FG, de Boer M, Roesler J, Kker N, Kker MY, Jakobsen M, Bustamante J, Garcia-Morato MB, Shephard JLV, Cagdas D, Tezcan I, Sherkat R, Mortaz E Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update).
Blood Cells Mol Dis. 2021 Jul 28;92:102596. doi: 10.1016/j.bcmd.2021.102596. Online ahead of print. (3.039)
51 Dongerdiye R, Sampagar A, Devendra R, Warang P, Kedar P. Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C?>?A, (Q101K), in the AK1 gene in an Indian family.
BMC Med Genomics. 2021 Jul 28;14(1):191. (IF : 2.931)
52 Kalantri M, Khopkar U, Shah A,Bargir UA, Hule G, Madkaikar M. A case of disseminated subcutaneous phaeohyphomycosis caused by Exserohilumrostratum with CARD9 mutation.
Indian J DermatolVenereolLeprol.2021 Jul 7:1-3. (IF : 2.545)
53 Setia P, Bargir UA, Aluri J, Sampagar A, Pandit A, Kumar V, Jodhawat N, Shabrish S, Sawant S, Kelkar M, Kambli P, Dalvi A, Madkaikar M. Novel CD3Z and CD3E Deficiency in Two Unrelated Females.
J ClinImmunol. 2021 Jul;41(5):1116-1118 (IF:8.317)
54 Kelkar MG, Bargir UA, Malik-Yadav R, Gupta M, Dalvi A, Jodhawat N, Shinde S,Madkaikar MR CD8 T Cells Exhibit an Exhausted Phenotype in Hemophagocytic Lymphohistiocytosis.
J ClinImmunol.2021 Aug 14.doi: 10.1007/s10875-021-01109-0. Online ahead of print. (IF : 8.317)
55 Panwar U, Mishra K, Patel P, Bharadva S, Vaniawala S, Shah A,Vundinti BR, Kothari SL, Ghosh K Assessment of Long-Term in vitro Multiplied Human Wharton's Jelly-Derived Mesenchymal Stem Cells prior to Their Use in Clinical Administration.
Cells Tissues Organs. 2021;210(4):239-249. doi: 10.1159/000517423. Epub 2021 Sep 14. (IF : 2.481)
56 Yadav RM, Pate A, Shankarkumar A, Athalye S, Shinde S, Bargir UA, Pate M, Ganpule M, Pruthi M, Patil H,Madkaikar MR. Serosurvey for Health-Care Workers Provides Supportive Evidence for the Effectiveness of Hydroxychloroquine Prophylaxis against SARS-CoV-2 Infection.
J Epidemiol Glob Health. 2021 Sep;11(3):283-288.(IF : 1.56)
57 Karimi E, Mahmoudian F, Reyes SOL,Bargir UA, Madkaikar M, Artac H, Sabzevari A, Lu N, Azizi G, Abolhassani H Approach to genetic diagnosis of inborn errors of immunity through next-generation sequencing.
MolImmunol. 2021 Sep;137:57-66.(IF : 4.407)
58 Sampagar A, Gosavi M,Kedar P, Patel T, Dongerdiye R, Mahantashetti N. Clinical, laboratory, and mutational profile of children with glucose phosphate isomerase deficiency: a single centre report.
Int J Hematol. 2021 Oct 27.doi: 10.1007/s12185-021-03240-5. Online ahead of print. ( IF : 2.49)
59 Dongerdiye R, Jagadeesh S, Suresh B, Rajendran A, Devendra R, Warang P,Kedar PS. Novel pathogenic variant c.2714C>A (p. Thr905Lys) in theHK1gene causing severe haemolyticanaemia with developmental delay in an Indian family.
J ClinPathol. 2021 Oct;74(10):620-624.(IF : 3.411)
60 Mohanty MC, Taur PD, Sawant UP, Yadav RM, Potdar V. Prolonged Fecal Shedding of SARS-CoV-2 in Asymptomatic Children with Inborn Errors of Immunity.
J Clin Immunol. 2021 Nov;41(8):1748-1753. (IF:8.317)
61 George M, Solanki A, Chavan N, Rajendran A, Raj R, Mohan S, Nemani S, Kanvinde S, Munirathnam D, Rao S, Radhakrishnan N, Lashkari HP, Ghildhiyal RG, Manglani M, Shanmukhaiah C, Bhat S, Ramesh S, Cherian A, Junagade P,Vundinti BR. A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects.
Hum Mutat. 2021 Dec;42(12):1648-1665. (IF : 4.878)

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