Rajni Kumrah

Post Graduate Institute of Medical Education and Research — India

Medicine · Health Sciences

12h-index514citations30works3.12yr avg
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Research Topics

Kawasaki Disease and Coronary Complications(14), Coronary Artery Anomalies(10), Immunodeficiency and Autoimmune Disorders(5), Inflammasome and immune disorders(4), Streptococcal Infections and Treatments(4)

Publications30 total

Deficiency of adenosine deaminase 2: Myriad faces in a single family
Pediatric Allergy and Immunology·2026
Flow Cytometric Expression of Nucleotide‐Binding Oligomerization Domain Containing 2 (<scp>NOD2</scp>) Protein: An Effective Screening Tool for Blau Syndrome
International Journal of Rheumatic Diseases·2025Open Access
Markers of T Lymphocyte Activation in Children With Kawasaki Disease: An Experimental Study From North India
International Journal of Rheumatic Diseases·2025· 1 citedOpen Access
Profile of patients with Juvenile Dermatomyositis and Anti-MDA5 autoantibodies
Pediatric Research·2024
Incidence of Kawasaki disease among children in Chandigarh, India during 2015–2019: a trend analysis
The Lancet Regional Health - Southeast Asia·2024· 7 citedOpen Access
Proteomics approach for biomarker discovery in Kawasaki disease
Expert Review of Clinical Immunology·2024· 1 cited
Markers of Endothelial Dysfunction in Kawasaki Disease: An Update
Clinical Reviews in Allergy & Immunology·2024· 13 cited
Intravenous Immunoglobulin in Kawasaki Disease—Evolution and Pathogenic Mechanisms
Diagnostics·2023· 25 citedOpen Access
Granulomatous inflammation and hypogammaglobulinemia: Clinical conundrum of familial hemophagocytic lymphohistiocytosis type 5
Immunobiology·2022
Juvenile dermatomyositis associated with autoantibodies to small ubiquitin-like modifier activating enzyme: a report of 4 cases from North India and a review of literature
Immunologic Research·2022· 7 cited
Blau syndrome: Lessons learned in a tertiary care centre at Chandigarh, North India
Frontiers in Immunology·2022· 19 citedOpen Access
Association of single nucleotide polymorphism rs113420705 of CASP3 in children with Kawasaki disease from North India
Journal of Family Medicine and Primary Care·2022· 6 citedOpen Access
Features of Hemophagocytic Lymphohistiocytosis in Infants With Severe Combined Immunodeficiency: Our Experience From Chandigarh, North India
Frontiers in Immunology·2022· 6 citedOpen Access
Association of SNP (rs1042579) in thrombomodulin gene and plasma thrombomodulin level in North Indian children with Kawasaki disease
Molecular Biology Reports·2022· 5 cited
Exploration of Potential Biomarker Genes and Pathways in Kawasaki Disease: An Integrated in-Silico Approach
Frontiers in Genetics·2022· 12 citedOpen Access
Deficiency of Human Adenosine Deaminase Type 2 – A Diagnostic Conundrum for the Hematologist
Frontiers in Immunology·2022· 25 citedOpen Access
Monocyte subsets and their activation markers in Kawasaki disease – A Study from a Tertiary care Center in North India
Research Square (Research Square)·2022Open Access
Features of nephrotic syndrome in infants with severe combined immunodeficiency
The Journal of Allergy and Clinical Immunology In Practice·2022Open Access
Association of ITPKC gene polymorphisms rs28493229 and rs2290692 in North Indian children with Kawasaki disease
Pediatric Research·2021· 7 cited
Deficiency of Adenosine Deaminase 2—a Monogenic Cause of Wunderlich Syndrome
Journal of Clinical Immunology·2021
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Frequent Co-authors

Amit Rawat(22), Pandiarajan Vignesh(17), Surjit Singh(15), Ankur Kumar Jindal(10), Rakesh Kumar Pilania(10), Deepti Suri(8), Gummadi Anjani(6), Surjit Singh(6), Deepti Suri(6), Nameirakpam Johnson(5), Anit Kaur(5), Sanjib Mondal(5), Anupriya Kaur(5), Ankita Singh(4), Kanika Arora(4), Priyanka Srivastava(4), Dharmagat Bhattarai(4), Himanshi Chaudhary(3), Pratap Kumar Patra(3), Madhubala Sharma(3)