OOIR: Observatory of International Research

Papers

(The H4-Index of Clinical Immunology is 30. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-06-01 to 2025-06-01.)

Article	Citations
Primary immunodeficiency associated with a SAMD9L mutation	152
Effectiveness of T2 biologics in patients with common variable immune deficiency and allergic respiratory disease	99
Exploring the role of insulin-like growth factor binding protein-1 in identifying idiopathic multicentric Castleman's disease types: Implications for the mTOR signaling pathway	90
Assessment of disease activity and management of patients with NFkB1 insufficiency	78
IgG Replacement Therapy Use in Patients with Hypogammaglobulinemia after Lung Transplant	61
Editorial Board	58
The possible involvement of sema3A and sema4A in the pathogenesis of multiple sclerosis	56
Results of a Phase 3 Trial of an Oral CXCR4 Antagonist, Mavorixafor, for Treatment of Patients With WHIM Syndrome	49
NLRP12-associated autoinflammatory disease: A novel causal mutation and bioinformatics analyses	46
Tissue resident cell processes determine organ damage in systemic lupus erythematosus	44
Anti-IL12p40 autoantibodies in a teenage girl with multiple recurrent abscesses	43
Determining reference ranges for lymphocyte proliferation responses to phytohemagglutinin and Bacillus Calmette–Guérin in Iranian children	42
USP18 induction regulates immunometabolism to attenuate M1 signal-polarized macrophages and enhance IL-4-polarized macrophages in systemic lupus erythematosus	41
2 Maternal and neonate outcomes following exposure to hyaluronidase-facilitated subcutaneous immunoglobulin 10% during pregnancy: a retrospective case series based on US claims data	40
17 Severe Cardiac Tamponade in an Unusual Case of CTLA-4 Haploinsufficiency	40
117 Clinical and Immunologic Phenotype of Prolidase Deficiency	38
94 Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulation	37
195 DHR-based Flow Cytometry Beyond CGD	37
87 Phenotypic variability of Circulating Natural Killer Cells in healthy donors	36
71 Two allelic variants in the SERPING1 gene associated with hereditary angioedema detected in one adult patient without clinical manifestation of the disease. Case report	35
Age-dependent transcriptomic profiles of leukocytes in pediatric population	34
142 A non-consanguineous family with hepatic veno-occlusive disease and immunodeficiency	33
Distinct innate and adaptive immunity phenotypic profile at the circulating single-cell level in Psoriatic Arthritis	33
IL-4 alters TLR7-induced B cell developmental program in lupus	33
Dok-1 regulates mast cell degranulation negatively through inhibiting calcium-dependent F-actin disassembly	33

Ionic reverberation modulates the cellular fate of CD8+tissue resident memory T cells (TRMs) in patients with renal cell carcinoma: A novel mechanism	32
Sialylated IVIg binding to DC-SIGN+ Hofbauer cells induces immune tolerance through the caveolin-1/NF-kB pathway and IL-10 secretion	32
Presence of ectopic germinal center structures in autoimmune hepatitis	32
Editorial Board	32
Novel biallelic mutations in the DUOX2 gene underlying very early-onset inflammatory bowel disease: A case report	31
PReS-endorsed international childhood lupus T2T task force definition of childhood lupus low disease activity state (cLLDAS)	30
5-HT is associated with the dysfunction of regulating T cells in patients with allergic rhinitis	30
Behçet's disease with a somatic UBA1 variant:Expanding spectrum of autoinflammatory phenotypes of VEXAS syndrome	30
AIM2 inflammasome: A potential therapeutic target in ischemic stroke	30