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 2022-05-01 to 2026-05-01.)

Article	Citations
2 Maternal and neonate outcomes following exposure to hyaluronidase-facilitated subcutaneous immunoglobulin 10% during pregnancy: a retrospective case series based on US claims data	139
17 Severe Cardiac Tamponade in an Unusual Case of CTLA-4 Haploinsufficiency	75
117 Clinical and Immunologic Phenotype of Prolidase Deficiency	73
94 Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulation	66
195 DHR-based Flow Cytometry Beyond CGD	60
BNT162b2 mRNA vaccination attenuates innate immune function in humans	58
87 Phenotypic variability of Circulating Natural Killer Cells in healthy donors	53
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	49
The possible involvement of sema3A and sema4A in the pathogenesis of multiple sclerosis	48
Novel biallelic mutations in the DUOX2 gene underlying very early-onset inflammatory bowel disease: A case report	48
Anti-IL12p40 autoantibodies in a teenage girl with multiple recurrent abscesses	45
Age-dependent transcriptomic profiles of leukocytes in pediatric population	39
AXL+SIGLEC6+ dendritic cells in cerebrospinal fluid and brain tissues of patients with autoimmune inflammatory demyelinating disease of CNS	39
USP18 induction regulates immunometabolism to attenuate M1 signal-polarized macrophages and enhance IL-4-polarized macrophages in systemic lupus erythematosus	39
Characterization of PANoptosis patterns predicts survival and immunotherapy response in gastric cancer	38
Behçet's disease with a somatic UBA1 variant:Expanding spectrum of autoinflammatory phenotypes of VEXAS syndrome	37
Ionic reverberation modulates the cellular fate of CD8+tissue resident memory T cells (TRMs) in patients with renal cell carcinoma: A novel mechanism	36
A spectrum of novel anti-vascular endothelial cells autoantibodies in idiopathic nephrotic syndrome patients	36
NLRP12-associated autoinflammatory disease: A novel causal mutation and bioinformatics analyses	35
Editorial Board	35
Sialylated IVIg binding to DC-SIGN+ Hofbauer cells induces immune tolerance through the caveolin-1/NF-kB pathway and IL-10 secretion	35
142 A non-consanguineous family with hepatic veno-occlusive disease and immunodeficiency	35
Aicardi-Goutières Syndrome caused by SAMHD1 mutation: Pathogenesis and Beyond	35
IgG Replacement Therapy Use in Patients with Hypogammaglobulinemia after Lung Transplant	34
Primary immunodeficiency associated with a SAMD9L mutation	33

Results of a Phase 3 Trial of an Oral CXCR4 Antagonist, Mavorixafor, for Treatment of Patients With WHIM Syndrome	32
Assessment of disease activity and management of patients with NFkB1 insufficiency	32
Effectiveness of T2 biologics in patients with common variable immune deficiency and allergic respiratory disease	31
5-HT is associated with the dysfunction of regulating T cells in patients with allergic rhinitis	30
Editorial Board	30