# Luigi D. Notarangelo

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/luigi-d-notarangelo/

## Facts

| Field | Value |
| --- | --- |
| Citations | 63,784 |
| Field | Immunodeficiency and Autoimmune Disorders |
| h-index | 122 |
| i10-index | 535 |
| Last Known Institution | National Institutes of Health |
| OpenAlex ID | https://openalex.org/A5029163913 |
| ORCID iD | https://orcid.org/0000-0002-8335-0262 |
| Works | 890 |

## Researcher papers

Showing 12 of 14.

- [Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID)](https://scholariq.org/papers/mutations-of-jak-3-gene-in-patients-with-autosomal-severe-combined-immune/)
- [Transplantation Outcomes for Severe Combined Immunodeficiency, 2000–2009](https://scholariq.org/papers/transplantation-outcomes-for-severe-combined-immunodeficiency-2000-2009/)
- [Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources](https://scholariq.org/papers/expansion-of-the-human-phenotype-ontology-hpo-knowledge-base-and-resources/)
- [Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis](https://scholariq.org/papers/defects-in-tcirg1-subunit-of-the-vacuolar-proton-pump-are-responsible-for-a/)
- [Partial V(D)J Recombination Activity Leads to Omenn Syndrome](https://scholariq.org/papers/partial-v-d-j-recombination-activity-leads-to-omenn-syndrome/)
- [A Modified γ-Retrovirus Vector for X-Linked Severe Combined Immunodeficiency](https://scholariq.org/papers/a-modified-retrovirus-vector-for-x-linked-severe-combined-immunodeficiency/)
- [Long-term outcome and lineage-specific chimerism in 194 patients with Wiskott-Aldrich syndrome treated by hematopoietic cell transplantation in the period 1980-2009: an international collaborative study](https://scholariq.org/papers/long-term-outcome-and-lineage-specific-chimerism-in-194-patients-with-wiskott/)
- [Preexisting autoantibodies to type I IFNs underlie critical COVID-19 pneumonia in patients with APS-1](https://scholariq.org/papers/preexisting-autoantibodies-to-type-i-ifns-underlie-critical-covid-19-pneumonia/)
- [Human Osteoclast-Poor Osteopetrosis with Hypogammaglobulinemia due to TNFRSF11A (RANK) Mutations](https://scholariq.org/papers/human-osteoclast-poor-osteopetrosis-with-hypogammaglobulinemia-due-to-tnfrsf11a/)
- [X–linked thrombocytopenia and Wiskott–Aldrich syndrome are allelic diseases with mutations in the WASP gene](https://scholariq.org/papers/x-linked-thrombocytopenia-and-wiskott-aldrich-syndrome-are-allelic-diseases-with/)
- [Immunopathological signatures in multisystem inflammatory syndrome in children and pediatric COVID-19](https://scholariq.org/papers/immunopathological-signatures-in-multisystem-inflammatory-syndrome-in-children/)
- [Long-term outcome following hematopoietic stem-cell transplantation in Wiskott-Aldrich syndrome: collaborative study of the European Society for Immunodeficiencies and European Group for Blood and Marrow Transplantation](https://scholariq.org/papers/long-term-outcome-following-hematopoietic-stem-cell-transplantation-in-wiskott/)

## Researcher topics

- [Immunodeficiency and Autoimmune Disorders](https://scholariq.org/topics/immunodeficiency-and-autoimmune-disorders/)
- [Immune Cell Function and Interaction](https://scholariq.org/topics/immune-cell-function-and-interaction/)
- [T-cell and B-cell Immunology](https://scholariq.org/topics/t-cell-and-b-cell-immunology/)
- [Blood disorders and treatments](https://scholariq.org/topics/blood-disorders-and-treatments/)
- [Hematopoietic Stem Cell Transplantation](https://scholariq.org/topics/hematopoietic-stem-cell-transplantation/)

## Researcher university

- [National Institutes of Health](https://scholariq.org/institutions/national-institutes-of-health/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.