# Anna Villa

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/anna-villa/

## Facts

| Field | Value |
| --- | --- |
| Citations | 18,162 |
| Field | Immunodeficiency and Autoimmune Disorders |
| h-index | 70 |
| i10-index | 229 |
| Last Known Institution | Vita-Salute San Raffaele University |
| OpenAlex ID | https://openalex.org/A5079738648 |
| ORCID iD | 0000-0003-4428-9013 |
| Works | 508 |

## Researcher papers

- [Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome](https://scholariq.org/papers/lentiviral-hematopoietic-stem-cell-gene-therapy-in-patients-with-wiskott-aldrich/)
- [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/)
- [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/)
- [The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity](https://scholariq.org/papers/the-european-society-for-immunodeficiencies-esid-registry-working-definitions/)
- [Osteopetrosis: genetics, treatment and new insights into osteoclast function](https://scholariq.org/papers/osteopetrosis-genetics-treatment-and-new-insights-into-osteoclast-function/)
- [Partial V(D)J Recombination Activity Leads to Omenn Syndrome](https://scholariq.org/papers/partial-v-d-j-recombination-activity-leads-to-omenn-syndrome/)
- [Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL](https://scholariq.org/papers/osteoclast-poor-human-osteopetrosis-due-to-mutations-in-the-gene-encoding-rankl/)
- [V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations](https://scholariq.org/papers/v-d-j-recombination-defects-in-lymphocytes-due-to-rag-mutations-severe/)
- [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/)
- [Preclinical modeling highlights the therapeutic potential of hematopoietic stem cell gene editing for correction of SCID-X1](https://scholariq.org/papers/preclinical-modeling-highlights-the-therapeutic-potential-of-hematopoietic-stem/)
- [Osteoclast rich osteopetrosis due to defects in the TCIRG1 gene](https://scholariq.org/papers/osteoclast-rich-osteopetrosis-due-to-defects-in-the-tcirg1-gene/)

## Researcher topics

- [Immunodeficiency and Autoimmune Disorders](https://scholariq.org/topics/immunodeficiency-and-autoimmune-disorders/)
- [Bone Metabolism and Diseases](https://scholariq.org/topics/bone-metabolism-and-diseases/)
- [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/)
- [Bone health and treatments](https://scholariq.org/topics/bone-health-and-treatments/)

## Researcher university

- [Vita-Salute San Raffaele University](https://scholariq.org/institutions/vita-salute-san-raffaele-university/)

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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.