Anna Villa - Concepedia

Author

Anna Villa

Institute of Genetic and Biomedical Research ORCID

Also Known As

A M Villa, A Villa, A. M. VILLA, A. M. Villa, A. Villa, A.M Villa, A.M. Villa, ANNA MARIA VILLA, ANNA VILLA, ANNA MARIA VILLA

510

Publications

17.7K

Citations

H-Index

219

Concepts

All Affiliations

Institute of Genetic and Biomedical Research Institute of Biomedical Technologies The San Raffaele Telethon Institute for Gene Therapy University of Brescia Humanitas University

About

Anna Villa is an author at Institute of Genetic and Biomedical Research specializing in medicine, pathology, and immunology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	39	87	8.6K
2	Natural Sciences	9	9	283
3	Health Sciences	5	5	1.4K
4	Engineering	4	4	203
5	Humanities	1	1	22

Anna Villa

182

Publications

14.4K

Citations

H-Index

Page 1

	Year	Citations
Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome Alessandro Aiuti, Luca Biasco, Samantha Scaramuzza, Science Cell TherapyLentiviral Gene TherapyImmunologyPathologyImmunotherapy	2013	1K
Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID) Paolo Macchi, Anna Villa, Silvia Giliani, Nature Primary ImmunodeficiencyImmunogeneticsImmune DeficiencyJak-3 GeneImmunology	1995	882
Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis Annalisa Frattini, Paul J. Orchard, Cristina Sobacchi, Nature Genetics Vacuolar Proton PumpBone Morphogenic ProteinGeneticsPathologyTcirg1 Subunit	2000	673
The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity Markus G. Seidel, Gerhard Kindle, Benjamin Gathmann, The Journal of Allergy and Clinical Immunology In Practice Primary ImmunodeficiencyVaccinationMaternal ImmunizationAutoimmune DiseaseImmunodeficiencies	2019	581
Partial V(D)J Recombination Activity Leads to Omenn Syndrome Anna Villa, Sandro Santagata, Fabio Bozzi, Cell Partial VGenetic DisorderGeneticsPathogenesisRecombination Dynamic	1998	460
Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL Cristina Sobacchi, Annalisa Frattini, Matteo M. Guerrini, Nature Genetics Bone DiseaseSclerostinDevelopmental BiologyOsteoclast-poor Human OsteopetrosisBone Morphogenic Protein	2007	378
V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations Anna Villa Blood	2001	343
Human Osteoclast-Poor Osteopetrosis with Hypogammaglobulinemia due to TNFRSF11A (RANK) Mutations Matteo M. Guerrini, Cristina Sobacchi, Barbara Cassani, The American Journal of Human Genetics Bone DiseaseRheumatologyImmunologyPathologyHuman Osteoclast-poor Osteopetrosis	2008	299
X–linked thrombocytopenia and Wiskott–Aldrich syndrome are allelic diseases with mutations in the WASP gene Anna Villa, Luigi D. Notarangelo, Paolo Macchi, Nature Genetics Autoimmune DiseaseDisease MechanismGenetic DisorderGeneticsPathogenesis	1995	281
Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human Nader Chalhoub, Nadia Benachenhou, Venkatesh Rajapurohitam, Nature Medicine Bone DiseaseSclerostinDevelopmental BiologyBone Morphogenic ProteinGenetic Disorder	2003	265

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