ScholarIQanswers from OpenAlex & ORCID
Luigi D. Notarangelo
ResearcherPublications, citations & collaboration network
Luigi D. Notarangelo is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Luigi D. Notarangelo have?
ScholarIQindexed works
Luigi D. Notarangelo has 890 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Luigi D. Notarangelo have?
ScholarIQcitation count
Luigi D. Notarangelo has 63,784 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Luigi D. Notarangelo?
ScholarIQh-index
Luigi D. Notarangelo has an h-index of 122 in OpenAlex.
What is the i10-index of Luigi D. Notarangelo?
ScholarIQi10-index
Luigi D. Notarangelo has an i10-index of 535 in OpenAlex.
What is the ORCID of Luigi D. Notarangelo?
ScholarIQorcid
The ORCID for Luigi D. Notarangelo is on the source record.
What is the OpenAlex record for Luigi D. Notarangelo?
ScholarIQopenalex
The OpenAlex for Luigi D. Notarangelo is on the source record.
What are the most-cited papers on Luigi D. Notarangelo?
ScholarIQmost cited works
Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID)
Paolo Macchi, Anna Villa, Silvia Giliani, Maria Grazia Sacco, Annalisa Frattini, Fulvio Porta, Alberto G. Ugazio, James A. Johnston, Fabio Candotti, John J. O'Sheai, Paolo Vezzoni, Luigi D. Notarangelo
Transplantation Outcomes for Severe Combined Immunodeficiency, 2000–2009
Sung‐Yun Pai, Brent R. Logan, Linda M. Griffith, Rebecca H. Buckley, Roberta Parrott, Christopher C. Dvorak, Neena Kapoor, I. Celine Hanson, Alexandra H. Filipovich, Soma Jyonouchi, Kathleen E. Sullivan, Trudy N. Small, Lauri M. Burroughs, Suzanne Skoda‐Smith, Ann E. Haight, Audrey Grizzle, Michael A. Pulsipher, Ka Wah Chan, Ramsay Fuleihan, Élie Haddad, Brett Loechelt, Victor M. Aquino, Alfred P. Gillio, Jeffrey Davis, Alan P. Knutsen, Angela R. Smith, Theodore B. Moore, Marlis L. Schroeder, Frederick D. Goldman, James A. Connelly, Matthew H. Porteus, Qun Xiang, William T. Shearer, Thomas A. Fleisher, Donald B. Kohn, Jennifer M. Puck, Luigi D. Notarangelo, Morton J. Cowan, Richard J. O’Reilly
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources
Sebastian Köhler, Leigh Carmody, Nicole Vasilevsky, Julius O.B. Jacobsen, Daniel Daniš, Jean-Philippe F. Gourdine, Michael Gargano, Nomi L. Harris, Nicolas Matentzoglu, Julie A. McMurry, David Osumi-Sutherland, Valentina Cipriani, James P. Balhoff, Tom Conlin, Hannah Blau, Gareth Baynam, R. Palmer, Dylan Gratian, Hugh Dawkins, Michael M. Segal, Anna Jansen, Ahmed Muaz, Willie Chang, Jenna Bergerson, Stanley J. F. Laulederkind, Zafer Yüksel, Sergi Beltrán, Alexandra F. Freeman, Panagiotis I. Sergouniotis, Daniel W. Durkin, Andrea L. Storm, Marc Hanauer, Michael Brudno, Susan M. Bello, Murat Sincan, Kayli Rageth, Matthew T. Wheeler, Renske Oegema, Halima Lourghi, Maria G. Della Rocca, Rachel Thompson, F Castellanos, James R. Priest, Charlotte Cunningham‐Rundles, Ayushi Hegde, Ruth C. Lovering, Catherine Hajek, Annie Olry, Luigi D. Notarangelo, Morgan Similuk, Xingmin Zhang, David Gómez‐Andrés, Hanns Lochmüller, Hélène Dollfus, Sergio D. Rosenzweig, Shruti Marwaha, Ana Rath, Kathleen E. Sullivan, Cynthia L. Smith, Joshua D. Milner, Dorothée Leroux, Cornelius F. Boerkoel, Amy D. Klion, Melody C. Carter, Tudor Groza, Damian Smedley, Melissa Haendel, Chris Mungall, Peter N. Robinson
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, Silvia Giliani, Mario Abinun, Jan P. Mattsson, David J. Keeling, Ann-Katrin Andersson, Pia Wallbrandt, Luigi Zecca, Luigi D. Notarangelo, Paolo Vezzoni, Anna Villa
Partial V(D)J Recombination Activity Leads to Omenn Syndrome
Anna Villa, Sandro Santagata, Fabio Bozzi, Silvia Giliani, Annalisa Frattini, Luisa Imberti, Luisa Benerini Gatta, Hans D. Ochs, Klaus Schwarz, Luigi D. Notarangelo, Paolo Vezzoni, Eugenia Spanopoulou