ScholarIQanswers from OpenAlex & ORCID
Jordan S. Orange
ResearcherPublications, citations & collaboration network
Jordan S. Orange is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Jordan S. Orange have?
ScholarIQindexed works
Jordan S. Orange has 881 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Jordan S. Orange have?
ScholarIQcitation count
Jordan S. Orange has 43,941 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Jordan S. Orange?
ScholarIQh-index
Jordan S. Orange has an h-index of 106 in OpenAlex.
What is the i10-index of Jordan S. Orange?
ScholarIQi10-index
Jordan S. Orange has an i10-index of 338 in OpenAlex.
What is the ORCID of Jordan S. Orange?
ScholarIQorcid
The ORCID for Jordan S. Orange is on the source record.
What is the OpenAlex record for Jordan S. Orange?
ScholarIQopenalex
The OpenAlex for Jordan S. Orange is on the source record.
What are the most-cited papers on Jordan S. Orange?
ScholarIQmost cited works
Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome
Alessandro Aiuti, Luca Biasco, Samantha Scaramuzza, Francesca Ferrua, Maria Pia Cicalese, Cristina Baricordi, Francesca Dionisio, Andrea Calabria, Stefania Giannelli, Maria Carmina Castiello, Marita Bosticardo, Costanza Evangelio, Andrea Assanelli, Miriam Casiraghi, Sara Di Nunzio, Luciano Callegaro, Claudia Benati, Paolo Rizzardi, Danilo Pellin, Clelia Di Serio, Manfred Schmidt, Christof von Kalle, Jason P. Gardner, Nalini Mehta, Victor Neduva, David J. Dow, Anne Galy, R Miniero, Andrea Finocchi, Ayşe Metìn, Pinaki P. Banerjee, Jordan S. Orange, Stefania Galimberti, Maria Grazia Valsecchi, Alessandra Biffi, Eugenio Montini, Anna Villa, Fabio Ciceri, Maria Grazia Roncarolo, Luigi Naldini
Human Decidual Natural Killer Cells Are a Unique NK Cell Subset with Immunomodulatory Potential
Louise A. Koopman, Hernan D. Kopcow, Basya Rybalov, Jonathan E. Boyson, Jordan S. Orange, Frederick Schatz, Rachel Masch, Charles J. Lockwood, Asher D. Schachter, Peter J. Park, Jack L. Strominger
Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome
Amy P. Hsu, Elizabeth P. Sampaio, Javed Khan, Katherine R. Calvo, Jacob E. Lemieux, Smita Y. Patel, David M. Frucht, Donald C. Vinh, Roger Auth, Alexandra F. Freeman, Kenneth N. Olivier, Gülbû Uzel, Christa S. Zerbe, Christine Spalding, Stefania Pittaluga, Mark Raffeld, Douglas B. Kuhns, Li Ding, Michelle L. Paulson, Beatriz E. Marciano, Juan Gea‐Banacloche, Jordan S. Orange, Jennifer Cuellar‐Rodríguez, Dennis D. Hickstein, Steven M. Holland
DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients
On behalf of the inborn errors working party of EBMT, Susanne Aydin, Sara Şebnem Kılıç, Caner Aytekin, Ashish Kumar, Óscar Porras, Leena Kainulainen, Larysa Kostyuchenko, Ferah Genel, Necil Kütükçüler, Neslihan Edeer Karaca, Luis Ignacio González‐Granado, Jordan K. Abbott, Daifulah Al-Zahrani, Nima Rezaei, Zeina Baz, Jens Thiel, Stephan Ehl, László Maródi, Jordan S. Orange, Julie Sawalle‐Belohradsky, Sevgi Keleş, Steven M. Holland, Özden Sanal, Deniz C. Ayvaz, İlhan Tezcan, Hamoud Al‐Mousa, Zobaida Alsum, Abbas Hawwari, Ayşe Metìn, Susanne Matthes‐Martin, Manfred Hönig, Ansgar Schulz, Capucine Pïcard, Vincent Barlogis, Andrew R. Gennery, Marianne Ifversen, Joris van Montfrans, Taco W. Kuijpers, Robbert G. M. Bredius, Gregor Dückers, Waleed Al–Herz, Sung‐Yun Pai, Raif S. Geha, Gundula Notheis, Carl-Philipp Schwarze, Betül Tavil, Fatih Azık, K. Bienemann, Bodo Grimbacher, Valerie Heinz, H. Bobby Gaspar, Roland C. Aydin, Beate Hagl, Benjamin Gathmann, Bernd H. Belohradsky, Hans D. Ochs, Talal A. Chatila, Ellen D. Renner, Helen C. Su, Alexandra F. Freeman, Karin R. Engelhardt, Michael H. Albert