ScholarIQanswers from OpenAlex & ORCID
Matthew Cook
ResearcherPublications, citations & collaboration network
Matthew Cook is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Matthew Cook have?
ScholarIQindexed works
Matthew Cook has 361 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Matthew Cook have?
ScholarIQcitation count
Matthew Cook has 20,740 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Matthew Cook?
ScholarIQh-index
Matthew Cook has an h-index of 68 in OpenAlex.
What is the i10-index of Matthew Cook?
ScholarIQi10-index
Matthew Cook has an i10-index of 168 in OpenAlex.
What is the ORCID of Matthew Cook?
ScholarIQorcid
The ORCID for Matthew Cook is on the source record.
What is the OpenAlex record for Matthew Cook?
ScholarIQopenalex
The OpenAlex for Matthew Cook is on the source record.
What are the most-cited papers on Matthew Cook?
ScholarIQmost cited works
Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies
S. Cindy, Natalie Wong, Geetha Rao, Danielle T. Avery, James Torpy, Thomas Hambridge, Jacinta Bustamante, Satoshi Okada, Jennifer Stoddard, Elissa K. Deenick, Simon J. Pelham, Kathryn Payne, Stéphanie Boisson‐Dupuis, Anne Puel, Masao Kobayashi, Peter D. Arkwright, Sara Şebnem Kılıç, Jamila El Baghdadi, Shigeaki Nonoyama, Yoshiyuki Minegishi, Seyed Alireza Mahdaviani, Davood Mansouri, Aziz Bousfiha, Annaliesse Blincoe, Martyn A. French, Peter Hsu, Dianne E. Campbell, Michael Stormon, Melanie Wong, Stephen Adelstein, Joanne Smart, David A. Fulcher, Matthew Cook, Tri Giang Phan, Polina Stepensky, Kaan Boztuǧ, Aydan Kansu, Aydan İkincioğulları, Ulrich Baumann, Rita Beier, Tony Roscioli, John B. Ziegler, Paul Gray, Capucine Pïcard, Bodo Grimbacher, Klaus Warnatz, Steven M. Holland, Jean‐Laurent Casanova, Gülbû Uzel, Stuart G. Tangye
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations
Tiziana Lorenzini, Manfred Fliegauf, Nils Klammer, Natalie Frede, Michele Proietti, Alla Bulashevska, Nadezhda Camacho-Ordóñez, Markku Varjosalo, Matias Kinnunen, Esther de Vries, J.W.M. van der Meer, Rohan Ameratunga, Chaim M. Roifman, Yael Dinur Schejter, Robin Kobbe, Timo Hautala, Faranaz Atschekzei, Reinhold E. Schmidt, Claudia Schröder, Polina Stepensky, Bella Shadur, Luis Alberto Pedroza, Michiel van der Flier, Mónica Martínez‐Gallo, Luis Ignacio González‐Granado, Luís M. Allende, Anna Shcherbina, N. B. Kuzmenko, V.P. Zakharova, João Farela Neves, Peter Švec, Ute Fischer, Winnie Ip, Oliver Bartsch, Safa Barış, Christoph Klein, Raif S. Geha, Janet Chou, Mohammed F. Alosaimi, Lauren Weintraub, Kaan Boztuǧ, Tatjana Hirschmugl, Maria Marluce dos Santos Vilela, Dirk Holzinger, Maximilian Seidl, Vassilios Lougaris, Alessandro Plebani, Laia Alsina, M. Piquer‐Gibert, Àngela Deyà‐Martínez, C Slade, Asghar Aghamohammadi, Hassan Abolhassani, Lennart Hammarström, Outi Kuismin, Merja Helminen, Hana Lango Allen, James E. Thaventhiran, Alexandra F. Freeman, Matthew Cook, Shahrzad Bakhtiar, Mette Christiansen, Charlotte Cunningham‐Rundles, Niraj Patel, William Rae, Tim Niehues, Nina Brauer, Jaana Syrjänen, Mikko Seppänen, Siobhan O. Burns, Paul Tuijnenburg, Taco W. Kuijpers, Klaus Warnatz, Bodo Grimbacher, Zoe Adhya, Hana Alachkar, Ariharan Anantharachagan, Richard Antrobus, Gururaj Arumugakani, Sofie Ashford, William J. Astle, Anthony Attwood, Chiara Bacchelli, Joana Batista, Helen Baxendale, Claire Bethune, Shahnaz Bibi, Marta Bleda, Barbara Boardman, Claire Booth, John R. Bradley, Gerome Breen, Matthew A. Brown, Michael J. Browning, Mary Brownlie, Matthew Buckland, Siobhan O. Burns, Oliver S. Burren, Keren Carss, John C. Chambers