ScholarIQanswers from OpenAlex & ORCID
Alexandra F. Freeman
ResearcherPublications, citations & collaboration network
Alexandra F. Freeman is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Alexandra F. Freeman have?
ScholarIQindexed works
Alexandra F. Freeman has 426 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Alexandra F. Freeman have?
ScholarIQcitation count
Alexandra F. Freeman has 21,631 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Alexandra F. Freeman?
ScholarIQh-index
Alexandra F. Freeman has an h-index of 78 in OpenAlex.
What is the i10-index of Alexandra F. Freeman?
ScholarIQi10-index
Alexandra F. Freeman has an i10-index of 217 in OpenAlex.
What is the ORCID of Alexandra F. Freeman?
ScholarIQorcid
The ORCID for Alexandra F. Freeman is on the source record.
What is the OpenAlex record for Alexandra F. Freeman?
ScholarIQopenalex
The OpenAlex for Alexandra F. Freeman is on the source record.
What are the most-cited papers on Alexandra F. Freeman?
ScholarIQmost cited works
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
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
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency
Karin R. Engelhardt, Michael E. Gertz, Sevgi Keleş, Alejandro A. Schäffer, Elena C. Sigmund, Cristina Glocker, Shiva Saghafi, Zahra Pourpak, R Ceja, Atfa Sassi, L Graham, Michel J. Massaad, Fethi Mellouli, Imen Ben‐Mustapha, Monia Khémiri, Sara Şebnem Kılıç, Amos Etzioni, Alexandra F. Freeman, Jens Thiel, Ilka Schulze, Waleed Al–Herz, Ayşe Metìn, Özden Sanal, İlhan Tezcan, Mehdi Yeganeh, Tim Niehues, Gregor Dueckers, Sebastian Weinspach, Türkan Patıroğlu, Ekrem Ünal, Majed Dasouki, M. Yılmaz, Ferah Genel, Caner Aytekin, Necil Kütükçüler, Ayper Somer, Mehmet Kılıç, İsmail Reisli, Yıldız Çamcıoğlu, Andrew R. Gennery, Andrew J. Cant, Alison Jones, Bobby Gaspar, Peter D. Arkwright, Maria Cristina Pietrogrande, Zeina Baz, Salem Al‐Tamemi, Vassilios Lougaris, Gerard Lefranc, André Mégarbané, Jeannette Boutros, Nermeen Galal, Mohamed Béjaoui, Mohamed‐Ridha Barbouche, Raif S. Geha, Talal A. Chatila, Bodo Grimbacher
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