Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Guidelines for genetic studies in single patients: lessons from primary immunodeficiencies
Jean‐Laurent Casanova, Mary Ellen Conley, Stephen Seligman, et al.
The Journal of Experimental Medicine (2014) Vol. 211, Iss. 11, pp. 2137-2149
Open Access | Times Cited: 235

Showing 1-25 of 235 citing articles:

Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
Stuart G. Tangye, Waleed Al–Herz, Aziz Bousfiha, et al.
Journal of Clinical Immunology (2020) Vol. 40, Iss. 1, pp. 24-64
Open Access | Times Cited: 1028
Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee
Stuart G. Tangye, Waleed Al–Herz, Aziz Bousfiha, et al.
Journal of Clinical Immunology (2022) Vol. 42, Iss. 7, pp. 1473-1507
Open Access | Times Cited: 846
International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity
Capucine Pïcard, H. Bobby Gaspar, Waleed Al–Herz, et al.
Journal of Clinical Immunology (2017) Vol. 38, Iss. 1, pp. 96-128
Open Access | Times Cited: 751
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities
Jessica X. Chong, Kati J. Buckingham, Shalini N. Jhangiani, et al.
The American Journal of Human Genetics (2015) Vol. 97, Iss. 2, pp. 199-215
Open Access | Times Cited: 655
Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants
Aziz Belkadi, Alexandre Bolze, Yuval Itan, et al.
Proceedings of the National Academy of Sciences (2015) Vol. 112, Iss. 17, pp. 5473-5478
Open Access | Times Cited: 561
Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency
Michael J. Ciancanelli, Sarah X.L. Huang, Priya Luthra, et al.
Science (2015) Vol. 348, Iss. 6233, pp. 448-453
Open Access | Times Cited: 434
Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis
Rajiv K. Khajuria, Mathias Munschauer, Jacob C. Ulirsch, et al.
Cell (2018) Vol. 173, Iss. 1, pp. 90-103.e19
Open Access | Times Cited: 356
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
Eric Scott, Anason Halees, Yuval Itan, et al.
Nature Genetics (2016) Vol. 48, Iss. 9, pp. 1071-1076
Open Access | Times Cited: 355
The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity
Aziz Bousfiha, Abderrahmane Moundir, Stuart G. Tangye, et al.
Journal of Clinical Immunology (2022) Vol. 42, Iss. 7, pp. 1508-1520
Closed Access | Times Cited: 347
Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome
Alexandra Y. Kreins, Michael J. Ciancanelli, Satoshi Okada, et al.
The Journal of Experimental Medicine (2015) Vol. 212, Iss. 10, pp. 1641-1662
Open Access | Times Cited: 330
Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasia
Bertrand Boisson, Emmanuel Laplantine, Kerry Dobbs, et al.
The Journal of Experimental Medicine (2015) Vol. 212, Iss. 6, pp. 939-951
Open Access | Times Cited: 264
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders
Asbjørg Stray‐Pedersen, Hanne Sørmo Sorte, Pubudu Samarakoon, et al.
Journal of Allergy and Clinical Immunology (2016) Vol. 139, Iss. 1, pp. 232-245
Open Access | Times Cited: 249
The human gene damage index as a gene-level approach to prioritizing exome variants
Yuval Itan, Lei Shang, Bertrand Boisson, et al.
Proceedings of the National Academy of Sciences (2015) Vol. 112, Iss. 44, pp. 13615-13620
Open Access | Times Cited: 244
A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection
Jean‐Laurent Casanova, Helen C. Su, Laurent Abel, et al.
Cell (2020) Vol. 181, Iss. 6, pp. 1194-1199
Open Access | Times Cited: 217
Severe infectious diseases of childhood as monogenic inborn errors of immunity
Jean‐Laurent Casanova
Proceedings of the National Academy of Sciences (2015) Vol. 112, Iss. 51
Open Access | Times Cited: 214
Comparison of predicted and actual consequences of missense mutations
Lisa A. Miosge, Matthew A. Field, Yovina Sontani, et al.
Proceedings of the National Academy of Sciences (2015) Vol. 112, Iss. 37
Open Access | Times Cited: 212
Functional IRF3 deficiency in a patient with herpes simplex encephalitis
Line Lykke Andersen, Nanna Mørk, Line S. Reinert, et al.
The Journal of Experimental Medicine (2015) Vol. 212, Iss. 9, pp. 1371-1379
Open Access | Times Cited: 199
The Ever-Increasing Array of Novel Inborn Errors of Immunity: an Interim Update by the IUIS Committee
Stuart G. Tangye, Waleed Al–Herz, Aziz Bousfiha, et al.
Journal of Clinical Immunology (2021) Vol. 41, Iss. 3, pp. 666-679
Open Access | Times Cited: 198
Genetics of intellectual disability in consanguineous families
Hao Hu, Kimia Kahrizi, Luciana Musante, et al.
Molecular Psychiatry (2018) Vol. 24, Iss. 7, pp. 1027-1039
Closed Access | Times Cited: 191
Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections
Kerry Dobbs, Cecilia Domínguez Conde, Shen‐Ying Zhang, et al.
New England Journal of Medicine (2015) Vol. 372, Iss. 25, pp. 2409-2422
Open Access | Times Cited: 182
Inherited IL-17RC deficiency in patients with chronic mucocutaneous candidiasis
Yun Ling, Sophie Cypowyj, Caner Aytekin, et al.
The Journal of Experimental Medicine (2015) Vol. 212, Iss. 5, pp. 619-631
Open Access | Times Cited: 181
Exome and genome sequencing for inborn errors of immunity
Isabelle Meyts, Barbara Bosch, Alexandre Bolze, et al.
Journal of Allergy and Clinical Immunology (2016) Vol. 138, Iss. 4, pp. 957-969
Open Access | Times Cited: 179
Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency
Nicholas Hernandez, Isabelle Melki, Huie Jing, et al.
The Journal of Experimental Medicine (2018) Vol. 215, Iss. 10, pp. 2567-2585
Open Access | Times Cited: 177
Severe influenza pneumonitis in children with inherited TLR3 deficiency
Hye Kyung Lim, Sarah X.L. Huang, Jie Chen, et al.
The Journal of Experimental Medicine (2019) Vol. 216, Iss. 9, pp. 2038-2056
Open Access | Times Cited: 165
Life-Threatening COVID-19: Defective Interferons Unleash Excessive Inflammation
Qian Zhang, Paul Bastard, Alexandre Bolze, et al.
Med (2020) Vol. 1, Iss. 1, pp. 14-20
Open Access | Times Cited: 150
Page 1 - Next Page

Scroll to top