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:
Immunologic, Molecular, and Clinical Profile of Patients with Chromosome 22q11.2 Duplications
Dharmagat Bhattarai, Daniel E. McGinn, T. Blaine Crowley, et al.
Journal of Clinical Immunology (2023) Vol. 43, Iss. 4, pp. 794-807
Closed Access | Times Cited: 7
Dharmagat Bhattarai, Daniel E. McGinn, T. Blaine Crowley, et al.
Journal of Clinical Immunology (2023) Vol. 43, Iss. 4, pp. 794-807
Closed Access | Times Cited: 7
Showing 7 citing articles:
Six at Sixty. ‘Have you tested for 22q?’
Peter Scambler
Journal of Medical Genetics (2025), pp. jmg-110504
Closed Access
Peter Scambler
Journal of Medical Genetics (2025), pp. jmg-110504
Closed Access
Review of the Pathophysiology and Clinical Manifestations of 22q11.2 Deletion and Duplication Syndromes
Jeremy Purow, Lauren Waidner, Hanadys Ale
Clinical Reviews in Allergy & Immunology (2025) Vol. 68, Iss. 1
Closed Access
Jeremy Purow, Lauren Waidner, Hanadys Ale
Clinical Reviews in Allergy & Immunology (2025) Vol. 68, Iss. 1
Closed Access
European Society of Immunodeficiencies guidelines for the management of patients with congenital athymia
Alexandra Y. Kreins, Fatima Dhalla, Aisling M. Flinn, et al.
Journal of Allergy and Clinical Immunology (2024)
Open Access | Times Cited: 3
Alexandra Y. Kreins, Fatima Dhalla, Aisling M. Flinn, et al.
Journal of Allergy and Clinical Immunology (2024)
Open Access | Times Cited: 3
Neurodevelopmental and other psychiatric disorders in 22q11.2 deletion syndrome from childhood to adult age: Prospective longitudinal study of 100 individuals
L. Wallin, Christopher Gillberg, Elisabeth Fernell, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023) Vol. 193, Iss. 2, pp. 172-182
Open Access | Times Cited: 5
L. Wallin, Christopher Gillberg, Elisabeth Fernell, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023) Vol. 193, Iss. 2, pp. 172-182
Open Access | Times Cited: 5
Severe T-cell lymphopenia in a patient with microduplication 22q11.2 identified by newborn screening
Maarja Soomann, Seraina Prader, Tiziana Lorenzini, et al.
The Journal of Allergy and Clinical Immunology In Practice (2024) Vol. 12, Iss. 8, pp. 2199-2200.e1
Open Access | Times Cited: 1
Maarja Soomann, Seraina Prader, Tiziana Lorenzini, et al.
The Journal of Allergy and Clinical Immunology In Practice (2024) Vol. 12, Iss. 8, pp. 2199-2200.e1
Open Access | Times Cited: 1
Differential inflammatory profiles in carriers of reciprocal 22q11.2 copy number variants
Kathleen O’Hora, Carolyn Amir, Emily Chiem, et al.
Psychoneuroendocrinology (2024) Vol. 169, pp. 107135-107135
Open Access | Times Cited: 1
Kathleen O’Hora, Carolyn Amir, Emily Chiem, et al.
Psychoneuroendocrinology (2024) Vol. 169, pp. 107135-107135
Open Access | Times Cited: 1
Comprehensive clinical, genome and transcriptomic analysis of primary ghost cell odontogenic carcinoma
Lirui Zhang, Qiaoshi Xu, Zhien Feng
Oral Oncology (2023) Vol. 148, pp. 106616-106616
Closed Access | Times Cited: 1
Lirui Zhang, Qiaoshi Xu, Zhien Feng
Oral Oncology (2023) Vol. 148, pp. 106616-106616
Closed Access | Times Cited: 1
