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OpenAlex Citation Counts

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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:

Somatic genetic rescue in Mendelian haematopoietic diseases
Patrick Revy, Caroline Kannengiesser, Alain Fischer
Nature Reviews Genetics (2019) Vol. 20, Iss. 10, pp. 582-598
Closed Access | Times Cited: 92

Showing 1-25 of 92 citing articles:

Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXAS
Caspar I. van der Made, Judith Potjewijd, Annemiek Hoogstins, et al.
Journal of Allergy and Clinical Immunology (2021) Vol. 149, Iss. 1, pp. 432-439.e4
Open Access | Times Cited: 167
Genetics of human telomere biology disorders
Patrick Revy, Caroline Kannengiesser, Alison A. Bertuch
Nature Reviews Genetics (2022) Vol. 24, Iss. 2, pp. 86-108
Closed Access | Times Cited: 131
Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes
Sushree Sangita Sahoo, Victor B. Pastor, Charnise Goodings, et al.
Nature Medicine (2021) Vol. 27, Iss. 10, pp. 1806-1817
Open Access | Times Cited: 123
Human hematopoietic stem cell vulnerability to ferroptosis
Jiawei Zhao, Yuemeng Jia, Dilnar Mahmut, et al.
Cell (2023) Vol. 186, Iss. 4, pp. 732-747.e16
Open Access | Times Cited: 81
Genetic variation across and within individuals
Zhi Yu, Tim H. H. Coorens, Md Mesbah Uddin, et al.
Nature Reviews Genetics (2024) Vol. 25, Iss. 8, pp. 548-562
Closed Access | Times Cited: 22
Human T-bet Governs Innate and Innate-like Adaptive IFN-γ Immunity against Mycobacteria
Rui Yang, Federico Mele, Lisa Worley, et al.
Cell (2020) Vol. 183, Iss. 7, pp. 1826-1847.e31
Open Access | Times Cited: 107
Gene therapy for severe combined immunodeficiencies and beyond
Alain Fischer, Salima Hacein‐Bey‐Abina
The Journal of Experimental Medicine (2019) Vol. 217, Iss. 2
Open Access | Times Cited: 90
Somatic genetic rescue of a germline ribosome assembly defect
Shengjiang Tan, Laëtitia Kermasson, Christine Hilcenko, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 59
The biology and management of dyskeratosis congenita and related disorders of telomeres
Hemanth Tummala, Amanda J. Walne, Inderjeet Dokal
Expert Review of Hematology (2022) Vol. 15, Iss. 8, pp. 685-696
Open Access | Times Cited: 52
Dyskeratosis congenita and telomere biology disorders
Sharon A. Savage
Hematology (2022) Vol. 2022, Iss. 1, pp. 637-648
Open Access | Times Cited: 52
Human embryonic genetic mosaicism and its effects on development and disease
Sarah M. Waldvogel, Jennifer E. Posey, Margaret A. Goodell
Nature Reviews Genetics (2024)
Closed Access | Times Cited: 13
An update on Fanconi anemia: Clinical, cytogenetic and molecular approaches (Review)
Olga Moreno, Angela Paredes, Fernando Suárez‐Obando, et al.
Biomedical Reports (2021) Vol. 15, Iss. 3
Open Access | Times Cited: 52
Somatic reversion impacts myelodysplastic syndromes and acute myeloid leukemia evolution in the short telomere disorders
Kristen E. Schratz, Valeriya Gaysinskaya, Zoe L. Cosner, et al.
Journal of Clinical Investigation (2021) Vol. 131, Iss. 18
Open Access | Times Cited: 49
Gain-of-function mutations in RPA1 cause a syndrome with short telomeres and somatic genetic rescue
Richa Sharma, Sushree Sangita Sahoo, Masayoshi Honda, et al.
Blood (2021) Vol. 139, Iss. 7, pp. 1039-1051
Open Access | Times Cited: 42
Gene therapy for inborn errors of immunity: past, present and future
Alain Fischer
Nature reviews. Immunology (2022) Vol. 23, Iss. 6, pp. 397-408
Closed Access | Times Cited: 31
Expanding the PRAAS spectrum: De novo mutations of immunoproteasome subunit β-type 10 in six infants with SCID-Omenn syndrome
Caspar I. van der Made, Simone Kersten, Odelia Chorin, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 4, pp. 791-804
Open Access | Times Cited: 6
Clonal landscape and clinical outcomes of telomere biology disorders: somatic rescuing and cancer mutations
Fernanda Gutierrez‐Rodrigues, Emma M. Groarke, Natthakan Thongon, et al.
Blood (2024) Vol. 144, Iss. 23, pp. 2402-2416
Open Access | Times Cited: 6
NHP2 deficiency impairs rRNA biogenesis and causes pulmonary fibrosis and Høyeraal–Hreidarsson syndrome
Maname Benyelles, Marie-Françoise O’Donohue, Laëtitia Kermasson, et al.
Human Molecular Genetics (2020) Vol. 29, Iss. 6, pp. 907-922
Closed Access | Times Cited: 45
Integrating germline variant assessment into routine clinical practice for myelodysplastic syndrome and acute myeloid leukaemia: current strategies and challenges
Kiran Tawana, Anna Brown, Jane E. Churpek
British Journal of Haematology (2021) Vol. 196, Iss. 6, pp. 1293-1310
Open Access | Times Cited: 40
Next-Generation Sequencing in the Field of Primary Immunodeficiencies: Current Yield, Challenges, and Future Perspectives
Emil E. Vorsteveld, Alexander Hoischen, Caspar I. van der Made
Clinical Reviews in Allergy & Immunology (2021) Vol. 61, Iss. 2, pp. 212-225
Open Access | Times Cited: 36
Clonal hematopoiesis in children with predisposing conditions
Enrico Attardi, Seth J. Corey, Marcin W. Włodarski
Seminars in Hematology (2024) Vol. 61, Iss. 1, pp. 35-42
Open Access | Times Cited: 5
Clonal Hematopoiesis and Myeloid Neoplasms in the Context of Telomere Biology Disorders
Alejandro Ferrer, Abhishek A. Mangaonkar, Mrinal M. Patnaik
Current Hematologic Malignancy Reports (2022) Vol. 17, Iss. 3, pp. 61-68
Open Access | Times Cited: 22
Germline predisposition traits in allogeneic hematopoietic stem-cell transplantation for myelodysplastic syndromes: a survey-based study and position paper on behalf of the Chronic Malignancies Working Party of the EBMT
Carmelo Gurnari, Marie Robin, Lucy A. Godley, et al.
The Lancet Haematology (2023) Vol. 10, Iss. 12, pp. e994-e1005
Closed Access | Times Cited: 12
Diamond-Blackfan anemia, the archetype of ribosomopathy: How distinct is it from the other constitutional ribosomopathies?
Lydie Da Costa, Narla Mohandas, Ludivine David-NGuyen, et al.
Blood Cells Molecules and Diseases (2024) Vol. 106, pp. 102838-102838
Open Access | Times Cited: 4
Discordant restoration of TCR expression and function by CD247 somatic reversions
Alejandro C. Briones, Ana V. Marín, Rebeca Chaparro-García, et al.
(2025)
Closed Access
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