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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:

Pathogenic TERT promoter variants in telomere diseases
Fernanda Gutierrez‐Rodrigues, Flávia S. Donaires, André Luiz Pinto Santos, et al.
Genetics in Medicine (2018) Vol. 21, Iss. 7, pp. 1594-1602
Open Access | Times Cited: 47

Showing 1-25 of 47 citing articles:

An update on the biology and management of dyskeratosis congenita and related telomere biology disorders
Marena R. Niewisch, Sharon A. Savage
Expert Review of Hematology (2019) Vol. 12, Iss. 12, pp. 1037-1052
Open Access | Times Cited: 146
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
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
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
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
The Genetic and Epigenetic Footprint in Idiopathic Pulmonary Fibrosis and Familial Pulmonary Fibrosis: A State-of-the-Art Review
Claudio Tirelli, Chiara Pesenti, Monica Miozzo, et al.
Diagnostics (2022) Vol. 12, Iss. 12, pp. 3107-3107
Open Access | Times Cited: 31
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
Machine Learning Approaches for the Prioritization of Genomic Variants Impacting Pre-mRNA Splicing
Charlie F Rowlands, Diana Baralle, Jamie M. Ellingford
Cells (2019) Vol. 8, Iss. 12, pp. 1513-1513
Open Access | Times Cited: 52
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
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
Impaired telomere integrity and rRNA biogenesis in PARN‐deficient patients and knock‐out models
Maname Benyelles, Harikleia Episkopou, Marie-Françoise O’Donohue, et al.
EMBO Molecular Medicine (2019) Vol. 11, Iss. 7
Open Access | Times Cited: 39
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
Tieing together loose ends: telomere instability in cancer and aging
Gustavo Borges, Mélanie Criqui, Lea Harrington
Molecular Oncology (2022) Vol. 16, Iss. 18, pp. 3380-3396
Open Access | Times Cited: 22
Genetic underpinning of idiopathic pulmonary fibrosis: the role of mucin
Seyedeh Zahra Fotook Kiaei, David A. Schwartz
Expert Review of Respiratory Medicine (2025)
Closed Access
Systematic identification of disease-causing promoter and untranslated region variants in 8040 undiagnosed individuals with rare disease
Alexandra C Martin-Geary, Alexander J. M. Blakes, Ruebena Dawes, et al.
Genome Medicine (2025) Vol. 17, Iss. 1
Open Access
Somatic genetic rescue in hematopoietic cells in GATA2 deficiency
Luiz Fernando Bazzo Catto, Gustavo Borges, André Luiz Pinto Santos, et al.
Blood (2020) Vol. 136, Iss. 8, pp. 1002-1005
Open Access | Times Cited: 31
Telomere Dysfunction in Idiopathic Pulmonary Fibrosis
Kexiong Zhang, Lu Xu, Yu‐Sheng Cong
Frontiers in Medicine (2021) Vol. 8
Open Access | Times Cited: 25
Lessons From Pediatric MDS: Approaches to Germline Predisposition to Hematologic Malignancies
Serine Avagyan, Akiko Shimamura
Frontiers in Oncology (2022) Vol. 12
Open Access | Times Cited: 17
Pulmonary Fibrosis and a TERT Founder Mutation With a Latency Period of 300 Years
Joanne J. van der Vis, Jasper J. van der Smagt, Frederic A. M. Hennekam, et al.
CHEST Journal (2020) Vol. 158, Iss. 2, pp. 612-619
Closed Access | Times Cited: 22
Occurrence, functionality and abundance of the TERT promoter mutations
Sivaramakrishna Rachakonda, Jörg D. Hoheisel, Rajiv Kumar
International Journal of Cancer (2021) Vol. 149, Iss. 11, pp. 1852-1862
Open Access | Times Cited: 19
Interstitial lung diseases associated with mutations of poly(A)‐specific ribonuclease: A multicentre retrospective study
Quentin Philippot, Caroline Kannengiesser, Marie‐Pierre Debray, et al.
Respirology (2022) Vol. 27, Iss. 3, pp. 226-235
Open Access | Times Cited: 13
Characterization of novel mutations in the TEL-patch domain of the telomeric factor TPP1 associated with telomere biology disorders
Alexis Bertrand, Ibrahima Ba, Laëtitia Kermasson, et al.
Human Molecular Genetics (2024)
Closed Access | Times Cited: 2
Somatic mosaicism in inherited bone marrow failure syndromes
Fernanda Gutierrez‐Rodrigues, Sushree Sangita Sahoo, Marcin W. Włodarski, et al.
Best Practice & Research Clinical Haematology (2021) Vol. 34, Iss. 2, pp. 101279-101279
Open Access | Times Cited: 15
Effects of nandrolone decanoate on telomere length and clinical outcome in patients with telomeropathies: a prospective trial
Diego V. Clé, Luiz Fernando Bazzo Catto, Fernanda Gutierrez‐Rodrigues, et al.
Haematologica (2022) Vol. 108, Iss. 5, pp. 1300-1312
Open Access | Times Cited: 11
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