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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:

Prevalence of germline GATA2 and SAMD9/9L variants in paediatric haematological disorders with monosomy 7
Masanori Yoshida, Kanako Tanase‐Nakao, Hirohito Shima, et al.
British Journal of Haematology (2020) Vol. 191, Iss. 5, pp. 835-843
Open Access | Times Cited: 23

Showing 23 citing articles:

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: 125
Advances in germline predisposition to acute leukaemias and myeloid neoplasms
Jeffery M. Klco, Charles G. Mullighan
Nature reviews. Cancer (2020) Vol. 21, Iss. 2, pp. 122-137
Open Access | Times Cited: 124
Germline Variants and Characteristic Features of Hereditary Hematological Malignancy Syndrome
Hironori Arai, Hirotaka Matsui, SungGi Chi, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 1, pp. 652-652
Open Access | Times Cited: 4
Of gains and losses: SAMD9/SAMD9L and monosomy 7 in myelodysplastic syndrome
Jörg Cammenga
Experimental Hematology (2024) Vol. 134, pp. 104217-104217
Open Access | Times Cited: 3
GATA2 Related Conditions and Predisposition to Pediatric Myelodysplastic Syndromes
Antonella Bruzzese, Davide Leardini, Riccardo Masetti, et al.
Cancers (2020) Vol. 12, Iss. 10, pp. 2962-2962
Open Access | Times Cited: 23
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: 17
Risk assessment and genetic counseling for hematologic malignancies—Practice resource of the National Society of Genetic Counselors
Brittany L. Stewart, Hannah L. Helber, Sarah A. Bannon, et al.
Journal of Genetic Counseling (2024)
Closed Access | Times Cited: 2
Enhanced ZNF521 expression induces an aggressive phenotype in human ovarian carcinoma cell lines
Stefania Scicchitano, Ylenia Montalcini, Valeria Lucchino, et al.
PLoS ONE (2022) Vol. 17, Iss. 10, pp. e0274785-e0274785
Open Access | Times Cited: 8
Decitabine-containing conditioning improved outcomes for children with higher-risk myelodysplastic syndrome undergoing allogeneic hematopoietic stem cell transplantation
Yuanyuan Ren, Fang Liu, Xia Chen, et al.
Annals of Hematology (2024) Vol. 103, Iss. 4, pp. 1345-1351
Closed Access | Times Cited: 1
Germline Predisposition in Hematologic Malignancies
Rina Kansal
Elsevier eBooks (2024), pp. 1-38
Closed Access | Times Cited: 1
From Basic Biology to Patient Mutational Spectra of GATA2 Haploinsufficiencies: What Are the Mechanisms, Hurdles, and Prospects of Genome Editing for Treatment
Cansu Koyunlar, Emma de Pater
Frontiers in Genome Editing (2020) Vol. 2
Open Access | Times Cited: 7
Clonal dynamics of hematopoietic stem cell compartment in aplastic anemia
Valeria Visconte, Jaroslaw P. Maciejewski
Seminars in Hematology (2022) Vol. 59, Iss. 1, pp. 47-53
Closed Access | Times Cited: 4
Germline Predisposition to Myeloid Neoplasms in Inherited Bone Marrow Failure Syndromes, Inherited Thrombocytopenias, Myelodysplastic Syndromes and Acute Myeloid Leukemia: Diagnosis and Progression to Malignancy
Rina Kansal
Journal of Hematology Research (2021) Vol. 8, pp. 11-38
Open Access | Times Cited: 4
Germline Predisposition to Myelodysplastic Syndromes
Georgina Gener‐Ricos, Yoheved Gerstein, Danielle Hammond, et al.
The Cancer Journal (2023) Vol. 29, Iss. 3, pp. 143-151
Closed Access | Times Cited: 1
[Pancytopenia in children caused by SAMD9/9L mutation: 5 cases report and literature review].
QianFeng Shang, Xue Li, L P Zhang, et al.
PubMed (2023) Vol. 44, Iss. 4, pp. 340-343
Closed Access | Times Cited: 1
The role of genetic factors in pediatric myelodysplastic syndromes with different outcomes
Ying Li, Cheng Li, Yun Peng, et al.
BMC Pediatrics (2024) Vol. 24, Iss. 1
Open Access
Impaired Mitochondrial Function and Marrow Failure in Patients Carrying a Variant of the SRSF4 Gene
Maurizio Miano, Nadia Bertola, Alice Grossi, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 4, pp. 2083-2083
Open Access
Germline Predisposition to Hematopoietic Malignancies: An Overview
Yogameenakshi Haribabu, Emma Bhote, Lucy A. Godley
Annual Review of Cancer Biology (2024) Vol. 8, Iss. 1, pp. 309-329
Open Access
Cord Blood Transplantation in 2 Infants Presenting Monosomy 7 Clonal Hematopoiesis: SAMD9/SAMD9L Germline Mutation
Maiko Hirai, Hiroshi Yagasaki, Koji Kanezawa, et al.
Journal of Pediatric Hematology/Oncology (2022) Vol. 45, Iss. 2, pp. e290-e293
Closed Access | Times Cited: 1
Acquired uniparental disomy of chromosome 7 in a patient with MIRAGE syndrome that veiled a pathogenic <i>SAMD9</i> variant
Kanako Tanase‐Nakao, Masanobu Kawai, Kazuko Wada, et al.
Clinical Pediatric Endocrinology (2021) Vol. 30, Iss. 4, pp. 163-169
Open Access | Times Cited: 1
Challenges to allogeneic hematopoietic stem cell transplantation in a patient with GATA2 deficiency and persistent Epstein-Barr virus infection
Naoki Sakata, Munehiro Okano, Ai Tanaka, et al.
Japanese Journal of Transplantation and Cellular Therapy (2023) Vol. 12, Iss. 1, pp. 59-64
Open Access
The Evolutionary Impact of Childhood Cancer on the Human Gene Pool
Ulrik Kristoffer Stoltze, Jon Foss-Skiftesvik, Thomas H. Hansen, et al.
Research Square (Research Square) (2023)
Open Access
The role of genetic factors in different outcomes of pediatric myelodysplastic syndromes
Ying Li, Cheng Li, Yun Peng, et al.
Research Square (Research Square) (2023)
Open Access
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