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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:

JAK2 p.G571S in B-cell precursor acute lymphoblastic leukemia: a synergizing germline susceptibility
Minhui Lin, Karin Nebral, Christoph G. W. Gertzen, et al.
Leukemia (2019) Vol. 33, Iss. 9, pp. 2331-2335
Open Access | Times Cited: 11

Showing 11 citing articles:

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
Comprehensive germline-genomic and clinical profiling in 160 unselected children and adolescents with cancer
Rabea Wagener, Julia Taeubner, Carolin Walter, et al.
European Journal of Human Genetics (2021) Vol. 29, Iss. 8, pp. 1301-1311
Open Access | Times Cited: 47
Risk Factors for Childhood Leukemia: Radiation and Beyond
J Schmidt, Sabine Hornhardt, Friederike Erdmann, et al.
Frontiers in Public Health (2021) Vol. 9
Open Access | Times Cited: 28
Spotlight on amino acid changing mutations in the JAK-STAT pathway: from disease-specific mutation to general mutation databases
Markus Hoffmann, Lothar Hennighausen
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
How I approach hereditary cancer predisposition in a child with cancer
Michaela Kuhlen, Dagmar Wieczorek, Reiner Siebert, et al.
Pediatric Blood & Cancer (2019) Vol. 66, Iss. 11
Closed Access | Times Cited: 9
A clinical screening tool to detect genetic cancer predisposition in pediatric oncology shows high sensitivity but can miss a substantial percentage of affected children
Ulrike Friedrich, Marc Bienias, Claudia Zinke, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 8, pp. 100875-100875
Open Access | Times Cited: 3
Elevated erythroferrone distinguishes erythrocytosis with inherited defects in oxygen‐sensing pathway from primary familial and congenital polycythaemia
Lucie Sochorcova, Katarina Kapralova, Jana Kučerová, et al.
British Journal of Haematology (2023) Vol. 202, Iss. 3, pp. 674-685
Open Access | Times Cited: 3
Disruption of R867 and Y613 interaction plays key roles in JAK2 R867Q mutation caused acute leukemia
Qingyun Wu, Mengmeng Ma, Sen Zhang, et al.
International Journal of Biological Macromolecules (2019) Vol. 136, pp. 209-219
Closed Access | Times Cited: 6
Molecular profiling of pediatric and adolescent ependymomas: identification of genetic variants using a next-generation sequencing panel
Débora Cabral de Carvalho Corrêa, Francine Tesser‐Gamba, Indhira Dias Oliveira, et al.
Journal of Neuro-Oncology (2021) Vol. 155, Iss. 1, pp. 13-23
Closed Access | Times Cited: 6
Resolving inherited and de novo germline predisposing sequence variants by means of whole exome trio analyses in childhood hematological malignancies
Triantafyllia Brozou, Layal Yasin, Danielle Brandes, et al.
Frontiers in Pediatrics (2023) Vol. 10
Open Access
Clinical criteria for genetic testing in pediatric oncology show a low specificity and miss every 4thchild carrying a cancer predisposition
Ulrike Friedrich, Marc Bienias, Claudia Zinke, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
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