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:
Incidence of the CHEK2 Germline Mutation and Its Impact on Clinicopathological Features, Treatment Responses, and Disease Course in Patients with Papillary Thyroid Carcinoma
Danuta Gąsior‐Perczak, Artur Kowalik, Krzysztof Gruszczyński, et al.
Cancers (2021) Vol. 13, Iss. 3, pp. 470-470
Open Access | Times Cited: 6
Danuta Gąsior‐Perczak, Artur Kowalik, Krzysztof Gruszczyński, et al.
Cancers (2021) Vol. 13, Iss. 3, pp. 470-470
Open Access | Times Cited: 6
Showing 6 citing articles:
Overview of the 2022 WHO Classification of Familial Endocrine Tumor Syndromes
Vânia Nosé, Anthony J. Gill, José Cameselle‐Teijeiro, et al.
Endocrine Pathology (2022) Vol. 33, Iss. 1, pp. 197-227
Closed Access | Times Cited: 45
Vânia Nosé, Anthony J. Gill, José Cameselle‐Teijeiro, et al.
Endocrine Pathology (2022) Vol. 33, Iss. 1, pp. 197-227
Closed Access | Times Cited: 45
Management of individuals with germline pathogenic/likely pathogenic variants in CHEK2: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Helen Hanson, Esteban Astiazaran‐Symonds, Laura M. Amendola, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 10, pp. 100870-100870
Open Access | Times Cited: 31
Helen Hanson, Esteban Astiazaran‐Symonds, Laura M. Amendola, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 10, pp. 100870-100870
Open Access | Times Cited: 31
Susceptibility Genes and Chromosomal Regions Associated With Non-Syndromic Familial Non-Medullary Thyroid Carcinoma: Some Pathogenetic and Diagnostic Keys
María Sánchez‐Ares, Soledad Cameselle‐García, Ihab Abdulkader, et al.
Frontiers in Endocrinology (2022) Vol. 13
Open Access | Times Cited: 11
María Sánchez‐Ares, Soledad Cameselle‐García, Ihab Abdulkader, et al.
Frontiers in Endocrinology (2022) Vol. 13
Open Access | Times Cited: 11
Insight of novel biomarkers for papillary thyroid carcinoma through multiomics
Wei Liu, Junkan Zhu, Zhen Wu, et al.
Frontiers in Oncology (2023) Vol. 13
Open Access | Times Cited: 4
Wei Liu, Junkan Zhu, Zhen Wu, et al.
Frontiers in Oncology (2023) Vol. 13
Open Access | Times Cited: 4
Relationship between the Expression of CHK2 and p53 in Tumor Tissue and the Course of Papillary Thyroid Cancer in Patients with CHEK2 Germline Mutations
Danuta Gąsior‐Perczak, Artur Kowalik, Janusz Kopczyński, et al.
Cancers (2024) Vol. 16, Iss. 4, pp. 815-815
Open Access | Times Cited: 1
Danuta Gąsior‐Perczak, Artur Kowalik, Janusz Kopczyński, et al.
Cancers (2024) Vol. 16, Iss. 4, pp. 815-815
Open Access | Times Cited: 1
CHEK2 mutations and papillary thyroid cancer: correlation or coincidence?
Koen Kortbeek, De Putter Robin, Eline Naert
Hereditary Cancer in Clinical Practice (2022) Vol. 20, Iss. 1
Open Access | Times Cited: 5
Koen Kortbeek, De Putter Robin, Eline Naert
Hereditary Cancer in Clinical Practice (2022) Vol. 20, Iss. 1
Open Access | Times Cited: 5
