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:
Impact of Different Selection Approaches for Identifying Lynch Syndrome-Related Colorectal Cancer Patients: Unity Is Strength
Daniele Fanale, Lidia Rita Corsini, Chiara Brando, et al.
Frontiers in Oncology (2022) Vol. 12
Open Access | Times Cited: 10
Daniele Fanale, Lidia Rita Corsini, Chiara Brando, et al.
Frontiers in Oncology (2022) Vol. 12
Open Access | Times Cited: 10
Showing 10 citing articles:
MUTYH-associated tumor syndrome: The other face of MAP
Luigi Magrin, Daniele Fanale, Chiara Brando, et al.
Oncogene (2022) Vol. 41, Iss. 18, pp. 2531-2539
Closed Access | Times Cited: 20
Luigi Magrin, Daniele Fanale, Chiara Brando, et al.
Oncogene (2022) Vol. 41, Iss. 18, pp. 2531-2539
Closed Access | Times Cited: 20
Screening and prevention of gynecologic malignancies in patients with lynch syndrome: following the guidelines
Chen Ben David, Yoav Siegler, Revital Linder, et al.
Frontiers in Oncology (2025) Vol. 15
Open Access
Chen Ben David, Yoav Siegler, Revital Linder, et al.
Frontiers in Oncology (2025) Vol. 15
Open Access
BRCA1/2 variants of unknown significance in hereditary breast and ovarian cancer (HBOC) syndrome: Looking for the hidden meaning
Daniele Fanale, Alessia Pivetti, D. Cancelliere, et al.
Critical Reviews in Oncology/Hematology (2022) Vol. 172, pp. 103626-103626
Closed Access | Times Cited: 14
Daniele Fanale, Alessia Pivetti, D. Cancelliere, et al.
Critical Reviews in Oncology/Hematology (2022) Vol. 172, pp. 103626-103626
Closed Access | Times Cited: 14
Genetic analysis of Japanese patients with small bowel adenocarcinoma using next-generation sequencing
Atsushi Tatsuguchi, Takeshi Yamada, Kohji Ueda, et al.
BMC Cancer (2022) Vol. 22, Iss. 1
Open Access | Times Cited: 8
Atsushi Tatsuguchi, Takeshi Yamada, Kohji Ueda, et al.
BMC Cancer (2022) Vol. 22, Iss. 1
Open Access | Times Cited: 8
BRCA-associated hereditary male cancers: can gender affect the prevalence and spectrum of germline pathogenic variants?
Daniele Fanale, Lidia Rita Corsini, Chiara Brando, et al.
Frontiers in Oncology (2024) Vol. 14
Open Access | Times Cited: 1
Daniele Fanale, Lidia Rita Corsini, Chiara Brando, et al.
Frontiers in Oncology (2024) Vol. 14
Open Access | Times Cited: 1
Potential agnostic role of BRCA alterations in patients with several solid tumors: One for all, all for one?
Daniele Fanale, Lidia Rita Corsini, Erika Pedone, et al.
Critical Reviews in Oncology/Hematology (2023) Vol. 190, pp. 104086-104086
Open Access | Times Cited: 3
Daniele Fanale, Lidia Rita Corsini, Erika Pedone, et al.
Critical Reviews in Oncology/Hematology (2023) Vol. 190, pp. 104086-104086
Open Access | Times Cited: 3
A new subtype of Lynch syndrome associated with MSH2 c.354T>A (p. Y118*) identified in a Chinese family: case report and literature review
Lan Zhong, Wenxiang Wang, Yuanqiong Duan, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access
Lan Zhong, Wenxiang Wang, Yuanqiong Duan, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access
Board Review Vignette-Hereditary Cancer Syndromes
Robin Wilson, Nicholas Bartell, Danielle Marino
The American Journal of Gastroenterology (2024)
Closed Access
Robin Wilson, Nicholas Bartell, Danielle Marino
The American Journal of Gastroenterology (2024)
Closed Access
Risk for Hereditary Neoplastic Syndromes in Women with Mismatch Repair-Proficient Endometrial Cancer
Jennifer Thalita Targino dos Santos, Reginaldo Cruz Alves Rosa, Álison Luís Eburnêo Pereira, et al.
Genes (2023) Vol. 14, Iss. 11, pp. 1999-1999
Open Access
Jennifer Thalita Targino dos Santos, Reginaldo Cruz Alves Rosa, Álison Luís Eburnêo Pereira, et al.
Genes (2023) Vol. 14, Iss. 11, pp. 1999-1999
Open Access
A novel mutation of MET in hereditary non-polyposis colorectal cancer identified by whole exome sequencing: report of a family
Natthapon Khongcharoen, Wison Laochareonsuk, Teeranut Boonpipattanapong, et al.
Research Square (Research Square) (2022)
Open Access
Natthapon Khongcharoen, Wison Laochareonsuk, Teeranut Boonpipattanapong, et al.
Research Square (Research Square) (2022)
Open Access
