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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:

Point/Counterpoint: Is It Time for Universal Germline Genetic Testing for All GI Cancers?
Heather Hampel, Matthew B. Yurgelun
Journal of Clinical Oncology (2022) Vol. 40, Iss. 24, pp. 2681-2692
Closed Access | Times Cited: 27

Showing 1-25 of 27 citing articles:

Does neoadjuvant treatment in resectable pancreatic cancer improve overall survival? A systematic review and meta-analysis of randomized controlled trials
Pedro Luiz Serrano Usón, Douglas Dias E Silva, Nicoly Marques de Castro, et al.
ESMO Open (2023) Vol. 8, Iss. 1, pp. 100771-100771
Open Access | Times Cited: 25
Potential pathogenic germline variant reporting from tumor comprehensive genomic profiling complements classic approaches to germline testing
Nadine Tung, Kali Chatham Dougherty, Emily Stern Gatof, et al.
npj Precision Oncology (2023) Vol. 7, Iss. 1
Open Access | Times Cited: 17
Saturation-scale functional evidence supports clinical variant interpretation in Lynch syndrome
Anthony Scott, Felicia Hernandez, Adam Chamberlin, et al.
Genome biology (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 26
Germline Variants Incidentally Detected via Tumor-Only Genomic Profiling of Patients With Mesothelioma
Owen Mitchell, Katie Gilliam, Daniela del Gaudio, et al.
JAMA Network Open (2023) Vol. 6, Iss. 8, pp. e2327351-e2327351
Open Access | Times Cited: 10
ItaLynch: an ongoing Italian study to evaluate the feasibility of mainstreaming the diagnosis of Lynch syndrome in colorectal cancer patients
Alberto Puccini, Federica Grillo, Matteo Fassan, et al.
ESMO Gastrointestinal Oncology (2024) Vol. 3, pp. 100044-100044
Open Access | Times Cited: 2
Comparison of Germline Genetic Testing Before and After a Medical Policy Covering Universal Testing Among Patients With Colorectal Cancer
Chad Moretz, Stacey DaCosta Byfield, Kathryn E. Hatchell, et al.
JAMA Network Open (2022) Vol. 5, Iss. 10, pp. e2238167-e2238167
Open Access | Times Cited: 10
Family Matters: Germline Testing in Thoracic Cancers
Feighanne Hathaway, Renato Martins, Steven Sorscher, et al.
American Society of Clinical Oncology Educational Book (2023), Iss. 43
Open Access | Times Cited: 5
Building on More Than 20 Years of Progress in Pancreatic Cancer Surveillance for High-Risk Individuals
Matthew B. Yurgelun
Journal of Clinical Oncology (2022) Vol. 40, Iss. 28, pp. 3230-3234
Open Access | Times Cited: 8
Do All Patients Diagnosed With Cancer Deserve Germline Testing?
Steven Sorscher
Journal of Clinical Oncology (2023) Vol. 41, Iss. 24, pp. 4057-4058
Closed Access | Times Cited: 4
Streamlining the diagnostic pathway for Lynch syndrome in colorectal cancer patients: a 10-year experience in a single Italian Cancer Center
Alberto Puccini, Simone Nardin, Lucia Trevisan, et al.
European Journal of Cancer Prevention (2024) Vol. 33, Iss. 4, pp. 355-362
Closed Access | Times Cited: 1
Feasibility and Clinical Utility of Reporting Hereditary Cancer Predisposition Pathogenic Variants Identified in Research Germline Sequencing: A Prospective Interventional Study
Megan L. Hutchcraft, Shulin Zhang, Nan Lin, et al.
JCO Precision Oncology (2024), Iss. 8
Open Access | Times Cited: 1
Invited Commentary
Kurt Schultz, Anne K. Mongiu
Journal of the American College of Surgeons (2024) Vol. 238, Iss. 6, pp. 1021-1022
Closed Access | Times Cited: 1
Genetic insights: High germline variant rate in an indigenous African cohort with early-onset colorectal cancer
Safiye Yıldız, Takudzwa N. Musarurwa, Ursula Algar, et al.
Frontiers in Oncology (2023) Vol. 13
Open Access | Times Cited: 2
Hereditäres kolorektales Karzinom
Isabel Spier, Stefan Aretz
coloproctology (2024) Vol. 46, Iss. 2, pp. 87-95
Closed Access
Outcomes of a universal germline screening program in a community urology practice
Neil Mendhiratta, Herman Hauver, Whitley Hatton, et al.
Clinical Genetics (2024) Vol. 106, Iss. 3, pp. 277-283
Closed Access
Consensus Guideline for the Management of Colorectal Cancer with Peritoneal Metastases
Kiran K. Turaga
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Universal screening of colorectal tumors for lynch syndrome: a survey of patient experiences and opinions
Alexander T Petterson, Jennifer Garbarini, Maria J. Baker
Hereditary Cancer in Clinical Practice (2024) Vol. 22, Iss. 1
Open Access
Poor compliance with germline testing recommendations in colorectal cancer patients undergoing molecular residual disease testing
Suzanne Schrock-Kelley, Vivienne Souter, Michael J. Hall, et al.
Communications Medicine (2024) Vol. 4, Iss. 1
Open Access
The Ethics of Genetic Testing for Inherited Cancer-Predisposing Genes
Steven Sorscher, Alisha T Detroye
Journal of the Advanced Practitioner in Oncology (2024) Vol. 15, Iss. 2, pp. 137-140
Open Access
Pilot Implementation Study of a Default Genetic Referral Process for Patients with Early-Onset Colorectal Cancer
Kelsey S. Lau‐Min, Shavon E. Rochester, Megan Grabill, et al.
Genetics in Medicine Open (2024) Vol. 3, pp. 101902-101902
Open Access
Refining the interpretation of Variants of Uncertain Significance in Hereditary Cancer Screening through Integrated RNA Sequencing
Youbao Sha, J. Bryce Ortiz, Sara L. Bristow, et al.
Genetics in Medicine Open (2024) Vol. 3, pp. 101914-101914
Open Access
Duty to recontact in genomic cancer care: A tool helping to assess the professional’s responsibility
Martine Corrette Ploem, Noor A. A. Giesbertz, Annelien L. Bredenoord, et al.
European Journal of Cancer (2023) Vol. 186, pp. 22-26
Open Access | Times Cited: 1
Report from the 24th Annual Western Canadian Gastrointestinal Cancer Consensus Conference on Colorectal Cancer, Richmond, British Columbia, 28–29, October 2022
Sharlene Gill, Shahid Ahmed, Brady Anderson, et al.
Current Oncology (2023) Vol. 30, Iss. 9, pp. 7964-7983
Open Access | Times Cited: 1
Genetic counselling referral practices for patients with pancreatic adenocarcinoma: A French retrospective multicentre observational cohort study (CAPANCOGEN)
Mathias Brügel, Thibault Marulier, Camille Evrard, et al.
Pancreatology (2023) Vol. 23, Iss. 6, pp. 622-629
Open Access
The Evolution of Genetic Testing from Focused Testing to Panel Testing and from Patient Focused to Population Testing: Are We There Yet?
Lauren Gima, Ilana Solomon, Heather Hampel
Clinics in Colon and Rectal Surgery (2023) Vol. 37, Iss. 03, pp. 133-139
Closed Access
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