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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:

Combined loss of CDH1 and downstream regulatory sequences drive early-onset diffuse gastric cancer and increase penetrance of hereditary diffuse gastric cancer
Celina São José, José Garcia‐Pelaez, Marta Ferreira, et al.
Gastric Cancer (2023) Vol. 26, Iss. 5, pp. 653-666
Open Access | Times Cited: 10

Showing 10 citing articles:

Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomes
German Demidov, Steven Laurie, Annalaura Torella, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 8, pp. 998-1004
Open Access | Times Cited: 7
Synergistic potential of CDH3 in targeting CRC metastasis and enhancing immunotherapy
Chen Fu, Fu Jia, Chaoyue Liu, et al.
BMC Cancer (2025) Vol. 25, Iss. 1
Open Access
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses
German Demidov, Burcu Yaldiz, José Garcia‐Pelaez, et al.
npj Genomic Medicine (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 3
Costs of Cancer Prevention: Physical and Psychosocial Sequelae of Risk-Reducing Total Gastrectomy
Amber F. Gallanis, Lauren A. Gamble, Sarah G. Samaranayake, et al.
Journal of Clinical Oncology (2023) Vol. 42, Iss. 4, pp. 421-430
Open Access | Times Cited: 7
Distinct characteristics of distant metastasis in early-onset gastric cancer patients compared to late-onset patients: An observational study
Feng Wu, Shuang Wu, Shujie Shuai
Medicine (2024) Vol. 103, Iss. 20, pp. e38098-e38098
Open Access | Times Cited: 1
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses
German Demidov, Burcu Yaldız, José Garcia‐Pelaez, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
Unravelling the Tumourigenesis Mechanisms of Oncocytic Cell Tumours: Discoveries from a Comparative Omics Study
Şule Canberk, Marta Ferreira, Arnaud Da Cruz Paula, et al.
Research Square (Research Square) (2024)
Open Access
Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomes
German Demidov, Steven Laurie, Annalaura Torella, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Spectrinopathies in rare neurological and neuromuscular diseases : large-scale efforts towards the identification of novel molecular causes
Liedewei Van de Vondel
(2024)
Open Access
Combined analysis of chromatin accessibility, promoter interactions and whole genome sequencing solved the missing heritability in gastric cancer
Celina São José, Marta Ferreira, Luis Rafael Martínez‐Córdova, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
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