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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:

Advancing Personalized Medicine Through the Application of Whole Exome Sequencing and Big Data Analytics
Pawel Suwinski, ChuangKee Ong, Maurice HT Ling, et al.
Frontiers in Genetics (2019) Vol. 10
Open Access | Times Cited: 187

Showing 1-25 of 187 citing articles:

Conserved pan-cancer microenvironment subtypes predict response to immunotherapy
Alexander Bagaev, Nikita Kotlov, Krystle Nomie, et al.
Cancer Cell (2021) Vol. 39, Iss. 6, pp. 845-865.e7
Open Access | Times Cited: 818
Cellular and molecular mechanisms of skin wound healing
Oscar A Peña, Paul Martin
Nature Reviews Molecular Cell Biology (2024) Vol. 25, Iss. 8, pp. 599-616
Closed Access | Times Cited: 299
Data Integration Challenges for Machine Learning in Precision Medicine
Mireya Martínez-García, Enrique Hernández-Lemus
Frontiers in Medicine (2022) Vol. 8
Open Access | Times Cited: 79
Personalised Medicine—Implementation to the Healthcare System in Europe (Focus Group Discussions)
Dorota Stefanicka-Wojtas, Donata Kurpas
Journal of Personalized Medicine (2023) Vol. 13, Iss. 3, pp. 380-380
Open Access | Times Cited: 42
PRECISION MEDICINE AND GENOMICS: A COMPREHENSIVE REVIEW OF IT-ENABLED APPROACHES
Francisca Chibugo Udegbe, Ogochukwu Roseline Ebulue, Charles Chukwudalu Ebulue, et al.
International Medical Science Research Journal (2024) Vol. 4, Iss. 4, pp. 509-520
Open Access | Times Cited: 26
Scalable and efficient DNA sequencing analysis on different compute infrastructures aiding variant discovery
Friederike Hanssen, M. Garcia, Lasse Folkersen, et al.
NAR Genomics and Bioinformatics (2024) Vol. 6, Iss. 2
Open Access | Times Cited: 23
The clinical impact of chronopharmacology on current medicine
Mert Kaşkal, Mustafa Sevım, Gökay Ülker, et al.
Naunyn-Schmiedeberg s Archives of Pharmacology (2025)
Open Access | Times Cited: 2
Precision and Personalized Medicine: How Genomic Approach Improves the Management of Cardiovascular and Neurodegenerative Disease
Oriana Strianese, Francesca Rizzo, Michele Ciccarelli, et al.
Genes (2020) Vol. 11, Iss. 7, pp. 747-747
Open Access | Times Cited: 120
Identification of pathogenic missense mutations using protein stability predictors
Lukas Gerasimavicius, Xin Liu, Joseph A. Marsh
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 103
Techniques for the Detection of Sickle Cell Disease: A Review
Wjdan A. Arishi, Hani A. Alhadrami, Mohammed Zourob
Micromachines (2021) Vol. 12, Iss. 5, pp. 519-519
Open Access | Times Cited: 86
Application of explainable artificial intelligence in the identification of Squamous Cell Carcinoma biomarkers
Jaishree Meena, Yasha Hasija
Computers in Biology and Medicine (2022) Vol. 146, pp. 105505-105505
Closed Access | Times Cited: 45
Big data: Historic advances and emerging trends in biomedical research
Conor J. Cremin, Sabyasachi Dash, Xiaofeng Huang
Current Research in Biotechnology (2022) Vol. 4, pp. 138-151
Open Access | Times Cited: 41
EULAR points to consider for the use of big data in rheumatic and musculoskeletal diseases
Laure Gossec, Joanna Kedra, H. Servy, et al.
Annals of the Rheumatic Diseases (2019) Vol. 79, Iss. 1, pp. 69-76
Open Access | Times Cited: 69
Burden of Rare Variants in the OTOG Gene in Familial Meniere’s Disease
Pablo Román-Naranjo, Alvaro Gallego‐Martinez, Andrés Soto-Varela, et al.
Ear and Hearing (2020) Vol. 41, Iss. 6, pp. 1598-1605
Closed Access | Times Cited: 58
Genetic predisposition in type 2 diabetes: A promising approach toward a personalized management of diabetes
Mahmoud M. Sirdah, N. Scott Reading
Clinical Genetics (2020) Vol. 98, Iss. 6, pp. 525-547
Closed Access | Times Cited: 52
Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics
Eloisa Arbustini, Elijah R. Behr, Lucie Carrier, et al.
European Heart Journal (2021) Vol. 43, Iss. 20, pp. 1901-1916
Open Access | Times Cited: 51
Gene Set Enrichment Analysis of Interaction Networks Weighted by Node Centrality
Alessandra Zito, Marta Lualdi, Paola Granata, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 50
Polygenic risk scores for predicting outcomes and treatment response in psychiatry: hope or hype?
Laura Fusar‐Poli, Bart P. F. Rutten, Jim van Os, et al.
International Review of Psychiatry (2022) Vol. 34, Iss. 7-8, pp. 663-675
Open Access | Times Cited: 36
Recent Advances in Machine Learning Variant Effect Prediction Tools for Protein Engineering
Jesse Horne, Diwakar Shukla
Industrial & Engineering Chemistry Research (2022) Vol. 61, Iss. 19, pp. 6235-6245
Open Access | Times Cited: 33
The promise and challenges of genomics‐informed periodontal disease diagnoses
Luigi Nibali, Kimon Divaris, Emily Ming‐Chieh Lu
Periodontology 2000 (2024) Vol. 95, Iss. 1, pp. 194-202
Open Access | Times Cited: 7
Drug development advances in human genetics‐based targets
X. Zhang, Wenjun Yu, Yan Li, et al.
MedComm (2024) Vol. 5, Iss. 2
Open Access | Times Cited: 6
The Use of Big Data in Personalized Healthcare to Reduce Inventory Waste and Optimize Patient Treatment
Yara Badr, Lamis Abdul Kader, Abdulrahim Shamayleh
Journal of Personalized Medicine (2024) Vol. 14, Iss. 4, pp. 383-383
Open Access | Times Cited: 6
Future Trends in Nebulized Therapies for Pulmonary Disease
S. McCarthy, H. Esteban, Brendan D. Higgins
Journal of Personalized Medicine (2020) Vol. 10, Iss. 2, pp. 37-37
Open Access | Times Cited: 49
Breast Cancer in Young Women: Status Quo and Advanced Disease Management by a Predictive, Preventive, and Personalized Approach
Erik Kúdela, Marek Samec, Peter Kubatka, et al.
Cancers (2019) Vol. 11, Iss. 11, pp. 1791-1791
Open Access | Times Cited: 47
Genome analysis and knowledge-driven variant interpretation with TGex
Dvir Dahary, Yaron Golan, Yaron Mazor, et al.
BMC Medical Genomics (2019) Vol. 12, Iss. 1
Open Access | Times Cited: 44
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