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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:

Clinical pharmacogenomic testing and reporting: A technical standard of the American College of Medical Genetics and Genomics (ACMG)
Marwan K. Tayeh, Andrea Gaedigk, Matthew P. Goetz, et al.
Genetics in Medicine (2022) Vol. 24, Iss. 4, pp. 759-768
Open Access | Times Cited: 36

Showing 1-25 of 36 citing articles:

CYP3A4 and CYP3A5 Genotyping Recommendations
Victoria M. Pratt, Larisa H. Cavallari, Makenzie L. Fulmer, et al.
Journal of Molecular Diagnostics (2023) Vol. 25, Iss. 9, pp. 619-629
Open Access | Times Cited: 36
DPYD Genotyping Recommendations
Victoria M. Pratt, Larisa H. Cavallari, Makenzie L. Fulmer, et al.
Journal of Molecular Diagnostics (2024) Vol. 26, Iss. 10, pp. 851-863
Closed Access | Times Cited: 11
Implementation of clopidogrel pharmacogenetic clinical decision support for a preemptive return of results program
Christina L. Aquilante, Katy E. Trinkley, Yee Ming Lee, et al.
American Journal of Health-System Pharmacy (2024) Vol. 81, Iss. 12, pp. 555-562
Closed Access | Times Cited: 6
Genome-wide association testing beyond SNPs
Laura Harris, Ellen M. McDonagh, Xiaolei Zhang, et al.
Nature Reviews Genetics (2024)
Closed Access | Times Cited: 5
Review of Precision Medicine and Diagnosis of Neonatal Illness
Safaa ELMeneza, Naglaa Agaba, Rasha Abd El Samad Fawaz, et al.
Diagnostics (2025) Vol. 15, Iss. 4, pp. 478-478
Open Access
Implementing Pharmacogenomics Clinical Decision Support: A Comprehensive Tutorial on how to Integrate the Epic Genomics Module
Bradley R. Hall, Eda Eken, Larisa H. Cavallari, et al.
Clinical Pharmacology & Therapeutics (2025)
Closed Access
Cardiovascular precision medicine – A pharmacogenomic perspective
Sandosh Padmanabhan, Clea du Toit, Anna F. Dominiczak
Cambridge Prisms Precision Medicine (2023) Vol. 1
Open Access | Times Cited: 11
Analytical Validation of a Computational Method for Pharmacogenetic Genotyping from Clinical Whole Exome Sequencing
Reynold C. Ly, Tyler Shugg, Ryan Ratcliff, et al.
Journal of Molecular Diagnostics (2022) Vol. 24, Iss. 6, pp. 576-585
Open Access | Times Cited: 13
Structural Protein Effects Underpinning Cognitive Developmental Delay of the PURA p.Phe233del Mutation Modelled by Artificial Intelligence and the Hybrid Quantum Mechanics–Molecular Mechanics Framework
Juan Javier López-Rivera, Luna Rodríguez‐Salazar, Alejandro Soto-Ospina, et al.
Brain Sciences (2022) Vol. 12, Iss. 7, pp. 871-871
Open Access | Times Cited: 12
Pharmacogenes that demonstrate high association evidence according to CPIC, DPWG, and PharmGKB
Mohammad A. Alshabeeb, Mesnad Alyabsi, Mohammad Aziz, et al.
Frontiers in Medicine (2022) Vol. 9
Open Access | Times Cited: 12
Screening program for familial hyperchylomicronemia syndrome detection: Experience of a university health system
Walter Masson, Leandro Barbagelata, Milagros Fleitas, et al.
Archives of Endocrinology and Metabolism (2023)
Open Access | Times Cited: 5
The Genetic Testing Reference Materials Coordination Program
Stuart A. Scott
Journal of Molecular Diagnostics (2023) Vol. 25, Iss. 9, pp. 630-633
Open Access | Times Cited: 5
Does Preoperative Pharmacogenomic Testing of Patients Undergoing TKA Improve Postoperative Pain? A Randomized Trial
Molly B. Kraus, Joshua S. Bingham, Adrijana Kekic, et al.
Clinical Orthopaedics and Related Research (2023)
Closed Access | Times Cited: 5
Comprehensive characterization of pharmacogenes in a Taiwanese Han population
Hsing‐Fang Lu, Ting‐Yuan Liu, Yu‐Pao Chou, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 8
Targeted haplotyping in pharmacogenomics using Oxford Nanopore Technologies’ adaptive sampling
Koen Deserranno, Laurentijn Tilleman, Kaat Rubben, et al.
Frontiers in Pharmacology (2023) Vol. 14
Open Access | Times Cited: 4
Customizing the electronic health record for delivery of pharmacogenetics
Glenda Hoffecker, Lisa A. Varughese, Joseph Bleznuck, et al.
Genetics in Medicine Open (2023) Vol. 1, Iss. 1, pp. 100779-100779
Closed Access | Times Cited: 3
Public Attitudes toward Pharmacogenomic Testing and Establishing a Statewide Pharmacogenomics Database in the State of Minnesota
Lusi Zhang, Pamala A. Jacobson, Alyssa N. K. Johnson, et al.
Journal of Personalized Medicine (2022) Vol. 12, Iss. 10, pp. 1615-1615
Open Access | Times Cited: 4
Applications of genome sequencing as a single platform for clinical constitutional genetic testing
Yao Yang, Daniela del Gaudio, Avni Santani, et al.
Genetics in Medicine Open (2024) Vol. 2, pp. 101840-101840
Open Access
Development of a comprehensive genome-wide cardiovascular disease genetic risk assessment test
Laura M. Amendola, Alison J. Coffey, Josh Lowry, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Techniques, procedures, and applications in host genetic analysis
Diego A. Bonilla, Carlos A. Orozco, Diego A. Forero, et al.
Advances in genetics (2024), pp. 1-79
Closed Access
Education of Future Pharmacogenomics Laboratory Directors
Reynold C. Ly, Marwan K. Tayeh, Yuan Ji
Advances in Molecular Pathology (2024) Vol. 7, Iss. 1, pp. 33-41
Closed Access
Genetic counseling
Wendy R. Uhlmann
Elsevier eBooks (2024), pp. 233-247
Closed Access
Bioinformatics for Precision Medicine
Akshaykumar Zawar, Arjun Gupta, Prakriti Arora, et al.
Elsevier eBooks (2024)
Closed Access
Genetics in the diagnosis and treatment of cardiovascular diseases
Kevin P. Bliden, Sahib Singh, Roni Shanoada, et al.
Journal of Translational Genetics and Genomics (2024) Vol. 8, Iss. 2, pp. 186-206
Open Access
Long-read Sequencing for Germline Pharmacogenomic Testing
Matthew B. Neu, Yao Yang, Stuart A. Scott
Advances in Molecular Pathology (2023) Vol. 6, Iss. 1, pp. 99-109
Open Access | Times Cited: 1
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