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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:

Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study
Iris Cohn, Tara Paton, Christian R. Marshall, et al.
npj Genomic Medicine (2017) Vol. 2, Iss. 1
Open Access | Times Cited: 51

Showing 26-50 of 51 citing articles:

Genome-wide sequencing technologies: A primer for paediatricians
Robin Z. Hayeems, Kym M. Boycott
Paediatrics & Child Health (2017) Vol. 23, Iss. 3, pp. 191-197
Open Access | Times Cited: 14
The Clinician-reported Genetic testing Utility InDEx (C-GUIDE): Preliminary evidence of validity and reliability
Robin Z. Hayeems, Stephanie Luca, Wendy J. Ungar, et al.
Genetics in Medicine (2021) Vol. 24, Iss. 2, pp. 430-438
Closed Access | Times Cited: 11
Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing data
Luciana Bertholim-Nasciben, Marília O. Scliar, Guilherme Debortoli, et al.
Frontiers in Pharmacology (2023) Vol. 14
Open Access | Times Cited: 4
Precision Child Health: an Emerging Paradigm for Paediatric Quality and Safety
Gregory Costain, Ronald D. Cohn, David Malkin
Current Treatment Options in Pediatrics (2020) Vol. 6, Iss. 4, pp. 317-324
Open Access | Times Cited: 11
Effects of Pharmacogenomic Testing in Clinical Pain Management: Retrospective Study
Christian Tagwerker, Mary Jane Carias-Marines, David J Smith
JMIRx Med (2022) Vol. 3, Iss. 2, pp. e32902-e32902
Open Access | Times Cited: 7
Pharmacogenetic profiling via genome sequencing in children with medical complexity
Amy Pan, Sierra Scodellaro, Tayyaba Khan, et al.
Pediatric Research (2022) Vol. 93, Iss. 4, pp. 905-910
Open Access | Times Cited: 7
Comprehensive Allele Genotyping in Critical Pharmacogenes Reduces Residual Clinical Risk in Diverse Populations
Shishi Luo, Ruomu Jiang, Joseph J. Grzymski, et al.
Clinical Pharmacology & Therapeutics (2021) Vol. 110, Iss. 3, pp. 759-767
Open Access | Times Cited: 9
Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing Ontario
Robin Z. Hayeems, Christian R. Marshall, Meredith Gillespie, et al.
CMAJ Open (2022) Vol. 10, Iss. 2, pp. E460-E465
Open Access | Times Cited: 6
Determination of the Duplicated CYP2D6 Allele Using Real-Time PCR Signal: An Alternative Approach
Mazen A. Atiq, Sandra E. Peterson, Loralie J. Langman, et al.
Journal of Personalized Medicine (2023) Vol. 13, Iss. 6, pp. 883-883
Open Access | Times Cited: 2
Comparison of variants in TPMT and NUDT15 between sequencing and genotyping methods in a multistate pediatric institution
Kelsey J. Cook, Victoria Grusauskas, Lucy Gloe, et al.
Clinical and Translational Science (2023) Vol. 16, Iss. 8, pp. 1352-1358
Open Access | Times Cited: 2
High-performance DNA sequencing to identify genetically determined diseases in pediatric practice
V. Yu. Voinova, Е. А. Николаева, N. V. Shсherbakova, et al.
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) (2019) Vol. 64, Iss. 1, pp. 103-109
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
Identifying Opioid-Related Pharmacogenomic Variants in High-Risk Hospitalized Infants: A Pilot Study
Rabab M. Barq, Shadassa Ourshalimian, Simran Maggo, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Update on next generation sequencing of pharmacokinetics-related genes: Development of the PKseq panel, a platform for amplicon sequencing of drug-metabolizing enzyme and drug transporter genes
Koya Fukunaga, Yukihide Momozawa, Taisei Mushiroda
Drug Metabolism and Pharmacokinetics (2020) Vol. 37, pp. 100370-100370
Open Access | Times Cited: 3
Pharmacogenomics
Zhuo Shao, Lianna Kyriakopoulou, Shinya Ito
Handbook of analytical separations (2019), pp. 321-353
Closed Access | Times Cited: 3
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
Pharmacogenetic Gene–Drug Associations in Pediatric Burn and Surgery Patients
Kristin Grimsrud, Ryan R. Davis, Clifford G. Tepper, et al.
Journal of Burn Care & Research (2022) Vol. 43, Iss. 5, pp. 987-996
Open Access | Times Cited: 2
Utilization of Whole Exome Sequencing Data to Identify Clinically Relevant Pharmacogenomic Variants in Pediatric Inflammatory Bowel Disease
Daniel J. Mulder, Sam Khalouei, Neil Warner, et al.
Clinical and Translational Gastroenterology (2020) Vol. 11, Iss. 12, pp. e00263-e00263
Open Access | Times Cited: 2
The Evolution of DNA Sequencing in Pharmacogenomics
Steven E. Scherer
Advances in Molecular Pathology (2019) Vol. 2, Iss. 1, pp. 119-131
Closed Access | Times Cited: 1
The Implementation of Personalized Medicine in the Republic of Moldova: Challenges and Opportunities in Cardiology
Alexei Leviţchi, Daniela Galea-Abduşa, Victor Sontea, et al.
IFMBE proceedings (2023), pp. 288-298
Closed Access
A Call for Increased Inclusivity and Global Representation in Pharmacogenetic Testing
Iris Cohn, April Kennedy, Gabriel Ma, et al.
Research Square (Research Square) (2023)
Open Access
Population Analysis of Pharmacogenetic Polymorphisms
Zen H. Lu, N. Shafqat, Nani Azman, et al.
Elsevier eBooks (2018), pp. 379-387
Closed Access
Population Analysis of Pharmacogenetic Polymorphisms
Zen H. Lu, N. Shafqat, Nani Azman, et al.
Elsevier eBooks (2019), pp. 484-493
Closed Access
DNA Technologies in Precision Medicine and Pharmacogenetics
Seyedeh Sedigheh Abedini, Niloofar Bazazzadegan, Mandana Hasanzad
(2022), pp. 129-149
Closed Access
Approaches to the comprehensive interpretation of genome-scale sequencing
Christina Austin‐Tse, Özge Ceyhan-Birsoy
Elsevier eBooks (2021), pp. 237-250
Closed Access

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