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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:

Re-analysis of genomic data: An overview of the mechanisms and complexities of clinical adoption
Alan J. Robertson, Natalie B. Tan, Amanda B. Spurdle, et al.
Genetics in Medicine (2022) Vol. 24, Iss. 4, pp. 798-810
Open Access | Times Cited: 41

Showing 1-25 of 41 citing articles:

Reanalysis of genomic data, how do we do it now and what if we automate it? A qualitative study
Zoe Fehlberg, Zornitza Stark, Stephanie Best
European Journal of Human Genetics (2024) Vol. 32, Iss. 5, pp. 521-528
Open Access | Times Cited: 6
Systematic reanalysis of genomic data by diagnostic laboratories: a scoping review of ethical, economic, legal and (psycho)social implications
Marije A. van der Geest, Els Maeckelberghe, Mariëlle van Gijn, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 5, pp. 489-497
Open Access | Times Cited: 6
Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services
Stephanie Best, Zoe Fehlberg, C. Richards, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 11, pp. 1428-1435
Open Access | Times Cited: 6
Newborn screening for neurodevelopmental diseases: Are we there yet?
Wendy K. Chung, Jonathan S. Berg, Jeffrey R. Botkin, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 2, pp. 222-230
Open Access | Times Cited: 23
Genetic Testing in Parkinson's Disease
Gian Pal, Lola Cook, Jeanine Schulze, et al.
Movement Disorders (2023) Vol. 38, Iss. 8, pp. 1384-1396
Open Access | Times Cited: 16
Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort
Estefanía Martinez-Barrios, Geòrgia Sarquella-Brugada, Alexandra Pérez‐Serra, et al.
International Journal of Legal Medicine (2023) Vol. 137, Iss. 2, pp. 345-351
Open Access | Times Cited: 15
All Patients With a Cerebral Palsy Diagnosis Merit Genomic Sequencing
Clare L. van Eyk, Suzanna C. MacLennan, Alastair H. MacLennan
JAMA Pediatrics (2023) Vol. 177, Iss. 5, pp. 455-455
Closed Access | Times Cited: 15
It Is in Our DNA: Bringing Electronic Health Records and Genomic Data Together for Precision Medicine
Alan J. Robertson, Andrew Mallett, Zornitza Stark, et al.
JMIR Bioinformatics and Biotechnology (2024) Vol. 5, pp. e55632-e55632
Open Access | Times Cited: 5
Challenges of variant reinterpretation: Opinions of stakeholders and need for guidelines
Sara M. Berger, Paul S. Appelbaum, Karolynn Siegel, et al.
Genetics in Medicine (2022) Vol. 24, Iss. 9, pp. 1878-1887
Open Access | Times Cited: 19
Is there a duty to routinely reinterpret genomic variant classifications?
Gabriel Watts, Ainsley J. Newson
Journal of Medical Ethics (2023) Vol. 49, Iss. 12, pp. 808-814
Open Access | Times Cited: 11
Genetic overlap between dystonia and other neurologic disorders: A study of 1,100 exomes
Ivana Dzinovic, Sylvia Boesch, Matěj Škorvánek, et al.
Parkinsonism & Related Disorders (2022) Vol. 102, pp. 1-6
Closed Access | Times Cited: 18
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
Reclassification of Genetic Testing Results: A Case Report Demonstrating the Need for Structured Re-Evaluation of Genetic Findings
Clara Schott, Samantha Colaiacovo, Cadence Baker, et al.
Canadian Journal of Kidney Health and Disease (2024) Vol. 11
Open Access | Times Cited: 3
The role of genetic testing in the diagnostic workflow of pediatric patients with kidney diseases: the experience of a single institution
Tiziana Vaisitti, Valeria Bracciamà, Angelo Corso Faini, et al.
Human Genomics (2023) Vol. 17, Iss. 1
Open Access | Times Cited: 9
Evolution of virtual gene panels over time and implications for genomic data re-analysis
Alan J. Robertson, Khoa Tran, Chirag Patel, et al.
Genetics in Medicine Open (2023) Vol. 1, Iss. 1, pp. 100820-100820
Open Access | Times Cited: 9
The clinical utility and costs of whole-genome sequencing to detect cancer susceptibility variants—a multi-site prospective cohort study
Aimee L. Davidson, Uwe Dressel, Sarah Norris, et al.
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 9
The Australian Genomics Mitochondrial Flagship: A National Program Delivering Mitochondrial Diagnoses.
Rocío Rius, Alison G. Compton, Naomi L. Baker, et al.
Genetics in Medicine (2024), pp. 101271-101271
Closed Access | Times Cited: 2
International Undiagnosed Diseases Programs (UDPs): components and outcomes
Ela Curic, Lisa Ewans, Ryan Pysar, et al.
Orphanet Journal of Rare Diseases (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 6
Emerging bone marrow failure syndromes- new pieces to an unsolved puzzle
Simone Feurstein
Frontiers in Oncology (2023) Vol. 13
Open Access | Times Cited: 5
The practice of genomic medicine: A delineation of the process and its governing principles
Julia Handra, Adrienne Elbert, Nour Gazzaz, et al.
Frontiers in Medicine (2023) Vol. 9
Open Access | Times Cited: 4
An In-Depth Single-Gene Worldwide Carrier Frequency and Genetic Prevalence Analysis of CYP4V2 as the Cause of Bietti Crystalline Dystrophy
Mor Hanany, Richard Rui Yang, Chun Man Lam, et al.
Translational Vision Science & Technology (2023) Vol. 12, Iss. 2, pp. 27-27
Open Access | Times Cited: 4
Next-generation sequencing and comprehensive data reassessment in 263 adult patients with neuromuscular disorders: insights into the gray zone of molecular diagnoses
Martin Krenn, Matias Wagner, Gudrun Zulehner, et al.
Journal of Neurology (2023) Vol. 271, Iss. 4, pp. 1937-1946
Open Access | Times Cited: 4
Implementation of a kidney genetic service into the diagnostic pathway for patients with chronic kidney disease in Canada.
Clara Schott, Monica Arnaldi, Cadence Baker, et al.
Kidney International Reports (2024)
Open Access | Times Cited: 1
A guide to gene–disease relationships in nephrology
Zornitza Stark, Alicia B. Byrne, Matthew G. Sampson, et al.
Nature Reviews Nephrology (2024)
Closed Access | Times Cited: 1
CNVizard—a lightweight streamlit application for an interactive analysis of copy number variants
Jeremias Krause, Carlos Classen, Daniela Dey, et al.
BMC Bioinformatics (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 1
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