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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:

Precision medicine in rare diseases: What is next?
Bianca Tesi, Cathérine Boileau, Kym M. Boycott, et al.
Journal of Internal Medicine (2023) Vol. 294, Iss. 4, pp. 397-412
Open Access | Times Cited: 17

Showing 17 citing articles:

Approaches of wearable and implantable biosensor towards of developing in precision medicine
Elham Ghazizadeh, Zahra Naseri, Hans-Peter Deigner, et al.
Frontiers in Medicine (2024) Vol. 11
Open Access | Times Cited: 8
Diagnostic yield and clinical impact of germline sequencing in children with CNS and extracranial solid tumors—a nationwide, prospective Swedish study
Bianca Tesi, Kristina Lagerstedt‐Robinson, Frida Abel, et al.
The Lancet Regional Health - Europe (2024) Vol. 39, pp. 100881-100881
Open Access | Times Cited: 5
Advancing personalized medicine: key priorities for clinical studies and funding systems based on a Europe–China collaborative Delphi survey
Tommaso Osti, C Savoia, Sara Farina, et al.
European Journal of Public Health (2025)
Open Access
Big data and transformative bioinformatics in genomic diagnostics and beyond
Alice Saparov, Michael Zech
Parkinsonism & Related Disorders (2025), pp. 107311-107311
Open Access
Omics and rare diseases: challenges, applications, and future perspectives
Daniela Braconi, Haidara Nadwa, Giulia Bernardini, et al.
Expert Review of Proteomics (2025)
Closed Access
International Precision Child Health Partnership (IPCHiP): an initiative to accelerate discovery and improve outcomes in rare pediatric disease
Katherine B. Howell, Susan M. White, Amy McTague, et al.
npj Genomic Medicine (2025) Vol. 10, Iss. 1
Open Access
Bioinformatics and AI/ML approaches using multi-omics data to accelerate diagnosis and delivery of precision care for patients with rare diseases
Kritika Singh, Sarah Usman, Saman Zeeshan, et al.
Methods in cell biology (2025)
Closed Access
Toward clinical long-read genome sequencing for rare diseases
Jesper Eisfeldt, Marlene Ek, Magnus Nordenskjöld, et al.
Nature Genetics (2025)
Closed Access
Pharmacology and Precision Medicine—Preparing for the Next Era in Clinical Medicine—Editorial
Rhian M. Touyz
Pharmacological Reviews (2024) Vol. 76, Iss. 4, pp. 559-560
Open Access | Times Cited: 2
The advantages of rare disease biobanking: A localised source of genetic knowledge to benefit the South African rare disease community and related stakeholders worldwide
Marli Dercksen, Engela H. Conradie, Christian J. Hendriksz, et al.
South African Medical Journal (2023) Vol. 113, Iss. 12, pp. 9-9
Open Access | Times Cited: 4
Genomic sequencing for newborn screening: current perspectives and challenges
Nidhi Shah, Petar Brlek, Luka Bulić, et al.
Croatian Medical Journal (2024) Vol. 65, Iss. 3, pp. 261-268
Open Access | Times Cited: 1
A combination of long- and short-read genomics reveals frequent p-arm breakpoints within chromosome 21 complex genomic rearrangements
Jakob Schuy, Kristine Bilgrav Sæther, Jasmin Lisfeld, et al.
Genetics in Medicine Open (2024) Vol. 2, pp. 101863-101863
Open Access | Times Cited: 1
Prioritizing educational initiatives on emerging technologies for Italian pediatricians: bibliometric review and a survey
Alberto Eugenio Tozzi, Francesco Gesualdo, Elisabetta Pandolfi, et al.
˜The œItalian Journal of Pediatrics/Italian journal of pediatrics (2023) Vol. 49, Iss. 1
Open Access | Times Cited: 3
ZNAČAJ PRECIZNE MEDICINE I FARMAKOGENOMIKE U PREVENTIVNOJ PEDIJATRIJI
Ivana Kavečan, Nataša Nikolić, Đerđi Erdeš-Kavečan, et al.
Deleted Journal (2024), pp. 060-064
Open Access
From Alpha-Thalassemia Trait to NPRL3-Related Epilepsy: A Genomic Diagnostic Odyssey
Maryam Nabavi Nouri, Lama Alandijani, Kalene van Engelen, et al.
Genes (2024) Vol. 15, Iss. 7, pp. 836-836
Open Access
Rare diseases load through the study of a regional population
Eliane Michel, Claudia Moreau, Laurence Gagnon, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Prioritizing Educational Initiatives on Emerging Technologies for Italian Pediatricians: bibliometric review and a survey
Alberto Eugenio Tozzi, Francesco Gesualdo, Elisabetta Pandolfi, et al.
Research Square (Research Square) (2023)
Open Access
A national pilot study: Clinical long-read sequencing of chromosomal rearrangements
Jesper Eisfeldt, Adam Ameur, Felix Lenner, et al.
(2023)
Closed Access
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