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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:

Rare versus common diseases: a false dichotomy in precision medicine
Brian Hon‐Yin Chung, Jeffrey Fong Ting Chau, Gane Ka‐Shu Wong
npj Genomic Medicine (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 22

Showing 22 citing articles:

Rare disease emerging as a global public health priority
Claudia Ching Yan Chung, Annie Chu, Brian Hon‐Yin Chung
Frontiers in Public Health (2022) Vol. 10
Open Access | Times Cited: 81
Unlocking life-threatening COVID-19 through two types of inborn errors of type I IFNs
Jean‐Laurent Casanova, Mark S. Anderson
Journal of Clinical Investigation (2023) Vol. 133, Iss. 3
Open Access | Times Cited: 46
Meta-analysis of the diagnostic and clinical utility of exome and genome sequencing in pediatric and adult patients with rare diseases across diverse populations
Claudia Ching Yan Chung, Shirley P.Y. Hue, Nicole Y.T. Ng, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 9, pp. 100896-100896
Open Access | Times Cited: 40
Development of Novel siRNA Therapeutics: A Review with a Focus on Inclisiran for the Treatment of Hypercholesterolemia
Oluwakemi Ebenezer, Pietro Comoglio, Gane Ka‐Shu Wong, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 4, pp. 4019-4019
Open Access | Times Cited: 26
The implementation of genome sequencing in rare genetic diseases diagnosis: a pilot study from the Hong Kong genome project
W.K. Lam, Chak Sing Lau, Ho‐Ming Luk, et al.
The Lancet Regional Health - Western Pacific (2025) Vol. 55, pp. 101473-101473
Closed Access | Times Cited: 1
The contribution of common regulatory and protein-coding TYR variants to the genetic architecture of albinism
Vincent Michaud, Eulalie Lasseaux, David Green, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 38
Targeting the Liver with Nucleic Acid Therapeutics for the Treatment of Systemic Diseases of Liver Origin
Anagha Gogate, Jordyn Belcourt, Milan Shah, et al.
Pharmacological Reviews (2023) Vol. 76, Iss. 1, pp. 49-89
Open Access | Times Cited: 13
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
Merritt-Putnam Symposium | Developmental and Epileptic Encephalopathies—Current Concepts and Novel Approaches
Rod C. Scott, Jenny Hsieh, Amy McTague, et al.
Epiliepsy currents/Epilepsy currents (2025)
Open Access
Unravelling disease complexity: integrative analysis of multi-omic data in clinical research
Ornella Cominetti, Loı̈c Dayon
Expert Review of Proteomics (2025)
Closed Access
Combining chromosome conformation capture and exome sequencing for simultaneous detection of structural and single-nucleotide variants
Maria Gridina, Timofey Lagunov, Polina Belokopytova, et al.
Genome Medicine (2025) Vol. 17, Iss. 1
Open Access
Variants of uncertain significance: At the crux of diagnostic odyssey
Akshaykumar Zawar, Gautham Manoj, Pramod P Nair, et al.
Gene (2025), pp. 149587-149587
Open Access
Potentials and challenges of launching the pilot phase of Hong Kong Genome Project
Annie Chu, Jasmine Lee Fong Fung, Amy H.Y. Tong, et al.
Journal of Translational Genetics and Genomics (2022) Vol. 6, pp. 290-303
Open Access | Times Cited: 12
Data Challenges for Externally Controlled Trials: Viewpoint
Russanthy Velummailum, Chelsea McKibbon, Darren M. Brenner, et al.
Journal of Medical Internet Research (2023) Vol. 25, pp. e43484-e43484
Open Access | Times Cited: 6
Disentangling multiple sclerosis phenotypes through Mendelian disorders: A network approach
Gianmarco Bellucci, Maria Chiara Buscarinu, Roberta Reniè, et al.
Multiple Sclerosis Journal (2024) Vol. 30, Iss. 3, pp. 325-335
Closed Access | Times Cited: 1
The Hong Kong genome project: building genome sequencing capacity and capability for advancing genomic science in Hong Kong
Annie Chu, Amy H.Y. Tong, Desiree M. S. Tse, et al.
Journal of Translational Genetics and Genomics (2023) Vol. 7, Iss. 4, pp. 196-212
Open Access | Times Cited: 3
Genetics and genomics: a frontier for clinicians
Hwei Wuen Chan, Shaun Seh Ern Loong, Roger Foo
Singapore Medical Journal (2023) Vol. 64, Iss. 1, pp. 2-3
Open Access | Times Cited: 1
Personalised genomic medicine is shaping the future of healthcare
Annie Chu, Brian Hon‐Yin Chung
Journal of Translational Genetics and Genomics (2024) Vol. 8, Iss. 1, pp. 49-54
Open Access
Co-existence of Myelin Oligodendrocyte Glycoprotien Antibody-associated Disease (MOGAD) and Spinocerebellar Ataxia type 1 (SCA1): A case report
Martina Nasello, Valeria Zancan, Roberta Reniè, et al.
Neurological Sciences (2024) Vol. 45, Iss. 8, pp. 4067-4070
Closed Access
Minimizing biological risk for novel inhibitory drug targets: One knockout is all you need
Alan Dimitriev, Lynne‐Marie Postovit, Amber L. Simpson, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
The contribution of common regulatory and protein-coding TYR variants in the genetic architecture of albinism
Vincent Michaud, Eulalie Lasseaux, David J. Green, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 1
Data Challenges for Externally Controlled Trials: Viewpoint (Preprint)
Russanthy Velummailum, Chelsea McKibbon, Darren M. Brenner, et al.
(2022)
Open Access
Association Analysis Using Set-Based Approaches in the Post-GWAS Era
Summaira Yasmeen
(2021)
Open Access
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