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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:

Analysis of clinically relevant variants from ancestrally diverse Asian genomes
Sock Hoai Chan, Yasmin Bylstra, Jing Xian Teo, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 46

Showing 26-50 of 46 citing articles:

It’s All in Your Genes: What Primary Care Should Know About Hereditary Cancer Syndromes
Rebecca Caeser, A Prof, Joanne Ngeow, et al.
The Singapore Family Physician (2024) Vol. 50, Iss. 1
Open Access | Times Cited: 1
The BIM deletion polymorphism potentiates the survival of leukemia stem and progenitor cells and impairs response to targeted therapies
Mengge Yu, Giselle Sek Suan Nah, Vaidehi Krishnan, et al.
Leukemia (2024)
Closed Access | Times Cited: 1
Ensemble and consensus approaches to prediction of recessive inheritance for missense variants in human disease
Ben Omega Petrazzini, Daniel J. Balick, Iain S. Forrest, et al.
Cell Reports Methods (2024), pp. 100914-100914
Closed Access | Times Cited: 1
Accelerating access to human genomics for public health: perspectives from the Western Pacific region
Kidong Park, Mengji Chen, Greco Mark Malijan, et al.
The Lancet Regional Health - Western Pacific (2024) Vol. 53, pp. 101265-101265
Open Access | Times Cited: 1
Identification of Novel and Recurrent Variants in BTD, GBE1, AGL and ASL Genes in Families with Metabolic Disorders in Saudi Arabia
Muhammad Latif, Jamil Amjad Hashmi, Abdulfatah M. Alayoubi, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 5, pp. 1193-1193
Open Access | Times Cited: 1
Frequency of actionable secondary findings in 7472 Korean genomes derived from the National Project of Bio Big Data pilot study
Young Jun Kim, Jeong‐Min Kim, Hye‐Won Cho, et al.
Human Genetics (2023) Vol. 142, Iss. 11, pp. 1561-1569
Open Access | Times Cited: 3
CYP2D6 and CYP2C19 Variant Coverage of Commercial Antidepressant Pharmacogenomic Testing Panels Available in Victoria, Australia
Malcolm Forbes, Malcolm Hopwood, Chad A. Bousman
Genes (2023) Vol. 14, Iss. 10, pp. 1945-1945
Open Access | Times Cited: 3
Diagnostic Challenges in ABCA4-Associated Retinal Degeneration: One Gene, Many Phenotypes
Tien‐En Tan, Rachael W. C. Tang, Choi Mun Chan, et al.
Diagnostics (2023) Vol. 13, Iss. 23, pp. 3530-3530
Open Access | Times Cited: 3
Retracing Human Genetic Histories and Natural Selection Using Precise Local Ancestry Inference
Jon Lerga-Jaso, Biljana Novković, Deepu Unnikrishnan, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Adiposity and metabolic health in Asian populations: An epidemiological study using Dual X-Ray Absorptiometry
Theresia Mina, Wubin Xie, Dorrain Low Yan Wen, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
A Catalogue of Structural Variation across Ancestrally Diverse Asian Genomes
Nicolas Bertin, Joanna Tan, Zhihui Li, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 1
Familial Hypercholesterolaemia: Saving Lives Through Early Detection and Intervention
Jeremy Hoe, Sharon Li Ting Pek, Andrew E ZAMANI Prof, et al.
The Singapore Family Physician (2024) Vol. 50, Iss. 1
Open Access
Pharmacogenomics in a Nutshell for General Practitioners
Ms Chua, Hui Min, Lo Ah, et al.
The Singapore Family Physician (2024) Vol. 50, Iss. 1
Open Access
Familial Cancers
Jeanette Yuen, Antonio Carlo D. De Guzman, Eliza Courtney, et al.
Elsevier eBooks (2024), pp. 237-260
Closed Access
Implementation of HLA-related genotype-guided prescribing in Singapore
Hui Min Chua, Lie Michael George Limenta, Carol Yee Leng Ng, et al.
American Journal of Health-System Pharmacy (2024)
Closed Access
Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population
Namanpreet Kaur, Michelle C. do Rosario, Purvi Majethia, et al.
American Journal of Medical Genetics Part A (2024)
Open Access
A Catalogue of Structural Variation across Ancestrally Diverse Asian Genomes
Joanna Tan, Zhihui Li, Mar Gonzalez Porta, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access
Pharmacogenomics in psychiatry: Practice recommendations from an Asian perspective (2024)
Shih Ee Goh, Saumya Shekhar Jamuar, Siew E. Chua, et al.
Annals of the Academy of Medicine Singapore (2024) Vol. 53, Iss. 12, pp. 734-741
Open Access
CYP2D6 and CYP2C19 Variant Coverage of Commercial Antidepressant Pharmacogenomic Testing Panels Available in Victoria, Australia
Malcolm Forbes, Malcolm Hopwood, Chad A. Bousman
(2023)
Open Access | Times Cited: 1
Population WGS-based spinal muscular atrophy carrier screening in a cohort of 1076 healthy Polish individuals
Mateusz Sypniewski, Dominika Kresa, Paula Dobosz, et al.
Journal of Applied Genetics (2022) Vol. 64, Iss. 1, pp. 135-139
Open Access | Times Cited: 2
Genomic landscape of drug binding and pharmacogenetic variation across diverse populations using SNPdrug3D
Sebastian Maurer‐Stroh, Ashar J. Malik, Dimitar Kenanov, et al.
Research Square (Research Square) (2023)
Open Access
Data Mining of Electronic Health Records to Identify Undiagnosed Patients with Rare Genetic Diseases
Daniel Patrick Moynihan, Sean Monaco, Teck Wah Ting, et al.
Research Square (Research Square) (2023)
Open Access
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