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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 1-25 of 46 citing articles:

Adiposity impacts cognitive function in Asian populations: an epidemiological and Mendelian Randomization study
Theresia Mina, Yik Weng Yew, Hong Kiat Ng, et al.
The Lancet Regional Health - Western Pacific (2023) Vol. 33, pp. 100710-100710
Open Access | Times Cited: 56
Epidemiology of the idiopathic inflammatory myopathies
Thomas Khoo, James B Lilleker, Bernard Yu‐Hor Thong, et al.
Nature Reviews Rheumatology (2023) Vol. 19, Iss. 11, pp. 695-712
Closed Access | Times Cited: 38
Blood-based epigenome-wide analyses of chronic low-grade inflammation across diverse population cohorts
Robert F. Hillary, Hong Kiat Ng, Daniel L. McCartney, et al.
Cell Genomics (2024) Vol. 4, Iss. 5, pp. 100544-100544
Open Access | Times Cited: 11
Multi-locus inherited neoplasia alleles syndromes in cancer: implications for clinical practice
Jeanette Yuen, Siqin Zhou, Rebecca Caeser, et al.
European Journal of Human Genetics (2025)
Open Access | Times Cited: 1
Analysis of 14,392 whole genomes reveals 3.5% of Qataris carry medically actionable variants
Amal Elfatih, Chadi Saad, Said I. Ismail, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 11, pp. 1465-1473
Open Access | Times Cited: 8
Pervasive ancestry bias in variant effect predictors
Ankit K. Pathak, Nikita Bora, Mihaly Badonyi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 6
Analysis and visualisation of electronic health records data to identify undiagnosed patients with rare genetic diseases
Daniel Patrick Moynihan, Sean Monaco, Teck Wah Ting, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 4
Adiposity and metabolic health in Asian populations: an epidemiological study using dual-energy x-ray absorptiometry in Singapore
Theresia Mina, Wubin Xie, Dorrain Yanwen Low, et al.
The Lancet Diabetes & Endocrinology (2024) Vol. 12, Iss. 10, pp. 704-715
Closed Access | Times Cited: 4
Genetics and Population Analysis
Prachi Balyan, Nismabi A Nisamudheen, Jan Zainab, et al.
Elsevier eBooks (2025)
Closed Access
The large-scale whole-genome sequencing era expedited medical discovery and clinical translation
Qingxin Yang, Shuhan Duan, Yuguo Huang, et al.
Deleted Journal (2025) Vol. 2, Iss. 1, pp. 100055-100055
Closed Access
Phenotypic Distinctions Between EYS- and USH2A-Associated Retinitis Pigmentosa in an Asian Population
Erik Yeo, Taro Kominami, Tien‐En Tan, et al.
Translational Vision Science & Technology (2025) Vol. 14, Iss. 2, pp. 16-16
Open Access
Pathogenic variants in the Alport genes are prevalent in the Singapore multiethnic population with highest frequency in the Chinese
Tina Si Ting Lim, Chee Teck Koh, Judy Savige, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Inherited retinal degeneration in Malay and Indian populations of Singapore and Malaysia: a prospective multicentre study
Shaobing Su, Choi Mun Chan, Yasmin Bylstra, et al.
Ophthalmic Genetics (2025), pp. 1-12
Closed Access
Determinants of diagnostic yield in a multi-ethnic Asian inherited retinal disease cohort
Jane A. Lieviant, Choi Mun Chan, Yasmin Bylstra, et al.
European Journal of Human Genetics (2025)
Open Access
Leveraging Electronic Health Records to Examine the Real-World Rates of Cancer Genetics Referrals in a Singapore Health Care Cluster
Jonathan Jian Hao Soon, Jaw‐Ching Wu, Nur Diana Binte Ishak, et al.
JCO Oncology Practice (2025)
Closed Access
A scoping review of the development of genetic counseling practices in Asia
Tiffany Qing Lim, Lisa Dive, Alison McEwen
Journal of Genetic Counseling (2025) Vol. 34, Iss. 3
Open Access
Unexpected genotypes associated with severe paediatric conditions identified in a healthy population cohort.
Saumya Shekhar Jamuar, Yasmin Bylstra, Weng Khong Lim, et al.
Research Square (Research Square) (2025)
Closed Access
Tracing human genetic histories and natural selection with precise local ancestry inference
Jon Lerga-Jaso, Biljana Novković, Deepu Unnikrishnan, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
The distribution of highly deleterious variants across human ancestry groups
Anastasia V. Stolyarova, Graham Coop, Molly Przeworski
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 21
Open Access
Blood-based epigenome-wide analyses of chronic low-grade inflammation across diverse population cohorts
Robert F. Hillary, Hong Kiat Ng, Daniel L. McCartney, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 7
Cascade testing for hereditary cancer in Singapore: how population genomics help guide clinical policy
Rebecca Caeser, Jianbang Chiang, Ee Shien Tan, et al.
Familial Cancer (2024) Vol. 23, Iss. 2, pp. 133-140
Closed Access | Times Cited: 2
Global carrier frequency and predicted genetic prevalence of patients with pathogenic sequence variants in autosomal recessive genetic neuromuscular diseases
Won-Jun Choi, Soo-Hyun Kim, Sung Rok Lee, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 2
South Asia: The Missing Diverse in Diversity
Deepika Dokuru, Tanya B. Horwitz, Samantha M. Freis, et al.
Behavior Genetics (2023) Vol. 54, Iss. 1, pp. 51-62
Open Access | Times Cited: 5
RETINITIS PIGMENTOSA ASSOCIATED WITH THE EYS C2139Y VARIANT
Choi Mun Chan, Tien‐En Tan, Kanika Jain, et al.
Retina (2023) Vol. 43, Iss. 10, pp. 1788-1796
Closed Access | Times Cited: 4
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
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