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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:

Exploring human genomic diversity with gnomAD
Linda Koch
Nature Reviews Genetics (2020) Vol. 21, Iss. 8, pp. 448-448
Open Access | Times Cited: 106

Showing 1-25 of 106 citing articles:

Simultaneous Copy Number Alteration and Single-Nucleotide Variation Analysis in Matched Aqueous Humor and Tumor Samples in Children with Retinoblastoma
J. Michael Schmidt, Rishvanth K. Prabakar, Sarah Pike, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 10, pp. 8606-8606
Open Access | Times Cited: 18
GenomeMUSter mouse genetic variation service enables multitrait, multipopulation data integration and analysis
Robyn L. Ball, Molly A. Bogue, Hongping Liang, et al.
Genome Research (2024) Vol. 34, Iss. 1, pp. 145-159
Open Access | Times Cited: 7
Genetic Risk Factors for Early-Onset Merkel Cell Carcinoma
Noreen Mohsin, Devin Hunt, Jia Yan, et al.
JAMA Dermatology (2024) Vol. 160, Iss. 2, pp. 172-172
Closed Access | Times Cited: 6
CSVS, a crowdsourcing database of the Spanish population genetic variability
María Peña-Chilet, Gema Roldán, Javier Pérez-Florido, et al.
Nucleic Acids Research (2020) Vol. 49, Iss. D1, pp. D1130-D1137
Open Access | Times Cited: 48
Identification and functional characterization of new missense SNPs in the coding region of the TP53 gene
Flora Doffe, Vincent Carbonnier, Manon Tissier, et al.
Cell Death and Differentiation (2020) Vol. 28, Iss. 5, pp. 1477-1492
Open Access | Times Cited: 41
The panoramic view of amyotrophic lateral sclerosis: A fatal intricate neurological disorder
Swati Dhasmana, Anupam Dhasmana, Acharan S. Narula, et al.
Life Sciences (2021) Vol. 288, pp. 120156-120156
Closed Access | Times Cited: 38
High diagnosis rate for nonimmune hydrops fetalis with prenatal clinical exome from the Hydrops-Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) Study
Huda B. Al‐Kouatly, Mona M. Makhamreh, Stephanie M. Rice, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 7, pp. 1325-1333
Open Access | Times Cited: 35
Exploiting deep transfer learning for the prediction of functional non-coding variants using genomic sequence
Li Chen, Ye Wang, Fengdi Zhao
Bioinformatics (2022) Vol. 38, Iss. 12, pp. 3164-3172
Open Access | Times Cited: 25
Lessons learned: next-generation sequencing applied to undiagnosed genetic diseases
Bryce Schuler, Erica T. Nelson, Mary Koziura, et al.
Journal of Clinical Investigation (2022) Vol. 132, Iss. 7
Open Access | Times Cited: 23
Comment on “Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals”
Roberto H. Herai, Katerina Semendeferi, Alysson R. Muotri
Science (2023) Vol. 379, Iss. 6636
Closed Access | Times Cited: 13
Advances in the study and treatment of genetic cardiomyopathies
Victoria N. Parikh, Sharlene M. Day, Neal K. Lakdawala, et al.
Cell (2025) Vol. 188, Iss. 4, pp. 901-918
Closed Access
Variations and Polymorphisms: The Human Pangenome Project
Shweta Pandey, Sanjiv S. Gambhir, Vipin Kumar Singh, et al.
Elsevier eBooks (2025), pp. 282-294
Closed Access
Exploring deleterious non-synonymous SNPs in FUT2 gene, and implications for norovirus susceptibility and gut microbiota composition
Muhammad Waleed Iqbal, Muneer Ahmad, Muhammad Shahab, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Clinical Utility of Comprehensive Genomic Profiling Tests Using MTB Management System at a Single Center in Japan
Chie Sarudate, Miki Dobashi, Maako Kawamura, et al.
Research Square (Research Square) (2025)
Closed Access
Predominant monomorphism of the RIT2 and GPM6B exceptionally long GA blocks in human and enriched divergent alleles in the disease compartment
Safoura Khamse, Masoud Arabfard, Mahmood Salesi, et al.
Genetica (2022) Vol. 150, Iss. 1, pp. 27-40
Closed Access | Times Cited: 17
Variant curation and interpretation in hereditary cancer genes: An institutional experience in Latin America
María Carolina Manotas, Ana Lucía Rivera, María Carolina Sanabria‐Salas
Molecular Genetics & Genomic Medicine (2023) Vol. 11, Iss. 5
Open Access | Times Cited: 10
A loss-of-function variant in ZCWPW1 causes human male infertility with sperm head defect and high DNA fragmentation
Yuelin Song, Juncen Guo, Yanling Zhou, et al.
Reproductive Health (2024) Vol. 21, Iss. 1
Open Access | Times Cited: 3
Discovery of novel predisposing coding and noncoding variants in familial Hodgkin lymphoma
Jamie E. Flerlage, Jason R. Myers, Jamie L. Maciaszek, et al.
Blood (2022) Vol. 141, Iss. 11, pp. 1293-1307
Open Access | Times Cited: 16
Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases
Wejdan M. Alenezi, Caitlin T. Fierheller, Corinne Serruya, et al.
Frontiers in Oncology (2023) Vol. 13
Open Access | Times Cited: 8
SAMD9L autoinflammatory or ataxia pancytopenia disease mutations activate cell-autonomous translational repression
Amanda J. Russell, Paul Gray, John B. Ziegler, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 34
Open Access | Times Cited: 20
Clinical decisions by the molecular tumor board on comprehensive genomic profiling tests in Japan: A retrospective observational study
Hidekazu Shirota, Keigo Komine, Masanobu Takahashi, et al.
Cancer Medicine (2022) Vol. 12, Iss. 5, pp. 6170-6181
Open Access | Times Cited: 14
Alzheimer’s Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer’s Disease
Pavel P. Kuksa, Chia‐Lun Liu, Wei Fu, et al.
Journal of Alzheimer s Disease (2022) Vol. 86, Iss. 1, pp. 461-477
Open Access | Times Cited: 13
Perception of personalized medicine, pharmacogenomics, and genetic testing among undergraduates in Hong Kong
Nicholas Yan Chai Cheung, Jasmine Lee Fong Fung, Yvette Nga Chung Ng, et al.
Human Genomics (2021) Vol. 15, Iss. 1
Open Access | Times Cited: 17
From bugs to bedside: functional annotation of human genetic variation for neurological disorders using invertebrate models
Melanie Mew, Kim A. Caldwell, Guy A. Caldwell
Human Molecular Genetics (2022) Vol. 31, Iss. R1, pp. R37-R46
Open Access | Times Cited: 11
Human Leukocyte Antigen Markers for Distinguishing Pustular Psoriasis and Adult-Onset Immunodeficiency with Pustular Reaction
Apiwat Sangphukieo, Patcharawadee Thongkumkoon, Pitiporn Noisagul, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 278-278
Open Access | Times Cited: 2
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