Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

The landscape of tolerated genetic variation in humans and primates
Hong Gao, Tobias Hamp, Jeffrey M. Ede, et al.
Science (2023) Vol. 380, Iss. 6648
Open Access | Times Cited: 100

Showing 1-25 of 100 citing articles:

CADD v1.7: using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions
Max Schubach, Thorben Maaß, Lusiné Nazaretyan, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. D1, pp. D1143-D1154
Open Access | Times Cited: 129
Machine learning-guided co-optimization of fitness and diversity facilitates combinatorial library design in enzyme engineering
Kerr Ding, M. A. Chin, Yunlong Zhao, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 18
A DNA language model based on multispecies alignment predicts the effects of genome-wide variants
Gonzalo Benegas, Carlos Albors, Alan J. Aw, et al.
Nature Biotechnology (2025)
Closed Access | Times Cited: 5
Rare penetrant mutations confer severe risk of common diseases
Petko Fiziev, Jeremy F. McRae, Jacob C. Ulirsch, et al.
Science (2023) Vol. 380, Iss. 6648
Open Access | Times Cited: 38
Identification of constrained sequence elements across 239 primate genomes
Lukas F. K. Kuderna, Jacob C. Ulirsch, Sabrina Mohd Rashid, et al.
Nature (2023) Vol. 625, Iss. 7996, pp. 735-742
Open Access | Times Cited: 38
Will variants of uncertain significance still exist in 2030?
Douglas M. Fowler, Heidi L. Rehm
The American Journal of Human Genetics (2023) Vol. 111, Iss. 1, pp. 5-10
Open Access | Times Cited: 32
COVID-19 annual update: a narrative review
Michela Biancolella, Vito Luigi Colona, Lucio Luzzatto, et al.
Human Genomics (2023) Vol. 17, Iss. 1
Open Access | Times Cited: 28
Applications of artificial intelligence in clinical laboratory genomics
Swaroop Aradhya, Flavia M. Facio, Hillery C. Metz, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023) Vol. 193, Iss. 3
Open Access | Times Cited: 28
Harnessing deep learning for population genetic inference
Xin Huang, Aigerim Rymbekova, Olga Dolgova, et al.
Nature Reviews Genetics (2023) Vol. 25, Iss. 1, pp. 61-78
Closed Access | Times Cited: 27
A foundational large language model for edible plant genomes
Javier Mendoza‐Revilla, Evan Trop, Liam Gonzalez, et al.
Communications Biology (2024) Vol. 7, Iss. 1
Open Access | Times Cited: 12
Joint genotypic and phenotypic outcome modeling improves base editing variant effect quantification
Jayoung Ryu, Sam Barkal, Tian Yu, et al.
Nature Genetics (2024) Vol. 56, Iss. 5, pp. 925-937
Closed Access | Times Cited: 10
Toward physics‐based precision medicine: Exploiting protein dynamics to design new therapeutics and interpret variants
Artur Meller, Devin Kelly, Louis G. Smith, et al.
Protein Science (2024) Vol. 33, Iss. 3
Open Access | Times Cited: 9
Genetic evidence for involvement of β2-adrenergic receptor in brown adipose tissue thermogenesis in humans
Yuka Ishida, Mami Matsushita, Takeshi Yoneshiro, et al.
International Journal of Obesity (2024) Vol. 48, Iss. 8, pp. 1110-1117
Open Access | Times Cited: 9
Guidelines for releasing a variant effect predictor
Benjamin Livesey, Mihaly Badonyi, Mafalda Dias, et al.
Genome biology (2025) Vol. 26, Iss. 1
Open Access | Times Cited: 1
The impact of systematized generation, evaluation, and incorporation of machine learning algorithms for clinical variant classification
Laure Frésard, Flavia M. Facio, Elaine Chen, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access | Times Cited: 1
Critical assessment of missense variant effect predictors on disease-relevant variant data
Ruchir Rastogi, Ryan Chung, Sindy Li, et al.
Human Genetics (2025)
Open Access | Times Cited: 1
High-throughput screening of human genetic variants by pooled prime editing
Michael Herger, Christina M. Kajba, Megan Buckley, et al.
Cell Genomics (2025), pp. 100814-100814
Open Access | Times Cited: 1
Predicting pathogenic protein variants
Joseph A. Marsh, Sarah A. Teichmann
Science (2023) Vol. 381, Iss. 6664, pp. 1284-1285
Open Access | Times Cited: 18
Functional genomics and small molecules in mitochondrial neurodevelopmental disorders
Daniel G. Calame, Lisa Emrick
Neurotherapeutics (2024) Vol. 21, Iss. 1, pp. e00316-e00316
Open Access | Times Cited: 7
Critical assessment of missense variant effect predictors on disease-relevant variant data
Ruchir Rastogi, Ryan Chung, Sindy Li, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 6
AlphaMissense is better correlated with functional assays of missense impact than earlier prediction algorithms
Alicia Ljungdahl, Sayeh Kohani, Nicholas F. Page, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 14
Envisioning a new era: Complete genetic information from routine, telomere-to-telomere genomes
Karen H. Miga, Evan E. Eichler
The American Journal of Human Genetics (2023) Vol. 110, Iss. 11, pp. 1832-1840
Open Access | Times Cited: 13
Biomedical Data Science, Artificial Intelligence, and Ethics: Navigating Challenges in the Face of Explosive Growth
Carole A. Federico, Artem A. Trotsyuk
Annual Review of Biomedical Data Science (2024) Vol. 7, Iss. 1, pp. 1-14
Closed Access | Times Cited: 5
Variant Impact Predictor database (VIPdb), version 2: trends from three decades of genetic variant impact predictors
Yu-Jen Lin, Arul S. Menon, Zhiqiang Hu, et al.
Human Genomics (2024) Vol. 18, Iss. 1
Open Access | Times Cited: 5
Promises and challenges of crop translational genomics
Martin Mascher, Murukarthick Jayakodi, Hyeonah Shim, et al.
Nature (2024)
Closed Access | Times Cited: 5
Page 1 - Next Page

Scroll to top