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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:

GAVIN: Gene-Aware Variant INterpretation for medical sequencing
K. Joeri van der Velde, Eddy N. de Boer, Cleo C. van Diemen, et al.
Genome biology (2017) Vol. 18, Iss. 1
Open Access | Times Cited: 63

Showing 1-25 of 63 citing articles:

CADD: predicting the deleteriousness of variants throughout the human genome
Philipp Rentzsch, Daniela Witten, Gregory M. Cooper, et al.
Nucleic Acids Research (2018) Vol. 47, Iss. D1, pp. D886-D894
Open Access | Times Cited: 3018
FATHMM-XF: accurate prediction of pathogenic point mutations via extended features
Mark F. Rogers, Hashem A. Shihab, Matthew Mort, et al.
Bioinformatics (2017) Vol. 34, Iss. 3, pp. 511-513
Open Access | Times Cited: 407
ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants
Najmeh Alirezaie, Kristin D. Kernohan, Taila Hartley, et al.
The American Journal of Human Genetics (2018) Vol. 103, Iss. 4, pp. 474-483
Open Access | Times Cited: 196
Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes
Sushree Sangita Sahoo, Victor B. Pastor, Charnise Goodings, et al.
Nature Medicine (2021) Vol. 27, Iss. 10, pp. 1806-1817
Open Access | Times Cited: 122
Molecular classification and diagnostics of upper urinary tract urothelial carcinoma
Yoichi Fujii, Yusuke Sato, Hiromichi Suzuki, et al.
Cancer Cell (2021) Vol. 39, Iss. 6, pp. 793-809.e8
Open Access | Times Cited: 108
Genotyping and population characteristics of the China Kadoorie Biobank
Robin Walters, Iona Y. Millwood, Kuang Lin, et al.
Cell Genomics (2023) Vol. 3, Iss. 8, pp. 100361-100361
Open Access | Times Cited: 70
Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis
Patrick Deelen, Sipko van Dam, Johanna C. Herkert, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 126
Genetic variation in human drug-related genes
Charlotta Schärfe, Roman Tremmel, Matthias Schwab, et al.
Genome Medicine (2017) Vol. 9, Iss. 1
Open Access | Times Cited: 119
MOLGENIS research: advanced bioinformatics data software for non-bioinformaticians
K. Joeri van der Velde, Floris Imhann, Bart Charbon, et al.
Bioinformatics (2018) Vol. 35, Iss. 6, pp. 1076-1078
Open Access | Times Cited: 90
Assessing performance of pathogenicity predictors using clinically relevant variant datasets
Adam C. Gunning, Verity Fryer, James Fasham, et al.
Journal of Medical Genetics (2020) Vol. 58, Iss. 8, pp. 547-555
Open Access | Times Cited: 88
New insights into the pathogenicity of non-synonymous variants through multi-level analysis
Hong Sun, Guangjun Yu
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 67
An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome
Michael Ferlaino, Mark F. Rogers, Hashem A. Shihab, et al.
BMC Bioinformatics (2017) Vol. 18, Iss. 1
Open Access | Times Cited: 66
An Improved Phenotype-Driven Tool for Rare Mendelian Variant Prioritization: Benchmarking Exomiser on Real Patient Whole-Exome Data
Valentina Cipriani, Nikolas Pontikos, Gavin Arno, et al.
Genes (2020) Vol. 11, Iss. 4, pp. 460-460
Open Access | Times Cited: 54
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: 35
CAPICE: a computational method for Consequence-Agnostic Pathogenicity Interpretation of Clinical Exome variations
Shuang� Li, K. Joeri van der Velde, Dick de Ridder, et al.
Genome Medicine (2020) Vol. 12, Iss. 1
Open Access | Times Cited: 46
Molecular alterations in the extracellular matrix in the brains of newborns with congenital Zika syndrome
Renato Santana Aguiar, Fabio Pohl, Guilherme Loss de Morais, et al.
Science Signaling (2020) Vol. 13, Iss. 635
Closed Access | Times Cited: 45
A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound
Nicole Corsten‐Janssen, Katelijne Bouman, Janouk C. D. Diphoorn, et al.
Prenatal Diagnosis (2020) Vol. 40, Iss. 10, pp. 1300-1309
Open Access | Times Cited: 43
GREB1L variants in familial and sporadic hereditary urogenital adysplasia and Mayer‐Rokitansky‐Kuster‐Hauser syndrome
Adeline Jacquinet, Bouchra Boujemla, Corinne Fasquelle, et al.
Clinical Genetics (2020) Vol. 98, Iss. 2, pp. 126-137
Open Access | Times Cited: 42
ZFP-CanPred: Predicting the effect of mutations in zinc-finger proteins in cancers using protein language models
Adhuna Phogat, Sowmya Ramaswamy Krishnan, Medha Pandey, et al.
Methods (2025)
Closed Access
A cellular assay to determine the fusion capacity of MFN2 variants linked to Charcot–Marie-Tooth disease of type 2 A
Chloe Barsa, Julian Perrin, Claudine David, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Principles and methods of in-silico prioritization of non-coding regulatory variants
Phil H. Lee, Christian Lee, Xihao Li, et al.
Human Genetics (2017) Vol. 137, Iss. 1, pp. 15-30
Open Access | Times Cited: 45
Investigating the genetic susceptibility to exertional heat illness
Lois Gardner, Dorota Miller, Catherine Daly, et al.
Journal of Medical Genetics (2020) Vol. 57, Iss. 8, pp. 531-541
Open Access | Times Cited: 30
Genotyping and population structure of the China Kadoorie Biobank
Robin Walters, Iona Y. Millwood, Kuang Lin, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 16
The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar
Sara Al‐Khawaga, Idris Mohammed, Saras Saraswathi, et al.
Molecular Genetics & Genomic Medicine (2019) Vol. 7, Iss. 10
Open Access | Times Cited: 27
Mutation screening of 17 candidate genes in a cohort of 67 probands with early‐onset high myopia
Fang Liu, Junwen Wang, Yiqiao Xing, et al.
Ophthalmic and Physiological Optics (2020) Vol. 40, Iss. 3, pp. 271-280
Closed Access | Times Cited: 21
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