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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:

The Ensembl Variant Effect Predictor
William McLaren, Laurent Gil, Sarah Hunt, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2016)
Open Access | Times Cited: 378

Showing 1-25 of 378 citing articles:

Technological Developments in lncRNA Biology
Sonali Jathar, Vikram Kumar, J.P. Srivastava, et al.
Advances in experimental medicine and biology (2017), pp. 283-323
Closed Access | Times Cited: 332
SNPnexus: assessing the functional relevance of genetic variation to facilitate the promise of precision medicine
Abu Z M Dayem Ullah, Jorge Oscanoa, Jun Wang, et al.
Nucleic Acids Research (2018) Vol. 46, Iss. W1, pp. W109-W113
Open Access | Times Cited: 161
ProGeM: a framework for the prioritization of candidate causal genes at molecular quantitative trait loci
David Stacey, Eric B. Fauman, Daniel Ziemek, et al.
Nucleic Acids Research (2018) Vol. 47, Iss. 1, pp. e3-e3
Open Access | Times Cited: 115
Review on the Computational Genome Annotation of Sequences Obtained by Next-Generation Sequencing
Girum Fitihamlak Ejigu, Jaehee Jung
Biology (2020) Vol. 9, Iss. 9, pp. 295-295
Open Access | Times Cited: 93
An online coronavirus analysis platform from the National Genomics Data Center
Zheng Gong, Jun-Wei Zhu, Cui-Ping Li, et al.
动物学研究 (2020) Vol. 41, Iss. 6, pp. 705-708
Open Access | Times Cited: 75
50,000 years of Evolutionary History of India: Insights from ~2,700 Whole Genome Sequences
Élise Kerdoncuff, Laurits Skov, Nick Patterson, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 17
Satellite glial GPR37L1 and its ligand maresin 1 regulate potassium channel signaling and pain homeostasis
Sangsu Bang, Changyu Jiang, Jing Xu, et al.
Journal of Clinical Investigation (2024)
Open Access | Times Cited: 15
Functional dissection of complex and molecular trait variants at single nucleotide resolution
Layla Siraj, Rodrigo Castro, Hannah B. Dewey, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 11
GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits
Dandan Huang, Xianfu Yi, Shijie Zhang, et al.
Nucleic Acids Research (2018) Vol. 46, Iss. W1, pp. W114-W120
Open Access | Times Cited: 80
Mutations in DNA repair genes are associated with increased neo-antigen load and activated T cell infiltration in lung adenocarcinoma
Young Kwang Chae, Jonathan F. Anker, Preeti Bais, et al.
Oncotarget (2017) Vol. 9, Iss. 8, pp. 7949-7960
Open Access | Times Cited: 56
ACE2gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population
Elisa Benetti, Tita Rossella, Ottavia Spiga, et al.
medRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 42
Nucleotide dependency analysis of DNA language models reveals genomic functional elements
Pedro Tomaz da Silva, Alexander Karollus, Johannes Hingerl, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 6
A novel deep targeted sequencing method for minimal residual disease monitoring in acute myeloid leukemia
Esther Onecha, María Linares, Inmaculada Rapado, et al.
Haematologica (2018) Vol. 104, Iss. 2, pp. 288-296
Open Access | Times Cited: 46
Whole‐exome sequencing of the BDR cohort: evidence to support the role of the PILRA gene in Alzheimer's disease
Tulsi Patel, Keeley J. Brookes, James Turton, et al.
Neuropathology and Applied Neurobiology (2017) Vol. 44, Iss. 5, pp. 506-521
Open Access | Times Cited: 45
Ex vivo culture of circulating tumour cells derived from non-small cell lung cancer
Joanna Kapeleris, Arutha Kulasinghe, Majid Ebrahimi Warkiani, et al.
Translational Lung Cancer Research (2020) Vol. 9, Iss. 5, pp. 1795-1809
Open Access | Times Cited: 38
Functional and population genetic features of copy number variations in two dairy cattle populations
Young-Lim Lee, Mirte Bosse, Erik Mullaart, et al.
BMC Genomics (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 35
Comparison of Multiple Imputation Algorithms and Verification Using Whole-Genome Sequencing in the CMUH Genetic Biobank
Ting‐Yuan Liu, Chih-Fan Lin, Hsing-Tsung Wu, et al.
Biomedicine (2021) Vol. 11, Iss. 4, pp. 57-65
Open Access | Times Cited: 31
Exploring public genomics data for population pharmacogenomics
Kleanthi Lakiotaki, Alexandros Kanterakis, Evgenia Kartsaki, et al.
PLoS ONE (2017) Vol. 12, Iss. 8, pp. e0182138-e0182138
Open Access | Times Cited: 39
Germline <em>BRCA1</em> and <em>BRCA2</em> deleterious mutations and variants of unknown clinical significance associated with breast/ovarian cancer: a report from North India
Anurag Mehta, Smreti Vasudevan, Sanjeev Kumar Sharma, et al.
Cancer Management and Research (2018) Vol. Volume 10, pp. 6505-6516
Open Access | Times Cited: 35
Genome-wide sequence analyses of ethnic populations across Russia
Daria V. Zhernakova, Vladimir Brukhin, Sergey V. Malov, et al.
Genomics (2019) Vol. 112, Iss. 1, pp. 442-458
Open Access | Times Cited: 35
Tumor-Based Genetic Testing and Familial Cancer Risk
Andrea Forman, Jilliane Sotelo
Cold Spring Harbor Perspectives in Medicine (2019) Vol. 10, Iss. 8, pp. a036590-a036590
Open Access | Times Cited: 35
DownstreamTRPM4Polymorphisms Are Associated with Intracranial Hypertension and Statistically Interact withABCC8Polymorphisms in a Prospective Cohort of Severe Traumatic Brain Injury
Ruchira M. Jha, Shashvat M. Desai, Benjamin E. Zusman, et al.
Journal of Neurotrauma (2018) Vol. 36, Iss. 11, pp. 1804-1817
Open Access | Times Cited: 33
Plasma Metabolomic Signatures of Chronic Obstructive Pulmonary Disease and the Impact of Genetic Variants on Phenotype-Driven Modules
Lucas A. Gillenwater, Katherine Pratte, Brian D. Hobbs, et al.
Network and Systems Medicine (2020) Vol. 3, Iss. 1, pp. 159-181
Open Access | Times Cited: 29
Aqueous Humor as a Liquid Biopsy for Retinoblastoma: Clear Corneal Paracentesis and Genomic Analysis
Mary E. Kim, Liya Xu, Rishvanth K. Prabakar, et al.
Journal of Visualized Experiments (2021), Iss. 175
Open Access | Times Cited: 27
PD-1 antibody camrelizumab for Epstein-Barr virus-positive metastatic gastric cancer: a single-arm, open-label, phase 2 trial.
Yuting Sun, Wen‐Long Guan, Qi Zhao, et al.
American Journal of Cancer Research (2021) Vol. 11, Iss. 10, pp. 5006-5015
Closed Access | Times Cited: 27
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