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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 mutational constraint spectrum quantified from variation in 141,456 humans
Konrad J. Karczewski, Laurent C. Francioli, Grace Tiao, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access | Times Cited: 1045

Showing 1-25 of 1045 citing articles:

The DisGeNET knowledge platform for disease genomics: 2019 update
Janet Piñero, Juan Manuel Ramírez‐Anguita, Josep Saüch-Pitarch, et al.
Nucleic Acids Research (2019)
Open Access | Times Cited: 2252
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Kyle Satterstrom, Jack A. Kosmicki, Jiebiao Wang, et al.
Cell (2020) Vol. 180, Iss. 3, pp. 568-584.e23
Open Access | Times Cited: 1886
Ensembl 2020
Andrew Yates, Premanand Achuthan, Wasiu Akanni, et al.
Nucleic Acids Research (2019)
Open Access | Times Cited: 1079
A brief history of human disease genetics
Melina Claussnitzer, Judy H. Cho, Rory Collins, et al.
Nature (2020) Vol. 577, Iss. 7789, pp. 179-189
Open Access | Times Cited: 606
Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework
Sarah E. Brnich, Ahmad Abou Tayoun, Fergus J. Couch, et al.
Genome Medicine (2019) Vol. 12, Iss. 1
Open Access | Times Cited: 437
A SARS-CoV-2-Human Protein-Protein Interaction Map Reveals Drug Targets and Potential Drug-Repurposing
David E. Gordon, Gwendolyn Μ. Jang, Mehdi Bouhaddou, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 433
Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks
Elizabeth K. Ruzzo, Laura Pérez‐Cano, Jae-Yoon Jung, et al.
Cell (2019) Vol. 178, Iss. 4, pp. 850-866.e26
Open Access | Times Cited: 396
Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseases
Mor Hanany, Carlo Rivolta, Dror Sharon
Proceedings of the National Academy of Sciences (2020) Vol. 117, Iss. 5, pp. 2710-2716
Open Access | Times Cited: 280
Genomic Analysis in the Age of Human Genome Sequencing
Tuuli Lappalainen, Alexandra J. Scott, Margot Brandt, et al.
Cell (2019) Vol. 177, Iss. 1, pp. 70-84
Open Access | Times Cited: 267
Programmed axon degeneration: from mouse to mechanism to medicine
Michael P. Coleman, Ahmet Höke
Nature reviews. Neuroscience (2020) Vol. 21, Iss. 4, pp. 183-196
Open Access | Times Cited: 260
The ChinaMAP analytics of deep whole genome sequences in 10,588 individuals
Yanan Cao, Lin Li, Min Xu, et al.
Cell Research (2020) Vol. 30, Iss. 9, pp. 717-731
Open Access | Times Cited: 243
Biological structure and function emerge from scaling unsupervised learning to 250 million protein sequences
Alexander Rives, Joshua Meier, Tom Sercu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access | Times Cited: 238
Cas9 activates the p53 pathway and selects for p53-inactivating mutations
Oana M. Enache, Verónica Rendo, Mai Abdusamad, et al.
Nature Genetics (2020) Vol. 52, Iss. 7, pp. 662-668
Open Access | Times Cited: 234
The impact of nonsense-mediated mRNA decay on genetic disease, gene editing and cancer immunotherapy
Rik G.H. Lindeboom, Michiel Vermeulen, Ben Lehner, et al.
Nature Genetics (2019) Vol. 51, Iss. 11, pp. 1645-1651
Open Access | Times Cited: 231
Initial whole-genome sequencing and analysis of the host genetic contribution to COVID-19 severity and susceptibility
Fang Wang, Shujia Huang, Rongsui Gao, et al.
Cell Discovery (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 210
Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel
Brian W. Kunkle, Michael A. Schmidt, Hans‐Ulrich Klein, et al.
JAMA Neurology (2020) Vol. 78, Iss. 1, pp. 102-102
Open Access | Times Cited: 207
Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy
James P. Pirruccello, Alexander G. Bick, Minxian Wang, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 204
A dual-deaminase CRISPR base editor enables concurrent adenine and cytosine editing
Julian Grünewald, Ronghao Zhou, Caleb A. Lareau, et al.
Nature Biotechnology (2020) Vol. 38, Iss. 7, pp. 861-864
Open Access | Times Cited: 201
SON and SRRM2 are essential for nuclear speckle formation
İbrahim Ilik, Michał Małszycki, Anna Katharina Lübke, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 195
Personalized neoantigen pulsed dendritic cell vaccine for advanced lung cancer
Zhenyu Ding, Qing Li, Rui Zhang, et al.
Signal Transduction and Targeted Therapy (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 190
Rare-variant collapsing analyses for complex traits: guidelines and applications
Gundula Povysil, Slavé Petrovski, Joseph Hostyk, et al.
Nature Reviews Genetics (2019) Vol. 20, Iss. 12, pp. 747-759
Closed Access | Times Cited: 183
Monogenic variants in dystonia: an exome-wide sequencing study
Michael Zech, Robert Jech, Sylvia Boesch, et al.
The Lancet Neurology (2020) Vol. 19, Iss. 11, pp. 908-918
Open Access | Times Cited: 179
Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease
Galen E.B. Wright, Jennifer A. Collins, Chris Kay, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 6, pp. 1116-1126
Open Access | Times Cited: 175
Mutations in COPA lead to abnormal trafficking of STING to the Golgi and interferon signaling
Alice Lepelley, Maria José Martin-Niclós, Melvin Le Bihan, et al.
The Journal of Experimental Medicine (2020) Vol. 217, Iss. 11
Open Access | Times Cited: 175
Is it time to change the reference genome?
Sara Ballouz, Alexander Dobin, Jesse Gillis
Genome biology (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 173
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