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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:

MichelaNglo: sculpting protein views on web pages without coding
Matteo P. Ferla, Alistair T. Pagnamenta, David Damerell, et al.
Bioinformatics (2020) Vol. 36, Iss. 10, pp. 3268-3270
Open Access | Times Cited: 26

Showing 1-25 of 26 citing articles:

Crystallographic and electrophilic fragment screening of the SARS-CoV-2 main protease
A. Douangamath, D. Fearon, Paul Gehrtz, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 486
Fragment binding to the Nsp3 macrodomain of SARS-CoV-2 identified through crystallographic screening and computational docking
M. Schuller, G.J. Correy, Stefan Gahbauer, et al.
Science Advances (2021) Vol. 7, Iss. 16
Open Access | Times Cited: 162
Pervasive cooperative mutational effects on multiple catalytic enzyme traits emerge via long-range conformational dynamics
Carlos G. Acevedo‐Rocha, Aitao Li, Lorenzo D’Amore, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 96
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases
Alistair T. Pagnamenta, Carlos Camps, Edoardo Giacopuzzi, et al.
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 31
Fragmenstein: predicting protein–ligand structures of compounds derived from known crystallographic fragment hits using a strict conserved-binding–based methodology
Matteo P. Ferla, Rubén Sánchez-García, R. Skyner, et al.
Journal of Cheminformatics (2025) Vol. 17, Iss. 1
Open Access | Times Cited: 1
Non-coding region variants upstream of MEF2C cause severe developmental disorder through three distinct loss-of-function mechanisms
Caroline F. Wright, Nicholas M. Quaife, Laura Ramos-Hernández, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 6, pp. 1083-1094
Open Access | Times Cited: 53
Crystallographic and electrophilic fragment screening of the SARS-CoV-2 main protease
A. Douangamath, D. Fearon, Paul Gehrtz, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 50
An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy
Alistair T. Pagnamenta, Rauan Kaiyrzhanov, Yaqun Zou, et al.
Brain (2020) Vol. 144, Iss. 2, pp. 584-600
Open Access | Times Cited: 36
MAST Kinases’ Function and Regulation: Insights from Structural Modeling and Disease Mutations
Michael C. Lemke, Nithin R. Avala, Mildred Rader, et al.
Biomedicines (2025) Vol. 13, Iss. 4, pp. 925-925
Open Access
Venus: Elucidating the Impact of Amino Acid Variants on Protein Function Beyond Structure Destabilisation
Matteo P. Ferla, Alistair T. Pagnamenta, Leonidas Koukouflis, et al.
Journal of Molecular Biology (2022) Vol. 434, Iss. 11, pp. 167567-167567
Open Access | Times Cited: 16
De novo variants in DENND5B cause a neurodevelopmental disorder
Marcello Scala, Valeria Tomati, Matteo P. Ferla, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 3, pp. 529-543
Open Access | Times Cited: 3
Expanding the phenotypic spectrum of BCS1L‐related mitochondrial disease
Omar Hikmat, Pirjo Isohanni, Nandaki Keshavan, et al.
Annals of Clinical and Translational Neurology (2021) Vol. 8, Iss. 11, pp. 2155-2165
Open Access | Times Cited: 22
Biallelic TLR4 deficiency in humans
Melania Capitani, Ahmad A. Al-Shaibi, Sumeet Pandey, et al.
Journal of Allergy and Clinical Immunology (2022) Vol. 151, Iss. 3, pp. 783-790.e5
Open Access | Times Cited: 14
Biallelic variants in SLC38A3 encoding a glutamine transporter cause epileptic encephalopathy
Dana Marafi, Jawid M. Fatih, Rauan Kaiyrzhanov, et al.
Brain (2021) Vol. 145, Iss. 3, pp. 909-924
Open Access | Times Cited: 19
Fragment Binding to the Nsp3 Macrodomain of SARS-CoV-2 Identified Through Crystallographic Screening and Computational Docking
M. Schuller, G.J. Correy, Stefan Gahbauer, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 19
Dominant negative variants in ITPR3 impair T cell Ca2+ dynamics causing combined immunodeficiency
Elena Blanco, Carme Camps, Sameer Bahal, et al.
The Journal of Experimental Medicine (2024) Vol. 222, Iss. 1
Open Access | Times Cited: 2
The multiple de novo copy number variant (MdnCNV) phenomenon presents with peri-zygotic DNA mutational signatures and multilocus pathogenic variation
Haowei Du, Angad Jolly, Christopher M. Grochowski, et al.
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 10
Biallelic MED27 variants lead to variable ponto-cerebello-lental degeneration with movement disorders
Reza Maroofian, Rauan Kaiyrzhanov, Elisa Calì, et al.
Brain (2023) Vol. 146, Iss. 12, pp. 5031-5043
Open Access | Times Cited: 6
Succinyl-CoA:3-oxoacid coenzyme A transferase (SCOT) deficiency: A rare and potentially fatal metabolic disease
Sarah C. Grünert, William R. Foster, Anke Schumann, et al.
Biochimie (2021) Vol. 183, pp. 55-62
Closed Access | Times Cited: 11
Structurally-informed human interactome reveals proteome-wide perturbations by disease mutations
Dapeng Xiong, Yunguang Qiu, Junfei Zhao, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
PIVOTAL: Prioritizing variants of uncertain significance with spatial genomic patterns in the 3D proteome
Siqi Liang, Matthew Mort, Peter D. Stenson, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 10
Pervasive cooperative mutational effects on multiple catalytic enzyme traits emerge via long-range conformational dynamics
Carlos G. Acevedo‐Rocha, Aitao Li, Lorenzo D’Amore, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 5
AroCageDB: A Web-Based Resource for Aromatic Cage Binding Sites and Their Intrinsic Ligands
Jianyu Li, Aurélien F. A. Moumbock, Ammar Qaseem, et al.
Journal of Chemical Information and Modeling (2021) Vol. 61, Iss. 11, pp. 5327-5330
Closed Access | Times Cited: 4
Experiences From Developing Software for Large X-Ray Crystallography-Driven Protein-Ligand Studies
Nicholas M. Pearce, R. Skyner, T. Krojer
Frontiers in Molecular Biosciences (2022) Vol. 9
Open Access | Times Cited: 3
Mutafy: A webserver to identify high quality mutant protein structures in the Protein Data Bank
Deborah Ness, Jiajing Hu, Munishikha Kalia, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
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