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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:

Mutation severity spectrum of rare alleles in the human genome is predictive of disease type
Jimin Pei, Lisa N. Kinch, Zbyszek Otwinowski, et al.
PLoS Computational Biology (2020) Vol. 16, Iss. 5, pp. e1007775-e1007775
Open Access | Times Cited: 17

Showing 17 citing articles:

Genome interpretation using in silico predictors of variant impact
Panagiotis Katsonis, Kevin Wilhelm, Amanda M. Williams, et al.
Human Genetics (2022) Vol. 141, Iss. 10, pp. 1549-1577
Open Access | Times Cited: 54
TransEFVP: A Two-Stage Approach for the Prediction of Human Pathogenic Variants Based on Protein Sequence Embedding Fusion
Zihao Yan, Fang Ge, Yan Liu, et al.
Journal of Chemical Information and Modeling (2024) Vol. 64, Iss. 4, pp. 1407-1418
Closed Access | Times Cited: 9
The expanding phenotypes of cohesinopathies: one ring to rule them all!
Jessica Piché, Patrick van Vliet, Michel Pucéat, et al.
Cell Cycle (2019) Vol. 18, Iss. 21, pp. 2828-2848
Open Access | Times Cited: 67
A Fifth of the Protein World: Rossmann-like Proteins as an Evolutionarily Successful Structural unit
Kirill E. Medvedev, Lisa N. Kinch, R. Dustin Schaeffer, et al.
Journal of Molecular Biology (2020) Vol. 433, Iss. 4, pp. 166788-166788
Open Access | Times Cited: 54
The DBSAV Database: Predicting Deleteriousness of Single Amino Acid Variations in the Human Proteome
Jimin Pei, Nick V. Grishin
Journal of Molecular Biology (2021) Vol. 433, Iss. 11, pp. 166915-166915
Open Access | Times Cited: 21
Molecular and in vivo phenotyping of missense variants of the human glucagon receptor
Wijnand J. C. van der Velden, Peter Lindquist, Jakob Sture Madsen, et al.
Journal of Biological Chemistry (2021) Vol. 298, Iss. 2, pp. 101413-101413
Open Access | Times Cited: 17
Assessment of variant effect predictors unveils variants difficulty as a critical performance indicator
Ragousandirane Radjasandirane, Julien Diharce, Jean‐Christophe Gelly, et al.
(2024)
Closed Access | Times Cited: 2
Loss of Function of Mutant IDS Due to Endoplasmic Reticulum-Associated Degradation: New Therapeutic Opportunities for Mucopolysaccharidosis Type II
Koji Matsuhisa, Kazunori Imaizumi
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 22, pp. 12227-12227
Open Access | Times Cited: 12
HSP90 buffers deleterious genetic variations inBRCA1
Brant Gracia, Patricia Montes, Min Huang, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
VariBench, new variation benchmark categories and data sets
Niloofar Shirvanizadeh, Mauno Vihinen
Frontiers in Bioinformatics (2023) Vol. 3
Open Access | Times Cited: 2
Estimation of CYP3A4*1B single nucleotide polymorphism using target-assembled in-situ detection by synthetic DNA-mounted excimers
Abdul M Gbaj, Inass A Sadawe, Nisreen H Meiqal, et al.
Journal of Clinical and Laboratory Research (2021) Vol. 2, Iss. 2, pp. 01-08
Open Access | Times Cited: 1
Identification of the Membrane-Associated Transporter Protein (MATP) Gene Polymorphism as Candidate Mutation for Albinism in Japanese Quail
Laksita Haniifah Pratiwi, Ratih Dewanti, Muhammad Cahyadi
Jurnal Ilmu-Ilmu Peternakan (2023) Vol. 33, Iss. 2, pp. 217-228
Open Access
ASCARIS: Positional feature annotation and protein structure-based representation of single amino acid variations
Fatma Cankara, Tunca Doğan
Computational and Structural Biotechnology Journal (2023) Vol. 21, pp. 4743-4758
Open Access
Membrane Anchorage‐Induced (MAGIC) Knockdown of Non‐synonymous Point Mutations**
Vijay K. Ulaganathan
ChemBioChem (2022) Vol. 23, Iss. 11
Open Access
Whole-genome sequencing identifies variants inANK1,LRRN1,HAS1,and other genes and regulatory regions for stroke in type 1 diabetes
Anni A. Antikainen, Jani K. Haukka, Anmol Kumar, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
Estimation of CYP3A4*1B Single Nucleotide Polymorphism Using Target-Assembled In-Situ Detection by Synthetic DNA-Mounted Excimers
Inass A Sadawe, Nisreen H Meiqal, Salah M Bensaber, et al.
(2021) Vol. 2, Iss. 1
Open Access
Predicting deleterious missense genetic variants via integrative supervised nonnegative matrix tri-factorization
Asieh Amousoltani Arani, Mohammadreza Sehhati, Mohammad Amin Tabatabaiefar
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access
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