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:
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
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
Showing 16 citing articles:
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
Alistair T. Pagnamenta, Carlos Camps, Edoardo Giacopuzzi, et al.
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 31
Characterizing the pathogenicity of genetic variants: the consequences of context
Timothy H. Ciesielski, Giorgio Sirugo, Sudha K. Iyengar, et al.
npj Genomic Medicine (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 8
Timothy H. Ciesielski, Giorgio Sirugo, Sudha K. Iyengar, et al.
npj Genomic Medicine (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 8
Assessing the clinical utility of protein structural analysis in genomic variant classification: experiences from a diagnostic laboratory
Richard Caswell, Adam C. Gunning, Martina Owens, et al.
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 22
Richard Caswell, Adam C. Gunning, Martina Owens, et al.
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 22
Comprehensive bioinformatics analysis of selected germline variants of uncertain significance identified in a cohort of Sri Lankan hereditary breast cancer patients
N. D. S. Arachchige, Nirmala D. Sirisena, Sumadee De Silva, et al.
Human Genomics (2025) Vol. 19, Iss. 1
Open Access
N. D. S. Arachchige, Nirmala D. Sirisena, Sumadee De Silva, et al.
Human Genomics (2025) Vol. 19, Iss. 1
Open Access
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
Michael C. Lemke, Nithin R. Avala, Mildred Rader, et al.
Biomedicines (2025) Vol. 13, Iss. 4, pp. 925-925
Open Access
WGS-Based Lineage and Antimicrobial Resistance Pattern of Salmonella Typhimurium Isolated during 2000–2017 in Peru
Raquel Hurtado, Debmalya Barh, Bart C. Weimer, et al.
Antibiotics (2022) Vol. 11, Iss. 9, pp. 1170-1170
Open Access | Times Cited: 18
Raquel Hurtado, Debmalya Barh, Bart C. Weimer, et al.
Antibiotics (2022) Vol. 11, Iss. 9, pp. 1170-1170
Open Access | Times Cited: 18
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
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
Unified access to up-to-date residue-level annotations from UniProtKB and other biological databases for PDB data
Preeti Choudhary, Stephen Anyango, John M. Berrisford, et al.
Scientific Data (2023) Vol. 10, Iss. 1
Open Access | Times Cited: 7
Preeti Choudhary, Stephen Anyango, John M. Berrisford, et al.
Scientific Data (2023) Vol. 10, Iss. 1
Open Access | Times Cited: 7
The use of pharmacological chaperones in rare diseases caused by reduced protein stability
Jon Gil‐Martínez, Ganeko Bernardo‐Seisdedos, José M. Mato, et al.
PROTEOMICS (2022) Vol. 22, Iss. 23-24
Closed Access | Times Cited: 12
Jon Gil‐Martínez, Ganeko Bernardo‐Seisdedos, José M. Mato, et al.
PROTEOMICS (2022) Vol. 22, Iss. 23-24
Closed Access | Times Cited: 12
PTRH2 Gene Variants: Recent Review of the Phenotypic Features and Their Bioinformatics Analysis
Rajech Sharkia, Sahil Jain, Muhammad Mahajnah, et al.
Genes (2023) Vol. 14, Iss. 5, pp. 1031-1031
Open Access | Times Cited: 6
Rajech Sharkia, Sahil Jain, Muhammad Mahajnah, et al.
Genes (2023) Vol. 14, Iss. 5, pp. 1031-1031
Open Access | Times Cited: 6
SCAF4 variants are associated with epilepsy with neurodevelopmental disorders
Yuanyuan Hu, Bingbing Zhang, Li Chen, et al.
Seizure (2023) Vol. 116, pp. 113-118
Closed Access | Times Cited: 3
Yuanyuan Hu, Bingbing Zhang, Li Chen, et al.
Seizure (2023) Vol. 116, pp. 113-118
Closed Access | Times Cited: 3
Investigation of polymorphism role in protein structure and function for selected cancer and diabetes disease; a rationale to selection of targets for insilico drug screening
Christopher Busayo Olowosoke, Tope Abraham Ibisanmi, Chioma Joy Eze, et al.
Informatics in Medicine Unlocked (2023) Vol. 42, pp. 101342-101342
Open Access | Times Cited: 2
Christopher Busayo Olowosoke, Tope Abraham Ibisanmi, Chioma Joy Eze, et al.
Informatics in Medicine Unlocked (2023) Vol. 42, pp. 101342-101342
Open Access | Times Cited: 2
Rare splice and missense variants with evidence of pathogenicity in consanguineous families with autosomal recessive intellectual disability from Pakistan
Abdül Waheed, Robert Eveleigh, Danielle Perley, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Abdül Waheed, Robert Eveleigh, Danielle Perley, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
The characterization of new de novo CACNA1G variants affecting the intracellular gate of Cav3.1 channel broadens the spectrum of neurodevelopmental phenotypes in SCA42ND
Leila Qebibo, Amaël Davakan, Mathilde Nesson-Dauphin, et al.
Genetics in Medicine (2024) Vol. 27, Iss. 3, pp. 101337-101337
Closed Access
Leila Qebibo, Amaël Davakan, Mathilde Nesson-Dauphin, et al.
Genetics in Medicine (2024) Vol. 27, Iss. 3, pp. 101337-101337
Closed Access
Impaired activity and membrane association of most calpain-5 mutants causal for neovascular inflammatory vitreoretinopathy
James W. Geddes, Vimala Bondada, Dorothy E. Croall, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2023) Vol. 1869, Iss. 6, pp. 166747-166747
Open Access | Times Cited: 1
James W. Geddes, Vimala Bondada, Dorothy E. Croall, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2023) Vol. 1869, Iss. 6, pp. 166747-166747
Open Access | Times Cited: 1
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
Deborah Ness, Jiajing Hu, Munishikha Kalia, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
