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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:

Phenotype-genotype comorbidity analysis of patients with rare disorders provides insight into their pathological and molecular bases
Elena Díaz-Santiago, Fernando M. Jabato, Elena Rojano, et al.
PLoS Genetics (2020) Vol. 16, Iss. 10, pp. e1009054-e1009054
Open Access | Times Cited: 17

Showing 17 citing articles:

Better understanding the phenotypic effects of drugs through shared targets in genetic disease networks
Elena Díaz-Santiago, Aurelio A. Moya‐García, José Manuel Pérez-García, et al.
Frontiers in Pharmacology (2025) Vol. 15
Open Access
Molecular bases of comorbidities: present and future perspectives
Jon Sánchez-Valle, Alfonso Valencia
Trends in Genetics (2023) Vol. 39, Iss. 10, pp. 773-786
Open Access | Times Cited: 10
Assigning protein function from domain-function associations using DomFun
Elena Rojano, Fernando M. Jabato, James R. Perkins, et al.
BMC Bioinformatics (2022) Vol. 23, Iss. 1
Open Access | Times Cited: 14
New Developments and Possibilities in Reanalysis and Reinterpretation of Whole Exome Sequencing Datasets for Unsolved Rare Diseases Using Machine Learning Approaches
Samarth Thonta Setty, Marie‐Pier Scott‐Boyer, Tania Cuppens, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 12, pp. 6792-6792
Open Access | Times Cited: 13
PheNominal: an EHR-integrated web application for structured deep phenotyping at the point of care
James M. Havrilla, Anbumalar Singaravelu, Dennis M. Driscoll, et al.
BMC Medical Informatics and Decision Making (2022) Vol. 22, Iss. S2
Open Access | Times Cited: 11
Network-Based Methods for Approaching Human Pathologies from a Phenotypic Point of View
Juan A. G. Ranea, James R. Perkins, Mónica Chagoyen, et al.
Genes (2022) Vol. 13, Iss. 6, pp. 1081-1081
Open Access | Times Cited: 7
Identification of cell type-specific gene targets underlying thousands of rare diseases and subtraits
Kitty B. Murphy, Robert Gordon-Smith, Jai Chapman, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Leveraging network analysis to evaluate biomedical named entity recognition tools
Eduardo P. García del Valle, Gerardo Lagunes García, Lucía Prieto Santamaría, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 7
Decoding Neuromuscular Disorders Using Phenotypic Clusters Obtained From Co-Occurrence Networks
Elena Díaz-Santiago, M. Gonzalo Claros, Raquel Yahyaoui, et al.
Frontiers in Molecular Biosciences (2021) Vol. 8
Open Access | Times Cited: 5
Evaluating, Filtering and Clustering Genetic Disease Cohorts Based on Human Phenotype Ontology Data with Cohort Analyzer
Elena Rojano, J. Caballero, Fernando M. Jabato, et al.
Journal of Personalized Medicine (2021) Vol. 11, Iss. 8, pp. 730-730
Open Access | Times Cited: 4
A scoping review finds a growing trend in studies validating multimorbidity patterns and identifies five broad types of validation methods
Thamer Ba Dhafari, Alexander Pate, Narges Azadbakht, et al.
Journal of Clinical Epidemiology (2023) Vol. 165, pp. 111214-111214
Open Access | Times Cited: 1
A Visual Phenotype-Based Differential Diagnosis Process for Rare Diseases
Jian Yang, Liqi Shu, Huilong Duan, et al.
Interdisciplinary Sciences Computational Life Sciences (2021) Vol. 14, Iss. 2, pp. 331-348
Closed Access | Times Cited: 2
Assigning Protein Function from Domain-Function Associations Using DomFun
Elena Rojano, Fernando M. Jabato, James R. Perkins, et al.
Research Square (Research Square) (2020)
Open Access
CRISPR and the Concept of Personhood
Michael W. Nestor, Richard L. Wilson
Springer eBooks (2022), pp. 65-76
Closed Access
Creation of Networks for the Analysis of Disease Similarities
Eduardo Pantaleón García del Valle
(2022)
Open Access
Meta-Analysis of Clinical Phenotype and Patient Survival in Neurodevelopmental Disorder with Microcephaly, Arthrogryposis, and Structural Brain Anomalies Due to Bi-allelic Loss of Function Variants in SMPD4
Dean Marchiori
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
Editorial: The genetics of human Mendelian skin disorders
Wei Hsum Yap, Jia Zhang, Ming Li, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access
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