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:
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
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
Showing 13 citing articles:
The genetics and pathogenesis of CAKUT
Caroline M. Kolvenbach, Shirlee Shril, Friedhelm Hildebrandt
Nature Reviews Nephrology (2023) Vol. 19, Iss. 11, pp. 709-720
Closed Access | Times Cited: 35
Caroline M. Kolvenbach, Shirlee Shril, Friedhelm Hildebrandt
Nature Reviews Nephrology (2023) Vol. 19, Iss. 11, pp. 709-720
Closed Access | Times Cited: 35
A systematic review on machine learning approaches in the diagnosis and prognosis of rare genetic diseases
Pablo Román-Naranjo, Alberto M. Parra‐Perez, José A. López‐Escámez
Journal of Biomedical Informatics (2023) Vol. 143, pp. 104429-104429
Open Access | Times Cited: 22
Pablo Román-Naranjo, Alberto M. Parra‐Perez, José A. López‐Escámez
Journal of Biomedical Informatics (2023) Vol. 143, pp. 104429-104429
Open Access | Times Cited: 22
Approaches to Evaluate Whole Exome Sequencing Data That Incorporate Genetic Intolerance Scores for Congenital Anomalies, Including Intronic Regions Adjacent to Exons
Kosuke Taniguchi, Fuyuki Hasegawa, Yuka Okazaki, et al.
Molecular Genetics & Genomic Medicine (2025) Vol. 13, Iss. 3
Open Access
Kosuke Taniguchi, Fuyuki Hasegawa, Yuka Okazaki, et al.
Molecular Genetics & Genomic Medicine (2025) Vol. 13, Iss. 3
Open Access
Resources and tools for rare disease variant interpretation
Luana Licata, Allegra Via, Paola Turina, et al.
Frontiers in Molecular Biosciences (2023) Vol. 10
Open Access | Times Cited: 9
Luana Licata, Allegra Via, Paola Turina, et al.
Frontiers in Molecular Biosciences (2023) Vol. 10
Open Access | Times Cited: 9
Identification and validation of cuproptosis related genes and signature markers in bronchopulmonary dysplasia disease using bioinformatics analysis and machine learning
Mingxuan Jia, Jieyi Li, Jingying Zhang, et al.
BMC Medical Informatics and Decision Making (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 6
Mingxuan Jia, Jieyi Li, Jingying Zhang, et al.
BMC Medical Informatics and Decision Making (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 6
International Undiagnosed Diseases Programs (UDPs): components and outcomes
Ela Curic, Lisa Ewans, Ryan Pysar, et al.
Orphanet Journal of Rare Diseases (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 6
Ela Curic, Lisa Ewans, Ryan Pysar, et al.
Orphanet Journal of Rare Diseases (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 6
Impact of dietary fiber on gut microbiota composition, function and gut-brain-modules in healthy adults – a systematic review protocol
David Antoine Lachmansingh, Benjamín Valderrama, Thomaz F. S. Bastiaanssen, et al.
HRB Open Research (2024) Vol. 6, pp. 62-62
Open Access | Times Cited: 1
David Antoine Lachmansingh, Benjamín Valderrama, Thomaz F. S. Bastiaanssen, et al.
HRB Open Research (2024) Vol. 6, pp. 62-62
Open Access | Times Cited: 1
Dating apps as tools for social engineering
Martin Beckstein, Bouke de Vries
Ethics and Information Technology (2024) Vol. 27, Iss. 1
Open Access
Martin Beckstein, Bouke de Vries
Ethics and Information Technology (2024) Vol. 27, Iss. 1
Open Access
Automated Shared Phenotype Discovery in Undiagnosed Cohorts for Rare Disease Research
Aaron J. Masino, Ranga Baminiwatte
(2024), pp. 1025-1030
Closed Access
Aaron J. Masino, Ranga Baminiwatte
(2024), pp. 1025-1030
Closed Access
A systematic review on machine learning approaches in the diagnosis of rare genetic diseases
Pablo Román-Naranjo, AM Parra-Perez, José A. López‐Escámez
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Pablo Román-Naranjo, AM Parra-Perez, José A. López‐Escámez
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Identification and Validation of Cuproptosis Related Genes and Signature Markers in Bronchopulmonary Dysplasia Disease using Bioinformatics Analysis and Machine Learning
Mingxuan Jia, Jieyi Li, Jingying Zhang, et al.
Research Square (Research Square) (2023)
Open Access
Mingxuan Jia, Jieyi Li, Jingying Zhang, et al.
Research Square (Research Square) (2023)
Open Access
Impact of dietary fiber on gut microbiota composition, function and gut-brain-modules in healthy adults – a systematic review protocol
David Antoine Lachmansingh, Benjamín Valderrama, Thomaz F. S. Bastiaanssen, et al.
HRB Open Research (2023) Vol. 6, pp. 62-62
Open Access
David Antoine Lachmansingh, Benjamín Valderrama, Thomaz F. S. Bastiaanssen, et al.
HRB Open Research (2023) Vol. 6, pp. 62-62
Open Access
Comparative Analysis of Machine Learning Algorithms for Genomic Data
Rohini Auti, Abhishek Bhatt, Shubhangi Tidake
(2023), pp. 1-6
Closed Access
Rohini Auti, Abhishek Bhatt, Shubhangi Tidake
(2023), pp. 1-6
Closed Access
