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:
Diagnosis of Rare Diseases: a scoping review of clinical decision support systems
Jannik Schaaf, Martin Sedlmayr, Johanna Schaefer, et al.
Orphanet Journal of Rare Diseases (2020) Vol. 15, Iss. 1
Open Access | Times Cited: 43
Jannik Schaaf, Martin Sedlmayr, Johanna Schaefer, et al.
Orphanet Journal of Rare Diseases (2020) Vol. 15, Iss. 1
Open Access | Times Cited: 43
Showing 1-25 of 43 citing articles:
Current Challenges and Future Opportunities for XAI in Machine Learning-Based Clinical Decision Support Systems: A Systematic Review
Anna Markella Antoniadi, Yuhan Du, Yasmine Guendouz, et al.
Applied Sciences (2021) Vol. 11, Iss. 11, pp. 5088-5088
Open Access | Times Cited: 381
Anna Markella Antoniadi, Yuhan Du, Yasmine Guendouz, et al.
Applied Sciences (2021) Vol. 11, Iss. 11, pp. 5088-5088
Open Access | Times Cited: 381
Establishing a second-generation artificial intelligence-based system for improving diagnosis, treatment, and monitoring of patients with rare diseases
Noa Hurvitz, Henny Azmanov, Asa Kesler, et al.
European Journal of Human Genetics (2021) Vol. 29, Iss. 10, pp. 1485-1490
Open Access | Times Cited: 68
Noa Hurvitz, Henny Azmanov, Asa Kesler, et al.
European Journal of Human Genetics (2021) Vol. 29, Iss. 10, pp. 1485-1490
Open Access | Times Cited: 68
Determinants of implementing artificial intelligence-based clinical decision support tools in healthcare: a scoping review protocol
Bishnu Bahadur Bajgain, Diane Lorenzetti, Joon Lee, et al.
BMJ Open (2023) Vol. 13, Iss. 2, pp. e068373-e068373
Open Access | Times Cited: 37
Bishnu Bahadur Bajgain, Diane Lorenzetti, Joon Lee, et al.
BMJ Open (2023) Vol. 13, Iss. 2, pp. e068373-e068373
Open Access | Times Cited: 37
Identifying Facilitators and Barriers to Implementation of AI-Assisted Clinical Decision Support in an Electronic Health Record System
Joseph Finkelstein, Aileen Gabriel, Susanna Schmer, et al.
Journal of Medical Systems (2024) Vol. 48, Iss. 1
Open Access | Times Cited: 10
Joseph Finkelstein, Aileen Gabriel, Susanna Schmer, et al.
Journal of Medical Systems (2024) Vol. 48, Iss. 1
Open Access | Times Cited: 10
Diagnostic delay in rare diseases: data from the Spanish rare diseases patient registry
Juan Benito-Lozano, Blanca López-Villalba, Greta Arias-Merino, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 24
Juan Benito-Lozano, Blanca López-Villalba, Greta Arias-Merino, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 24
Clinical decision support systems to improve drug prescription and therapy optimisation in clinical practice: a scoping review
Lucrezia Greta Armando, Gianluca Miglio, Pierluigi de Cosmo, et al.
BMJ Health & Care Informatics (2023) Vol. 30, Iss. 1, pp. e100683-e100683
Open Access | Times Cited: 14
Lucrezia Greta Armando, Gianluca Miglio, Pierluigi de Cosmo, et al.
BMJ Health & Care Informatics (2023) Vol. 30, Iss. 1, pp. e100683-e100683
Open Access | Times Cited: 14
Initial User-Centred Design of an AI-Based Clinical Decision Support System for Primary Care
Michaela Neff, Jannik Schaaf, Richard Noll, et al.
Studies in health technology and informatics (2024)
Open Access | Times Cited: 4
Michaela Neff, Jannik Schaaf, Richard Noll, et al.
Studies in health technology and informatics (2024)
Open Access | Times Cited: 4
High-throughput assays to assess variant effects on disease
Kaiyue Ma, L. Gauthier, Frances Cheung, et al.
Disease Models & Mechanisms (2024) Vol. 17, Iss. 6
Open Access | Times Cited: 4
Kaiyue Ma, L. Gauthier, Frances Cheung, et al.
Disease Models & Mechanisms (2024) Vol. 17, Iss. 6
Open Access | Times Cited: 4
Kurze Wege zur Diagnose mit künstlicher Intelligenz – systematische Literaturrecherche zu „diagnostic decision support systems“
Julia Sellin, Jean Tori Pantel, Natalie Börsch, et al.
Zeitschrift für Pneumologie (2025)
Closed Access
Julia Sellin, Jean Tori Pantel, Natalie Börsch, et al.
Zeitschrift für Pneumologie (2025)
Closed Access
The impact of rare diseases on the quality of life in paediatric patients: current status
John Sieh Dumbuya, Cizheng Zeng, Linhong Deng, et al.
Frontiers in Public Health (2025) Vol. 13
Open Access
John Sieh Dumbuya, Cizheng Zeng, Linhong Deng, et al.
Frontiers in Public Health (2025) Vol. 13
Open Access
CADA: phenotype-driven gene prioritization based on a case-enriched knowledge graph
Chengyao Peng, Simon Dieck, Alexander Schmid, et al.
NAR Genomics and Bioinformatics (2021) Vol. 3, Iss. 3
Open Access | Times Cited: 26
Chengyao Peng, Simon Dieck, Alexander Schmid, et al.
NAR Genomics and Bioinformatics (2021) Vol. 3, Iss. 3
Open Access | Times Cited: 26
Evaluation of a clinical decision support system for rare diseases: a qualitative study
Jannik Schaaf, Martin Sedlmayr, Brita Sedlmayr, et al.
BMC Medical Informatics and Decision Making (2021) Vol. 21, Iss. 1
Open Access | Times Cited: 23
Jannik Schaaf, Martin Sedlmayr, Brita Sedlmayr, et al.
BMC Medical Informatics and Decision Making (2021) Vol. 21, Iss. 1
Open Access | Times Cited: 23
Requirements analysis for an AI-based clinical decision support system for general practitioners: a user-centered design process
Dania Schütze, Svea Holtz, Michaela Neff, et al.
BMC Medical Informatics and Decision Making (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 8
Dania Schütze, Svea Holtz, Michaela Neff, et al.
BMC Medical Informatics and Decision Making (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 8
Kurze Wege zur Diagnose mit künstlicher Intelligenz – systematische Literaturrecherche zu „diagnostic decision support systems“
Julia Sellin, Jean Tori Pantel, Natalie Börsch, et al.
Der Schmerz (2024) Vol. 38, Iss. 1, pp. 19-27
Closed Access | Times Cited: 2
Julia Sellin, Jean Tori Pantel, Natalie Börsch, et al.
Der Schmerz (2024) Vol. 38, Iss. 1, pp. 19-27
Closed Access | Times Cited: 2
``It Is a Moving Process": Understanding the Evolution of Explainability Needs of Clinicians in Pulmonary Medicine
Lorenzo Corti, Rembrandt Oltmans, Jiwon Jung, et al.
(2024), pp. 1-21
Open Access | Times Cited: 2
Lorenzo Corti, Rembrandt Oltmans, Jiwon Jung, et al.
(2024), pp. 1-21
Open Access | Times Cited: 2
The Power of Clinical Diagnosis for Deciphering Complex Genetic Mechanisms in Rare Diseases
Li Shu, Tatiana Maroilley, Maja Tarailo‐Graovac
Genes (2023) Vol. 14, Iss. 1, pp. 196-196
Open Access | Times Cited: 6
Li Shu, Tatiana Maroilley, Maja Tarailo‐Graovac
Genes (2023) Vol. 14, Iss. 1, pp. 196-196
Open Access | Times Cited: 6
Adaption of the OMOP CDM for Rare Diseases
Michéle Zoch, Christian Gierschner, Yuan Peng, et al.
Studies in health technology and informatics (2021)
Open Access | Times Cited: 11
Michéle Zoch, Christian Gierschner, Yuan Peng, et al.
Studies in health technology and informatics (2021)
Open Access | Times Cited: 11
Rare diseases and pyruvate kinase M2: a promising therapeutic connection
Saumya Kapoor, Vaishnavi Kalmegh, Hemant Kumar, et al.
Drug Discovery Today (2024) Vol. 29, Iss. 5, pp. 103949-103949
Closed Access | Times Cited: 1
Saumya Kapoor, Vaishnavi Kalmegh, Hemant Kumar, et al.
Drug Discovery Today (2024) Vol. 29, Iss. 5, pp. 103949-103949
Closed Access | Times Cited: 1
Synthetic protein protease sensor platform
Ciarán Devoy, Yensi Flores Bueso, Stephen Buckley, et al.
Frontiers in Bioengineering and Biotechnology (2024) Vol. 12
Open Access | Times Cited: 1
Ciarán Devoy, Yensi Flores Bueso, Stephen Buckley, et al.
Frontiers in Bioengineering and Biotechnology (2024) Vol. 12
Open Access | Times Cited: 1
Objectivizing issues in the diagnosis of complex rare diseases: lessons learned from testing existing diagnosis support systems on ciliopathies
Carole Faviez, Xiaoyi Chen, Nicolas Garcelon, et al.
BMC Medical Informatics and Decision Making (2024) Vol. 24, Iss. 1
Open Access | Times Cited: 1
Carole Faviez, Xiaoyi Chen, Nicolas Garcelon, et al.
BMC Medical Informatics and Decision Making (2024) Vol. 24, Iss. 1
Open Access | Times Cited: 1
Review of Key Elements in Developing a Common Data Model for Rare Diseases: Identifying Common Success Factors
Adam S.L. Graefe, Filip Rehburg, Miriam Hübner, et al.
Studies in health technology and informatics (2024)
Open Access | Times Cited: 1
Adam S.L. Graefe, Filip Rehburg, Miriam Hübner, et al.
Studies in health technology and informatics (2024)
Open Access | Times Cited: 1
Diet and Nutrients in Rare Neurological Disorders: Biological, Biochemical, and Pathophysiological Evidence
Marilena Briglia, Fabio Allia, Rosanna Avola, et al.
Nutrients (2024) Vol. 16, Iss. 18, pp. 3114-3114
Open Access | Times Cited: 1
Marilena Briglia, Fabio Allia, Rosanna Avola, et al.
Nutrients (2024) Vol. 16, Iss. 18, pp. 3114-3114
Open Access | Times Cited: 1
Development and expert inspections of the user interface for a primary care decision support system
Michaela Neff, Dania Schütze, Svea Holtz, et al.
International Journal of Medical Informatics (2024) Vol. 192, pp. 105651-105651
Open Access | Times Cited: 1
Michaela Neff, Dania Schütze, Svea Holtz, et al.
International Journal of Medical Informatics (2024) Vol. 192, pp. 105651-105651
Open Access | Times Cited: 1
The Experience of a Tertiary Reference Hospital in the Study of Rare Neurological Diseases
Styliani-Aggeliki Sintila, Marina Boziki, Christos Bakirtzis, et al.
Medicina (2023) Vol. 59, Iss. 2, pp. 266-266
Open Access | Times Cited: 3
Styliani-Aggeliki Sintila, Marina Boziki, Christos Bakirtzis, et al.
Medicina (2023) Vol. 59, Iss. 2, pp. 266-266
Open Access | Times Cited: 3
