Patient Registries
Patient Registries is a systematic data collection infrastructure that prospectively gathers standardized information on individuals with a specific condition or exposure, distinguished by its longitudinal design and primary focus on characterizing disease progression, treatment patterns, and outcomes in real-world clinical contexts.
1.6K
Publications
111.2K
Citations
11.8K
Authors
3.3K
Institutions
Publications per year
2017–2026
659
1.6K
ClinVar: improving access to variant interpretations and supporting evidence
Melissa Landrum, Jennifer M. Lee, Mark J. Benson et al. · Nucleic Acids Research · 2017 · 4.5K citations · Full text
Real-World Evidence — What Is It and What Can It Tell Us?
Rachel E. Sherman, Steven A. Anderson, Gerald J. Dal Pan et al. · New England Journal of Medicine · 2016 · 2.1K citations
1–5 of 1.6K
11.8K
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12
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10
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10
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1–5 of 11.8K
3.3K
National Cancer Institute
Bethesda, United States
37 h-index
182 publications
37.1K citations

Karolinska Institutet
Stockholm, Sweden
36 h-index
190 publications
10.3K citations
Harvard University
Cambridge, United States
33 h-index
134 publications
8.3K citations
Inserm
Paris, France
32 h-index
99 publications
7.1K citations

Aarhus University Hospital
Aarhus, Denmark
31 h-index
143 publications
10.8K citations

Lund University
Lund, Sweden
29 h-index
87 publications
7.1K citations

Karolinska University Hospital
Stockholm, Sweden
29 h-index
94 publications
5.8K citations
National Institutes of Health
Bethesda, United States
27 h-index
82 publications
104.4K citations
1–8 of 3.3K
55 publications · 7K citations
40
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Repository · 117 publications · 7.9K citations
36
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OJRD · 26 publications · 1.6K citations
22
h-index
23 publications · 894 citations
18
h-index
16 publications · 2.5K citations
14
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1–5