Shared Disease Phenotypes
Shared Disease Phenotypes is a scientific construct that identifies homologous pathological manifestations across different species, enabling comparative analysis of disease mechanisms by emphasizing common clinical, molecular, or physiological traits rooted in conserved biological pathways.
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2017–2026
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Yanick J. Crow, Diana Chase, Johanna L. Schmidt et al. · American Journal of Medical Genetics Part A · 2015 · 613 citations · Full text
Prioritization of disease microRNAs through a human phenome-microRNAome network
Qinghua Jiang, Yangyang Hao, Guohua Wang et al. · BMC Systems Biology · 2010 · 400 citations · Full text
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Harvard University
Cambridge, United States
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55 publications
8.7K citations

Brigham and Women's Hospital
Boston, United States
10 h-index
31 publications
3.4K citations
University College London
London, United Kingdom
8 h-index
92 publications
7.9K citations
Case Western Reserve University
Cleveland, United States
7 h-index
17 publications
5.1K citations
Inserm
Paris, France
7 h-index
37 publications
4.4K citations
Stanford University
Stanford, United States
7 h-index
92 publications
3.4K citations

University of Manchester
Manchester, United Kingdom
7 h-index
45 publications
8K citations
University of California, Los Angeles
Los Angeles, United States
7 h-index
54 publications
4.7K citations
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