Werner Syndrome
Werner Syndrome is a rare autosomal recessive disorder belonging to the class of human diseases characterized by premature aging and caused by mutations in the WRN gene, which encodes a DNA helicase involved in DNA repair and genomic stability.
713
Publications
47.1K
Citations
2.7K
Authors
797
Institutions
Publications per year
2017–2026
76
Variants
Adult Progeria
Parents
713
Positional Cloning of the Werner's Syndrome Gene
Chang-En Yu, Junko Oshima, Ying‐Hui Fu et al. · Science · 1996 · 1.7K citations
The Werner syndrome protein is a DNA helicase
Matthew D. Gray, Jiang-Cheng Shen, Ashwini S. Kamath‐Loeb et al. · Nature Genetics · 1997 · 612 citations
Defective Telomere Lagging Strand Synthesis in Cells Lacking WRN Helicase Activity
Laure Crabbé, Ramiro E. Verdún, Candy Haggblom et al. · Science · 2004 · 601 citations
A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging
Weiqi Zhang, Jingyi Li, Keiichiro Suzuki et al. · Science · 2015 · 546 citations · Full text
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797
University of Washington
Seattle, United States
56 h-index
360 publications
37.3K citations
National Institute on Aging
Baltimore, United States
49 h-index
295 publications
31K citations
National Institutes of Health
Bethesda, United States
46 h-index
296 publications
32.1K citations
GeneCare Research Institute (Japan)
Kamakura, Japan
20 h-index
116 publications
8.4K citations

Chiba University
Chiba, Japan
19 h-index
133 publications
3.9K citations
The University of Osaka
Osaka, Japan
16 h-index
92 publications
7.3K citations
Otsuka (Japan)
Tokyo, Japan
16 h-index
40 publications
4.3K citations

University of Arkansas for Medical Sciences
Little Rock, United States
15 h-index
65 publications
3.6K citations
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JBC · 58 publications · 6.3K citations
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38 publications · 2.6K citations
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Repository · 43 publications · 2.1K citations
24
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PNAS · 21 publications · 3.8K citations
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20 publications · 1.7K citations
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