JACKSON-WEISS SYNDROME

Known as: Acrocephalosyndactyly Jackson Weiss type, Enlarged great toes and craniofacial abnormalities, JWS 
A rare, autosomal dominant inherited disorder caused by mutations in the FGFR2 gene. It is characterized by the premature fusion of the bones of the… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1976-2016
024619762016

Papers overview

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Highly Cited
2011
Highly Cited
2011
Tarun Dua, Corrado Barbui, Nicolas Clark, Alexandra Fleischmann, Vladimir Poznyak, Mark van Ommeren, M. Taghi Yasamy, Jose Luis… (More)
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2009
2009
The primary purpose of this study was to analyze the sequential relationships proposed by the fear-avoidance model of pain… (More)
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2006
2006
Systems Biology aims to understand quantitatively how properties of biological systems can be understood as functions of the… (More)
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2006
2006
The cognitive-behavioral, fear-avoidance (FA) model of chronic pain (Vlaeyen JWS, Kole-Snijders AMJ, Boeren RGB, van Eek H. Fear… (More)
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Highly Cited
2004
Highly Cited
2004
UNLABELLED JWS Online is a repository of kinetic models, describing biological systems, which can be interactively run and… (More)
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1997
1997
Jackson-Weiss syndrome is a rare skeletal disorder characterized by craniosynostosis associated with foot malformations. This… (More)
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1995
1995
Mutations have been reported for several craniosynostotic disorders in exon IIIa (exon U or 7) or IIIc (exon B or 9) of the… (More)
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1995
1995
Dominant mutations in the fibroblast growth factor receptor 2 (FGFR2) gene have been recently identified as causes of four… (More)
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Highly Cited
1994
Highly Cited
1994
Jackson-Weiss syndrome is an autosomal dominant condition characterized by craniosynostosis, foot anomalies and great phenotypic… (More)
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1994
1994
Crouzon syndrome (MIM 123500) is a common autosomal dominant form of craniosynostosis with shallow orbits, ocular proptosis, and… (More)
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