Facioscapulohumeral muscular dystrophy 1 patients participating in the UK FSHD registry can be subdivided into 4 patterns of self-reported symptoms

ConsensusClusterPlus: a class discovery tool with confidence assessments and item tracking

Matthew D. Wilkerson, D. Neil Hayes · Bioinformatics · 2010 · 6.3K citations · Full text

Life Sciences, Bioinformatics, Oncology +11

Somatic symptom reporting in women and men

Arthur J. Barsky, Heli M. Peekna, Jonathan F. Borus · Journal of General Internal Medicine · 2001 · 791 citations

Nursing, Psychiatry, Psychology +12

A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy

Richard J.L.F. Lemmers, Patrick J. van der Vliet, Rinse Klooster et al. · Science · 2010 · 783 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

Richard J.L.F. Lemmers, Rabi Tawil, Lisa M. Petek et al. · Nature Genetics · 2012 · 664 citations

Life Sciences, Genetics, Molecular Genetics +12

Population-based incidence and prevalence of facioscapulohumeral dystrophy

Johanna C.W. Deenen, Hisse Arnts, Silvère M. van der Maarel et al. · Neurology · 2014 · 387 citations · Full text

Veterinary Medicine, Health Sciences, Population Health Sciences +14