S Spranger

High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome

Stefan Aretz, Dietlinde Stienen, Siegfried Uhlhaas et al. · Journal of Medical Genetics · 2007 · 246 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Mutation and phenotypic spectrum in patients with cardio‐facio‐cutaneous and Costello syndrome

AL Schulz, Beate Albrecht, I. van der Bürgt et al. · Clinical Genetics · 2007 · 109 citations

Life Sciences, Genetics, Molecular Genetics +14

Familial Hemiplegic Migraine with Cerebellar Ataxia and Paroxysmal Psychosis

Matthias Spranger, S Spranger, Sibylle G. Schwab et al. · European Neurology · 1999 · 48 citations

Life Sciences, Genetics, Neurology +17

SCA17 caused by homozygous repeat expansion in TBP due to partial isodisomy 6

Christine Zühlke, Matthias Spranger, S Spranger et al. · European Journal of Human Genetics · 2003 · 40 citations

Medicine, Genetics, Molecular Genetics +8

Schema avoidance in bulimic and non–eating‐disordered women

S Spranger, Glenn Waller, Rachel Bryant‐Waugh · International Journal of Eating Disorders · 2001 · 32 citations · Full text

Medicine, Psychiatry, Psychology +9