Frank Tiecke

Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype–phenotype correlations in FBN1 exons 24–40

Frank Tiecke, Stefanie Katzke, Patrick Booms et al. · European Journal of Human Genetics · 2001 · 157 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +10

Novel exon skipping mutation in the fibrillin‐1 gene: Two ‘hot spots’ for the neonatal Marfan syndrome

Patrick Booms, Jason Cisler, Kurt R. Mathews et al. · Clinical Genetics · 1999 · 103 citations

Decentral gene expression analysis for ER+/Her2− breast cancer: results of a proficiency testing program for the EndoPredict assay

Carsten Denkert, Ralf Kronenwett, W. Schlake et al. · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · 2012 · 90 citations · Full text

Breast Oncology, Engineering, Pathology +18

TGGE screening of the entire<i>FBN1</i>coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies

Stefanie Katzke, Patrick Booms, Frank Tiecke et al. · Human Mutation · 2002 · 74 citations

Genetics, Genetic Epidemiology, Pathology +18

Clustering of mutations associated with mild Marfan-like phenotypes in the 3? region ofFBN1 suggests a potential genotype-phenotype correlation

Monika Palz, Frank Tiecke, Patrick Booms et al. · American Journal of Medical Genetics · 2000 · 63 citations

Genetics, Pathology, Disease Gene Identification +19