Jutta Becker

Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta

Jutta Becker, Oliver Semler, Christian Gilissen et al. · The American Journal of Human Genetics · 2011 · 354 citations · Full text

Sclerostin, Developmental Biology, Mendelian Disorder +10

Mutations in WNT1 Cause Different Forms of Bone Fragility

Katharina Keupp, Filippo Beleggia, Hülya Kayserili et al. · The American Journal of Human Genetics · 2013 · 277 citations · Full text

Bone Disease, Bone Fragility, Bone Morphogenic Protein +4

Enhanced apoptotic cell death of renal epithelial cells in mice lacking transcription factor AP-2β

Markus Moser, Armin Pscherer, Christina Roth et al. · Genes & Development · 1997 · 272 citations · Full text

Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): Molecular genetics, clinical experience, and fetal morphology

Klaus Zerres, Gabi M�cher, Jutta Becker et al. · American Journal of Medical Genetics · 1998 · 263 citations

Fetal Morphology, Renal Pathology, Pathology +16

A Mutation in the 5′-UTR of IFITM5 Creates an In-Frame Start Codon and Causes Autosomal-Dominant Osteogenesis Imperfecta Type V with Hyperplastic Callus

Oliver Semler, Lutz Garbes, Katharina Keupp et al. · The American Journal of Human Genetics · 2012 · 236 citations · Full text

Developmental Biology, Genetic Disorder, Medicine +7