Andreas Hehr

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

Maximilian Muenke, Ute Schell, Andreas Hehr et al. · Nature Genetics · 1994 · 622 citations

Fibrosis, Mendelian Disorder, Common Mutation +8

Mutations in <i>FGFR1</i> and <i>FGFR2</i> cause familial and sporadic Pfeiffer syndrome

Ute Schell, Andreas Hehr, George Feldman et al. · Human Molecular Genetics · 1995 · 232 citations

Long‐term course and mutational spectrum of <i>spatacsin</i>‐linked spastic paraplegia

Ute Hehr, Peter Bauer, Beate Winner et al. · Annals of Neurology · 2007 · 116 citations

Neurological Disorder, Genetics, Motor Development +22

Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly

Ute Hehr, Daniel Pineda‐Alvarez, Goekhan Uyanik et al. · Human Genetics · 2010 · 62 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

Wide phenotypic variability in families with holoprosencephaly and a sonic hedgehog mutation

Ute Hehr, Uta Diebold, Dagmar Wahl et al. · European Journal of Pediatrics · 2004 · 55 citations

Developmental Biology, Genetic Disorder, Medicine +7