W Schönberger

Partial deficiency of Thyroid transcription factor 1 produces predominantly neurological defects in humans and mice

Joachim Pohlenz, A Dumitrescu, Dorothee Zundel et al. · Journal of Clinical Investigation · 2002 · 179 citations · Full text

Genetics, Molecular Genetics, Disease Gene Identification +16

Partial deficiency of Thyroid transcription factor 1 produces predominantly neurological defects in humans and mice

Joachim Pohlenz, A Dumitrescu, Dorothee Zundel et al. · Journal of Clinical Investigation · 2002 · 160 citations

Genetics, Reporter Gene, Molecular Genetics +16

Familial insulin resistant diabetes associated with acanthosis nigricans, polycystic ovaries, hypogonadism, pigmentary retinopathy, labyrinthine deafness, and mental retardation

Rainer Boor, J. Herwig, Jürgen Schrezenmeir et al. · American Journal of Medical Genetics · 1993 · 29 citations

New point mutation (R243W) in the hormone binding domain of the c-erbA β1 gene in a family with generalized resistance to thyroid hormone

Joachim Pohlenz, W Schönberger, Heike Wemme et al. · Human Mutation · 1996 · 23 citations

Systems Biology, Signal Transduction, Hormone Binding Domain +15

Effect of oestrogen/gestagen replacement therapy on liver enzymes in patients with Ullrich-Turner Syndrome

Heike Wemme, Joachim Pohlenz, W Schönberger · European Journal of Pediatrics · 1995 · 22 citations

Urology, Hepatology, Liver Physiology +8