Pia Staedt

Analysis of the GNAS1 Gene in Albright’s Hereditary Osteodystrophy

Wiebke Ahrens, Olaf Hiort, Pia Staedt et al. · The Journal of Clinical Endocrinology & Metabolism · 2001 · 92 citations · Full text

Medicine, Genetics, Molecular Genetics +15

A positive genotype–phenotype correlation in a large cohort of patients with Pseudohypoparathyroidism Type Ia and Pseudo‐pseudohypoparathyroidism and 33 newly identified mutations in the <i><scp>GNAS</scp></i> gene

Susanne Thiele, Ralf Werner, Joachim Grötzinger et al. · Molecular Genetics & Genomic Medicine · 2014 · 54 citations · Full text

Medicine, Endocrinology, Genetics +14

A Disruptive Mutation in Exon 3 of the GNAS Gene with Albright Hereditary Osteodystrophy, Normocalcemic Pseudohypoparathyroidism, and Selective Long Transcript Variant Gsα-L Deficiency

Susanne Thiele, Ralf Werner, Wiebke Ahrens et al. · The Journal of Clinical Endocrinology & Metabolism · 2007 · 36 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Different Pattern of Epigenetic Changes of the<i>GNAS</i>Gene Locus in Patients With Pseudohypoparathyroidism Type Ic Confirm the Heterogeneity of Underlying Pathomechanisms in This Subgroup of Pseudohypoparathyroidism and the Demand for a New Classification of<i>GNAS</i>-Related Disorders

Bettina Brix, Ralf Werner, Pia Staedt et al. · The Journal of Clinical Endocrinology & Metabolism · 2014 · 30 citations · Full text

Life Sciences, Endocrinology, Genetics +9