Stephanie Groß

Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect

Karin Buiting, Stephanie Groß, Christina Lich et al. · The American Journal of Human Genetics · 2003 · 366 citations · Full text

Imprinting Defect, Molecular Study, Angelman Syndromes

Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis

Karin Buiting, Bärbel Dittrich, Stephanie Groß et al. · The American Journal of Human Genetics · 1998 · 215 citations · Full text

Developmental Anomaly, Genetic Disorder, Genetics +8

Characterization of a methylation imprint in the Prader — Willi syndrome chromosome region

Bärbel Dittrich, Karin Buiting, Stephanie Groß et al. · Human Molecular Genetics · 1993 · 85 citations

Identification of a Testis-Specific Gene (C15orf2) in the Prader–Willi Syndrome Region on Chromosome 15

Claudia Färber, Stephanie Groß, Jürgen Neesen et al. · Genomics · 2000 · 49 citations

Developmental Biology, Chromosome 15, Genetic Disorder +11

Identification of cis- and trans-acting factors possibly modifying the risk of epimutations on chromosome 15

Corinna Zogel, Stefan Böhringer, Stephanie Groß et al. · European Journal of Human Genetics · 2006 · 38 citations · Full text

Chromatin, Chromosome 15, Genetic Disorder +9