Claudia Färber

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

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

Construction of a Detailed Physical and Transcript Map of the Candidate Region for Russell–Silver Syndrome on Chromosome 17q23–q24

Sylvia Dörr, Alina T. Midro, Claudia Färber et al. · Genomics · 2001 · 38 citations

Russell–silver Syndrome, Cytogenetics, Genetic Disorder +9

Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselling

Karin Buiting, Claudia Färber, Peter M. Kroisel et al. · Clinical Genetics · 2000 · 36 citations

Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15

Maren Runte, Claudia Färber, Christina Lich et al. · European Journal of Human Genetics · 2001 · 14 citations · Full text

Chromatin, Epigenetic Change, Genetics +11