Karin Buiting

Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

Karin Buiting, Shinji Saitoh, Bärbel Dittrich et al. · Nature Genetics · 1995 · 598 citations

Developmental Biology, Genetic Disorder, Developmental Genetics +8

Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

Jérôme Cavaillé, Karin Buiting, Martin Kiefmann et al. · Proceedings of the National Academy of Sciences · 2000 · 576 citations

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

Imprinting-Mutation Mechanisms in Prader-Willi Syndrome

Tohru Ohta, Todd A. Gray, Peter K. Rogan et al. · The American Journal of Human Genetics · 1999 · 276 citations · Full text

Developmental Biology, Genetic Disorder, Genetics +5

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

Bärbel Dittrich, Karin Buiting, Bernd Korn et al. · Nature Genetics · 1996 · 257 citations

Chromatin, Transcriptional Regulation, Developmental Biology +9