Shinji Saitoh

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

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

Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy

Lucie Gueneau, A. Bertrand, Jean-Philippe Jaı̈s et al. · The American Journal of Human Genetics · 2009 · 236 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +3

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.

Christopher C. Glenn, Shinji Saitoh, M T Jong et al. · PubMed · 1996 · 236 citations