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

Life Sciences, Genetics, Molecular Genetics +16

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

Life Sciences, Genetics, Molecular Genetics +13

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

Life Sciences, Genetics, Molecular Genetics +11

Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy

Lucie Gueneau, A. Bertrand, Jean‐Philippe Jaïs et al. · The American Journal of Human Genetics · 2009 · 238 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

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

Medicine, Genetics, Molecular Genetics +15