Kensaku Sasaki

Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair

Yuka Nakazawa, Kensaku Sasaki, Norisato Mitsutake et al. · Nature Genetics · 2012 · 212 citations · Full text

Life Sciences, Genetics, Molecular Biology +15

Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia

Kazuya Kashiyama, Yuka Nakazawa, Daniela T. Pilz et al. · The American Journal of Human Genetics · 2013 · 205 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Maternal uniparental isodisomy and heterodisomy on chromosome 6 encompassing a CUL7 gene mutation causing 3M syndrome

Kensaku Sasaki, Nobuhiko Okamoto, Kenjiro Kosaki et al. · Clinical Genetics · 2010 · 59 citations

Life Sciences, Genetics, Molecular Genetics +17

Autosomal recessive cystinuria caused by genome‐wide paternal uniparental isodisomy in a patient with Beckwith–Wiedemann syndrome

Yasufumi Ohtsuka, Ken Higashimoto, Kensaku Sasaki et al. · Clinical Genetics · 2014 · 52 citations

Life Sciences, Genetics, Molecular Genetics +15

Japanese and North American/European patients with Beckwith–Wiedemann syndrome have different frequencies of some epigenetic and genetic alterations

Kensaku Sasaki, Hidenobu Soejima, Ken Higashimoto et al. · European Journal of Human Genetics · 2007 · 43 citations

Life Sciences, Genetics, Molecular Genetics +8