Keiko Shimojima Yamamoto

13PUBLICATIONS
10CO-AUTHORS
Cell and nuclear divisionFoetal development and medicineAcoustics and noise control (excl. architectural acoustics)Developmental genetics (incl. sex determination)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (13)

|Sep 24, 2025
Balanced chromosomal insertions as the mechanism of recurrent familial microstructural abnormalities: detailed analyses using long-read whole-genome sequencing.

Hironao Shirai, Keiko Shimojima Yamamoto, Hirokazu Arai

|Aug 16, 2024
Uniparental maternal tetrasomy X co-occurrence with paternal nondisjunction: investigation of the origin of 48,XXXX.

Keiko Shimojima Yamamoto, Sakurako Yamamoto, Taichi Imaizumi

|Aug 09, 2024
Reciprocal chromosome translocation t(3;4)(q27;q31.2) with deletion of 3q27 and reduced FBXW7 expression in a patient with developmental delay, hypotonia, and seizures.

Takeaki Tamura, Keiko Shimojima Yamamoto, Jun Tohyama

|May 15, 2024
Xq22 deletion involving TCEAL1 in a female patient with early-onset neurological disease trait.

Keiko Shimojima Yamamoto, Yusuke Itagaki, Kazuki Tanaka

|Jan 14, 2024
Rare mosaic variant of GJA1 in a patient with a neurodevelopmental disorder.

Rina Shimomura, Tomoe Yanagishita, Kumiko Ishiguro

|Oct 23, 2023
Preimplantation genetic testing using comprehensive genomic copy number analysis is beneficial for balanced translocation carriers.

Aya Yamazaki, Tomoko Kuroda, Nami Kawasaki

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Frequent Collaborators

12 joint publications

Toshiyuki Yamamoto

4 joint publications

Hitoshi Kanno

2 joint publications

Takuya Hirade

2 joint publications

Tadashi Kaname