Toshiki Takenouchi

48PUBLICATIONS
50CO-AUTHORS
NeonatologyMedical molecular engineering of nucleic acids and proteinsHaematological tumoursMolecular targetsNutrigenomics and personalised nutrition
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Publications (48)

|Apr 15, 2026
Refining the Neonatal Phenotypic Spectrum of Distal Deletion 14q Syndrome: Early Genomic Diagnosis in Infancy.

Koji Nakae, Shiori Hamada, Junpei Kawamura

|Jan 22, 2026
Identification of new human monogenic disorders and implementation of genomic medicine in sick newborn infants.

Toshiki Takenouchi

|Oct 30, 2025
Missense variants in homeobox domain of PBX1 cause coracoclavicular ankylosis.

Maki Iwai, Kyra E Stuurman, Kirsten Meagher

|Sep 25, 2025
Haploinsufficiency of Runx2 restores the cranial sutures in a mouse model of Pdgfrb-related craniosynostosis.

Eri Ogawa, Tomona Oikawa, Shinya Ayabe

|May 28, 2025
De novo CDKN1C variant in Beckwith-Wiedermann spectrum with atypical complications.

Yuri Moriura, Yosuke Nishio, Shintaro Ichimura

|Apr 24, 2025
Prenatal Brain Abnormalities in Sodium-Dependent Multivitamin Transporter Deficiency.

Eri Ogawa, Kenjiro Kosaki, Toshiki Takenouchi

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Frequent Collaborators

22 joint publications

Tomoko Uehara

16 joint publications

Hisato Suzuki

12 joint publications

Mamiko Yamada

8 joint publications

Kenjiro Kosaki