Takeo Yoshikawa

15PUBLICATIONS
58CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Central nervous systemNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Molecular targets
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Publications (15)

|Feb 24, 2024
De Novo Variants Found in Three Distinct Schizophrenia Populations Hit a Common Core Gene Network Related to Microtubule and Actin Cytoskeleton Gene Ontology Classes.

Yann Loe-Mie, Christine Plançon, Caroline Dubertret

|Oct 09, 2023
Impairment of serine transport across the blood-brain barrier by deletion of Slc38a5 causes developmental delay and motor dysfunction.

Inna Radzishevsky, Maali Odeh, Oded Bodner

|Sep 09, 2022
SLITRK1-mediated noradrenergic projection suppression in the neonatal prefrontal cortex.

Minoru Hatayama, Kei-Ichi Katayama, Yukie Kawahara

|Feb 27, 2022
Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder.

Chenyao Wang, Shin-Ichiro Horigane, Minoru Wakamori

|Jul 15, 2021
A loss-of-function variant in SUV39H2 identified in autism-spectrum disorder causes altered H3K9 trimethylation and dysregulation of protocadherin β-cluster genes in the developing brain.

Shabeesh Balan, Yoshimi Iwayama, Tetsuo Ohnishi

|May 09, 2021
Glyoxalase I disruption and external carbonyl stress impair mitochondrial function in human induced pluripotent stem cells and derived neurons.

Tomonori Hara, Manabu Toyoshima, Yasuko Hisano

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Frequent Collaborators

8 joint publications

Shabeesh Balan

3 joint publications

Tetsuo Ohnishi

2 joint publications

Haruhiko Bito

2 joint publications

Manabu Toyoshima