Ken Saida

10PUBLICATIONS
117CO-AUTHORS
NeurogeneticsNeurology and neuromuscular diseasesMolecular targetsGene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (10)

|Nov 27, 2025
Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatment.

Florian Buerger, Daanya Salmanullah, Lorrin Liang

|Mar 14, 2024
Quantitative phenotyping of Nphs1 knockout mice as a prerequisite for gene replacement studies.

Florian Buerger, Lea M Merz, Ken Saida

|Sep 27, 2021
Pathogenic variants in the survival of motor neurons complex gene GEMIN5 cause cerebellar atrophy.

Ken Saida, Junya Tamaoki, Masayuki Sasaki

|Jul 07, 2021
Novel CLTC variants cause new brain and kidney phenotypes.

Toshiyuki Itai, Satoko Miyatake, Naomi Tsuchida

|Feb 01, 2021
Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation.

David B Beck, Mohammed A Basar, Anthony J Asmar

|Nov 01, 2020
Efficient detection of copy-number variations using exome data: Batch- and sex-based analyses.

Yuri Uchiyama, Daisuke Yamaguchi, Kazuhiro Iwama

Pageof 2

Frequent Collaborators

3 joint publications

Friedhelm Hildebrandt

3 joint publications

Takeshi Mizuguchi

3 joint publications

Naomichi Matsumoto

2 joint publications

Noriko Miyake