Yukiko Kuroda

18PUBLICATIONS
11CO-AUTHORS
Cell and nuclear divisionPaediatrics not elsewhere classifiedGene and molecular therapyNeurogeneticsEpigenetics (incl. genome methylation and epigenomics)
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Publications (18)

|May 24, 2025
Genotype-phenotype correlations and phenotypic expansion in a case series of ReNU syndrome associated with RNU4-2 variants.

Yukiko Kuroda, Koki Nagai, Yasuhiro Kawai

|Jun 26, 2024
GPC4 truncating variant associated with Keipert syndrome and lacrimal punctal agenesis.

Yukiko Kuroda, Takeshi Uehara, Yumi Enomoto

|May 14, 2024
Noonan syndrome-like phenotype associated with an ERF frameshift variant.

Yasuhiro Hirano, Yukiko Kuroda, Yumi Enomoto

|Apr 11, 2024
Role of TOE1 variants at the nuclear localization motif in pontocerebellar hypoplasia 7.

Yukiko Kuroda, Takuya Naruto, Yu Tsuyusaki

|Aug 30, 2023
A Japanese patient with Teebi hypertelorism syndrome and a novel CDH11 EC1 domain variant.

Yukiko Kuroda, Yoko Saito, Yumi Enomoto

|May 15, 2023
PHACES-like syndrome with TMEM260 compound heterozygous variants.

Yukiko Kuroda, Yoko Saito, Yumi Enomoto

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