Yukiko Kuroda

18PUBLICATIONS
11CO-AUTHORS
Cell and nuclear divisionEpigenetics (incl. genome methylation and epigenomics)TribologyMicroelectromechanical systems (MEMS)Paediatrics not elsewhere classified
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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

|Dec 23, 2024
Polysplenia and developmental delay in a case of microduplication in the 1p36.11 region involving the ARID1A gene.

Machiko Kataoka, Yukiko Kuroda, Hiroyuki Tanaka

|Dec 20, 2024
Recurrent FLNA p.Gly1554Arg Variant Associated With Familial Ebstein Anomaly and Joint Stiffness.

Yukiko Kuroda, Koki Nagai, Yasuhiro Kawai

|Jul 18, 2024
Subtle phenotypes of Mowat-Wilson syndrome in a patient with a novel ZEB2 C-ZF domain variant.

Yukiko Kuroda, Takuya Naruto, Kenji Kurosawa

|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

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