Kenji Kurosawa

55PUBLICATIONS
70CO-AUTHORS
Pacific Peoples youth and familyGene expression (incl. microarray and other genome-wide approaches)Medical biotechnology not elsewhere classifiedInfant and child healthHaematological tumours
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Publications (55)

|Jun 01, 2026
Health-Related Quality of Life and Its Related Factors in Adolescents and Adults With Prader-Willi Syndrome in Japan.

|May 20, 2026
Aberrant Splicing From an HDAC8 Intronic Variant c.112-15C>A Causes Familial Cornelia de Lange Syndrome in Heterozygous and Hemizygous Individuals.

|Nov 06, 2025
Homozygous LZTR1 Variant Lacking the Second BTB Domain Associated With Bone Marrow Failure and Multiple Congenital Anomalies Distinct From Those of Noonan Syndrome.

Yukiko Kuroda, Tomoko Yokosuka, Koki Nagai

|Nov 05, 2025
Age-related changes in thyroid hormone profile in pediatric patients with Down syndrome.

Machiko Toki, Satoshi Narumi, Junko Hanakawa

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

Maki Iwai, Kyra E Stuurman, Kirsten Meagher

|Jul 24, 2025
A questionnaire-based survey on hyperphagia in individuals with Prader-Willi syndrome in Japan.

Makiko Tachibana, Yuji Oto, Kenichi Kashimada

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Frequent Collaborators

11 joint publications

Yukiko Kuroda

9 joint publications

Hiroaki Murakami

6 joint publications

Yumi Enomoto

5 joint publications

Yuichi Kimura