Yoshihiro Maruo

Shiga University of Medical Science — Japan

Medicine · Health Sciences

25h-index2.6kcitations142works1.22yr avg
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Research Topics

Neonatal Health and Biochemistry(52), Methemoglobinemia and Tumor Lysis Syndrome(24), Heme Oxygenase-1 and Carbon Monoxide(21), Metabolism and Genetic Disorders(18), Erythrocyte Function and Pathophysiology(9)

Publications141 total

Accuracy of Death Certificates for Children: A Population-Based Retrospective Analysis
Pediatric Reports·2025Open Access
Japanese siblings with neuronal ceroid lipofuscinosis type 7 showing different initial symptoms due to biallelic MFSD8 variants: A case report
Brain and Development Case Reports·2025Open Access
Improving Perinatal Palliative Care in the Communities: A Regional Population-Based Study
Maternal and Child Health Journal·2025Open Access
National survey of Hutchinson-Gilford progeria syndrome and progeroid laminopathy in Japan
Aging·2025Open Access
Clinical factors related to bilirubin encephalopathy in preterm infants: A case-control study
Brain and Development·2025· 2 cited
Increased intracellular stress responses and decreased KLF2 in adult patients with atopic dermatitis
Cell Stress and Chaperones·2025· 2 citedOpen Access
KNTC1 introduces segmental heterogeneity to mitochondria
Disease Models & Mechanisms·2025Open Access
Dolutegravir metabolism: impact of genetic variations on uridine diphosphate glucuronosyltransferase subfamilies
Xenobiotica·2025
Continuous increase in podocyte numbers in the first 36 months of life—insights from forensic autopsies in Japanese children
Pediatric Nephrology·2025
Radiological changes in <scp>STING</scp> ‐associated vasculopathy of infancy treated with a <scp>JAK</scp> inhibitor
Pediatrics International·2025Open Access
Incidence of Bloodstream Infections in Pediatric Patients with Cancer during Febrile Neutropenia: A Retrospective Study
JMA Journal·2025Open Access
Defibrillation in a newborn immediately post‐birth for severe asphyxia
Pediatrics International·2025Open Access
Identification of a novel missense variant in the &lt;i&gt;AVP&lt;/i&gt; gene in a Japanese pedigree with familial neurohypophyseal diabetes insipidus
Clinical Pediatric Endocrinology·2024Open Access
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities
Nature Genetics·2024· 15 citedOpen Access
Moesin deficiency leads to lupus-like nephritis with accumulation of CXCL13-producing patrolling monocytes
Biochemical and Biophysical Research Communications·2024· 2 cited
Allogeneic Hematopoietic Cell Transplantation Ameliorated Asymptomatic Granulomatous and Lymphocytic Interstitial Lung Disease in a Patient With XIAP Deficiency
Journal of Pediatric Hematology/Oncology·2024· 1 cited
Challenges in the management of Turner syndrome with Y chromosome material: a case report of prophylactic gonadectomy revealing dysgerminoma
International Cancer Conference Journal·2024Open Access
Use of a long-term continuous glucose monitor for predicting sulfonylurea dose in patients with neonatal diabetes mellitus: a case series
Clinical Pediatric Endocrinology·2024Open Access
Siblings of neonatal hyperbilirubinemia with &lt;i&gt;UGT1A1&lt;/i&gt; double missense variants
Clinical Pediatric Endocrinology·2024Open Access
(Epi)genetic and clinical characteristics in 84 patients with pseudohypoparathyroidism type 1B
European Journal of Endocrinology·2023· 2 cited
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Frequent Co-authors

Yoshihiro Takeuchi(18), Hiroshi Satō(15), Asami Mori(12), Hiroshi Sato(8), Katsuyuki Matsui(8), Yu Mimura(7), Masaru Iwai(7), Hiroko Takahashi(5), Sayuri Nakahara(5), Takahide Yanagi(5), Masaki Ito(4), Morimi Shimada(4), Noriko Nishikura(3), Yoriko Ota(3), Tomoaki Kunitsu(3), Tohru Yorifuji(3), Yuki Hosokawa(3), Katsuya Aizu(3), Tatsuhiko Urakami(3), Kazuo Yamamoto(3)