Agustini Utari is an expert in Endocrinology at Dr. Kariadi Hospital (Indonesia). As of October 2026, ScienceLeadR ranks Agustini Utari in the top 1% of experts in Indonesia for Adrenal Gland Diseases, Gonadal Disorders and Congenital Abnormalities. Agustini Utari has authored 85 publications, the most recent in 2026. SLR score: 268 (community average: 125). How the SLR is computed.

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Agustini Utari Dr. Kariadi Hospital Indonesia
268 ScienceLeadR Reputation 268
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Endocrinology

Subspecialties: Pediatrics - Genetics - Public Health

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Expert Rankings

Top experts on the MeSH terms this expert works on

Organizations

Career arc: 2011 - 2026

Source: PubMed

Diponegoro University

Publications Synthesis

Sources: PubMed, OpenAlex

Breakdown by type

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
A novel microdeletion syndrome involving 17q23.3 region in a child with short stature and multiple congenital anomalies: A Case Report.
PMID 42862774 — genes, growth, phenotype, chromosomes, child
Cytogenet Genome Res20260
Exploring Factors Associated With Parental Acceptance-Rejection Among Parents of Children With Congenital Adrenal Hyperplasia in Central Java, Indonesia.
PMID 42745617 — schools, genetic counseling, adrenal hyperplasia, congenital, hostility, hyperplasia, education, child
J Genet Couns20260
Global perspective of the management of patients with Differences of Sex Development in Low- and Middle- Income Countries; a scoping review.
PMID 42721113 — sex differentiation, income, sex, sexual development
Sex Dev20260
Adaptation of Parental Perception of Uncertainty Scale (PPUS): A psychometric study in a genetic research center in Indonesia.
PMID 42666837 — diabetes mellitus, genetic research, chronic disease, perception, uncertainty, research, psychometrics, diabetes mellitus, type 1, child
Belitung Nurs J20260
Phenotypic variability of Fragile-X syndrome in Asian population: A systematic review.
PMID 42643713 — fragile x syndrome, phenotype, ear, intellectual disability
Intractable Rare Dis Res20260

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