Agustini Utari

Congenital adrenal hyperplasia - current insights in pathophysiology, diagnostics and management.

P. White, L. Guasti, H. Falhammar, 2021, Endocrine reviews.

Broad clinical involvement in a family affected by the fragile X premutation.

D. Hessl, F. Tassone, R. Hagerman, 2009, Journal of developmental and behavioral pediatrics : JDBP.

Side effects of minocycline treatment in patients with fragile X syndrome and exploration of outcome measures.

S. Rivera, D. Nguyen, I. Ethell, 2010, American journal on intellectual and developmental disabilities.

Surveillance and prevalence of fragile X syndrome in Indonesia.

H. van Bokhoven, R. Hagerman, S. Faradz, 2021, Intractable & rare diseases research.

Robust Screening and Cascade Testing for Fragile X Expansions in a Large Multigenerational Family Identify Many Affected Individuals: An Experience in the Remote Area of Indonesia

F. Tassone, S. Faradz, T. Winarni, 2020, Journal of Intellectual Disability - Diagnosis and Treatment.

Identification of expanded alleles of the FMR1 gene among high-risk population in Indonesia by using blood spot screening.

F. Tassone, B. Durbin-Johnson, S. Faradz, 2012, Genetic testing and molecular biomarkers.

Insulin-like growth factor-1 and growth in infants 0-6 months of age

A. Utari, M. Mexitalia, Bob Kevin Pardede, 2021 .

Familiarity and genetic literacy among medical students in Indonesia

T. Winarni, Yolanda Marthia Swandayani, F. Cayami, 2021, BMC medical education.