Agustini Utari

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 13

Top Venues

International journal of neonatal screening

International journal of molecular sciences

American journal of medical genetics. Part A

Cardiology research

Universitas Diponegoro Fakultas Kedokteran

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Universitas Diponegoro Fakultas Kedokteran

Indonesia

Lecturer :: Department of Pediatrics

Publications

Tri Indah Winarni, Ye Hyun Hwang, Susan M Rivera, David R Hessl, Blythe P Durbin-Johnson, Agustini Utari, Randi J Hagerman, Flora Tassone
Apolipoproteine and KLOTHO Gene Variants Do Not Affect the Penetrance of Fragile X-Associated Tremor/Ataxia Syndrome. International journal of molecular sciences 25 (15) (2024)
Aman Bhakti Pulungan, Helena Arnetta Puteri, Muhammad Faizi, Paul Leslie Hofman, Agustini Utari, Jean-Pierre Chanoine
Experiences and Challenges with Congenital Hypothyroidism Newborn Screening in Indonesia: A National Cross-Sectional Survey. International journal of neonatal screening 10 (1) (2024)
Aman Bhakti Pulungan, Helena Arnetta Puteri, Muhammad Faizi, Paul Leslie Hofman, Agustini Utari, Jean-Pierre Chanoine
Experiences and Challenges with Congenital Hypothyroidism Newborn Screening in Indonesia: A National Cross-Sectional Survey. International journal of neonatal screening 10 (1) (2024)
Tri Indah Winarni, Ye Hyun Hwang, Susan M Rivera, David R Hessl, Blythe P Durbin-Johnson, Agustini Utari, Randi J Hagerman, Flora Tassone
Apolipoproteine and KLOTHO Gene Variants Do Not Affect the Penetrance of Fragile X-Associated Tremor/Ataxia Syndrome. International journal of molecular sciences 25 (15) (2024)
Tri Indah Winarni, Ye Hyun Hwang, Susan M Rivera, David R Hessl, Blythe P Durbin-Johnson, Agustini Utari, Randi J Hagerman, Flora Tassone
Apolipoproteine and KLOTHO Gene Variants Do Not Affect the Penetrance of Fragile X-Associated Tremor/Ataxia Syndrome. International journal of molecular sciences 25 (15) (2024)
Bas P H Adriaansen, Agustini Utari, André J Olthaar, Rob C B M van der Steen, Karijn J Pijnenburg-Kleizen, Lizanne Berkenbosch, Paul N Span, Fred C G J Sweep, Hedi L Claahsen-van der Grinten, Antonius E van Herwaarden
Free cortisol and free 21-deoxycortisol in the clinical evaluation of congenital adrenal hyperplasia. The Journal of clinical endocrinology and metabolism (2024)
Aman Bhakti Pulungan, Helena Arnetta Puteri, Muhammad Faizi, Paul Leslie Hofman, Agustini Utari, Jean-Pierre Chanoine
Experiences and Challenges with Congenital Hypothyroidism Newborn Screening in Indonesia: A National Cross-Sectional Survey. International journal of neonatal screening 10 (1) (2024)
Irene Astrid Larasati, Fanti Saktini, Tri Indah Winarni, Annastasia Ediati, Agustini Utari
Factors influencing illness uncertainty in parents of children with congenital adrenal hyperplasia in a developing country: A cross-sectional study. Belitung nursing journal 9 (1) (2023)
Yolanda Marthia Swandayani, Ferdy Kurniawan Cayami, Tri Indah Winarni, Agustini Utari
Familiarity and genetic literacy among medical students in Indonesia. BMC medical education 21 (1) (2021)
Nani Maharani, Anindita Soetadji, Agustini Utari, Izumi Naka, Jun Ohashi, Maria Mexitalia
Cytochrome b-245 Alpha Chain Gene Variants and Arterial Function in Indonesian Short Stature Children. Cardiology research 12 (6) (2021)
Kate Armstrong, Alain Benedict Yap, Sioksoan Chan-Cua, Maria E Craig, Catherine Cole, Vu Chi Dung, Joseph Hansen, Mohsina Ibrahim, Hassana Nadeem, Aman Pulungan, Jamal Raza, Agustini Utari, Paul Russell Ward
We All Have a Role to Play: Redressing Inequities for Children Living with CAH and Other Chronic Health Conditions of Childhood in Resource-Poor Settings. International journal of neonatal screening 6 (4) (2020)
Gara Samara Brajadenta, Agustini Utari, Sylvie Patri, Frederic Bilan, Sultana Muhammad Hussein Faradz, Alain Kitzis, Vincent Thoreau
Identification of a Novel CHD7 Mutation in a CHARGE Syndrome Patient in Indonesia. Annals of laboratory medicine 39 (5) (2019)
Paul S Kruszka, Yonit A Addissie, Cedrik Tekendo-Ngongang, Kelly L Jones, Sarah K Savage, Neerja Gupta, Nirmala D Sirisena, Vajira H W Dissanayake, C Sampath Paththinige, Teresa Aravena, Sheela Nampoothiri, Dhanya Yesodharan, Katta Mohan Girisha, Siddaramappa Jagdish Patil, Saumya Shekhar Jamuar, Jasmine Chew-Yin Goh, Agustini Utari, Nydia Sihombing, Rupesh Mishra, Neer Shoba Chitrakar, Brenda C Iriele, Ezana Lulseged, Andre Megarbane, Annette Uwineza, Elizabeth Eberechi Oyenusi, Oluwarotimi Bolaji Olopade, Olufemi Adetola Fasanmade, Milagros M Duenas-Roque, Meow-Keong Thong, Joanna Y L Tung, Gary T K Mok, Nicole Fleischer, Godfrey M Rwegerera, María Beatriz de Herreros, Johnathan Watts, Karen Fieggen, Victoria Huckstadt, Angélica Moresco, María Gabriela Obregon, Dalia Farouk Hussen, Neveen A Ashaat, Engy A Ashaat, Brian H Y Chung, Eben Badoe, Sultana M H Faradz, Mona O El Ruby, Vorasuk Shotelersuk, Ambroise Wonkam, Ekanem Nsikak Ekure, Shubha Rao Phadke, Antonio Richieri-Costa, Maximilian Muenke
Turner syndrome in diverse populations. American journal of medical genetics. Part A 182 (2) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Agustini Utari