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Cited by in CrossRef
For: Mundhofir FE, Winarni TI, Nillesen W, Bon BWV, Schepens M, Ruiterkamp-Versteeg M, Hamel BC, Yntema HG, Faradz SM. Prevalence of fragile X syndrome in males and females in Indonesia. World J Med Genet 2012; 2(3): 15-22 [DOI: 10.5496/wjmg.v2.i3.15]
URL: https://www.wjgnet.com/2220-3184/full/v2/i3/15.htm
Number Citing Articles
Tri Indah Winarni, Tanjung Ayu Sumekar, Susilo Wibowo, Randi J. Hagerman, Sultana M.H. Faradz. Premutation Allele Combined with Caregiver Distress Factor Increase the Risk of Depression in Fragile X Carriers: Indonesia SettingJournal of Intellectual Disability - Diagnosis and Treatment 2019; 7(4): 200 doi: 10.6000/2292-2598.2019.07.04.1
Agustini Utari, Kirin Basuta, Tri Indah Winarni, Joyce Lo, Guadalupe Mendoza Morales, Sultana M.H. Faradz, Flora Tassone. 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 IndonesiaJournal of Intellectual Disability - Diagnosis and Treatment 2020; 8(1): 9 doi: 10.6000/2292-2598.2020.08.01.2
Grace X.Y. Lim, Yu Ling Loo, Farmaditya E.P. Mundhofir, Ferdy K. Cayami, Sultana M.H. Faradz, Indhu-Shree Rajan-Babu, Samuel S. Chong, Yvonne Y. Koh, Ming Guan. Validation of a Commercially Available Screening Tool for the Rapid Identification of CGG Trinucleotide Repeat Expansions in FMR1The Journal of Molecular Diagnostics 2015; 17(3): 302 doi: 10.1016/j.jmoldx.2014.12.005
NRB Sihombing, S Cai, DPW Wong, M Guan, SS Chong, SMH Faradz, TI Winarni. Repeat expansion and methylation-sensitive triplet-primed polymerase chain reaction for fragile X mental retardation 1 gene screening in institutionalised intellectually disabled individualsSingapore Medical Journal 2021; 62(3): 143 doi: 10.11622/smedj.2020009
Nydia Rena Benita Sihombing, Tri Indah Winarni, Agustini Utari, Hans van Bokhoven, Randi J Hagerman, Sultana MH Faradz. Surveillance and prevalence of fragile X syndrome in IndonesiaIntractable & Rare Diseases Research 2021; 10(1): 11 doi: 10.5582/irdr.2020.03101
Grace X. Y. Lim, Minli Yeo, Yvonne Y. Koh, Tri Indah Winarni, Indhu-Shree Rajan-Babu, Samuel S. Chong, Sultana M. H. Faradz, Ming Guan, Maya Koronyo-Hamaoui. Validation of a commercially available test that enables the quantification of the numbers of CGG trinucleotide repeat expansion in FMR1 genePLOS ONE 2017; 12(3): e0173279 doi: 10.1371/journal.pone.0173279
Akash Rajaratnam, Jasdeep Shergill, Maria Salcedo-Arellano, Wilmar Saldarriaga, Xianlai Duan, Randi Hagerman. Fragile X syndrome and fragile X-associated disordersF1000Research 2017; 6: 2112 doi: 10.12688/f1000research.11885.1