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Jun 27, 2012 (publication date) through Nov 6, 2024
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Publication Name
World Journal of Medical Genetics
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2220-3184
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| 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] |
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| URL: | https://www.wjgnet.com/2220-3184/full/v2/i3/15.htm |
| Number | Citing Articles |
| 1 |
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 Setting. Journal of Intellectual Disability - Diagnosis and Treatment 2019; 7(4): 200 doi: 10.6000/2292-2598.2019.07.04.1
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| 2 |
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 Indonesia. Journal of Intellectual Disability - Diagnosis and Treatment 2020; 8(1): 9 doi: 10.6000/2292-2598.2020.08.01.2
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| 3 |
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 FMR1. The Journal of Molecular Diagnostics 2015; 17(3): 302 doi: 10.1016/j.jmoldx.2014.12.005
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| 4 |
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 individuals. Singapore Medical Journal 2021; 62(3): 143 doi: 10.11622/smedj.2020009
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| 5 |
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 Indonesia. Intractable & Rare Diseases Research 2021; 10(1): 11 doi: 10.5582/irdr.2020.03101
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| 6 |
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 gene. PLOS ONE 2017; 12(3): e0173279 doi: 10.1371/journal.pone.0173279
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| 7 |
Akash Rajaratnam, Jasdeep Shergill, Maria Salcedo-Arellano, Wilmar Saldarriaga, Xianlai Duan, Randi Hagerman. Fragile X syndrome and fragile X-associated disorders. F1000Research 2017; 6: 2112 doi: 10.12688/f1000research.11885.1
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