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Catherine Lynn T. Silao
Catherine Lynn T. Silao
Institute of Human Genetics, NIH Philippines; Dept. of Pediatrics, UPPGH
Verified email at post.upm.edu.ph
Title
Cited by
Cited by
Year
Diversity of approaches to classic galactosemia around the world: a comparison of diagnosis, intervention, and outcomes
PP Jumbo-Lucioni, K Garber, J Kiel, I Baric, GT Berry, A Bosch, A Burlina, ...
Journal of inherited metabolic disease 35, 1037-1049, 2012
942012
PD1 as a common candidate susceptibility gene of subacute sclerosing panencephalitis
Y Ishizaki, N Yukaya, K Kusuhara, R Kira, H Torisu, K Ihara, Y Sakai, ...
Human genetics 127, 411-419, 2010
532010
Maple syrup urine disease (MSUD)—clinical profile of 47 Filipino patients
JY Lee, MA Chiong, SC Estrada, EM Cutiongco-De la Paz, CLT Silao, ...
Journal of inherited metabolic disease 31, 281-285, 2008
522008
Clinical, biochemical and molecular characteristics of Filipino patients with mucopolysaccharidosis type II-Hunter syndrome
MAD Chiong, DM Canson, MAR Abacan, MMP Baluyot, CP Cordero, ...
Orphanet Journal of Rare Diseases 12, 1-11, 2017
292017
A novel deletion creating a new terminal exon of the dihydrolipoyl transacylase gene is a founder mutation of Filipino maple syrup urine disease
CLT Silao, CD Padilla, M Matsuo
Molecular genetics and metabolism 81 (2), 100-104, 2004
282004
Molecular basis of glucose‐6‐phosphate dehydrogenase deficiency among Filipinos
CL Silao, T Shirakawa, K Nishiyama, CPAM Matsuo
Pediatrics international 41 (2), 138-141, 1999
201999
Association of carbamazepine-induced Stevens–Johnson syndrome/toxic epidermal necrolysis with the HLA-B75 serotype or HLA-B*15:21 allele in Filipino patients
F Capule, P Tragulpiankit, S Mahasirimongkol, J Jittikoon, ...
The Pharmacogenomics Journal 20 (3), 533-541, 2020
192020
Prevalence of pharmacogenomic variants in 100 pharmacogenes among Southeast Asian populations under the collaboration of the Southeast Asian Pharmacogenomics Research Network …
C Runcharoen, K Fukunaga, I Sensorn, N Iemwimangsa, S Klumsathian, ...
Human genome variation 8 (1), 7, 2021
142021
Screening pathways through China, the Asia Pacific region, the World
V Wiley, D Webster, G Loeber
International Journal of Neonatal Screening 5 (3), 26, 2019
142019
Analysis of MxA, IL-4, and IRF-1 genes in Filipino patients with subacute sclerosing panencephalitis
JR Pipo-Deveza, K Kusuhara, CLT Silao, MB Lukban, AM Salonga, ...
Neuropediatrics 37 (04), 222-228, 2006
132006
Novel cystathionine β‐synthase gene mutations in a Filipino patient with classic homocystinuria
CLT Silao, TDF Fabella, KID Rama, SC Estrada
Pediatrics International 57 (5), 884-887, 2015
112015
Mutations of the phenylalanine hydroxylase (PAH) gene in Filipino patients with phenylketonuria
CLT Silao, DM Canson, KN Hernandez, MAD Chiong, ...
Acta Medica Philippina 43 (2), 2009
82009
Early diagnosis of maple syrup urine disease using polymerase chain reaction‐based mutation detection
CLT Silao, CD Padilla, M Matsuo
Pediatrics International 50 (3), 312-314, 2008
72008
A Master of Science in Genetic Counseling Program in the Philippines
MY Laurino, CD Padilla, MMB Alcausin, CLT Silao, EM dela Paz
ACTA Medica Philippina 45 (4), 7-8, 2011
62011
Mutational Analysis of the GALT gene in Filipino patients
SC Estrada, DM Canson, C Silao, T Lynn
Kobe J. Med. Sci 59 (3), E106-E111, 2013
52013
Molecular analysis of the MUT gene in Filipino patients with methylmalonic acidemia
CLT Silao, KN Hernandez, DM Canson, SC Estrada, MAD Chiong, ...
Acta Medica Philippina 43 (1), 2009
52009
Glucose-6-phosphate dehydrogenase deficiency in Filipino neonates with jaundice
CLT Silao, C David-Padilla, EV Uy, R Ernesto
Acta Medica Philippina 43 (2), 2009
52009
Characterization of Mutations and Polymorhisms in the G6PD gene Among Filipino Newborns with Glucose-6-Phosphate Dehydrogenase Deficiency
CD Padilla, CES Abaya, EMC de la Paz, CLT Silao, T Shirakawa, ...
ACTA Medica Philippina 45 (4), 53-57, 2011
42011
Maple syrup urine disease: a report of 26 cases in the Philippines
CD PADILLA, CLT SILAO, JOYY LEE
Frontiers in Human Genetics: Diseases and Technologies, 185-193, 2001
42001
HLA-A*24:07 as a potential biomarker for carbamazepine-induced Stevens–Johnson syndrome/toxic epidermal necrolysis in Filipino patients
F Capule, P Tragulpiankit, S Mahasirimongkol, J Jittikoon, ...
Pharmacogenomics 22 (8), 465-472, 2021
22021
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