Eva Maria Cutiongco-de la Paz
Eva Maria Cutiongco-de la Paz
National Institutes of Health, University of the Philippines Manila
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Mapping human genetic diversity in Asia
HUGO Pan-Asian SNP Consortium, MA Abdulla, I Ahmed, ...
Science 326 (5959), 1541-1545, 2009
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24. 2, 17q23 and 19q13
EJ Leslie, JC Carlson, JR Shaffer, E Feingold, G Wehby, CA Laurie, ...
Human molecular genetics 25 (13), 2862-2872, 2016
Decreased elastin deposition and high proliferation of fibroblasts from Costello Syndrome are related to functional deficiency in the 67 KDa elastin binding protein
A Hinek, A Smith, EM Cutiongco, J Callahan, K Gripp, R Weksberg
American Journal of Human Genetics 66 (3), 859-872, 2000
GPC 3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome
M Li, C Shuman, EMC Cutiongco, HA Bender, C Stevens, L Willins-Hary, ...
American Journal of Medical Genetics 102 (2), 161-168, 2001
BRCA 1 and BRCA 2 Mutations Among Breast Cancer Patients from the Philippines
ML De Leon Matsuda, A Liede, E Kwan, EM Mapua,CA, Cutiongco, A Tan, ...
International Journal of Cancer 98 (4), 596-603, 2002
New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3)
A Domingo, A Westenberger, L Lee, I BrŠnne, T Liu, ...
European Journal of Human Genetic, 1-7, 2015
Maple syrup urine disease (MSUD) - clinical profile of 47 Filipino patients
JY Lee, MD Chiong, SC Estrada, EMC Cutiongco-de la Paz, CLT Silao, ...
Journal of Inherited Metabolic Disease 31 (2), 281-285, 2008
Rare A2ML1 variants confer susceptibility to otitis media
RL Santos-Cortez, CM Chiong, MR Reyes-Quintos, ML Tantoco, W X, ...
Nature Genetics 7 (8), 917-20, 2015
Genome sequencing and analysis of an emergent SARS-CoV-2 variant characterized by multiple spike protein mutations detected from the Central Visayas Region of the Philippines
FA Tablizo, KM Kim, CM Lapid, MJR Castro, MSL Yangzon, BA Maralit, ...
MedRxiv, 2021.03. 03.21252812, 2021
Genomics and health in the developing world
D Kumar
Oxford University Press, USA, 2012
FUT2 variants confer susceptibility to familial otitis media
RLP Santos-Cortez, CM Chiong, DN Frank, AF Ryan, APJ Giese, ...
The American Journal of Human Genetics 103 (5), 679-690, 2018
Low Density Lipoprotien Receptor (LDLR) Gene Mutation Among Filipinos with Familial Hypercholesterolemia
F Punzalan, R Sy, R Santos, E Cutiongco, S Gosengfiao, E Fadreguilan, ...
Journal of Atherosclerosis and Thrombosis 12 (5), 276-283, 2005
Screening for Congenital Hypothyroidism (CH) among Filipino newborn infants. Philippine Newborn Screening Study Group
C Fagela-Domingo, C Padilla, EM Cutiongco
The Southeast Asia Journal of Tropical Medicine and Public Health 30, 20-22, 1998
Middle ear microbiome differences in indigenous Filipinos with chronic otitis media due to a duplication in the A2ML1 gene
RLP Santos-Cortez, DS Hutchinson, NJ Ajami, MRT Reyes-Quintos, ...
Infectious Diseases of Poverty 5 (06), 86-94, 2016
Genetic counseling/consultation in South-East Asia: a report from the workshop at the 10th Asia Pacific conference human genetics
O Zayts, S Sarangi, MK Thong, ...
J Genet Couns 22 (6), 917-24, 2013
Genetic and environmental determinants of otitis media in an indigenous Filipino population
RLP Santos-Cortez, MRT Reyes-Quintos, MLC Tantoco, I Abbe, ...
Otolaryngology–Head and Neck Surgery 155 (5), 856-862, 2016
Genetics and genomic medicine in the Philippines
CD Padilla, EM Cutiongco‐de la Paz
Molecular genetics & genomic medicine 4 (5), 494, 2016
Birth defects ascertainment in the Philippines.
EM Cutiongco, JM Sia
The Southeast Asian Journal of Tropical Medicine and Public Health 34, 239-243, 2003
A genome wide pattern of population structure and admixture in peninsular Malaysia Malays
WI Hatin, AR Nur-Shafawati, A Etemad, W Jin, P Qin, S Xu, L Jin, SG Tan, ...
The HUGO journal 8, 1-18, 2014
Genetic Services and Testing in the Philippines
CD Padilla, E Cutiongco-de la Paz
Journal of Community Genetics 4 (3), 399-411, 2013
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