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1.
Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes.
Genet Epidemiol
; 46(3-4): 182-198, 2022 04.
Article
in English
| MEDLINE | ID: mdl-35191549
2.
Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts.
Hum Hered
; 2022 Feb 16.
Article
in English
| MEDLINE | ID: mdl-35172313
3.
Methylation changes in the peripheral blood of Filipinos with type 2 diabetes suggest spurious transcription initiation at TXNIP.
Hum Mol Genet
; 28(24): 4208-4218, 2019 12 15.
Article
in English
| MEDLINE | ID: mdl-31691802
4.
Estimating the annual dengue force of infection from the age of reporting primary infections across urban centres in endemic countries.
BMC Med
; 19(1): 217, 2021 09 30.
Article
in English
| MEDLINE | ID: mdl-34587957
5.
TRMU deficiency: A broad clinical spectrum responsive to cysteine supplementation.
Mol Genet Metab
; 132(2): 146-153, 2021 02.
Article
in English
| MEDLINE | ID: mdl-33485800
6.
The Influence of Sex and Ancestry on Three-Dimensional Palate Shape.
J Craniofac Surg
; 32(8): 2883-2887, 2021.
Article
in English
| MEDLINE | ID: mdl-34231514
7.
Parents of Children With Nonsyndromic Orofacial Clefting Show Altered Palate Shape.
Cleft Palate Craniofac J
; 58(7): 847-853, 2021 07.
Article
in English
| MEDLINE | ID: mdl-33111571
8.
Genome-Wide Association Study (GWAS) of dental caries in diverse populations.
BMC Oral Health
; 21(1): 377, 2021 07 26.
Article
in English
| MEDLINE | ID: mdl-34311721
9.
A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals.
Genet Epidemiol
; 43(6): 704-716, 2019 09.
Article
in English
| MEDLINE | ID: mdl-31172578
10.
A serological framework to investigate acute primary and post-primary dengue cases reporting across the Philippines.
BMC Med
; 18(1): 364, 2020 11 27.
Article
in English
| MEDLINE | ID: mdl-33243267
11.
Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts.
Genet Epidemiol
; 42(7): 664-672, 2018 10.
Article
in English
| MEDLINE | ID: mdl-30277614
12.
Asia Pacific Society of Human Genetics (APSHG) from conception to 2019: 13 years of collaboration to tackle congenital malformation and genetic disorders in Asia.
Am J Med Genet C Semin Med Genet
; 181(2): 155-165, 2019 06.
Article
in English
| MEDLINE | ID: mdl-31050142
13.
Training in clinical genetics and genetic counseling in Asia.
Am J Med Genet C Semin Med Genet
; 181(2): 177-186, 2019 06.
Article
in English
| MEDLINE | ID: mdl-31037827
14.
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.
Am J Hum Genet
; 98(4): 744-54, 2016 Apr 07.
Article
in English
| MEDLINE | ID: mdl-27018472
15.
Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts.
Am J Med Genet A
; 179(3): 467-474, 2019 03.
Article
in English
| MEDLINE | ID: mdl-30582786
16.
Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes.
Genet Epidemiol
; 41(8): 887-897, 2017 12.
Article
in English
| MEDLINE | ID: mdl-29124805
17.
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.
Hum Mol Genet
; 25(13): 2862-2872, 2016 07 01.
Article
in English
| MEDLINE | ID: mdl-27033726
18.
Newborn screening in the developing countries.
Curr Opin Pediatr
; 30(6): 734-739, 2018 12.
Article
in English
| MEDLINE | ID: mdl-30124582
19.
A Report on Ten Asia Pacific Countries on Current Status and Future Directions of the Genetic Counseling Profession: The Establishment of the Professional Society of Genetic Counselors in Asia.
J Genet Couns
; 27(1): 21-32, 2018 02.
Article
in English
| MEDLINE | ID: mdl-28699126
20.
Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate.
Hum Genet
; 136(3): 275-286, 2017 03.
Article
in English
| MEDLINE | ID: mdl-28054174