Detalhe da pesquisa
1.
Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios.
PLoS Genet
; 17(7): e1009584, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34242216
2.
Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios.
Am J Hum Genet
; 107(1): 124-136, 2020 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32574564
3.
Damaging Mutations in AFDN Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate.
Cleft Palate Craniofac J
; : 10556656221135926, 2022 Nov 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36384317
4.
Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants.
Genet Epidemiol
; 43(1): 37-49, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30246882
5.
Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21.
Hum Genet
; 139(2): 215-226, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31848685
6.
Evidence for SNP-SNP interaction identified through targeted sequencing of cleft case-parent trios.
Genet Epidemiol
; 41(3): 244-250, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28019042
7.
Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci.
Am J Hum Genet
; 96(3): 397-411, 2015 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25704602
8.
Identifying a Deletion Affecting Total Lung Capacity Among Subjects in the COPDGene Study Cohort.
Genet Epidemiol
; 40(1): 81-8, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26643968
9.
Gene-Gene Interaction Among WNT Genes for Oral Cleft in Trios.
Genet Epidemiol
; 39(5): 385-94, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25663376
10.
Admixture mapping identifies a quantitative trait locus associated with FEV1/FVC in the COPDGene Study.
Genet Epidemiol
; 38(7): 652-9, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25112515
11.
Novel evidence of association with nonsyndromic cleft lip with or without cleft palate was shown for single nucleotide polymorphisms in FOXF2 gene in an Asian population.
Birth Defects Res A Clin Mol Teratol
; 103(10): 857-62, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26278207
12.
A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13.
Hum Mol Genet
; 21(4): 947-57, 2012 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22080838
13.
Examining markers in 8q24 to explain differences in evidence for association with cleft lip with/without cleft palate between Asians and Europeans.
Genet Epidemiol
; 36(4): 392-9, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22508319
14.
X-linked markers in the Duchenne muscular dystrophy gene associated with oral clefts.
Eur J Oral Sci
; 121(2): 63-8, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23489894
15.
The FGF and FGFR Gene Family and Risk of Cleft Lip With or Without Cleft Palate.
Cleft Palate Craniofac J
; 50(1): 96-103, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22074045
16.
Clinically actionable secondary findings in 130 triads from sub-Saharan African families with non-syndromic orofacial clefts.
Mol Genet Genomic Med
; 11(10): e2237, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37496383
17.
Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate.
Genet Epidemiol
; 35(6): 469-78, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21618603
18.
Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts.
Am J Med Genet A
; 158A(4): 784-94, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22419666
19.
Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate.
Birth Defects Res A Clin Mol Teratol
; 94(2): 76-83, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22241686
20.
Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate.
Sci Rep
; 12(1): 11743, 2022 07 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35817949