Search details
1.
Shared genetic risk between major orofacial cleft phenotypes in an African population.
Genet Epidemiol
; 2024 Apr 18.
Article
in English
| MEDLINE | ID: mdl-38634654
2.
Perceptions and beliefs of community gatekeepers about genomic risk information in African cleft research.
BMC Public Health
; 24(1): 507, 2024 Feb 17.
Article
in English
| MEDLINE | ID: mdl-38365612
3.
Variant analyses of candidate genes in orofacial clefts in multi-ethnic populations.
Oral Dis
; 28(7): 1921-1935, 2022 Oct.
Article
in English
| MEDLINE | ID: mdl-34061439
4.
Novel GRHL3 Variants in a South African Cohort With Cleft Lip and Palate.
Cleft Palate Craniofac J
; 59(9): 1125-1130, 2022 09.
Article
in English
| MEDLINE | ID: mdl-34459660
5.
Genome-Wide Scan for Parent-of-Origin Effects in a sub-Saharan African Cohort With Nonsyndromic Cleft Lip and/or Cleft Palate (CL/P).
Cleft Palate Craniofac J
; 59(7): 841-851, 2022 07.
Article
in English
| MEDLINE | ID: mdl-34382870
6.
Damaging Mutations in AFDN Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate.
Cleft Palate Craniofac J
; : 10556656221135926, 2022 Nov 16.
Article
in English
| MEDLINE | ID: mdl-36384317
7.
Six2 regulates Pax9 expression, palatogenesis and craniofacial bone formation.
Dev Biol
; 458(2): 246-256, 2020 02 15.
Article
in English
| MEDLINE | ID: mdl-31765609
8.
Genomic analyses in African populations identify novel risk loci for cleft palate.
Hum Mol Genet
; 28(6): 1038-1051, 2019 03 15.
Article
in English
| MEDLINE | ID: mdl-30452639
9.
Parents and Provider Perspectives on the Return of Genomic Findings for Cleft Families in Africa.
AJOB Empir Bioeth
; 15(2): 133-146, 2024.
Article
in English
| MEDLINE | ID: mdl-38236653
10.
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate.
HGG Adv
; 4(4): 100234, 2023 10 12.
Article
in English
| MEDLINE | ID: mdl-37719664
11.
Investigating the relationship between cancer and orofacial clefts using GWAS significant loci for cancers: A case-control and case-triad study.
Front Oral Health
; 3: 915361, 2022.
Article
in English
| MEDLINE | ID: mdl-35990505
12.
Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate.
Sci Rep
; 12(1): 11743, 2022 07 11.
Article
in English
| MEDLINE | ID: mdl-35817949
13.
Co-occurrence of orofacial clefts and clubfoot phenotypes in a sub-Saharan African cohort: Whole-exome sequencing implicates multiple syndromes and genes.
Mol Genet Genomic Med
; 9(4): e1655, 2021 04.
Article
in English
| MEDLINE | ID: mdl-33719213
14.
Non-random distribution of deleterious mutations in the DNA and protein-binding domains of IRF6 are associated with Van Der Woude syndrome.
Mol Genet Genomic Med
; 8(8): e1355, 2020 08.
Article
in English
| MEDLINE | ID: mdl-32558391
15.
Missense Pathogenic variants in KIF4A Affect Dental Morphogenesis Resulting in X-linked Taurodontism, Microdontia and Dens-Invaginatus.
Front Genet
; 10: 800, 2019.
Article
in English
| MEDLINE | ID: mdl-31616463
16.
Identification of paternal uniparental disomy on chromosome 22 and a de novo deletion on chromosome 18 in individuals with orofacial clefts.
Mol Genet Genomic Med
; 6(6): 924-932, 2018 11.
Article
in English
| MEDLINE | ID: mdl-30141273
17.
Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate.
Birth Defects Res
; 109(1): 27-37, 2017 01 20.
Article
in English
| MEDLINE | ID: mdl-28029220
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