Search details
1.
Limb development genes underlie variation in human fingerprint patterns.
Cell
; 185(1): 95-112.e18, 2022 01 06.
Article
in English
| MEDLINE | ID: mdl-34995520
2.
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.
Article
in English
| MEDLINE | ID: mdl-34242216
3.
Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.
PLoS Genet
; 17(8): e1009695, 2021 08.
Article
in English
| MEDLINE | ID: mdl-34411106
4.
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
5.
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes.
Hum Genet
; 142(10): 1531-1541, 2023 Oct.
Article
in English
| MEDLINE | ID: mdl-37676273
6.
Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios.
Am J Hum Genet
; 107(1): 124-136, 2020 07 02.
Article
in English
| MEDLINE | ID: mdl-32574564
7.
FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research.
Development
; 147(18)2020 09 21.
Article
in English
| MEDLINE | ID: mdl-32958507
8.
Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting.
Genet Med
; 25(10): 100918, 2023 10.
Article
in English
| MEDLINE | ID: mdl-37330696
9.
Using data-driven phenotyping to investigate the impact of sex on 3D human facial surface morphology.
J Anat
; 243(2): 274-283, 2023 08.
Article
in English
| MEDLINE | ID: mdl-36943032
10.
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?
Am J Med Genet A
; 191(10): 2558-2570, 2023 10.
Article
in English
| MEDLINE | ID: mdl-37350193
11.
A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature.
Am J Med Genet A
; 191(5): 1227-1239, 2023 05.
Article
in English
| MEDLINE | ID: mdl-36751037
12.
Mother's Experience of Conflict Within Their Family Social Network when Advocating for Children's oral Health.
Matern Child Health J
; 27(1): 151-157, 2023 Jan.
Article
in English
| MEDLINE | ID: mdl-36352279
13.
Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts.
Hum Hered
; 2022 Feb 16.
Article
in English
| MEDLINE | ID: mdl-35172313
14.
A Retrospective and Prospective Cohort Study Comparing Pediatric Patients With Cleft Lip and Palate From the United States and Guatemala.
J Craniofac Surg
; 34(7): 1978-1984, 2023 Oct 01.
Article
in English
| MEDLINE | ID: mdl-37449578
15.
FAT4 identified as a potential modifier of orofacial cleft laterality.
Genet Epidemiol
; 45(7): 721-735, 2021 10.
Article
in English
| MEDLINE | ID: mdl-34130359
16.
Tools for standardized data collection: Speech, Language, and Hearing measurement protocols in the PhenX Toolkit.
Ann Hum Genet
; 86(1): 45-51, 2022 01.
Article
in English
| MEDLINE | ID: mdl-34582045
17.
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
18.
Correction: Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay.
PLoS Genet
; 15(6): e1008230, 2019 Jun.
Article
in English
| MEDLINE | ID: mdl-31233495
19.
Facial Anthropometry Measurements Using Three-Dimensional Stereophotogrammetry Analysis Among Nigerians.
J Craniofac Surg
; 33(4): 1178-1181, 2022 Jun 01.
Article
in English
| MEDLINE | ID: mdl-34310429
20.
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