Detalhe da pesquisa
1.
SPECC1L regulates palate development downstream of IRF6.
Hum Mol Genet
; 29(5): 845-858, 2020 03 27.
Artigo
Inglês
| MEDLINE | ID: mdl-31943082
2.
Facial Anthropometry Measurements Using Three-Dimensional Stereophotogrammetry Analysis Among Nigerians.
J Craniofac Surg
; 33(4): 1178-1181, 2022 Jun 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34310429
3.
Novel GRHL3 Variants in a South African Cohort With Cleft Lip and Palate.
Cleft Palate Craniofac J
; 59(9): 1125-1130, 2022 09.
Artigo
Inglês
| MEDLINE | ID: mdl-34459660
4.
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.
Artigo
Inglês
| MEDLINE | ID: mdl-34382870
5.
The TFAP2A-IRF6-GRHL3 genetic pathway is conserved in neurulation.
Hum Mol Genet
; 28(10): 1726-1737, 2019 05 15.
Artigo
Inglês
| MEDLINE | ID: mdl-30689861
6.
Genomic analyses in African populations identify novel risk loci for cleft palate.
Hum Mol Genet
; 28(6): 1038-1051, 2019 03 15.
Artigo
Inglês
| MEDLINE | ID: mdl-30452639
7.
Novel GREM1 Variations in Sub-Saharan African Patients With Cleft Lip and/or Cleft Palate.
Cleft Palate Craniofac J
; 55(5): 736-742, 2018 05.
Artigo
Inglês
| MEDLINE | ID: mdl-29489415
8.
Association of candidate gene polymorphisms with clinical subtypes of preterm birth in a Latin American population.
Pediatr Res
; 82(3): 554-559, 2017 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-28426651
9.
Polymorphisms in NR5A2, gene encoding liver receptor homolog-1 are associated with preterm birth.
Pediatr Res
; 79(5): 776-80, 2016 05.
Artigo
Inglês
| MEDLINE | ID: mdl-26761123
10.
Genetic variation in CYB5R3 is associated with methemoglobin levels in preterm infants receiving nitric oxide therapy.
Pediatr Res
; 77(3): 472-6, 2015 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-25521918
11.
Maternal coding variants in complement receptor 1 and spontaneous idiopathic preterm birth.
Hum Genet
; 132(8): 935-42, 2013 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-23591632
12.
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate.
Hum Mol Genet
; 18(24): 4879-96, 2009 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-19779022
13.
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.
Artigo
Inglês
| MEDLINE | ID: mdl-30141273
14.
The prevalence, penetrance, and expressivity of etiologic IRF6 variants in orofacial clefts patients from sub-Saharan Africa.
Mol Genet Genomic Med
; 5(2): 164-171, 2017 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-28361103
15.
Siglec-5 and Siglec-14 are polymorphic paired receptors that modulate neutrophil and amnion signaling responses to group B Streptococcus.
J Exp Med
; 211(6): 1231-42, 2014 Jun 02.
Artigo
Inglês
| MEDLINE | ID: mdl-24799499