Detalhe da pesquisa
1.
Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts.
Genet Epidemiol
; 42(7): 664-672, 2018 10.
Artigo
Inglês
| MEDLINE | ID: mdl-30277614
2.
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.
Artigo
Inglês
| MEDLINE | ID: mdl-27018472
3.
Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts.
Am J Med Genet A
; 179(3): 467-474, 2019 03.
Artigo
Inglês
| MEDLINE | ID: mdl-30582786
4.
Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes.
Genet Epidemiol
; 41(8): 887-897, 2017 12.
Artigo
Inglês
| MEDLINE | ID: mdl-29124805
5.
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.
Artigo
Inglês
| MEDLINE | ID: mdl-27033726
6.
Induction and activation of antiviral enzyme 2',5'-oligoadenylate synthetase by in vitro transcribed insulin mRNA and other cellular RNAs.
Mol Biol Rep
; 39(7): 7813-22, 2012 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-22547268
7.
Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results.
Hum Hered
; 68(3): 151-70, 2009.
Artigo
Inglês
| MEDLINE | ID: mdl-19521098
8.
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate.
N Engl J Med
; 351(8): 769-80, 2004 Aug 19.
Artigo
Inglês
| MEDLINE | ID: mdl-15317890
9.
X-chromosome inactivation patterns in monozygotic twins and sib pairs discordant for nonsyndromic cleft lip and/or palate.
Am J Med Genet A
; 143A(24): 3267-72, 2007 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-18000982
10.
OAS1 splice site polymorphism controlling antiviral enzyme activity influences susceptibility to type 1 diabetes.
Diabetes
; 54(5): 1588-91, 2005 May.
Artigo
Inglês
| MEDLINE | ID: mdl-15855350
11.
Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts.
Genetics
; 197(3): 1039-44, 2014 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-24793288
12.
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.
Nat Genet
; 42(6): 525-9, 2010 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-20436469
13.
The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P.
Eur J Hum Genet
; 17(6): 774-84, 2009 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-19092777
14.
Variation in antiviral 2',5'-oligoadenylate synthetase (2'5'AS) enzyme activity is controlled by a single-nucleotide polymorphism at a splice-acceptor site in the OAS1 gene.
Am J Hum Genet
; 76(4): 623-33, 2005 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-15732009
15.
Confirmation of a dyslexia susceptibility locus on chromosome 1p34-p36 in a set of 100 Canadian families.
Am J Med Genet B Neuropsychiatr Genet
; 127B(1): 117-24, 2004 May 15.
Artigo
Inglês
| MEDLINE | ID: mdl-15108193
16.
Chromosome 17: gene mapping studies of cleft lip with or without cleft palate in Chinese families.
Cleft Palate Craniofac J
; 40(1): 71-9, 2003 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-12498608
17.
Genome scan for loci involved in nonsyndromic cleft lip with or without cleft palate in families from West Bengal, India.
Am J Med Genet A
; 130A(3): 265-71, 2004 Oct 15.
Artigo
Inglês
| MEDLINE | ID: mdl-15378549
18.
Genome-scan for loci involved in cleft lip with or without cleft palate in consanguineous families from Turkey.
Am J Med Genet A
; 126A(2): 111-22, 2004 Apr 15.
Artigo
Inglês
| MEDLINE | ID: mdl-15057975
19.
A dyslexia susceptibility locus (DYX7) linked to dopamine D4 receptor (DRD4) region on chromosome 11p15.5.
Am J Med Genet B Neuropsychiatr Genet
; 125B(1): 112-9, 2004 Feb 15.
Artigo
Inglês
| MEDLINE | ID: mdl-14755455
20.
Absence of age effect on meiotic recombination between human X and Y chromosomes.
Am J Hum Genet
; 71(2): 254-61, 2002 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-12046006