Detalhe da pesquisa
1.
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.
Am J Hum Genet
; 110(10): 1704-1717, 2023 10 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37802043
2.
Multivariate analysis of a missense variant in CREBRF reveals associations with measures of adiposity in people of Polynesian ancestries.
Genet Epidemiol
; 47(1): 105-118, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36352773
3.
Exploratory assessment of the effect of systemic administration of soluble glycoprotein 130 on cognitive performance and chemokine levels in a mouse model of experimental traumatic brain injury.
J Neuroinflammation
; 21(1): 149, 2024 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38840141
4.
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes.
Hum Genet
; 142(10): 1531-1541, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37676273
5.
Association of rs9939609 in FTO with BMI among Polynesian peoples living in Aotearoa New Zealand and other Pacific nations.
J Hum Genet
; 68(7): 463-468, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-36864286
6.
Epilepsy panel testing criteria: A clinical assessment.
J Genet Couns
; 2023 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37246482
7.
FAT4 identified as a potential modifier of orofacial cleft laterality.
Genet Epidemiol
; 45(7): 721-735, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34130359
8.
Correction: Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay.
PLoS Genet
; 15(6): e1008230, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-31233495
9.
Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels.
J Hum Genet
; 66(2): 111-121, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-32759990
10.
Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay.
PLoS Genet
; 14(1): e1007168, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29357356
11.
A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals.
Genet Epidemiol
; 43(6): 704-716, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31172578
12.
Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment.
Am J Hum Genet
; 101(6): 913-924, 2017 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29198719
13.
A missense variant in CREBRF is associated with taller stature in Samoans.
Am J Hum Biol
; 32(6): e23414, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32190945
14.
Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts.
Genet Epidemiol
; 42(7): 664-672, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30277614
15.
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
em Inglês
| MEDLINE | ID: mdl-27018472
16.
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
em Inglês
| MEDLINE | ID: mdl-30582786
17.
Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes.
Genet Epidemiol
; 41(8): 887-897, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29124805
18.
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
em Inglês
| MEDLINE | ID: mdl-27033726
19.
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
20.
Exploring the genomic basis of early childhood caries: a pilot study.
Int J Paediatr Dent
; 28(2): 217-225, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29057527