Detalhe da pesquisa
1.
Human nonsense-mediated RNA decay initiates widely by endonucleolysis and targets snoRNA host genes.
Genes Dev
; 28(22): 2498-517, 2014 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25403180
2.
Consortium-based genome-wide meta-analysis for childhood dental caries traits.
Hum Mol Genet
; 27(17): 3113-3127, 2018 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29931343
3.
A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma.
PLoS Genet
; 13(3): e1006659, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28273074
4.
A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria.
Diabetologia
; 62(2): 292-305, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30547231
5.
Fish Oil-Derived Fatty Acids in Pregnancy and Wheeze and Asthma in Offspring.
N Engl J Med
; 375(26): 2530-9, 2016 12 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-28029926
6.
Cadherin-related Family Member 3 Genetics and Rhinovirus C Respiratory Illnesses.
Am J Respir Crit Care Med
; 197(5): 589-594, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29121479
7.
UPF2-Dependent Nonsense-Mediated mRNA Decay Pathway Is Essential for Spermatogenesis by Selectively Eliminating Longer 3'UTR Transcripts.
PLoS Genet
; 12(5): e1005863, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27149259
8.
Corrigendum: Human nonsense-mediated RNA decay initiates widely by endonucleolysis and targets snoRNA host genes.
Genes Dev
; 30(9): 1128-34, 2016 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27151980
9.
A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.
Hum Mol Genet
; 25(18): 4127-4142, 2016 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27559109
10.
NKG2D gene variation and susceptibility to viral bronchiolitis in childhood.
Pediatr Res
; 84(3): 451-457, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29967528
11.
Shared genetic variants suggest common pathways in allergy and autoimmune diseases.
J Allergy Clin Immunol
; 140(3): 771-781, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28188724
12.
A novel common variant in DCST2 is associated with length in early life and height in adulthood.
Hum Mol Genet
; 24(4): 1155-68, 2015 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25281659
13.
C/EBPα is required for long-term self-renewal and lineage priming of hematopoietic stem cells and for the maintenance of epigenetic configurations in multipotent progenitors.
PLoS Genet
; 10(1): e1004079, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24415956
14.
Temporal mapping of CEBPA and CEBPB binding during liver regeneration reveals dynamic occupancy and specific regulatory codes for homeostatic and cell cycle gene batteries.
Genome Res
; 23(4): 592-603, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23403033
15.
UBL5 is essential for pre-mRNA splicing and sister chromatid cohesion in human cells.
EMBO Rep
; 15(9): 956-64, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25092792
16.
Amplification of pico-scale DNA mediated by bacterial carrier DNA for small-cell-number transcription factor ChIP-seq.
BMC Genomics
; 16: 46, 2015 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25652644
17.
spliceR: an R package for classification of alternative splicing and prediction of coding potential from RNA-seq data.
BMC Bioinformatics
; 15: 81, 2014 Mar 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-24655717
18.
CDHR3 gene variation and childhood bronchiolitis.
J Allergy Clin Immunol
; 140(5): 1469-1471.e7, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28782631
19.
The trans-ancestral genomic architecture of glycemic traits.
Nat Genet
; 53(6): 840-860, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34059833
20.
Distinct immune phenotypes in infants developing asthma during childhood.
Sci Transl Med
; 12(529)2020 02 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32024797