Detalhe da pesquisa
1.
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Nature
; 616(7958): 755-763, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37046083
2.
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program.
Am J Hum Genet
; 109(5): 857-870, 2022 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35385699
3.
A statistical physics approach for disease module detection.
Genome Res
; 32(10): 1918-1929, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36220609
4.
A robust and adaptive framework for interaction testing in quantitative traits between multiple genetic loci and exposure variables.
PLoS Genet
; 18(11): e1010464, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36383614
5.
Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence data.
Hum Mol Genet
; 31(22): 3873-3885, 2022 11 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35766891
6.
Association of clonal hematopoiesis with chronic obstructive pulmonary disease.
Blood
; 139(3): 357-368, 2022 01 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34855941
7.
Genome-wide association analysis of COVID-19 mortality risk in SARS-CoV-2 genomes identifies mutation in the SARS-CoV-2 spike protein that colocalizes with P.1 of the Brazilian strain.
Genet Epidemiol
; 45(7): 685-693, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34159627
8.
C FTR variants are associated with chronic bronchitis in smokers.
Eur Respir J
; 60(2)2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34996830
9.
A polygenic risk score and age of diagnosis of COPD.
Eur Respir J
; 60(3)2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35115341
10.
Interstitial lung abnormalities are associated with decreased mean telomere length.
Eur Respir J
; 60(2)2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35115336
11.
Multiethnic genome-wide and HLA association study of total serum IgE level.
J Allergy Clin Immunol
; 148(6): 1589-1595, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34536413
12.
Connecting COPD GWAS Genes: FAM13A Controls TGFß2 Secretion by Modulating AP-3 Transport.
Am J Respir Cell Mol Biol
; 65(5): 532-543, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34166600
13.
Statistical considerations for the analysis of massively parallel reporter assays data.
Genet Epidemiol
; 44(7): 785-794, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32681690
14.
Whole exome sequencing analysis in severe chronic obstructive pulmonary disease.
Hum Mol Genet
; 27(21): 3801-3812, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30060175
15.
Identification of Functional Variants in the FAM13A Chronic Obstructive Pulmonary Disease Genome-Wide Association Study Locus by Massively Parallel Reporter Assays.
Am J Respir Crit Care Med
; 199(1): 52-61, 2019 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30079747
16.
Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees.
Am J Hum Genet
; 99(4): 846-859, 2016 Oct 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27666371
17.
Whole-Genome Sequencing in Severe Chronic Obstructive Pulmonary Disease.
Am J Respir Cell Mol Biol
; 59(5): 614-622, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29949718
18.
Gene-based segregation method for identifying rare variants in family-based sequencing studies.
Genet Epidemiol
; 41(4): 309-319, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28191685
19.
FARVATX: Family-Based Rare Variant Association Test for X-Linked Genes.
Genet Epidemiol
; 40(6): 475-85, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27325607
20.
Family-Based Rare Variant Association Analysis: A Fast and Efficient Method of Multivariate Phenotype Association Analysis.
Genet Epidemiol
; 40(6): 502-11, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27312886