Detalhe da pesquisa
1.
X chromosome associations with chronic obstructive pulmonary disease and related phenotypes: an X chromosome-wide association study.
Respir Res
; 24(1): 38, 2023 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36726148
2.
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
3.
A unifying framework for rare variant association testing in family-based designs, including higher criticism approaches, SKATs, and burden tests.
Bioinformatics
; 36(22-23): 5432-5438, 2021 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33367522
4.
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
5.
Genome-Wide Association Study of the Genetic Determinants of Emphysema Distribution.
Am J Respir Crit Care Med
; 195(6): 757-771, 2017 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27669027
6.
Exome Array Analysis Identifies a Common Variant in IL27 Associated with Chronic Obstructive Pulmonary Disease.
Am J Respir Crit Care Med
; 194(1): 48-57, 2016 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26771213
7.
A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes.
Am J Respir Crit Care Med
; 192(5): 559-69, 2015 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26030696
8.
Integrating Multiple Correlated Phenotypes for Genetic Association Analysis by Maximizing Heritability.
Hum Hered
; 79(2): 93-104, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26111731
9.
Statistical Methods in the Journal - An Update.
N Engl J Med
; 376(11): 1086-1087, 2017 03 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-28296608
10.
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.
BMC Genet
; 16: 138, 2015 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26634245
11.
Heritability of chronic obstructive pulmonary disease and related phenotypes in smokers.
Am J Respir Crit Care Med
; 188(8): 941-7, 2013 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23972146
12.
A new testing strategy to identify rare variants with either risk or protective effect on disease.
PLoS Genet
; 7(2): e1001289, 2011 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-21304886
13.
Genomic screening and replication using the same data set in family-based association testing.
Nat Genet
; 37(7): 683-91, 2005 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15937480
14.
Ozone exposure, vitamin C intake, and genetic susceptibility of asthmatic children in Mexico City: a cohort study.
Respir Res
; 14: 14, 2013 Feb 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-23379631
15.
Differentiating population stratification from genotyping error using family data.
Ann Hum Genet
; 76(1): 42-52, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22111716
16.
Tests for compositional epistasis under single interaction-parameter models.
Ann Hum Genet
; 75(1): 146-56, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20726965
17.
Estimating the effect of a predictor measured by two informants on a continuous outcome: a comparison of methods.
Epidemiology
; 22(3): 390-9, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21403520
18.
Gene-environment interaction tests for family studies with quantitative phenotypes: A review and extension to longitudinal measures.
Hum Genomics
; 4(5): 302-26, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20650819
19.
Combining disease models to test for gene-environment interaction in nuclear families.
Biometrics
; 67(4): 1260-70, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21401569
20.
Alternative methods for testing treatment effects on the basis of multiple outcomes: simulation and case study.
Stat Med
; 30(16): 1917-32, 2011 Jul 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-21538986