Detalhe da pesquisa
1.
Whole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium.
Hum Mol Genet
; 2024 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38747556
2.
RAREsim: A simulation method for very rare genetic variants.
Am J Hum Genet
; 109(4): 680-691, 2022 04 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35298919
3.
Family history aggregation unit-based tests to detect rare genetic variant associations with application to the Framingham Heart Study.
Am J Hum Genet
; 109(4): 738-749, 2022 04 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35316615
4.
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
5.
SharePro: an accurate and efficient genetic colocalization method accounting for multiple causal signals.
Bioinformatics
; 40(5)2024 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38688586
6.
Genetically Predicted Body Mass Index and Mortality in COPD.
Am J Respir Crit Care Med
; 2024 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38471013
7.
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
8.
Genome-wide association study of preserved ratio impaired spirometry (PRISm).
Eur Respir J
; 63(1)2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38097206
9.
Investigating Associations of Omega-3 Fatty Acids, Lung Function Decline, and Airway Obstruction.
Am J Respir Crit Care Med
; 208(8): 846-857, 2023 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37470492
10.
A Polygenic Risk Score for Idiopathic Pulmonary Fibrosis and Interstitial Lung Abnormalities.
Am J Respir Crit Care Med
; 208(7): 791-801, 2023 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37523715
11.
Key variants via the Alzheimer's Disease Sequencing Project whole genome sequence data.
Alzheimers Dement
; 20(5): 3290-3304, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38511601
12.
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts.
Am J Hum Genet
; 106(1): 112-120, 2020 01 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31883642
13.
The relationship between interstitial lung abnormalities, mortality, and multimorbidity: a cohort study.
Thorax
; 78(6): 559-565, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35777957
14.
Bronchial epithelial gene expression and interstitial lung abnormalities.
Respir Res
; 24(1): 245, 2023 Oct 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37817229
15.
Identifying important gene signatures of BMI using network structure-aided nonparametric quantile regression.
Stat Med
; 42(10): 1625-1639, 2023 05 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36822218
16.
Host and gut microbial tryptophan metabolism and type 2 diabetes: an integrative analysis of host genetics, diet, gut microbiome and circulating metabolites in cohort studies.
Gut
; 71(6): 1095-1105, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34127525
17.
JEM: A joint test to estimate the effect of multiple genetic variants on DNA methylation.
Genet Epidemiol
; 45(3): 280-292, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33038041
18.
Assisted clustering of gene expression data using regulatory data from partially overlapping sets of individuals.
BMC Genomics
; 23(1): 819, 2022 Dec 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36496393
19.
Leveraging family history in genetic association analyses of binary traits.
BMC Genomics
; 23(1): 678, 2022 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36182916
20.
Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program.
Am J Hum Genet
; 105(4): 706-718, 2019 10 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31564435