Detalhe da pesquisa
1.
Quality control and analytic best practices for testing genetic models of sex differences in large populations.
Cell
; 186(10): 2044-2061, 2023 05 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37172561
2.
Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep Apnea.
Am J Respir Crit Care Med
; 206(10): 1271-1280, 2022 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35822943
3.
Rare coding variants in RCN3 are associated with blood pressure.
BMC Genomics
; 23(1): 148, 2022 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35183128
4.
Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level.
Am J Hum Genet
; 105(5): 1057-1068, 2019 11 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31668705
5.
Detecting fitness epistasis in recently admixed populations with genome-wide data.
BMC Genomics
; 21(1): 476, 2020 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32652930
6.
Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure.
PLoS Genet
; 13(3): e1006678, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28346479
7.
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data.
Hum Genet
; 138(2): 199-210, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30671673
8.
Big Data Analytics for Genomic Medicine.
Int J Mol Sci
; 18(2)2017 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28212287
9.
Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.
Hypertension
; 79(8): 1656-1667, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35652341
10.
Variant Interpretation for Cancer (VIC): a computational tool for assessing clinical impacts of somatic variants.
Genome Med
; 11(1): 53, 2019 08 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-31443733
11.
Characterization of APOE Christchurch carriers in 455,306 UK Biobank participants.
Mol Neurodegener
; 18(1): 92, 2023 Nov 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38017580
12.
Multivariate Analysis of Anthropometric Traits Using Summary Statistics of Genome-Wide Association Studies from GIANT Consortium.
PLoS One
; 11(10): e0163912, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27701450
13.
SparkText: Biomedical Text Mining on Big Data Framework.
PLoS One
; 11(9): e0162721, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27685652
14.
Pathogenic Mutations in Cancer-Predisposing Genes: A Survey of 300 Patients with Whole-Genome Sequencing and Lifetime Electronic Health Records.
PLoS One
; 11(12): e0167847, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27930734