Detalhe da pesquisa
1.
Genomic Analyses from Non-invasive Prenatal Testing Reveal Genetic Associations, Patterns of Viral Infections, and Chinese Population History.
Cell
; 175(2): 347-359.e14, 2018 10 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30290141
2.
The Born in Guangzhou Cohort Study enables generational genetic discoveries.
Nature
; 626(7999): 565-573, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38297123
3.
CMDB: the comprehensive population genome variation database of China.
Nucleic Acids Res
; 51(D1): D890-D895, 2023 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35871305
4.
Genome-wide association and Mendelian randomisation analysis among 30,699 Chinese pregnant women identifies novel genetic and molecular risk factors for gestational diabetes and glycaemic traits.
Diabetologia
; 67(4): 703-713, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38372780
5.
Sequencing and de novo assembly of 150 genomes from Denmark as a population reference.
Nature
; 548(7665): 87-91, 2017 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28746312
6.
Effect of Surface Morphology Changes on Optical Properties of Silicon Nanowire Arrays.
Sensors (Basel)
; 22(7)2022 Mar 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-35408069
7.
Identifying occult maternal malignancies from 1.93 million pregnant women undergoing noninvasive prenatal screening tests.
Genet Med
; 21(10): 2293-2302, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30976098
8.
Verifying the accuracy of self-reported smoking behavior in female volunteer soldiers.
Sci Rep
; 13(1): 3438, 2023 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36859420
9.
Initial whole-genome sequencing and analysis of the host genetic contribution to COVID-19 severity and susceptibility.
Cell Discov
; 6(1): 83, 2020 Nov 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33298875
10.
Validation of Self-reported Smoking with Urinary Cotinine Levels and Influence of Second-hand Smoke among Conscripts.
Sci Rep
; 7(1): 15462, 2017 11 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-29133917
11.
Stochastic anomaly of methylome but persistent SRY hypermethylation in disorder of sex development in canine somatic cell nuclear transfer.
Sci Rep
; 6: 31088, 2016 08 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27501986
12.
Discovery, genotyping and characterization of structural variation and novel sequence at single nucleotide resolution from de novo genome assemblies on a population scale.
Gigascience
; 4: 64, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26705468
13.
De novo assembly of a haplotype-resolved human genome.
Nat Biotechnol
; 33(6): 617-22, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26006006
14.
Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios.
Nat Commun
; 6: 5969, 2015 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25597990
15.
Rapid detection of structural variation in a human genome using nanochannel-based genome mapping technology.
Gigascience
; 3(1): 34, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25671094
16.
Systematic assessment of reduced representation bisulfite sequencing to human blood samples: A promising method for large-sample-scale epigenomic studies.
J Biotechnol
; 157(1): 1-6, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21763364
17.
Bisulfite sequencing reveals that Aspergillus flavus holds a hollow in DNA methylation.
PLoS One
; 7(1): e30349, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22276181
18.
Effectiveness of a smoking restriction policy on smoking behaviour in the military.
Addict Behav
; 67: 53-57, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28012966
19.
An atlas of DNA methylomes in porcine adipose and muscle tissues.
Nat Commun
; 3: 850, 2012 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-22617290
20.
Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly.
Nat Biotechnol
; 29(8): 723-30, 2011 Jul 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-21785424