Detalhe da pesquisa
1.
Genomic insights into the formation of human populations in East Asia.
Nature;
591(7850): 413-419, 2021 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33618348
2.
Enhancer variants on chromosome 2p14 regulating SPRED2 and ACTR2 act as a signal amplifier to protect against rheumatoid arthritis.
Am J Hum Genet;
110(4): 625-637, 2023 04 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36924774
3.
High-throughput functional dissection of noncoding SNPs with biased allelic enhancer activity for insulin resistance-relevant phenotypes.
Am J Hum Genet;
110(8): 1266-1288, 2023 08 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37506691
4.
Transcriptome-wide association study identifies multiple genes and pathways associated with thyroid function.
Hum Mol Genet;
31(11): 1871-1883, 2022 06 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34962261
5.
ExsgRNA: reduce off-target efficiency by on-target mismatched sgRNA.
Brief Bioinform;
23(5)2022 09 20.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35580855
6.
Two-sample Mendelian randomization analysis reveals causal relationships between blood lipids and venous thromboembolism.
Haematologica;
2024 May 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38695130
7.
Multi-tissue transcriptome-wide association study reveals susceptibility genes and drug targets for insulin resistance-relevant phenotypes.
Diabetes Obes Metab;
26(1): 135-147, 2024 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37779362
8.
Assessment of bidirectional relationships between brain imaging-derived phenotypes and stroke: a Mendelian randomization study.
BMC Med;
21(1): 271, 2023 07 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37491271
9.
LDBlockShow: a fast and convenient tool for visualizing linkage disequilibrium and haplotype blocks based on variant call format files.
Brief Bioinform;
22(4)2021 07 20.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33126247
10.
Application of Hi-C technology in three-dimensional genomics research and disease pathogenesis analysis.
Yi Chuan;
45(4): 279-294, 2023 Apr 20.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37077163
11.
Causal Associations Between Blood Lipids and COVID-19 Risk: A Two-Sample Mendelian Randomization Study.
Arterioscler Thromb Vasc Biol;
41(11): 2802-2810, 2021 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34496635
12.
An Osteoporosis Risk SNP at 1p36.12 Acts as an Allele-Specific Enhancer to Modulate LINC00339 Expression via Long-Range Loop Formation.
Am J Hum Genet;
102(5): 776-793, 2018 05 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29706346
13.
Integrating regulatory features data for prediction of functional disease-associated SNPs.
Brief Bioinform;
20(1): 26-32, 2019 01 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28968709
14.
Modeling circRNA expression pattern with integrated sequence and epigenetic features demonstrates the potential involvement of H3K79me2 in circRNA expression.
Bioinformatics;
36(18): 4739-4748, 2020 09 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32539144
15.
PopLDdecay: a fast and effective tool for linkage disequilibrium decay analysis based on variant call format files.
Bioinformatics;
35(10): 1786-1788, 2019 05 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30321304
16.
Genetic substructure and admixture of Mongolians and Kazakhs inferred from genome-wide array genotyping.
Ann Hum Biol;
47(7-8): 620-628, 2020 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33059477
17.
The osteoporosis susceptible SNP rs4325274 remotely regulates the SOX6 gene through enhancers.
Yi Chuan;
42(9): 889-897, 2020 Sep 20.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32952123
18.
Detecting epistasis within chromatin regulatory circuitry reveals CAND2 as a novel susceptibility gene for obesity.
Int J Obes (Lond);
43(3): 450-456, 2019 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29717274
19.
A functional SNP regulated by miR-196a-3p in the 3'UTR of FGF2 is associated with bone mineral density in the Chinese population.
Hum Mutat;
38(6): 725-735, 2017 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28317323
20.
Identification of a novel FGFRL1 MicroRNA target site polymorphism for bone mineral density in meta-analyses of genome-wide association studies.
Hum Mol Genet;
24(16): 4710-27, 2015 Aug 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25941324