Detalhe da pesquisa
1.
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
2.
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
3.
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
4.
ExsgRNA: reduce off-target efficiency by on-target mismatched sgRNA.
Brief Bioinform
; 23(5)2022 09 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35580855
5.
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
6.
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
7.
Surgical methods influence on the risk of anastomotic fistula after pancreaticoduodenectomy: a systematic review and network meta-analysis.
Surg Endosc
; 37(5): 3380-3397, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36627536
8.
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
9.
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
10.
Transcriptome-wide association study identifies multiple genes associated with childhood body mass index.
Int J Obes (Lond)
; 45(5): 1105-1113, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33627773
11.
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
12.
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
13.
Phosphorus Co-Existing in Water: A New Mechanism to Boost Boron Removal by Calcined Oyster Shell Powder.
Molecules
; 27(1)2021 Dec 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35011286
14.
Sex-specific SNP-SNP interaction analyses within topologically associated domains reveals ANGPT1 as a novel tumor suppressor gene for lung cancer.
Genes Chromosomes Cancer
; 59(1): 13-22, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31385379
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.
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
17.
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
18.
Regulatory element-based prediction identifies new susceptibility regulatory variants for osteoporosis.
Hum Genet
; 136(8): 963-974, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28634715
19.
Modeling circRNA expression pattern with integrated sequence and epigenetic features demonstrates the potential involvement of H3K79me2 in circRNA expression.
Bioinformatics
; 37(19): 3386, 2021 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34430971
20.
Association analyses of FGFR2 gene polymorphisms with femoral neck bone mineral density in Chinese Han population.
Mol Genet Genomics
; 290(2): 485-91, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25300516