Detalhe da pesquisa
1.
Powerful and robust inference of complex phenotypes' causal genes with dependent expression quantitative loci by a median-based Mendelian randomization.
Am J Hum Genet
; 109(5): 838-856, 2022 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35460606
2.
Noncoding SNP at rs1663689 represses ADGRG6 via interchromosomal interaction and reduces lung cancer progression.
EMBO Rep
; 24(7): e56212, 2023 Jul 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37154297
3.
QTLbase2: an enhanced catalog of human quantitative trait loci on extensive molecular phenotypes.
Nucleic Acids Res
; 51(D1): D1122-D1128, 2023 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36330927
4.
ADAR1 links R-loop homeostasis to ATR activation in replication stress response.
Nucleic Acids Res
; 51(21): 11668-11687, 2023 Nov 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37831098
5.
Target genes regulated by CLEC16A intronic region associated with common variable immunodeficiency.
J Allergy Clin Immunol
; 2024 Jan 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38191060
6.
Shared molecular mechanisms and transdiagnostic potential of neurodevelopmental disorders and immune disorders.
Brain Behav Immun
; 119: 767-780, 2024 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38677625
7.
webTWAS: a resource for disease candidate susceptibility genes identified by transcriptome-wide association study.
Nucleic Acids Res
; 50(D1): D1123-D1130, 2022 01 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34669946
8.
VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseases.
Nucleic Acids Res
; 50(D1): D1408-D1416, 2022 01 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34570217
9.
Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases.
Nucleic Acids Res
; 50(6): e34, 2022 04 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34931221
10.
Hippocampal transcriptome-wide association study and neurobiological pathway analysis for Alzheimer's disease.
PLoS Genet
; 17(2): e1009363, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33630843
11.
eaQTLdb: An atlas of enhancer activity quantitative trait loci across cancer types.
Int J Cancer
; 153(1): 111-119, 2023 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36840614
12.
Genome-wide analysis of genetic pleiotropy and causal genes across three age-related ocular disorders.
Hum Genet
; 142(4): 507-522, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36917350
13.
Ultrafast and scalable variant annotation and prioritization with big functional genomics data.
Genome Res
; 30(12): 1789-1801, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33060171
14.
A causal association of ANKRD37 with human hippocampal volume.
Mol Psychiatry
; 27(11): 4432-4445, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36195640
15.
Methods and resources to access mutation-dependent effects on cancer drug treatment.
Brief Bioinform
; 21(6): 1886-1903, 2020 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31750520
16.
vSampler: fast and annotation-based matched variant sampling tool.
Bioinformatics
; 37(13): 1915-1917, 2021 07 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33270826
17.
HRP2-DPF3a-BAF complex coordinates histone modification and chromatin remodeling to regulate myogenic gene transcription.
Nucleic Acids Res
; 48(12): 6563-6582, 2020 07 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32459350
18.
QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes.
Nucleic Acids Res
; 48(D1): D983-D991, 2020 01 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31598699
19.
CAUSALdb: a database for disease/trait causal variants identified using summary statistics of genome-wide association studies.
Nucleic Acids Res
; 48(D1): D807-D816, 2020 01 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31691819
20.
CHIMGEN: a Chinese imaging genetics cohort to enhance cross-ethnic and cross-geographic brain research.
Mol Psychiatry
; 25(3): 517-529, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31827248