Suppr超能文献

相似文献

1
Pathway analysis for genome-wide genetic variation data: Analytic principles, latest developments, and new opportunities.
J Genet Genomics. 2021 Mar 20;48(3):173-183. doi: 10.1016/j.jgg.2021.01.007. Epub 2021 Feb 26.
2
Genomics meets proteomics: identifying the culprits in disease.
Hum Genet. 2014 Jun;133(6):689-700. doi: 10.1007/s00439-013-1376-2. Epub 2013 Oct 18.
3
Systems Genetics for Mechanistic Discovery in Heart Diseases.
Circ Res. 2020 Jun 5;126(12):1795-1815. doi: 10.1161/CIRCRESAHA.119.315863. Epub 2020 Jun 4.
4
HGV2011: personalized genomic medicine meets the incidentalome.
Hum Mutat. 2012 Mar;33(3):582-5. doi: 10.1002/humu.22008. Epub 2012 Jan 17.
5
Functional genomics complements quantitative genetics in identifying disease-gene associations.
PLoS Comput Biol. 2010 Nov 11;6(11):e1000991. doi: 10.1371/journal.pcbi.1000991.
7
qtlXplorer: an online systems genetics browser in the Eucalyptus Genome Integrative Explorer (EucGenIE).
BMC Bioinformatics. 2021 Dec 15;22(1):595. doi: 10.1186/s12859-021-04514-9.
8
Research progress of plant population genomics based on high-throughput sequencing.
Yi Chuan. 2016 Aug;38(8):688-99. doi: 10.16288/j.yczz.16-061.
9
Multi-omics study for interpretation of genome-wide association study.
J Hum Genet. 2021 Jan;66(1):3-10. doi: 10.1038/s10038-020-00842-5. Epub 2020 Sep 18.
10
Molecular mechanisms underlying noncoding risk variations in psychiatric genetic studies.
Mol Psychiatry. 2017 Apr;22(4):497-511. doi: 10.1038/mp.2016.241. Epub 2017 Jan 3.

引用本文的文献

1
Plasma microRNAs to Select Optimal Patients for Antibody Production from Anti-Addiction Vaccines.
Vaccines (Basel). 2025 Feb 13;13(2):181. doi: 10.3390/vaccines13020181.
2
BridGE: a pathway-based analysis tool for detecting genetic interactions from GWAS.
Nat Protoc. 2024 May;19(5):1400-1435. doi: 10.1038/s41596-024-00954-8. Epub 2024 Mar 21.
3
SPP2 plays a role in the tumorigenesis of hepatocellular carcinoma: A bioinformatic based analysis.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2023 Dec 28;48(12):1779-1792. doi: 10.11817/j.issn.1672-7347.2023.230077.
4
bioGWAS: A Simple and Flexible Tool for Simulating GWAS Datasets.
Biology (Basel). 2023 Dec 23;13(1):0. doi: 10.3390/biology13010010.
5
Polymorphism of IL-12/IL-23 axis is associated with coronary heart disease.
J Cell Mol Med. 2024 Feb;28(3):e18100. doi: 10.1111/jcmm.18100. Epub 2024 Jan 8.
6
Stage-specific coexpression network analysis of Myc in cohorts of renal cancer.
Sci Rep. 2023 Jul 22;13(1):11848. doi: 10.1038/s41598-023-38681-x.

本文引用的文献

1
H-MAGMA, inheriting a shaky statistical foundation, yields excess false positives.
Ann Hum Genet. 2021 May;85(3-4):97-100. doi: 10.1111/ahg.12412. Epub 2020 Dec 29.
2
The GTEx Consortium atlas of genetic regulatory effects across human tissues.
Science. 2020 Sep 11;369(6509):1318-1330. doi: 10.1126/science.aaz1776.
3
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
Cell. 2020 Sep 3;182(5):1214-1231.e11. doi: 10.1016/j.cell.2020.08.008.
4
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease.
Nature. 2020 Aug;584(7822):619-623. doi: 10.1038/s41586-020-2436-0. Epub 2020 Jun 24.
5
Beyond SNP heritability: Polygenicity and discoverability of phenotypes estimated with a univariate Gaussian mixture model.
PLoS Genet. 2020 May 19;16(5):e1008612. doi: 10.1371/journal.pgen.1008612. eCollection 2020 May.
6
Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders.
Mol Psychiatry. 2021 Jun;26(6):2070-2081. doi: 10.1038/s41380-020-0705-9. Epub 2020 May 12.
7
GOMCL: a toolkit to cluster, evaluate, and extract non-redundant associations of Gene Ontology-based functions.
BMC Bioinformatics. 2020 Apr 10;21(1):139. doi: 10.1186/s12859-020-3447-4.
10
Integrative pathway enrichment analysis of multivariate omics data.
Nat Commun. 2020 Feb 5;11(1):735. doi: 10.1038/s41467-019-13983-9.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验