Suppr超能文献

相似文献

2
ssSNPer: identifying statistically similar SNPs to aid interpretation of genetic association studies.
Bioinformatics. 2006 Dec 1;22(23):2960-1. doi: 10.1093/bioinformatics/btl518. Epub 2006 Oct 12.
3
LDA--a java-based linkage disequilibrium analyzer.
Bioinformatics. 2003 Nov 1;19(16):2147-8. doi: 10.1093/bioinformatics/btg276.
4
LDkit: a parallel computing toolkit for linkage disequilibrium analysis.
BMC Bioinformatics. 2020 Oct 16;21(1):461. doi: 10.1186/s12859-020-03754-5.
7
Linkage disequilibrium patterns and functional analysis of RGS4 polymorphisms in relation to schizophrenia.
Schizophr Bull. 2008 Jan;34(1):118-26. doi: 10.1093/schbul/sbm042. Epub 2007 May 21.
8
Analysis of single-locus tests to detect gene/disease associations.
Genet Epidemiol. 2005 Apr;28(3):207-19. doi: 10.1002/gepi.20050.
9
Haplotype and linkage disequilibrium architecture for human cancer-associated genes.
Genome Res. 2002 Dec;12(12):1846-53. doi: 10.1101/gr.483802.
10
ArchiLD: hierarchical visualization of linkage disequilibrium in human populations.
PLoS One. 2014 Jan 21;9(1):e86761. doi: 10.1371/journal.pone.0086761. eCollection 2014.

引用本文的文献

1
Investigating the Role of Gene Polymorphisms in Hypertension: Evidence from the Jordanian Population.
Vasc Health Risk Manag. 2025 Sep 3;21:705-717. doi: 10.2147/VHRM.S536434. eCollection 2025.
3
Efficient gene set analysis for DNA methylation addressing probe dependency and bias.
Bioinformatics. 2025 Aug 2;41(8). doi: 10.1093/bioinformatics/btaf422.
4
Mapping Cerebellar Morphology in 15q11.2 CNV Carriers Using Normative Modeling.
medRxiv. 2025 May 28:2025.05.28.25328353. doi: 10.1101/2025.05.28.25328353.
5
Saliency Models Reveal Reduced Top-Down Attention in Attention-Deficit/Hyperactivity Disorder: A Naturalistic Eye-Tracking Study.
JAACAP Open. 2024 Apr 3;3(2):192-204. doi: 10.1016/j.jaacop.2024.03.001. eCollection 2025 Jun.
6
Copy Number Variant Architecture of Child Psychopathology and Cognitive Development in the ABCD Study.
Am J Psychiatry. 2025 Jun 11:appiajp20240445. doi: 10.1176/appi.ajp.20240445.
9
metacp: a versatile software package for combining dependent or independent p-values.
BMC Bioinformatics. 2025 Apr 19;26(1):109. doi: 10.1186/s12859-025-06126-z.
10
Intergenerational transmission of complex traits and the offspring methylome.
Mol Psychiatry. 2025 Apr 3. doi: 10.1038/s41380-025-02981-7.

本文引用的文献

2
Linkage disequilibrium in finite populations.
Theor Appl Genet. 1968 Jun;38(6):226-31. doi: 10.1007/BF01245622.
3
Selection of genetic markers for association analyses, using linkage disequilibrium and haplotypes.
Am J Hum Genet. 2003 Jul;73(1):115-30. doi: 10.1086/376561. Epub 2003 Jun 5.
5
The allelic architecture of human disease genes: common disease-common variant...or not?
Hum Mol Genet. 2002 Oct 1;11(20):2417-23. doi: 10.1093/hmg/11.20.2417.
6
Merlin--rapid analysis of dense genetic maps using sparse gene flow trees.
Nat Genet. 2002 Jan;30(1):97-101. doi: 10.1038/ng786. Epub 2001 Dec 3.
7
A simple correction for multiple comparisons in interval mapping genome scans.
Heredity (Edinb). 2001 Jul;87(Pt 1):52-8. doi: 10.1046/j.1365-2540.2001.00901.x.
9
Haplotypes vs single marker linkage disequilibrium tests: what do we gain?
Eur J Hum Genet. 2001 Apr;9(4):291-300. doi: 10.1038/sj.ejhg.5200619.
10
The relative power of SNPs and haplotype as genetic markers for association tests.
Pharmacogenomics. 2001 Feb;2(1):11-24. doi: 10.1517/14622416.2.1.11.

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