Decoding NF1 Intragenic Copy-Number Variations
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference71 articles.
1. Impacts of variation in the human genome on gene regulation;Haraksingh;J. Mol. Biol.,2013
2. What have studies of genomic disorders taught us about our genome?;Simmons;Methods Mol. Biol.,2012
3. Human genome sequencing in health and disease;Gonzaga-Jauregui;Annu. Rev. Med.,2012
4. Human copy number variation and complex genetic disease;Girirajan;Annu. Rev. Genet.,2011
5. Structural variation in the human genome and its role in disease;Stankiewicz;Annu. Rev. Med.,2010
Cited by 24 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Epigenetic Gene-Regulatory Loci in Alu Elements Associated with Autism Susceptibility in the Prefrontal Cortex of ASD;International Journal of Molecular Sciences;2023-04-19
2. Childhood-Onset Refractory Hypertension Results from Neurofibromatosis Type 1 Caused by a Splicing <i>NF1</i> Mutation;Kidney and Blood Pressure Research;2023
3. Investigation of the mechanism of copy number variations involving the α-globin gene cluster on chromosome 16: two case reports and literature review;Molecular Genetics and Genomics;2022-11-03
4. Genotype-Phenotype Correlations in Neurofibromatosis Type 1: Identification of Novel and Recurrent NF1 Gene Variants and Correlations with Neurocognitive Phenotype;Genes;2022-06-23
5. Relationship of TP53 gene with retroelements in urogenital organs carcinogenesis;Cancer Urology;2022-05-06
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3