Gene-based association study reveals a distinct female genetic signal in primary hypertension
Author:
Funder
Israel Science Foundation
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://link.springer.com/content/pdf/10.1007/s00439-023-02567-9.pdf
Reference50 articles.
1. Arteche-Lopez A, Alvarez-Mora MI, Sanchez Calvin MT, Lezana Rosales JM, Palma Milla C, Gomez Rodriguez MJ, Gomez Manjon I, Blazquez A, Juarez Rufian A, Ramos Gomez P, Sierra Tomillo O, Hidalgo Mayoral I, Perez de la Fuente R, Posada Rodriguez IJ, Gonzalez Granado LI, Martin MA, Quesada-Espinosa JF, Moreno-Garcia M (2021) Biallelic variants in genes previously associated with dominant inheritance: CACNA1A, RET and SLC20A2. Eur J Hum Genet 29:1520–1526. https://doi.org/10.1038/s41431-021-00919-5
2. Bohnen MS, Roman-Campos D, Terrenoire C, Jnani J, Sampson KJ, Chung WK, Kass RS (2017) The impact of heterozygous KCNK3 mutations associated with pulmonary arterial hypertension on channel function and pharmacological recovery. J Am Heart Assoc. https://doi.org/10.1161/JAHA.117.006465
3. Brandes N, Linial N, Linial M (2019) Quantifying gene selection in cancer through protein functional alteration bias. Nucl Acids Res 47:6642–6655. https://doi.org/10.1093/nar/gkz546
4. Brandes N, Linial N, Linial M (2020) PWAS: proteome-wide association study-linking genes and phenotypes by functional variation in proteins. Genome Biol 21:173. https://doi.org/10.1186/s13059-020-02089-x
5. Brandes N, Linial N, Linial M (2021) Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition. Sci Rep 11:14901. https://doi.org/10.1038/s41598-021-94252-y
Cited by 4 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. Revealing the genetic complexity of hypothyroidism: integrating complementary association methods;Frontiers in Genetics;2024-06-11
2. PWAS Hub: Exploring Gene-Based Associations of Common Complex Diseases;2024-01-22
3. Immune and inflammatory mechanisms in hypertension;Nature Reviews Cardiology;2024-01-03
4. The genetics of idiopathic intracranial hypertension (IIH): Integration of population studies and clinical data;2023-06-05
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