WHOLE-EXOME SEQUENCING IN FAMILIAL HYPERCHOLESTEROLEMIA REVEALS NEWLY IDENTIFIED VARIANTS ASSOCIATED WITH CARDIOVASCULAR-EVENT FREE SURVIVAL

被引：0
|
作者：
Khoury, Etienne [1 ,2 ]
Brisson, Diane [1 ,2 ]
Larouche, Miriam [1 ,2 ]
Ere, Alex Lauzi [1 ,2 ]
Gallo, Antonio [3 ]
Gaudet, Daniel [1 ,2 ]
机构：
[1] Univ Montreal, Med, Chicoutimi, PQ, Canada
[2] ECOGENE 21, Chicoutimi, PQ, Canada
[3] Sorbonne Univ, AP HP, Lipidol & Cardiovascular Prevent Unit, Hop Pitie Salpetriere,Inserm UMR1166, Paris, France
来源：
ATHEROSCLEROSIS | 2024年 / 395卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
SaaG097
引用
收藏
页数：2
相关论文
共 50 条
  • [31] Whole-exome sequencing analysis of NSCLC reveals the pathogenic missense variants from cancer-associated genes
    Kumar, S. Udhaya
    Balasundaram, Ambritha
    Cathryn, R. Hephzibah
    Varghese, Rinku Polachirakkal
    Siva, R.
    Gnanasambandan, R.
    Younes, Salma
    Zayed, Hatem
    Doss, George Priya
    COMPUTERS IN BIOLOGY AND MEDICINE, 2022, 148
  • [32] Whole-exome sequencing study identifies rare variants associated with intraocular pressure
    Lin, Yizi
    Williams, Kara
    Moroi, Sayoko E.
    Gao, Xiaoyi Raymond
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2021, 62 (08)
  • [33] Whole-exome sequencing reveals novel variants associated with abnormal uterine bleeding caused by copper intrauterine device
    Shen, Yupei
    Liu, Xiaoli
    Xu, Linfen
    Zhu, Weiqiang
    Zhang, Zhaofeng
    Liu, Junwei
    Jiang, Lifang
    Mao, Yanyan
    Xu, Jianhua
    Yan, Xiaoqin
    Sun, Junjie
    Liu, Fang
    Xiong, Xiumei
    Chen, Xiujuan
    Che, Yan
    Du, Jing
    PERSONALIZED MEDICINE, 2022, 19 (06) : 523 - 534
  • [34] Whole-Exome Sequencing Identified DLG1 as a Candidate Gene for Familial Exudative Vitreoretinopathy
    Zhang, Shanshan
    Li, Xiao
    Liu, Wenjing
    Zhang, Xiang
    Huang, Lulin
    Li, Shujin
    Yang, Mu
    Zhao, Peiquan
    Yang, Jiyun
    Fei, Ping
    Zhu, Xianjun
    Yang, Zhenglin
    GENETIC TESTING AND MOLECULAR BIOMARKERS, 2021, 25 (05) : 309 - 316
  • [35] Genetic variants in familial abdominal aortic aneurysms identified by Whole Genome and Exome sequencing
    IJpma, A.
    Heijsman, D.
    Bruggenwirth, H.
    van den Boogert, I.
    Majoor-Krakauer, D.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 257 - 258
  • [36] Novel variants in women with premature ovarian function decline identified via whole-exome sequencing
    Ruiyi Tang
    Qi Yu
    Journal of Assisted Reproduction and Genetics, 2020, 37 : 2487 - 2502
  • [37] Pathogenic variants identified using whole-exome sequencing in Chinese patients with primary ciliary dyskinesia
    Ye, Yutian
    Huang, Qijun
    Chen, Lipeng
    Yuan, Fang
    Liu, Shengguo
    Zhang, Xiangxia
    Chen, Rongchang
    Fu, Yingyun
    Yue, Yongjian
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2022, 188 (10) : 3024 - 3031
  • [38] Sequencing: The Next Generation-What Is the Role of Whole-Exome Sequencing in the Diagnosis of Familial Cardiovascular Diseases?
    Farhan, Sali M. K.
    Hegele, Robert A.
    CANADIAN JOURNAL OF CARDIOLOGY, 2014, 30 (02) : 152 - 154
  • [39] Novel variants in women with premature ovarian function decline identified via whole-exome sequencing
    Tang, Ruiyi
    Yu, Qi
    JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2020, 37 (10) : 2487 - 2502
  • [40] Whole-Exome Sequencing Identified Novel de Novo SON Variants: Two Case Reports
    Popa, Andreea
    Bell, Sarah M.
    Stubbs, Douglas
    Ward, Scott
    Agrawal, Neena S.
    Christensen, Michael D.
    Jacoby, Ellie J.
    Mayo, Ping C.
    Vilt, Michelle L.
    Wang, Lijun
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2024, 26 (06): : S9 - S9
12345