Whole exome sequencing of Chagas disease cardiomyopathy families reveals accumulation of rare variants in mitochondrial and inflammation-associated genes

被引:0
|
作者
Cunha-Neto, E. [1 ]
Marquet, S. [2 ]
Farage Frade, A. [1 ]
Mota Ferreira, A. [3 ]
Ouarhache, M. [4 ]
Ianni, B. [5 ]
Rodrigues Pinto Ferreira, L. [6 ]
Oliveira-Carvalho Rigaud, V. [6 ]
Ribeiro Almeida, R. [1 ]
Candido, D. [6 ]
Torres, M. [7 ]
Gallardo, F. [8 ]
Fernandes, R. [6 ]
Mady, C. [5 ]
Buck, P. [5 ]
Cardoso, C. [9 ]
Santos-Junior, O. R. [10 ]
Oliveira, L. C. [11 ]
Oliveira, C. D. L. [12 ]
do Carmo Nunes, M. [10 ]
Abel, L. [13 ]
Kalil, J. [6 ]
Ribeiro, A. L. P. [14 ]
Sabino, E. C. [15 ,16 ]
Chevillard, C. [17 ]
机构
[1] Univ Sao Paulo, Div Clin Immunol & Allergy, Heart Inst InCor, Sao Paulo, Brazil
[2] Aix Marseille Univ, Labex ParaFrap, INSERM, GIMP,UMR906, Marseille, France
[3] Univ Estadual Montes Claros, Hlth Sci Programme, Montes Claros, Brazil
[4] Aix Marseille Univ, URMITE, IHU Mediterranee Infect, UM63,CNRS 7278,IRD 198,INSERM 1095, Marseille, France
[5] Univ Sao Paulo, Sch Med, Heart Inst InCor, Myocardiopathies Unit, Sao Paulo, Brazil
[6] Univ Sao Paulo, Inst Invest Immunol, Inst Nacl Ciencia & Tecnol, Lab Immunol,Heart Inst InCor,Div Clin Immunol &, Sao Paulo, Brazil
[7] Aix Marseille Univ, INSERM, UMR 1090, Marseille, France
[8] Aix Marseille Univ, INSERM, TAGC UMR S1090, Marseille, France
[9] Univ Fed Sao Joao del Rei, Sch Med, Divinopolis, Brazil
[10] Univ Fed Minas Gerais, Belo Horizonte, MG, Brazil
[11] Univ Sao Paulo, Sch Med, Gen Hosp, Lab Med Laboratorial LIM03, Sao Paulo, Brazil
[12] Univ Fed Sao Joao del Rei, Sch Med, Divinopolis, Brazil
[13] Paris Descartes Univ, Sorbonne Paris Cite, Lab Human Genet Infect Dis, Necker Branch,INSERM,U1163, Paris, France
[14] Univ Fed Minas Gerais, Dept Internal Med, Belo Horizonte, MG, Brazil
[15] Univ Sao Paulo, Sch Med, Dept Infect Dis, Sao Paulo, Brazil
[16] Univ Sao Paulo, Inst Trop Med, Sao Paulo, Brazil
[17] Aix Marseille Univ, INSERM, GIMP UMR S906, Marseille, France
关键词
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
O092
引用
收藏
页码:1171 / 1172
页数:2
相关论文
共 50 条
  • [41] Whole-exome sequencing study reveals common copy number variants in protocadherin genes associated with childhood obesity in Koreans
    Moon, S.
    Hwang, M. Y.
    Jang, H. B.
    Han, S.
    Kim, Y. J.
    Hwang, J-Y
    Lee, H-J
    Park, S. I.
    Song, J.
    Kim, B-J
    INTERNATIONAL JOURNAL OF OBESITY, 2017, 41 (04) : 660 - 663
  • [42] Whole exome sequencing reveals novel variants associated with diminished ovarian reserve in young women
    Li, Na
    Xu, Wanxue
    Liu, Huimin
    Zhou, Rui
    Zou, Siqi
    Wang, Shiqing
    Li, Siyu
    Yang, Zexin
    Piao, Yongjun
    Zhang, Yunshan
    FRONTIERS IN GENETICS, 2023, 14
  • [43] Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies
    Avigail Beryozkin
    Elia Shevah
    Adva Kimchi
    Liliana Mizrahi-Meissonnier
    Samer Khateb
    Rinki Ratnapriya
    Csilla H. Lazar
    Anat Blumenfeld
    Tamar Ben-Yosef
    Yitzhak Hemo
    Jacob Pe’er
    Eduard Averbuch
    Michal Sagi
    Alexis Boleda
    Linn Gieser
    Abraham Zlotogorski
    Tzipora Falik-Zaccai
    Ola Alimi-Kasem
    Samuel G. Jacobson
    Itay Chowers
    Anand Swaroop
    Eyal Banin
    Dror Sharon
    Scientific Reports, 5
  • [44] Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies
    Beryozkin, Avigail
    Shevah, Elia
    Kimchi, Adva
    Mizrahi-Meissonnier, Liliana
    Khateb, Samer
    Ratnapriya, Rinki
    Lazar, Csilla H.
    Blumenfeld, Anat
    Ben-Yosef, Tamar
    Hemo, Yitzhak
    Pe'er, Jacob
    Averbuch, Eduard
    Sagi, Michal
    Boleda, Alexis
    Gieser, Linn
    Zlotogorski, Abraham
    Falik-Zaccai, Tzipora
    Alimi-Kasem, Ola
    Jacobson, Samuel G.
    Chowers, Itay
    Swaroop, Anand
    Banin, Eyal
    Sharon, Dror
    SCIENTIFIC REPORTS, 2015, 5
  • [45] Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency
    Turkyilmaz, Ayberk
    Alavanda, Ceren
    Ates, Esra Arslan
    Geckinli, Bilgen Bilge
    Polat, Hamza
    Gokcu, Mehmet
    Karakaya, Taner
    Cebi, Alper Han
    Soylemez, Mehmet Ali
    Guney, Ahmet Ilter
    Ata, Pinar
    Arman, Ahmet
    JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2022, 39 (03) : 695 - 710
  • [46] Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome
    Warejko, Jillian K.
    Schueler, Markus
    Vivante, Asaf
    Tan, Weizhen
    Daga, Ankana
    Lawson, Jennifer A.
    Braun, Daniela A.
    Shril, Shirlee
    Amann, Kassaundra
    Somers, Michael J. G.
    Rodig, Nancy M.
    Baum, Michelle A.
    Daouk, Ghaleb
    Traum, Avram Z.
    Kim, Heung Bae
    Vakili, Khashayar
    Porras, Diego
    Lock, James
    Rivkin, Michael J.
    Chaudry, Gulraiz
    Smoot, Leslie B.
    Singh, Michael N.
    Smith, Edward R.
    Mane, Shrikant M.
    Lifton, Richard P.
    Stein, Deborah R.
    Ferguson, Michael A.
    Hildebrandt, Friedhelm
    HYPERTENSION, 2018, 71 (04) : 691 - 699
  • [47] Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency
    Ayberk Turkyilmaz
    Ceren Alavanda
    Esra Arslan Ates
    Bilgen Bilge Geckinli
    Hamza Polat
    Mehmet Gokcu
    Taner Karakaya
    Alper Han Cebi
    Mehmet Ali Soylemez
    Ahmet İlter Guney
    Pinar Ata
    Ahmet Arman
    Journal of Assisted Reproduction and Genetics, 2022, 39 : 695 - 710
  • [48] Rare variants in novel and known genes associated with primary angle closure glaucoma based on whole exome sequencing of 549 probands
    Sun, Wenmin
    Xiao, Xueshan
    Li, Shiqiang
    Ouyang, Jiamin
    Li, Xueqing
    Jia, Xiaoyun
    Liu, Xing
    Zhang, Qingjiong
    JOURNAL OF GENETICS AND GENOMICS, 2019, 46 (07) : 353 - 357
  • [49] Rare variants in novel and known genes associated with primary angle closure glaucoma based on whole exome sequencing of 549 probands
    Wenmin Sun
    Xueshan Xiao
    Shiqiang Li
    Jiamin Ouyang
    Xueqing Li
    Xiaoyun Jia
    Xing Liu
    Qingjiong Zhang
    JournalofGeneticsandGenomics, 2019, 46 (07) : 353 - 357
  • [50] Exome Sequencing Of β2-Adrenergic Receptor Pathway Genes Reveals Rare Variants Associated With Asthma Severity In African Americans
    Ortega, V. E.
    Slager, R. E.
    Hawkins, G.
    Moore, W. C.
    Busse, W. W.
    Erzurum, S. C.
    Wenzel, S. E.
    Barnes, K. C.
    Mathias, R. A.
    Bamshad, M. J.
    Nickerson, D.
    Peters, S. P.
    Meyers, D. A.
    Bleecker, E. R.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2013, 187