Identification of novel variants and candidate genes in women with familial idiopathic premature ovarian failure using whole-exome sequencing

被引:0
|
作者
Morale Sabater, R. [1 ]
Lledo, B. [1 ]
Ortiz, J. A. [1 ]
Lozano, F. [1 ]
Bernabeu, A. [2 ]
Fuentes, A. [2 ]
Llacer, J. [2 ]
Bernabeu, R. [2 ]
机构
[1] Inst Bernabeu, Biotech, Alicante, Spain
[2] Inst Bernabeu, Reprod Med, Alicante, Spain
关键词
D O I
暂无
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
P-541
引用
收藏
页码:383 / 384
页数:2
相关论文
共 50 条
  • [41] Novel rare genetic variants of familial and sporadic pulmonary atresia identified by whole-exome sequencing
    Xing, Junyue
    Wang, Hongdan
    Xie, Yuanyuan
    Fan, Taibing
    Cui, Cunying
    Li, Yanan
    Wang, Shuai
    Gu, Weiyue
    Wang, Chengzeng
    Tang, Hao
    Liu, Lin
    OPEN LIFE SCIENCES, 2023, 18 (01):
  • [42] Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis
    Dinckan, N.
    Du, R.
    Petty, L. E.
    Coban-Akdemir, Z.
    Jhangiani, S. N.
    Paine, I.
    Baugh, E. H.
    Erdem, A. P.
    Kayserili, H.
    Doddapaneni, H.
    Hu, J.
    Muzny, D. M.
    Boerwinkle, E.
    Gibbs, R. A.
    Lupski, J. R.
    Uyguner, Z. O.
    Below, J. E.
    Letra, A.
    JOURNAL OF DENTAL RESEARCH, 2018, 97 (01) : 49 - 59
  • [43] Identification of Novel Gene Variants for Autism Spectrum Disorders in the Lebanese Population Using Whole-Exome Sequencing
    Gerges, Perla
    Bitar, Tania
    Laumonnier, Frederic
    Marouillat, Sylviane
    Nemer, Georges
    Andres, Christian R.
    Hleihel, Walid
    GENES, 2022, 13 (02)
  • [44] Identification of potential candidate genes and pathways in atrioventricular nodal reentry tachycardia by whole-exome sequencing
    Luo, Rong
    Zheng, Chenqing
    Yang, Hao
    Chen, Xuepin
    Jiang, Panpan
    Wu, Xiushan
    Yang, Zhenglin
    Shen, Xia
    Li, Xiaoping
    CLINICAL AND TRANSLATIONAL MEDICINE, 2020, 10 (01): : 238 - 257
  • [45] Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration
    Narta, Kiran
    Teltumbade, Manoj Ramesh
    Vishal, Mansi
    Sadaf, Samreen
    Faruq, Mohd.
    Jama, Hodan
    Waseem, Naushin
    Rao, Aparna
    Sen, Abhijit
    Ray, Kunal
    Mukhopadhyay, Arijit
    GENES, 2023, 14 (02)
  • [46] Whole-exome sequencing screening for candidate genes and variants associated with primary sporadic keratoconus in Chinese patients
    Song, Chunyuan
    Li, Ling
    Liu, Chang
    Hu, Luping
    Bai, Jie
    Liang, Weiyan
    Zhao, Lin
    Song, Wenxiu
    Li, Shaowei
    EXPERIMENTAL EYE RESEARCH, 2024, 245
  • [47] Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer
    Esteban-Jurado, Clara
    Vila-Casadesus, Maria
    Garre, Pilar
    Lozano, Juan Jose
    Pristoupilova, Anna
    Beltran, Sergi
    Munoz, Jenifer
    Ocana, Teresa
    Balaguer, Francesc
    Lopez-Ceron, Maria
    Cuatrecasas, Miriam
    Franch-Exposito, Sebastia
    Pique, Josep M.
    Castells, Antoni
    Carracedo, Angel
    Ruiz-Ponte, Clara
    Abuli, Anna
    Bessa, Xavier
    Andreu, Montserrat
    Bujanda, Luis
    Caldes, Trinidad
    Castellvi-Bel, Sergi
    GENETICS IN MEDICINE, 2015, 17 (02) : 131 - 142
  • [48] Novel candidate genes putatively involved in stress fracture predisposition detected by whole-exome sequencing
    Friedman, Eitan
    Moran, Daniel S.
    Ben-Avraham, Danny
    Yanovich, Ran
    Atzmon, Gil
    GENETICS RESEARCH, 2014, 96 : e004
  • [49] Whole-exome Sequencing Identifies Rare Variants and Genes Associated with Glaucoma
    Chiariglione, Marion
    Arch, Alexander J.
    Gao, XIaoyi R.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2023, 64 (08)
  • [50] Identification of NID1 as a novel candidate susceptibility gene for familial non-medullary thyroid carcinoma using whole-exome sequencing
    Barbalho de Mello, Luis Eduardo
    Ribeiro Carneiro, Thaise Nayane
    Araujo, Aline Neves
    Alves, Camila Xavier
    Favoretto Galante, Pedro Alexandre
    Buzatto, Vanessa Candiotti
    de Almeida, Maria das Gracas
    Vermeulen-Serpa, Karina Marques
    de Lima Vale, Sancha Helena
    de Pinto Paiva, Fernando Jose
    Brandao-Neto, Jose
    Cerutti, Janete Maria
    ENDOCRINE CONNECTIONS, 2022, 11 (01)