BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

319 related articles for article (PubMed ID: 36732629)

  • 61. Exome Sequencing Reveals the POLR3H Gene as a Novel Cause of Primary Ovarian Insufficiency.
    Franca MM; Han X; Funari MFA; Lerario AM; Nishi MY; Fontenele EGP; Domenice S; Jorge AAL; Garcia-Galiano D; Elias CF; Mendonca BB
    J Clin Endocrinol Metab; 2019 Jul; 104(7):2827-2841. PubMed ID: 30830215
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Premature Ovarian Insufficiency: Phenotypic Characterization Within Different Etiologies.
    Jiao X; Zhang H; Ke H; Zhang J; Cheng L; Liu Y; Qin Y; Chen ZJ
    J Clin Endocrinol Metab; 2017 Jul; 102(7):2281-2290. PubMed ID: 28368522
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Role of microRNAs in premature ovarian insufficiency.
    Guo Y; Sun J; Lai D
    Reprod Biol Endocrinol; 2017 May; 15(1):38. PubMed ID: 28499456
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Rare variants in FANCA induce premature ovarian insufficiency.
    Yang X; Zhang X; Jiao J; Zhang F; Pan Y; Wang Q; Chen Q; Cai B; Tang S; Zhou Z; Chen S; Yin H; Fu W; Luo Y; Li D; Li G; Shang L; Yang J; Jin L; Shi Q; Wu Y
    Hum Genet; 2019 Dec; 138(11-12):1227-1236. PubMed ID: 31535215
    [TBL] [Abstract][Full Text] [Related]  

  • 65. An exome-wide exploration of cases of primary ovarian insufficiency uncovers novel sequence variants and candidate genes.
    Alvarez-Mora MI; Todeschini AL; Caburet S; Perets LP; Mila M; Younis JS; Shalev S; Veitia RA
    Clin Genet; 2020 Sep; 98(3):293-298. PubMed ID: 32613604
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Bi-allelic recessive loss-of-function mutations in FIGLA cause premature ovarian insufficiency with short stature.
    Yuan P; He Z; Sun S; Li Y; Wang W; Liang X; Xie X; Jiang Y; Yang D
    Clin Genet; 2019 Mar; 95(3):409-414. PubMed ID: 30474133
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Rare deleterious BUB1B variants induce premature ovarian insufficiency and early menopause.
    Chen Q; Ke H; Luo X; Wang L; Wu Y; Tang S; Li J; Jin L; Zhang F; Qin Y; Chen X
    Hum Mol Genet; 2020 Sep; 29(16):2698-2707. PubMed ID: 32716490
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Pathogenic bi-allelic variants of meiotic ZMM complex gene SPO16 in premature ovarian insufficiency.
    Qi Y; Wang Y; Li W; Zhuang S; Li S; Xu K; Qin Y; Guo T
    Clin Genet; 2023 Oct; 104(4):486-490. PubMed ID: 37270785
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Premature Ovarian Insufficiency in CLPB Deficiency: Transcriptomic, Proteomic and Phenotypic Insights.
    Tucker EJ; Baker MJ; Hock DH; Warren JT; Jaillard S; Bell KM; Sreenivasan R; Bakhshalizadeh S; Hanna CA; Caruana NJ; Wortmann SB; Rahman S; Pitceathly RDS; Donadieu J; Alimi A; Launay V; Coppo P; Christin-Maitre S; Robevska G; van den Bergen J; Kline BL; Ayers KL; Stewart PN; Stroud DA; Stojanovski D; Sinclair AH
    J Clin Endocrinol Metab; 2022 Nov; 107(12):3328-3340. PubMed ID: 36074910
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Gene variants identified by whole-exome sequencing in 33 French women with premature ovarian insufficiency.
    Yang X; Touraine P; Desai S; Humphreys G; Jiang H; Yatsenko A; Rajkovic A
    J Assist Reprod Genet; 2019 Jan; 36(1):39-45. PubMed ID: 30406445
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Variations of C14ORF39 and SYCE1 Identified in Idiopathic Premature Ovarian Insufficiency and Nonobstructive Azoospermia.
    Hou D; Yao C; Xu B; Luo W; Ke H; Li Z; Qin Y; Guo T
    J Clin Endocrinol Metab; 2022 Feb; 107(3):724-734. PubMed ID: 34718620
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Molecular Genetics of Premature Ovarian Insufficiency.
    Jiao X; Ke H; Qin Y; Chen ZJ
    Trends Endocrinol Metab; 2018 Nov; 29(11):795-807. PubMed ID: 30078697
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Integral Role of the Mitochondrial Ribosome in Supporting Ovarian Function: MRPS7 Variants in Syndromic Premature Ovarian Insufficiency.
    Kline BL; Jaillard S; Bell KM; Bakhshalizadeh S; Robevska G; van den Bergen J; Dulon J; Ayers KL; Christodoulou J; Tchan MC; Touraine P; Sinclair AH; Tucker EJ
    Genes (Basel); 2022 Nov; 13(11):. PubMed ID: 36421788
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Consanguineous familial study revealed biallelic FIGLA mutation associated with premature ovarian insufficiency.
    Chen B; Li L; Wang J; Li T; Pan H; Liu B; Zhou Y; Cao Y; Wang B
    J Ovarian Res; 2018 Jun; 11(1):48. PubMed ID: 29914564
    [TBL] [Abstract][Full Text] [Related]  

  • 75. A novel missense variant in LAMC1 identified in a POI family by whole exome sequencing.
    Xu H; Wang C; Wei H; Li T; Fang Y; Wang B
    Gynecol Endocrinol; 2023 Oct; 39(1):2265507. PubMed ID: 37839437
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Limited contribution of NR5A1 (SF-1) mutations in women with primary ovarian insufficiency (POI).
    Janse F; de With LM; Duran KJ; Kloosterman WP; Goverde AJ; Lambalk CB; Laven JS; Fauser BC; Giltay JC;
    Fertil Steril; 2012 Jan; 97(1):141-6.e2. PubMed ID: 22100173
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Biallelic loss of function variants in STAG3 result in primary ovarian insufficiency.
    Demain LAM; Boetje E; Edgerley JJ; Miles E; Fitzgerald CT; Busby G; Beaman GM; O'Sullivan J; O'Keefe RT; Newman WG
    Reprod Biomed Online; 2021 Nov; 43(5):899-902. PubMed ID: 34497033
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Genetic landscape of a large cohort of Primary Ovarian Insufficiency: New genes and pathways and implications for personalized medicine.
    Heddar A; Ogur C; Da Costa S; Braham I; Billaud-Rist L; Findikli N; Beneteau C; Reynaud R; Mahmoud K; Legrand S; Marchand M; Cedrin-Durnerin I; Cantalloube A; Peigne M; Bretault M; Dagher-Hayeck B; Perol S; Droumaguet C; Cavkaytar S; Nicolas-Bonne C; Elloumi H; Khrouf M; Rougier-LeMasle C; Fradin M; Le Boette E; Luigi P; Guerrot AM; Ginglinger E; Zampa A; Fauconnier A; Auger N; Paris F; Brischoux-Boucher E; Cabrol C; Brun A; Guyon L; Berard M; Riviere A; Gruchy N; Odent S; Gilbert-Dussardier B; Isidor B; Piard J; Lambert L; Hamamah S; Guedj AM; Brac de la Perriere A; Fernandez H; Raffin-Sanson ML; Polak M; Letur H; Epelboin S; Plu-Bureau G; Wołczyński S; Hieronimus S; Aittomaki K; Catteau-Jonard S; Misrahi M
    EBioMedicine; 2022 Oct; 84():104246. PubMed ID: 36099812
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform.
    Norling A; Hirschberg AL; Rodriguez-Wallberg KA; Iwarsson E; Wedell A; Barbaro M
    Hum Reprod; 2014 Aug; 29(8):1818-27. PubMed ID: 24939957
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Meiotic genes in premature ovarian insufficiency: variants in HROB and REC8 as likely genetic causes.
    Tucker EJ; Bell KM; Robevska G; van den Bergen J; Ayers KL; Listyasari N; Faradz SM; Dulon J; Bakhshalizadeh S; Sreenivasan R; Nouyou B; Carre W; Akloul L; Duros S; Domin-Bernhard M; Belaud-Rotureau MA; Touraine P; Jaillard S; Sinclair AH
    Eur J Hum Genet; 2022 Feb; 30(2):219-228. PubMed ID: 34707299
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.