249 related articles for article (PubMed ID: 33095795)
1. Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency.
França MM; Funari MFA; Lerario AM; Santos MG; Nishi MY; Domenice S; Moraes DR; Costalonga EF; Maciel GAR; Maciel-Guerra AT; Guerra-Junior G; Mendonca BB
PLoS One; 2020; 15(10):e0240795. PubMed ID: 33095795
[TBL] [Abstract][Full Text] [Related]
2. Genetics of ovarian insufficiency and defects of folliculogenesis.
França MM; Mendonca BB
Best Pract Res Clin Endocrinol Metab; 2022 Jan; 36(1):101594. PubMed ID: 34794894
[TBL] [Abstract][Full Text] [Related]
3. Two rare loss-of-function variants in the STAG3 gene leading to primary ovarian insufficiency.
França MM; Nishi MY; Funari MFA; Lerario AM; Baracat EC; Hayashida SAY; Maciel GAR; Jorge AAL; Mendonca BB
Eur J Med Genet; 2019 Mar; 62(3):186-189. PubMed ID: 30006057
[TBL] [Abstract][Full Text] [Related]
4. Screening of premature ovarian insufficiency associated genes in Hungarian patients with next generation sequencing.
Illés A; Pikó H; Árvai K; Donka V; Szepesi O; Kósa J; Lakatos P; Beke A
BMC Med Genomics; 2024 Apr; 17(1):98. PubMed ID: 38649916
[TBL] [Abstract][Full Text] [Related]
5. High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function.
Bestetti I; Castronovo C; Sironi A; Caslini C; Sala C; Rossetti R; Crippa M; Ferrari I; Pistocchi A; Toniolo D; Persani L; Marozzi A; Finelli P
Hum Reprod; 2019 Mar; 34(3):574-583. PubMed ID: 30689869
[TBL] [Abstract][Full Text] [Related]
6. Identification of the first homozygous 1-bp deletion in GDF9 gene leading to primary ovarian insufficiency by using targeted massively parallel sequencing.
França MM; Funari MFA; Nishi MY; Narcizo AM; Domenice S; Costa EMF; Lerario AM; Mendonca BB
Clin Genet; 2018 Feb; 93(2):408-411. PubMed ID: 29044499
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Targeted Next-Generation Sequencing Indicates a Frequent Oligogenic Involvement in Primary Ovarian Insufficiency Onset.
Rossetti R; Moleri S; Guizzardi F; Gentilini D; Libera L; Marozzi A; Moretti C; Brancati F; Bonomi M; Persani L
Front Endocrinol (Lausanne); 2021; 12():664645. PubMed ID: 34803902
[TBL] [Abstract][Full Text] [Related]
9. Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency.
Bestetti I; Barbieri C; Sironi A; Specchia V; Yatsenko SA; De Donno MD; Caslini C; Gentilini D; Crippa M; Larizza L; Marozzi A; Rajkovic A; Toniolo D; Bozzetti MP; Finelli P
Hum Reprod; 2021 Oct; 36(11):2975-2991. PubMed ID: 34480478
[TBL] [Abstract][Full Text] [Related]
10. Genetics of primary ovarian insufficiency: new developments and opportunities.
Qin Y; Jiao X; Simpson JL; Chen ZJ
Hum Reprod Update; 2015; 21(6):787-808. PubMed ID: 26243799
[TBL] [Abstract][Full Text] [Related]
11. Next-generation sequencing of 500 POI patients identified novel responsible monogenic and oligogenic variants.
Luo W; Ke H; Tang S; Jiao X; Li Z; Zhao S; Zhang F; Guo T; Qin Y
J Ovarian Res; 2023 Feb; 16(1):39. PubMed ID: 36793102
[TBL] [Abstract][Full Text] [Related]
12. Landscape of pathogenic mutations in premature ovarian insufficiency.
Ke H; Tang S; Guo T; Hou D; Jiao X; Li S; Luo W; Xu B; Zhao S; Li G; Zhang X; Xu S; Wang L; Wu Y; Wang J; Zhang F; Qin Y; Jin L; Chen ZJ
Nat Med; 2023 Feb; 29(2):483-492. PubMed ID: 36732629
[TBL] [Abstract][Full Text] [Related]
13. Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian Insufficiency.
Hyon C; Mansour-Hendili L; Chantot-Bastaraud S; Donadille B; Kerlan V; Dodé C; Jonard S; Delemer B; Gompel A; Reznik Y; Touraine P; Siffroi JP; Christin-Maitre S
J Clin Endocrinol Metab; 2016 May; 101(5):2099-104. PubMed ID: 27003306
[TBL] [Abstract][Full Text] [Related]
14. Genetic etiologic analysis in 74 Chinese Han women with idiopathic premature ovarian insufficiency by combined molecular genetic testing.
Shen J; Qu D; Gao Y; Sun F; Xie J; Sun X; Wang D; Ma X; Cui Y; Liu J; Diao F
J Assist Reprod Genet; 2021 Apr; 38(4):965-978. PubMed ID: 33538981
[TBL] [Abstract][Full Text] [Related]
15. Next Generation Sequencing Should Be Proposed to Every Woman With "Idiopathic" Primary Ovarian Insufficiency.
Eskenazi S; Bachelot A; Hugon-Rodin J; Plu-Bureau G; Gompel A; Catteau-Jonard S; Molina-Gomes D; Dewailly D; Dodé C; Christin-Maitre S; Touraine P
J Endocr Soc; 2021 Jul; 5(7):bvab032. PubMed ID: 34095689
[TBL] [Abstract][Full Text] [Related]
16. Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention.
Liu H; Wei X; Sha Y; Liu W; Gao H; Lin J; Li Y; Tang Y; Wang Y; Wang Y; Su Z
J Ovarian Res; 2020 Sep; 13(1):114. PubMed ID: 32962729
[TBL] [Abstract][Full Text] [Related]
17. "Evaluation of four genes associated with primary ovarian insufficiency in a cohort of Mexican women".
Juárez-Rendón KJ; García-Ortiz JE
J Assist Reprod Genet; 2018 Aug; 35(8):1483-1488. PubMed ID: 29916099
[TBL] [Abstract][Full Text] [Related]
18. Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency.
Bouilly J; Beau I; Barraud S; Bernard V; Azibi K; Fagart J; Fèvre A; Todeschini AL; Veitia RA; Beldjord C; Delemer B; Dodé C; Young J; Binart N
J Clin Endocrinol Metab; 2016 Dec; 101(12):4541-4550. PubMed ID: 27603904
[TBL] [Abstract][Full Text] [Related]
19. New insights into the genetic basis of premature ovarian insufficiency: Novel causative variants and candidate genes revealed by genomic sequencing.
Jaillard S; Bell K; Akloul L; Walton K; McElreavy K; Stocker WA; Beaumont M; Harrisson C; Jääskeläinen T; Palvimo JJ; Robevska G; Launay E; Satié AP; Listyasari N; Bendavid C; Sreenivasan R; Duros S; van den Bergen J; Henry C; Domin-Bernhard M; Cornevin L; Dejucq-Rainsford N; Belaud-Rotureau MA; Odent S; Ayers KL; Ravel C; Tucker EJ; Sinclair AH
Maturitas; 2020 Nov; 141():9-19. PubMed ID: 33036707
[TBL] [Abstract][Full Text] [Related]
20. NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency.
Bouali N; Francou B; Bouligand J; Lakhal B; Malek I; Kammoun M; Warszawski J; Mougou S; Saad A; Guiochon-Mantel A
Clin Genet; 2016 May; 89(5):608-13. PubMed ID: 26848058
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]