357 related articles for article (PubMed ID: 32381463)
1. Primary ovarian insufficiency, meiosis and DNA repair.
Veitia RA
Biomed J; 2020 Apr; 43(2):115-123. PubMed ID: 32381463
[TBL] [Abstract][Full Text] [Related]
2. The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing.
Laissue P
Mol Cell Endocrinol; 2018 Jan; 460():170-180. PubMed ID: 28743519
[TBL] [Abstract][Full Text] [Related]
3. Homozygous missense variant in MEIOSIN causes premature ovarian insufficiency.
Zhang Q; Zhang W; Wu X; Ke H; Qin Y; Zhao S; Guo T
Hum Reprod; 2023 Nov; 38(Supplement_2):ii47-ii56. PubMed ID: 37982418
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency.
Huhtaniemi I; Hovatta O; La Marca A; Livera G; Monniaux D; Persani L; Heddar A; Jarzabek K; Laisk-Podar T; Salumets A; Tapanainen JS; Veitia RA; Visser JA; Wieacker P; Wolczynski S; Misrahi M
Trends Endocrinol Metab; 2018 Jun; 29(6):400-419. PubMed ID: 29706485
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. A kaleidoscopic view of ovarian genes associated with premature ovarian insufficiency and senescence.
Yang Q; Mumusoglu S; Qin Y; Sun Y; Hsueh AJ
FASEB J; 2021 Aug; 35(8):e21753. PubMed ID: 34233068
[TBL] [Abstract][Full Text] [Related]
9. Meiotic Recombination Defects and Premature Ovarian Insufficiency.
Huang C; Guo T; Qin Y
Front Cell Dev Biol; 2021; 9():652407. PubMed ID: 33763429
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Pathogenic variants of meiotic double strand break (DSB) formation genes PRDM9 and ANKRD31 in premature ovarian insufficiency.
Wang Y; Guo T; Ke H; Zhang Q; Li S; Luo W; Qin Y
Genet Med; 2021 Dec; 23(12):2309-2315. PubMed ID: 34257419
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. ZSWIM7 Is Associated With Human Female Meiosis and Familial Primary Ovarian Insufficiency.
McGlacken-Byrne SM; Le Quesne Stabej P; Del Valle I; Ocaka L; Gagunashvili A; Crespo B; Moreno N; James C; Bacchelli C; Dattani MT; Williams HJ; Kelberman D; Achermann JC; Conway GS
J Clin Endocrinol Metab; 2022 Jan; 107(1):e254-e263. PubMed ID: 34402903
[TBL] [Abstract][Full Text] [Related]
15. Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency.
Turkyilmaz A; Alavanda C; Ates EA; Geckinli BB; Polat H; Gokcu M; Karakaya T; Cebi AH; Soylemez MA; Guney Aİ; Ata P; Arman A
J Assist Reprod Genet; 2022 Mar; 39(3):695-710. PubMed ID: 35066699
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.
Riera-Escamilla A; Enguita-Marruedo A; Moreno-Mendoza D; Chianese C; Sleddens-Linkels E; Contini E; Benelli M; Natali A; Colpi GM; Ruiz-Castañé E; Maggi M; Baarends WM; Krausz C
Hum Reprod; 2019 Jun; 34(6):978-988. PubMed ID: 31125047
[TBL] [Abstract][Full Text] [Related]
18. [Genes and ovarian insufficiency].
Christin-Maitre S; Bouchard P
Ann Endocrinol (Paris); 1999 Jul; 60(2):118-22. PubMed ID: 10456183
[TBL] [Abstract][Full Text] [Related]
19. AMH mutations with reduced in vitro bioactivity are related to premature ovarian insufficiency.
Alvaro Mercadal B; Imbert R; Demeestere I; Gervy C; De Leener A; Englert Y; Costagliola S; Delbaere A
Hum Reprod; 2015 May; 30(5):1196-202. PubMed ID: 25750103
[TBL] [Abstract][Full Text] [Related]
20. Premature ovarian insufficiency: clinical orientations for genetic testing and genetic counseling.
Barros F; Carvalho F; Barros A; Dória S
Porto Biomed J; 2020; 5(3):e62. PubMed ID: 33299945
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
