These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
1077 related articles for article (PubMed ID: 30689869)
1. 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]
2. 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]
3. Gene dosage as a relevant mechanism contributing to the determination of ovarian function in Turner syndrome. Castronovo C; Rossetti R; Rusconi D; Recalcati MP; Cacciatore C; Beccaria E; Calcaterra V; Invernizzi P; Larizza D; Finelli P; Persani L Hum Reprod; 2014 Feb; 29(2):368-79. PubMed ID: 24324027 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Chromosomal instability in women with primary ovarian insufficiency. Katari S; Aarabi M; Kintigh A; Mann S; Yatsenko SA; Sanfilippo JS; Zeleznik AJ; Rajkovic A Hum Reprod; 2018 Mar; 33(3):531-538. PubMed ID: 29425284 [TBL] [Abstract][Full Text] [Related]
6. Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases. Tšuiko O; Nõukas M; Žilina O; Hensen K; Tapanainen JS; Mägi R; Kals M; Kivistik PA; Haller-Kikkatalo K; Salumets A; Kurg A Hum Reprod; 2016 Aug; 31(8):1913-25. PubMed ID: 27301361 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. A homozygous NOBOX truncating variant causes defective transcriptional activation and leads to primary ovarian insufficiency. Li L; Wang B; Zhang W; Chen B; Luo M; Wang J; Wang X; Cao Y; Kee K Hum Reprod; 2017 Jan; 32(1):248-255. PubMed ID: 27836978 [TBL] [Abstract][Full Text] [Related]
9. CAV1 regulates primordial follicle formation via the Notch2 signalling pathway and is associated with premature ovarian insufficiency in humans. Huang K; Dang Y; Zhang P; Shen C; Sui X; Xia G; Qin Y; Jiao X; Wang C; Huo R; Chen ZJ Hum Reprod; 2018 Nov; 33(11):2087-2095. PubMed ID: 30304446 [TBL] [Abstract][Full Text] [Related]
10. A high-resolution X chromosome copy-number variation map in fertile females and women with primary ovarian insufficiency. Yatsenko SA; Wood-Trageser M; Chu T; Jiang H; Rajkovic A Genet Med; 2019 Oct; 21(10):2275-2284. PubMed ID: 30948856 [TBL] [Abstract][Full Text] [Related]
11. Sequence variants of KHDRBS1 as high penetrance susceptibility risks for primary ovarian insufficiency by mis-regulating mRNA alternative splicing. Wang B; Li L; Zhu Y; Zhang W; Wang X; Chen B; Li T; Pan H; Wang J; Kee K; Cao Y Hum Reprod; 2017 Oct; 32(10):2138-2146. PubMed ID: 28938739 [TBL] [Abstract][Full Text] [Related]
12. New mutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing. Patiño LC; Beau I; Carlosama C; Buitrago JC; González R; Suárez CF; Patarroyo MA; Delemer B; Young J; Binart N; Laissue P Hum Reprod; 2017 Jul; 32(7):1512-1520. PubMed ID: 28505269 [TBL] [Abstract][Full Text] [Related]
13. Association of genetic disorders and congenital malformations with premature ovarian insufficiency: a nationwide register-based study. Silvén H; Savukoski SM; Pesonen P; Pukkala E; Ojaniemi M; Gissler M; Suvanto E; Niinimäki M Hum Reprod; 2023 Jun; 38(6):1224-1230. PubMed ID: 37018629 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
19. Incidence and familial risk of premature ovarian insufficiency in the Finnish female population. Silvén H; Savukoski SM; Pesonen P; Pukkala E; Gissler M; Suvanto E; Niinimäki M Hum Reprod; 2022 May; 37(5):1030-1036. PubMed ID: 35134918 [TBL] [Abstract][Full Text] [Related]
20. The significance of fragile X mental retardation gene 1 CGG repeat sizes in the normal and intermediate range in women with primary ovarian insufficiency. Voorhuis M; Onland-Moret NC; Janse F; Ploos van Amstel HK; Goverde AJ; Lambalk CB; Laven JS; van der Schouw YT; Broekmans FJ; Fauser BC; Hum Reprod; 2014 Jul; 29(7):1585-93. PubMed ID: 24812319 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]