1025 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]
16. 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]
17. Improving diagnostic precision in primary ovarian insufficiency using comprehensive genetic and autoantibody testing.
Vogt EC; Bratland E; Berland S; Berentsen R; Lund A; Björnsdottir S; Husebye E; Øksnes M
Hum Reprod; 2024 Jan; 39(1):177-189. PubMed ID: 37953503
[TBL] [Abstract][Full Text] [Related]
18. Primary Ovarian Insufficiency.
Laven JS
Semin Reprod Med; 2016 Jul; 34(4):230-4. PubMed ID: 27513024
[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. Heterozygous TP63 pathogenic variants in isolated primary ovarian insufficiency.
Vanderschelden RK; Rodriguez-Escriba M; Chan SH; Berman AJ; Rajkovic A; Yatsenko SA
J Assist Reprod Genet; 2023 Sep; 40(9):2211-2218. PubMed ID: 37453019
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]