339 related articles for article (PubMed ID: 30406445)
1. 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]
2. 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]
3. Novel variants in women with premature ovarian function decline identified via whole-exome sequencing.
Tang R; Yu Q
J Assist Reprod Genet; 2020 Oct; 37(10):2487-2502. PubMed ID: 32789750
[TBL] [Abstract][Full Text] [Related]
4. Biallelic mutations in PSMC3IP are associated with secondary amenorrhea: expanding the spectrum of premature ovarian insufficiency.
Sirchia F; Giorgio E; Cucinella L; Valente EM; Nappi RE
J Assist Reprod Genet; 2022 May; 39(5):1177-1181. PubMed ID: 35352317
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Identification of new variants and candidate genes in women with familial premature ovarian insufficiency using whole-exome sequencing.
Morales R; Lledo B; Ortiz JA; Lozano FM; Garcia EM; Bernabeu A; Fuentes A; Bernabeu R
J Assist Reprod Genet; 2022 Nov; 39(11):2595-2605. PubMed ID: 36208357
[TBL] [Abstract][Full Text] [Related]
7. Identification of potential causal variants for premature ovarian failure by whole exome sequencing.
Jin H; Ahn J; Park Y; Sim J; Park HS; Ryu CS; Kim NK; Kwack K
BMC Med Genomics; 2020 Oct; 13(1):159. PubMed ID: 33109206
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease.
Jolly A; Bayram Y; Turan S; Aycan Z; Tos T; Abali ZY; Hacihamdioglu B; Coban Akdemir ZH; Hijazi H; Bas S; Atay Z; Guran T; Abali S; Bas F; Darendeliler F; Colombo R; Barakat TS; Rinne T; White JJ; Yesil G; Gezdirici A; Gulec EY; Karaca E; Pehlivan D; Jhangiani SN; Muzny DM; Poyrazoglu S; Bereket A; Gibbs RA; Posey JE; Lupski JR
J Clin Endocrinol Metab; 2019 Aug; 104(8):3049-3067. PubMed ID: 31042289
[TBL] [Abstract][Full Text] [Related]
10. Novel pathogenic mutations in minichromosome maintenance complex component 9 (MCM9) responsible for premature ovarian insufficiency.
Guo T; Zheng Y; Li G; Zhao S; Ma J; Qin Y
Fertil Steril; 2020 Apr; 113(4):845-852. PubMed ID: 32145932
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Two novel biallelic mutations in
Mei L; Huang L; Huang Y; Wu X; He H; He X; Su Z; Li P
Mol Med Rep; 2022 Feb; 25(2):. PubMed ID: 34878148
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Novel PMM2 missense mutation in a Chinese family with non-syndromic premature ovarian insufficiency.
Peng T; Lv C; Tan H; Huang J; He H; Wang Y; Zeng M; Yi D; Li J; Deng H; Shi X; Xiao H
J Assist Reprod Genet; 2020 Feb; 37(2):443-450. PubMed ID: 31902100
[TBL] [Abstract][Full Text] [Related]
15. Whole exome sequencing in a cohort of familial premature ovarian insufficiency cases reveals a broad array of pathogenic or likely pathogenic variants in 50% of families.
Rouen A; Rogers E; Kerlan V; Delemer B; Catteau-Jonard S; Reznik Y; Gompel A; Cedrin I; Guedj AM; Grouthier V; Brue T; Pienkowski C; Bachelot A; Chantot-Bastaraud S; Rousseau A; Simon T; Kott E; Siffroi JP; Touraine P; Christin-Maitre S
Fertil Steril; 2022 Apr; 117(4):843-853. PubMed ID: 35115167
[TBL] [Abstract][Full Text] [Related]
16. MCM8 and MCM9 Nucleotide Variants in Women With Primary Ovarian Insufficiency.
Desai S; Wood-Trageser M; Matic J; Chipkin J; Jiang H; Bachelot A; Dulon J; Sala C; Barbieri C; Cocca M; Toniolo D; Touraine P; Witchel S; Rajkovic A
J Clin Endocrinol Metab; 2017 Feb; 102(2):576-582. PubMed ID: 27802094
[TBL] [Abstract][Full Text] [Related]
17. Novel loss-of-function mutation in MCM8 causes premature ovarian insufficiency.
Zhang YX; He WB; Xiao WJ; Meng LL; Tan C; Du J; Lu GX; Lin G; Tan YQ
Mol Genet Genomic Med; 2020 Apr; 8(4):e1165. PubMed ID: 32048466
[TBL] [Abstract][Full Text] [Related]
18. Whole-exome sequencing reveals SALL4 variants in premature ovarian insufficiency: an update on genotype-phenotype correlations.
Wang Q; Li D; Cai B; Chen Q; Li C; Wu Y; Jin L; Wang X; Zhang X; Zhang F
Hum Genet; 2019 Jan; 138(1):83-92. PubMed ID: 30603774
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency.
Fauchereau F; Shalev S; Chervinsky E; Beck-Fruchter R; Legois B; Fellous M; Caburet S; Veitia RA
Clin Genet; 2016 May; 89(5):603-7. PubMed ID: 26771056
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]