170 related articles for article (PubMed ID: 36373164)
1. Genetic screening in patients with ovarian dysfunction.
Zeng Y; Li L; Li Q; Hu J; Zhang N; Wu L; Yan Z; Qu R; Dong J; Liu R; Choy KW; Wang L; Sang Q; Guan Y; Chen B
Clin Genet; 2023 Mar; 103(3):352-357. PubMed ID: 36373164
[TBL] [Abstract][Full Text] [Related]
2. Analysis of NR5A1 in 142 patients with premature ovarian insufficiency, diminished ovarian reserve, or unexplained infertility.
Jaillard S; Sreenivasan R; Beaumont M; Robevska G; Dubourg C; Knarston IM; Akloul L; van den Bergen J; Odent S; Croft B; Jouve G; Grover SR; Duros S; Pimentel C; Belaud-Rotureau MA; Ayers KL; Ravel C; Tucker EJ; Sinclair AH
Maturitas; 2020 Jan; 131():78-86. PubMed ID: 31787151
[TBL] [Abstract][Full Text] [Related]
3. A novel heterozygous splice-altering mutation in HFM1 may be a cause of premature ovarian insufficiency.
Zhe J; Chen S; Chen X; Liu Y; Li Y; Zhou X; Zhang J
J Ovarian Res; 2019 Jul; 12(1):61. PubMed ID: 31279343
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Exome sequencing reveals SYCE1 mutation associated with autosomal recessive primary ovarian insufficiency.
de Vries L; Behar DM; Smirin-Yosef P; Lagovsky I; Tzur S; Basel-Vanagaite L
J Clin Endocrinol Metab; 2014 Oct; 99(10):E2129-32. PubMed ID: 25062452
[TBL] [Abstract][Full Text] [Related]
6. Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.
Fan S; Jiao Y; Khan R; Jiang X; Javed AR; Ali A; Zhang H; Zhou J; Naeem M; Murtaza G; Li Y; Yang G; Zaman Q; Zubair M; Guan H; Zhang X; Ma H; Jiang H; Ali H; Dil S; Shah W; Ahmad N; Zhang Y; Shi Q
Am J Hum Genet; 2021 Feb; 108(2):324-336. PubMed ID: 33508233
[TBL] [Abstract][Full Text] [Related]
7. A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiency.
Carlosama C; Elzaiat M; Patiño LC; Mateus HE; Veitia RA; Laissue P
Hum Mol Genet; 2017 Aug; 26(16):3161-3166. PubMed ID: 28541421
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Variations of C14ORF39 and SYCE1 Identified in Idiopathic Premature Ovarian Insufficiency and Nonobstructive Azoospermia.
Hou D; Yao C; Xu B; Luo W; Ke H; Li Z; Qin Y; Guo T
J Clin Endocrinol Metab; 2022 Feb; 107(3):724-734. PubMed ID: 34718620
[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. A novel EIF4ENIF1 mutation associated with a diminished ovarian reserve and premature ovarian insufficiency identified by whole-exome sequencing.
Zhao M; Feng F; Chu C; Yue W; Li L
J Ovarian Res; 2019 Dec; 12(1):119. PubMed ID: 31810472
[TBL] [Abstract][Full Text] [Related]
12. Oligogenic basis of premature ovarian insufficiency: an observational study.
Long P; Wang L; Tan H; Quan R; Hu Z; Zeng M; Deng Z; Huang H; Greenbaum J; Deng H; Xiao H
J Ovarian Res; 2024 Feb; 17(1):32. PubMed ID: 38310280
[TBL] [Abstract][Full Text] [Related]
13. Homozygous variants in
He WB; Tan C; Zhang YX; Meng LL; Gong F; Lu GX; Lin G; Du J; Tan YQ
J Med Genet; 2021 Mar; 58(3):168-172. PubMed ID: 32303603
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Are FSHR polymorphisms risk factors to premature ovarian insufficiency?
Cordts EB; Santos MC; Bianco B; Barbosa CP; Christofolini DM
Gynecol Endocrinol; 2015; 31(8):663-6. PubMed ID: 26291798
[TBL] [Abstract][Full Text] [Related]
16. A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing.
Bramble MS; Goldstein EH; Lipson A; Ngun T; Eskin A; Gosschalk JE; Roach L; Vashist N; Barseghyan H; Lee E; Arboleda VA; Vaiman D; Yuksel Z; Fellous M; Vilain E
Hum Reprod; 2016 Apr; 31(4):905-14. PubMed ID: 26911863
[TBL] [Abstract][Full Text] [Related]
17. Primary Ovarian Insufficiency.
Laven JS
Semin Reprod Med; 2016 Jul; 34(4):230-4. PubMed ID: 27513024
[TBL] [Abstract][Full Text] [Related]
18. Consanguineous familial study revealed biallelic FIGLA mutation associated with premature ovarian insufficiency.
Chen B; Li L; Wang J; Li T; Pan H; Liu B; Zhou Y; Cao Y; Wang B
J Ovarian Res; 2018 Jun; 11(1):48. PubMed ID: 29914564
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Penetrance of pathogenic genetic variants associated with premature ovarian insufficiency.
Shekari S; Stankovic S; Gardner EJ; Hawkes G; Kentistou KA; Beaumont RN; Mörseburg A; Wood AR; Prague JK; Mishra GD; Day FR; Baptista J; Wright CF; Weedon MN; Hoffmann ER; Ruth KS; Ong KK; Perry JRB; Murray A
Nat Med; 2023 Jul; 29(7):1692-1699. PubMed ID: 37349538
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]