287 related articles for article (PubMed ID: 27798098)
21. Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency.
Chen A; Tiosano D; Guran T; Baris HN; Bayram Y; Mory A; Shapiro-Kulnane L; Hodges CA; Akdemir ZC; Turan S; Jhangiani SN; van den Akker F; Hoppel CL; Salz HK; Lupski JR; Buchner DA
Hum Mol Genet; 2018 Jun; 27(11):1913-1926. PubMed ID: 29566152
[TBL] [Abstract][Full Text] [Related]
22. New MCM8 mutation associated with premature ovarian insufficiency and chromosomal instability in a highly consanguineous Tunisian family.
Bouali N; Francou B; Bouligand J; Imanci D; Dimassi S; Tosca L; Zaouali M; Mougou S; Young J; Saad A; Guiochon-Mantel A
Fertil Steril; 2017 Oct; 108(4):694-702. PubMed ID: 28863940
[TBL] [Abstract][Full Text] [Related]
23. "Evaluation of four genes associated with primary ovarian insufficiency in a cohort of Mexican women".
Juárez-Rendón KJ; García-Ortiz JE
J Assist Reprod Genet; 2018 Aug; 35(8):1483-1488. PubMed ID: 29916099
[TBL] [Abstract][Full Text] [Related]
24. Mutation analysis of NOBOX homeodomain in Chinese women with premature ovarian failure.
Qin Y; Shi Y; Zhao Y; Carson SA; Simpson JL; Chen ZJ
Fertil Steril; 2009 Apr; 91(4 Suppl):1507-9. PubMed ID: 18930203
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency.
Bouilly J; Beau I; Barraud S; Bernard V; Azibi K; Fagart J; Fèvre A; Todeschini AL; Veitia RA; Beldjord C; Delemer B; Dodé C; Young J; Binart N
J Clin Endocrinol Metab; 2016 Dec; 101(12):4541-4550. PubMed ID: 27603904
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. GDF9 is transiently expressed in oocytes before follicle formation in the human fetal ovary and is regulated by a novel NOBOX transcript.
Bayne RA; Kinnell HL; Coutts SM; He J; Childs AJ; Anderson RA
PLoS One; 2015; 10(3):e0119819. PubMed ID: 25790371
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. 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]
31. TP63 truncating mutation causes increased cell apoptosis and premature ovarian insufficiency by enhanced transcriptional activation of CLCA2.
Fan Y; Chen S; Chu C; Yin X; Jin J; Zhang L; Yan H; Cao Z; Liu R; Xin M; Li L; Yin C
J Ovarian Res; 2024 Mar; 17(1):67. PubMed ID: 38528613
[TBL] [Abstract][Full Text] [Related]
32. The Potential Synergic Effect of a Complex Pattern of Multiple Inherited Genetic Variants as a Pathogenic Factor for Ovarian Dysgenesis: A Case Report.
Cattoni A; Spano A; Tulone A; Boneschi A; Masera N; Maitz S; Di Blasio AM; Persani L; Guizzardi F; Rossetti R
Front Endocrinol (Lausanne); 2020; 11():540683. PubMed ID: 33101191
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Identification of novel biallelic variants in BMP15 in two siblings with premature ovarian insufficiency.
Zhang T; Ma Q; Shen Q; Jiang C; Zou F; Shen Y; Wang Y
J Assist Reprod Genet; 2022 Sep; 39(9):2125-2134. PubMed ID: 35861920
[TBL] [Abstract][Full Text] [Related]
35. Genetics of primary ovarian insufficiency.
Rossetti R; Ferrari I; Bonomi M; Persani L
Clin Genet; 2017 Feb; 91(2):183-198. PubMed ID: 27861765
[TBL] [Abstract][Full Text] [Related]
36. Mutational analysis of the homeobox region of the human NOBOX gene in Japanese women who exhibit premature ovarian failure.
Zhao XX; Suzumori N; Yamaguchi M; Suzumori K
Fertil Steril; 2005 Jun; 83(6):1843-4. PubMed ID: 15950662
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. 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]
39. 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]
40. [NR5A1 and ovarian failure].
Bashamboo A; Ravel C; Brauner R; McElreavey K
Med Sci (Paris); 2009 Oct; 25(10):809-13. PubMed ID: 19849982
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
