326 related articles for article (PubMed ID: 36732629)
41. 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]
42. The landscape of genetic variations in non-syndromic primary ovarian insufficiency in the MENA region: a systematic review.
Allouch A; Al-Barazenji T; Al-Shafai M; Abdallah AM
Front Endocrinol (Lausanne); 2023; 14():1289333. PubMed ID: 38737775
[TBL] [Abstract][Full Text] [Related]
43. Pathogenic variants of meiotic double strand break (DSB) formation genes PRDM9 and ANKRD31 in premature ovarian insufficiency.
Wang Y; Guo T; Ke H; Zhang Q; Li S; Luo W; Qin Y
Genet Med; 2021 Dec; 23(12):2309-2315. PubMed ID: 34257419
[TBL] [Abstract][Full Text] [Related]
44. Primary ovarian insufficiency, meiosis and DNA repair.
Veitia RA
Biomed J; 2020 Apr; 43(2):115-123. PubMed ID: 32381463
[TBL] [Abstract][Full Text] [Related]
45. DIS3 Variants are Associated With Primary Ovarian Insufficiency: Importance of Transcription/Translation in Oogenesis.
Johnstone EB; Gorsi B; Coelho E; Moore B; Farr AM; Cooper AR; Mardis ER; Rajkovic A; Chow CY; Yandell M; Welt CK
J Clin Endocrinol Metab; 2023 Aug; 108(9):2330-2335. PubMed ID: 36869713
[TBL] [Abstract][Full Text] [Related]
46. Diverse genetic causes of amenorrhea in an ethnically homogeneous cohort and an evolving approach to diagnosis.
Bakhshalizadeh S; Afkhami F; Bell KM; Robevska G; van den Bergen J; Cronin S; Jaillard S; Ayers KL; Kumar P; Siebold C; Xiao Z; Tate EW; Danaei S; Farzadi L; Shahbazi S; Sinclair AH; Tucker EJ
Mol Cell Endocrinol; 2024 Jun; 587():112212. PubMed ID: 38521400
[TBL] [Abstract][Full Text] [Related]
47. Premature ovarian insufficiency may be associated with the mutations in mitochondrial tRNA genes.
Ding Y; Xia BH; Zhuo GC; Zhang CJ; Leng JH
Endocr J; 2019 Jan; 66(1):81-88. PubMed ID: 30404982
[TBL] [Abstract][Full Text] [Related]
48. Homozygous Variant in KASH5 Causes Premature Ovarian Insufficiency by Disordered Meiotic Homologous Pairing.
Zhang Q; Tao C; Gao S; Li S; Xu B; Ke H; Wang Y; Zhang F; Qin Y; Zhang L; Guo T
J Clin Endocrinol Metab; 2022 Aug; 107(9):2589-2597. PubMed ID: 35708642
[TBL] [Abstract][Full Text] [Related]
49. miR-21 and Pellino-1 Expression Profiling in Autoimmune Premature Ovarian Insufficiency.
Li X; Xie J; Wang Q; Cai H; Xie C; Fu X
J Immunol Res; 2020; 2020():3582648. PubMed ID: 32352018
[TBL] [Abstract][Full Text] [Related]
50. EIF4ENIF1 variants in two patients with non-syndromic premature ovarian insufficiency.
Shang L; Ren S; Yang X; Zhang F; Jin L; Zhang X; Wu Y
Eur J Med Genet; 2022 Oct; 65(10):104597. PubMed ID: 36030004
[TBL] [Abstract][Full Text] [Related]
51.
Ramos L
Genes (Basel); 2022 Mar; 13(4):. PubMed ID: 35456418
[TBL] [Abstract][Full Text] [Related]
52. NOTCH2 variant D1853H is mutated in two non-syndromic premature ovarian insufficiency patients from a Chinese pedigree.
Li L; Feng F; Zhao M; Li T; Yue W; Ma X; Wang B; Yin C
J Ovarian Res; 2020 Apr; 13(1):41. PubMed ID: 32312275
[TBL] [Abstract][Full Text] [Related]
53. 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]
54. 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]
55. LARS2 variants can present as premature ovarian insufficiency in the absence of overt hearing loss.
Neyroud AS; Rudinger-Thirion J; Frugier M; Riley LG; Bidet M; Akloul L; Simpson A; Gilot D; Christodoulou J; Ravel C; Sinclair AH; Belaud-Rotureau MA; Tucker EJ; Jaillard S
Eur J Hum Genet; 2023 Apr; 31(4):453-460. PubMed ID: 36450801
[TBL] [Abstract][Full Text] [Related]
56. Rare variants in GPR3 in POI patients: a case series with review of literature.
Ren S; Zhang F; Shang L; Yang X; Pan Y; Zhang X; Wu Y
J Ovarian Res; 2023 Nov; 16(1):210. PubMed ID: 37919810
[TBL] [Abstract][Full Text] [Related]
57. Premature Ovarian Insufficiency: New Perspectives on Genetic Cause and Phenotypic Spectrum.
Tucker EJ; Grover SR; Bachelot A; Touraine P; Sinclair AH
Endocr Rev; 2016 Dec; 37(6):609-635. PubMed ID: 27690531
[TBL] [Abstract][Full Text] [Related]
58. CPEB1 deletion is not a common explanation for premature ovarian insufficiency in a Chinese cohort.
Jiao W; Zhao S; Liu R; Guo T; Qin Y
J Ovarian Res; 2020 Apr; 13(1):49. PubMed ID: 32354341
[TBL] [Abstract][Full Text] [Related]
59. Mutation in ALOX12B likely cause of POI and also ichthyosis in a large Iranian pedigree.
Alavi A; Darki F; Bidgoli MMR; Zare-Abdollahi D; Moini A; Shahshahani MM; Fischer J; Elahi E
Mol Genet Genomics; 2020 Jul; 295(4):1039-1053. PubMed ID: 32253496
[TBL] [Abstract][Full Text] [Related]
60. Premature ovarian insufficiency as a variable feature of blepharophimosis, ptosis, and epicanthus inversus syndrome associated with c.223C > T p.(Leu75Phe) FOXL2 mutation: a case report.
Grzechocińska B; Warzecha D; Wypchło M; Ploski R; Wielgoś M
BMC Med Genet; 2019 Jul; 20(1):132. PubMed ID: 31366388
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
