663 related articles for article (PubMed ID: 30078697)
21. Prediction of premature ovarian insufficiency: foolish fallacy or feasible foresight?
Nelson SM; Anderson RA
Climacteric; 2021 Oct; 24(5):438-443. PubMed ID: 33522318
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing.
Laissue P
Mol Cell Endocrinol; 2018 Jan; 460():170-180. PubMed ID: 28743519
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. 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]
27. Rare deleterious BUB1B variants induce premature ovarian insufficiency and early menopause.
Chen Q; Ke H; Luo X; Wang L; Wu Y; Tang S; Li J; Jin L; Zhang F; Qin Y; Chen X
Hum Mol Genet; 2020 Sep; 29(16):2698-2707. PubMed ID: 32716490
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. Next-generation sequencing of 500 POI patients identified novel responsible monogenic and oligogenic variants.
Luo W; Ke H; Tang S; Jiao X; Li Z; Zhao S; Zhang F; Guo T; Qin Y
J Ovarian Res; 2023 Feb; 16(1):39. PubMed ID: 36793102
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. 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]
33. Variants in Homologous Recombination Genes EXO1 and RAD51 Related with Premature Ovarian Insufficiency.
Luo W; Guo T; Li G; Liu R; Zhao S; Song M; Zhang L; Wang S; Chen ZJ; Qin Y
J Clin Endocrinol Metab; 2020 Oct; 105(10):. PubMed ID: 32772095
[TBL] [Abstract][Full Text] [Related]
34. Meiotic Recombination Defects and Premature Ovarian Insufficiency.
Huang C; Guo T; Qin Y
Front Cell Dev Biol; 2021; 9():652407. PubMed ID: 33763429
[TBL] [Abstract][Full Text] [Related]
35. Pathogenic Variations of Homologous Recombination Gene
Li S; Xu W; Xu B; Gao S; Zhang Q; Qin Y; Guo T
Front Cell Dev Biol; 2021; 9():768123. PubMed ID: 35174157
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Whole exome sequencing identified a rare WT1 loss-of-function variant in a non-syndromic POI patient.
Wang Y; Chen Q; Zhang F; Yang X; Shang L; Ren S; Pan Y; Zhou Z; Li G; Fang Y; Jin L; Wu Y; Zhang X
Mol Genet Genomic Med; 2022 Jan; 10(1):e1820. PubMed ID: 34845858
[TBL] [Abstract][Full Text] [Related]
38. Single-cell RNA-seq identified novel genes involved in primordial follicle formation.
Tan HJ; Deng ZH; Shen H; Deng HW; Xiao HM
Front Endocrinol (Lausanne); 2023; 14():1285667. PubMed ID: 38149096
[TBL] [Abstract][Full Text] [Related]
39. DNA double-strand break genetic variants in patients with premature ovarian insufficiency.
Ding X; Gong X; Fan Y; Cao J; Zhao J; Zhang Y; Wang X; Meng K
J Ovarian Res; 2023 Jul; 16(1):135. PubMed ID: 37430352
[TBL] [Abstract][Full Text] [Related]
40. Genetics of Reproductive Aging from Gonadal Dysgenesis through Menopause.
Desai S; Rajkovic A
Semin Reprod Med; 2017 Mar; 35(2):147-159. PubMed ID: 28278532
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
