172 related articles for article (PubMed ID: 38672141)
1. Exome Sequencing to Identify Novel Variants Associated with Secondary Amenorrhea and Premature Ovarian Insufficiency (POI) in Saudi Women.
Almatrafi AM; Hibshi AM; Basit S
Biomedicines; 2024 Apr; 12(4):. PubMed ID: 38672141
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
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. Sequence variants of KHDRBS1 as high penetrance susceptibility risks for primary ovarian insufficiency by mis-regulating mRNA alternative splicing.
Wang B; Li L; Zhu Y; Zhang W; Wang X; Chen B; Li T; Pan H; Wang J; Kee K; Cao Y
Hum Reprod; 2017 Oct; 32(10):2138-2146. PubMed ID: 28938739
[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. Compound heterozygous null mutations of NOBOX in sisters with delayed puberty and primary amenorrhea.
Sassi A; Désir J; Duerinckx S; Soblet J; Van Dooren S; Bonduelle M; Abramowicz M; Delbaere A
Mol Genet Genomic Med; 2021 Oct; 9(10):e1776. PubMed ID: 34480423
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Landscape of pathogenic mutations in premature ovarian insufficiency.
Ke H; Tang S; Guo T; Hou D; Jiao X; Li S; Luo W; Xu B; Zhao S; Li G; Zhang X; Xu S; Wang L; Wu Y; Wang J; Zhang F; Qin Y; Jin L; Chen ZJ
Nat Med; 2023 Feb; 29(2):483-492. PubMed ID: 36732629
[TBL] [Abstract][Full Text] [Related]
11. Targeted Next-Generation Sequencing Indicates a Frequent Oligogenic Involvement in Primary Ovarian Insufficiency Onset.
Rossetti R; Moleri S; Guizzardi F; Gentilini D; Libera L; Marozzi A; Moretti C; Brancati F; Bonomi M; Persani L
Front Endocrinol (Lausanne); 2021; 12():664645. PubMed ID: 34803902
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Homozygous missense variant in MEIOSIN causes premature ovarian insufficiency.
Zhang Q; Zhang W; Wu X; Ke H; Qin Y; Zhao S; Guo T
Hum Reprod; 2023 Nov; 38(Supplement_2):ii47-ii56. PubMed ID: 37982418
[TBL] [Abstract][Full Text] [Related]
15. Novel
Wang Y; Liu L; Tan C; Meng G; Meng L; Nie H; Du J; Lu GX; Lin G; He WB; Tan YQ
Front Genet; 2022; 13():936264. PubMed ID: 35991565
[No Abstract] [Full Text] [Related]
16. 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]
17. Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency.
Turkyilmaz A; Alavanda C; Ates EA; Geckinli BB; Polat H; Gokcu M; Karakaya T; Cebi AH; Soylemez MA; Guney Aİ; Ata P; Arman A
J Assist Reprod Genet; 2022 Mar; 39(3):695-710. PubMed ID: 35066699
[TBL] [Abstract][Full Text] [Related]
18. Improving diagnostic precision in primary ovarian insufficiency using comprehensive genetic and autoantibody testing.
Vogt EC; Bratland E; Berland S; Berentsen R; Lund A; Björnsdottir S; Husebye E; Øksnes M
Hum Reprod; 2024 Jan; 39(1):177-189. PubMed ID: 37953503
[TBL] [Abstract][Full Text] [Related]
19. High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function.
Bestetti I; Castronovo C; Sironi A; Caslini C; Sala C; Rossetti R; Crippa M; Ferrari I; Pistocchi A; Toniolo D; Persani L; Marozzi A; Finelli P
Hum Reprod; 2019 Mar; 34(3):574-583. PubMed ID: 30689869
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
