327 related articles for article (PubMed ID: 28938739)
21. Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform.
Norling A; Hirschberg AL; Rodriguez-Wallberg KA; Iwarsson E; Wedell A; Barbaro M
Hum Reprod; 2014 Aug; 29(8):1818-27. PubMed ID: 24939957
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. 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]
25. 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]
26. Whole-exome sequencing identifies a homozygous donor splice-site mutation in STAG3 that causes primary ovarian insufficiency.
He WB; Banerjee S; Meng LL; Du J; Gong F; Huang H; Zhang XX; Wang YY; Lu GX; Lin G; Tan YQ
Clin Genet; 2018 Feb; 93(2):340-344. PubMed ID: 28393351
[TBL] [Abstract][Full Text] [Related]
27. Successful fertility preservation following ovarian tissue vitrification in patients with primary ovarian insufficiency.
Suzuki N; Yoshioka N; Takae S; Sugishita Y; Tamura M; Hashimoto S; Morimoto Y; Kawamura K
Hum Reprod; 2015 Mar; 30(3):608-15. PubMed ID: 25567618
[TBL] [Abstract][Full Text] [Related]
28. Differentiation of primordial germ cells from induced pluripotent stem cells of primary ovarian insufficiency.
Leng L; Tan Y; Gong F; Hu L; Ouyang Q; Zhao Y; Lu G; Lin G
Hum Reprod; 2015 Mar; 30(3):737-48. PubMed ID: 25586786
[TBL] [Abstract][Full Text] [Related]
29. Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations.
Amiri-Yekta A; Coutton C; Kherraf ZE; Karaouzène T; Le Tanno P; Sanati MH; Sabbaghian M; Almadani N; Sadighi Gilani MA; Hosseini SH; Bahrami S; Daneshipour A; Bini M; Arnoult C; Colombo R; Gourabi H; Ray PF
Hum Reprod; 2016 Dec; 31(12):2872-2880. PubMed ID: 27798045
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Rare missense variant in MSH4 associated with primary gonadal failure in both 46, XX and 46, XY individuals.
Akbari A; Padidar K; Salehi N; Mashayekhi M; Almadani N; Sadighi Gilani MA; Bashambou A; McElreavey K; Totonchi M
Hum Reprod; 2021 Mar; 36(4):1134-1145. PubMed ID: 33448284
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Novel alanyl-tRNA synthetase 2 (AARS2) homozygous mutation in a consanguineous Chinese family with premature ovarian insufficiency.
Zhou Y; Chen B; Li L; Pan H; Liu B; Li T; Wang R; Ma X; Wang B; Cao Y
Fertil Steril; 2019 Sep; 112(3):569-576.e2. PubMed ID: 31280959
[TBL] [Abstract][Full Text] [Related]
34. Whole-exome sequencing of consanguineous families with infertile men and women identifies homologous mutations in SPATA22 and MEIOB.
Wu Y; Li Y; Murtaza G; Zhou J; Jiao Y; Gong C; Hu C; Han Q; Zhang H; Zhang Y; Shi B; Ma H; Jiang X; Shi Q
Hum Reprod; 2021 Sep; 36(10):2793-2804. PubMed ID: 34392356
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. ZSWIM7 Is Associated With Human Female Meiosis and Familial Primary Ovarian Insufficiency.
McGlacken-Byrne SM; Le Quesne Stabej P; Del Valle I; Ocaka L; Gagunashvili A; Crespo B; Moreno N; James C; Bacchelli C; Dattani MT; Williams HJ; Kelberman D; Achermann JC; Conway GS
J Clin Endocrinol Metab; 2022 Jan; 107(1):e254-e263. PubMed ID: 34402903
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. A novel missense variant in LAMC1 identified in a POI family by whole exome sequencing.
Xu H; Wang C; Wei H; Li T; Fang Y; Wang B
Gynecol Endocrinol; 2023 Oct; 39(1):2265507. PubMed ID: 37839437
[TBL] [Abstract][Full Text] [Related]
39. Consanguineous Chinese Familial Study Reveals that a Gross Deletion that Includes the SYCE1 Gene Region Is Associated with Premature Ovarian Insufficiency.
Zhe J; Ye D; Chen X; Liu Y; Zhou X; Li Y; Zhang J; Chen S
Reprod Sci; 2020 Feb; 27(2):461-467. PubMed ID: 31925770
[TBL] [Abstract][Full Text] [Related]
40. Mutations in the stromal antigen 3 (STAG3) gene cause male infertility due to meiotic arrest.
van der Bijl N; Röpke A; Biswas U; Wöste M; Jessberger R; Kliesch S; Friedrich C; Tüttelmann F
Hum Reprod; 2019 Nov; 34(11):2112-2119. PubMed ID: 31682730
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]