342 related articles for article (PubMed ID: 30406445)
21. No mutations in the PSMC3IP gene identified in a Swedish cohort of women with primary ovarian insufficiency.
Norling A; Hirschberg AL; Karlsson L; Rodriguez-Wallberg KA; Iwarsson E; Wedell A; Barbaro M
Sex Dev; 2014; 8(4):146-50. PubMed ID: 24481226
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Two rare loss-of-function variants in the STAG3 gene leading to primary ovarian insufficiency.
França MM; Nishi MY; Funari MFA; Lerario AM; Baracat EC; Hayashida SAY; Maciel GAR; Jorge AAL; Mendonca BB
Eur J Med Genet; 2019 Mar; 62(3):186-189. PubMed ID: 30006057
[TBL] [Abstract][Full Text] [Related]
24. Causal and Candidate Gene Variants in a Large Cohort of Women With Primary Ovarian Insufficiency.
Gorsi B; Hernandez E; Moore MB; Moriwaki M; Chow CY; Coelho E; Taylor E; Lu C; Walker A; Touraine P; Nelson LM; Cooper AR; Mardis ER; Rajkovic A; Yandell M; Welt CK
J Clin Endocrinol Metab; 2022 Feb; 107(3):685-714. PubMed ID: 34718612
[TBL] [Abstract][Full Text] [Related]
25. Primary ovarian insufficiency in a female with phosphomannomutase-2 gene (PMM2) mutations for congenital disorder of glycosylation.
Masunaga Y; Mochizuki M; Kadoya M; Wada Y; Okamoto N; Fukami M; Kato F; Saitsu H; Ogata T
Endocr J; 2021 May; 68(5):605-611. PubMed ID: 33583911
[TBL] [Abstract][Full Text] [Related]
26. Heterozygous FMN2 missense variant found in a family case of premature ovarian insufficiency.
Li J; Peng T; Wang L; Long P; Quan R; Tan H; Zeng M; Wu X; Yang J; Xiao H; Shi X
J Ovarian Res; 2022 Feb; 15(1):31. PubMed ID: 35227295
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. 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]
30. 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]
31. Variations of C14ORF39 and SYCE1 Identified in Idiopathic Premature Ovarian Insufficiency and Nonobstructive Azoospermia.
Hou D; Yao C; Xu B; Luo W; Ke H; Li Z; Qin Y; Guo T
J Clin Endocrinol Metab; 2022 Feb; 107(3):724-734. PubMed ID: 34718620
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. 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]
34. TP63-truncating variants cause isolated premature ovarian insufficiency.
Tucker EJ; Jaillard S; Grover SR; van den Bergen J; Robevska G; Bell KM; Sadedin S; Hanna C; Dulon J; Touraine P; Sinclair AH
Hum Mutat; 2019 Jul; 40(7):886-892. PubMed ID: 30924587
[TBL] [Abstract][Full Text] [Related]
35. A novel EIF4ENIF1 mutation associated with a diminished ovarian reserve and premature ovarian insufficiency identified by whole-exome sequencing.
Zhao M; Feng F; Chu C; Yue W; Li L
J Ovarian Res; 2019 Dec; 12(1):119. PubMed ID: 31810472
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. Molecular Genetics of Premature Ovarian Insufficiency.
Jiao X; Ke H; Qin Y; Chen ZJ
Trends Endocrinol Metab; 2018 Nov; 29(11):795-807. PubMed ID: 30078697
[TBL] [Abstract][Full Text] [Related]
39.
He WB; Tu CF; Liu Q; Meng LL; Yuan SM; Luo AX; He FS; Shen J; Li W; Du J; Zhong CG; Lu GX; Lin G; Fan LQ; Tan YQ
J Med Genet; 2018 Mar; 55(3):198-204. PubMed ID: 29331980
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
