222 related articles for article (PubMed ID: 35285020)
1. Bi-allelic SPATA22 variants cause premature ovarian insufficiency and nonobstructive azoospermia due to meiotic arrest.
Yao C; Hou D; Ji Z; Pang D; Li P; Tian R; Zhang Y; Ou N; Bai H; Zhi E; Huang Y; Qin Y; Zhao J; Wang C; Zhou Z; Guo T; Li Z
Clin Genet; 2022 May; 101(5-6):507-516. PubMed ID: 35285020
[TBL] [Abstract][Full Text] [Related]
2.
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]
3. 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]
4. 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]
5. Bi-allelic
Yao C; Yang C; Zhao L; Li P; Tian R; Chen H; Guo Y; Huang Y; Zhi E; Zhai J; Sun H; Zhang J; Hong Y; Zhang L; Ji Z; Zhang F; Zhou Z; Li Z
J Med Genet; 2021 Oct; 58(10):679-686. PubMed ID: 32900840
[TBL] [Abstract][Full Text] [Related]
6. A novel homozygote nonsense variant of MSH4 leads to primary ovarian insufficiency and non-obstructive azoospermia.
Hashemi Sheikhshabani S; Ghafouri-Fard S; Hosseini E; Omrani MD
Mol Biol Rep; 2024 Jan; 51(1):68. PubMed ID: 38175272
[TBL] [Abstract][Full Text] [Related]
7. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.
Riera-Escamilla A; Enguita-Marruedo A; Moreno-Mendoza D; Chianese C; Sleddens-Linkels E; Contini E; Benelli M; Natali A; Colpi GM; Ruiz-Castañé E; Maggi M; Baarends WM; Krausz C
Hum Reprod; 2019 Jun; 34(6):978-988. PubMed ID: 31125047
[TBL] [Abstract][Full Text] [Related]
8. Novel bi-allelic MSH4 variants causes meiotic arrest and non-obstructive azoospermia.
Li P; Ji Z; Zhi E; Zhang Y; Han S; Zhao L; Tian R; Chen H; Huang Y; Zhang J; Chen H; Zhao F; Zhou Z; Li Z; Yao C
Reprod Biol Endocrinol; 2022 Jan; 20(1):21. PubMed ID: 35090489
[TBL] [Abstract][Full Text] [Related]
9. A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest.
Okutman O; Boivin M; Muller J; Charlet-Berguerand N; Viville S
Hum Reprod; 2023 Feb; 38(2):306-314. PubMed ID: 36524333
[TBL] [Abstract][Full Text] [Related]
10. Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humans.
Wu H; Zhang X; Hua R; Li Y; Cheng L; Li K; Liu Y; Gao Y; Shen Q; Wang G; Lv M; Xu Y; He X; Cao Y; Liu M
Hum Genet; 2022 Nov; 141(11):1795-1809. PubMed ID: 35587281
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. A pathogenic DMC1 frameshift mutation causes nonobstructive azoospermia but not primary ovarian insufficiency in humans.
Cao D; Shi F; Guo C; Liu Y; Lin Z; Zhang J; Li RHW; Yao Y; Liu K; Ng EHY; Yeung WSB; Wang T
Mol Hum Reprod; 2021 Sep; 27(9):. PubMed ID: 34515795
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Novel MEIOB pathogenic variants including a homozygous non-canonical splicing variant, cause meiotic arrest and human non-obstructive azoospermia.
Zhu X; Hu K; Cheng H; Wu H; Li K; Gao Y; Lv M; Xu C; Geng H; Shen Q; Cao Y; He X; Tang D; Guo R
Clin Genet; 2024 Jan; 105(1):99-105. PubMed ID: 37715646
[TBL] [Abstract][Full Text] [Related]
15. Novel STAG3 variant associated with primary ovarian insufficiency and non-obstructive azoospermia in an Iranian consanguineous family.
Akbari A; Zoha Tabatabaei S; Salehi N; Padidar K; Almadani N; Ali Sadighi Gilani M; Mashayekhi M; Motevaseli E; Totonchi M
Gene; 2022 May; 821():146281. PubMed ID: 35176428
[TBL] [Abstract][Full Text] [Related]
16. STAG3 homozygous missense variant causes primary ovarian insufficiency and male non-obstructive azoospermia.
Jaillard S; McElreavy K; Robevska G; Akloul L; Ghieh F; Sreenivasan R; Beaumont M; Bashamboo A; Bignon-Topalovic J; Neyroud AS; Bell K; Veron-Gastard E; Launay E; van den Bergen J; Nouyou B; Vialard F; Belaud-Rotureau MA; Ayers KL; Odent S; Ravel C; Tucker EJ; Sinclair AH
Mol Hum Reprod; 2020 Sep; 26(9):665-677. PubMed ID: 32634216
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Whole-exome sequencing in patients with maturation arrest: a potential additional diagnostic tool for prevention of recurrent negative testicular sperm extraction outcomes.
Ghieh F; Barbotin AL; Swierkowski-Blanchard N; Leroy C; Fortemps J; Gerault C; Hue C; Mambu Mambueni H; Jaillard S; Albert M; Bailly M; Izard V; Molina-Gomes D; Marcelli F; Prasivoravong J; Serazin V; Dieudonne MN; Delcroix M; Garchon HJ; Louboutin A; Mandon-Pepin B; Ferlicot S; Vialard F
Hum Reprod; 2022 May; 37(6):1334-1350. PubMed ID: 35413094
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.
Fan S; Jiao Y; Khan R; Jiang X; Javed AR; Ali A; Zhang H; Zhou J; Naeem M; Murtaza G; Li Y; Yang G; Zaman Q; Zubair M; Guan H; Zhang X; Ma H; Jiang H; Ali H; Dil S; Shah W; Ahmad N; Zhang Y; Shi Q
Am J Hum Genet; 2021 Feb; 108(2):324-336. PubMed ID: 33508233
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
