304 related articles for article (PubMed ID: 32900840)
1. 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]
2. 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]
3. 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]
4. Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice.
Wang W; Meng L; He J; Su L; Li Y; Tan C; Xu X; Nie H; Zhang H; Du J; Lu G; Luo M; Lin G; Tu C; Tan YQ
Mol Hum Reprod; 2022 May; 28(6):. PubMed ID: 35485979
[TBL] [Abstract][Full Text] [Related]
5. Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia.
Kasak L; Punab M; Nagirnaja L; Grigorova M; Minajeva A; Lopes AM; Punab AM; Aston KI; Carvalho F; Laasik E; Smith LB; ; Conrad DF; Laan M
Am J Hum Genet; 2018 Aug; 103(2):200-212. PubMed ID: 30075111
[TBL] [Abstract][Full Text] [Related]
6. 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]
7.
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]
8. A homozygous frameshift variant in SYCP2 caused meiotic arrest and non-obstructive azoospermia.
Xu J; Sun Y; Zhang Y; Ou N; Bai H; Zhao J; Xu S; Luo J; Han S; Li P; Tian R; Zhi E; Huang Y; Zhang J; Liu G; Li Z; Yao C
Clin Genet; 2023 Nov; 104(5):577-581. PubMed ID: 37337432
[TBL] [Abstract][Full Text] [Related]
9. A homozygous loss-of-function mutation in FBXO43 causes human non-obstructive azoospermia.
Wu H; Zhang X; Shen Q; Liu Y; Gao Y; Wang G; Lv M; Hua R; Xu Y; Zhou P; Wei Z; Tao F; He X; Cao Y; Liu M
Clin Genet; 2022 Jan; 101(1):55-64. PubMed ID: 34595750
[TBL] [Abstract][Full Text] [Related]
10. Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility.
Wyrwoll MJ; Temel ŞG; Nagirnaja L; Oud MS; Lopes AM; van der Heijden GW; Heald JS; Rotte N; Wistuba J; Wöste M; Ledig S; Krenz H; Smits RM; Carvalho F; Gonçalves J; Fietz D; Türkgenç B; Ergören MC; Çetinkaya M; Başar M; Kahraman S; McEleny K; Xavier MJ; Turner H; Pilatz A; Röpke A; Dugas M; Kliesch S; Neuhaus N; ; Aston KI; Conrad DF; Veltman JA; Friedrich C; Tüttelmann F
Am J Hum Genet; 2020 Aug; 107(2):342-351. PubMed ID: 32673564
[TBL] [Abstract][Full Text] [Related]
11. A new MEIOB mutation is a recurrent cause for azoospermia and testicular meiotic arrest.
Gershoni M; Hauser R; Barda S; Lehavi O; Arama E; Pietrokovski S; Kleiman SE
Hum Reprod; 2019 Apr; 34(4):666-671. PubMed ID: 30838384
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermia.
Huang Y; Tian R; Xu J; Ji Z; Zhang Y; Zhao L; Yang C; Li P; Zhi E; Bai H; Han S; Luo J; Zhao J; Zhang J; Zhou Z; Li Z; Yao C
BMC Med Genomics; 2022 Jun; 15(1):137. PubMed ID: 35718780
[TBL] [Abstract][Full Text] [Related]
14. Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia.
Salas-Huetos A; Tüttelmann F; Wyrwoll MJ; Kliesch S; Lopes AM; Goncalves J; Boyden SE; Wöste M; Hotaling JM; ; Nagirnaja L; Conrad DF; Carrell DT; Aston KI
Hum Genet; 2021 Jan; 140(1):217-227. PubMed ID: 33211200
[TBL] [Abstract][Full Text] [Related]
15. A bi-allelic REC114 loss-of-function variant causes meiotic arrest and nonobstructive azoospermia.
Xu S; Zhao J; Gao F; Zhang Y; Luo J; Zhang C; Tian R; Zhi E; Zhang J; Bai F; Sun H; Zhao F; Huang Y; Li P; Jiang L; Li Z; Yao C; Zhou Z
Clin Genet; 2024 Apr; 105(4):440-445. PubMed ID: 38148155
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. A recurrent ZSWIM7 mutation causes male infertility resulting from decreased meiotic recombination.
Li Y; Wu Y; Zhou J; Zhang H; Zhang Y; Ma H; Jiang X; Shi Q
Hum Reprod; 2021 Apr; 36(5):1436-1445. PubMed ID: 33713115
[TBL] [Abstract][Full Text] [Related]
18. Biallelic HFM1 variants cause non-obstructive azoospermia with meiotic arrest in humans by impairing crossover formation to varying degrees.
Xie X; Murtaza G; Li Y; Zhou J; Ye J; Khan R; Jiang L; Khan I; Zubair M; Yin H; Jiang H; Liu W; Shi B; Hou X; Gong C; Fan S; Wang Y; Jiang X; Zhang Y; Zhang H; Ma H; Shi Q
Hum Reprod; 2022 Jun; 37(7):1664-1677. PubMed ID: 35526155
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
