387 related articles for article (PubMed ID: 29790874)
1. Point-of-care whole-exome sequencing of idiopathic male infertility.
Fakhro KA; Elbardisi H; Arafa M; Robay A; Rodriguez-Flores JL; Al-Shakaki A; Syed N; Mezey JG; Abi Khalil C; Malek JA; Al-Ansari A; Al Said S; Crystal RG
Genet Med; 2018 Nov; 20(11):1365-1373. PubMed ID: 29790874
[TBL] [Abstract][Full Text] [Related]
2. 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]
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. 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]
5. Whole-exome sequencing of a large Chinese azoospermia and severe oligospermia cohort identifies novel infertility causative variants and genes.
Chen S; Wang G; Zheng X; Ge S; Dai Y; Ping P; Chen X; Liu G; Zhang J; Yang Y; Zhang X; Zhong A; Zhu Y; Chu Q; Huang Y; Zhang Y; Shen C; Yuan Y; Yuan Q; Pei X; Cheng CY; Sun F
Hum Mol Genet; 2020 Aug; 29(14):2451-2459. PubMed ID: 32469048
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Whole-exome sequencing identifies novel homozygous mutation in NPAS2 in family with nonobstructive azoospermia.
Ramasamy R; Bakırcıoğlu ME; Cengiz C; Karaca E; Scovell J; Jhangiani SN; Akdemir ZC; Bainbridge M; Yu Y; Huff C; Gibbs RA; Lupski JR; Lamb DJ
Fertil Steril; 2015 Aug; 104(2):286-91. PubMed ID: 25956372
[TBL] [Abstract][Full Text] [Related]
8.
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]
9. Two Novel TEX15 Mutations in a Family with Nonobstructive Azoospermia.
Colombo R; Pontoglio A; Bini M
Gynecol Obstet Invest; 2017; 82(3):283-286. PubMed ID: 28355598
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. The second mutation of SYCE1 gene associated with autosomal recessive nonobstructive azoospermia.
Pashaei M; Rahimi Bidgoli MM; Zare-Abdollahi D; Najmabadi H; Haji-Seyed-Javadi R; Fatehi F; Alavi A
J Assist Reprod Genet; 2020 Feb; 37(2):451-458. PubMed ID: 31916078
[TBL] [Abstract][Full Text] [Related]
13. Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia.
Tang D; Li K; Geng H; Xu C; Lv M; Gao Y; Wang G; Yu H; Shao Z; Shen Q; Jiang H; Zhang X; He X; Cao Y
Reprod Biol Endocrinol; 2022 Apr; 20(1):63. PubMed ID: 35366911
[TBL] [Abstract][Full Text] [Related]
14. Genetic variants in Ser-Arg protein-coding genes are associated with the risk of nonobstructive azoospermia in Chinese men.
Ni B; Ma H; Lin Y; Dai J; Guo X; Xia Y; Sha J; Hu Z
Fertil Steril; 2014 Jun; 101(6):1711-7.e1-2. PubMed ID: 24661730
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Whole-genome sequencing identifies new candidate genes for nonobstructive azoospermia.
Malcher A; Stokowy T; Berman A; Olszewska M; Jedrzejczak P; Sielski D; Nowakowski A; Rozwadowska N; Yatsenko AN; Kurpisz MK
Andrology; 2022 Nov; 10(8):1605-1624. PubMed ID: 36017582
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Systematic molecular analyses for 115 karyotypically normal men with isolated non-obstructive azoospermia.
Muranishi Y; Kobori Y; Katoh-Fukui Y; Tamaoka S; Hattori A; Osaka A; Okada H; Nakabayashi K; Hata K; Kawai T; Ogata-Kawata H; Iwahata T; Saito K; Kon M; Shinohara N; Fukami M
Hum Reprod; 2024 May; 39(5):1131-1140. PubMed ID: 38511217
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]