208 related articles for article (PubMed ID: 30878252)
1. A novel homozygous FBXO43 mutation associated with male infertility and teratozoospermia in a consanguineous Chinese family.
Ma Y; Xie N; Xie D; Sun L; Li S; Li P; Li Y; Li J; Dong Z; Xie X
Fertil Steril; 2019 May; 111(5):909-917.e1. PubMed ID: 30878252
[TBL] [Abstract][Full Text] [Related]
2. A homozygous RPL10L missense mutation associated with male factor infertility and severe oligozoospermia.
Tu C; Meng L; Nie H; Yuan S; Wang W; Du J; Lu G; Lin G; Tan YQ
Fertil Steril; 2020 Mar; 113(3):561-568. PubMed ID: 32111475
[TBL] [Abstract][Full Text] [Related]
3. FBXO43 variants in patients with female infertility characterized by early embryonic arrest.
Wang W; Wang W; Xu Y; Shi J; Fu J; Chen B; Mu J; Zhang Z; Zhao L; Lin J; Du J; Li Q; He L; Jin L; Sun X; Wang L; Sang Q
Hum Reprod; 2021 Jul; 36(8):2392-2402. PubMed ID: 34052850
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella.
Martinez G; Kherraf ZE; Zouari R; Fourati Ben Mustapha S; Saut A; Pernet-Gallay K; Bertrand A; Bidart M; Hograindleur JP; Amiri-Yekta A; Kharouf M; Karaouzène T; Thierry-Mieg N; Dacheux-Deschamps D; Satre V; Bonhivers M; Touré A; Arnoult C; Ray PF; Coutton C
Hum Reprod; 2018 Oct; 33(10):1973-1984. PubMed ID: 30137358
[TBL] [Abstract][Full Text] [Related]
7. A novel homozygous missense mutation of PMFBP1 causes acephalic spermatozoa syndrome.
Lu M; Kong S; Xiang M; Wang Y; Zhang J; Duan Z; Zha X; Wang F; Cao Y; Zhu F
J Assist Reprod Genet; 2021 Apr; 38(4):949-955. PubMed ID: 33484382
[TBL] [Abstract][Full Text] [Related]
8. Whole-exome sequencing identified a novel mutation of AURKC in a Chinese family with macrozoospermia.
Hua J; Wan YY
J Assist Reprod Genet; 2019 Mar; 36(3):529-534. PubMed ID: 30594972
[TBL] [Abstract][Full Text] [Related]
9. Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia.
Oud MS; Okutman Ö; Hendricks LAJ; de Vries PF; Houston BJ; Vissers LELM; O'Bryan MK; Ramos L; Chemes HE; Viville S; Veltman JA
Hum Reprod; 2020 Jan; 35(1):240-252. PubMed ID: 31985809
[TBL] [Abstract][Full Text] [Related]
10. Whole-exome sequencing of a cohort of infertile men reveals novel causative genes in teratozoospermia that are chiefly related to sperm head defects.
Li Y; Wang Y; Wen Y; Zhang T; Wang X; Jiang C; Zheng R; Zhou F; Chen D; Yang Y; Shen Y
Hum Reprod; 2021 Dec; 37(1):152-177. PubMed ID: 34791246
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Biallelic mutations in KATNAL2 cause male infertility due to oligo-astheno-teratozoospermia.
Wei X; Liu W; Zhu X; Li Y; Zhang X; Chen J; Isachenko V; Sha Y; Lu Z
Clin Genet; 2021 Oct; 100(4):376-385. PubMed ID: 34096614
[TBL] [Abstract][Full Text] [Related]
14. Whole Exome Sequencing of a Consanguineous Turkish Family Identifies a Mutation in GTF2H3 in Brothers With Spermatogenic Failure.
Clavijo RI; Arora H; Gibbs E; Cohen S; Griswold A; Bakircioglu E; Bademci G; Tekin M; Ramasamy R
Urology; 2018 Oct; 120():86-89. PubMed ID: 29966603
[TBL] [Abstract][Full Text] [Related]
15. DNAH1 gene mutations and their potential association with dysplasia of the sperm fibrous sheath and infertility in the Han Chinese population.
Sha Y; Yang X; Mei L; Ji Z; Wang X; Ding L; Li P; Yang S
Fertil Steril; 2017 Jun; 107(6):1312-1318.e2. PubMed ID: 28577616
[TBL] [Abstract][Full Text] [Related]
16. Loss-of-function mutations in centrosomal protein 112 is associated with human acephalic spermatozoa phenotype.
Sha Y; Wang X; Yuan J; Zhu X; Su Z; Zhang X; Xu X; Wei X
Clin Genet; 2020 Feb; 97(2):321-328. PubMed ID: 31654588
[TBL] [Abstract][Full Text] [Related]
17. A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.
Okutman O; Muller J; Skory V; Garnier JM; Gaucherot A; Baert Y; Lamour V; Serdarogullari M; Gultomruk M; Röpke A; Kliesch S; Herbepin V; Aknin I; Benkhalifa M; Teletin M; Bakircioglu E; Goossens E; Charlet-Berguerand N; Bahceci M; Tüttelmann F; Viville S
J Assist Reprod Genet; 2017 May; 34(5):683-694. PubMed ID: 28401488
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing.
Wei C; Yang L; Cheng J; Imani S; Fu S; Lv H; Li Y; Chen R; Leung EL; Fu J
BMC Med Genet; 2018 Jun; 19(1):99. PubMed ID: 29890953
[TBL] [Abstract][Full Text] [Related]
20. Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player.
Celse T; Cazin C; Mietton F; Martinez G; Martinez D; Thierry-Mieg N; Septier A; Guillemain C; Beurois J; Clergeau A; Mustapha SFB; Kharouf M; Zoghmar A; Chargui A; Papaxanthos A; Dorphin B; Foliguet B; Triki C; Sifer C; Lauton D; Tachdjian G; Schuler G; Lejeune H; Puechberty J; Bessonnat J; Pasquier L; Mery L; Poulain M; Chaabouni M; Sermondade N; Cabry R; Benbouhadja S; Veau S; Frapsauce C; Mitchell V; Achard V; Satre V; Hennebicq S; Zouari R; Arnoult C; Kherraf ZE; Coutton C; Ray PF
Hum Genet; 2021 Jan; 140(1):43-57. PubMed ID: 33108537
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
