147 related articles for article (PubMed ID: 29966603)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
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. 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]
9. Pathogenic variants of ATG4D in infertile men with non-obstructive azoospermia identified using whole-exome sequencing.
Sha Y; Liu W; Wei X; Zhu X; Tang B; Zhang X; Yang X; Wang Y; Wang X
Clin Genet; 2021 Sep; 100(3):280-291. PubMed ID: 33988247
[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. Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family.
Okutman O; Muller J; Baert Y; Serdarogullari M; Gultomruk M; Piton A; Rombaut C; Benkhalifa M; Teletin M; Skory V; Bakircioglu E; Goossens E; Bahceci M; Viville S
Hum Mol Genet; 2015 Oct; 24(19):5581-8. PubMed ID: 26199321
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A novel missense variant in CDK5RAP2 associated with non-obstructive azoospermia.
Rahimian M; Askari M; Salehi N; Riccio A; Jaafarinia M; Almadani N; Totonchi M
Taiwan J Obstet Gynecol; 2023 Nov; 62(6):830-837. PubMed ID: 38008501
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. A Novel Frameshift Microdeletion of the TEX12 Gene Caused Infertility in Two Brothers with Nonobstructive Azoospermia.
Bui MD; Luong TLA; Tran HD; Duong TTH; Nguyen TN; Nguyen DT; Nguyen TD; Nong VH
Reprod Sci; 2023 Sep; 30(9):2876-2881. PubMed ID: 37012491
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans.
Tan YQ; Tu C; Meng L; Yuan S; Sjaarda C; Luo A; Du J; Li W; Gong F; Zhong C; Deng HX; Lu G; Liang P; Lin G
Genet Med; 2019 May; 21(5):1209-1217. PubMed ID: 31048812
[TBL] [Abstract][Full Text] [Related]
19. 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]
20.
Wan YY; Guo L; Yao Y; Shi XY; Jiang H; Xu B; Hua J; Zhang XS
Asian J Androl; 2022; 24(2):186-190. PubMed ID: 34596601
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
