These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
216 related articles for article (PubMed ID: 25956372)
1. 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]
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. 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]
4. 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]
5. 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]
6. 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]
7. 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]
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. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. Whole-exome sequencing identifies novel compound heterozygous mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa. Méndez-Vidal C; González-Del Pozo M; Vela-Boza A; Santoyo-López J; López-Domingo FJ; Vázquez-Marouschek C; Dopazo J; Borrego S; Antiñolo G Mol Vis; 2013; 19():2187-95. PubMed ID: 24227914 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
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. 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]
19. 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]
20. 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] [Next] [New Search]