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.
217 related articles for article (PubMed ID: 35013161)
1. A de novo paradigm for male infertility. Oud MS; Smits RM; Smith HE; Mastrorosa FK; Holt GS; Houston BJ; de Vries PF; Alobaidi BKS; Batty LE; Ismail H; Greenwood J; Sheth H; Mikulasova A; Astuti GDN; Gilissen C; McEleny K; Turner H; Coxhead J; Cockell S; Braat DDM; Fleischer K; D'Hauwers KWM; Schaafsma E; ; Nagirnaja L; Conrad DF; Friedrich C; Kliesch S; Aston KI; Riera-Escamilla A; Krausz C; Gonzaga-Jauregui C; Santibanez-Koref M; Elliott DJ; Vissers LELM; Tüttelmann F; O'Bryan MK; Ramos L; Xavier MJ; van der Heijden GW; Veltman JA Nat Commun; 2022 Jan; 13(1):154. PubMed ID: 35013161 [TBL] [Abstract][Full Text] [Related]
2. De novo mutations in idiopathic male infertility-A pilot study. Hodžić A; Maver A; Plaseska-Karanfilska D; Ristanović M; Noveski P; Zorn B; Terzic M; Kunej T; Peterlin B Andrology; 2021 Jan; 9(1):212-220. PubMed ID: 32860660 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. A hemizygous loss-of-function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia. Luo C; Chen Z; Meng L; Tan C; He W; Tu C; Du J; Lu GX; Lin G; Tan YQ; Hu TY Clin Genet; 2024 Jul; 106(1):27-36. PubMed ID: 38342987 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. RBM5 is a male germ cell splicing factor and is required for spermatid differentiation and male fertility. O'Bryan MK; Clark BJ; McLaughlin EA; D'Sylva RJ; O'Donnell L; Wilce JA; Sutherland J; O'Connor AE; Whittle B; Goodnow CC; Ormandy CJ; Jamsai D PLoS Genet; 2013; 9(7):e1003628. PubMed ID: 23935508 [TBL] [Abstract][Full Text] [Related]
9. Mutations of NANOS1, a human homologue of the Drosophila morphogen, are associated with a lack of germ cells in testes or severe oligo-astheno-teratozoospermia. Kusz-Zamelczyk K; Sajek M; Spik A; Glazar R; Jędrzejczak P; Latos-Bieleńska A; Kotecki M; Pawelczyk L; Jaruzelska J J Med Genet; 2013 Mar; 50(3):187-93. PubMed ID: 23315541 [TBL] [Abstract][Full Text] [Related]
10. 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]
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. 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]
13. Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations. Kataoka M; Matoba N; Sawada T; Kazuno AA; Ishiwata M; Fujii K; Matsuo K; Takata A; Kato T Mol Psychiatry; 2016 Jul; 21(7):885-93. PubMed ID: 27217147 [TBL] [Abstract][Full Text] [Related]
14. [Mutation of KLHL-10 in idiopathic infertile males with azoospermia, oligospermia or asthenospermia]. Qiu QM; Liu G; Li WN; Shi QW; Zhu FX; Lu GX Zhonghua Nan Ke Xue; 2009 Nov; 15(11):974-9. PubMed ID: 20218307 [TBL] [Abstract][Full Text] [Related]
15. Germline Mutations for Novel Candidate Predisposition Genes in Sporadic Schwannomatosis. Min BJ; Kang YK; Chung YG; Seo ME; Chang KB; Joo MW Clin Orthop Relat Res; 2020 Nov; 478(11):2442-2450. PubMed ID: 32281771 [TBL] [Abstract][Full Text] [Related]
16. CHD7 missense variants and clinical characteristics of Chinese males with infertility. Li L; Wang R; Yu Y; Zhang H; Jiang Y; Yang X; Liu R Mol Genet Genomic Med; 2020 Sep; 8(9):e1372. PubMed ID: 32573075 [TBL] [Abstract][Full Text] [Related]
17. [Mutations and polymorphisms in CFTR genes in infertile men with oligospermia or azoospermia]. Kusić J; Radojković D; Maletić V; Branković S; Savić A Srp Arh Celok Lek; 2002; 130(1-2):1-6. PubMed ID: 12073281 [TBL] [Abstract][Full Text] [Related]
18. Toward clinical exomes in diagnostics and management of male infertility. Lillepea K; Juchnewitsch AG; Kasak L; Valkna A; Dutta A; Pomm K; Poolamets O; Nagirnaja L; Tamp E; Mahyari E; Vihljajev V; Tjagur S; Papadimitriou S; Riera-Escamilla A; Versbraegen N; Farnetani G; Castillo-Madeen H; Sütt M; Kübarsepp V; Tennisberg S; Korrovits P; Krausz C; Aston KI; Lenaerts T; Conrad DF; Punab M; Laan M Am J Hum Genet; 2024 May; 111(5):877-895. PubMed ID: 38614076 [TBL] [Abstract][Full Text] [Related]
19. A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review. Sha Y; Zheng L; Ji Z; Mei L; Ding L; Lin S; Wang X; Yang X; Li P BMC Med Genet; 2018 Apr; 19(1):63. PubMed ID: 29661171 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]