412 related articles for article (PubMed ID: 36524333)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. Biallelic HFM1 variants cause non-obstructive azoospermia with meiotic arrest in humans by impairing crossover formation to varying degrees.
Xie X; Murtaza G; Li Y; Zhou J; Ye J; Khan R; Jiang L; Khan I; Zubair M; Yin H; Jiang H; Liu W; Shi B; Hou X; Gong C; Fan S; Wang Y; Jiang X; Zhang Y; Zhang H; Ma H; Shi Q
Hum Reprod; 2022 Jun; 37(7):1664-1677. PubMed ID: 35526155
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Rare missense variant in MSH4 associated with primary gonadal failure in both 46, XX and 46, XY individuals.
Akbari A; Padidar K; Salehi N; Mashayekhi M; Almadani N; Sadighi Gilani MA; Bashambou A; McElreavey K; Totonchi M
Hum Reprod; 2021 Mar; 36(4):1134-1145. PubMed ID: 33448284
[TBL] [Abstract][Full Text] [Related]
9. Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes.
Wyrwoll MJ; van Walree ES; Hamer G; Rotte N; Motazacker MM; Meijers-Heijboer H; Alders M; Meißner A; Kaminsky E; Wöste M; Krallmann C; Kliesch S; Hunt TJ; Clark AT; Silber S; Stallmeyer B; Friedrich C; van Pelt AMM; Mathijssen IB; Tüttelmann F
Hum Reprod; 2021 Dec; 37(1):178-189. PubMed ID: 34755185
[TBL] [Abstract][Full Text] [Related]
10. Actionable secondary findings following exome sequencing of 836 non-obstructive azoospermia cases and their value in patient management.
Kasak L; Lillepea K; Nagirnaja L; Aston KI; Schlegel PN; Gonçalves J; Carvalho F; Moreno-Mendoza D; Almstrup K; Eisenberg ML; Jarvi KA; O'Bryan MK; Lopes AM; Conrad DF; ; Punab M; Laan M
Hum Reprod; 2022 Jun; 37(7):1652-1663. PubMed ID: 35535697
[TBL] [Abstract][Full Text] [Related]
11. A recurrent ZSWIM7 mutation causes male infertility resulting from decreased meiotic recombination.
Li Y; Wu Y; Zhou J; Zhang H; Zhang Y; Ma H; Jiang X; Shi Q
Hum Reprod; 2021 Apr; 36(5):1436-1445. PubMed ID: 33713115
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia.
Wang W; Su L; Meng L; He J; Tan C; Yi D; Cheng D; Zhang H; Lu G; Du J; Lin G; Zhang Q; Tu C; Tan YQ
Hum Reprod; 2023 Jul; 38(7):1399-1411. PubMed ID: 37192818
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. 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]
18. Effects of
Olszewska M; Malcher A; Stokowy T; Pollock N; Berman AJ; Budkiewicz S; Kamieniczna M; Jackowiak H; Suszynska-Zajczyk J; Jedrzejczak P; Yatsenko AN; Kurpisz M
Hum Reprod Open; 2024; 2024(2):hoae020. PubMed ID: 38650655
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
