| Bi-allelic mutations in M1AP are a frequent cause of meiotic arrest and severely impaired spermatogenesis leading to male infertility MJ Wyrwoll, ŞG Temel, L Nagirnaja, MS Oud, AM Lopes, ... The American Journal of Human Genetics 107 (2), 342-351, 2020 | 84 | 2020 |
| Genetic architecture of azoospermia—time to advance the standard of care MJ Wyrwoll, N Köckerling, M Vockel, AK Dicke, N Rotte, E Pohl, J Emich, ... European urology 83 (5), 452-462, 2023 | 66 | 2023 |
| Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failure JJ Hardy, MJ Wyrwoll, W Mcfadden, A Malcher, N Rotte, NC Pollock, ... Human genetics 140 (8), 1169-1182, 2021 | 33 | 2021 |
| Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes MJ Wyrwoll, ES Van Walree, G Hamer, N Rotte, MM Motazacker, ... Human Reproduction 37 (1), 178-189, 2022 | 32 | 2022 |
| A novel xeno-organoid approach: exploring the crosstalk between human iPSC-derived PGC-like and rat testicular cells EM Mall, N Rotte, J Yoon, R Sandhowe-Klaverkamp, A Röpke, J Wistuba, ... Molecular Human Reproduction 26 (12), 879-893, 2020 | 16 | 2020 |
| The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans MJ Wyrwoll, CM Gaasbeek, I Golubickaite, R Stakaitis, MS Oud, ... The American Journal of Human Genetics 109 (10), 1850-1866, 2022 | 14 | 2022 |
| Analysis of copy number variation in men with non‐obstructive azoospermia MJ Wyrwoll, R Wabschke, A Röpke, M Wöste, C Ruckert, S Perrey, ... Andrology 10 (8), 1593-1604, 2022 | 9 | 2022 |
| C19ORF84 connects piRNA and DNA methylation machineries to defend the mammalian germ line A Zoch, G Konieczny, T Auchynnikava, B Stallmeyer, N Rotte, M Heep, ... Molecular Cell 84 (6), 1021-1035. e11, 2024 | 4 | 2024 |
| Biallelic mutations in M1AP are a frequent cause of meiotic arrest leading to male infertility MJ Wyrwoll, ŞG Temel, L Nagirnaja, MS Oud, AM Lopes, ... bioRxiv, 803346, 2019 | 1 | 2019 |
| Genotype-specific differences in infertile men due to loss-of-function variants in M1AP or ZZS genes N Rotte, JEM Dunleavy, MD Runkel, D Fietz, A Pilatz, J Kuss, AK Dicke, ... medRxiv, 2024.03. 20.24304490, 2024 | | 2024 |
| FKBP6 has an essential role in human spermatogenesis GW Van der Heijden, M Oud, R Stakaitis, I Golubickaite, C Gaasbeek, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 100-100, 2022 | | 2022 |
| Biallelic mutations in M1AP are associated with meiotic arrest, severely impaired spermatogenesis and male infertility C Friedrich, SG Temel, L Nagirnaja, MS Oud, AM Lopes, ... | | 2020 |
