| A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene-disease relationships BJ Houston, A Riera, MJ Wyrwoll, A Salas-Huetos, MJ Xavier, L Nagirnaja, ... medRxiv, 2021 | 154 | 2021 |
| Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic men C Krausz, A Riera-Escamilla, D Moreno-Mendoza, K Holleman, F Cioppi, ... Genetics in Medicine 22 (12), 1956-1966, 2020 | 103 | 2020 |
| 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 | 72 | 2020 |
| Nanomechanics of the endothelial glycocalyx contribute to Na+-induced vascular inflammation F Schierke, MJ Wyrwoll, M Wisdorf, L Niedzielski, M Maase, T Ruck, ... Scientific reports 7 (1), 1-11, 2017 | 50 | 2017 |
| Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes TF Araujo, C Friedrich, CHP Grangeiro, LR Martelli, JD Grzesiuk, J Emich, ... Andrology 8 (2), 434-441, 2020 | 48 | 2020 |
| Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia A Salas-Huetos, F Tüttelmann, MJ Wyrwoll, S Kliesch, AM Lopes, ... Human genetics 140 (1), 217-227, 2021 | 37 | 2021 |
| 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, 1-14, 2021 | 32 | 2021 |
| Genetic counseling and diagnostic guidelines for couples with infertility and/or recurrent miscarriage MJ Wyrwoll, S Rudnik-Schöneborn, F Tüttelmann Medizinische Genetik 33 (1), 3-12, 2021 | 5 | 2021 |
| EGR4-dependent decrease of UTF1 is associated with failure to reserve spermatogonial stem cells in infertile men S Di Persio, T Tekath, LM Siebert-Kuss, JF Cremers, J Wistuba, X Li, ... bioRxiv, 2021 | 2 | 2021 |
| Genetic dissection of spermatogenic arrest through exome analysis. Clinical implications for the management of azoospermic men A Riera-Escamilla, D Moreno-Mendoza, K Holleman, F Cioppi, F Algaba, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 1000-1000, 2020 | 1 | 2020 |
| 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 |
| Correction to: Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia A Salas-Huetos, F Tüttelmann, MJ Wyrwoll, S Kliesch, AM Lopes, ... Human genetics 140 (1), 229, 2021 | | 2021 |
| Improved classification of testicular histopathology to promote uniform diagnosis and discovery of genetic causes for male infertility GW van der Heijden, MJ Wyrwoll, L Ramos, J Veltman, F Tuettelmann EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 157-158, 2020 | | 2020 |
| Identification of novel causes for male infertility: loss-of-function variants in MSH4 and MSH5 MJ Wyrwoll, C Friedrich, E Kaminsky, C Krallmann, S Kliesch, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 30-30, 2020 | | 2020 |
| 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, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 1002-1003, 2020 | | 2020 |
| Genetic analysis of 24 candidate genes validates TEX14, TEX11, NR5A1 and DMRT1 as clinically relevant for non-obstructive azoospermia A Roepke, N Koeckerling, MJ Wyrwoll, J Emich, M Woeste, M Dugas, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1191-1191, 2019 | | 2019 |
| Salt triggers monocyte-adhesion on vascular endothelium: P072 M Wyrwoll, F Schierke, N Oelkers, V Hofschröer, K Kusche-Vihrog Acta Physiologica 213, 2015 | | 2015 |
