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Author Details

Margot J Wyrwoll
Institute of Reproductive Genetics, University of Munster
2017
19
8
PMIDPaper TitleJournal TitlePublished Year
37723288Improved phenotypic classification of male infertility to promote discovery of genetic causes.Nat Rev Urol2024
37594251Scrutinizing the human TEX genes in the context of human male infertility.Andrology2024
37953324The Human Phenotype Ontology in 2024: phenotypes around the world.Nucleic Acids Res2024
36807972Linking human Dead end 1 (DND1) variants to male infertility employing zebrafish embryos.Hum Reprod2023
35690514Genetic Architecture of Azoospermia-Time to Advance the Standard of Care.Eur Urol2023
37086090WWC2 expression in the testis: Implications for spermatogenesis and male fertility.FASEB J2023
37208861Bi-allelic variants in INSL3 and RXFP2 cause bilateral cryptorchidism and male infertility.Hum Reprod2023
36997603DDX3Y is likely the key spermatogenic factor in the AZFa region that contributes to human non-obstructive azoospermia.Commun Biol2023
35022746Human INHBB Gene Variant (c.1079T>C:p.Met360Thr) Alters Testis Germ Cell Content, but Does Not Impact Fertility in Mice.Endocrinology2022
36446526Transcriptome analyses in infertile men reveal germ cell-specific expression and splicing patterns.Life Sci Alliance2022
36150389The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans.Am J Hum Genet2022
36041235Analysis of copy number variation in men with non-obstructive azoospermia.Andrology2022
34622232Single-cell RNA-seq unravels alterations of the human spermatogonial stem cell compartment in patients with impaired spermatogenesis.Cell Rep Med2021
34498060A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene-disease relationships.Hum Reprod Update2021
34755185Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes.Hum Reprod2021
31479588Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes.Andrology2020
32741963Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic men.Genet Med2020
32673564Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility.Am J Hum Genet2020
28406245Nanomechanics of the endothelial glycocalyx contribute to Na<sup>+</sup>-induced vascular inflammation.Sci Rep2017
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Harvard Medical School
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