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Author Details
Full Name
Margot J Wyrwoll
Affiliation
Institute of Reproductive Genetics, University of Munster
ORCID
Career Start Year
2017
Papers
19
H Index
8
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37723288
Improved phenotypic classification of male infertility to promote discovery of genetic causes.
Nat Rev Urol
2024
37594251
Scrutinizing the human TEX genes in the context of human male infertility.
Andrology
2024
37953324
The Human Phenotype Ontology in 2024: phenotypes around the world.
Nucleic Acids Res
2024
36807972
Linking human Dead end 1 (DND1) variants to male infertility employing zebrafish embryos.
Hum Reprod
2023
35690514
Genetic Architecture of Azoospermia-Time to Advance the Standard of Care.
Eur Urol
2023
37086090
WWC2 expression in the testis: Implications for spermatogenesis and male fertility.
FASEB J
2023
37208861
Bi-allelic variants in INSL3 and RXFP2 cause bilateral cryptorchidism and male infertility.
Hum Reprod
2023
36997603
DDX3Y is likely the key spermatogenic factor in the AZFa region that contributes to human non-obstructive azoospermia.
Commun Biol
2023
35022746
Human INHBB Gene Variant (c.1079T>C:p.Met360Thr) Alters Testis Germ Cell Content, but Does Not Impact Fertility in Mice.
Endocrinology
2022
36446526
Transcriptome analyses in infertile men reveal germ cell-specific expression and splicing patterns.
Life Sci Alliance
2022
36150389
The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans.
Am J Hum Genet
2022
36041235
Analysis of copy number variation in men with non-obstructive azoospermia.
Andrology
2022
34622232
Single-cell RNA-seq unravels alterations of the human spermatogonial stem cell compartment in patients with impaired spermatogenesis.
Cell Rep Med
2021
34498060
A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene-disease relationships.
Hum Reprod Update
2021
34755185
Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes.
Hum Reprod
2021
31479588
Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes.
Andrology
2020
32741963
Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic men.
Genet Med
2020
32673564
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility.
Am J Hum Genet
2020
28406245
Nanomechanics of the endothelial glycocalyx contribute to Na<sup>+</sup>-induced vascular inflammation.
Sci Rep
2017
1 - 19 of 19
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