Author

Ewa Rajpert‐De Meyts

University of CopenhagenORCID 0000-0002-5946-7559Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genetic & Genomic Medicine· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 4 Research Focus:differential expression· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1 Assay:scRNA-seq· 1

Frequent Co-Authors

Kristian AlmstrupiD· 3 shared Alberto BarrosiD· 2 shared Alexandra Manuel LopesiD· 2 shared Anders JuuliD· 2 shared Antoni Riera‐EscamillaiD· 2 shared Corinna FriedrichiD· 2 shared Csilla Gabriella KrausziD· 2 shared Donald F. ConradiD· 2 shared

Activity by Year

2022-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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3 shared papersGenetics

Kristian AlmstrupORCID

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4 papers

Recent·Most cited

Changes in local mineral homeostasis facilitate the formation of benign and malignant testicular microcalcifications

Ida Marie Boisen, Nadia Krarup Knudsen, John E. Nielsen, Ireen Kooij, Mathilde Louise Bagger, Jovanna Kaludjerovic, Peter J. O’Shaughnessy, Peter W. Andrews, Noriko Ide, Birgitte Grønkær Toft, Anders Juul, Arnela Mehmedbašić, Anne Jørgensen, Lee B. Smith, Richard Norman, , Martin Blomberg Jensen

The paper shows that local mineral homeostasis changes lead to testicular microcalcifications, associated with both benign and malignant conditions.

eLife · Apr 25, 2025Peer-reviewedMolecular Biology

X-chromosome loss rescues Sertoli cell maturation and spermatogenesis in Klinefelter syndrome

Sofia Boeg Winge, Niels Erik Skakkebæk, Lise Aksglæde, Gülizar Saritaş, Ewa Rajpert‐De Meyts, Ellen Goossens, Anders Juul, Kristian Almstrup

The paper shows that X-chromosome loss in Sertoli cells enables maturation and focal spermatogenesis in Klinefelter syndrome.

Cell Death and Disease · Jun 5, 2024Peer-reviewedGenetics

Diverse Monogenic Subforms of Human Spermatogenic Failure

Liina Nagirnaja, Alexandra Manuel Lopes, Wu‐Lin Charng, Brian Miller, Rytis Stakaitis, Ieva Golubickaitė, Alexandra M. Stendahl, Tianpengcheng Luan, Corinna Friedrich, Eisa Mahyari, Eloise Fadial, Laura Kasak, Katinka A. Vigh‐Conrad, Manon S. Oud, Miguel Joao Xavier, , Donald F. Conrad

This study identifies genetic subforms of non-obstructive azoospermia using exome sequencing and single-cell RNA sequencing, revealing molecular groups of genes involved in spermatogenesis.

Nature Communications · Dec 26, 2022Peer-reviewedGenetic & Genomic Medicine

A de novo paradigm for male infertility

Manon S. Oud, RM Smits, H E Smith, Francesco Kumara Mastrorosa, Giles S. Holt, Brendan J. Houston, Petra F. de Vries, B. Alobaidi, Lois E. Batty, H. Ismail, J. Greenwood, Harsh J. Sheth, Aneta Mikulášová, Galuh Astuti, Christian Gilissen, , Joris Andre Veltman

The paper identifies de novo mutations as a significant genetic cause of male infertility, finding several candidate genes and an enrichment of loss-of-function and missense mutations in intolerant genes.

Nature Communications · Jan 10, 2022Peer-reviewedGenetics