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Dr. Claudia Krallmann

Current affiliations

Klinik für Andrologie

Publications

NXT2 is a key component of the RNA nuclear export factor complex in the human testis and essential for spermatogenesis Dicke, Ann-Kristin; Ahmedani, Ammar; Ma, Lin; Herrmann, Leonie; van der Heijden, Godfried W.; Koser, Sophie A.; Krallmann, Claudia; Kalyon, Oguzhan; Xavier, Miguel J.; Veltman, Joris A.; Kliesch, Sabine; Neuhaus, Nina; Kotaja, Noora; Tüttelmann, Frank; Stallmeyer, Birgit (2025) In: Nature Communications, 16(6254). doi:10.1038/s41467-025-61463-0 Research article (journal) \| Peer reviewed \| Published
Functional and clinical insights into nuclear receptor variants for advancing precision diagnostics in male infertility Gaikwad, Avinash S; Wyrwoll, Margot J; Koser, Sophie A; Emich, Jana; Kuß, Johanna; Aravina, Mariya; Krallmann, Claudia; Gromoll, Jörg; Kliesch, Sabine; Laurentino, Sandra; Stallmeyer, Birgit; Friedrich, Corinna; Tüttelmann, Frank (2025) In: EBioMedicine, 119. doi:10.1016/j.ebiom.2025.105899 Research article (journal) \| Peer reviewed \| Published
Human fertilization in vivo and in vitro requires the CatSper channel to initiate sperm hyperactivation Young S; Schiffer C; Wagner A; Patz J; Potapenko A; Herrmann L; Nordhoff V; Pock T; Krallmann C; Stallmeyer B; Röpke A; Kierzek M; Biagioni C; Wang T; Haalck L; Deuster D; Hansen JN; Wachten D; Risse B; Behre HM; Schlatt S; Kliesch S; Tüttelmann F; Brenker C; Strünker T (2024) In: Journal of Clinical Investigation, 134(1). doi:10.1172/JCI173564 Research article (journal) \| Peer reviewed \| Published
Decreased spermatogonial numbers in boys with severe haematological diseases. Lahtinen AK; Funke M; Krallmann C; Wyrwoll MJ; Jarisch A; Yang Y; Bjarnason R; Romerius P; Sundin M; Norén-Nyström U; Langenskiöld C; Cremers JF; Kliesch S; Stukenborg JB; Neuhaus N; Jahnukainen K (2024) In: British Journal of Haematology, 205(1), 229-235. doi:10.1111/bjh.19572 Research article (journal) \| Peer reviewed \| Published
Pathogenic gene variants in CCDC39, CCDC40, RSPH1, RSPH9, HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility. Aprea, I; Wilken, A; Krallmann, C; Nöthe-Menchen, T; Olbrich, H; Loges, NT; Dougherty, GW; Bracht, D; Brenker, C; Kliesch, S; Strünker, T; Tüttelmann, F; Raidt, J; Omran, H (2023) In: Frontiers in Genetics, 14. doi:10.3389/fgene.2023.1117821 Research article (journal) \| Peer reviewed \| Published

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