Publications of Lena Wartosch

Stauber, T.; Wartosch, L.; Vishnolia, S.; Schulz, A.; Kornak, U.: CLCN7, a gene shared by autosomal recessive and autosomal dominant osteopetrosis. Bone 168, 116639 (2023)

Wartosch, L.; Schindler, K.; Schuh, M.; Gruhn, J. R.; Hoffmann, E.R.; McCoy, R. C.; Xing, J.: Origins and mechanisms leading to aneuploidy in human eggs. Prenatal Diagnosis 41 (5), pp. 620 - 630 (2021)

Pavlova, E. V.; Shatunov, A.; Wartosch, L.; Moskvina, A. I.; Nikolaeva, L. E.; Bright, N. A.; Tylee, K. L.; Church, H. J.; Ballabio, A.; Luzio, J. P. et al.; Cox, T. M.: The lysosomal disease caused by mutant VPS33A. Human Molecular Genetics 28 (15), pp. 2514 - 2530 (2019)

Hesketh, G. G.; Wartosch, L.; Davis, L. J.; Bright, N. A.; Luzio, J. P.: The Lysosome and Intracellular Signalling. In: Endocytosis and Signaling, pp. 151 - 180 (Eds. Lamaze , C.; Prior, I.). Springer, Cham (2018)