PD.Dr. Nadja Bogdanova Markov

Current affiliations

Institute of Human Genetics

Publications

Genetic analysis of the M2/ANXA5 haplotype as recurrent pregnancy loss predisposition in the Malay population Ang K., Kathirgamanathan S., Ch’ng E., Lee Y., Roslani A., Naidu B., Kumar K., Abdullah R., Kadir S., Yusoff N., Abdullah W., Bogdanova N., Wieacker P., Markoff A., Tang T. (2017) In: Journal of Assisted Reproduction and Genetics, null(null), 1-8. doi:10.1007/s10815-017-0871-0 Research article (journal) \| Peer reviewed \| Published
The RAD51C exonic splice-site mutations c.404G>C and c.404G>T are associated with familial breast and ovarian cancer Neidhardt G., Becker A., Hauke J., Horváth J., Bogdanova Markov N., Heilmann-Heimbach S., Hellebrand H., Thiele H., Altmüller J., Nürnberg P., Meindl A., Rhiem K., Blümcke B., Wappenschmidt B., Schmutzler R., Hahnen E. (2017) In: European Journal of Cancer Prevention, 26(2), 165-169. doi:10.1097/CEJ.0000000000000240 Research article (journal) \| Peer reviewed \| Published
Elevated annexin A5 plasma levels in term pregnancies of M2/ANXA5 carriers Ang K., Kathirgamanathan S., Ch'ng E., Abdullah W., Yusoff N., Jahnke C., Schmitz R., Bogdanova N., Wieacker P., Tang T., Markoff A. (2017) In: Thrombosis Research, 156(null), 87-90. doi:10.1016/j.thromres.2017.06.008 Research article (journal) \| Peer reviewed \| Published
Intrafamilial phenotypic variability of Specific Language Impairment Bartha-Doering L., Regele S., Deuster D., Seidl R., Bogdanova N., Röpke A., Wieacker P., am Zehnhoff-Dinnesen A. (2016) In: Brain and Language, 159(null), 102-108. doi:10.1016/j.bandl.2016.06.005 Research article (journal) \| Peer reviewed \| Published
Functional characterisation of the CFTR mutations M348V and A1087P from patients with pancreatitis suggests functional interaction between CFTR monomers. Weiss FU, Simon P, Bogdanova N, Shcheynikov N, Muallem S, Lerch MM (2009) In: Gut, 58(5), 733-734. doi:10.1136/gut.2008.167650 Research article (journal) \| Published

Projects

Molecular analysis of the M2/ANXA5 haplotype as a new marker for infertility and thrombophilia predisposition

Duration: 15/07/2014 - 14/07/2017

Funded by: DFG - Individual Grants Programme

Type of project: Individual project