H. Shima, K. Koehler, Y. Nomura, K. Sugimoto, A. Satoh, T. Ogata, M. Fukami, R. Juhlen, M. Schuelke, K. Mohnike, A. Huebner, S. Narumi:

Two patients with MIRAGE syndrome lacking haematological features: role of somatic second-site reversion SAMD9 mutations

Journal of Medical Genetics 55(2) (2018), 81-85

C. Tatsi, A. Gkourogianni, K. Mohnike, D. DeArment, S. Witchel, A. C. Andrade, T. C. Markello, J. Baron, O. Nilsson, Y. H. Jee:

Aggrecan Mutations in Nonfamilial Short Stature and Short Stature Without Accelerated Skeletal Maturation

Journal of the Endocrine Society 1(8) (2017), 1006-1011

K. Mohnike:

Exceedingly Rare

Deutsches Ärzteblatt International 113(27-28) (2016), 487

D. Papathemeli, K. Mohnike, A. Ambach:

Multiple Polycyclic Brownish to Reddish Macules on the Skin in an Infant

JAMA Dermatology 151(11) (2015), 1249-50