K. Sanggaard

Branchio–oto–renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analyses

K. Lage, H. Eiberg, K. Kjaer, 2007, European Journal of Human Genetics.

A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family

H. Eiberg, G. Nürnberg, P. Nürnberg, 2008, American journal of medical genetics. Part A.

Serotonin inhibits glutamate‐ but not PACAP‐induced per gene expression in the rat suprachiasmatic nucleus at night

J. Hannibal, J. Fahrenkrug, K. Sanggaard, 2003, The European journal of neuroscience.