Equine Multiple Congenital Ocular Anomalies and Silver Coat Colour Result from the Pleiotropic Effects of Mutant PMEL

Por Andersson, Lisa S., Wilbe, Maria, Viluma, Agnese, Cothran, Gus, Ekesten, Björn, Ewart, Susan, Lindgren, Gabriella
Publicado em 2013

Mutation in NRAS in familial Noonan syndrome – case report and review of the literature

Por Ekvall, Sara, Wilbe, Maria, Dahlgren, Jovanna, Legius, Eric, van Haeringen, Arie, Westphal, Otto, Annerén, Göran, Bondeson, Marie-Louise
Publicado no BMC Med Genet (2015)

DLA Class II Alleles Are Associated with Risk for Canine Symmetrical Lupoid Onychodystropy (SLO)

Por Wilbe, Maria, Ziener, Martine Lund, Aronsson, Anita, Harlos, Charlotte, Sundberg, Katarina, Norberg, Elin, Andersson, Lisa, Lindblad-Toh, Kerstin, Hedhammar, Åke, Andersson, Göran, Lingaas, Frode
Publicado em 2010

Correction: DLA Class II Alleles Are Associated with Risk for Canine Symmetrical Lupoid Onychodystrophy (SLO)

Por Wilbe, Maria, Ziener, Martine Lund, Aronsson, Anita, Harlos, Charlotte, Sundberg, Katarina, Norberg, Elin, Andersson, Lisa, Lindblad-Toh, Kerstin, Hedhammar, Åke, Andersson, Göran, Lingaas, Frode
Publicado em 2010

Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26

Por Gudmundsson, Sanna, Wilbe, Maria, Ekvall, Sara, Ameur, Adam, Cahill, Nicola, Alexandrov, Ludmil B., Virtanen, Marie, Hellström Pigg, Maritta, Vahlquist, Anders, Törmä, Hans, Bondeson, Marie-Louise
Publicado no Hum Mol Genet (2017)

Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease

Por Wilbe, Maria, Kozyrev, Sergey V., Farias, Fabiana H. G., Bremer, Hanna D., Hedlund, Anna, Pielberg, Gerli R., Seppälä, Eija H., Gustafson, Ulla, Lohi, Hannes, Carlborg, Örjan, Andersson, Göran, Hansson-Hamlin, Helene, Lindblad-Toh, Kerstin
Publicado no PLoS Genet (2015)