Christina Lissewski
5PUBLICATIONS
25CO-AUTHORS
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Publications (5)
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|Oct 21, 2020
The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered.Julia Brinkmann, Christina Lissewski, Valentina Pinna
|Aug 14, 2020
Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications.Christina Lissewski, Valérie Chune, Francesca Pantaleoni
|Mar 01, 2020
Pathogenic PTPN11 variants involving the poly-glutamine Gln255 -Gln256 -Gln257 stretch highlight the relevance of helix B in SHP2's functional regulation.Simone Martinelli, Luca Pannone, Christina Lissewski
|Apr 22, 2016
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation.Karim Kouz, Christina Lissewski, Stephanie Spranger
|Apr 09, 2016
Germline RRAS2 mutations are not associated with Noonan syndrome.John J Ceremsak, Ariel Yu, Emilio Esquivel
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Frequent Collaborators
3 joint publications
Marco Tartaglia
2 joint publications
Martin Zenker
2 joint publications
Hélène Cave
2 joint publications
Yoann Vial
2 joint publications
Julia Brinkmann
2 joint publications
Francesca Pantaleoni
2 joint publications
Alessandro De Luca
1 joint publications
Mignon L Loh
1 joint publications
Alain Verloes
1 joint publications
Andreas Hahn
