Publications and scholarly work

Guzmán C, Šolman M, Ligabue A, Blaževitš O, Andrade DM, Reymond L, Eggeling C, Abankwa D.

The efficacy of Raf kinase recruitment to the GTPase H-ras depends on H-ras membrane conformer-specific nanoclustering

J Biol Chem, 2014

Ensina LF, de Lacerda AE, de Andrade DM, Machado L, Camelo-Nunes I, Solé D.

Drug-induced anaphylaxis in children: nonsteroidal anti-inflammatory drugs and drug provocation test

J Allergy Clin Immunol Pract, 2014

Andrade DM, Krings T, Chow EW, Kiehl TR, Bassett AS.

Hippocampal malrotation is associated with chromosome 22q11.2 microdeletion

Can J Neurol Sci, 2013

Carvill GL, Heavin SB, Yendle SC, McMahon JM, O'Roak BJ, Cook J, Khan A, Dorschner MO, Weaver M, Calvert S, Malone S, Wallace G, Stanley T, Bye AM, Bleasel A, Howell KB, Kivity S, Mackay MT, Rodriguez-Casero V, Webster R, Korczyn A, Afawi Z, Zelnick N, Lerman-Sagie T, Lev D, Møller RS, Gill D, Andrade DM, Freeman JL, Sadleir LG, Shendure J, Berkovic SF, Scheffer IE, Mefford HC.

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1

Nat Genet, 2013

Andrade DM.

Nonlesional focal epilepsy: a challenge from genes to surgery

Can J Neurol Sci, 2013

Rilstone JJ, Coelho FM, Minassian BA, Andrade DM.

Dravet syndrome: seizure control and gait in adults with different SCN1A mutations

Epilepsia, 2012

Thompson MD, Roscioli T, Marcelis C, Nezarati MM, Stolte-Dijkstra I, Sharom FJ, Lu P, Phillips JA, Sweeney E, Robinson PN, Krawitz P, Yntema HG, Andrade DM, Brunner HG, Cole DE.

Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome)

Am J Med Genet A, 2012

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