Publications and scholarly work
Marin R, Rulo G, Andrade DM, Inuzuka LM, Castro MAA, Vincentiis S, Guerreiro MM, Valente KD.
A new developmental and epileptic encephalopathy: PUM1-neurodevelopmental disorder with epilepsy with myoclonic-atonic seizures
Seizure, 2025
Andrade DM, Bailey LD, Meskis MA, Hood V, Ferreira S, Dixon-Salazar T, Griffin J, Perry MS.
A survey of adult caregivers of people with developmental and epileptic encephalopathies: A long-term care planning needs assessment
Epilepsy Behav, 2025
Van Winssen C, Andrade AV, Andrade DM, Burneo JG, de Ribaupierre S, Donner E, Hassan A, Ibrahim G, Jones KC, Lomax LB, Muir K, Nouri MN, Porter N, Ramachandrannair R, Raymond P, Rutka J, Shapiro MJ, Steven DA, Swain D, Valiante T, Whiting S, Whitney R, Yau I, Fantaneanu TA.
Evaluating the Current State of Epilepsy Care in the Province of Ontario
Can J Neurol Sci, 2025
Andrade DM.
Out with prolactin, in with neurofilament light and glial fibrillary acidic protein
Epilepsy Curr, 2025
Rong M, Zulfiqar Ali Q, Aledo-Serrano A, Bayat A, Devinsky O, Qaiser F, Chandran I, Ali A, Fasano A, Bassett AS, Andrade DM.
Adult Phenotype of CHD2-Associated Disorders
Neurol Genet, 2024
Chen S, Abou-Khalil BW, Afawi Z, Ali QZ, Amadori E, Anderson A, Anderson J, Andrade DM, Annesi G, Arslan M, Auce P, Bahlo M, Baker MD, Balagura G, Balestrini S, Banks E, Barba C, Barboza K, Bartolomei F, Bass N, Baum LW, Baumgartner TH, Baykan B, Bebek N, Becker F, Bennett CA, Beydoun A, Bianchini C, Bisulli F, Blackwood D, Blatt I, Borggräfe I, Bosselmann C, Braatz V, Brand H, Brockmann K, Buono RJ, Busch RM, Caglayan SH, Canafoglia L, Canavati C, Castellotti B, Cavalleri GL, Cerrato F, Chassoux F, Cherian C, Cherny SS, Cheung CL, Chou IJ, Chung SK, Churchhouse C, Ciullo V, Clark PO, Cole AJ, Cosico M, Cossette P, Cotsapas C, Cusick C, Daly MJ, Davis LK, Jonghe P, Delanty N, Dennig D, Depondt C, Derambure P, Devinsky O, Di Vito L, Dickerson F, Dlugos DJ, Doccini V, Doherty CP, El-Naggar H, Ellis CA, Epstein L, Evans M, Faucon A, Feng YA, Ferguson L, Ferraro TN, Da Silva IF, Ferri L, Feucht M, Fields MC, Fitzgerald M, Fonferko-Shadrach B, Fortunato F, Franceschetti S, French JA, Freri E, Fu JM, Gabriel S, Gagliardi M, Gambardella A, Gauthier L, Giangregorio T, Gili T, Glauser TA, Goldberg E, Goldman A, Goldstein DB, et al.
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
medRxiv, 2024