Danielle Andrade

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Recent Publications

Journal Articles

1. Andrade DM. Dravet syndrome, lamotrigine, and personalized medicine. Dev Med Child Neurol. 2015; 57(2): 118-9.

2. Lowther C, Costain G, Stavropoulos DJ, Melvin R, Silversides CK, Andrade DM, So J, Faghfoury H, Lionel AC, Marshall CR, Scherer SW, Bassett AS. Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature. Gen Med. 2015; 17(2): 149-157.

3. Fung WL, Butcher NJ, Costain G, Andrade DM, Boot E, Chow EW, Chung B, Cytrynbaum C, Faghfoury H, Fishman L, García-Miñaúr S, George S, Lang AE, Repetto G, Shugar A, Silversides C, Swillen A, van Amelsvoort T, McDonald-McGinn DM, Bassett AS. Practical guidelines for managing adults with 22q11.2 deletion syndrome. Genet Med. 2015; Epub ahead of print

4. Muona M, Berkovic SF, Dibbens LM, Oliver KL, Maljevic S, Bayly MA, Joensuu T, Canafoglia L, Franceschetti S, Michelucci R, Markkinen S, Heron SE, Hildebrand MS, Andermann E, Andermann F, Gambardella A, Tinuper P, Licchetta L, Scheffer IE, Criscuolo C, Filla A, Ferlazzo E, Ahmad J, Ahmad A, Baykan B, Said E, Topcu M, Riguzzi P, King MD, Ozkara C, Andrade DM, Engelsen BA, Crespel A, Lindenau M, Lohmann E, Saletti V, Massano J, Privitera M, Espay AJ, Kauffmann B, Duchowny M, Møller RS, Straussberg R, Afawi Z, Ben-Zeev B, Samocha KE, Daly MJ, Petrou S, Lerche H, Palotie A, Lehesjoki AE. A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy. Nat Genet. 2015; 47(1): 39-46.

5. Law R, Dixon-Salazar T, Jerber J, Cai N, Abbasi AA, Zaki MS, Mittal K, Gabriel SB, Rafiq MA, Khan V, Nguyen M, Ali G, Copeland B, Scott E, Vasli N, Mikhailov A, Khan MN, Andrade DM, Ayaz M, AnsarM, Ayub M, Vincent JB, Gleeson JG. Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability. Am J of Hum Genet. 2014; 95(6): 721-8.

6. Borlot F, Wither RG, Ali A, Wu N, Verocai F, Andrade DM. A pilot double-blind trial using verapamil as adjuvant therapy for refractory seizures. Epilepsy Res. 2014; 108(9): 1652-51.

7. Borlot F, Tellez-Zenteno JF, Allen A, Ali A, Snead OC III, Andrade DM. Epilepsy transition: challenges of caring for adults with childhood-onset seizures. Epilepsia. 2014; 55(10): 1659-66.

8. Mansouri A, Fallah A, McAndrews MP, Cohn M, Mayor D, Andrade D, Carlen P, Del Campo JM,Tai P, Wennberg RA, Valiante TA. Neurocognitive and Seizure Outcomes of Selective Amygdalohippocampectomy versus Anterior Temporal Lobectomy for Mesial Temporal Lobe Epilepsy. Epilepsy Res Treat. 2014; 2014: 306382.

9. Wu N, Borlot F, Ali A, Krings T, Andrade DM. Hemimegalencephaly: what happens when children get older? Dev Med Child Neurol. 2014; 56(9): 905-9.

10. Cheung EN, George SR, Costain GA, Andrade DM, Chow EW, Silversides CK, Bassett AS. Prevalence of hypocalcaemia and its associated features in 22q11•2 deletion syndrome. Clin endocrinol. 2014; 81(2): 190-6.

11. Vincent JB, Jamil T, Rafiq MA, Anwar Z, Ayaz M, Hameed A, Nasr T, Naeem F, Khattak NA, Carter M, Ahmed I, John P, Wiame E, Andrade DM, Schaftingen EV, Mir A, Ayub M. Phosphoserine phosphatase (PSPH) gene mutation in an intellectual disability family from Pakistan. Clin Genet. 2014; Epub ahead of print.

12. Fasano A, Borlot F, Lang AE, Andrade DM. Antecollis and levodopa-responsive parkinsonism are late features of Dravet syndrome. Neurology. 2014; 82(24): 2250-1.

13. Nascimento FA, Faghfoury H, Krings T, Ali A, Fridhandler JD, Lozano A, Wennberg R, Andrade DM. Deep brain stimulation for the management of seizures in MECP2 duplication syndrome. Seizure. 2014; 23(5): 405-7.

14. Steriade C, Andrade DM, Faghfoury H, Tarnopolsky MA, Tai P. Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) may respond to adjunctive ketogenic diet. Pediatr Neurol. 2014; 50(5): 498-502.

15. Cheung EN, George SR, Andrade DM, Chow EW, Silversides CK, Bassett AS. Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome. Genet Med. 2014; 16(1): 40-4.

16. Andrade DM, Krings T, Chow EW, Kiehl TR, Bassett AS. Hippocampal malrotation is associated with chromosome 22q11.2 microdeletion. Can J Neurol Sci. 2013; 40(5): 652-6.

17. Carvill GL1, 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; 45(7): 825-30.

18. Andrade DM. Nonlesional focal epilepsy: a challenge from genes to surgery. Can J Neurol Sci. 2013; 40(2): 137-8.

19. Téllez-Zenteno JF, Ronquillo LH, Jette N, Burneo JG, Nguyen DK, Donner EJ, Sadler M, Javidan M M, Gross DW, Wiebe S; Canadian Epilepsy Surgery Study Group. Collaborators: Ahmed N, Andermann F, Appendino JP, Andrade D et al. Discontinuation of antiepileptic drugs after successful epilepsy surgery. A Canadian survey. Epilepsy Res. 2012; 102(1-2): 23-33.

20. Mandzia J, Andrade D, Burneo JG, Jenkins ME, University Of Western Ontario Evidence Based Neurology Group. Critically appraised topic. Temporal lobe epilepsy and hippocampal stimulation. Can J Neurol Sci. 2012; 39(6): 830-2.

21. Fridhandler J, Coelho FM, Tai P, Jette N, Andrade DM. A comparison of antiepileptic drug therapy in patients with severe intellectual disability and patients with normal intellect. Epilepsy Behav. 2012; 25(2): 196-199.

22. Chiu AWL, Gadi H, Moller DW, Valiante TA, Andrade DM. Multistage preictal seizure analysis using Hidden Markov Model. Int J Biomed Eng Tech. 2012; 10(2): 160-173.

23. Andrade DM, Paton T, Turnbull J, Marshal CR, Scherer SW, Minassian BA. Mutation of the CLN6 gene in teenage-onset progressive myoclonus epilepsy. Pediatr Neurol. 2012; 47(3): 205-8.

24. Rilstone JJ, Coelho FM, Minassian BA, Andrade DM. Dravet syndrome: seizure control and gait in adults with different SCN1A mutations. Epilepsia. 2012; 53(8): 1421-8

25. 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. Part A. 2012; 158A(3): 553-8.

26. Thompson MD, Noble-Topham S, Percy ME, Andrade DM, Ebers GC. Chromosome 1p36 in migraine with aura: association study of the 5HT(1D) locus. Neuroreport. 2012; 23(1): 45-8.

27. Andrade DM, Tai P, Dalmau J, Wennberg R. Tonic seizures: a diagnostic clue of anti-LGI1 encephalitis? Neurology. 2011; 76(15): 1355-7.

28. Andrade DM, Hamani C, Lozano AM, Wennberg RA. Dravet syndrome and deep brain stimulation: seizure control after 10 years of treatment. Epilepsia. 2010; 51(7): 1314-6.

29. Bittencourt S, Dubiela FP, Queiroz C, Covolan L, Andrade D, Lozano A, Mello LE, Hamani C. Microinjection of GABAergic agents into the anterior nucleus of the thalamus modulates pilocarpineinduced seizures and status epilepticus. Seizure. 2010; 19(4): 242-6.

30. Tai P, Poochikian-Sarkissian S, Andrade D, Valiante T, del Campo M, Wennberg R. Postictal wandering is common after temporal lobe seizures. Neurology. 2010; 74(11): 932-3.

31. Andrade DM, McAndrews MP, Hamani C, Poublanc J, Angel M, Wennberg R. Seizure recurrence 29 years after hemispherectomy for Sturge Weber syndrome. Can J Neurol Sci. 2010; 37(1):141-4.

32. Andrade DM, Hamani C., Minassian BA. Treatment options for epileptic myoclonus and epilepsy syndromes associated with myoclonus. Expert Opin Pharmacother. 2009; 10(10):1549-60.

33. Hamani C, Andrade D, Hodaie M, Wennberg R, Lozano A. Deep brain stimulation for the treatment of epilepsy. Int J Neur Syst. 2009; 19(3):213-26.

34. Andrade DM. Genetic basis in epilepsies caused by malformations of cortical development and in those with structurally normal brain. Hum Genet. 2009;126(1):173-93.

35. Poochikian-Sarkissian S, Tai P, del Campo M, Andrade DM, Carlen PL, Valiante T, Wennberg RA. Patient awareness of seizures as documented in the epilepsy monitoring unit. Can J Neurosci Nurs. 2009; 31(4):22-23.

36. Raghavan LV, Valiante T, Adhikary S, Andrade D. Alfentanil induced electrocorticographic activation: a promising tool for presurgical evaluation of temporal lobe epilepsy (TLE) patients. Can J Anaesth. 55 (S1): 4736991-4736992.

37. Hamani C, Hodaie M, Chiang J, del Campo M, Andrade DM, Sherman D, Mirski M, Mello LE, Lozano AM. Deep brain stimulation of the anterior nucleus of the thalamus: effects of electrical stimulation on pilocarpine-induced seizures and status epilepticus. Epilepsy Res. 2008;78(2-3):117-23.

38. Andrade DM, Turnbull J, Minassian BA. Lafora disease, seizures and sugars. Acta Myologica. 2007; 26(1):83-6.

39. Andrade DM, Carlen PL. Novel antiseizure drug mechanisms. Future Neurology. 2007; 2(1):73-86. Principal Author.

40. Andrade DM, Minassian BA. Genetics of Epilepsies. Expert Rev Neurother. 2007; 7(6): 727-34.

41. Andrade DM, Zumsteg D, Hamani C, Hodaie M, Sarkissian S, Lozano AM, Wennberg RA. Long-term follow-up of patients with thalamic deep brain stimulation for epilepsy. Neurology. 2006; 66(10):1571-3.

42. Zumsteg D, Andrade DM, Wennberg RA. Source Localization of small sharp spikes: low resolution electromagnetic tomography (LORETA) reveals two distinct cortical sources. Clin Neurophysiol. 2006; 117(6):1380-7.

43. Zumsteg D, Andrade DM, Del Campo JM, Wennberg R. Parietal lobe source localization and sensitivity to hyperventilation in a patient with subclinical rhythmic electrographic discharges of adults (SREDA). Clin Neurophysiol. 2006; 117(10):2257-63.

44. Zumsteg D, Andrade DM, Wennberg RA. Clinical electrophysiology factors indicative of intractability in patients with temporal lobe epilepsy. Adv Neurol. 2006; 97:45-62.

45. Andrade DM, Scherer SW, Minassian BA. Protein therapy for Unverricht-Lundborg disease using cystatin B transduction by TAT-PTD. Is it that simple? Epilepsy Res. 2006; 72(1):75-9.

46. Andrade DM, Zumsteg D, Sutula TP, Wennberg RA. Clinical aspects of temporal/limbic epilepsy and their relationships to intractability. Adv Neurol. 2006; 97:39-44.

47. Andrade DM, del Campo JM, Moro E, Minassian BA, Wennberg RA. Non-epileptic visual hallucinations in Lafora disease. Neurology. 2005; 64(7):1311-2.

48. Espay AJ, Andrade DM, Wennberg RA, Lang AE. Atypical absences and recurrent absence status in an adult with Angelman syndrome due to UBE3A mutation. Epileptic Disord. 2005; 7(3):227-30.

49. Chan EM, Andrade DM, Franceschetti S, Minassian B. Progressive myoclonus epilepsies: EPM1, EPM2A, EPM2B. Adv Neurol. 2005; 95:47-57.

50. Andrade DM, Ackerley CA, Minett TS, Teive HA, Bohlega S, Scherer SW, Minassian BA. Skin biopsy in Lafora disease: genotype-phenotype correlations and diagnostic pitfalls. Neurology. 2003; 61(11):1611-4.

51. Minassian BA, Andrade DM, Ianzano L, Young EJ, Chan E, Ackerley CA, Scherer SW. Laforin is a cell membrane and endoplasmic reticulum-associated protein tyrosine phosphatase. Annals of neurology. 2001; 49(2):271-5.

52. Meneses M., Molinari D, Fortes M., Pedroso A., Ramina R. Surgical considerations about the anterior syphon knee of the internal carotid artery. Arq Neuropsiquiatr. 1995; 53(1):34-7.

Book Chapters

1. Andrade DM. Genetic causes of epilepsies in women. In: Bui E, Klein EM (Eds). Women with epilepsy: A practical management handbook. Cambridge, United Kingdom: Cambridge University Press; 2014.

2. Andrade DM. Epilepsy, Biomarkers and Genes. In: Ritsner MS (Ed). The handbook of neuropsychiatric biomarkers, endophenotypes, and genes: Volume IV: Molecular genetic and genomic markers. Vol 4. Springer; 2009.

3. Andrade DM, Minassian BA. Unverricht-Lundborg disease. In: Chapman K, Rho JM  (Eds). Pediatric Case Studies: From infancy and childhood through adolescence. CRC press; Boca Raton, USA; 2008.

4. Hodaie M, Hamani C, Zumsteg D, Andrade DM, Wennberg R, Lozano AM. Deep brain stimulation in a patient with medically intractable generalized seizures. In: Luders HO (Ed). Textbook of Epilepsy Surgery. London, United Kingdom: Informa UK Ltd.; 2008.