Research
Read how they describe their research on their McGill University profile.
Latest papers
Diverse Genetic Etiologies of Unilateral Polymicrogyria.
Annals of neurology · 2026
Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria
JAMA Neurology · 2023
Comparative analysis of the safety and tolerability of eslicarbazepine acetate in older (≥60 years) and younger (18-59 years) adults.
Epilepsy research · 2021 · first author
22 publications.
Diverse Genetic Etiologies of Unilateral Polymicrogyria.
Lai A, Neil JE, Akula SK, Amrom D, Andermann E, Bergin A, Caraballo R, Chen AY, Gaitanis J, Mochida GH, Gotoff JM, Kuchukhidze G, Marom D, ElAchkar CM, Regev M, Rodan LH, Olson H, Zhang B, Poduri A, Shao DD, Walsh CA, Yang E
Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria
Shyam K. Akula, Allen Y. Chen, Jennifer E. Neil, Diane D. Shao, Alisa Mo, Norma K. Hylton, Stephanie P. DiTroia, Vijay S Ganesh, Richard Scott Smith, Katherine O’kane, Rebecca C. Yeh, Jack H. Marciano, Samantha L. Kirkham, Connor J. Kenny, Janet H. T. Song, Muna Al Saffar, Francisca Millan, David James Harris, Andrea V. Murphy, Kara C. Klemp, Stephen R. Braddock, Harrison Brand, Isaac Wong, Michael E. Talkowski, Anne O’Donnell‐Luria, Abbe Lai, Robert Sean Hill, Ganeshwaran H. Mochida, Ryan N. Doan, Anthony James Barkovich, et al. (131 authors)
Comparative analysis of the safety and tolerability of eslicarbazepine acetate in older (≥60 years) and younger (18-59 years) adults.
Andermann E, Rosenfeld W, Penovich P, Rogin J, Cendes F, Carreño M, Ramsay RE, Ben-Menachem E, Gama H, Rocha F, Soares-da-Silva P, Tosiello R, Blum D, Grinnell T
Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes.
Courage C, Oliver KL, Park EJ, Cameron JM, Grabińska KA, Muona M, Canafoglia L, Gambardella A, Said E, Afawi Z, Baykan B, Brandt C, di Bonaventura C, Chew HB, Criscuolo C, Dibbens LM, Castellotti B, Riguzzi P, Labate A, Filla A, Giallonardo AT, Berecki G, Jackson CB, Joensuu T, Damiano JA, Kivity S, Korczyn A, Palotie A, Striano P, Uccellini D, Giuliano L, Andermann E, Scheffer IE, Michelucci R, Bahlo M, Franceschetti S, Sessa WC, Berkovic SF, Lehesjoki AE
Autosomal-dominant adult neuronal ceroid lipofuscinosis caused by duplication in DNAJC5 initially missed by Sanger and whole-exome sequencing
Ivana Jedličková, Maxime Cadieux‐Dion, Anna Přistoupilová, Viktor Stránecký, Hana Hartmannová, Kateřina Hodaňová, Veronika Barešová, Helena Hůlková, Jakub Sikora, Lenka Nosková, Dita Mušálková, Petr Vyleťal, Jana Sovová, Patrick Cossette, Eva Andermann, Frédérick Andermann, Stanislav Kmoch
Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features.
Berkovic SF, Oliver KL, Canafoglia L, Krieger P, Damiano JA, Hildebrand MS, Morbin M, Vears DF, Sofia V, Giuliano L, Garavaglia B, Simonati A, Santorelli FM, Gambardella A, Labate A, Belcastro V, Castellotti B, Ozkara C, Zeman A, Rankin J, Mole SE, Aguglia U, Farrell M, Rajagopalan S, McDougall A, Brammah S, Andermann F, Andermann E, Dahl HM, Franceschetti S, Carpenter S
Duplication 2p16 is associated with perisylvian polymicrogyria.
Amrom D, Poduri A, Goldman JS, Dan B, Deconinck N, Pichon B, Nadaf J, Andermann F, Andermann E, Walsh CA, Dobyns WB
Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development
Richard Scott Smith, Connor J. Kenny, Vijay S Ganesh, Ahram Jang, Rebeca Borges-Monroy, Jennifer N. Partlow, Robert Sean Hill, Taehwan Shin, Allen Y. Chen, Ryan N. Doan, Anna‐Kaisa Anttonen, Jaakko Ignatius, Līvija Medne, Carsten G. Bönnemann, Jonathan L. Hecht, Oili L. M. Salonen, Anthony James Barkovich, Annapurna H. Poduri, Martina Wilke, Marie‐Claire Y. de Wit, Grazia M. S. Mancini, László Sztriha, Kiho Im, Dina Amrom, Eva Andermann, Ritva Paetau, Anna‐Elina Lehesjoki, Christopher A. Walsh, Maria K. Lehtinen
Psychiatric and cognitive adverse events: A pooled analysis of three phase III trials of adjunctive eslicarbazepine acetate for partial-onset seizures.
Andermann E, Biton V, Benbadis SR, Shneker B, Shah AK, Carreño M, Trinka E, Ben-Menachem E, Biraben A, Rocha F, Gama H, Cheng H, Blum D, Study 301, 302 and 304 Investigators
Research conference summary from the 2014 International Task Force on ATP1A3-Related Disorders.
Rosewich H, Sweney MT, DeBrosse S, Ess K, Ozelius L, Andermann E, Andermann F, Andrasco G, Belgrade A, Brashear A, Ciccodicola S, Egan L, George AL, Lewelt A, Magelby J, Merida M, Newcomb T, Platt V, Poncelin D, Reyna S, Sasaki M, Sotero de Menezes M, Sweadner K, Viollet L, Zupanc M, Silver K, Swoboda K
Frequent collaborators
- Massimo Pandolfo and Amanpreet Badhwar: 4 shared papers
- Gabriella Gobbi and Massimo Pandolfo: 2 shared papers
- Gabriella Gobbi and Amanpreet Badhwar: 2 shared papers
- Amanpreet Badhwar and Eva Andermann: 2 shared papers
- Vijay Ganesh and Eva Andermann: 2 shared papers
- Dang Nguyen and Vijay Ganesh: 1 shared paper
- Dang Nguyen and Micheil Innes: 1 shared paper
- Dang Nguyen and Harvey Sarnat: 1 shared paper
- Dang Nguyen and Eva Andermann: 1 shared paper
- Gabriella Gobbi and Robert Koenekoop: 1 shared paper
- Gabriella Gobbi and Eva Andermann: 1 shared paper
- Robert Koenekoop and Massimo Pandolfo: 1 shared paper
- Robert Koenekoop and Amanpreet Badhwar: 1 shared paper
- Robert Koenekoop and Eva Andermann: 1 shared paper
- Massimo Pandolfo and Harvey Sarnat: 1 shared paper
- Massimo Pandolfo and Eva Andermann: 1 shared paper
- Vijay Ganesh and Micheil Innes: 1 shared paper
- Vijay Ganesh and Harvey Sarnat: 1 shared paper
- Micheil Innes and Harvey Sarnat: 1 shared paper
- Micheil Innes and Eva Andermann: 1 shared paper
- Harvey Sarnat and Eva Andermann: 1 shared paper
- Department of Human Genetics
- Département de pharmacologie et physiologie
- Cheriton School of Computer Science
- Neurologie, Service de
- Department of Psychiatry
- Cumming School of Medicine
- Department of Neurology and Neurosurgery
- Other
Co-authors at McGill University, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
Amanpreet Badhwar
Département de pharmacologie et physiologie
2 shared papers, latest 2006
Vijay Ganesh
Cheriton School of Computer Science
2 shared papers, latest 2023
Amit Bar-Or
Rheumatology
1 shared papers, latest 2014
Patrick Cossette
Faculty
1 shared papers, latest 2020
Robert Koenekoop
Department of Human Genetics
1 shared papers, latest 2006
Massimo Pandolfo
Department of Neurology and Neurosurgery
1 shared papers, latest 2006
Micheil Innes
Department of Medical Genetics
1 shared papers, latest 2023
Dang Nguyen
Neurologie, Service de
1 shared papers, latest 2023
Harvey Sarnat
Cumming School of Medicine
1 shared papers, latest 2023
Gabriella Gobbi
Department of Psychiatry
1 shared papers, latest 2006
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Profile data last refreshed on September 29, 2026 from the university directory, publication records and public research funding records.