Not logged in Posterior Fossa Malformations in a Cohort of 116 Fetuses: A Retrospective Analysis of Imaging Characteristics, Postnatal Imaging Concordance, Pregnancy Outcomes and Yield of Genetic Testing Malta, Maisa; Fortin, Olivier; Badner, Braeden; Charouf, Daniel; Addour-Boudrahem, Nassima; Beaudet-Leclair, Olivier; Rampakakis, Emmanouil; Rosenblatt, David S.; Nedelchev, Atanas Angelov; Shear, Roberta; Carpineta, Lucia; Srour, Myriam Share Save
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Age and Maturation Stage Linked Consequences of Fibrinogen on Human Oligodendroglia Blaszczyk, Gabriela J.; Weng, Chao; Mohammadnia, Abdulshakour; Cui, Qiao-Ling; Giurleo, Arianna; Groh, Adam M. R.; Plouffe, Chloe; Sirois, Julien; Piscopo, Valerio E. C.; Yaqubi, Moein; Taqvi, Asad; Cassidy, Erin; Martin, Liam Callahan; Hall, Jeffery A.; Dudley, Roy W. R.; Srour, Myriam; Zandee, Stephanie E. J.; Klement, Wendy; Larouche, Sandra; Prat, Alexandre; Durcan, Thomas M.; Stratton, Jo Anne; Antel, Jack P.; Moore, G. R. Wayne Share Save
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A human DCC variant causing mirror movement disorder reveals that the WAVE regulatory complex mediates axon guidance by netrin-1-DCC Chaudhari, Karina; Zhang, Kaiyue; Yam, Patricia T.; Zang, Yixin; Kramer, Daniel A.; Gagnon, Sarah; Schlienger, Sabrina; Calabretta, Sara; Michaud, Jean-Francois; Collins, Meagan; Wang, Junmei; Srour, Myriam; Chen, Baoyu; Charron, Frederic; Bashaw, Greg J. Share Save
Biallelic loss-of-function variants of SLC12A9 cause lysosome dysfunction and a syndromic neurodevelopmental disorder Accogli, Andrea; Park, Young N.; Lenk, Guy M.; Severino, Mariasavina; Scala, Marcello; Denecke, Jonas; Hempel, Maja; Lessel, Davor; Kortuem, Fanny; Salpietro, Vincenzo; de Marco, Patrizia; Guerrisi, Sara; Torella, Annalaura; Nigro, Vincenzo; Srour, Myriam; Turro, Ernest; Labarque, Veerle; Freson, Kathleen; Piatelli, Gianluca; Capra, Valeria; Kitzman, Jacob O.; Meisler, Miriam H. Share Save
Genotype-phenotype correlation in CLCN4-related developmental and epileptic encephalopathy Sahly, Ahmed N.; Sierra-Marquez, Juan; Bungert-Pluemke, Stefanie; Franzen, Arne; Mougharbel, Lina; Berrahmoune, Saoussen; Dassi, Christelle; Poulin, Chantal; Srour, Myriam; Guzman, Raul E.; Myers, Kenneth A. Share Save
Mono-allelic KCNB2 variants lead to a neurodevelopmental syndrome caused by altered channel inactivation Bhat, Shreyas; Rousseau, Justine; Michaud, Coralie; Lourenco, Charles Marques; Stoler, Joan M.; Louie, Raymond J.; Clarkson, Lola K.; Lichty, Angie; Koboldt, Daniel C.; Reshmi, Shalini C.; Sisodiya, Sanjay M.; van Konijnenburg, Eva M. M. Hoytema; Koop, Klaas; Hasselt, Peter M. van; Demurger, Florence; Dubourg, Christele; Sullivan, Bonnie R.; Hughes, Susan S.; Thiffault, Isabelle; Tremblay, Elisabeth Simard; Accogli, Andrea; Srour, Myriam; Blunck, Rikard; Campeau, Philippe M. Share Save
Age-dependent effects of metformin on human oligodendrocyte lineage cell ensheathment capacity Mohammadnia, Abdulshakour; Cui, Qiao-Ling; Weng, Chao; Yaqubi, Moein; Fernandes, Milton G. F.; Hall, Jeffery A.; Dudley, Roy; Srour, Myriam; Kennedy, Timothy E.; Stratton, Jo Anne; Antel, Jack P. Share Save
Regulation of stress granule formation in human oligodendrocytes Pernin, Florian; Cui, Qiao-Ling; Mohammadnia, Abdulshakour; Fernandes, Milton G. F.; Hall, Jeffery A.; Srour, Myriam; Dudley, Royw. R.; Zandee, Stephanie E. J.; Klement, Wendy; Prat, Alexandre; Salapa, Hannah E.; Levin, Michael C.; Moore, G. R. Wayne; Kennedy, Timothy E.; Vande Velde, Christine; Antel, Jack P. Share Save
Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals Hutchinson, Meagan L. Collins; St-Onge, Judith; Schlienger, Sabrina; Boudrahem-Addour, Nassima; Mougharbel, Lina; Michaud, Jean-Francois; Lloyd, Clara; Bruneau, Elena; Roux, Cedric; Sahly, Ahmed N.; Osterman, Bradley; Myers, Kenneth A.; Rouleau, Guy A.; Cruz, Daniel Alexander Jimenez; Riviere, Jean-Baptiste; Accogli, Andrea; Charron, Frederic; Srour, Myriam Share Save
mTOR Pathway Somatic Pathogenic Variants in Focal Malformations of Cortical Development Krochmalnek, Eric; Accogli, Andrea; St-Onge, Judith; Addour-Boudrahem, Nassima; Prakash, Gyan; Kim, Sung-Hoon; Brunette-Clement, Tristan; Alhajaj, Ghadd; Mougharbel, Lina; Bruneau, Elena; Myers, Kenneth A.; Dubeau, Francois; Karamchandani, Jason; Farmer, Jean-Pierre; Atkinson, Jeffrey; Hall, Jeffrey; Poulin, Chantal Chantal; Rosenblatt, Bernard; Lafond-Lapalme, Joel; Weil, Alexander; Fallet-Bianco, Catherine; Albrecht, Steffen; Sonenberg, Nahum; Riviere, Jean-Baptiste; Dudley, Roy W.; Srour, Myriam Share Save
Mechanisms of metabolic stress induced cell death of human oligodendrocytes: relevance for progressive multiple sclerosis Fernandes, Milton Guilherme Forestieri; Mohammadnia, Abdulshakour; Pernin, Florian; Schmitz-Gielsdorf, Laura Eleonora; Hodgins, Caroline; Cui, Qiao-Ling; Yaqubi, Moein; Blain, Manon; Hall, Jeffery; Dudley, Roy; Srour, Myriam; Zandee, Stephanie E. J.; Klement, Wendy; Prat, Alexandre; Stratton, Jo Anne; Rodriguez, Moses; Kuhlmann, Tanja; Moore, Wayne; Kennedy, Timothy. E. E.; Antel, Jack. P. P. Share Save
Analysis of the microglia transcriptome across the human lifespan using single cell RNA sequencing Yaqubi, Moein; Groh, Adam M. R.; Dorion, Marie-France; Afanasiev, Elia; Luo, Julia Xiao Xuan; Hashemi, Hadi; Sinha, Sarthak; Kieran, Nicholas W.; Blain, Manon; Cui, Qiao-Ling; Biernaskie, Jeff; Srour, Myriam; Dudley, Roy; Hall, Jeffery A.; Sonnen, Joshua A.; Arbour, Nathalie; Prat, Alexandre; Stratton, Jo Anne; Antel, Jack; Healy, Luke M. Share Save
Genotype-phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder D'Onofrio, Gianluca; Accogli, Andrea; Severino, Mariasavina; Caliskan, Haluk; Kokotovic, Tomislav; Blazekovic, Antonela; Jercic, Kristina Gotovac; Markovic, Silvana; Zigman, Tamara; Goran, Krnjak; Barisic, Nina; Duranovic, Vlasta; Ban, Ana; Borovecki, Fran; Ramadza, Danijela Petkovic; Baric, Ivo; Fazeli, Walid; Herkenrath, Peter; Marini, Carla; Vittorini, Roberta; Gowda, Vykuntaraju; Bouman, Arjan; Rocca, Clarissa; Alkhawaja, Issam Azmi; Murtaza, Bibi Nazia; Rehman, Malik Mujaddad Ur; Al Alam, Chadi; Nader, Gisele; Mancardi, Maria Margherita; Giacomini, Thea; Srivastava, Siddharth; Alvi, Javeria Raza; Tomoum, Hoda; Matricardi, Sara; Iacomino, Michele; Riva, Antonella; Scala, Marcello; Madia, Francesca; Pistorio, Angela; Salpietro, Vincenzo; Minetti, Carlo; Riviere, Jean-Baptiste; Srour, Myriam; Efthymiou, Stephanie; Maroofian, Reza; Houlden, Henry; Vernes, Sonja Catherine; Zara, Federico; Striano, Pasquale; Nagy, Vanja Share Save
Genetics of mirror movements identifies a multifunctional complex required for Netrin-1 guidance and lateralization of motor control Schlienger, Sabrina; Yam, Patricia T.; Balekoglu, Nursen; Ducuing, Hugo; Michaud, Jean-Francois; Makihara, Shirin; Kramer, Daniel K.; Chen, Baoyu; Fasano, Alfonso; Berardelli, Alfredo; Hamdan, Fadi F.; Rouleau, Guy A.; Srour, Myriam; Charron, Frederic Share Save
Genetic and metabolic investigations for neurodevelopmental disorders: position statement of the Canadian College of Medical Geneticists (CCMG) Carter, Melissa T.; Srour, Myriam; Au, Ping-Yee Billie; Buhas, Daniela; Dyack, Sarah; Eaton, Alison; Inbar-Feigenberg, Michal; Howley, Heather; Kawamura, Anne; Lewis, Suzanne M. E.; McCready, Elizabeth; Nelson, Tanya N.; Vallance, Hilary Share Save
Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals Saida, Ken; Marootain, Reza; Sengoku, Toru; Mitani, Tadahiro; Pagnamenta, Alistair T.; Marafi, Dana; Zaki, Maha S.; O'Brian, Thomas J.; Karimiani, Ehsan Ghayoor; Kaiyrzhanov, Rauan; Takizawa, Marina; Ohori, Sachiko; Leong, Huey Yin; Akay, Gulsen; Galehdari, Hamid; Zamani, Mina; Romy, Ratna; Carroll, Christopher J.; Toosi, Mehran Beiraghi; Ashrafzadeh, Farah; Imannezhad, Shima; Malek, Hadis; Ahangari, Najmeh; Tomoum, Hoda; Gowda, Vykuntaraju K.; Srinivasan, Varunvenkat M.; Murphy, David; Dominik, Natalia; Elbendary, Hasnaa M.; Rafat, Karima; Yilmaz, Sanem; Kanmaz, Seda; Serin, Mine; Krishnakumar, Deepa; Gardham, Alice; Maw, Anna; Rao, Tekki Sreenivasa; Alsubhi, Sarah; Srour, Myriam; Buhas, Daniela; Jewett, Tamison; Goldberg, Rachel E.; Shamseldin, Hanan; Frengen, Eirik; Misceo, Doriana; Stromme, Petter; Ceroni, Jose Ricardo Magliocco; Kim, Chong Ae; Yesil, Gozde; Sengenc, Esma; Guler, Serhat; Hull, Mariam; Parnes, Mered; Aktas, Dilek; Anlar, Banu; Bayram, Yavuz; Pehlivan, Davut; Posey, Jennifer E.; Alayi, Shahryar; Manshadi, Seyed Ali Madani; Alzaidan, Hamad; Al-Owain, Mohammad; Alabdi, Lama; Abdulwahab, Ferdous; Sekiguchi, Futoshi; Hamanaka, Kohei; Fujita, Atsushi; Uchiyama, Yuri; Mizuguchi, Takeshi; Miyatake, Satoko; Miyake, Noriko; Elshafie, Reem M.; Salayev, Kamran; Guliyeva, Ulviyya; Alkuraya, Fowzan S.; Gleeson, Joseph G.; Monaghan, Kristin G.; Langley, Katherine G.; Yang, Hui; Motavaf, Mahsa; Safari, Saeid; Alipour, Mozhgan; Ogata, Kazuhiro; Brown, Andre E. X.; Lupski, James R.; Houlden, Henry; Matsumoto, Naomichi Share Save
Regional and age-related diversity of human mature oligodendrocytes Yaqubi, Moein; Luo, Julia Xiao Xuan; Baig, Salma; Cui, Qiao-Ling; Petrecca, Kevin; Desu, Haritha; Larochelle, Catherine; Afanasiev, Elia; Hall, Jeffery A.; Dudley, Roy; Srour, Myriam; Haglund, Lisbet; Ouellet, Jean; Georgiopoulos, Miltiadis; Santaguida, Carlo; Sonnen, Joshua A.; Healy, Luke M.; Stratton, Jo Anne; Kennedy, Timothy E.; Antel, Jack P. Share Save
Diverse injury responses of human oligodendrocyte to mediators implicated in multiple sclerosis Pernin, Florian; Luo, Julia Xiao Xuan; Cui, Qiao-Ling; Blain, Manon; Fernandes, Milton G. F.; Yaqubi, Moein; Srour, Myriam; Hall, Jeff; Dudley, Roy; Jamann, Helene; Larochelle, Catherine; Zandee, Stephanie E. J.; Prat, Alexandre; Stratton, Jo Anne; Kennedy, Timothy E.; Antel, Jack P. Share Save
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