Accounting for long-range correlations in genome-wide simulations of large cohorts by Nelson, Dominic, Kelleher, Jerome, Ragsdale, Aaron P, Moreau, Claudia, McVean, Gil, Gravel, Simon

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Unraveling the role of non-coding rare variants in epilepsy by Girard, Alexandre, Moreau, Claudia, Michaud, Jacques L, Minassian, Berge, Cossette, Patrick, Girard, Simon L

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P607: Identification of pathogenic genetic variants using whole genome sequencing in patients with epilepsy by Olifir, Oleksandr, Moreau, Claudia, Cadieux-Dion, Maxime, Minassian, Berge, Cossette, Patrick, Girard, Simon

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The role of common genetic variation in presumed monogenic epilepsies by Campbell, Ciarán, Leu, Costin, Feng, Yen-Chen Anne, Wolking, Stefan, Moreau, Claudia, Ellis, Colin, Ganesan, Shiva, Martins, Helena, Oliver, Karen, Boothman, Isabelle, Benson, Katherine, Molloy, Anne, Brody, Lawrence, Michaud, Jacques L., Hamdan, Fadi F., Minassian, Berge A., Lerche, Holger, Scheffer, Ingrid E., Sisodiya, Sanjay, Girard, Simon, Cosette, Patrick, Delanty, Norman, Lal, Dennis, Cavalleri, Gianpiero L.

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Assessment of burden and segregation profiles of CNVs in patients with epilepsy by Moreau, Claudia, Tremblay, Frédérique, Wolking, Stefan, Girard, Alexandre, Laprise, Catherine, Hamdan, Fadi F., Michaud, Jacques L., Minassian, Berge A., Cossette, Patrick, Girard, Simon L.

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Assessing the role of rare genetic variants in drug‐resistant, non‐lesional focal epilepsy by Wolking, Stefan, Moreau, Claudia, McCormack, Mark, Krause, Roland, Krenn, Martin, Berkovic, Samuel, Cavalleri, Gianpiero L., Delanty, Norman, Depondt, Chantal, Johnson, Michael R., Koeleman, Bobby P. C., Kunz, Wolfram S., Lerche, Holger, Marson, Anthony G., O’Brien, Terence J., Petrovski, Slave, Sander, Josemir W., Sills, Graeme J., Striano, Pasquale, Zara, Federico, Zimprich, Fritz, Sisodiya, Sanjay M., Girard, Simon L., Cossette, Patrick

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X-linked MTMR8 diversity and evolutionary history of sub-Saharan populations by Labuda, Damian, Yotova, Vania, Lefebvre, Jean-François, Moreau, Claudia, Utermann, Gerd, Williams, Scott M

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Native American admixture in the Quebec founder population by Moreau, Claudia, Lefebvre, Jean-François, Jomphe, Michèle, Bhérer, Claude, Ruiz-Linares, Andres, Vézina, Hélène, Roy-Gagnon, Marie-Hélène, Labuda, Damian

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Genomic inference using diffusion models and the allele frequency spectrum by Ragsdale, Aaron P., Moreau, Claudia, Gravel, Simon

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Deciphering the genetic structure of the Quebec founder population using genealogies by Gagnon, Laurence, Moreau, Claudia, Laprise, Catherine, Vézina, Hélène, Girard, Simon L

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Deep Human Genealogies Reveal a Selective Advantage to Be on an Expanding Wave Front by Moreau, Claudia, Bhérer, Claude, Vézina, Hélène, Jomphe, Michèle, Labuda, Damian, Excoffier, Laurent

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Inferring Transmission Histories of Rare Alleles in Population-Scale Genealogies by Nelson, Dominic, Moreau, Claudia, de Vriendt, Marianne, Zeng, Yixiao, Preuss, Christoph, Vézina, Hélène, Milot, Emmanuel, Andelfinger, Gregor, Labuda, Damian, Gravel, Simon

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Unraveling the role of non-coding rare variants in epilepsy by Alexandre Girard, Claudia Moreau, Jacques L Michaud, Berge Minassian, Patrick Cossette, Simon L Girard

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Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study by Stanley, Kate E., Bobbili, Dheeraj R., Dhindsa, Ryan S., May, Patrick, Alldredge, Brian K., Allen, Andrew S., Altmüller, Janine, Amrom, Dina, Andermann, Eva, Auce, Pauls, Avbersek, Andreja, Bautista, Jocelyn F., Becker, Felicitas, Bellows, Susannah T., Berghuis, Bianca, Bluvstein, Judith, Boro, Alex, Burgess, Rosemary, Caglayan, Hande, Cascino, Gregory D., Chung, Seo‐Kyung, Cieuta‐Walti, Cécile, Consalvo, Damian, Cossette, Patrick, Crumrine, Patricia, Delanty, Norman, Depondt, Chantal, Desbiens, Richard, Dlugos, Dennis, Epstein, Michael P., Everett, Kate, Fountain, Nathan B., Francis, Ben, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Girard, Simon, Glauser, Tracy, Glynn, Simon, Gravel, Micheline, Haas, Kevin, Haut, Sheryl R., Heinzen, Erin L., Helbig, Ingo, Hildebrand, Michael S., Jorgensen, Andrea, Joshi, Sucheta, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Kossoff, Eric H., Krause, Roland, Kunz, Wolfram S., Langley, Sarah R., LeGuern, Eric, Lerche, Holger, Leu, Costin, Lortie, Anne, Marson, Anthony G., Mebane, Caroline, Mefford, Heather C., Meloche, Caroline, Motika, Paul V., Muhle, Hiltrud, Nabbout, Rima, Nguyen, Dang K., Nikanorova, Marina, Novotny, Edward J., Ottman, Ruth, O’Brien, Terence J., Paolicchi, Juliann M., Parent, Jack M., Peter, Sarah, Petrou, Steven, Pickrell, William O., Poduri, Annapurna, Radtke, Rodney A., Rees, Mark I., Regan, Brigid M., Sadleir, Lynette G., Sander, Josemir W., Sander, Thomas, Scheffer, Ingrid E., Singh, Rani K., Sirven, Joseph, Sisodiya, Sanjay M., Smith, Michael C., Sonsma, Anja C. M., Sullivan, Joseph, Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Von Allmen, Gretchen K., Wang, Quanli, Weber, Yvonne G., Weckhuysen, Sarah, Widdess‐Walsh, Peter, Winawer, Melodie R., Wolking, Stefan, Zimprich, Fritz

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Historical human remains identification through maternal and paternal genetic signatures in a founder population with extensive genealogical record by Harding, Tommy, Milot, Emmanuel, Moreau, Claudia, Lefebvre, Jean‐Francois, Bournival, Jean‐Sébastien, Vézina, Hélène, Laprise, Catherine, Lalueza‐Fox, Carles, Anglada, Roger, Loewen, Brad, Casals, Ferran, Ribot, Isabelle, Labuda, Damian

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Genomic and genealogical investigation of the French Canadian founder population structure by Roy-Gagnon, Marie-Hélène, Moreau, Claudia, Bherer, Claude, St-Onge, Pascal, Sinnett, Daniel, Laprise, Catherine, Vézina, Hélène, Labuda, Damian

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Endothelin ETA receptor blockade prevents the progression of renal failure and hypertension in uraemic rats by Brochu, Edith, Lacasse-M., Sonia, Moreau, Claudia, Lebel, Marcel, Kingma, Iris, Grose, John H., Larivière, Richard

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Genome-wide patterns of identity-by-descent sharing in the French Canadian founder population by Gauvin, Héloïse, Moreau, Claudia, Lefebvre, Jean-François, Laprise, Catherine, Vézina, Hélène, Labuda, Damian, Roy-Gagnon, Marie-Hélène

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Polygenic risk scores of several subtypes of epilepsies in a founder population by Moreau, Claudia, Rébillard, Rose-Marie, Wolking, Stefan, Michaud, Jacques, Tremblay, Frédérique, Girard, Alexandre, Bouchard, Joanie, Minassian, Berge, Laprise, Catherine, Cossette, Patrick, Girard, Simon L

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GENLIB: an R package for the analysis of genealogical data by Gauvin, Héloïse, Lefebvre, Jean-François, Moreau, Claudia, Lavoie, Eve-Marie, Labuda, Damian, Vézina, Hélène, Roy-Gagnon, Marie-Hélène

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