Search Results - Fadi F Hamdan
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Assessment of burden and segregation profiles of CNVs in patients with epilepsy by Claudia Moreau, Frédérique Tremblay, Stefan Wolking, Alexandre Girard, Catherine Laprise, Fadi F. Hamdan, Jacques L. Michaud, Berge A. Minassian, Patrick Cossette, Simon L. Girard
Published in Annals of Clinical and Translational Neurology (2022-07-01)Get full text
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Global characterization of copy number variants in epilepsy patients from whole genome sequencing. by Jean Monlong, Simon L Girard, Caroline Meloche, Maxime Cadieux-Dion, Danielle M Andrade, Ron G Lafreniere, Micheline Gravel, Dan Spiegelman, Alexandre Dionne-Laporte, Cyrus Boelman, Fadi F Hamdan, Jacques L Michaud, Guy Rouleau, Berge A Minassian, Guillaume Bourque, Patrick Cossette
Published in PLoS Genetics (2018-04-01)Get full text
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A population genetic approach to mapping neurological disorder genes using deep resequencing. by Rachel A Myers, Ferran Casals, Julie Gauthier, Fadi F Hamdan, Jon Keebler, Adam R Boyko, Carlos D Bustamante, Amelie M Piton, Dan Spiegelman, Edouard Henrion, Martine Zilversmit, Julie Hussin, Jacklyn Quinlan, Yan Yang, Ronald G Lafrenière, Alexander R Griffing, Eric A Stone, Guy A Rouleau, Philip Awadalla
Published in PLoS Genetics (2011-02-01)Get full text
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Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans. by Ferran Casals, Alan Hodgkinson, Julie Hussin, Youssef Idaghdour, Vanessa Bruat, Thibault de Maillard, Jean-Christophe Grenier, Elias Gbeha, Fadi F Hamdan, Simon Girard, Jean-François Spinella, Mathieu Larivière, Virginie Saillour, Jasmine Healy, Isabel Fernández, Daniel Sinnett, Jacques L Michaud, Guy A Rouleau, Elie Haddad, Françoise Le Deist, Philip Awadalla
Published in PLoS Genetics (2013-01-01)Get full text
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