Integrated genomic analysis of mitochondrial RNA processing in human cancers

by Idaghdour, Youssef, Hodgkinson, Alan
Published in Genome Med (2017)

Human Triallelic Sites: Evidence for a New Mutational Mechanism?

by Hodgkinson, Alan, Eyre-Walker, Adam
Published 2010

The Genomic Distribution and Local Context of Coincident SNPs in Human and Chimpanzee

by Hodgkinson, Alan, Eyre-Walker, Adam
Published 2010

Cryptic Variation in the Human Mutation Rate

by Hodgkinson, Alan, Ladoukakis, Emmanuel, Eyre-Walker, Adam
Published 2009

Analysis of mitochondrial m1A/G RNA modification reveals links to nuclear genetic variants and associated disease processes

by Ali, Aminah Tasnim, Idaghdour, Youssef, Hodgkinson, Alan
Published in Commun Biol (2020)

A haplotype-based normalization technique for the analysis and detection of allele specific expression

by Hodgkinson, Alan, Grenier, Jean-Christophe, Gbeha, Elias, Awadalla, Philip
Published in BMC Bioinformatics (2016)

Nuclear genetic regulation of the human mitochondrial transcriptome

by Ali, Aminah T, Boehme, Lena, Carbajosa, Guillermo, Seitan, Vlad C, Small, Kerrin S, Hodgkinson, Alan
Published in eLife (2019)

Selective constraint, background selection, and mutation accumulation variability within and between human populations

by Hodgkinson, Alan, Casals, Ferran, Idaghdour, Youssef, Grenier, Jean-Christophe, Hernandez, Ryan D, Awadalla, Philip
Published 2013

Intellectual disability-associated factor Zbtb11 cooperates with NRF-2/GABP to control mitochondrial function

by Wilson, Brooke C., Boehme, Lena, Annibali, Ambra, Hodgkinson, Alan, Carroll, Thomas S., Oakey, Rebecca J., Seitan, Vlad C.
Published in Nat Commun (2020)

Gene-by-environment interactions in urban populations modulate risk phenotypes

by Favé, Marie-Julie, Lamaze, Fabien C., Soave, David, Hodgkinson, Alan, Gauvin, Héloïse, Bruat, Vanessa, Grenier, Jean-Christophe, Gbeha, Elias, Skead, Kimberly, Smargiassi, Audrey, Johnson, Markey, Idaghdour, Youssef, Awadalla, Philip
Published in Nat Commun (2018)

Relaxed Selection During a Recent Human Expansion

by Peischl, Stephan, Dupanloup, Isabelle, Foucal, Adrien, Jomphe, Michèle, Bruat, Vanessa, Grenier, Jean-Christophe, Gouy, Alexandre, Gilbert, K. J., Gbeha, Elias, Bosshard, Lars, Hip-Ki, Elodie, Agbessi, Mawussé, Hodgkinson, Alan, Vézina, Hélène, Awadalla, Philip, Excoffier, Laurent
Published in Genetics (2018)

Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia

by Samuels, Mark E, Majewski, Jacek, Alirezaie, Najmeh, Fernandez, Isabel, Casals, Ferran, Patey, Natalie, Decaluwe, Hélène, Gosselin, Isabelle, Haddad, Elie, Hodgkinson, Alan, Idaghdour, Youssef, Marchand, Valerie, Michaud, Jacques L, Rodrigue, Marc-André, Desjardins, Sylvie, Dubois, Stéphane, Le Deist, Francoise, Awadalla, Philip, Raymond, Vincent, Maranda, Bruno
Published 2013

Whole-Exome Sequencing Reveals a Rapid Change in the Frequency of Rare Functional Variants in a Founding Population of Humans

by Casals, Ferran, Hodgkinson, Alan, Hussin, Julie, Idaghdour, Youssef, Bruat, Vanessa, de Maillard, Thibault, Grenier, Jean-Cristophe, Gbeha, Elias, Hamdan, Fadi F., Girard, Simon, Spinella, Jean-François, Larivière, Mathieu, Saillour, Virginie, Healy, Jasmine, Fernández, Isabel, Sinnett, Daniel, Michaud, Jacques L., Rouleau, Guy A., Haddad, Elie, Le Deist, Françoise, Awadalla, Philip
Published 2013

Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsy

by Kahle, Kristopher T, Merner, Nancy D, Friedel, Perrine, Silayeva, Liliya, Liang, Bo, Khanna, Arjun, Shang, Yuze, Lachance-Touchette, Pamela, Bourassa, Cynthia, Levert, Annie, Dion, Patrick A, Walcott, Brian, Spiegelman, Dan, Dionne-Laporte, Alexandre, Hodgkinson, Alan, Awadalla, Philip, Nikbakht, Hamid, Majewski, Jacek, Cossette, Patrick, Deeb, Tarek Z, Moss, Stephen J, Medina, Igor, Rouleau, Guy A
Published 2014