Integrated genomic analysis of mitochondrial RNA processing in human cancers

Autor Idaghdour, Youssef, Hodgkinson, Alan
Vydáno v Genome Med (2017)

Human Triallelic Sites: Evidence for a New Mutational Mechanism?

Autor Hodgkinson, Alan, Eyre-Walker, Adam
Vydáno 2010

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

Autor Hodgkinson, Alan, Eyre-Walker, Adam
Vydáno 2010

Cryptic Variation in the Human Mutation Rate

Autor Hodgkinson, Alan, Ladoukakis, Emmanuel, Eyre-Walker, Adam
Vydáno 2009

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

Autor Ali, Aminah Tasnim, Idaghdour, Youssef, Hodgkinson, Alan
Vydáno v Commun Biol (2020)

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

Autor Hodgkinson, Alan, Grenier, Jean-Christophe, Gbeha, Elias, Awadalla, Philip
Vydáno v BMC Bioinformatics (2016)

Nuclear genetic regulation of the human mitochondrial transcriptome

Autor Ali, Aminah T, Boehme, Lena, Carbajosa, Guillermo, Seitan, Vlad C, Small, Kerrin S, Hodgkinson, Alan
Vydáno v eLife (2019)

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

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

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

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

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

Autor 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
Vydáno v Nat Commun (2018)

Relaxed Selection During a Recent Human Expansion

Autor 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
Vydáno v Genetics (2018)

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

Autor 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
Vydáno 2013

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

Autor 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
Vydáno 2013

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

Autor 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
Vydáno 2014