Torthaí cuardaigh - Alan Hodgkinson
- 1 - 9 toradh as 9 á dtaispeáint
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1
Human Triallelic Sites: Evidence for a New Mutational Mechanism? de réir Alan Hodgkinson, Adam Eyre‐Walker
Foilsithe / Cruthaithe 2009Artigo -
2
Cryptic Variation in the Human Mutation Rate de réir Alan Hodgkinson, Emmanuel D. Ladoukakis, Adam Eyre‐Walker
Foilsithe / Cruthaithe 2009Artigo -
3
Nuclear genetic regulation of the human mitochondrial transcriptome de réir Aminah T. Ali, Lena Boehme, Guillermo Carbajosa, Vlad C. Seitan, Kerrin S. Small, Alan Hodgkinson
Foilsithe / Cruthaithe 2019Artigo -
4
Recombination affects accumulation of damaging and disease-associated mutations in human populations de réir Julie Hussin, Alan Hodgkinson, Youssef Idaghdour, Jean‐Christophe Grenier, Jean-Philippe Goulet, Elias Gbeha, Elodie Hip-Ki, Philip Awadalla
Foilsithe / Cruthaithe 2015Artigo -
5
Relaxed Selection During a Recent Human Expansion de réir Stephan Peischl, Isabelle Dupanloup, Adrien Foucal, Michèle Jomphe, Vanessa Bruat, Jean‐Christophe Grenier, Alexandre Gouy, Kimberly J. Gilbert, Elias Gbeha, Lars Bosshard, Elodie Hip-Ki, Mawussé Agbessi, Alan Hodgkinson, Hélène Vézina, Philip Awadalla, Laurent Excoffier
Foilsithe / Cruthaithe 2017Artigo -
6
Genetic variation at mouse and human ribosomal DNA influences associated epigenetic states de réir Francisco Rodríguez-Algarra, Robert A. Seaborne, Amy F. Danson, Selin Yildizoglu, Harunori Yoshikawa, Pui Pik Law, Zakaryya Ahmad, Victoria A. Maudsley, Ama Brew, Nadine Holmes, Mateus Ochôa, Alan Hodgkinson, Sarah J. Marzi, Madapura M. Pradeepa, Matthew Loose, Michelle L. Holland, Vardhman K. Rakyan
Foilsithe / Cruthaithe 2022Artigo -
7
Exome sequencing identifies mutations in the gene<i>TTC7A</i>in French-Canadian cases with hereditary multiple intestinal atresia de réir Mark E. Samuels, Jacek Majewski, Najmeh Alirezaie, Isabel Fernández, Ferrán Casals, Natalie Patey, Hélène Decaluwe, Isabelle Gosselin, Élie Haddad, Alan Hodgkinson, Youssef Idaghdour, Valérie Marchand, Jacques L. Michaud, Marc‐André Rodrigue, Sylvie Desjardins, Stéphane Dubois, Françoise Le Deist, Philip Awadalla, Vincent Raymond, Bruno Maranda
Foilsithe / Cruthaithe 2013Artigo -
8
Whole-Exome Sequencing Reveals a Rapid Change in the Frequency of Rare Functional Variants in a Founding Population of Humans de réir Ferrán 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, Élie Haddad, Françoise Le Deist, Philip Awadalla
Foilsithe / Cruthaithe 2013Artigo -
9
Genetically encoded impairment of neuronal <scp>KCC</scp> 2 cotransporter function in human idiopathic generalized epilepsy de réir Kristopher T. Kahle, Nancy D. Merner, Perrine Friedel, Liliya Silayeva, Bo Liang, Arjun Khanna, Yuze Shang, Pamela Lachance‐Touchette, Cynthia V. Bourassa, Annie Levert, Patrick A. Dion, Brian P. Walcott, Dan Spiegelman, Alexandre Dionne‐Laporte, Alan Hodgkinson, Philip Awadalla, Hamid Nikbakht, Jacek Majewski, Patrick Cossette, Tarek Z. Deeb, Stephen J. Moss, Igor Medina, Guy A. Rouleau
Foilsithe / Cruthaithe 2014Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Gene
Genetics
Evolutionary biology
Mutation
Haplotype
Allele
Genetic variation
Genome
Demography
Exome
Exome sequencing
Founder effect
Gene expression
Human genome
Mutation rate
Population
Recombination
Sociology
Artificial intelligence
Astronomy
Chemistry
Composite material
Compound heterozygosity
Computational biology
Computer science
Cotransporter
DNA
DNA methylation
DNA sequencing