Articles with public access mandates - Alan HodgkinsonLearn more
Not available anywhere: 2
Recombination affects accumulation of damaging and disease-associated mutations in human populations
JG Hussin, A Hodgkinson, Y Idaghdour, JC Grenier, JP Goulet, E Gbeha, ...
Nature genetics 47 (4), 400-404, 2015
Mandates: Fonds de recherche du Québec - Santé, Genome Canada
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis
CS Leblond, Z Gan-Or, D Spiegelman, SB Laurent, A Szuto, ...
Neurobiology of aging 37, 209. e17-209. e21, 2016
Mandates: Canadian Institutes of Health Research, Genome Canada
Available somewhere: 20
A global reference for human genetic variation
TGP Consortium
Nature 526, 68-74, 2015
Mandates: Swiss National Science Foundation, US National Institutes of Health, Howard …
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56-65, 2012
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, British …
Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsy
KT Kahle, ND Merner, P Friedel, L Silayeva, B Liang, A Khanna, Y Shang, ...
EMBO reports 15 (7), 766-774, 2014
Mandates: US National Institutes of Health, Canadian Institutes of Health Research
Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia
ME Samuels, J Majewski, N Alirezaie, I Fernandez, F Casals, N Patey, ...
Journal of medical genetics 50 (5), 324-329, 2013
Mandates: Canadian Institutes of Health Research, Fonds de recherche du Québec - Santé …
Gene-by-environment interactions in urban populations modulate risk phenotypes
MJ Favé, FC Lamaze, D Soave, A Hodgkinson, H Gauvin, V Bruat, ...
Nature communications 9 (1), 827, 2018
Mandates: Canadian Institutes of Health Research, Fonds de recherche du Québec - Santé …
High-Resolution Genomic Analysis of Human Mitochondrial RNA Sequence Variation
A Hodgkinson, Y Idaghdour, E Gbeha, JC Grenier, E Hip-Ki, V Bruat, ...
Science 344 (6182), 413-415, 2014
Mandates: US National Institutes of Health, Fonds de recherche du Québec - Santé …
Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans
F Casals, A Hodgkinson, J Hussin, Y Idaghdour, V Bruat, T de Maillard, ...
PLoS genetics 9 (9), e1003815, 2013
Mandates: Canadian Institutes of Health Research, Fonds de recherche du Québec - Santé …
Nuclear genetic regulation of the human mitochondrial transcriptome
AT Ali, L Boehme, G Carbajosa, VC Seitan, KS Small, A Hodgkinson
eLife 8, e41927, 2019
Mandates: US National Institutes of Health, UK Biotechnology and Biological Sciences …
Relaxed selection during a recent human expansion
S Peischl, I Dupanloup, A Foucal, M Jomphe, V Bruat, JC Grenier, A Gouy, ...
Genetics, genetics. 300551.2017, 2017
Mandates: Swiss National Science Foundation, Fonds de recherche du Québec - Santé …
Integrated genomic analysis of mitochondrial RNA processing in human cancers
Y Idaghdour, A Hodgkinson
Genome Medicine 9 (1), 36, 2017
Mandates: UK Medical Research Council, National Institute for Health Research, UK
Analysis of mitochondrial m1A/G RNA modification reveals links to nuclear genetic variants and associated disease processes
AT Ali, Y Idaghdour, A Hodgkinson
Communications biology 3 (1), 1-11, 2020
Mandates: US National Institutes of Health, UK Medical Research Council, National …
Genetic variation at mouse and human ribosomal DNA influences associated epigenetic states
F Rodriguez-Algarra, RAE Seaborne, AF Danson, S Yildizoglu, ...
Genome Biology 23 (1), 1-17, 2022
Mandates: UK Biotechnology and Biological Sciences Research Council, UK Medical …
Selective constraint, background selection, and mutation accumulation variability within and between human populations
A Hodgkinson, F Casals, Y Idaghdour, JC Grenier, RD Hernandez, ...
BMC genomics 14 (1), 495, 2013
Mandates: Genome Canada
Intellectual disability-associated factor Zbtb11 cooperates with NRF-2/GABP to control mitochondrial function
BC Wilson, L Boehme, A Annibali, A Hodgkinson, TS Carroll, RJ Oakey, ...
Nature communications 11 (1), 1-20, 2020
Mandates: UK Medical Research Council
A haplotype-based normalization technique for the analysis and detection of allele specific expression
A Hodgkinson, JC Grenier, E Gbeha, P Awadalla
BMC bioinformatics 17 (1), 364, 2016
Mandates: Fonds de recherche du Québec - Santé, Genome Canada, UK Medical Research …
Mitochondrial-nuclear cross-talk in the human brain is modulated by cell type and perturbed in neurodegenerative disease
A Fairbrother-Browne, AT Ali, RH Reynolds, S Garcia-Ruiz, D Zhang, ...
Communications Biology 4 (1), 1-14, 2021
Mandates: US National Institutes of Health, UK Biotechnology and Biological Sciences …
Highly accurate quantification of allelic gene expression for population and disease genetics
A Saukkonen, H Kilpinen, A Hodgkinson
Genome Research, gr. 276296.121, 2022
Mandates: US National Institutes of Health, UK Biotechnology and Biological Sciences …
ensemblQueryR: fast, flexible and high-throughput querying of Ensembl LD API endpoints in R
A Fairbrother-Browne, S García-Ruiz, RH Reynolds, M Ryten, ...
GigaByte 2023, 1, 2023
Mandates: UK Biotechnology and Biological Sciences Research Council
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