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Antona, G-C, Ali, A.T., Hodgkinson, A. 2022. Identification of human mitochondrial RNA cleavage sites and candidate RNA processing factors. BMC Biology 20:168.
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Fairbrother-Browne, A., Ali, A., Reynolds, R., Garcia-Ruiz, S., Zhang, D., Chen, Z., Ryten, M. and Hodgkinson, A. 2021, Mitochondrial-nuclear cross-talk in the human brain is modulated by cell type and perturbed in neurodegenerative disease. Communications Biology 4: 1262.
Wilson B.C., Boehme L., Annibali A., Hodgkinson A., Carroll T.S., Oakey R.J., Seitan V.C. 2020. Intellectual disability-associated factor Zbtb11 cooperates with NRF-2/GABP to control mitochondrial function. Nature Communications 11: 5469.
Ali, A.T., Idaghdour, Y, Hodgkinson, A. 2020. Analysis of mitochondrial m1A/G RNA modification reveals links to nuclear genetic variants and associated disease processes. Communications Biology 3: 147.
Ali, A.T., Boehme, L., Antona, G-C, Seitan, V.C., Small, K.S., Hodgkinson, A. 2019. Nuclear Genetic Regulation of the Human Mitochondrial Transcriptome. eLife 8: e41927.
Favé, M.-J. et al (including Hodgkinson, A.). 2018. Gene-by-environment interactions in urban populations modulate risk phenotypes. Nature Communications 9: 827.
Peischl, S. et al (including Hodgkinson, A.). 2018. Relaxed Selection During a Recent Human Expansion. Genetics 2018: 763-777.
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Leblond, C. et al (including Hodgkinson, A.). 2016. Replication study of MATR3 in familial and sporadic amyotrphic lateral sclerosis. Neurobiology of aging 37: 209.
The 1000 Genomes Project Consortium (including Hodgkinson, A.). 2015. A global reference for human genetic variation. Nature 526: 68-74.
Hussin, J.G., Hodgkinson, A. et al. 2015 Recombination affects accumulation of damaging and disease-associated mutations in human populations. Nature Genetics 47(4): 400-4
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Casals, F.*, Hodgkinson, A.*, et al. 2013. Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans. PLoS Genetics 9: e1003815.
Hodgkinson, A., Casals, F., Idaghdour, Y., Grenier, J.C., Hernandez, R. and Awadalla, P. 2013. Selective constraint, background selection, and mutation accumulation variability within and between human populations. BMC Genomics. 14:495-504.
Samuels, M.A. et al (including Hodgkinson, A.). 2013. Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia. J Med Genet. 50: 324-329.
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Hodgkinson, A., and A. Eyre-Walker. 2011. Variation in the Mutation Rate Across Mammalian Genomes. Nature Reviews Genetics 12:756-766.
Hodgkinson, A., and A. Eyre-Walker. 2011. The Large-Scale Distribution of Somatic Mutations in Cancer Genomes. Human Mutation 33: 136-143.
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