Julie Hussin
Julie Hussin
Montreal Heart Institute, University of Montreal
Adresse e-mail validée de umontreal.ca - Page d'accueil
TitreCitée parAnnée
Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4
DL Guernsey, H Jiang, J Hussin, M Arnold, K Bouyakdan, S Perry, ...
The American Journal of Human Genetics 87 (1), 40-51, 2010
Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in mice
B Davies, E Hatton, N Altemose, JG Hussin, F Pratto, G Zhang, AG Hinch, ...
Nature 530 (7589), 171, 2016
A population genetic approach to mapping neurological disorder genes using deep resequencing
RA Myers, F Casals, J Gauthier, FF Hamdan, J Keebler, AR Boyko, ...
PLoS genetics 7 (2), e1001318, 2011
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
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, 2015
Plasmodium falciparum Genetic Diversity Maintained and Amplified Over 5 Years of a Low Transmission Endemic in the Peruvian Amazon
OLH Branch, PL Sutton, C Barnes, JC Castro, J Hussin, P Awadalla, ...
Molecular Biology and Evolution 28 (7), 1973-1986, 2010
Rare allelic forms of PRDM9 associated with childhood leukemogenesis
J Hussin, D Sinnett, F Casals, Y Idaghdour, V Bruat, V Saillour, J Healy, ...
Genome research 23 (3), 419-430, 2013
Age-dependent recombination rates in human pedigrees
J Hussin, MH Roy-Gagnon, R Gendron, G Andelfinger, P Awadalla
PLoS genetics 7 (9), e1002251, 2011
Next-generation sequencing approaches for genetic mapping of complex diseases
F Casals, Y Idaghdour, J Hussin, P Awadalla
Journal of neuroimmunology 248 (1-2), 10-22, 2012
A family-based probabilistic method for capturing de novo mutations from high-throughput short-read sequencing data
RA Cartwright, J Hussin, JEM Keebler, EA Stone, P Awadalla
Statistical applications in genetics and molecular biology 11 (2), 2012
Haplotype allelic classes for detecting ongoing positive selection
J Hussin, P Nadeau, JF Lefebvre, D Labuda
BMC bioinformatics 11 (1), 65, 2010
Diet networks: Thin parameters for fat genomics
A Romero, PL Carrier, A Erraqabi, T Sylvain, A Auvolat, E Dejoie, ...
arXiv preprint arXiv:1611.09340, 2016
Multicohort analysis of the maternal age effect on recombination
HC Martin, R Christ, JG Hussin, J O’Connell, S Gordon, H Mbarek, ...
Nature communications 6, 7846, 2015
Insights into platypus population structure and history from whole-genome sequencing
HC Martin, EM Batty, J Hussin, P Westall, T Daish, S Kolomyjec, P Piazza, ...
Molecular biology and evolution 35 (5), 1238-1252, 2018
The impact of recombination on human mutation load and disease
I Alves, AA Houle, JG Hussin, P Awadalla
Philosophical Transactions of the Royal Society B: Biological Sciences 372 …, 2017
Reprogramming meiotic recombination in the mouse
B Davies, E Hatton, J Hussin, N Altemose, F Pratto, D Moralli, A Gupta, ...
Recombination impacts damaging and disease mutations accumulation in human populations
JG Hussin, A Hodgkinson, Y Idaghdour, JC Grenier, JP Goulet, E Gbeha, ...
bioRxiv, 006064, 2014
Genomic variation in recombination patterns: implications for disease and cancer
J Hussin
Correction: Rare Copy Number Variants Contribute to Congenital Left-Sided Heart Disease
MP Hitz, LP Lemieux-Perreault, C Marshall, Y Feroz-Zada, R Davies, ...
PLoS genetics 9 (3), 2013
Classes Alléliques d’Haplotypes et Sélection Positive dans le Génome Humain
J Hussin
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