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Julie Hussin, Ph.D. - Publications

Affiliations: 
2013 Biochemistry Université de Montréal, Montréal, Canada 
Area:
Genetics, Bioinformatics Biology, Biochemistry
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26 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Legault MA, Barhdadi A, Gamache I, Lemaçon A, Lemieux Perreault LP, Grenier JC, Sylvestre MP, Hussin JG, Rhainds D, Tardif JC, Dubé MP. Study of effect modifiers of genetically predicted CETP reduction. Genetic Epidemiology. PMID 36701426 DOI: 10.1002/gepi.22514  0.738
2022 Besse S, Poujol R, Hussin JG. Comparative Study of Protein Aggregation Propensity and Mutation Tolerance Between Naked Mole-Rat and Mouse. Genome Biology and Evolution. 14. PMID 35482036 DOI: 10.1093/gbe/evac057  0.728
2022 Mostefai F, Gamache I, N'Guessan A, Pelletier J, Huang J, Murall CL, Pesaranghader A, Gaonac'h-Lovejoy V, Hamelin DJ, Poujol R, Grenier JC, Smith M, Caron E, Craig M, Wolf G, ... ... Hussin JG, et al. Population Genomics Approaches for Genetic Characterization of SARS-CoV-2 Lineages. Frontiers in Medicine. 9: 826746. PMID 35265640 DOI: 10.3389/fmed.2022.826746  0.336
2022 Levinsson A, de Denus S, Sandoval J, Lemieux Perreault LP, Rouleau J, Tardif JC, Hussin J, Dubé MP. Construction of a femininity score in the UK Biobank and its association with angina diagnosis prior to myocardial infarction. Scientific Reports. 12: 1780. PMID 35110607 DOI: 10.1038/s41598-022-05713-x  0.718
2021 Gamache I, Legault MA, Grenier JC, Sanchez R, Rhéaume E, Asgari S, Barhdadi A, Zada YF, Trochet H, Luo Y, Lecca L, Murray M, Raychaudhuri S, Tardif JC, Dubé MP, ... Hussin J, et al. A sex-specific evolutionary interaction between and . Elife. 10. PMID 34609279 DOI: 10.7554/eLife.69198  0.766
2021 Tremblay J, Haloui M, Attaoua R, Tahir R, Hishmih C, Harvey F, Marois-Blanchet FC, Long C, Simon P, Santucci L, Hizel C, Chalmers J, Marre M, Harrap S, Cífková R, ... ... Hussin JG, et al. Correction to: Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control. Diabetologia. PMID 34448881 DOI: 10.1007/s00125-021-05544-x  0.733
2021 Tremblay J, Haloui M, Attaoua R, Tahir R, Hishmih C, Harvey F, Marois-Blanchet FC, Long C, Simon P, Santucci L, Hizel C, Chalmers J, Marre M, Harrap S, Cífková R, ... ... Hussin JG, et al. Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control. Diabetologia. PMID 34226943 DOI: 10.1007/s00125-021-05491-7  0.743
2021 Dubé MP, Lemaçon A, Barhdadi A, Lemieux Perreault LP, Oussaïd E, Asselin G, Provost S, Sun M, Sandoval J, Legault MA, Mongrain I, Dubois A, Valois D, Dedelis E, Lousky J, ... ... Hussin J, et al. Genetics of symptom remission in outpatients with COVID-19. Scientific Reports. 11: 10847. PMID 34035401 DOI: 10.1038/s41598-021-90365-6  0.731
2018 Martin HC, Batty EM, Hussin J, Westall P, Daish T, Kolomyjec S, Piazza P, Bowden R, Hawkins M, Grant T, Moritz C, Grutzner F, Gongora J, Donnelly P. Insights into Platypus Population Structure and History from Whole-Genome Sequencing. Molecular Biology and Evolution. 35: 1238-1252. PMID 29688544 DOI: 10.1093/Molbev/Msy041  0.581
2017 Alves I, Houle AA, Hussin JG, Awadalla P. The impact of recombination on human mutation load and disease. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 372. PMID 29109227 DOI: 10.1098/Rstb.2016.0465  0.697
2016 Davies B, Hatton E, Altemose N, Hussin JG, Pratto F, Zhang G, Hinch AG, Moralli D, Biggs D, Diaz R, Preece C, Li R, Bitoun E, Brick K, Green CM, et al. Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in mice. Nature. PMID 26840484 DOI: 10.1038/Nature16931  0.452
2015 Martin HC, Christ R, Hussin JG, O'Connell J, Gordon S, Mbarek H, Hottenga JJ, McAloney K, Willemsen G, Gasparini P, Pirastu N, Montgomery GW, Navarro P, Soranzo N, Toniolo D, et al. Multicohort analysis of the maternal age effect on recombination. Nature Communications. 6: 7846. PMID 26242864 DOI: 10.1038/Ncomms8846  0.443
2015 Hussin JG, Hodgkinson A, Idaghdour Y, Grenier JC, Goulet JP, Gbeha E, Hip-Ki E, Awadalla P. Recombination affects accumulation of damaging and disease-associated mutations in human populations. Nature Genetics. 47: 400-4. PMID 25685891 DOI: 10.1038/Ng.3216  0.802
2015 Martin HC, Christ R, Hussin JG, O'Connell J, Gordon S, Mbarek H, Hottenga JJ, McAloney K, Willemsen G, Gasparini P, Pirastu N, Montgomery GW, Navarro P, Soranzo N, Toniolo D, et al. Multicohort analysis of the maternal age effect on recombination Nature Communications. 6. DOI: 10.1038/ncomms8846  0.399
2014 Davies B, Hatton E, Hussin J, Altemose N, Pratto F, Moralli D, Gupta A, Biggs D, Brick K, Green C, Camerini-Otero D, Myers S, Donnelly P. Reprogramming meiotic recombination in the mouse Transgenic Research. 23: 854-854. DOI: 10.1007/S11248-014-9820-1  0.491
2013 Casals F, Hodgkinson A, Hussin J, Idaghdour Y, Bruat V, de Maillard T, Grenier JC, Grenier JC, Gbeha E, Hamdan FF, Girard S, Spinella JF, Larivière M, Saillour V, Healy J, et al. Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans. Plos Genetics. 9: e1003815. PMID 24086152 DOI: 10.1371/Journal.Pgen.1003815  0.774
2013 Hussin J, Sinnett D, Casals F, Idaghdour Y, Bruat V, Saillour V, Healy J, Grenier JC, de Malliard T, Busche S, Spinella JF, Larivière M, Gibson G, Andersson A, Holmfeldt L, et al. Rare allelic forms of PRDM9 associated with childhood leukemogenesis. Genome Research. 23: 419-30. PMID 23222848 DOI: 10.1101/Gr.144188.112  0.784
2013 Hitz M, Lemieux-Perreault L, Marshall C, Feroz-Zada Y, Davies R, Yang SW, Lionel AC, D'Amours G, Lemyre E, Cullum R, Bigras J, Thibeault M, Chetaille P, Montpetit A, Khairy P, ... ... Hussin J, et al. Correction: Rare Copy Number Variants Contribute to Congenital Left-Sided Heart Disease Plos Genetics. 9. DOI: 10.1371/Annotation/8Bc63544-9Ed4-42Ca-A830-E8058Ab13Bab  0.715
2012 Hitz MP, Lemieux-Perreault LP, Marshall C, Feroz-Zada Y, Davies R, Yang SW, Lionel AC, D'Amours G, Lemyre E, Cullum R, Bigras JL, Thibeault M, Chetaille P, Montpetit A, Khairy P, ... ... Hussin J, et al. Rare copy number variants contribute to congenital left-sided heart disease. Plos Genetics. 8: e1002903. PMID 22969434 DOI: 10.1371/Journal.Pgen.1002903  0.74
2012 Cartwright RA, Hussin J, Keebler JE, Stone EA, Awadalla P. A family-based probabilistic method for capturing de novo mutations from high-throughput short-read sequencing data. Statistical Applications in Genetics and Molecular Biology. 11. PMID 22499693 DOI: 10.2202/1544-6115.1713  0.788
2012 Casals F, Idaghdour Y, Hussin J, Awadalla P. Next-generation sequencing approaches for genetic mapping of complex diseases. Journal of Neuroimmunology. 248: 10-22. PMID 22285396 DOI: 10.1016/J.Jneuroim.2011.12.017  0.772
2011 Hussin J, Roy-Gagnon MH, Gendron R, Andelfinger G, Awadalla P. Age-dependent recombination rates in human pedigrees. Plos Genetics. 7: e1002251. PMID 21912527 DOI: 10.1371/Journal.Pgen.1002251  0.619
2011 Myers RA, Casals F, Gauthier J, Hamdan FF, Keebler J, Boyko AR, Bustamante CD, Piton AM, Spiegelman D, Henrion E, Zilversmit M, Hussin J, Quinlan J, Yang Y, Lafrenière RG, et al. A population genetic approach to mapping neurological disorder genes using deep resequencing. Plos Genetics. 7: e1001318. PMID 21383861 DOI: 10.1371/Journal.Pgen.1001318  0.721
2011 Branch OH, Sutton PL, Barnes C, Castro JC, Hussin J, Awadalla P, Hijar G. Plasmodium falciparum genetic diversity maintained and amplified over 5 years of a low transmission endemic in the Peruvian Amazon. Molecular Biology and Evolution. 28: 1973-86. PMID 21109587 DOI: 10.1093/Molbev/Msq311  0.633
2010 Guernsey DL, Jiang H, Hussin J, Arnold M, Bouyakdan K, Perry S, Babineau-Sturk T, Beis J, Dumas N, Evans SC, Ferguson M, Matsuoka M, Macgillivray C, Nightingale M, Patry L, et al. Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4. American Journal of Human Genetics. 87: 40-51. PMID 20598275 DOI: 10.1016/J.Ajhg.2010.06.003  0.668
2010 Hussin J, Nadeau P, Lefebvre JF, Labuda D. Haplotype allelic classes for detecting ongoing positive selection. Bmc Bioinformatics. 11: 65. PMID 20109229 DOI: 10.1186/1471-2105-11-65  0.345
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