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 |
0.739 |
|
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 |
0.36 |
|
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 |
0.717 |
|
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 |
0.764 |
|
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 |
0.73 |
|
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 |
0.741 |
|
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 |
0.732 |
|
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 |
0.429 |
|
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 |
0.682 |
|
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 |
0.799 |
|
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 |
0.772 |
|
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 |
0.783 |
|
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 |
0.716 |
|
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 |
0.745 |
|
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 |
0.787 |
|
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 |
0.771 |
|
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 |
0.612 |
|
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 |
0.711 |
|
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 |
0.641 |
|
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 |
0.67 |
|
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 |
0.358 |
|
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