Jon Keebler - Publications

Affiliations: 
University of Montreal (Canada) 

11 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, 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
2015 Cirulli ET, Lasseigne BN, Petrovski S, Sapp PC, Dion PA, Leblond CS, Couthouis J, Lu YF, Wang Q, Krueger BJ, Ren Z, Keebler J, Han Y, Levy SE, Boone BE, et al. Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways. Science (New York, N.Y.). 347: 1436-41. PMID 25700176 DOI: 10.1126/science.aaa3650  0.48
2013 Zhang J, Franks RG, Liu X, Kang M, Keebler JE, Schaff JE, Huang HW, Xiang QY. De novo sequencing, characterization, and comparison of inflorescence transcriptomes of Cornus canadensis and C. florida (Cornaceae). Plos One. 8: e82674. PMID 24386108 DOI: 10.1371/journal.pone.0082674  0.48
2013 Goldstein DB, Allen A, Keebler J, Margulies EH, Petrou S, Petrovski S, Sunyaev S. Sequencing studies in human genetics: design and interpretation. Nature Reviews. Genetics. 14: 460-70. PMID 23752795 DOI: 10.1038/nrg3455  0.48
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  0.48
2011 Conrad DF, Keebler JE, DePristo MA, Lindsay SJ, Zhang Y, Casals F, Idaghdour Y, Hartl CL, Torroja C, Garimella KV, Zilversmit M, Cartwright R, Rouleau GA, Daly M, Stone EA, et al. Variation in genome-wide mutation rates within and between human families. Nature Genetics. 43: 712-4. PMID 21666693 DOI: 10.1038/ng.862  0.48
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  0.48
2010 Awadalla P, Gauthier J, Myers RA, Casals F, Hamdan FF, Griffing AR, Côté M, Henrion E, Spiegelman D, Tarabeux J, Piton A, Yang Y, Boyko A, Bustamante C, Xiong L, ... ... Keebler J, et al. Direct measure of the de novo mutation rate in autism and schizophrenia cohorts. American Journal of Human Genetics. 87: 316-24. PMID 20797689 DOI: 10.1016/j.ajhg.2010.07.019  0.48
2008 Prugnolle F, McGee K, Keebler J, Awadalla P. Selection shapes malaria genomes and drives divergence between pathogens infecting hominids versus rodents. Bmc Evolutionary Biology. 8: 223. PMID 18667061 DOI: 10.1186/1471-2148-8-223  0.48
2007 Bockhorst J, Lu F, Janes JH, Keebler J, Gamain B, Awadalla P, Su Xz, Samudrala R, Jojic N, Smith JD. Structural polymorphism and diversifying selection on the pregnancy malaria vaccine candidate VAR2CSA Molecular and Biochemical Parasitology. 155: 103-112. PMID 17669514 DOI: 10.1016/j.molbiopara.2007.06.007  0.48
2007 Mu J, Awadalla P, Duan J, McGee KM, Keebler J, Seydel K, McVean GA, Su XZ. Genome-wide variation and identification of vaccine targets in the Plasmodium falciparum genome. Nature Genetics. 39: 126-30. PMID 17159981 DOI: 10.1038/ng1924  0.48
2006 Jackson M, Watt AJ, Gautier P, Gilchrist D, Driehaus J, Graham GJ, Keebler J, Prugnolle F, Awadalla P, Forrester LM. A murine specific expansion of the Rhox cluster involved in embryonic stem cell biology is under natural selection. Bmc Genomics. 7: 212. PMID 16916441 DOI: 10.1186/1471-2164-7-212  0.48
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