Corey T. Watson, Ph.D. - Publications

2012 Simon Fraser University, Burnaby, British Columbia, Canada 
Evolution, Ecology, Genetics

31 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
2019 Ohlin M, Scheepers C, Corcoran M, Lees WD, Busse CE, Bagnara D, Thörnqvist L, Bürckert JP, Jackson KJL, Ralph D, Schramm CA, Marthandan N, Breden F, Scott J, Matsen Iv FA, ... ... Watson CT, et al. Inferred Allelic Variants of Immunoglobulin Receptor Genes: A System for Their Evaluation, Documentation, and Naming. Frontiers in Immunology. 10: 435. PMID 30936866 DOI: 10.3389/fimmu.2019.00435  1
2017 Breden F, Watson CT. Using High-Throughput Sequencing to Characterize the Development of the Antibody Repertoire During Infections: A Case Study of HIV-1. Advances in Experimental Medicine and Biology. 1053: 245-263. PMID 29549643 DOI: 10.1007/978-3-319-72077-7_12  1
2017 Breden F, Luning Prak ET, Peters B, Rubelt F, Schramm CA, Busse CE, Vander Heiden JA, Christley S, Bukhari SAC, Thorogood A, Matsen Iv FA, Wine Y, Laserson U, Klatzmann D, Douek DC, ... ... Watson CT, et al. Reproducibility and Reuse of Adaptive Immune Receptor Repertoire Data. Frontiers in Immunology. 8: 1418. PMID 29163494 DOI: 10.3389/fimmu.2017.01418  1
2017 Rubelt F, Busse CE, Bukhari SAC, Bürckert JP, Mariotti-Ferrandiz E, Cowell LG, Watson CT, Marthandan N, Faison WJ, Hershberg U, Laserson U, Corrie BD, Davis MM, Peters B, Lefranc MP, et al. Adaptive Immune Receptor Repertoire Community recommendations for sharing immune-repertoire sequencing data. Nature Immunology. 18: 1274-1278. PMID 29144493 DOI: 10.1038/ni.3873  1
2017 Sandkam BA, Joy JB, Watson CT, Breden F. Genomic environment impacts color vision evolution in a family with visually-based sexual selection. Genome Biology and Evolution. PMID 29121209 DOI: 10.1093/gbe/evx228  1
2017 Watson CT, Matsen FA, Jackson KJL, Bashir A, Smith ML, Glanville J, Breden F, Kleinstein SH, Collins AM, Busse CE. Comment on "A Database of Human Immune Receptor Alleles Recovered from Population Sequencing Data". Journal of Immunology (Baltimore, Md. : 1950). 198: 3371-3373. PMID 28416712 DOI: 10.4049/jimmunol.1700306  1
2016 Avnir Y, Watson CT, Glanville J, Peterson EC, Tallarico AS, Bennett AS, Qin K, Fu Y, Huang CY, Beigel JH, Breden F, Zhu Q, Marasco WA. Erratum: IGHV1-69 polymorphism modulates anti-influenza antibody repertoires, correlates with IGHV utilization shifts and varies by ethnicity. Scientific Reports. 6: 23876. PMID 27125899 DOI: 10.1038/srep23876  1
2016 Avnir Y, Watson CT, Glanville J, Peterson EC, Tallarico AS, Bennett AS, Qin K, Fu Y, Huang CY, Beigel JH, Breden F, Zhu Q, Marasco WA. IGHV1-69 polymorphism modulates anti-influenza antibody repertoires, correlates with IGHV utilization shifts and varies by ethnicity. Scientific Reports. 6: 20842. PMID 26880249 DOI: 10.1038/srep20842  1
2016 Watson CT, Roussos P, Garg P, Ho DJ, Azam N, Katsel PL, Haroutunian V, Sharp AJ. Genome-wide12 DNA methylation profiling in the superior temporal gyrus reveals epigenetic signatures associated with Alzheimer's disease. Genome Medicine. 8: 5. PMID 26787419 DOI: 10.1186/s13073-015-0258-8  1
2015 Watson CT, Szutorisz H, Garg P, Martin Q, Landry JA, Sharp AJ, Hurd YL. Genome-Wide DNA Methylation Profiling Reveals Epigenetic Changes in the Rat Nucleus Accumbens Associated with Cross-Generational Effects of Adolescent THC Exposure. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 26044905 DOI: 10.1038/npp.2015.155  1
2015 Watson CT, Steinberg KM, Graves TA, Warren RL, Malig M, Schein J, Wilson RK, Holt RA, Eichler EE, Breden F. Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversity. Genes and Immunity. 16: 24-34. PMID 25338678 DOI: 10.1038/gene.2014.56  1
2014 Watson CT, Marques-Bonet T, Sharp AJ, Mefford HC. The genetics of microdeletion and microduplication syndromes: an update. Annual Review of Genomics and Human Genetics. 15: 215-44. PMID 24773319 DOI: 10.1146/annurev-genom-091212-153408  1
2014 Bala Tannan N, Brahmachary M, Garg P, Borel C, Alnefaie R, Watson CT, Thomas NS, Sharp AJ. DNA methylation profiling in X;autosome translocations supports a role for L1 repeats in the spread of X chromosome inactivation. Human Molecular Genetics. 23: 1224-36. PMID 24186870 DOI: 10.1093/hmg/ddt553  1
2014 Disanto G, Kjetil Sandve G, Ricigliano VA, Pakpoor J, Berlanga-Taylor AJ, Handel AE, Kuhle J, Holden L, Watson CT, Giovannoni G, Handunnetthi L, Ramagopalan SV. DNase hypersensitive sites and association with multiple sclerosis. Human Molecular Genetics. 23: 942-8. PMID 24092328 DOI: 10.1093/hmg/ddt489  1
2013 Disanto G, Watson CT, Meier UC, Ebers GC, Giovannoni G, Ramagopalan SV. Month of birth and thymic output. Jama Neurology. 70: 527-8. PMID 23568650 DOI: 10.1001/jamaneurol.2013.2116  1
2013 Watson CT, Steinberg KM, Huddleston J, Warren RL, Malig M, Schein J, Willsey AJ, Joy JB, Scott JK, Graves TA, Wilson RK, Holt RA, Eichler EE, Breden F. Complete haplotype sequence of the human immunoglobulin heavy-chain variable, diversity, and joining genes and characterization of allelic and copy-number variation. American Journal of Human Genetics. 92: 530-46. PMID 23541343 DOI: 10.1016/j.ajhg.2013.03.004  1
2013 Watson CT, Garg P, Sharp AJ. Comment on "genomic hypomethylation in the human germline associates with selective structural mutability in the human genome". Plos Genetics. 9: e1003332. PMID 23468658 DOI: 10.1371/journal.pgen.1003332  1
2013 Sandkam BA, Joy JB, Watson CT, Gonzalez-Bendiksen P, Gabor CR, Breden F. Hybridization leads to sensory repertoire expansion in a gynogenetic fish, the Amazon molly (poecilia formosa): a test of the hybrid-sensory expansion hypothesis. Evolution; International Journal of Organic Evolution. 67: 120-30. PMID 23289566 DOI: 10.1111/j.1558-5646.2012.01779.x  1
2012 Watson CT, Disanto G, Breden F, Giovannoni G, Ramagopalan SV. Estimating the proportion of variation in susceptibility to multiple sclerosis captured by common SNPs. Scientific Reports. 2: 770. PMID 23105968 DOI: 10.1038/srep00770  1
2012 Watson CT, Disanto G, Sandve GK, Breden F, Giovannoni G, Ramagopalan SV. Age-associated hyper-methylated regions in the human brain overlap with bivalent chromatin domains. Plos One. 7: e43840. PMID 23028473 DOI: 10.1371/journal.pone.0043840  1
2012 Disanto G, Sandve GK, Berlanga-Taylor AJ, Ragnedda G, Morahan JM, Watson CT, Giovannoni G, Ebers GC, Ramagopalan SV. Vitamin D receptor binding, chromatin states and association with multiple sclerosis. Human Molecular Genetics. 21: 3575-86. PMID 22595971 DOI: 10.1093/hmg/dds189  1
2012 Watson CT, Breden F. The immunoglobulin heavy chain locus: genetic variation, missing data, and implications for human disease. Genes and Immunity. 13: 363-73. PMID 22551722 DOI: 10.1038/gene.2012.12  1
2011 Tam KJ, Watson CT, Massah S, Kolybaba AM, Breden F, Prefontaine GG, Beischlag TV. Regulatory function of conserved sequences upstream of the long-wave sensitive opsin genes in teleost fishes. Vision Research. 51: 2295-303. PMID 21971525 DOI: 10.1016/j.visres.2011.09.010  1
2011 Murphy TR, Vihtelic TS, Ile KE, Watson CT, Willer GB, Gregg RG, Bankaitis VA, Hyde DR. Phosphatidylinositol synthase is required for lens structural integrity and photoreceptor cell survival in the zebrafish eye. Experimental Eye Research. 93: 460-74. PMID 21722635 DOI: 10.1016/j.exer.2011.06.010  1
2011 Watson CT, Para AE, Lincoln MR, Ramagopalan SV, Orton SM, Morrison KM, Handunnetthi L, Handel AE, Chao MJ, Morahan J, Sadovnick AD, Breden F, Ebers GC. Revisiting the T-cell receptor alpha/delta locus and possible associations with multiple sclerosis. Genes and Immunity. 12: 59-66. PMID 21270827 DOI: 10.1038/gene.2010.65  1
2011 Watson CT, Gray SM, Hoffmann M, Lubieniecki KP, Joy JB, Sandkam BA, Weigel D, Loew E, Dreyer C, Davidson WS, Breden F. Gene duplication and divergence of long wavelength-sensitive opsin genes in the guppy, Poecilia reticulata. Journal of Molecular Evolution. 72: 240-52. PMID 21170644 DOI: 10.1007/s00239-010-9426-z  1
2010 Ramagopalan SV, Heger A, Berlanga AJ, Maugeri NJ, Lincoln MR, Burrell A, Handunnetthi L, Handel AE, Disanto G, Orton SM, Watson CT, Morahan JM, Giovannoni G, Ponting CP, Ebers GC, et al. A ChIP-seq defined genome-wide map of vitamin D receptor binding: associations with disease and evolution. Genome Research. 20: 1352-60. PMID 20736230 DOI: 10.1101/gr.107920.110  1
2010 Watson CT, Ramagopalan SV, Morrison KM, Ebers GC, Breden F. IGHV4-39 deletion polymorphism does not associate with risk or outcome of multiple sclerosis. Journal of Neuroimmunology. 225: 164-6. PMID 20471699 DOI: 10.1016/j.jneuroim.2010.04.012  1
2010 Handel AE, Handunnetthi L, Berlanga AJ, Watson CT, Morahan JM, Ramagopalan SV. The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression. Plos One. 5: e10142. PMID 20405052 DOI: 10.1371/journal.pone.0010142  1
2010 Watson CT, Lubieniecki KP, Loew E, Davidson WS, Breden F. Genomic organization of duplicated short wave-sensitive and long wave-sensitive opsin genes in the green swordtail, Xiphophorus helleri. Bmc Evolutionary Biology. 10: 87. PMID 20353595 DOI: 10.1186/1471-2148-10-87  1
2009 Song Y, Selak MA, Watson CT, Coutts C, Scherer PC, Panzer JA, Gibbs S, Scott MO, Willer G, Gregg RG, Ali DW, Bennett MJ, Balice-Gordon RJ. Mechanisms underlying metabolic and neural defects in zebrafish and human multiple acyl-CoA dehydrogenase deficiency (MADD). Plos One. 4: e8329. PMID 20020044 DOI: 10.1371/journal.pone.0008329  1
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