| A ChIP-seq defined genome-wide map of vitamin D receptor binding: associations with disease and evolution SV Ramagopalan, A Heger, AJ Berlanga, NJ Maugeri, MR Lincoln, ... Genome research 20 (10), 1352-1360, 2010 | 914 | 2010 |
| Complete haplotype sequence of the human immunoglobulin heavy-chain variable, diversity, and joining genes and characterization of allelic and copy-number variation CT Watson, KM Steinberg, J Huddleston, RL Warren, M Malig, J Schein, ... The American Journal of Human Genetics 92 (4), 530-546, 2013 | 171 | 2013 |
| The immunoglobulin heavy chain locus: genetic variation, missing data, and implications for human disease CT Watson, F Breden Genes and immunity 13 (5), 363-373, 2012 | 130 | 2012 |
| Genetics of Microdeletion and Duplication Syndromes: An Update CT Watson, T Marques-Bonet, AJ Sharp, HC Mefford Annual Review of Genomics and Human Genetics 15 (1), 2014 | 121 | 2014 |
| Genome-wide DNA methylation profiling in the superior temporal gyrus reveals epigenetic signatures associated with Alzheimer’s disease CT Watson, P Roussos, P Garg, DJ Ho, N Azam, PL Katsel, ... Genome Medicine 8 (1), 1-14, 2016 | 105 | 2016 |
| Slow delivery immunization enhances HIV neutralizing antibody and germinal center responses via modulation of immunodominance KM Cirelli, DG Carnathan, B Nogal, JT Martin, OL Rodriguez, ... Cell, 2019 | 87 | 2019 |
| Genome-Wide DNA Methylation Profiling Reveals Epigenetic Changes in the Rat Nucleus Accumbens Associated with Cross-Generational Effects of Adolescent THC Exposure. HYL Watson CT, Szutorisz H, Garg P, Martin Q, Landry JA, Sharp AJ Neuropsychopharmacology, 2015 | 86 | 2015 |
| IGHV1-69 polymorphism modulates anti-influenza antibody repertoires, correlates with IGHV utilization shifts and varies by ethnicity Y Avnir, CT Watson, J Glanville, EC Peterson, AS Tallarico, AS Bennett, ... Scientific Reports, 20842, 2016 | 82 | 2016 |
| Adaptive Immune Receptor Repertoire Community recommendations for sharing immune-repertoire sequencing data F Rubelt, CE Busse, SAC Bukhari, JP Bürckert, E Mariotti-Ferrandiz, ... Nature immunology 18 (12), 1274, 2017 | 80 | 2017 |
| The Individual and Population Genetics of Antibody Immunity CT Watson, J Glanville, WA Marasco Trends in Immunology, 2017 | 60 | 2017 |
| Perspective: Reproducibility and Reuse of Adaptive Immune Receptor Repertoire Data F Breden, ET Luning Prak, B Peters, F Rubelt, CA Schramm, C Busse, ... Frontiers in Immunology 8, 1418, 2017 | 55 | 2017 |
| Mechanisms underlying metabolic and neural defects in zebrafish and human multiple acyl-CoA dehydrogenase deficiency (MADD) Y Song, MA Selak, CT Watson, C Coutts, PC Scherer, JA Panzer, S Gibbs, ... PloS one 4 (12), e8329, 2009 | 53 | 2009 |
| A Potently Neutralizing Antibody Protects Mice against SARS-CoV-2 Infection WB Alsoussi, JS Turner, JB Case, H Zhao, AJ Schmitz, JQ Zhou, RE Chen, ... The Journal of Immunology, 2020 | 51 | 2020 |
| Vitamin D receptor binding, chromatin states and association with multiple sclerosis G Disanto, GK Sandve, AJ Berlanga-Taylor, G Ragnedda, JM Morahan, ... Human molecular genetics 21 (16), 3575-3586, 2012 | 49 | 2012 |
| DNA methylation profiling in X; autosome translocations supports a role for L1 repeats in the spread of X chromosome inactivation N Bala Tannan, M Brahmachary, P Garg, C Borel, R Alnefaie, CT Watson, ... Human molecular genetics 23 (5), 1224-1236, 2013 | 48 | 2013 |
| Gene duplication and divergence of long wavelength-sensitive opsin genes in the guppy, Poecilia reticulata CT Watson, SM Gray, M Hoffmann, KP Lubieniecki, JB Joy, BA Sandkam, ... Journal of molecular evolution 72 (2), 240-252, 2011 | 44 | 2011 |
| The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression AE Handel, L Handunnetthi, AJ Berlanga, CT Watson, JM Morahan, ... PloS one 5 (4), e10142, 2010 | 40 | 2010 |
| Genomic organization of duplicated short wave-sensitive and long wave-sensitive opsin genes in the green swordtail, Xiphophorus helleri CT Watson, KP Lubieniecki, E Loew, WS Davidson, F Breden BMC evolutionary biology 10 (1), 87, 2010 | 38 | 2010 |
| Identification of rare de novo epigenetic variations in congenital disorders M Barbosa, RS Joshi, P Garg, A Martin-Trujillo, N Patel, B Jadhav, ... Nature communications 9 (1), 2064, 2018 | 37 | 2018 |
| DNA methylation profiling of uniparental disomy subjects provides a map of parental epigenetic bias in the human genome RS Joshi, P Garg, N Zaitlen, T Lappalainen, CT Watson, N Azam, D Ho, ... The American Journal of Human Genetics 99 (3), 555-566, 2016 | 37 | 2016 |
Felix BredenProfessor of Biological Sciences, Simon Fraser UniversityVerified email at sfu.ca
