Catarina Campbell, Ph.D.
Affiliations: | Genome Sciences | University of Washington, Seattle, Seattle, WA |
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"Catarina Campbell"
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Publications
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| Mohajeri K, Cantsilieris S, Huddleston J, et al. (2016) Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region. Genome Research. 26: 1453-1467 |
| Baffour-Awuah NY, Fleet S, Montgomery RK, et al. (2015) Functional significance of single nucleotide polymorphisms in the lactase gene in diverse US patients and evidence for a novel lactase persistence allele at -13909 in those of European ancestry. Journal of Pediatric Gastroenterology and Nutrition. 60: 182-91 |
| Pino-Yanes M, Gignoux CR, Galanter JM, et al. (2015) Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos. The Journal of Allergy and Clinical Immunology. 135: 1502-10 |
| Seoane JA, Campbell C, Day IN, et al. (2014) Canonical correlation analysis for gene-based pleiotropy discovery. Plos Computational Biology. 10: e1003876 |
| Campbell CD, Mohajeri K, Malig M, et al. (2014) Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthma. Plos One. 9: e104396 |
| Campbell CD, Eichler EE. (2013) Properties and rates of germline mutations in humans. Trends in Genetics : Tig. 29: 575-84 |
| Girirajan S, Dennis MY, Baker C, et al. (2013) Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder. American Journal of Human Genetics. 92: 221-37 |
| Campbell CD, Chong JX, Malig M, et al. (2012) Estimating the human mutation rate using autozygosity in a founder population. Nature Genetics. 44: 1277-81 |
| Steinberg KM, Antonacci F, Sudmant PH, et al. (2012) Structural diversity and African origin of the 17q21.31 inversion polymorphism. Nature Genetics. 44: 872-80 |
| Girirajan S, Campbell CD, Eichler EE. (2011) Human copy number variation and complex genetic disease. Annual Review of Genetics. 45: 203-26 |