Catarina Campbell, Ph.D.

Genome Sciences University of Washington, Seattle, Seattle, WA 
"Catarina Campbell"
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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
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
Campbell CD, Sampas N, Tsalenko A, et al. (2011) Population-genetic properties of differentiated human copy-number polymorphisms. American Journal of Human Genetics. 88: 317-32
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