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Items: 5

1.

Genotyping-by-sequencing and SNP-arrays are complementary for detecting quantitative trait loci by tagging different haplotypes in association studies.

Negro SS, Millet EJ, Madur D, Bauland C, Combes V, Welcker C, Tardieu F, Charcosset A, Nicolas SD.

BMC Plant Biol. 2019 Jul 16;19(1):318. doi: 10.1186/s12870-019-1926-4.

2.

Genetic Evidence of a Population Bottleneck and Inbreeding in the Endangered New Zealand Sea Lion, Phocarctos hookeri.

Osborne AJ, Negro SS, Chilvers BL, Robertson BC, Kennedy MA, Gemmell NJ.

J Hered. 2016 Sep;107(5):392-402. doi: 10.1093/jhered/esw015. Epub 2016 Mar 19.

PMID:
26995741
3.

Heterozygote advantage at MHC DRB may influence response to infectious disease epizootics.

Osborne AJ, Pearson J, Negro SS, Chilvers BL, Kennedy MA, Gemmell NJ.

Mol Ecol. 2015 Apr;24(7):1419-32. doi: 10.1111/mec.13128. Epub 2015 Mar 19.

PMID:
25728376
4.

Extensive variation at MHC DRB in the New Zealand sea lion (Phocarctos hookeri) provides evidence for balancing selection.

Osborne AJ, Zavodna M, Chilvers BL, Robertson BC, Negro SS, Kennedy MA, Gemmell NJ.

Heredity (Edinb). 2013 Jul;111(1):44-56. doi: 10.1038/hdy.2013.18. Epub 2013 Apr 10.

5.

Correlation between male social status, testosterone levels, and parasitism in a dimorphic polygynous mammal.

Negro SS, Caudron AK, Dubois M, Delahaut P, Gemmell NJ.

PLoS One. 2010 Sep 13;5(9):e12507. doi: 10.1371/journal.pone.0012507.

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