Emma Whitelaw
Affiliations: | University of Sydney, Camperdown, New South Wales, Australia |
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"Emma Whitelaw"
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| Daxinger L, Oey H, Isbel L, et al. (2016) Hypomethylation of ERVs in the sperm of mice haploinsufficient for the histone methyltransferase Setdb1 correlates with a paternal effect on phenotype. Scientific Reports. 6: 25004 |
| Oey H, Isbel L, Hickey P, et al. (2015) Genetic and epigenetic variation among inbred mouse littermates: identification of inter-individual differentially methylated regions. Epigenetics & Chromatin. 8: 54 |
| Harten SK, Oey H, Bourke LM, et al. (2015) The recently identified modifier of murine metastable epialleles, Rearranged L-Myc Fusion, is involved in maintaining epigenetic marks at CpG island shores and enhancers. Bmc Biology. 13: 21 |
| Harten SK, Bruxner TJ, Bharti V, et al. (2014) The first mouse mutants of D14Abb1e (Fam208a) show that it is critical for early development. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 25: 293-303 |
| Blewitt M, Whitelaw E. (2013) The use of mouse models to study epigenetics. Cold Spring Harbor Perspectives in Biology. 5: a017939 |
| Daxinger L, Harten SK, Oey H, et al. (2013) An ENU mutagenesis screen identifies novel and known genes involved in epigenetic processes in the mouse. Genome Biology. 14: R96 |
| Youngson NA, Epp T, Roberts AR, et al. (2013) No evidence for cumulative effects in a Dnmt3b hypomorph across multiple generations. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 24: 206-17 |
| Brown FC, Scott N, Rank G, et al. (2013) ENU mutagenesis identifies the first mouse mutants reproducing human β-thalassemia at the genomic level. Blood Cells, Molecules & Diseases. 50: 86-92 |
| Daxinger L, Whitelaw E. (2012) Understanding transgenerational epigenetic inheritance via the gametes in mammals. Nature Reviews. Genetics. 13: 153-62 |
| Ashe A, Butterfield NC, Town L, et al. (2012) Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies. Human Molecular Genetics. 21: 1808-23 |