Lilian Elizabeth Hunt
Affiliations: | The Francis Crick Institute, London, England, United Kingdom |
Area:
conserved noncoding elements, genomics, genetics, polymorphisms, SNPs, human variation, developmental biology, genomic regulation, evolutionary biology, systems biologyGoogle:
"Lilian Hunt"
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Publications
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| Polubothu S, Zecchin D, Al-Olabi L, et al. (2021) Inherited duplications of PPP2R3B predispose to nevi and melanoma via a C21orf91-driven proliferative phenotype. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Abah SE, Burté F, Marquet S, et al. (2018) Low plasma haptoglobin is a risk factor for life-threatening childhood severe malarial anemia and not an exclusive consequence of hemolysis. Scientific Reports. 8: 17527 |
| Moss CF, Dalla Rosa I, Hunt LE, et al. (2017) Aberrant ribonucleotide incorporation and multiple deletions in mitochondrial DNA of the murine MPV17 disease model. Nucleic Acids Research |
| Dalla Rosa I, Cámara Y, Durigon R, et al. (2016) MPV17 Loss Causes Deoxynucleotide Insufficiency and Slow DNA Replication in Mitochondria. Plos Genetics. 12: e1005779 |
| Hunt LE, Noyvert B, Bhaw-Rosun L, et al. (2015) Complete re-sequencing of a 2Mb topological domain encompassing the FTO/IRXB genes identifies a novel obesity-associated region upstream of IRX5. Genome Medicine. 7: 126 |