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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2015 | 1 |
2016 | 1 |
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2022 | 2 |
2024 | 0 |
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Page 1
Sex differences and sex bias in human circadian and sleep physiology research.
Elife. 2022 Feb 18;11:e65419. doi: 10.7554/eLife.65419.
Elife. 2022.
PMID: 35179486
Free PMC article.
Review.
A framework for sex, gender, and diversity analysis in research.
Hunt L, Nielsen MW, Schiebinger L.
Hunt L, et al.
Science. 2022 Sep 30;377(6614):1492-1495. doi: 10.1126/science.abp9775. Epub 2022 Sep 29.
Science. 2022.
PMID: 36173857
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Inherited duplications of PPP2R3B predispose to nevi and melanoma via a C21orf91-driven proliferative phenotype.
Polubothu S, Zecchin D, Al-Olabi L, Lionarons DA, Harland M, Horswell S, Thomas AC, Hunt L, Wlodarchak N, Aguilera P, Brand S, Bryant D, Carrera C, Chen H, Elgar G, Harwood CA, Howell M, Larue L, Loughlin S, MacDonald J, Malvehy J, Barberan SM, da Silva VM, Molina M, Morrogh D, Moulding D, Nsengimana J, Pittman A, Puig-Butillé JA, Parmar K, Sebire NJ, Scherer S, Stadnik P, Stanier P, Tell G, Waelchli R, Zarrei M, Puig S, Bataille V, Xing Y, Healy E, Moore GE, Di WL, Newton-Bishop J, Downward J, Kinsler VA.
Polubothu S, et al. Among authors: hunt l.
Genet Med. 2021 Sep;23(9):1636-1647. doi: 10.1038/s41436-021-01204-y. Epub 2021 Jun 18.
Genet Med. 2021.
PMID: 34145395
Free PMC article.
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MPV17 Loss Causes Deoxynucleotide Insufficiency and Slow DNA Replication in Mitochondria.
Dalla Rosa I, Cámara Y, Durigon R, Moss CF, Vidoni S, Akman G, Hunt L, Johnson MA, Grocott S, Wang L, Thorburn DR, Hirano M, Poulton J, Taylor RW, Elgar G, Martí R, Voshol P, Holt IJ, Spinazzola A.
Dalla Rosa I, et al. Among authors: hunt l.
PLoS Genet. 2016 Jan 13;12(1):e1005779. doi: 10.1371/journal.pgen.1005779. eCollection 2016 Jan.
PLoS Genet. 2016.
PMID: 26760297
Free PMC article.
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Aberrant ribonucleotide incorporation and multiple deletions in mitochondrial DNA of the murine MPV17 disease model.
Moss CF, Dalla Rosa I, Hunt LE, Yasukawa T, Young R, Jones AWE, Reddy K, Desai R, Virtue S, Elgar G, Voshol P, Taylor MS, Holt IJ, Reijns MAM, Spinazzola A.
Moss CF, et al. Among authors: hunt le.
Nucleic Acids Res. 2017 Dec 15;45(22):12808-12815. doi: 10.1093/nar/gkx1009.
Nucleic Acids Res. 2017.
PMID: 29106596
Free PMC article.
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Low plasma haptoglobin is a risk factor for life-threatening childhood severe malarial anemia and not an exclusive consequence of hemolysis.
Abah SE, Burté F, Marquet S, Brown BJ, Akinkunmi F, Oyinloye G, Afolabi NK, Omokhodion S, Lagunju I, Shokunbi WA, Wahlgren M, Dessein H, Argiro L, Dessein AJ, Noyvert B, Hunt L, Elgar G, Sodeinde O, Holder AA, Fernandez-Reyes D.
Abah SE, et al. Among authors: hunt l.
Sci Rep. 2018 Dec 3;8(1):17527. doi: 10.1038/s41598-018-35944-w.
Sci Rep. 2018.
PMID: 30510258
Free PMC article.
Clinical Trial.
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Complete re-sequencing of a 2Mb topological domain encompassing the FTO/IRXB genes identifies a novel obesity-associated region upstream of IRX5.
Hunt LE, Noyvert B, Bhaw-Rosun L, Sesay AK, Paternoster L, Nohr EA, Davey Smith G, Tommerup N, Sørensen TI, Elgar G.
Hunt LE, et al.
Genome Med. 2015 Dec 7;7:126. doi: 10.1186/s13073-015-0250-3.
Genome Med. 2015.
PMID: 26642925
Free PMC article.
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