Year |
Citation |
Score |
2024 |
Aguilar C, Williams D, Kurapati R, Bains RS, Mburu P, Parker A, Williams J, Concas D, Tateossian H, Haynes AR, Banks G, Vikhe P, Heise I, Hutchison M, Atkins G, et al. Pleiotropic brain function of whirlin identified by a novel mutation. Iscience. 27: 110170. PMID 38974964 DOI: 10.1016/j.isci.2024.110170 |
0.489 |
|
2020 |
Banks GT, Guillaumin MCC, Heise I, Lau P, Yin M, Bourbia N, Aguilar C, Bowl MR, Esapa C, Brown LA, Hasan S, Tagliatti E, Nicholson E, Bains RS, Wells S, et al. Forward genetics identifies a novel sleep mutant with sleep state inertia and REM sleep deficits. Science Advances. 6: eabb3567. PMID 32851175 DOI: 10.1126/Sciadv.Abb3567 |
0.567 |
|
2016 |
Potter PK, Bowl MR, Jeyarajan P, Wisby L, Blease A, Goldsworthy ME, Simon MM, Greenaway S, Michel V, Barnard A, Aguilar C, Agnew T, Banks G, Blake A, Chessum L, ... ... Heise I, et al. Novel gene function revealed by mouse mutagenesis screens for models of age-related disease. Nature Communications. 7: 12444. PMID 27534441 DOI: 10.1038/Ncomms12444 |
0.644 |
|
2015 |
Heise I, Fisher SP, Banks GT, Wells S, Peirson SN, Foster RG, Nolan PM. Sleep-like behavior and 24-h rhythm disruption in the Tc1 mouse model of Down syndrome. Genes, Brain, and Behavior. 14: 209-16. PMID 25558895 DOI: 10.1111/Gbb.12198 |
0.59 |
|
2015 |
Joyce PI, Mcgoldrick P, Saccon RA, Weber W, Fratta P, West SJ, Zhu N, Carter S, Phatak V, Stewart M, Simon M, Kumar S, Heise I, Bros-Facer V, Dick J, et al. A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity. Human Molecular Genetics. 24: 1883-97. PMID 25468678 DOI: 10.1093/Hmg/Ddu605 |
0.678 |
|
2015 |
Banks G, Heise I, Starbuck B, Osborne T, Wisby L, Potter P, Jackson IJ, Foster RG, Peirson SN, Nolan PM. Genetic background influences age-related decline in visual and nonvisual retinal responses, circadian rhythms, and sleep. Neurobiology of Aging. 36: 380-93. PMID 25179226 DOI: 10.1016/J.Neurobiolaging.2014.07.040 |
0.565 |
|
2015 |
Potter PK, Laura W, Blease A, Simon MM, Aguilar C, Agnew T, Banks G, Blake A, Chessum L, Dorning J, Falcone S, Goosey L, Greenaway S, Harris S, Haynes A, ... Heise I, et al. Discovering gene function from development to ageing Reproductive Toxicology. 56: 10. DOI: 10.1016/J.Reprotox.2015.07.024 |
0.549 |
|
2014 |
Tucci V, Kleefstra T, Hardy A, Heise I, Maggi S, Willemsen MH, Hilton H, Esapa C, Simon M, Buenavista MT, McGuffin LJ, Vizor L, Dodero L, Tsaftaris S, Romero R, et al. Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features. The Journal of Clinical Investigation. 124: 1468-82. PMID 24614104 DOI: 10.1172/Jci70372 |
0.331 |
|
2014 |
Mandillo S, Heise I, Garbugino L, Tocchini-Valentini GP, Giuliani A, Wells S, Nolan PM. Early motor deficits in mouse disease models are reliably uncovered using an automated home-cage wheel-running system: a cross-laboratory validation. Disease Models & Mechanisms. 7: 397-407. PMID 24423792 DOI: 10.1242/Dmm.013946 |
0.578 |
|
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