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David Keays
David Keays
Professor of Neurobiology, LMU, Munich. Principal Research Associate, PDN, University of Cambridge.
Verified email at bio.lmu.de - Homepage
Title
Cited by
Cited by
Year
Mutations in α-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans
DA Keays, G Tian, K Poirier, GJ Huang, C Siebold, J Cleak, PL Oliver, ...
Cell 128 (1), 45-57, 2007
4682007
Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria
XH Jaglin, K Poirier, Y Saillour, E Buhler, G Tian, N Bahi-Buisson, ...
Nature genetics 41 (6), 746-752, 2009
3692009
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits
M Groszer, DA Keays, RMJ Deacon, JP De Bono, S Prasad-Mulcare, ...
Current Biology 18 (5), 354-362, 2008
3672008
Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A)
K Poirier, DA Keays, F Francis, Y Saillour, N Bahi, S Manouvrier, ...
Human mutation 28 (11), 1055-1064, 2007
2662007
A novel α-conotoxin identified by gene sequencing is active in suppressing the vascular response to selective stimulation of sensory nerves in vivo
DW Sandall, N Satkunanathan, DA Keays, MA Polidano, X Liping, ...
Biochemistry 42 (22), 6904-6911, 2003
2232003
Clusters of iron-rich cells in the upper beak of pigeons are macrophages not magnetosensitive neurons
CD Treiber, MC Salzer, J Riegler, N Edelman, C Sugar, M Breuss, ...
Nature 484 (7394), 367-370, 2012
2142012
Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities
M Breuss, JIT Heng, K Poirier, G Tian, XH Jaglin, Z Qu, A Braun, T Gstrein, ...
Cell reports 2 (6), 1554-1562, 2012
1912012
A gene-driven ENU-based approach to generating an allelic series in any gene
MM Quwailid, A Hugill, N Dear, L Vizor, S Wells, E Horner, S Fuller, ...
Mammalian Genome 15, 585-591, 2004
1812004
Therapeutic applications of conotoxins that target the neuronal nicotinic acetylcholine receptor
BG Livett, DW Sandall, D Keays, J Down, KR Gayler, N Satkunanathan, ...
Toxicon 48 (7), 810-829, 2006
1682006
Unexpected complexity in the haplotypes of commonly used inbred strains of laboratory mice
B Yalcin, J Fullerton, S Miller, DA Keays, S Brady, A Bhomra, A Jefferson, ...
Proceedings of the National Academy of Sciences 101 (26), 9734-9739, 2004
1332004
Magnetoreception—a sense without a receptor
GC Nordmann, T Hochstoeger, DA Keays
PLoS biology 15 (10), e2003234, 2017
1302017
Mutations in the HECT domain of NEDD4L lead to AKT–mTOR pathway deregulation and cause periventricular nodular heterotopia
L Broix, H Jagline, E L Ivanova, S Schmucker, N Drouot, J Clayton-Smith, ...
Nature genetics 48 (11), 1349-1358, 2016
1112016
Mutations in PGAP3 impair GPI-anchor maturation, causing a subtype of hyperphosphatasia with mental retardation
MF Howard, Y Murakami, AT Pagnamenta, C Daumer-Haas, B Fischer, ...
The American Journal of Human Genetics 94 (2), 278-287, 2014
1052014
Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene
V Conti, A Carabalona, E Pallesi-Pocachard, E Parrini, RJ Leventer, ...
Brain 136 (11), 3378-3394, 2013
992013
No evidence for intracellular magnetite in putative vertebrate magnetoreceptors identified by magnetic screening
NB Edelman, T Fritz, S Nimpf, P Pichler, M Lauwers, RW Hickman, ...
Proceedings of the National Academy of Sciences 112 (1), 262-267, 2015
852015
Genetic discrimination in Australia.
D Keays, K BARLOW-STEWART
Journal of Law and Medicine 8 (3), 250-262, 2001
852001
Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies
AT Pagnamenta, S Lise, V Harrison, H Stewart, S Jayawant, ...
Journal of human genetics 57 (1), 70-72, 2012
842012
Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome
A Hempel, AT Pagnamenta, M Blyth, S Mansour, V McConnell, I Kou, ...
Journal of medical genetics 53 (3), 152-162, 2016
832016
Tubulins and brain development–The origins of functional specification
MW Breuss, I Leca, T Gstrein, AH Hansen, DA Keays
Molecular and Cellular Neuroscience 84, 58-67, 2017
822017
Estimating the number of coding mutations in genotypic- and phenotypic-driven N-ethyl-N-nitrosourea (ENU) screens
DA Keays, TG Clark, J Flint
Mammalian genome 17, 230-238, 2006
802006
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