FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

David Keays

Research Profile

Physiology

Living Beings

Chemicals & Drugs

Disorders

Genes & Molecular Sequences

Alleles

Procedures

Phenomena

Dimerization

Co-author Network

Publications

TOP 3
Dawn E Watkins-Chow; Ruth M Arkell; Laura L Baxter; Laura Biondini; Thomas G Campbell; Jamel Chelly; Joanna Cooke; Andrew Edwards; Jonathan Flint; Gretchen Gibney; Karen E Leeds; Fabrizio Loreni; Mark F Lythgoe; H Douglas Morris; Raymond Mullen; William J Pavan; Françoise Phan Dinh Tuy; Ruth Pidsley; Johannes Riegler; Marion C Salzer; Rebecca Slotkin; David A Keays
Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes.
Martin Breuss; Jamel Chelly; Tim Clausen; Nicholas Justin Cowan; Pierre Gressens; Thomas Gstrein; Matilda Haas; Julian Ik-Tsen Heng; Xavier Hubert Jaglin; Marie-Laure Moutard; Linh Ngo; Sandrine Passemard; Karine Poirier; Zhengdong Qu; Deepa Selvi Rani; Kathryn J H Robson; Kumarasamy Thangaraj; Guoling Tian; Alain Verloes; Yunli Xie; Nadia Bahi-Buisson; Andreas Braun; David A Keays
Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.
Alistair T Pagnamenta; Elham Sadighi Akha; Helen Stewart; Jenny C Taylor; Grace Yoon; Kaseem Ajilogba; Louise S Bicknell; Victoria Harrison; Andrew P Jackson; David A Keays; Usha Kini; Jennie E Murray; Samantha J L Knight
A novel nonsense CDK5RAP2 mutation in a Somali child with primary microcephaly and sensorineural hearing loss.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of David Keays (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Dawn E Watkins-Chow; Ruth M Arkell; Laura L Baxter; Laura Biondini; Thomas G Campbell; Jamel Chelly; Joanna Cooke; Andrew Edwards; Jonathan Flint; Gretchen Gibney; Karen E Leeds; Fabrizio Loreni; Mark F Lythgoe; H Douglas Morris; Raymond Mullen; William J Pavan; Françoise Phan Dinh Tuy; Ruth Pidsley; Johannes Riegler; Marion C Salzer; Rebecca Slotkin; David A Keays
Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes.
PLoS genetics 2013;9(1):e1003094.
2012: Martin Breuss; Jamel Chelly; Tim Clausen; Nicholas Justin Cowan; Pierre Gressens; Thomas Gstrein; Matilda Haas; Julian Ik-Tsen Heng; Xavier Hubert Jaglin; Marie-Laure Moutard; Linh Ngo; Sandrine Passemard; Karine Poirier; Zhengdong Qu; Deepa Selvi Rani; Kathryn J H Robson; Kumarasamy Thangaraj; Guoling Tian; Alain Verloes; Yunli Xie; Nadia Bahi-Buisson; Andreas Braun; David A Keays
Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.
Cell reports 2012;2(6):1554-62.
2012: Alistair T Pagnamenta; Elham Sadighi Akha; Helen Stewart; Jenny C Taylor; Grace Yoon; Kaseem Ajilogba; Louise S Bicknell; Victoria Harrison; Andrew P Jackson; David A Keays; Usha Kini; Jennie E Murray; Samantha J L Knight
A novel nonsense CDK5RAP2 mutation in a Somali child with primary microcephaly and sensorineural hearing loss.
American journal of medical genetics. Part A 2012;158A(10):2577-82.
2012: Alistair T Pagnamenta; Gerardine Quaghebeur; Andy Rimmer; Helen Stewart; Jenny C Taylor; Elham Sadighi Akha; Alexander T Deng; Victoria Harrison; Sandeep Jayawant; Usha Kini; Samantha J L Knight; Stefano Lise; Iain Mathieson; Valerie Elizabeth Murphy; David A Keays
Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies.
Journal of human genetics 2012;57(1):70-2.
2011: A Edwards; Jonathan Flint; Guo-Jen Huang; M Breuss; J Cleak; Peter L Oliver; R Pidsley; C D Treiber; David A Keays
Cytoarchitectural disruption of the superior colliculus and an enlarged acoustic startle response in the Tuba1a mutant mouse.
Neuroscience 2011;195():191-200.
2009: Xavier Hubert Jaglin; Karine Poirier; Yoann Saillour; Emmanuelle Buhler; Guoling Tian; Nadia Bahi-Buisson; Catherine Fallet-Bianco; Françoise Phan Dinh Tuy; Xiang-Peng Kong; Pascale Bomont; Laëtitia Castelnau-Ptakhine; Sylvie Odent; Philippe Loget; Manoelle Kossorotoff; Irina Snoeck; Ghislaine Plessis; Philippe Parent; Cherif Beldjord; Carlos Cardoso; Alfonso Represa; Jonathan Flint; David A Keays; Nicholas Justin Cowan; Jamel Chelly
Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria.
Nature genetics 2009;41(6):746-52.
2008: Matthias Groszer; David A Keays; Robert M J Deacon; Joseph P de Bono; Shweta Prasad-Mulcare; Simone Gaub; Muriel G Baum; Catherine A French; Jérôme Nicod; Julie A Coventry; Wolfgang Enard; Martin Fray; Steve D M Brown; Patrick M Nolan; Svante Pääbo; Keith M Channon; Rui M Costa; Jens Eilers; Günter Ehret; J Nicholas P Rawlins; Simon E Fisher
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits.
Current biology : CB 2008;18(5):354-62.
2008: Guoling Tian; Xiang-Peng Kong; Xavier H Jaglin; Jamel Chelly; David A Keays; Nicholas J Cowan
A pachygyria-causing alpha-tubulin mutation results in inefficient cycling with CCT and a deficient interaction with TBCB.
Molecular biology of the cell 2008;19(3):1152-61.
2007: Karine Poirier; David A Keays; Fiona Francis; Yoann Saillour; Nadia Bahi; Sylvie Manouvrier; Catherine Fallet-Bianco; Laurent Pasquier; Annick Toutain; Françoise Phan Dinh Tuy; Thierry Bienvenu; Sylvie Joriot; Sylvie Odent; Dorothée Ville; Isabelle Desguerre; Alice Goldenberg; Marie-Laure Moutard; Jean-Pierre Fryns; Hilde Van Esch; Robert Justin Harvey; Christian Siebold; Jonathan Flint; Cherif Beldjord; Jamel Chelly
Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A).
Human mutation 2007;28(11):1055-64.
2007: Peter L Oliver; David A Keays; Kay E Davies
Behavioural characterisation of the robotic mouse mutant.
Behavioural brain research 2007;181(2):239-47.
2007: David A Keays
Neuronal migration: unraveling the molecular pathway with humans, mice, and a fungus.
Mammalian genome : official journal of the International Mammalian Genome Society 2007;18(6-7):425-30.
2007: David A Keays; Taane G Clark; Thomas G Campbell; John Broxholme; William Valdar
Estimating the number of coding mutations in genotypic and phenotypic driven N-ethyl-N-nitrosourea (ENU) screens: revisited.
Mammalian genome : official journal of the International Mammalian Genome Society 2007;18(2):123-4.
2007: David A Keays; Guoling Tian; Karine Poirier; Guo-Jen Huang; Christian Siebold; James Cleak; Peter L Oliver; Martin Fray; Robert Justin Harvey; Zoltán Molnár; Maria C Piñon; Neil Dear; William Valdar; Steve D M Brown; Kay E Davies; J N P Rawlins; Nicholas J Cowan; Patrick Nolan; Jamel Chelly; Jonathan Flint
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans.
Cell 2007;128(1):45-57.
2006: David A Keays; Taane G Clark; Jonathan Flint
Estimating the number of coding mutations in genotypic- and phenotypic-driven N-ethyl-N-nitrosourea (ENU) screens.
Mammalian genome : official journal of the International Mammalian Genome Society 2006;17(3):230-8.
2004: Debora Bogani; Nick Warr; Paul Elms; Jennifer Davies; Zuzanna Tymowska-Lalanne; Michelle Goldsworthy; Roger D Cox; David A Keays; Jonathan Flint; Valerie Wilson; Pat Nolan; Ruth Arkell
New semidominant mutations that affect mouse development.
Genesis (New York, N.Y. : 2000) 2004;40(2):109-117.
2004: Mohamed Mohideen Quwailid; Alison Hugill; Neil Dear; Lucie Vizor; Sara Wells; Emma Horner; Shelly Fuller; Jessica Weedon; Hamish McMath; Paul Woodman; David Edwards; David Campbell; Susan Rodger; Joanne Carey; Ann Roberts; Peter Glenister; Zuzanna Lalanne; Nick Parkinson; Emma L Coghill; Richard McKeone; Sam Cox; John Willan; Andy Greenfield; David A Keays; Saffron Brady; Nigel K Spurr; Ian C Gray; Jackie Hunter; Steve D M Brown; Roger D Cox
A gene-driven ENU-based approach to generating an allelic series in any gene.
Mammalian genome : official journal of the International Mammalian Genome Society 2004;15(8):585-91.
2004: Binnaz Yalcin; Jan Fullerton; Susette Miller; David A Keays; S Brady; Amarjit Bhomra; A Jefferson; E Volpi; Richard R Copley; Jonathan Flint; Richard Mott
Unexpected complexity in the haplotypes of commonly used inbred strains of laboratory mice.
Proceedings of the National Academy of Sciences of the United States of America 2004;101(26):9734-9.