David Keays
#121,793
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Australian neuroscientist
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David Keaysbiology Degrees
Biology
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Genetics
#1843
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#1959
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Neuroscience
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#2725
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Biology
Why Is David Keays Influential?
(Suggest an Edit or Addition)According to Wikipedia, David Anthony Keays is an Australian neuroscientist who studies magnetoreception and neurodevelopment. He is currently Chair of Organismal and Developmental Neurobiology at the Ludwig Maximilians University in Munich, and a Principle Research Associate at the University of Cambridge. He was formerly a group leader at the Research Institute of Molecular Pathology in Vienna, Austria,
David Keays's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans (2007) (416)
- Impaired Synaptic Plasticity and Motor Learning in Mice with a Point Mutation Implicated in Human Speech Deficits (2008) (274)
- Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria (2009) (238)
- A gene-driven ENU-based approach to generating an allelic series in any gene (2004) (178)
- A novel alpha-conotoxin identified by gene sequencing is active in suppressing the vascular response to selective stimulation of sensory nerves in vivo. (2003) (166)
- Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities (2012) (161)
- Clusters of iron-rich cells in the upper beak of pigeons are macrophages not magnetosensitive neurons (2012) (153)
- Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria (2011) (151)
- Therapeutic applications of conotoxins that target the neuronal nicotinic acetylcholine receptor. (2006) (126)
- Unexpected complexity in the haplotypes of commonly used inbred strains of laboratory mice. (2004) (121)
- Magnetoreception—A sense without a receptor (2017) (86)
- Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies (2011) (71)
- Mutations in PIGY: expanding the phenotype of inherited glycosylphosphatidylinositol deficiencies (2015) (68)
- No evidence for intracellular magnetite in putative vertebrate magnetoreceptors identified by magnetic screening (2014) (66)
- Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type. (2015) (64)
- Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway. (2010) (62)
- Microtubules and neurodevelopmental disease: the movers and the makers. (2014) (61)
- Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome (2015) (61)
- Tubulins and brain development – The origins of functional specification (2017) (58)
- Estimating the number of coding mutations in genotypic and phenotypic driven N-ethyl-N-nitrosourea (ENU) screens: revisited (2006) (55)
- Estimating the number of coding mutations in genotypic- and phenotypic-driven N-ethyl-N-nitrosourea (ENU) screens (2005) (54)
- Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes (2013) (52)
- A pachygyria-causing alpha-tubulin mutation results in inefficient cycling with CCT and a deficient interaction with TBCB. (2007) (51)
- Germline recessive mutations in PI4KA are associated with perisylvian polymicrogyria, cerebellar hypoplasia and arthrogryposis (2015) (49)
- An Iron-Rich Organelle in the Cuticular Plate of Avian Hair Cells (2013) (48)
- Determining sequences and post-translational modifications of novel conotoxins in Conus victoriae using cDNA sequencing and mass spectrometry. (2004) (47)
- A Putative Mechanism for Magnetoreception by Electromagnetic Induction in the Pigeon Inner Ear (2019) (45)
- A Novel Nonsense CDK5RAP2 Mutation in a Somali Child With Primary Microcephaly and Sensorineural Hearing Loss (2012) (42)
- Is magnetogenetics the new optogenetics? (2017) (42)
- Tuba8 is expressed at low levels in the developing mouse and human brain. (2010) (41)
- Improved Genome Assembly and Annotation for the Rock Pigeon (Columba livia) (2017) (38)
- TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons. (2014) (36)
- The biophysical, molecular, and anatomical landscape of pigeon CRY4: A candidate light-based quantal magnetosensor (2020) (35)
- Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans (2018) (29)
- New semidominant mutations that affect mouse development (2004) (28)
- De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation (2016) (27)
- Mutations in the murine homologue of TUBB5 cause microcephaly by perturbing cell cycle progression and inducing p53-associated apoptosis (2016) (25)
- The expression of tubb2b undergoes a developmental transition in murine cortical neurons (2015) (24)
- High resolution anatomical mapping confirms the absence of a magnetic sense system in the rostral upper beak of pigeons (2013) (23)
- N-ethyl-N-nitrosourea mouse mutants in the dissection of behavioural and psychiatric disorders. (2003) (23)
- Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations (2018) (23)
- Behavioural characterisation of the robotic mouse mutant (2007) (23)
- The Role of Tuba1a in Adult Hippocampal Neurogenesis and the Formation of the Dentate Gyrus (2010) (19)
- Neuronal migration: unraveling the molecular pathway with humans, mice, and a fungus (2007) (17)
- EMCD real space maps of Magnetospirillum magnetotacticum. (2011) (16)
- Why (and how) we should publish negative data (2019) (16)
- No evidence for a magnetite-based magnetoreceptor in the lagena of pigeons (2019) (15)
- Cryptochrome: The magnetosensor with a sinister side? (2018) (14)
- Molecular prospecting for drugs from the sea (2005) (13)
- Lidocaine is a nocebo treatment for trigeminally mediated magnetic orientation in birds (2018) (13)
- Comment on "Magnetosensitive neurons mediate geomagnetic orientation in Caenorhabditis elegans" (2018) (12)
- Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability (2016) (12)
- Activation of an exonic splice‐donor site in exon 30 of CDK5RAP2 in a patient with severe microcephaly and pigmentary abnormalities (2016) (10)
- Subcellular analysis of pigeon hair cells implicates vesicular trafficking in cuticulosome formation and maintenance (2017) (10)
- UNSOLVED MYSTERY Unsolved mysteries : Magnetoreception — A sense without a receptor (2017) (10)
- Quantum magnetic imaging of iron organelles within the pigeon cochlea (2021) (9)
- Molecular prospecting for drugs from the sea. Isolating therapeutic peptides and proteins from cone snail venom. (2005) (7)
- A high sensitivity ZENK monoclonal antibody to map neuronal activity in Aves (2020) (7)
- A proteomic survey of microtubule-associated proteins in a R402H TUBA1A mutant mouse (2020) (7)
- ISCA1 and CRY4: An improbable proposition (2016) (7)
- Genetic testing and insurance: When is discrimination justified? (2000) (7)
- Cytoarchitectural disruption of the superior colliculus and an enlarged acoustic startle response in the Tuba1a mutant mouse (2011) (6)
- The legal implications of genetic testing: Insurance, employment and privacy (1999) (6)
- Brain-specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition (2017) (5)
- The expression, localisation and interactome of pigeon CRY2 (2021) (3)
- The Biggest Challenges Facing Young Scientists (2014) (3)
- Mutations in Human Beta-2 b Tubulin Result in Asymmetrical Polymicrogyria (2011) (3)
- Patenting DNA and amino acid sequences--an Australian perspective. (1999) (3)
- Neuronal circuits and the magnetic sense: central questions (2020) (3)
- Myths in magnetosensation (2022) (2)
- Ectopic otoconial formation in the lagena of the pigeon inner ear (2018) (2)
- Mutations in the murine homologue of TUBB5 cause microcephaly by perturbing cell cycle progression and inducing p53-associated apoptosis (2016) (2)
- Revised testing procedures do not elicit magnetoreceptive behavior in C. elegans (2018) (2)
- Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans (2018) (1)
- Correction: Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes (2015) (1)
- Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans (2018) (0)
- Mutations in themurine homologue of TUBB 5 causemicrocephaly by perturbing cell cycle progression and inducing p 53-associated apoptosis (2016) (0)
- Author response: Subcellular analysis of pigeon hair cells implicates vesicular trafficking in cuticulosome formation and maintenance (2017) (0)
- A forward genetic screen for mice with defects in neuronal migration (2015) (0)
- De Novo Mutations in DEN R Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation Graphical (2016) (0)
- Supplementary material from "Lidocaine is a nocebo treatment for trigeminally mediated magnetic orientation in birds" (2018) (0)
- Fainzilber M. et al., “A New Neurotoxin Receptor Site on Sodium Channels is Identified by a Conotoxin That Affects Sodium Channel Inactivation in Molluses and Acts as an Antagonist in Rat Brain' (2017) (0)
- Genomic analysis of sporadic neurological disease using family trios: learning to expect the unexpected (2012) (0)
- Author response: Comment on "Magnetosensitive neurons mediate geomagnetic orientation in Caenorhabditis elegans" (2017) (0)
- Codon modification of Tuba1a alters mRNA levels and causes a severe neurodevelopmental phenotype in mice (2023) (0)
- Treating drug-dependent patients in hospitals. (2002) (0)
- The mysterious magnetic sense (2019) (0)
- Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans (2018) (0)
- Temperature and angle dependent magnetic imaging of biological iron nanoparticles using quantum diamond microscopy (2023) (0)
- Exome sequencing in patients with circumferential skin creases Kunze type: evidence for locus heterogeneity (2014) (0)
- Impaired Synaptic Plasticity and Motor t Mutation Implicated in Human Speech Deficits (0)
- Mutations in MAST 1 Caus e Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations Graphical (2018) (0)
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