| Year |
Citation |
Score |
| 2023 |
Cushion TD, Leca I, Keays DA. MAPping tubulin mutations. Frontiers in Cell and Developmental Biology. 11: 1136699. PMID 36875768 DOI: 10.3389/fcell.2023.1136699 |
0.31 |
|
| 2023 |
Leca I, Phillips AW, Ushakova L, Cushion TD, Keays DA. Codon modification of Tuba1a alters mRNA levels and causes a severe neurodevelopmental phenotype in mice. Scientific Reports. 13: 1215. PMID 36681692 DOI: 10.1038/s41598-023-27782-2 |
0.333 |
|
| 2020 |
Leca I, Phillips A, Hofer I, Landler L, Ushakova L, Cushion TD, Dürnberger G, Stejskal K, Mechtler K, Keays DA. A proteomic survey of microtubule-associated proteins in a R402H TUBA1A mutant mouse. Plos Genetics. 16: e1009104. PMID 33137126 DOI: 10.1371/journal.pgen.1009104 |
0.418 |
|
| 2020 |
Hochstoeger T, Al Said T, Maestre D, Walter F, Vilceanu A, Pedron M, Cushion TD, Snider W, Nimpf S, Nordmann GC, Landler L, Edelman N, Kruppa L, Dürnberger G, Mechtler K, ... ... Keays DA, et al. The biophysical, molecular, and anatomical landscape of pigeon CRY4: A candidate light-based quantal magnetosensor. Science Advances. 6: eabb9110. PMID 32851187 DOI: 10.1126/sciadv.abb9110 |
0.702 |
|
| 2018 |
Tripathy R, Leca I, van Dijk T, Weiss J, van Bon BW, Sergaki MC, Gstrein T, Breuss M, Tian G, Bahi-Buisson N, Paciorkowski AR, Pagnamenta AT, Wenninger-Weinzierl A, Martinez-Reza MF, Landler L, ... ... Keays DA, et al. Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations. Neuron. PMID 30449657 DOI: 10.1016/J.Neuron.2018.10.044 |
0.718 |
|
| 2018 |
Engels S, Treiber CD, Salzer MC, Michalik A, Ushakova L, Keays DA, Mouritsen H, Heyers D. Lidocaine is a nocebo treatment for trigeminally mediated magnetic orientation in birds. Journal of the Royal Society, Interface. 15. PMID 30089685 DOI: 10.1098/rsif.2018.0124 |
0.309 |
|
| 2018 |
Gstrein T, Edwards A, Přistoupilová A, Leca I, Breuss M, Pilat-Carotta S, Hansen AH, Tripathy R, Traunbauer AK, Hochstoeger T, Rosoklija G, Repic M, Landler L, Stránecký V, Dürnberger G, ... ... Keays DA, et al. Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans. Nature Neuroscience. PMID 29875394 DOI: 10.1038/S41593-018-0170-9 |
0.693 |
|
| 2018 |
Holt C, Campbell M, Keays DA, Edelman N, Kapusta A, Maclary E, Domyan E, Suh A, Warren WC, Yandell M, Gilbert MTP, Shapiro MD. Improved Genome Assembly and Annotation for the Rock Pigeon (). G3 (Bethesda, Md.). PMID 29519939 DOI: 10.1534/G3.117.300443 |
0.7 |
|
| 2018 |
Gstrein T, Edwards A, Přistoupilová A, Leca I, Breuss M, Pilat-Carotta S, Hansen AH, Tripathy R, Traunbauer AK, Hochstoeger T, Rosoklija G, Repic M, Landler L, Stránecký V, Dürnberger G, ... ... Keays DA, et al. Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans. Nature Neuroscience. PMID 29311744 DOI: 10.1038/S41593-017-0053-5 |
0.736 |
|
| 2017 |
Nimpf S, Malkemper EP, Lauwers M, Ushakova L, Nordmann G, Wenninger-Weinzierl A, Burkard TR, Jacob S, Heuser T, Resch GP, Keays DA. Subcellular analysis of pigeon hair cells implicates vesicular trafficking in cuticulosome formation and maintenance. Elife. 6. PMID 29140244 DOI: 10.7554/Elife.29959 |
0.314 |
|
| 2017 |
Breuss MW, Leca I, Gstrein T, Hansen AH, Keays DA. Tubulins and brain development - The origins of functional specification. Molecular and Cellular Neurosciences. 84: 58-67. PMID 28347630 DOI: 10.1016/j.mcn.2017.03.002 |
0.692 |
|
| 2017 |
Breuss MW, Hansen AH, Landler L, Keays DA. Brain-specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition. Behavioural Brain Research. PMID 28130172 DOI: 10.1016/j.bbr.2017.01.029 |
0.713 |
|
| 2016 |
Breuss MW, Nguyen T, Srivatsan A, Leca I, Tian G, Fritz T, Hansen AH, Musaev D, McEvoy-Venneri J, James KN, Rosti RO, Scott E, Tan U, Kolodner RD, Cowan NJ, ... Keays DA, et al. Uner Tan Syndrome Caused by a Homozygous TUBB2B Mutation Affecting Microtubule Stability. Human Molecular Genetics. PMID 28013290 DOI: 10.1093/Hmg/Ddw383 |
0.739 |
|
| 2016 |
Broix L, Jagline H, L Ivanova E, Schmucker S, Drouot N, Clayton-Smith J, Pagnamenta AT, Metcalfe KA, Isidor B, Louvier UW, Poduri A, Taylor JC, Tilly P, Poirier K, Saillour Y, ... ... Keays D, et al. Mutations in the HECT domain of NEDD4L lead to AKT-mTOR pathway deregulation and cause periventricular nodular heterotopia. Nature Genetics. PMID 27694961 DOI: 10.1038/Ng.3676 |
0.318 |
|
| 2016 |
Haas MA, Ngo L, Li SS, Schleich S, Qu Z, Vanyai HK, Cullen HD, Cardona-Alberich A, Gladwyn-Ng IE, Pagnamenta AT, Taylor JC, Stewart H, Kini U, Duncan KE, Teleman AA, ... Keays DA, et al. De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation. Cell Reports. PMID 27239039 DOI: 10.1016/J.Mod.2017.04.122 |
0.333 |
|
| 2016 |
Breuss M, Fritz T, Gstrein T, Chan K, Ushakova L, Yu N, Vonberg FW, Werner B, Elling U, Keays DA. Mutations in the murine homologue of TUBB5 cause microcephaly by perturbing cell cycle progression and inducing p53 associated apoptosis. Development (Cambridge, England). PMID 26903504 DOI: 10.1242/dev.131516 |
0.741 |
|
| 2015 |
Isrie M, Breuss M, Tian G, Hansen AH, Cristofoli F, Morandell J, Kupchinsky ZA, Sifrim A, Rodriguez-Rodriguez CM, Dapena EP, Doonanco K, Leonard N, Tinsa F, Moortgat S, Ulucan H, ... ... Keays DA, et al. Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type. American Journal of Human Genetics. 97: 790-800. PMID 26637975 DOI: 10.1016/J.Ajhg.2015.10.014 |
0.711 |
|
| 2015 |
Breuss M, Morandell J, Nimpf S, Gstrein T, Lauwers M, Hochstoeger T, Braun A, Chan K, Sánchez Guajardo ER, Zhang L, Suplata M, Heinze KG, Elsayad K, Keays DA. The expression of Tubb2b undergoes a developmental transition in murine cortical neurons. The Journal of Comparative Neurology. PMID 26105993 DOI: 10.1002/cne.23836 |
0.723 |
|
| 2015 |
Edelman NB, Fritz T, Nimpf S, Pichler P, Lauwers M, Hickman RW, Papadaki-Anastasopoulou A, Ushakova L, Heuser T, Resch GP, Saunders M, Shaw JA, Keays DA. No evidence for intracellular magnetite in putative vertebrate magnetoreceptors identified by magnetic screening. Proceedings of the National Academy of Sciences of the United States of America. 112: 262-7. PMID 25535350 DOI: 10.1073/Pnas.1407915112 |
0.731 |
|
| 2014 |
Ngo L, Haas M, Qu Z, Li SS, Zenker J, Teng KS, Gunnersen JM, Breuss M, Habgood M, Keays DA, Heng JI. TUBB5 and its disease-associated mutations influence the terminal differentiation and dendritic spine densities of cerebral cortical neurons. Human Molecular Genetics. 23: 5147-58. PMID 24833723 DOI: 10.1093/Hmg/Ddu238 |
0.728 |
|
| 2014 |
Breuss M, Keays DA. Microtubules and neurodevelopmental disease: the movers and the makers. Advances in Experimental Medicine and Biology. 800: 75-96. PMID 24243101 DOI: 10.1007/978-94-007-7687-6_5 |
0.709 |
|
| 2013 |
Conti V, Carabalona A, Pallesi-Pocachard E, Parrini E, Leventer RJ, Buhler E, McGillivray G, Michel FJ, Striano P, Mei D, Watrin F, Lise S, Pagnamenta AT, Taylor JC, Kini U, ... ... Keays DA, et al. Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene. Brain : a Journal of Neurology. 136: 3378-94. PMID 24056535 DOI: 10.1093/Brain/Awt249 |
0.341 |
|
| 2013 |
Treiber CD, Salzer M, Breuss M, Ushakova L, Lauwers M, Edelman N, Keays DA. High resolution anatomical mapping confirms the absence of a magnetic sense system in the rostral upper beak of pigeons. Communicative & Integrative Biology. 6: e24859. PMID 23940826 DOI: 10.4161/cib.24859 |
0.742 |
|
| 2013 |
Lauwers M, Pichler P, Edelman NB, Resch GP, Ushakova L, Salzer MC, Heyers D, Saunders M, Shaw J, Keays DA. An iron-rich organelle in the cuticular plate of avian hair cells. Current Biology : Cb. 23: 924-9. PMID 23623555 DOI: 10.1016/J.Cub.2013.04.025 |
0.734 |
|
| 2013 |
Watkins-Chow DE, Cooke J, Pidsley R, Edwards A, Slotkin R, Leeds KE, Mullen R, Baxter LL, Campbell TG, Salzer MC, Biondini L, Gibney G, Phan Dinh Tuy F, Chelly J, Morris HD, ... ... Keays DA, et al. Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes. Plos Genetics. 9: e1003094. PMID 23382688 DOI: 10.1371/Journal.Pgen.1003094 |
0.327 |
|
| 2012 |
Breuss M, Heng JI, Poirier K, Tian G, Jaglin XH, Qu Z, Braun A, Gstrein T, Ngo L, Haas M, Bahi-Buisson N, Moutard ML, Passemard S, Verloes A, Gressens P, ... ... Keays DA, et al. Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities. Cell Reports. 2: 1554-62. PMID 23246003 DOI: 10.1016/J.Celrep.2012.11.017 |
0.75 |
|
| 2012 |
Treiber CD, Salzer MC, Riegler J, Edelman N, Sugar C, Breuss M, Pichler P, Cadiou H, Saunders M, Lythgoe M, Shaw J, Keays DA. Clusters of iron-rich cells in the upper beak of pigeons are macrophages not magnetosensitive neurons. Nature. 484: 367-70. PMID 22495303 DOI: 10.1038/Nature11046 |
0.751 |
|
| 2011 |
Edwards A, Treiber CD, Breuss M, Pidsley R, Huang GJ, Cleak J, Oliver PL, Flint J, Keays DA. Cytoarchitectural disruption of the superior colliculus and an enlarged acoustic startle response in the Tuba1a mutant mouse. Neuroscience. 195: 191-200. PMID 21875651 DOI: 10.1016/J.Neuroscience.2011.08.035 |
0.725 |
|
| 2010 |
Keays DA, Cleak J, Huang GJ, Edwards A, Braun A, Treiber CD, Pidsley R, Flint J. The role of Tuba1a in adult hippocampal neurogenesis and the formation of the dentate gyrus. Developmental Neuroscience. 32: 268-77. PMID 21041996 DOI: 10.1159/000319663 |
0.316 |
|
| 2010 |
Tian G, Jaglin XH, Keays DA, Francis F, Chelly J, Cowan NJ. Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway. Human Molecular Genetics. 19: 3599-613. PMID 20603323 DOI: 10.1093/Hmg/Ddq276 |
0.352 |
|
| 2010 |
Braun A, Breuss M, Salzer MC, Flint J, Cowan NJ, Keays DA. Tuba8 is expressed at low levels in the developing mouse and human brain. American Journal of Human Genetics. 86: 819-22; author reply. PMID 20466094 DOI: 10.1016/J.Ajhg.2010.03.019 |
0.697 |
|
| 2009 |
Jaglin XH, Poirier K, Saillour Y, Buhler E, Tian G, Bahi-Buisson N, Fallet-Bianco C, Phan-Dinh-Tuy F, Kong XP, Bomont P, Castelnau-Ptakhine L, Odent S, Loget P, Kossorotoff M, Snoeck I, ... ... Keays DA, et al. Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria. Nature Genetics. 41: 746-52. PMID 19465910 DOI: 10.1038/Ng.380 |
0.392 |
|
| 2007 |
Poirier K, Keays DA, Francis F, Saillour Y, Bahi N, Manouvrier S, Fallet-Bianco C, Pasquier L, Toutain A, Tuy FP, Bienvenu T, Joriot S, Odent S, Ville D, Desguerre I, et al. Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A). Human Mutation. 28: 1055-64. PMID 17584854 DOI: 10.1002/humu.20572 |
0.333 |
|
| 2007 |
Keays DA, Tian G, Poirier K, Huang GJ, Siebold C, Cleak J, Oliver PL, Fray M, Harvey RJ, Molnár Z, Piñon MC, Dear N, Valdar W, Brown SD, Davies KE, et al. Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans. Cell. 128: 45-57. PMID 17218254 DOI: 10.1016/J.Cell.2006.12.017 |
0.369 |
|
| 2004 |
Bogani D, Warr N, Elms P, Davies J, Tymowska-Lalanne Z, Goldsworthy M, Cox RD, Keays DA, Flint J, Wilson V, Nolan P, Arkell R. New semidominant mutations that affect mouse development Genesis. 40: 109-117. PMID 15384171 DOI: 10.1002/gene.20071 |
0.313 |
|
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