BETA: Related publications

Publications

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Tripathy R, Leca I, van Dijk T, et al. (2018) Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations. Neuron
Engels S, Treiber CD, Salzer MC, et al. (2018) Lidocaine is a nocebo treatment for trigeminally mediated magnetic orientation in birds. Journal of the Royal Society, Interface. 15
Gstrein T, Edwards A, Přistoupilová A, et al. (2018) Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans. Nature Neuroscience
Gstrein T, Edwards A, Přistoupilová A, et al. (2018) Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans. Nature Neuroscience
Breuss MW, Nguyen T, Srivatsan A, et al. (2016) Uner Tan Syndrome Caused by a Homozygous TUBB2B Mutation Affecting Microtubule Stability. Human Molecular Genetics
Haas MA, Ngo L, Li SS, et al. (2016) De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation. Cell Reports
Breuss M, Fritz T, Gstrein T, et al. (2016) Mutations in the murine homologue of TUBB5 cause microcephaly by perturbing cell cycle progression and inducing p53 associated apoptosis. Development (Cambridge, England)
Isrie M, Breuss M, Tian G, et al. (2015) Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type. American Journal of Human Genetics. 97: 790-800
Hempel A, Pagnamenta AT, Blyth M, et al. (2015) Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome. Journal of Medical Genetics
Ilkovski B, Pagnamenta AT, O'Grady GL, et al. (2015) Mutations in PIGY: expanding the phenotype of inherited glycosylphosphatidylinositol (GPI) deficiencies. Human Molecular Genetics
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