11 Publications

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[11]
2020 | Journal Article | IST-REx-ID: 7815 | OA
Beattie, R. J., Streicher, C., Amberg, N., Cheung, G. T., Contreras, X., Hansen, A. H., & Hippenmeyer, S. (2020). Lineage tracing and clonal analysis in developing cerebral cortex using mosaic analysis with double markers (MADM). Journal of Visual Experiments (JoVE), (159). https://doi.org/10.3791/61147
View | Files available | DOI
 
[10]
2020 | Preprint | IST-REx-ID: 8546 | OA
Zhang, T., Liu, T., Mora, N., Guegan, J., Bertrand, M., Contreras, X., … Hassan, B. A. (n.d.). Generation of neuronal diversity from common progenitors via Notch signaling in the cerebellum. BioRxiv. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2020.03.18.997205
View | DOI | Download Preprint (ext.)
 
[9]
2020 | Preprint | IST-REx-ID: 8545 | OA
Contreras, X., Davaatseren, A., Amberg, N., Hansen, A. H., Sonntag, J., Andersen, L., … Hippenmeyer, S. (2020). A genome-wide library of MADM mice for single-cell genetic mosaic analysis. BioRxiv. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2020.06.05.136192
View | DOI | Download Preprint (ext.)
 
[8]
2020 | Journal Article | IST-REx-ID: 8162 | OA
Laukoter, S., Pauler, F., Beattie, R. J., Amberg, N., Hansen, A. H., Streicher, C., … Hippenmeyer, S. (n.d.). Cell-type specificity of genomic imprinting in cerebral cortex. Neuron, 107(9), 1–20. https://doi.org/10.1016/j.neuron.2020.06.031
View | Files available | DOI | Download Published Version (ext.)
 
[7]
2020 | Journal Article | IST-REx-ID: 8569 | OA
Hansen, A. H., & Hippenmeyer, S. (2020). Non-cell-autonomous mechanisms in radial projection neuron migration in the developing cerebral cortex. Frontiers in Cell and Developmental Biology, 8(9). https://doi.org/10.3389/fcell.2020.574382
View | Files available | DOI | PubMed | Europe PMC
 
[6]
2018 | Journal Article | IST-REx-ID: 547
Gstrein, T., Edwards, A., Přistoupilová, A., Leca, I., Breuss, M., Pilat Carotta, S., … Keays, D. (2018). Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans. Nature Neuroscience, 21(2), 207–217. https://doi.org/10.1038/s41593-017-0053-5
View | DOI
 
[5]
2017 | Journal Article | IST-REx-ID: 960 | OA
Hansen, A. H., Düllberg, C. F., Mieck, C., Loose, M., & Hippenmeyer, S. (2017). Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks. Frontiers in Cellular Neuroscience, 11. https://doi.org/10.3389/fncel.2017.00176
View | Files available | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 1016
Breuss, M., Nguyen, T., Srivatsan, A., Leca, I., Tian, G., Fritz, T., … Gleeson, J. (2017). Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability. Human Molecular Genetics, 26(2), 258–269. https://doi.org/10.1093/hmg/ddw383
View | DOI
 
[3]
2017 | Journal Article | IST-REx-ID: 1017 | OA
Breuss, M., Leca, I., Gstrein, T., Hansen, A. H., & Keays, D. (2017). Tubulins and brain development: The origins of functional specification. Molecular and Cellular Neuroscience, 84, 58–67. https://doi.org/10.1016/j.mcn.2017.03.002
View | Files available | DOI
 
[2]
2017 | Journal Article | IST-REx-ID: 1107 | OA
Breuss, M., Hansen, A. H., Landler, L., & Keays, D. (2017). Brain specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition. Behavioural Brain Research, 323, 47–55. https://doi.org/10.1016/j.bbr.2017.01.029
View | Files available | DOI
 
[1]
2015 | Journal Article | IST-REx-ID: 1106
Isrie, M., Breuss, M., Tian, G., Hansen, A. H., Cristofoli, F., Morandell, J., … Van Esch, H. (2015). Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type. The American Journal of Human Genetics, 97(6), 790–800. https://doi.org/10.1016/j.ajhg.2015.10.014
View | DOI
 

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11 Publications

Mark all

[11]
2020 | Journal Article | IST-REx-ID: 7815 | OA
Beattie, R. J., Streicher, C., Amberg, N., Cheung, G. T., Contreras, X., Hansen, A. H., & Hippenmeyer, S. (2020). Lineage tracing and clonal analysis in developing cerebral cortex using mosaic analysis with double markers (MADM). Journal of Visual Experiments (JoVE), (159). https://doi.org/10.3791/61147
View | Files available | DOI
 
[10]
2020 | Preprint | IST-REx-ID: 8546 | OA
Zhang, T., Liu, T., Mora, N., Guegan, J., Bertrand, M., Contreras, X., … Hassan, B. A. (n.d.). Generation of neuronal diversity from common progenitors via Notch signaling in the cerebellum. BioRxiv. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2020.03.18.997205
View | DOI | Download Preprint (ext.)
 
[9]
2020 | Preprint | IST-REx-ID: 8545 | OA
Contreras, X., Davaatseren, A., Amberg, N., Hansen, A. H., Sonntag, J., Andersen, L., … Hippenmeyer, S. (2020). A genome-wide library of MADM mice for single-cell genetic mosaic analysis. BioRxiv. Cold Spring Harbor Laboratory. https://doi.org/10.1101/2020.06.05.136192
View | DOI | Download Preprint (ext.)
 
[8]
2020 | Journal Article | IST-REx-ID: 8162 | OA
Laukoter, S., Pauler, F., Beattie, R. J., Amberg, N., Hansen, A. H., Streicher, C., … Hippenmeyer, S. (n.d.). Cell-type specificity of genomic imprinting in cerebral cortex. Neuron, 107(9), 1–20. https://doi.org/10.1016/j.neuron.2020.06.031
View | Files available | DOI | Download Published Version (ext.)
 
[7]
2020 | Journal Article | IST-REx-ID: 8569 | OA
Hansen, A. H., & Hippenmeyer, S. (2020). Non-cell-autonomous mechanisms in radial projection neuron migration in the developing cerebral cortex. Frontiers in Cell and Developmental Biology, 8(9). https://doi.org/10.3389/fcell.2020.574382
View | Files available | DOI | PubMed | Europe PMC
 
[6]
2018 | Journal Article | IST-REx-ID: 547
Gstrein, T., Edwards, A., Přistoupilová, A., Leca, I., Breuss, M., Pilat Carotta, S., … Keays, D. (2018). Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans. Nature Neuroscience, 21(2), 207–217. https://doi.org/10.1038/s41593-017-0053-5
View | DOI
 
[5]
2017 | Journal Article | IST-REx-ID: 960 | OA
Hansen, A. H., Düllberg, C. F., Mieck, C., Loose, M., & Hippenmeyer, S. (2017). Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks. Frontiers in Cellular Neuroscience, 11. https://doi.org/10.3389/fncel.2017.00176
View | Files available | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 1016
Breuss, M., Nguyen, T., Srivatsan, A., Leca, I., Tian, G., Fritz, T., … Gleeson, J. (2017). Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability. Human Molecular Genetics, 26(2), 258–269. https://doi.org/10.1093/hmg/ddw383
View | DOI
 
[3]
2017 | Journal Article | IST-REx-ID: 1017 | OA
Breuss, M., Leca, I., Gstrein, T., Hansen, A. H., & Keays, D. (2017). Tubulins and brain development: The origins of functional specification. Molecular and Cellular Neuroscience, 84, 58–67. https://doi.org/10.1016/j.mcn.2017.03.002
View | Files available | DOI
 
[2]
2017 | Journal Article | IST-REx-ID: 1107 | OA
Breuss, M., Hansen, A. H., Landler, L., & Keays, D. (2017). Brain specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition. Behavioural Brain Research, 323, 47–55. https://doi.org/10.1016/j.bbr.2017.01.029
View | Files available | DOI
 
[1]
2015 | Journal Article | IST-REx-ID: 1106
Isrie, M., Breuss, M., Tian, G., Hansen, A. H., Cristofoli, F., Morandell, J., … Van Esch, H. (2015). Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type. The American Journal of Human Genetics, 97(6), 790–800. https://doi.org/10.1016/j.ajhg.2015.10.014
View | DOI
 

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