6 Publications

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[6]
2018 | Journal Article | IST-REx-ID: 547
Gstrein, Thomas, Andrew Edwards, Anna Přistoupilová, Ines Leca, Martin Breuss, Sandra Pilat Carotta, Andi H Hansen, et al. “Mutations in Vps15 Perturb Neuronal Migration in Mice and Are Associated with Neurodevelopmental Disease in Humans.” Nature Neuroscience 21, no. 2 (2018): 207–17. https://doi.org/10.1038/s41593-017-0053-5.
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[5]
2017 | Journal Article | IST-REx-ID: 960   OA
Hansen, Andi H, Christian F Düllberg, Christine Mieck, Martin Loose, and Simon Hippenmeyer. “Cell Polarity in Cerebral Cortex Development - Cellular Architecture Shaped by Biochemical Networks.” Frontiers in Cellular Neuroscience 11 (2017). https://doi.org/10.3389/fncel.2017.00176.
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[4]
2017 | Journal Article | IST-REx-ID: 1016
Breuss, Martin, Thai Nguyen, Anjana Srivatsan, Ines Leca, Guoling Tian, Tanja Fritz, Andi H Hansen, et al. “Uner Tan Syndrome Caused by a Homozygous TUBB2B Mutation Affecting Microtubule Stability.” Human Molecular Genetics 26, no. 2 (2017): 258–69. https://doi.org/10.1093/hmg/ddw383.
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[3]
2017 | Journal Article | IST-REx-ID: 1017   OA
Breuss, Martin, Ines Leca, Thomas Gstrein, Andi H Hansen, and David Keays. “Tubulins and Brain Development: The Origins of Functional Specification.” Molecular and Cellular Neuroscience 84 (2017): 58–67. https://doi.org/10.1016/j.mcn.2017.03.002.
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[2]
2017 | Journal Article | IST-REx-ID: 1107   OA
Breuss, Martin, Andi H Hansen, Lukas Landler, and David Keays. “Brain Specific Knockin of the Pathogenic Tubb5 E401K Allele Causes Defects in Motor Coordination and Prepulse Inhibition.” Behavioural Brain Research 323 (2017): 47–55. https://doi.org/10.1016/j.bbr.2017.01.029.
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[1]
2015 | Journal Article | IST-REx-ID: 1106
Isrie, Mala, Martin Breuss, Guoling Tian, Andi H Hansen, Francesca Cristofoli, Jasmin Morandell, Zachari A Kupchinsky, et al. “Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.” The American Journal of Human Genetics 97, no. 6 (2015): 790–800. https://doi.org/10.1016/j.ajhg.2015.10.014.
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6 Publications

Mark all

[6]
2018 | Journal Article | IST-REx-ID: 547
Gstrein, Thomas, Andrew Edwards, Anna Přistoupilová, Ines Leca, Martin Breuss, Sandra Pilat Carotta, Andi H Hansen, et al. “Mutations in Vps15 Perturb Neuronal Migration in Mice and Are Associated with Neurodevelopmental Disease in Humans.” Nature Neuroscience 21, no. 2 (2018): 207–17. https://doi.org/10.1038/s41593-017-0053-5.
View | DOI
 
[5]
2017 | Journal Article | IST-REx-ID: 960   OA
Hansen, Andi H, Christian F Düllberg, Christine Mieck, Martin Loose, and Simon Hippenmeyer. “Cell Polarity in Cerebral Cortex Development - Cellular Architecture Shaped by Biochemical Networks.” Frontiers in Cellular Neuroscience 11 (2017). https://doi.org/10.3389/fncel.2017.00176.
View | Files available | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 1016
Breuss, Martin, Thai Nguyen, Anjana Srivatsan, Ines Leca, Guoling Tian, Tanja Fritz, Andi H Hansen, et al. “Uner Tan Syndrome Caused by a Homozygous TUBB2B Mutation Affecting Microtubule Stability.” Human Molecular Genetics 26, no. 2 (2017): 258–69. https://doi.org/10.1093/hmg/ddw383.
View | DOI
 
[3]
2017 | Journal Article | IST-REx-ID: 1017   OA
Breuss, Martin, Ines Leca, Thomas Gstrein, Andi H Hansen, and David Keays. “Tubulins and Brain Development: The Origins of Functional Specification.” Molecular and Cellular Neuroscience 84 (2017): 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, Martin, Andi H Hansen, Lukas Landler, and David Keays. “Brain Specific Knockin of the Pathogenic Tubb5 E401K Allele Causes Defects in Motor Coordination and Prepulse Inhibition.” Behavioural Brain Research 323 (2017): 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, Mala, Martin Breuss, Guoling Tian, Andi H Hansen, Francesca Cristofoli, Jasmin Morandell, Zachari A Kupchinsky, et al. “Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.” The American Journal of Human Genetics 97, no. 6 (2015): 790–800. https://doi.org/10.1016/j.ajhg.2015.10.014.
View | DOI
 

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