Andi H Hansen

Graduate School
Hippenmeyer Group

14 Publications

Mark all

[14]
2024 | Journal Article | IST-REx-ID: 14794 | OA
Hansen AH, Hippenmeyer S. Time-lapse imaging of cortical projection neuron migration in mice using mosaic analysis with double markers. STAR Protocols. 2024;5(1). doi:10.1016/j.xpro.2023.102795
[Published Version] View | Files available | DOI | Download Published Version (ext.) | PubMed | Europe PMC
 
[13]
2022 | Journal Article | IST-REx-ID: 10791 | OA
Hansen AH, Pauler F, Riedl M, et al. Tissue-wide effects override cell-intrinsic gene function in radial neuron migration. Oxford Open Neuroscience. 2022;1(1). doi:10.1093/oons/kvac009
[Published Version] View | Files available | DOI
 
[12]
2021 | Journal Article | IST-REx-ID: 8546 | OA
Zhang T, Liu T, Mora N, et al. Generation of excitatory and inhibitory neurons from common progenitors via Notch signaling in the cerebellum. Cell Reports. 2021;35(10). doi:10.1016/j.celrep.2021.109208
[Published Version] View | Files available | DOI | WoS | PubMed | Europe PMC
 
[11]
2021 | Journal Article | IST-REx-ID: 9603 | OA
Contreras X, Amberg N, Davaatseren A, et al. A genome-wide library of MADM mice for single-cell genetic mosaic analysis. Cell Reports. 2021;35(12). doi:10.1016/j.celrep.2021.109274
[Published Version] View | Files available | DOI | WoS
 
[10]
2021 | Thesis | IST-REx-ID: 9962 | OA
Hansen AH. Cell-autonomous gene function and non-cell-autonomous effects in radial projection neuron migration. 2021. doi:10.15479/at:ista:9962
[Published Version] View | Files available | DOI
 
[9]
2020 | Journal Article | IST-REx-ID: 8162 | OA
Laukoter S, Pauler F, Beattie RJ, et al. Cell-type specificity of genomic imprinting in cerebral cortex. Neuron. 2020;107(6):1160-1179.e9. doi:10.1016/j.neuron.2020.06.031
[Published Version] View | Files available | DOI | WoS
 
[8]
2020 | Journal Article | IST-REx-ID: 8569 | OA
Hansen AH, Hippenmeyer S. Non-cell-autonomous mechanisms in radial projection neuron migration in the developing cerebral cortex. Frontiers in Cell and Developmental Biology. 2020;8(9). doi:10.3389/fcell.2020.574382
[Published Version] View | Files available | DOI | WoS | PubMed | Europe PMC
 
[7]
2020 | Journal Article | IST-REx-ID: 7815 | OA
Beattie RJ, Streicher C, Amberg N, et al. Lineage tracing and clonal analysis in developing cerebral cortex using mosaic analysis with double markers (MADM). Journal of Visual Experiments. 2020;(159). doi:10.3791/61147
[Published Version] View | Files available | DOI | WoS
 
[6]
2018 | Journal Article | IST-REx-ID: 547
Gstrein T, Edwards A, Přistoupilová A, Leca I, Breuss M, Pilat Carotta S, Hansen AH, Tripathy R, Traunbauer A, Hochstoeger T, Rosoklija G, Repic M, Landler L, Stránecký V, Dürnberger G, Keane T, Zuber J, Adams D, Flint J, Honzik T, Gut M, Beltran S, Mechtler K, Sherr E, Kmoch S, Gut I, 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.
View | DOI | WoS
 
[5]
2017 | Journal Article | IST-REx-ID: 1107 | OA
Breuss M, Hansen AH, Landler L, Keays D. Brain specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition. Behavioural Brain Research. 2017;323:47-55. doi:10.1016/j.bbr.2017.01.029
[Published Version] View | Files available | DOI | WoS
 
[4]
2017 | Journal Article | IST-REx-ID: 1017 | OA
Breuss M, Leca I, Gstrein T, Hansen AH, Keays D. Tubulins and brain development: The origins of functional specification. Molecular and Cellular Neuroscience. 2017;84:58-67. doi:10.1016/j.mcn.2017.03.002
[Published Version] View | Files available | DOI | WoS
 
[3]
2017 | Journal Article | IST-REx-ID: 1016
Breuss M, Nguyen T, Srivatsan A, et al. Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability. Human Molecular Genetics. 2017;26(2):258-269. doi:10.1093/hmg/ddw383
View | DOI | WoS
 
[2]
2017 | Journal Article | IST-REx-ID: 960 | OA
Hansen AH, Düllberg CF, Mieck C, Loose M, Hippenmeyer S. Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks. Frontiers in Cellular Neuroscience. 2017;11. doi:10.3389/fncel.2017.00176
[Published Version] View | Files available | DOI | WoS
 
[1]
2015 | Journal Article | IST-REx-ID: 1106
Isrie M, Breuss M, Tian G, Hansen AH, Cristofoli F, Morandell J, Kupchinsky ZA, Sifrim A, Rodriguez Rodriguez C, Dapena EP, Doonanco K, Leonard N, Tinsa F, Moortgat S, Ulucan H, Koparir E, Karaca E, Katsanis N, Marton V, Vermeesch JR, Davis EE, Cowan NJ, Keays D, 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.
View | DOI
 
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14 Publications

Mark all

[14]
2024 | Journal Article | IST-REx-ID: 14794 | OA
Hansen AH, Hippenmeyer S. Time-lapse imaging of cortical projection neuron migration in mice using mosaic analysis with double markers. STAR Protocols. 2024;5(1). doi:10.1016/j.xpro.2023.102795
[Published Version] View | Files available | DOI | Download Published Version (ext.) | PubMed | Europe PMC
 
[13]
2022 | Journal Article | IST-REx-ID: 10791 | OA
Hansen AH, Pauler F, Riedl M, et al. Tissue-wide effects override cell-intrinsic gene function in radial neuron migration. Oxford Open Neuroscience. 2022;1(1). doi:10.1093/oons/kvac009
[Published Version] View | Files available | DOI
 
[12]
2021 | Journal Article | IST-REx-ID: 8546 | OA
Zhang T, Liu T, Mora N, et al. Generation of excitatory and inhibitory neurons from common progenitors via Notch signaling in the cerebellum. Cell Reports. 2021;35(10). doi:10.1016/j.celrep.2021.109208
[Published Version] View | Files available | DOI | WoS | PubMed | Europe PMC
 
[11]
2021 | Journal Article | IST-REx-ID: 9603 | OA
Contreras X, Amberg N, Davaatseren A, et al. A genome-wide library of MADM mice for single-cell genetic mosaic analysis. Cell Reports. 2021;35(12). doi:10.1016/j.celrep.2021.109274
[Published Version] View | Files available | DOI | WoS
 
[10]
2021 | Thesis | IST-REx-ID: 9962 | OA
Hansen AH. Cell-autonomous gene function and non-cell-autonomous effects in radial projection neuron migration. 2021. doi:10.15479/at:ista:9962
[Published Version] View | Files available | DOI
 
[9]
2020 | Journal Article | IST-REx-ID: 8162 | OA
Laukoter S, Pauler F, Beattie RJ, et al. Cell-type specificity of genomic imprinting in cerebral cortex. Neuron. 2020;107(6):1160-1179.e9. doi:10.1016/j.neuron.2020.06.031
[Published Version] View | Files available | DOI | WoS
 
[8]
2020 | Journal Article | IST-REx-ID: 8569 | OA
Hansen AH, Hippenmeyer S. Non-cell-autonomous mechanisms in radial projection neuron migration in the developing cerebral cortex. Frontiers in Cell and Developmental Biology. 2020;8(9). doi:10.3389/fcell.2020.574382
[Published Version] View | Files available | DOI | WoS | PubMed | Europe PMC
 
[7]
2020 | Journal Article | IST-REx-ID: 7815 | OA
Beattie RJ, Streicher C, Amberg N, et al. Lineage tracing and clonal analysis in developing cerebral cortex using mosaic analysis with double markers (MADM). Journal of Visual Experiments. 2020;(159). doi:10.3791/61147
[Published Version] View | Files available | DOI | WoS
 
[6]
2018 | Journal Article | IST-REx-ID: 547
Gstrein T, Edwards A, Přistoupilová A, Leca I, Breuss M, Pilat Carotta S, Hansen AH, Tripathy R, Traunbauer A, Hochstoeger T, Rosoklija G, Repic M, Landler L, Stránecký V, Dürnberger G, Keane T, Zuber J, Adams D, Flint J, Honzik T, Gut M, Beltran S, Mechtler K, Sherr E, Kmoch S, Gut I, 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.
View | DOI | WoS
 
[5]
2017 | Journal Article | IST-REx-ID: 1107 | OA
Breuss M, Hansen AH, Landler L, Keays D. Brain specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition. Behavioural Brain Research. 2017;323:47-55. doi:10.1016/j.bbr.2017.01.029
[Published Version] View | Files available | DOI | WoS
 
[4]
2017 | Journal Article | IST-REx-ID: 1017 | OA
Breuss M, Leca I, Gstrein T, Hansen AH, Keays D. Tubulins and brain development: The origins of functional specification. Molecular and Cellular Neuroscience. 2017;84:58-67. doi:10.1016/j.mcn.2017.03.002
[Published Version] View | Files available | DOI | WoS
 
[3]
2017 | Journal Article | IST-REx-ID: 1016
Breuss M, Nguyen T, Srivatsan A, et al. Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability. Human Molecular Genetics. 2017;26(2):258-269. doi:10.1093/hmg/ddw383
View | DOI | WoS
 
[2]
2017 | Journal Article | IST-REx-ID: 960 | OA
Hansen AH, Düllberg CF, Mieck C, Loose M, Hippenmeyer S. Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks. Frontiers in Cellular Neuroscience. 2017;11. doi:10.3389/fncel.2017.00176
[Published Version] View | Files available | DOI | WoS
 
[1]
2015 | Journal Article | IST-REx-ID: 1106
Isrie M, Breuss M, Tian G, Hansen AH, Cristofoli F, Morandell J, Kupchinsky ZA, Sifrim A, Rodriguez Rodriguez C, Dapena EP, Doonanco K, Leonard N, Tinsa F, Moortgat S, Ulucan H, Koparir E, Karaca E, Katsanis N, Marton V, Vermeesch JR, Davis EE, Cowan NJ, Keays D, 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.
View | DOI
 
Marked Publication(s)

Search

Filter Publications

    • Display / Sort

    Citation Style: AMA

    Export / Embed