11 Publications

Mark all

[11]
2020 | Journal Article | IST-REx-ID: 7815 | OA
Lineage tracing and clonal analysis in developing cerebral cortex using mosaic analysis with double markers (MADM)
R.J. Beattie, C. Streicher, N. Amberg, G.T. Cheung, X. Contreras, A.H. Hansen, S. Hippenmeyer, Journal of Visual Experiments (JoVE) (2020).
View | Files available | DOI
 
[10]
2020 | Preprint | IST-REx-ID: 8546 | OA
Generation of neuronal diversity from common progenitors via Notch signaling in the cerebellum
T. Zhang, T. Liu, N. Mora, J. Guegan, M. Bertrand, X. Contreras, A.H. Hansen, C. Streicher, M. Anderle, L. Tiberi, S. Hippenmeyer, B.A. Hassan, BioRxiv (n.d.).
View | DOI | Download Preprint (ext.)
 
[9]
2020 | Preprint | IST-REx-ID: 8545 | OA
A genome-wide library of MADM mice for single-cell genetic mosaic analysis
X. Contreras, A. Davaatseren, N. Amberg, A.H. Hansen, J. Sonntag, L. Andersen, T. Bernthaler, A.-M. Heger, R. Johnson, L.A. Schwarz, L. Luo, T. Rülicke, S. Hippenmeyer, BioRxiv (2020).
View | DOI | Download Preprint (ext.)
 
[8]
2020 | Journal Article | IST-REx-ID: 8569 | OA
Non-cell-autonomous mechanisms in radial projection neuron migration in the developing cerebral cortex
A.H. Hansen, S. Hippenmeyer, Frontiers in Cell and Developmental Biology 8 (2020).
View | Files available | DOI
 
[7]
2020 | Journal Article | IST-REx-ID: 8162 | OA
Cell-type specificity of genomic imprinting in cerebral cortex
S. Laukoter, F. Pauler, R.J. Beattie, N. Amberg, A.H. Hansen, C. Streicher, T. Penz, C. Bock, S. Hippenmeyer, Neuron 107 (n.d.) 1–20.
View | Files available | DOI | Download Published Version (ext.)
 
[6]
2018 | Journal Article | IST-REx-ID: 547
Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans
T. Gstrein, A. Edwards, A. Přistoupilová, I. Leca, M. Breuss, S. Pilat Carotta, A.H. Hansen, R. Tripathy, A. Traunbauer, T. Hochstoeger, G. Rosoklija, M. Repic, L. Landler, V. Stránecký, G. Dürnberger, T. Keane, J. Zuber, D. Adams, J. Flint, T. Honzik, M. Gut, S. Beltran, K. Mechtler, E. Sherr, S. Kmoch, I. Gut, D. Keays, Nature Neuroscience 21 (2018) 207–217.
View | DOI
 
[5]
2017 | Journal Article | IST-REx-ID: 960 | OA
Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks
A.H. Hansen, C.F. Düllberg, C. Mieck, M. Loose, S. Hippenmeyer, Frontiers in Cellular Neuroscience 11 (2017).
View | Files available | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 1016
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability
M. Breuss, T. Nguyen, A. Srivatsan, I. Leca, G. Tian, T. Fritz, A.H. Hansen, D. Musaev, J. Mcevoy Venneri, J. Kiely, R. Rosti, E. Scott, U. Tan, R. Kolodner, N. Cowan, D. Keays, J. Gleeson, Human Molecular Genetics 26 (2017) 258–269.
View | DOI
 
[3]
2017 | Journal Article | IST-REx-ID: 1017 | OA
Tubulins and brain development: The origins of functional specification
M. Breuss, I. Leca, T. Gstrein, A.H. Hansen, D. Keays, Molecular and Cellular Neuroscience 84 (2017) 58–67.
View | Files available | DOI
 
[2]
2017 | Journal Article | IST-REx-ID: 1107 | OA
Brain specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition
M. Breuss, A.H. Hansen, L. Landler, D. Keays, Behavioural Brain Research 323 (2017) 47–55.
View | Files available | DOI
 
[1]
2015 | Journal Article | IST-REx-ID: 1106
Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type
M. Isrie, M. Breuss, G. Tian, A.H. Hansen, F. Cristofoli, J. Morandell, Z.A. Kupchinsky, A. Sifrim, C. Rodriguez Rodriguez, E.P. Dapena, K. Doonanco, N. Leonard, F. Tinsa, S. Moortgat, H. Ulucan, E. Koparir, E. Karaca, N. Katsanis, V. Marton, J.R. Vermeesch, E.E. Davis, N.J. Cowan, D. Keays, H. Van Esch, The American Journal of Human Genetics 97 (2015) 790–800.
View | DOI
 

Search

Filter Publications

11 Publications

Mark all

[11]
2020 | Journal Article | IST-REx-ID: 7815 | OA
Lineage tracing and clonal analysis in developing cerebral cortex using mosaic analysis with double markers (MADM)
R.J. Beattie, C. Streicher, N. Amberg, G.T. Cheung, X. Contreras, A.H. Hansen, S. Hippenmeyer, Journal of Visual Experiments (JoVE) (2020).
View | Files available | DOI
 
[10]
2020 | Preprint | IST-REx-ID: 8546 | OA
Generation of neuronal diversity from common progenitors via Notch signaling in the cerebellum
T. Zhang, T. Liu, N. Mora, J. Guegan, M. Bertrand, X. Contreras, A.H. Hansen, C. Streicher, M. Anderle, L. Tiberi, S. Hippenmeyer, B.A. Hassan, BioRxiv (n.d.).
View | DOI | Download Preprint (ext.)
 
[9]
2020 | Preprint | IST-REx-ID: 8545 | OA
A genome-wide library of MADM mice for single-cell genetic mosaic analysis
X. Contreras, A. Davaatseren, N. Amberg, A.H. Hansen, J. Sonntag, L. Andersen, T. Bernthaler, A.-M. Heger, R. Johnson, L.A. Schwarz, L. Luo, T. Rülicke, S. Hippenmeyer, BioRxiv (2020).
View | DOI | Download Preprint (ext.)
 
[8]
2020 | Journal Article | IST-REx-ID: 8569 | OA
Non-cell-autonomous mechanisms in radial projection neuron migration in the developing cerebral cortex
A.H. Hansen, S. Hippenmeyer, Frontiers in Cell and Developmental Biology 8 (2020).
View | Files available | DOI
 
[7]
2020 | Journal Article | IST-REx-ID: 8162 | OA
Cell-type specificity of genomic imprinting in cerebral cortex
S. Laukoter, F. Pauler, R.J. Beattie, N. Amberg, A.H. Hansen, C. Streicher, T. Penz, C. Bock, S. Hippenmeyer, Neuron 107 (n.d.) 1–20.
View | Files available | DOI | Download Published Version (ext.)
 
[6]
2018 | Journal Article | IST-REx-ID: 547
Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans
T. Gstrein, A. Edwards, A. Přistoupilová, I. Leca, M. Breuss, S. Pilat Carotta, A.H. Hansen, R. Tripathy, A. Traunbauer, T. Hochstoeger, G. Rosoklija, M. Repic, L. Landler, V. Stránecký, G. Dürnberger, T. Keane, J. Zuber, D. Adams, J. Flint, T. Honzik, M. Gut, S. Beltran, K. Mechtler, E. Sherr, S. Kmoch, I. Gut, D. Keays, Nature Neuroscience 21 (2018) 207–217.
View | DOI
 
[5]
2017 | Journal Article | IST-REx-ID: 960 | OA
Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks
A.H. Hansen, C.F. Düllberg, C. Mieck, M. Loose, S. Hippenmeyer, Frontiers in Cellular Neuroscience 11 (2017).
View | Files available | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 1016
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability
M. Breuss, T. Nguyen, A. Srivatsan, I. Leca, G. Tian, T. Fritz, A.H. Hansen, D. Musaev, J. Mcevoy Venneri, J. Kiely, R. Rosti, E. Scott, U. Tan, R. Kolodner, N. Cowan, D. Keays, J. Gleeson, Human Molecular Genetics 26 (2017) 258–269.
View | DOI
 
[3]
2017 | Journal Article | IST-REx-ID: 1017 | OA
Tubulins and brain development: The origins of functional specification
M. Breuss, I. Leca, T. Gstrein, A.H. Hansen, D. Keays, Molecular and Cellular Neuroscience 84 (2017) 58–67.
View | Files available | DOI
 
[2]
2017 | Journal Article | IST-REx-ID: 1107 | OA
Brain specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition
M. Breuss, A.H. Hansen, L. Landler, D. Keays, Behavioural Brain Research 323 (2017) 47–55.
View | Files available | DOI
 
[1]
2015 | Journal Article | IST-REx-ID: 1106
Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type
M. Isrie, M. Breuss, G. Tian, A.H. Hansen, F. Cristofoli, J. Morandell, Z.A. Kupchinsky, A. Sifrim, C. Rodriguez Rodriguez, E.P. Dapena, K. Doonanco, N. Leonard, F. Tinsa, S. Moortgat, H. Ulucan, E. Koparir, E. Karaca, N. Katsanis, V. Marton, J.R. Vermeesch, E.E. Davis, N.J. Cowan, D. Keays, H. Van Esch, The American Journal of Human Genetics 97 (2015) 790–800.
View | DOI
 

Search

Filter Publications