11 Publications

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[11]
2020 | Journal Article | IST-REx-ID: 7815 | OA
Beattie RJ, Streicher C, Amberg N, Cheung GT, Contreras X, Hansen AH, 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).
View | Files available | DOI
 
[10]
2020 | Preprint | IST-REx-ID: 8546 | OA
Zhang T, Liu T, Mora N, Guegan J, Bertrand M, Contreras X, Hansen AH, Streicher C, Anderle M, Tiberi L, Hippenmeyer S, Hassan BA. Generation of neuronal diversity from common progenitors via Notch signaling in the cerebellum. bioRxiv.
View | DOI | Download Preprint (ext.)
 
[9]
2020 | Preprint | IST-REx-ID: 8545 | OA
Contreras X, Davaatseren A, Amberg N, Hansen AH, Sonntag J, Andersen L, Bernthaler T, Heger A-M, Johnson R, Schwarz LA, Luo L, Rülicke T, Hippenmeyer S. 2020. A genome-wide library of MADM mice for single-cell genetic mosaic analysis. bioRxiv.
View | DOI | Download Preprint (ext.)
 
[8]
2020 | Journal Article | IST-REx-ID: 8569 | OA
Hansen AH, 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).
View | Files available | DOI | PubMed | Europe PMC
 
[7]
2020 | Journal Article | IST-REx-ID: 8162 | OA
Laukoter S, Pauler F, Beattie RJ, Amberg N, Hansen AH, Streicher C, Penz T, Bock C, Hippenmeyer S. 2020. Cell-type specificity of genomic imprinting in cerebral cortex. Neuron. 107(6), 1160–1179.e9.
View | Files available | DOI
 
[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
 
[5]
2017 | Journal Article | IST-REx-ID: 960 | OA
Hansen AH, Düllberg CF, Mieck C, Loose M, Hippenmeyer S. 2017. Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks. Frontiers in Cellular Neuroscience. 11.
View | Files available | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 1016
Breuss M, Nguyen T, Srivatsan A, Leca I, Tian G, Fritz T, Hansen AH, Musaev D, Mcevoy Venneri J, Kiely J, Rosti R, Scott E, Tan U, Kolodner R, Cowan N, Keays D, Gleeson J. 2017. Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability. Human Molecular Genetics. 26(2), 258–269.
View | DOI
 
[3]
2017 | Journal Article | IST-REx-ID: 1017 | OA
Breuss M, Leca I, Gstrein T, Hansen AH, Keays D. 2017. Tubulins and brain development: The origins of functional specification. Molecular and Cellular Neuroscience. 84, 58–67.
View | Files available | DOI
 
[2]
2017 | Journal Article | IST-REx-ID: 1107 | OA
Breuss M, Hansen AH, 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.
View | Files available | DOI
 
[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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11 Publications

Mark all

[11]
2020 | Journal Article | IST-REx-ID: 7815 | OA
Beattie RJ, Streicher C, Amberg N, Cheung GT, Contreras X, Hansen AH, 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).
View | Files available | DOI
 
[10]
2020 | Preprint | IST-REx-ID: 8546 | OA
Zhang T, Liu T, Mora N, Guegan J, Bertrand M, Contreras X, Hansen AH, Streicher C, Anderle M, Tiberi L, Hippenmeyer S, Hassan BA. Generation of neuronal diversity from common progenitors via Notch signaling in the cerebellum. bioRxiv.
View | DOI | Download Preprint (ext.)
 
[9]
2020 | Preprint | IST-REx-ID: 8545 | OA
Contreras X, Davaatseren A, Amberg N, Hansen AH, Sonntag J, Andersen L, Bernthaler T, Heger A-M, Johnson R, Schwarz LA, Luo L, Rülicke T, Hippenmeyer S. 2020. A genome-wide library of MADM mice for single-cell genetic mosaic analysis. bioRxiv.
View | DOI | Download Preprint (ext.)
 
[8]
2020 | Journal Article | IST-REx-ID: 8569 | OA
Hansen AH, 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).
View | Files available | DOI | PubMed | Europe PMC
 
[7]
2020 | Journal Article | IST-REx-ID: 8162 | OA
Laukoter S, Pauler F, Beattie RJ, Amberg N, Hansen AH, Streicher C, Penz T, Bock C, Hippenmeyer S. 2020. Cell-type specificity of genomic imprinting in cerebral cortex. Neuron. 107(6), 1160–1179.e9.
View | Files available | DOI
 
[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
 
[5]
2017 | Journal Article | IST-REx-ID: 960 | OA
Hansen AH, Düllberg CF, Mieck C, Loose M, Hippenmeyer S. 2017. Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks. Frontiers in Cellular Neuroscience. 11.
View | Files available | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 1016
Breuss M, Nguyen T, Srivatsan A, Leca I, Tian G, Fritz T, Hansen AH, Musaev D, Mcevoy Venneri J, Kiely J, Rosti R, Scott E, Tan U, Kolodner R, Cowan N, Keays D, Gleeson J. 2017. Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability. Human Molecular Genetics. 26(2), 258–269.
View | DOI
 
[3]
2017 | Journal Article | IST-REx-ID: 1017 | OA
Breuss M, Leca I, Gstrein T, Hansen AH, Keays D. 2017. Tubulins and brain development: The origins of functional specification. Molecular and Cellular Neuroscience. 84, 58–67.
View | Files available | DOI
 
[2]
2017 | Journal Article | IST-REx-ID: 1107 | OA
Breuss M, Hansen AH, 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.
View | Files available | DOI
 
[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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