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Andrew E Timms

Showing results (31-40 of 47) with videos related to

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Nature Neuroscience|June 18, 2021
Spatial and cell type transcriptional landscape of human cerebellar developmentKimberly A Aldinger, Zachary Thomson, Ian G Phelps, et al.
Science (New York, N.Y.)|October 19, 2019
Spatiotemporal expansion of primary progenitor zones in the developing human cerebellumParthiv Haldipur, Kimberly A Aldinger, Silvia Bernardo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 20, 2018
Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephalyNataliya Di Donato, Andrew E Timms, Kimberly A Aldinger, et al.
Brain : a Journal of Neurology|March 31, 2022
Profiling PI3K-AKT-MTOR variants in focal brain malformations reveals new insights for diagnostic careFilomena Pirozzi, Matthew Berkseth, Rylee Shear, et al.
Acta Neuropathologica|August 4, 2021
Evidence of disrupted rhombic lip development in the pathogenesis of Dandy-Walker malformationParthiv Haldipur, Silvia Bernardo, Kimberly A Aldinger, et al.
American Journal of Human Genetics|March 5, 2016
Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous LipomatosisJames T Bennett, Tiong Yang Tan, Diana Alcantara, et al.
Brain : a Journal of Neurology|June 30, 2022
Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disordersNataliya Di Donato, Renzo Guerrini, Charles J Billington, et al.
The Lancet. Neurology|November 2, 2015
Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing studyGhayda M Mirzaa, Valerio Conti, Andrew E Timms, et al.
Nature Genetics|September 6, 2011
Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemiaChristopher N Hahn, Chan-Eng Chong, Catherine L Carmichael, et al.
Brain : a Journal of Neurology|October 4, 2017
Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephalyDiana Alcantara, Andrew E Timms, Karen Gripp, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Nature Neuroscience|June 18, 2021
Spatial and cell type transcriptional landscape of human cerebellar developmentKimberly A Aldinger, Zachary Thomson, Ian G Phelps, et al.
Science (New York, N.Y.)|October 19, 2019
Spatiotemporal expansion of primary progenitor zones in the developing human cerebellumParthiv Haldipur, Kimberly A Aldinger, Silvia Bernardo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 20, 2018
Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephalyNataliya Di Donato, Andrew E Timms, Kimberly A Aldinger, et al.
Brain : a Journal of Neurology|March 31, 2022
Profiling PI3K-AKT-MTOR variants in focal brain malformations reveals new insights for diagnostic careFilomena Pirozzi, Matthew Berkseth, Rylee Shear, et al.
Acta Neuropathologica|August 4, 2021
Evidence of disrupted rhombic lip development in the pathogenesis of Dandy-Walker malformationParthiv Haldipur, Silvia Bernardo, Kimberly A Aldinger, et al.
American Journal of Human Genetics|March 5, 2016
Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous LipomatosisJames T Bennett, Tiong Yang Tan, Diana Alcantara, et al.
Brain : a Journal of Neurology|June 30, 2022
Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disordersNataliya Di Donato, Renzo Guerrini, Charles J Billington, et al.
The Lancet. Neurology|November 2, 2015
Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing studyGhayda M Mirzaa, Valerio Conti, Andrew E Timms, et al.
Nature Genetics|September 6, 2011
Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemiaChristopher N Hahn, Chan-Eng Chong, Catherine L Carmichael, et al.
Brain : a Journal of Neurology|October 4, 2017
Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephalyDiana Alcantara, Andrew E Timms, Karen Gripp, et al.
Pageof 5