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Showing results (611-620 of 809) with videos related to

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Frontiers in Neuroscience|December 5, 2022
Linear discriminant analysis of phenotypic data for classifying autism spectrum disorder by diagnosis and sexZachary Jacokes, Allison Jack, Catherine A W Sullivan, et al.
Plos One|February 27, 2009
Association and mutation analyses of 16p11.2 autism candidate genesRavinesh A Kumar, Christian R Marshall, Judith A Badner, et al.
Elife|December 14, 2022
The injured sciatic nerve atlas (iSNAT), insights into the cellular and molecular basis of neural tissue degeneration and regenerationXiao-Feng Zhao, Lucas D Huffman, Hannah Hafner, et al.
Nature Genetics|June 2, 2022
Genetic correlates of phenotypic heterogeneity in autismVarun Warrier, Xinhe Zhang, Patrick Reed, et al.
Nature Genetics|April 11, 2018
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insightsAlexander Gusev, Nicholas Mancuso, Hyejung Won, et al.
Nature Communications|June 26, 2021
Conservation and divergence of vulnerability and responses to stressors between human and mouse astrocytesJiwen Li, Lin Pan, William G Pembroke, et al.
Human Molecular Genetics|April 25, 2014
Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2Brent L Fogel, Ellen Cho, Amanda Wahnich, et al.
Neuron|July 4, 2014
A quantitative framework to evaluate modeling of cortical development by neural stem cellsJason L Stein, Luis de la Torre-Ubieta, Yuan Tian, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17L N Clark, P Poorkaj, Z Wszolek, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 2, 2015
Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonismStanley B Prusiner, Amanda L Woerman, Daniel A Mordes, et al.
Pageof 81

Showing results (611-620 of 809) with videos related to

Sort By:
Pageof 81
Frontiers in Neuroscience|December 5, 2022
Linear discriminant analysis of phenotypic data for classifying autism spectrum disorder by diagnosis and sexZachary Jacokes, Allison Jack, Catherine A W Sullivan, et al.
Plos One|February 27, 2009
Association and mutation analyses of 16p11.2 autism candidate genesRavinesh A Kumar, Christian R Marshall, Judith A Badner, et al.
Elife|December 14, 2022
The injured sciatic nerve atlas (iSNAT), insights into the cellular and molecular basis of neural tissue degeneration and regenerationXiao-Feng Zhao, Lucas D Huffman, Hannah Hafner, et al.
Nature Genetics|June 2, 2022
Genetic correlates of phenotypic heterogeneity in autismVarun Warrier, Xinhe Zhang, Patrick Reed, et al.
Nature Genetics|April 11, 2018
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insightsAlexander Gusev, Nicholas Mancuso, Hyejung Won, et al.
Nature Communications|June 26, 2021
Conservation and divergence of vulnerability and responses to stressors between human and mouse astrocytesJiwen Li, Lin Pan, William G Pembroke, et al.
Human Molecular Genetics|April 25, 2014
Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2Brent L Fogel, Ellen Cho, Amanda Wahnich, et al.
Neuron|July 4, 2014
A quantitative framework to evaluate modeling of cortical development by neural stem cellsJason L Stein, Luis de la Torre-Ubieta, Yuan Tian, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17L N Clark, P Poorkaj, Z Wszolek, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 2, 2015
Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonismStanley B Prusiner, Amanda L Woerman, Daniel A Mordes, et al.
Pageof 81