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Showing results (741-750 of 809) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|March 22, 2023
Cross-ancestry, cell-type-informed atlas of gene, isoform, and splicing regulation in the developing human brainCindy Wen, Michael Margolis, Rujia Dai, et al.
Science (New York, N.Y.)|April 24, 2004
Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesisJoanna C Jen, Wai-Man Chan, Thomas M Bosley, et al.
Biorxiv : the Preprint Server for Biology|March 18, 2024
Deep sequencing of proteotoxicity modifier genes uncovers a Presenilin-2/beta-amyloid-actin genetic risk module shared among alpha-synucleinopathiesSumaiya Nazeen, Xinyuan Wang, Dina Zielinski, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 23, 2024
Psychotropic medication usage in sporadic versus genetic behavioral-variant frontotemporal dementiaJuan-Camilo Vargas-Gonzalez, Nico Dimal, Kasey Cortez, et al.
Neurology|July 5, 2022
Differences in Motor Features of <i>C9orf72</i>, <i>MAPT</i>, or <i>GRN</i> Variant Carriers With Familial Frontotemporal Lobar DegenerationPhilip Wade Tipton, Angela B Deutschlaender, Rodolfo Savica, et al.
Nature Genetics|May 5, 2015
Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate exportAndrea Legati, Donatella Giovannini, Gaël Nicolas, et al.
Neurology|December 24, 2010
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriersN Finch, M M Carrasquillo, M Baker, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 2012
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autismPatrícia B S Celestino-Soper, Sara Violante, Emily L Crawford, et al.
Medrxiv : the Preprint Server for Health Sciences|December 3, 2025
Common and rare variant genetic contributions in African Americans with autismMatilde Cirnigliaro, Jennifer K Lowe, Alexander O Flynn-Carroll, et al.
Nature|January 17, 2025
Brain-wide neuronal circuit connectome of human glioblastomaYusha Sun, Xin Wang, Daniel Y Zhang, et al.
Pageof 81

Showing results (741-750 of 809) with videos related to

Sort By:
Pageof 81
Medrxiv : the Preprint Server for Health Sciences|March 22, 2023
Cross-ancestry, cell-type-informed atlas of gene, isoform, and splicing regulation in the developing human brainCindy Wen, Michael Margolis, Rujia Dai, et al.
Science (New York, N.Y.)|April 24, 2004
Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesisJoanna C Jen, Wai-Man Chan, Thomas M Bosley, et al.
Biorxiv : the Preprint Server for Biology|March 18, 2024
Deep sequencing of proteotoxicity modifier genes uncovers a Presenilin-2/beta-amyloid-actin genetic risk module shared among alpha-synucleinopathiesSumaiya Nazeen, Xinyuan Wang, Dina Zielinski, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 23, 2024
Psychotropic medication usage in sporadic versus genetic behavioral-variant frontotemporal dementiaJuan-Camilo Vargas-Gonzalez, Nico Dimal, Kasey Cortez, et al.
Neurology|July 5, 2022
Differences in Motor Features of <i>C9orf72</i>, <i>MAPT</i>, or <i>GRN</i> Variant Carriers With Familial Frontotemporal Lobar DegenerationPhilip Wade Tipton, Angela B Deutschlaender, Rodolfo Savica, et al.
Nature Genetics|May 5, 2015
Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate exportAndrea Legati, Donatella Giovannini, Gaël Nicolas, et al.
Neurology|December 24, 2010
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriersN Finch, M M Carrasquillo, M Baker, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 2012
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autismPatrícia B S Celestino-Soper, Sara Violante, Emily L Crawford, et al.
Medrxiv : the Preprint Server for Health Sciences|December 3, 2025
Common and rare variant genetic contributions in African Americans with autismMatilde Cirnigliaro, Jennifer K Lowe, Alexander O Flynn-Carroll, et al.
Nature|January 17, 2025
Brain-wide neuronal circuit connectome of human glioblastomaYusha Sun, Xin Wang, Daniel Y Zhang, et al.
Pageof 81