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Daniel H Geschwind

Showing results (431-440 of 474) with videos related to

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Nature Communications|September 9, 2024
Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genesKurt Farrell, Jack Humphrey, Timothy Chang, et al.
Annals of Clinical and Translational Neurology|September 17, 2025
Functional Connectivity Associations With Markers of Disease Progression in GRN Pathogenic Variant CarriersTaru M Flagan, Stephanie A Chu, Suvi Häkkinen, et al.
Science (New York, N.Y.)|December 15, 2018
Integrative functional genomic analysis of human brain development and neuropsychiatric risksMingfeng Li, Gabriel Santpere, Yuka Imamura Kawasawa, et al.
Neurogenetics|January 22, 2013
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcificationSandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.
Neuron|September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk LociStephan J Sanders, Xin He, A Jeremy Willsey, et al.
Nature Genetics|May 13, 2008
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentLeanne M Dibbens, Patrick S Tarpey, Kim Hynes, et al.
Neurology|September 25, 2024
Gene-Specific Effects on Brain Volume and Cognition of <i>TMEM106B</i> in Frontotemporal Lobar DegenerationMarijne Vandebergh, Eliana Marisa Ramos, Nick Corriveau-Lecavalier, et al.
Nature|May 1, 2009
Common genetic variants on 5p14.1 associate with autism spectrum disordersKai Wang, Haitao Zhang, Deqiong Ma, et al.
Molecular Neurodegeneration|August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear PalsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Pageof 48

Showing results (431-440 of 474) with videos related to

Sort By:
Pageof 48
Nature Communications|September 9, 2024
Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genesKurt Farrell, Jack Humphrey, Timothy Chang, et al.
Annals of Clinical and Translational Neurology|September 17, 2025
Functional Connectivity Associations With Markers of Disease Progression in GRN Pathogenic Variant CarriersTaru M Flagan, Stephanie A Chu, Suvi Häkkinen, et al.
Science (New York, N.Y.)|December 15, 2018
Integrative functional genomic analysis of human brain development and neuropsychiatric risksMingfeng Li, Gabriel Santpere, Yuka Imamura Kawasawa, et al.
Neurogenetics|January 22, 2013
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcificationSandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.
Neuron|September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk LociStephan J Sanders, Xin He, A Jeremy Willsey, et al.
Nature Genetics|May 13, 2008
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentLeanne M Dibbens, Patrick S Tarpey, Kim Hynes, et al.
Neurology|September 25, 2024
Gene-Specific Effects on Brain Volume and Cognition of <i>TMEM106B</i> in Frontotemporal Lobar DegenerationMarijne Vandebergh, Eliana Marisa Ramos, Nick Corriveau-Lecavalier, et al.
Nature|May 1, 2009
Common genetic variants on 5p14.1 associate with autism spectrum disordersKai Wang, Haitao Zhang, Deqiong Ma, et al.
Molecular Neurodegeneration|August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear PalsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Pageof 48