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Sebastian Guelfi

Showing results (1-10 of 22) with videos related to

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Neurogenetics|April 10, 2017
Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson's disease on chromosome 7p15.3Megha N Murthy, Cornelis Blauwendraat, , et al.
Nature Communications|April 28, 2022
Leveraging omic features with F3UTER enables identification of unannotated 3'UTRs for synaptic genesSiddharth Sethi, David Zhang, Sebastian Guelfi, et al.
BMC Systems Biology|April 14, 2017
An additional k-means clustering step improves the biological features of WGCNA gene co-expression networksJuan A Botía, Jana Vandrovcova, Paola Forabosco, et al.
Human Brain Mapping|June 20, 2020
Imaging genomics discovery of a new risk variant for Alzheimer's disease in the postsynaptic SHARPIN geneSourena Soheili-Nezhad, Neda Jahanshad, Sebastian Guelfi, et al.
Molecular Neurodegeneration|February 26, 2016
Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysisRaffaele Ferrari, Paola Forabosco, Jana Vandrovcova, et al.
Scientific Reports|August 24, 2023
Analysis of subcellular RNA fractions demonstrates significant genetic regulation of gene expression in human brain post-transcriptionallyKarishma D'Sa, Sebastian Guelfi, Jana Vandrovcova, et al.
JAMA Neurology|February 1, 2021
Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data SetsDemis A Kia, David Zhang, Sebastian Guelfi, et al.
Brain : a Journal of Neurology|April 2, 2019
Transcriptomic and genetic analyses reveal potential causal drivers for intractable partial epilepsySebastian Guelfi, Juan A Botia, Maria Thom, et al.
Nature Neuroscience|September 1, 2014
Genetic variability in the regulation of gene expression in ten regions of the human brainAdaikalavan Ramasamy, Daniah Trabzuni, Sebastian Guelfi, et al.
Science Advances|September 12, 2020
Incomplete annotation has a disproportionate impact on our understanding of Mendelian and complex neurogenetic disordersDavid Zhang, Sebastian Guelfi, Sonia Garcia-Ruiz, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Neurogenetics|April 10, 2017
Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson's disease on chromosome 7p15.3Megha N Murthy, Cornelis Blauwendraat, , et al.
Nature Communications|April 28, 2022
Leveraging omic features with F3UTER enables identification of unannotated 3'UTRs for synaptic genesSiddharth Sethi, David Zhang, Sebastian Guelfi, et al.
BMC Systems Biology|April 14, 2017
An additional k-means clustering step improves the biological features of WGCNA gene co-expression networksJuan A Botía, Jana Vandrovcova, Paola Forabosco, et al.
Human Brain Mapping|June 20, 2020
Imaging genomics discovery of a new risk variant for Alzheimer's disease in the postsynaptic SHARPIN geneSourena Soheili-Nezhad, Neda Jahanshad, Sebastian Guelfi, et al.
Molecular Neurodegeneration|February 26, 2016
Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysisRaffaele Ferrari, Paola Forabosco, Jana Vandrovcova, et al.
Scientific Reports|August 24, 2023
Analysis of subcellular RNA fractions demonstrates significant genetic regulation of gene expression in human brain post-transcriptionallyKarishma D'Sa, Sebastian Guelfi, Jana Vandrovcova, et al.
JAMA Neurology|February 1, 2021
Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data SetsDemis A Kia, David Zhang, Sebastian Guelfi, et al.
Brain : a Journal of Neurology|April 2, 2019
Transcriptomic and genetic analyses reveal potential causal drivers for intractable partial epilepsySebastian Guelfi, Juan A Botia, Maria Thom, et al.
Nature Neuroscience|September 1, 2014
Genetic variability in the regulation of gene expression in ten regions of the human brainAdaikalavan Ramasamy, Daniah Trabzuni, Sebastian Guelfi, et al.
Science Advances|September 12, 2020
Incomplete annotation has a disproportionate impact on our understanding of Mendelian and complex neurogenetic disordersDavid Zhang, Sebastian Guelfi, Sonia Garcia-Ruiz, et al.
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