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Author Details
Full Name
Brian M Schilder
Affiliation
UK Dementia Research Institute, Imperial College London
ORCID
Career Start Year
2014
Papers
17
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37250110
EpiCompare: R package for the comparison and quality control of epigenomic peak files.
Bioinform Adv
2023
37606627
Artificial intelligence for dementia genetics and omics.
Alzheimers Dement
2023
37768001
Artificial intelligence for neurodegenerative experimental models.
Alzheimers Dement
2023
37250110
EpiCompare: R package for the comparison and quality control of epigenomic peak files.
Bioinform Adv
2023
37606627
Artificial intelligence for dementia genetics and omics.
Alzheimers Dement
2023
37768001
Artificial intelligence for neurodegenerative experimental models.
Alzheimers Dement
2023
34529038
echolocatoR: an automated end-to-end statistical and functional genomic fine-mapping pipeline.
Bioinformatics
2022
34992268
Genetic analysis of the human microglial transcriptome across brain regions, aging and disease pathologies.
Nat Genet
2022
34617105
Fine-mapping of Parkinson's disease susceptibility loci identifies putative causal variants.
Hum Mol Genet
2022
34871738
Multi-omic insights into Parkinson's Disease: From genetic associations to functional mechanisms.
Neurobiol Dis
2022
34529038
echolocatoR: an automated end-to-end statistical and functional genomic fine-mapping pipeline.
Bioinformatics
2022
34992268
Genetic analysis of the human microglial transcriptome across brain regions, aging and disease pathologies.
Nat Genet
2022
34871738
Multi-omic insights into Parkinson's Disease: From genetic associations to functional mechanisms.
Neurobiol Dis
2022
34617105
Fine-mapping of Parkinson's disease susceptibility loci identifies putative causal variants.
Hum Mol Genet
2022
34027315
Phenome-wide and expression quantitative trait locus associations of coronavirus disease 2019 genetic risk loci.
iScience
2021
34002096
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.
Nat Genet
2021
34027315
Phenome-wide and expression quantitative trait locus associations of coronavirus disease 2019 genetic risk loci.
iScience
2021
35005630
Dysregulation of mitochondrial and proteolysosomal genes in Parkinson's disease myeloid cells.
Nat Aging
2021
35005630
Dysregulation of mitochondrial and proteolysosomal genes in Parkinson's disease myeloid cells.
Nat Aging
2021
34002096
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.
Nat Genet
2021
31756266
Evolutionary shifts dramatically reorganized the human hippocampal complex.
J Comp Neurol
2020
31756266
Evolutionary shifts dramatically reorganized the human hippocampal complex.
J Comp Neurol
2020
31114885
Geneshot: search engine for ranking genes from arbitrary text queries.
Nucleic Acids Res
2019
31677972
FAIRshake: Toolkit to Evaluate the FAIRness of Research Digital Resources.
Cell Syst
2019
31114885
Geneshot: search engine for ranking genes from arbitrary text queries.
Nucleic Acids Res
2019
31677972
FAIRshake: Toolkit to Evaluate the FAIRness of Research Digital Resources.
Cell Syst
2019
29800326
eXpression2Kinases (X2K) Web: linking expression signatures to upstream cell signaling networks.
Nucleic Acids Res
2018
29800326
eXpression2Kinases (X2K) Web: linking expression signatures to upstream cell signaling networks.
Nucleic Acids Res
2018
25545051
Becoming a high-fidelity - super - imitator: what are the contributions of social and individual learning?
Dev Sci
2015
25545051
Becoming a high-fidelity - super - imitator: what are the contributions of social and individual learning?
Dev Sci
2015
25835199
Take the monkey and run.
J Neurosci Methods
2015
25835199
Take the monkey and run.
J Neurosci Methods
2015
25161051
Working memory constraints on imitation and emulation.
J Exp Child Psychol
2014
25161051
Working memory constraints on imitation and emulation.
J Exp Child Psychol
2014
1 - 34 of 34
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Co-authored papers
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1
Markus M N??then
Institute of Human Genetics, University Hospital Bonn
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Center for Quantitative Health, Massachusetts General Hospital
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