Author

Adaikalavan Ramasamy

Agency for Science, Technology and ResearchORCID 0000-0002-7598-2892Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 3 Systems Biology· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 4 Research Focus:gene regulatory network inference· 3 Organism:human· 3 Research Focus:differential expression· 2 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1

Frequent Co-Authors

John HardyiD· 3 shared Agustı́n RuiziD· 2 shared Alberto LleóiD· 2 shared Alessandro PadovaniiD· 2 shared Anders Martin DaleiD· 2 shared Barbara BorroniiD· 2 shared Bruce L. MilleriD· 2 shared Carlos CruchagaiD· 2 shared

Activity by Year

2018-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetics

John HardyORCID

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Author profile →

4 papers

Recent·Most cited

Systems BiologybioRxivPreprintApr 23, 2021

Developmental and Intergenerational Landscape of Human Circulatory Lipidome and its Association with Obesity Risk

Sartaj Ahmad Mir, Li Chen, Satvika Burugupalli…·Neerja Karnani

The paper maps the developmental and intergenerational changes in the human circulatory lipidome and identifies lipid signatures associated with obesity risk in mothers and offspring.

2 citations

humanmetabolomics

𝕏 PostBluesky

GeneticsBrainPeer-reviewedJun 17, 2020

Transcriptomic analysis of dystonia-associated genes reveals functional convergence within specific cell types and shared neurobiology with psychiatric disorders

Niccolò Emanuele Mencacci, Regina Hertfelder Reynolds, Sonia García-Ruiz…·Caleb Webber

This study identifies cell-type-specific expression of dystonia-associated genes and links them to shared genetic and biological mechanisms with psychiatric disorders.

64 citationstop 3%

mousebulk RNA-seq

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GeneticsTranslational PsychiatryPeer-reviewedApr 11, 2018

CXCR4 involvement in neurodegenerative diseases

Luke W. Bonham, Celeste M M. Karch, Chun Chieh Fan…·Murray Grossman

The paper identifies a genetic variant near CXCR4 associated with increased risk for PSP and PD, showing dysregulation of CXCR4 and microglia-related genes in neurodegenerative diseases.

95 citationstop 5%

humanGWAS summary statistics

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GeneticsPLoS MedicinePeer-reviewedJan 9, 2018

Immune-related genetic enrichment in frontotemporal dementia

Iris Broce, Celeste M M. Karch, Natalie Wen…·John Collinge

This study identifies genetic overlaps between frontotemporal dementia and immune-mediated diseases, finding strong enrichment with rheumatoid arthritis and moderate enrichment with other immune conditions.

184 citationstop 1%

humanGWAS summary statistics

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