Author

Olivia Belbin

Universitat Autònoma de BarcelonaORCID 0000-0002-6109-6371Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 3 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 4 Research Focus:differential expression· 2 Research Focus:GWAS / association mapping· 2 Assay:whole-exome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Alberto LleóiD· 3 shared Juan ForteaiD· 3 shared Oriol Dols‐IcardoiD· 3 shared Itziar de RojasiD· 2 shared Jordi ClarimóniD· 2 shared Laura Molina‐PorceliD· 2 shared Marc HulsmaniD· 2 shared Afina Willemina LemstraiD· 1 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Alberto LleóORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 28, 2024

Exome analysis of 22,319 individuals links extremely rare CNVs and 22q11.21 dosage to Alzheimer's risk

Olivier Quenez, Catherine Schramm, Kévin Cassinari…·Betty Marije Tijms

The paper analyzes exome data from 22,319 individuals to identify rare CNVs and 22q11.21 dosage as risk factors for Alzheimer's disease.

DOI 10.1101/2024.10.28.24314051

humanwhole-exome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJun 21, 2024

A Novel Susceptibility Locus in NFASC Highlights Oligodendrocytes and Myelination in Progressive Supranuclear Palsy Pathology

Pablo García‐González, Héctor Rodrigo Lara, Yaroslau Compta…·Agustı́n Ruiz

The paper performs a GWAS on PSP in the Iberian population, replicates known risk variants, and identifies a novel locus in NFASC/CNTN2 associated with oligodendrocyte and myelination processes.

3 citations

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJul 12, 2022

Polygenic risk score analysis identifies deleterious protein-coding variants in novel immune pathway genes ATP8B4, FCGR1A, and LILRB1 that associate with Alzheimer's disease.

Joseph S. Reddy, Xue Wang, Mariet Allen…·Steven G. Younkin

The paper identifies three novel immune pathway genes with deleterious variants associated with Alzheimer's disease using polygenic risk scores in whole exome sequence data.

2 citations

humanwhole-exome sequencing

𝕏 PostBluesky

NeurosciencebioRxivPreprintFeb 7, 2020

Characterization of the motor cortex transcriptome supports microgial-related key events in amyotrophic lateral sclerosis

Oriol Dols‐Icardo, Víctor Montal, Sònia Sirisi…·Jordi Clarimón

The paper characterizes transcriptional changes in ALS motor cortex, identifying microglial activation and synapse-related pathway alterations as key features.

2 citations

humanbulk RNA-seq

𝕏 PostBluesky