Author

Nadia Dehghani

Van Andel InstituteORCID 0000-0002-0385-7267Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:GWAS summary statistics· 2 Research Focus:benchmarking· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

José BrásiD· 3 shared Rita João GuerreiroiD· 3 shared Afina Willemina LemstraiD· 1 shared Alberto LleóiD· 1 shared Andrew John LeesiD· 1 shared Andrew SingletoniD· 1 shared Anne BraaeiD· 1 shared Başar BılgıçiD· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

José BrásORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintFeb 13, 2023

Genetic analysis of VCP variants in a Turkish dementia cohort

Nadia Dehghani, Zeynep Tüfekçıoğlu, Gamze Güven…·José Brás

The paper screens a Turkish dementia cohort for VCP variants and identifies a missense variant associated with prodromal dementia with Lewy bodies.

DOI 10.1101/2023.02.13.23285395

humanwhole-exome sequencing

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GeneticsAlzheimer s & DementiaPeer-reviewedDec 1, 2020

How understudied populations have contributed to our understanding of Alzheimer's disease genetics

Nadia Dehghani, José Brás, Rita João Guerreiro

This study highlights how understudied populations have contributed to identifying genetic factors in Alzheimer's disease and compares SNP effects across populations.

1 citation

humanGWAS summary statistics

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NeuroscienceNeurobiology of DiseasePeer-reviewedApr 3, 2019

Heritability and genetic variance of dementia with Lewy bodies

Rita João Guerreiro, Valentina Escott‐Price, Dena G. Hernandez…·José Brás

This study estimates the heritability of dementia with Lewy bodies (DLB) and finds it to be higher than previous estimates, with low variance explained by polygenic risk scores from Parkinson's or Alzheimer's disease.

45 citationstop 4%

humanGWAS summary statistics

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