Author

Javad Nadaf

McGill Genome CentreORCID 0000-0001-9393-810XUnclaimed ORCID profile · follow to get notified of new preprints

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Javad Nadaf1 paper

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Assay:scRNA-seq· 1 Research Focus:trajectory inference· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alexandre PratiD· 1 shared Andriniaina Andy Nkili-Meyong· 1 shared Anne‐Marie Mes‐MassoniD· 1 shared Annisa Djedid· 1 shared Caitlin T. FierhelleriD· 1 shared Celia M.T. GreenwoodiD· 1 shared Corinne Serruya· 1 shared Deepak SubramanianiD· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperNeuroscience

Alexandre PratORCID

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2 papers

Recent·Most cited

NeuroscienceiSciencePeer-reviewedFeb 26, 2024

Identity and Nature of Neural Stem Cells in the Adult Human Subventricular Zone

Salma Baig, Javad Nadaf, Redouane Allache…·Kevin Petrecca

This study creates a cell atlas of the adult human subventricular zone using single-cell transcriptomics, identifying multipotent neural stem cells and their lineage potential.

27 citationstop 4%

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Genetic & Genomic MedicineGenome MedicinePeer-reviewedDec 1, 2021

The genetic analysis of a founder Northern American population of European descent identifies FANCI as a candidate familial ovarian cancer risk gene

Caitlin T. Fierheller, Laure Guitton-Sert, Wejdan M. Alenezi…·Patricia N. Tonin

This paper identifies FANCI c.1813C>T as a candidate familial ovarian cancer risk allele in a French Canadian population with founder effects.

23 citations

humanwhole-exome sequencing

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