Author

Kelly Nicole Holohan Nudelman

Indiana University IndianapolisORCID 0000-0003-4040-1717Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:cell type annotation· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Assay:imaging· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Tatiana ForoudiD· 2 shared Alzheimer’s Disease Neuroimaging Initiative· 1 shared Andrew J. SaykiniD· 1 shared Andrew SingletoniD· 1 shared Bradford Clark DickersoniD· 1 shared Brenna C. McDonaldiD· 1 shared Brent J. SmalliD· 1 shared Claire Wegel· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Tatiana ForoudORCID

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3 papers

Recent·Most cited

NeurosciencebioRxivPreprintJun 23, 2026

Characterisation of Posterior Predominant Amyloid PET Binding Across Multiple Cohorts

Joseph Giorgio, Ganna Blazhenets, Susan M. Landau…·Alzheimer’s Disease Neuroimaging Initiative

This paper identifies a posterior predominant amyloid PET binding pattern in multiple cohorts, showing its clinical and biological relevance and suggesting the need for more nuanced analysis methods.

1 citation

𝕏 PostBluesky

Genetic & Genomic MedicineCancersPeer-reviewedMay 23, 2023

Genetic variants associated with longitudinal cognitive performance in older breast cancer patients and controls

Kelly Nicole Holohan Nudelman, Kwangsik T. Nho, Michael Zhang…·the Thinking and Living with Cancer (TLC) Study

This study identifies genetic variants associated with cognitive decline in older breast cancer patients compared to controls using longitudinal cognitive data.

4 citations

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintMar 21, 2022

Dystonia-Parkinsonism Gene Variants in Individuals with Parkinsonism and Brain Scans without Evidence for Dopaminergic Deficit (SWEDD)

Kelly Nicole Holohan Nudelman, Yajing Yan Yan Xiong, Lola P. Cook…·The Parkinson’s Progression Markers Initiative

This study identifies pathogenic variants in dystonia-parkinsonism genes in 12.5% of SWEDD cases in the PPMI cohort, highlighting the importance of genetic testing in this patient group.

1 citation

humanwhole-genome sequencing

𝕏 PostBluesky