Author

Sushma Narayan

Albert Einstein College of Medicine

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Neuroscience· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:differential expression· 2 Assay:proteomics· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Roy N. AlcalayiD· 2 shared Alex DésautelsiD· 1 shared Alison P. Joyce· 1 shared Bin ZhangiD· 1 shared Caitlin M. Kehoe· 1 shared Carlos Cabrera· 1 shared Cheryl WatersiD· 1 shared Chris GaiteriiD· 1 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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2 shared papersNeuroscience

Roy N. AlcalayORCID

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3 papers

Recent·Most cited

Human brain aging heterogeneity observed from multi-region omics data reveals a subtype closely related to Alzheimer's disease

Shouneng Peng, Erming Wang, Minghui Wang, Xusheng Wang, Kaiwen Yu, Yingxue Fu, Suresh Poudel, Lap Ho, Sushma Narayan, Derek M. Huffman, Chris Gaiteri, David A. Bennet, Michelle E. Ehrlich, Vahram H. Haroutunian, Junmin Peng, , Zhidong Tu

The paper identifies an AD-like subtype in brain aging across multiple regions, showing overlap with AD gene signatures and regional differences in gene expression.

bioRxiv · Mar 1, 2024 · PreprintNeuroscience

An assessment of LRRK2 serine 935 phosphorylation in human peripheral blood mononuclear cells in idiopathic Parkinson’s disease and G2019S LRRK2 cohorts

Shalini Padmanabhan, Thomas A. Lanz, Donal N. Gorman, Michele Wolfe, Alison P. Joyce, Carlos Cabrera, Rosemary F. Lawrence-Henderson, Najah Levers, Neal Joshi, Thong Chi Ma, Christopher Liong, Sushma Narayan, Roy N. Alcalay, Samantha J. Hutten, Marco A. S. Baptista, Kalpana Merchant

The paper assesses pS935 LRRK2 levels in PBMCs of iPD and G2019S LRRK2 carriers, finding reduced levels in G2019S carriers with PD compared to those without PD or iPD.

Journal of Parkinson s Disease · Jan 28, 2020Peer-reviewedNeuroscience

Analysis of common and rare VPS13C variants in late onset Parkinson disease

Uladzislau Rudakou, Jennifer A. Ruskey, Lynne Krohn, Sandra B. Laurent, Dan Spiegelman, Lior Greenbaum, Gilad Yahalom, Alex Désautels, Jacques Yves Montplaisir, Stanley Fahn, Cheryl Waters, Oren Levy, Caitlin M. Kehoe, Sushma Narayan, Yves A Dauvilliers, , Ziv Gan‐Or

The paper investigates the role of VPS13C variants in late-onset Parkinson disease, finding no significant association with rare variants but a nominal association with a haplotype.

Neurology Genetics · Jan 9, 2020Peer-reviewedGenetics