Author

Paul Nyquist

Johns Hopkins UniversityORCID 0000-0001-6078-3543Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genomics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 4 Organism:human· 4 Approach:statistical model· 4 Assay:GWAS summary statistics· 2 Assay:whole-genome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:fine-mapping· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Alexa BeiseriD· 3 shared Charles S DeCarliiD· 3 shared Claudia Liliana SatizábaliD· 3 shared Lisa R. YanekiD· 3 shared Myriam FornageiD· 3 shared Sudha S. SeshadriiD· 3 shared Albert V. SmithiD· 2 shared Aniket MishraiD· 2 shared

Activity by Year

2019-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Alexa BeiserORCID

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Author profile →

4 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJun 11, 2025

The Ethnic/Racial Variations of Intracerebral Hemorrhage Genetics (ERICH-GENE) Study Protocol

Guido J. Falcone, Stacey Q Wolfe, Marialuisa Zedde…·the ERICH-Gene Investigators

ERICH-GENE collects and analyzes genomic and neuroimaging data from over 10,000 multi-ethnic ICH cases to identify genetic risk factors and trans-ethnic variation in ICH.

1 citation

humanwhole-genome sequencing

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Genetic & Genomic MedicinemedRxivPreprintJun 11, 2025

Whole genome sequence association analysis of brain structural volume measures in the NHLBI TOPMed Program highlights novel loci in diverse participants

Lincoln M. P. Shade, Mohsen Sharifitabar, Alexa Beiser…·Chloé Sarnowski

This study uses whole-genome sequence data from diverse participants to identify novel genetic loci associated with brain structural volumes, highlighting the importance of diverse cohorts in uncovering genetic architecture.

DOI 10.1101/2025.06.11.25329426

humanwhole-genome sequencing

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GenomicsCell Reports MedicinePeer-reviewedMay 1, 2024

Genetic variants for head size share genes and pathways with cancer

Maria J. Knol, Raymond A. Poot, Tavia E. Evans…·Saud Alhusaini

This study identifies 67 genetic loci associated with head size, finding strong overlaps with cancer pathways and genes, suggesting shared genetic mechanisms between head growth and cancer risk.

10 citations

humanGWAS summary statistics

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NeurosciencebioRxivPreprintJun 27, 2019

Common genetic variation indicates separate etiologies for periventricular and deep white matter hyperintensities

Nicola J. Armstrong, Karen A. Mather, Muralidharan Sargurupremraj…·Paul Nyquist

This study identifies genetic loci specific to periventricular and deep white matter hyperintensities, revealing distinct genetic architectures and potential biological mechanisms.

1 citation

humanGWAS summary statistics

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