Niall Lennon

13PUBLICATIONS
227CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Major global burdens of diseasePredictive and prognostic markersGenomicsEpigenetics (incl. genome methylation and epigenomics)
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Publications (13)

|Oct 24, 2026
A 515,579-Genome Reference Panel Improves Rare-Variant Imputation Across Multiple Underrepresented Populations.

|Oct 10, 2026
Generalizability of proteomic risk prediction across biobanks reveals dependence on phenotype definitions.

|Sep 24, 2026
Genomic Research as a Critical Pathway to Diagnosis for Individuals with Rare Disease.

|Jul 08, 2026
A blended genome and exome sequencing method captures genetic variation in an unbiased and cost-effective manner.

|Jul 03, 2026
Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencing.

|Jan 26, 2026
Genomic risk model to implement precision prostate cancer screening in clinical care: the ProGRESS study.

Jason L Vassy, Anna M Dornisch, Roshan Karunamuni

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Frequent Collaborators

5 joint publications

Christopher Kachulis

4 joint publications

Michael E Talkowski

4 joint publications

Benjamin M Neale

3 joint publications

Robert Ye