Author

Ravi Duggirala

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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Genetic & Genomic Medicine· 1 Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:whole-genome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1

Frequent Co-Authors

John BlangeroiD· 3 shared Joanne E. CurraniD· 2 shared Adel El Boueiz· 1 shared Ahmad R. HaririiD· 1 shared Allison Ashley-Koch· 1 shared Allison E. Ashley‐KochiD· 1 shared Álvaro AlonsoiD· 1 shared Amber Beitelshees· 1 shared

Activity by Year

2015-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 23 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

John BlangeroORCID

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Author profile →

3 papers

Recent·Most cited

Local ancestry-aware genome-wide meta-analysis uncovers novel genetic loci for sickle cell disease nephropathy

Melanie E. Garrett, Seyed Mehdi Nouraie, Roberto F. Machado, Victor R. Gordeuk, Mark T. Gladwin, Marilyn J. Telen, Allison E. Ashley‐Koch, Gonçalo Abecasis, François Aguet, Christine Albert, Laura Almasy, Álvaro Alonso, Seth Ament, Peter Anderson, Pramod Anugu, , Mao Fu

This paper performs a local ancestry-aware GWAS on SCD cohorts to identify novel genetic loci associated with eGFR, uncovering regions linked to inflammation, ECM integrity, and other pathways relevant to SCD nephropathy.

Blood Advances · Aug 19, 2026Peer-reviewedGenetic & Genomic Medicine

Do Candidate Genes Affect the Brain’s White Matter Microstructure? Large-Scale Evaluation of 6,165 Diffusion MRI Scans

Neda Jahanshad, Habib Ganjgahi, Janita Bralten, Anouk den Braber, Joshua Faskowitz, Annchen R. Knodt, Hervé Lemaître, Talia M. Nir, Binish Patel, Stuart Richie, Emma Sprooten, Martine Hoogman, Kimm J. E. van Hulzen, Artemis Zavaliangos‐Petropulu, Marcel P. Zwiers, , Peter V Kochunov

The paper evaluates 15 candidate SNPs associated with psychiatric disorders using 6,165 diffusion MRI scans, finding no significant associations after correction for multiple testing.

bioRxiv · Feb 20, 2017 · PreprintNeuroscience

Non-crossover gene conversions show strong GC bias and unexpected clustering in humans

Amy L. Williams, Giulio Geneovese, Thomas Dyer, Nicolas Altemose, Katherine Truax, Goo Jun, Nick Patterson, Simon R. Myers, Joanne E. Curran, Ravi Duggirala, John Blangero, David Reich, Molly Przeworski, the T2D-GENES Consortium

The paper identifies and analyzes non-crossover gene conversion events in humans, finding strong GC bias and unexpected clustering of conversion tracts.

bioRxiv · Jan 8, 2015Genetics