Author

David B. Rye

Emory University

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

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Organism:human· 2 Approach:statistical model· 2 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Aditya AmbatiiD· 2 shared Birgit HögliD· 2 shared Emmanuel Jean-Marie MignotiD· 2 shared Fabio PizzaiD· 2 shared Fang Han· 2 shared Geert MayeriD· 2 shared Giuseppe PlazziiD· 2 shared Hanna Maria OllilaiD· 2 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Aditya AmbatiORCID

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2 papers

Recent·Most cited

Kleine Levin syndrome is associated with birth difficulties and genetic variants in the TRANK1 gene loci.

Aditya Ambati, Ryan P. Hillary, Smaranda Leu‐Semenescu, Hanna Maria Ollila, Ling Lin, Emmanuel During, Neal M. Farber, Thomas J Rico, Juliette H. Faraco, Eileen B. Leary, Andrea N. Goldstein‐Piekarski, Yu‐Shu Huang, Fang Han, Yakov Sivan, Michel Lecendreux, , Emmanuel Jean-Marie Mignot

This study identifies a genetic association between Kleine-Levin Syndrome and variants in the TRANK1 gene, with increased risk linked to birth difficulties.

Proceedings of the National Academy of Sciences · Mar 18, 2021Peer-reviewedGenetic & Genomic Medicine

Narcolepsy risk loci are enriched in immune cells and suggest autoimmune modulation of the T cell receptor repertoire

Hanna Maria Ollila, Eilon Sharon, Ling Lin, Nasa Sinnott-Armstrong, Aditya Ambati, Ryan P. Hillary, Otto Jolanki, Juliette H. Faraco, Mali A. Einen, Guo Luo, Jing Zhang, Fang Han, Han Yan, Xiao Song Dong, Jing Li, , Emmanuel Jean-Marie Mignot

This study identifies genetic risk loci for narcolepsy, showing enrichment in immune cells and suggesting autoimmune modulation via T cell receptor chains and influenza-A infection.

bioRxiv · Jul 22, 2018 · PreprintGenetics