Author

Ryan Richholt

Translational Genomics Research Institute

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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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Matthew J. HuentelmaniD· 2 shared Ana M. ClaaseniD· 1 shared Ashley L. Siniard· 1 shared Brittany GeraldiD· 1 shared Catherine Cook KaczorowskiiD· 1 shared Chris BalakiD· 1 shared David Alan BennettiD· 1 shared David Wesley CraigiD· 1 shared

Activity by Year

2017-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenomics

Matthew J. HuentelmanORCID

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2 papers

Recent·Most cited

Complex genetic network underlying the convergent of Rett Syndrome like (RTT-L) phenotype in neurodevelopmental disorders

Eric Frankel, Julius Dodson, Megan Sharifi, Roshan Pillai, Keri M. Ramsey, Raj Gupta, Molly Brzezinski, Pooja Venugopal, Lorida Llaci, Brittany Gerald, Gabrielle Mills, Newell Belnap, Meredith Sanchez‐Castillo, Chris Balak, Ana M. Claasen, , Sampathkumar Rangasamy

The paper identifies genes associated with Rett syndrome-like (RTT-L) phenotype through whole exome sequencing and protein-protein interaction network analysis, revealing shared pathways with classical Rett syndrome.

bioRxiv · Jan 11, 2020 · PreprintGenomics

Systems genetics identifies modifiers of Alzheimer’s disease risk and resilience

Sarah M. Neuner, Timothy J. Hohman, Ryan Richholt, David Alan Bennett, Julie A. Schneider, Philip L. De Jager, Matthew J. Huentelman, Kristen M. S. O’Connell, Catherine Cook Kaczorowski

This study identifies genetic modifiers of Alzheimer’s disease using a humanized mouse model and finds Trpc3 as a novel therapeutic target.

bioRxiv · Nov 27, 2017 · PreprintGenetics