Author

Eric Frankel

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.

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Genomics· 1

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Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Ana M. ClaaseniD· 1 shared Ashley L. Siniard· 1 shared Brittany GeraldiD· 1 shared Chris BalakiD· 1 shared David Wesley CraigiD· 1 shared Gabrielle Mills· 1 shared Ignazio Stefano PirasiD· 1 shared Isabelle SchrauweniD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Ana M. ClaasenORCID

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1 paper

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