Author

Gabrielle Mills

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 Eric Frankel· 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

GenomicsbioRxivPreprintJan 11, 2020

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

Eric Frankel, Julius Dodson, Megan Sharifi…·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.

DOI 10.1101/2020.01.11.899658

humanwhole-exome sequencing

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