Author

Ashley L. Siniard

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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Genomics· 2 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ignazio Stefano PirasiD· 3 shared Matt D. De BothiD· 3 shared Matthew J. HuentelmaniD· 3 shared Keri M. RamseyiD· 2 shared Marcus NaymikiD· 2 shared Wayne M. JepseniD· 2 shared Adrienne Henderson-SmithiD· 1 shared Alvaro Gonzalo HernandeziD· 1 shared

Activity by Year

2020-2020 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 34 mutual co-author links

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3 shared papersGenomics

Ignazio Stefano PirasORCID

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Author profile →

3 papers

Recent·Most cited

Association of common genetic variants in the CPSF7 and SDHAF2 genes with Canine Idiopathic Pulmonary Fibrosis in the West Highland White Terrier

Ignazio Stefano Piras, Christiane Bleul, Ashley L. Siniard, Amanda J. Wolfe, Matt D. De Both, Alvaro Gonzalo Hernandez, Matthew J. Huentelman

Genes · May 30, 2020Peer-reviewedGenomics

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

Adenosine triphosphate Binding Cassette subfamily C member 1 (ABCC1) overexpression reduces APP processing and increases alpha- versus beta-secretase activity, in vitro

Wayne M. Jepsen, Matt D. De Both, Ashley L. Siniard, Keri M. Ramsey, Ignazio Stefano Piras, Marcus Naymik, Adrienne Henderson-Smith, Matthew J. Huentelman

Biology Open · Jan 1, 2020Peer-reviewedMolecular Biology