Author

Ashley D. Cannon

University of Alabama at BirminghamORCID 0000-0002-2319-208XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Anna HurstiD· 2 shared Gregory M. CooperiD· 2 shared Stephanie A. FelkeriD· 2 shared Susan M. HiattiD· 2 shared Alexandre ReymondiD· 1 shared Alfredo BruscoiD· 1 shared Amanda G. NoyesiD· 1 shared Amanda Luedecke· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Anna HurstORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 29, 2022

Deleterious, protein-altering variants in the X-linked transcriptional coregulator ZMYM3 in 22 individuals with a neurodevelopmental delay phenotype

Susan M. Hiatt, Slavica Trajkova, Matteo Rossi Sebastiano…·Gregory M. Cooper

The paper identifies ZMYM3 variants in 22 individuals with neurodevelopmental delay, showing recurrent mutations, phenotypic overlap, and functional effects, supporting ZMYM3 as a novel NDD gene.

DOI 10.1101/2022.09.29.22279724

humanstatistical model

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Genetic & Genomic MedicinemedRxivPreprintAug 31, 2021

Genome sequencing as a first-line diagnostic test for hospitalized newborns

Kevin M. Bowling, Michelle L. Thompson, Candice R. Finnila…·Gregory M. Cooper

This study evaluates genome sequencing in hospitalized newborns, finding it more effective than standard care in identifying genetic diagnoses, especially in those with specific phenotypes.

1 citation

humanwhole-genome sequencing

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