Author

Cheryl L. Maslen

Oregon Health & Science UniversityORCID 0000-0003-3976-6284Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Benjamin L. Rambo‐MartiniD· 1 shared Clifford L. CuaiD· 1 shared David J. CutleriD· 1 shared George T. CaponeiD· 1 shared Jennifer Gladys MulleiD· 1 shared Kenneth J. Dooley· 1 shared Lora Jh BeaniD· 1 shared Michael E. ZwickiD· 1 shared

Activity by Year

2017-2017 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Benjamin L. Rambo‐MartinORCID

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1 paper

Recent·Most cited

GenomicsG3 Genes Genomes GeneticsPeer-reviewedNov 15, 2017

Analysis of copy number variants on chromosome 21 in Down syndrome-associated congenital heart defects

Benjamin L. Rambo‐Martin, Jennifer Gladys Mulle, David J. Cutler…·Michael E. Zwick

This study investigates the association between copy number variants on chromosome 21 and congenital heart defects in Down syndrome, finding no direct link but suggesting ethnic differences in CNV patterns.

21 citations

humanwhole-genome sequencing

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