Author

Oguzhan Atay

BillionToOne (United States)ORCID 0000-0002-7203-9575Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant calling· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Brian P. LandryiD· 2 shared David TsaoiD· 2 shared Vivien SheehaniD· 2 shared Akila SubramaniamiD· 1 shared Amy B. NguyeniD· 1 shared Brian D. AlfordiD· 1 shared Celeste K. KanneiD· 1 shared Devon B. Chandler-BrowniD· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Brian P. LandryORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Clinical validity of single-gene non-invasive prenatal testing for sickle cell disease and beta thalassemia

Erik R. Westin, David Tsao, Oguzhan Atay, Brian P. Landry, Patrick Peiyong Ye, Devon B. Chandler-Brown, Brian D. Alford, Jennifer M. Hoskovec, Akila Subramaniam, Kevin M. Pawlik, Spencer G. Kuper, Frederick D. Goldman, Tim M. Townes, Vivien Sheehan

This study validates a single-gene non-invasive prenatal test (NIPT) for sickle cell disease and beta thalassemia, showing 100% concordance with newborn screening in 79 pregnancies.

medRxiv · Sep 2, 2021 · PreprintGenetic & Genomic Medicine

A novel high-throughput molecular counting method with single base-pair resolution enables accurate single-gene NIPT

David Tsao, Sukrit Silas, Brian P. Landry, Nelda P. Itzep, Amy B. Nguyen, Samuel Greenberg, Celeste K. Kanne, Vivien Sheehan, Rani Sharma, Rahul Shukla, Prem N. Arora, Oguzhan Atay

This paper introduces a high-throughput molecular counting method with single base-pair resolution for accurate single-gene NIPT, achieving high sensitivity and specificity in detecting genetic disorders.

Scientific Reports · Oct 7, 2019Peer-reviewedGenetics