Author

Talia S. Schwartz

Boston Children's HospitalORCID 0000-0001-5339-4451Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Alan H. BeggsiD· 1 shared Amy L. McGuireiD· 1 shared Bethany ZettleriD· 1 shared Casie A. GenettiiD· 1 shared Heidi L. RehmiD· 1 shared Ingrid A. HolmiD· 1 shared Kurt Derek ChristenseniD· 1 shared Matthew S. LeboiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alan H. BeggsORCID

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1 paper

Recent·Most cited

Medical Evaluation of Unanticipated Monogenic Disease Risks Identified through Newborn Genomic Screening: Findings from the BabySeq Project

Robert C. Green, Nidhi D Shah, Casie A. Genetti, Timothy W. Yu, Bethany Zettler, Talia S. Schwartz, Melissa Kurtz Uveges, Ozge Ceyhan‐Birsoy, Matthew S. Lebo, Stacey Pereira, Pankaj B. Agrawal, Richard B. Parad, Amy L. McGuire, Kurt Derek Christensen, Heidi L. Rehm, , the BabySeq Project

The paper evaluates unanticipated monogenic disease risks found in newborns through genomic screening, finding most risks are actionable and lead to medical interventions.

medRxiv · Mar 18, 2022 · PreprintGenetic & Genomic Medicine