Publications by authors named "Sara Caylor"

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Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselection.
Stephen F Kingsmore, Meredith Wright, Laurie D Smith, Yupu Liang, William R Mowrey, Sara Caylor

Am J Hum Genet· December 2024

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Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trial.
Stephen F Kingsmore, Meredith Wright, Lauren Olsen, Brandan Schultz, Liana Protopsaltis, Sara Caylor

Am J Hum Genet· December 2024

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Assessing Diversity in Newborn Genomic Sequencing Research Recruitment: Race/Ethnicity and Primary Spoken Language Variation in Eligibility, Enrollment, and Reasons for Declining.
Julie A Cakici, David Dimmock, Sara Caylor, Mary Gaughran, Christina Clarke

Clin Ther· August 2023

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Response to Grosse et al.
Stephen F Kingsmore, Laurie D Smith, Chris M Kunard, Matthew Bainbridge, Sergey Batalov, Sara Caylor

Am J Hum Genet· June 2023

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Breaking Barriers to Rapid Whole Genome Sequencing in Pediatrics: Michigan's Project Baby Deer.
Caleb P Bupp, Elizabeth G Ames, Madison K Arenchild, Sara Caylor, David P Dimmock

Children (Basel)· January 2023

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A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases.
Stephen F Kingsmore, Laurie D Smith, Chris M Kunard, Matthew Bainbridge, Sergey Batalov, Sara Caylor

Am J Hum Genet· September 2022

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Project Baby Bear: Rapid precision care incorporating rWGS in 5 California children's hospitals demonstrates improved clinical outcomes and reduced costs of care.
David Dimmock, Sara Caylor, Bryce Waldman, Wendy Benson, Christina Ashburner

Am J Hum Genet· July 2021

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Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease.
Nathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, Sergey Batalov, Michelle Clark, Sara Caylor

NPJ Genom Med· May 2021

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Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease.
Nathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, Sergey Batalov, Michelle Clark, Sara Caylor

NPJ Genom Med· May 2021

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Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease.
Nathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, Sergey Batalov, Michelle Clark, Sara Caylor

NPJ Genom Med· April 2021

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An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm.
David P Dimmock, Michelle M Clark, Mary Gaughran, Julie A Cakici, Sara A Caylor

Am J Hum Genet· November 2020

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A Prospective Study of Parental Perceptions of Rapid Whole-Genome and -Exome Sequencing among Seriously Ill Infants.
Julie A Cakici, David P Dimmock, Sara A Caylor, Mary Gaughran, Christina Clarke

Am J Hum Genet· November 2020

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A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants.
Stephen F Kingsmore, Julie A Cakici, Michelle M Clark, Mary Gaughran, Michele Feddock, Sara A Caylor

Am J Hum Genet· October 2019

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Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation.
Michelle M Clark, Amber Hildreth, Sergey Batalov, Yan Ding, Shimul Chowdhury, Sara A Caylor

Sci Transl Med· April 2019

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