Sara A Caylor - Rady Children's Institute for Genomic Medicine, Rady Children's Hospital

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论文共 12 篇作者统计合作学者相似作者

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P146: BeginNGS, an Artificial Intelligence-Enabled Genome Sequencing System for Newborn Screening of 409 Childhood Genetic Disorders*

Jennifer Schleit,Meredith Wright, Lauren Olsen, Eric Blincow,Sara Caylor,Christina Chambers,Guillermo del Angel,Katarzyna (Kasia) Ellsworth,Annette Feigenbaum,Erwin Frise,Lucia Guidugli,Kevin Hall,Christian Hansen,Charlotte Hobbs,Mark Kiel, Chad Krilow,Chris Kunard,YongHyun Kwon, Rao Madhavrao, Shyamal Mehtalia

Genetics in Medicine Open (2024): 101043

引用0浏览0引用

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,Joseph D. Fakhoury, Padmani Karna,April Lehman,Cristian I. Meghea,Vinod Misra,Danielle A. Nolan, Jessica O'Shea, Aditi Sharangpani,Linda S. Franck,Andrea Scheurer-Monaghan

Children (Basel)（2023）

引用4浏览0WOS引用

Response to Grosse Et Al

Stephen F Kingsmore,Laurie D Smith,Chris M Kunard,Matthew Bainbridge,Sergey Batalov,Wendy Benson, Eric Blincow,Sara Caylor,Christina Chambers,Guillermo Del Angel,David P Dimmock,Yan Ding,Katarzyna Ellsworth,Annette Feigenbaum,Erwin Frise,Robert C Green,Lucia Guidugli,Kevin P Hall,Christian Hansen,Charlotte A Hobbs, Scott D Kahn,Mark Kiel, Lucita Van Der Kraan, Chad Krilow,Yong H Kwon, Lakshminarasimha Madhavrao,Jennie Le,Sebastien Lefebvre,Rebecca Mardach, William R Mowrey, Danny Oh,Mallory J Owen, George Powley,Gunter Scharer, Seth Shelnutt,Mari Tokita, Shyamal S Mehtalia,Albert Oriol,Stavros Papadopoulos, James Perry,Edwin Rosales,Erica Sanford,Steve Schwartz, Duke Tran,Martin G Reese,Meredith Wright,Narayanan Veeraraghavan,Kristen Wigby,Mary J Willis,Aaron R Wolen,Thomas Defay

American journal of human geneticsno. 6 (2023): 1017-1017

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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,Cynthia Triplett,Michelle M. Clark,Stephen F. Kingsmore,Cinnamon S. Bloss

Clinical Therapeutics（2023）

引用1浏览0WOS引用

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,Wendy Benson, Eric Blincow,Sara Caylor,Christina Chambers,Guillermo Del Angel,David P. Dimmock,Yan Ding,Katarzyna Ellsworth,Annette Feigenbaum,Erwin Frise,Robert C. Green,Lucia Guidugli,Kevin P. Hall,Christian Hansen,Charlotte A. Hobbs, Scott D. Kahn,Mark Kiel, Lucita Van Der Kraan, Chad Krilow,Yong H. Kwon, Lakshminarasimha Madhavrao,Jennie Le,Sebastien Lefebvre,Rebecca Mardach, William R. Mowrey, Danny Oh,Mallory J. Owen, George Powley,Gunter Scharer, Seth Shelnutt,Mari Tokita, Shyamal S. Mehtalia,Albert Oriol,Stavros Papadopoulos,James Perry,Edwin Rosales,Erica Sanford,Steve Schwartz, Duke Tran,Martin G. Reese,Meredith Wright,Narayanan Veeraraghavan,Kristen Wigby,Mary J. Willis,Aaron R. Wolen,Thomas Defay

American journal of human genetics（2022）

引用39浏览0WOS引用

Rapid Whole Genome Sequencing Impacts Care and Resource Utilization in Infants with Congenital Heart Disease

Nathaly M. Sweeney,Shareef A. Nahas, Sh. Chowdhury,Sergey Batalov,Michelle Clark,Sara Caylor,Julie Cakici,John J. Nigro,Yan Ding,Narayanan Veeraraghavan,Charlotte Hobbs,David Dimmock,Stephen F. Kingsmore

npj Genomic Medicine（2021）

引用30浏览0WOS引用

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,Christina Clarke, Michele Feddock,Shimul Chowdhury,Lisa Salz,Cynthia Cheung,Lynne M. Bird,Charlotte Hobbs,Kristen Wigby,Lauge Farnaes,Cinnamon S. Bloss,Stephen F. Kingsmore

American journal of human genetics（2020）

引用98浏览0WOS引用

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,Cynthia Triplett,Michelle M. Clark,Stephen F. Kingsmore,Cinnamon S. Bloss

American journal of human geneticsno. 5 (2020): 953-962

引用60浏览0WOS引用

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