O18: BabyFORce: A pioneering program translating variants identified via rapid genome sequencing to targeted therapeutics for neonatal intensive care unit patients

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Main Authors: Whitney Thompson, Christopher Schmitz, Filippo Pinto e Vairo, Andrew Haak, Brandi Smith, Eric Klee, Christopher Colby, Lisa Schimmenti, Christopher Moxham, Natalie Downs, Nicole Perfito, Laura Lambert
Format: Article
Language:English
Published: Elsevier 2025-01-01
Series:Genetics in Medicine Open
Online Access:http://www.sciencedirect.com/science/article/pii/S2949774425001335
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author Whitney Thompson
Christopher Schmitz
Filippo Pinto e Vairo
Andrew Haak
Brandi Smith
Eric Klee
Christopher Colby
Lisa Schimmenti
Christopher Moxham
Natalie Downs
Nicole Perfito
Laura Lambert
author_facet Whitney Thompson
Christopher Schmitz
Filippo Pinto e Vairo
Andrew Haak
Brandi Smith
Eric Klee
Christopher Colby
Lisa Schimmenti
Christopher Moxham
Natalie Downs
Nicole Perfito
Laura Lambert
author_sort Whitney Thompson
collection DOAJ
format Article
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institution OA Journals
issn 2949-7744
language English
publishDate 2025-01-01
publisher Elsevier
record_format Article
series Genetics in Medicine Open
spelling doaj-art-2b5bf8071cab45ed948443fe5535850a2025-08-20T02:19:22ZengElsevierGenetics in Medicine Open2949-77442025-01-01310209410.1016/j.gimo.2025.102094O18: BabyFORce: A pioneering program translating variants identified via rapid genome sequencing to targeted therapeutics for neonatal intensive care unit patientsWhitney Thompson0Christopher Schmitz1Filippo Pinto e Vairo2Andrew Haak3Brandi Smith4Eric Klee5Christopher Colby6Lisa Schimmenti7Christopher Moxham8Natalie Downs9Nicole Perfito10Laura Lambert11Mayo ClinicMayo ClinicMayo ClinicMayo ClinicMayo ClinicMayo ClinicMayo ClinicMayo ClinicTranscriptaBioTranscriptaBioTranscriptaBioMayo Clinichttp://www.sciencedirect.com/science/article/pii/S2949774425001335
spellingShingle Whitney Thompson
Christopher Schmitz
Filippo Pinto e Vairo
Andrew Haak
Brandi Smith
Eric Klee
Christopher Colby
Lisa Schimmenti
Christopher Moxham
Natalie Downs
Nicole Perfito
Laura Lambert
O18: BabyFORce: A pioneering program translating variants identified via rapid genome sequencing to targeted therapeutics for neonatal intensive care unit patients
Genetics in Medicine Open
title O18: BabyFORce: A pioneering program translating variants identified via rapid genome sequencing to targeted therapeutics for neonatal intensive care unit patients
title_full O18: BabyFORce: A pioneering program translating variants identified via rapid genome sequencing to targeted therapeutics for neonatal intensive care unit patients
title_fullStr O18: BabyFORce: A pioneering program translating variants identified via rapid genome sequencing to targeted therapeutics for neonatal intensive care unit patients
title_full_unstemmed O18: BabyFORce: A pioneering program translating variants identified via rapid genome sequencing to targeted therapeutics for neonatal intensive care unit patients
title_short O18: BabyFORce: A pioneering program translating variants identified via rapid genome sequencing to targeted therapeutics for neonatal intensive care unit patients
title_sort o18 babyforce a pioneering program translating variants identified via rapid genome sequencing to targeted therapeutics for neonatal intensive care unit patients
url http://www.sciencedirect.com/science/article/pii/S2949774425001335
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