Parent- and Intensivist-Reported Utility for Neonatal Genomic Testing
Katharine Press Callahan, K. Taylor Wild, Alexandra Heck, Laura K. Conlin et autres
us (code pays fourni par la source)
0 citations
JAMA Network Open
Nancy B. Spinner
Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.
303Publications signalées
25052Citations signalées
1Affiliations récentes
Les institutions déclarées
Les domaines associés
Pediatric Hepatobiliary Diseases and TreatmentsGenomic variations and chromosomal abnormalitiesGallbladder and Bile Duct DisordersGenomics and Rare DiseasesPrenatal Screening and Diagnostics
Les publications récentes
Response to Sansom et al
Katharine Press Callahan, Rebecca Mueller, Steven Joffe, Cara Skraban et autres
us (code pays fourni par la source)
0 citations
Genetics in Medicine
Rapid targeted analysis of the genome: Rapid genomic sequencing in critically ill infants
K. Taylor Wild, Sara L. Reichert, Matthew C. Dulik, Alexandra Heck et autres
us (code pays fourni par la source)
1 citation
Genetics in Medicine Open
Placental Malperfusion Is Associated With Adverse Outcomes in Congenital Heart Disease and With Genetic Variants in Placental Developmental Pathways
Rebecca Josowitz, Stacy Woyciechowski, Tanaya Jadhav, Tejas Jammihal et autres
us (code pays fourni par la source)
6 citations
Journal of the American College of Cardiology
Phenotypic Divergence of JAG1 ‐ and NOTCH2 ‐Associated Alagille Syndrome & Disease‐Specific NOTCH2 Variant Classification Guidelines
Shannon M. Vandriel, Liting Li, Huiyu She, Jian‐She Wang et autres
ca, cn, us, pl, it, fr, be, kr, se, au, in, jp, de, at, gb, nl, my, th, ch, il, nz, es, tr, dk, gr, pt, si, ar, ae (code pays fourni par la source)
5 citations
Liver International
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
Ane Miren Sagardia, Katrina A.B. Goddard, Jason L. Vassy, Gail P. Jarvik et autres
us (code pays fourni par la source)
0 citations
Carolina Digital Repository (University of North Carolina at Chapel Hill)
Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
Lucia A. Hindorff, Tia L. Kauffman, Sawona Biswas, Jason L. Vassy et autres
us (code pays fourni par la source)
0 citations
Carolina Digital Repository (University of North Carolina at Chapel Hill)
Reporting ABCD1 variants as actionable secondary findings on exome and genome sequencing
Nancy B. Spinner, Rebecca C. Ahrens‐Nicklas, Lisa R. Young, Laura Voss et autres
us (code pays fourni par la source)
1 citation
Genetics in Medicine
Parents’ perceptions of the utility of genetic testing in the NICU
Katharine Press Callahan, Rebecca Mueller, Steven Joffe, Cara Skraban et autres
us (code pays fourni par la source)
6 citations
Genetics in Medicine
How Neonatologists Use Genetic Information
Katharine Press Callahan, Rebecca Mueller, Steven Joffe, Cara Skraban et autres
us (code pays fourni par la source)
1 citation
The Journal of Pediatrics
P741: Recurrent 2q11.2 deletions and duplications: A look at segregation, clinical presentation, and additional genetic testing
Elizabeth A. Fanning, Sara Reichert, Brooke Weckselblatt, Matthew C. Dulik et autres
us (code pays fourni par la source)
0 citations
Genetics in Medicine Open
P640: Reevaluating the standard approach to genomic testing in infants: Targeted genomic testing vs exome/genome sequencing as a first-tier test
Sara Reichert, Emma Bedoukian, K. Taylor Wild, J.W.M. van Lent et autres
us (code pays fourni par la source)
0 citations
Genetics in Medicine Open
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