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Author

Lisa Salz

Observed name: Salz, Lisa
Institution: Baylor Genetics
ORCID: 0000-0002-6380-4984
Observed ORCID: 0000-0002-6380-4984
OpenAlex ID: A5081498113
A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants
2019 · Stephen F. Kingsmore, Julie A. Cakici, et al. · The American Journal of Human Genetics · 357
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Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation
2019 · Michelle M. Clark, Amber Hildreth, et al. · Science Translational Medicine · 308
An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm
2020 · David P. Dimmock, Michelle M. Clark, et al. · The American Journal of Human Genetics · 190
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Rapid Whole-Genome Sequencing and Clinical Management in the PICU: A Multicenter Cohort, 2016–2023*
2024 · Katherine M. Rodriguez, Jordan Vaught, et al. · Pediatric Critical Care Medicine · 32
Multi-center implementation of rapid whole genome sequencing provides additional evidence of its utility in the pediatric inpatient setting
2024 · Lauren Thompson, Austin Larson, et al. · Frontiers in Pediatrics · 16
Moving Genomics to Routine Care: An Initial Pilot in Acute Cardiovascular Disease
2020 · Zahra Aryan, Attila Szanto, et al. · Circulation Genomic and Precision Medicine · 16
Failure to thrive - an overlooked manifestation of KMT2B-related dystonia: a case presentation
2020 · Andrew Ng, Serena Galosi, et al. · BMC Neurology · 12
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O46: Diagnostic yield of rapid genome sequencing in critically ill infants with cardiac indications
2026 · Xiaonan Zhao, Liesbeth Vossaert, et al. · Genetics in Medicine Open
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P561: Expanding the genotypic spectrum for ReNU syndrome: A clinical laboratory experience*
2026 · Eileen Barr, Morgan Driver, et al. · Genetics in Medicine Open
P564: Genome and exome sequencing reanalysis: Improvement to diagnostic yield and classification of variants over time*
2026 · Morgan Driver, Liesbeth Vossaert, et al. · Genetics in Medicine Open
25: a Multicenter Cohort Analysis of Rapid Genome Sequencing in the Picu
2022 · Katherine Rodriguez, Erica Sanford Kobayashi, et al. · Critical Care Medicine
OP020: Demonstrating the value of genome sequencing in a pediatric neurology cohort: A successful partnership between a patient organization and industry
2022 · Holly Snyder, Lisa Salz, et al. · Genetics in Medicine
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Additional file 7 of Failure to thrive - an overlooked manifestation of KMT2B-related dystonia: a case presentation
2020 · Ng, Andrew, Galosi, Serena, et al. · Figshare
KMT2B early childhood onset dystonia presenting as failure to thrive (P4.6-034)
2019 · Andrew Ng, Serena Galosi, et al. · Neurology
Works count: 15
Citation count: 931
H-index: 7
I10-index: 7
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