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Author Details
Full Name
Amy Brower
Affiliation
American College of Medical Genetics and Genomics
ORCID
Career Start Year
1998
Papers
31
H Index
13
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36594517
Data sharing to advance gene-targeted therapies in rare diseases.
Am J Med Genet C Semin Med Genet
2023
37663526
Newborn sequencing is only part of the solution for better child health.
Lancet Reg Health Am
2023
37479106
Factors influencing creatine kinase-MM concentrations in newborns and implications for newborn screening for Duchenne muscular dystrophy.
Clin Biochem
2023
37987476
NBSTRN Tools to Advance Newborn Screening Research and Support Newborn Screening Stakeholders.
Int J Neonatal Screen
2023
37350320
Newborn screening for Duchenne muscular dystrophy: A two-year pilot study.
Ann Clin Transl Neurol
2023
36738469
Moving away from one disease at a time: Screening, trial design, and regulatory implications of novel platform technologies.
Am J Med Genet C Semin Med Genet
2023
36152336
Newborn screening for Duchenne muscular dystrophy-early detection and diagnostic algorithm for female carriers of Duchenne muscular dystrophy.
Am J Med Genet C Semin Med Genet
2022
35692825
Using Long-Term Follow-Up Data to Classify Genetic Variants in Newborn Screened Conditions.
Front Genet
2022
36214312
Special issue: Newborn screening research.
Am J Med Genet C Semin Med Genet
2022
36278620
Newborn Screening for Duchenne Muscular Dystrophy: First Year Results of a Population-Based Pilot.
Int J Neonatal Screen
2022
35938011
Population-Based Screening of Newborns: Findings From the NBS Expansion Study (Part One).
Front Genet
2022
36118861
Population-based screening of newborns: Findings from the newborn screening expansion study (part two).
Front Genet
2022
33264411
The Human Phenotype Ontology in 2021.
Nucleic Acids Res
2021
35619984
Accelerating the Pace of Newborn Screening Research to Advance Disease Understanding and Improve Health Outcomes:: Key Efforts of the Newborn Screening Translational Research Network (NBSTRN).
Dela J Public Health
2021
34208910
The Longitudinal Pediatric Data Resource: Facilitating Longitudinal Collection of Health Information to Inform Clinical Care and Guide Newborn Screening Efforts.
Int J Neonatal Screen
2021
30393376
Foundation of the Newborn Screening Translational Research Network and its tools for research.
Genet Med
2019
31839987
FDA oversight of NSIGHT genomic research: the need for an integrated systems approach to regulation.
NPJ Genom Med
2019
30100612
Including ELSI research questions in newborn screening pilot studies.
Genet Med
2019
33072932
Duchenne Muscular Dystrophy Newborn Screening, a Case Study for Examining Ethical and Legal Issues for Pilots for Emerging Disorders: Considerations and Recommendations.
Int J Neonatal Screen
2018
28096516
Newborn Sequencing in Genomic Medicine and Public Health.
Pediatrics
2017
27268406
A framework for assessing outcomes from newborn screening: on the road to measuring its promise.
Mol Genet Metab
2016
24139498
Primary Immune Deficiency Treatment Consortium (PIDTC) report.
J Allergy Clin Immunol
2014
25138334
Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States.
JAMA
2014
21150372
Long-term follow-up in newborn screening: A systems approach for improving health outcomes.
Genet Med
2010
18250228
CYP4F2 genetic variant alters required warfarin dose.
Blood
2008
17873728
Impact of oral hygiene on prevention of ventilator-associated pneumonia in neuroscience patients.
J Nurs Care Qual
2007
18007148
Committee Report: advancing the current recommended panel of conditions for newborn screening.
Genet Med
2007
15503566
Reading disability and chromosome 6p21.3: evaluation of MOG as a candidate gene.
J Learn Disabil
2001
9915954
Quantitative-trait locus for specific language and reading deficits on chromosome 6p.
Am J Hum Genet
1999
10088931
Prediction of early-onset asthma in genetically at-risk children.
Pediatr Pulmonol
1999
9549238
Molecular approaches to the genetic analysis of specific reading disability.
Hum Biol
1998
1 - 31 of 31
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