Alexandra C. Keefe
Pediatrics | Medical Genetics
4800 Sand Point Way NE # Oc.7830
Seattle, WA 98105
Seattle, WA 98105
Last Updated: 09/26/2026
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Found 12 publications
Development of a pediatric urgent care research infrastructure to facilitate human immunology studies.
Journal: Journal of clinical and translational science
Published: April 24, 2026
The Spectrum of Mosaic Double Aneuploidy of Monosomy X and Trisomy 18: Two New Cases and Review of the Literature.
Journal: Cytogenetic and genome research
Published: January 08, 2026
Hospital-wide implementation of inpatient first-tier rapid genome sequencing.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 14, 2025
RNU4ATAC-opathy: Clinical, molecular and transcriptomic insights from a large cohort.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 13, 2025
RNU4ATAC-opathy: Clinical, molecular, and transcriptomic insights from a large cohort.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 13, 2025
Implementation of First-Line Rapid Genome Sequencing for Children in Pediatric and Cardiac Intensive Care Units.
Journal: American journal of medical genetics. Part A
Published: August 24, 2025
Case Report: An atypical case of ARPKD highlights the utility and challenges of implementing genetic testing in cystic kidney disease.
Journal: Frontiers in pediatrics
Published: July 31, 2025
Implementation of First-Line Rapid Genome Sequencing in Non-Critical Care Pediatric Wards.
Journal: The Journal of pediatrics
Published: April 05, 2025
Expanding implementation of pediatric whole-genome sequencing: Insights from SeqFirst providers to inform equitable access to a precise genetic diagnosis.
Journal: HGG advances
Published: March 11, 2025
Mosaic X-linked adrenoleukodystrophy in males identified by newborn screening and next-generation sequencing.
Journal: NPJ genomic medicine
Published: September 18, 2024
SeqFirst: Building equity access to a precise genetic diagnosis in critically ill newborns.
Journal: American journal of human genetics
Published: September 13, 2024
First a Provider, Now a Patient: Receiving a Devastating Diagnosis Through the Patient Portal.
Journal: American journal of medical genetics. Part C, Seminars in medical genetics
Published: March 30, 2024
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Last Updated: 09/26/2026