Last Updated: 09/26/2026
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Found 75 publications
High Diagnosis Rate for Nonimmune Hydrops Fetalis With Prenatal Clinical Genome: Expanded Results From the Hydrops-Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) Study.
Journal: American journal of medical genetics. Part A
Published: May 15, 2026
Kauro, a graph-based chatbot for high-fidelity information transmission conversations.
Journal: medRxiv : the preprint server for health sciences
Published: February 12, 2026
Sequencing approaches in hereditary cancer testing: strengths, limitations and future directions.
Journal: European journal of human genetics : EJHG
Published: October 31, 2025
Large Class of Neurodevelopmental Disorders Requires Genome Sequencing for Diagnosis.
Journal: Annals of neurology
Published: October 30, 2025
Identification of de novo variants from parent-proband duos via long-read sequencing.
Journal: American journal of human genetics
Published: October 05, 2025
Response to Spurdle et al.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 03, 2025
Incorporating Rare Disease Growth Monitoring Into Routine Practice to Improve Early Recognition and Diagnosis of Genetic Conditions.
Journal: Pediatric annals
Published: September 09, 2025
Genetic Variants Associated with Persistent Pulmonary Hypertension of Newborn: A Systematic Review.
Journal: Neonatology
Published: September 05, 2025
Hereditary Anemias as a Monogenic Etiology for Nonimmune Hydrops Fetalis.
Journal: Clinical therapeutics
Published: July 31, 2025
Rare heterozygous de novo variants in RAPGEF2 are associated with a neurodevelopmental disorder.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 12, 2025
Computer vision techniques for high-speed atomic force microscopy of DNA molecules.
Journal: Nanotechnology
Published: April 01, 2025
Last Updated: 09/26/2026