Christine M. Eng

Career Trajectory

Research Cluster Map

Direct collaborators. Node size = influence, colour = community, dashed = past collaboration.

• Clinical significance of mRNA nonstop decay in rare disease diagnosis and recommendations for its application in variant classificationPreprint

  Research Square · 2026-03-26

• Biallelic LAMP3 variants in 5 families with interstitial lung disease: Evidence of a disease-gene association

  Genetics in Medicine · 2026-02-03 · 3 citations

• Diagnostic Yield of Exome Sequencing for Pregnancies With and Without Fetal Anomalies and for Stillbirth

  Prenatal Diagnosis · 2025-05-27 · 2 citations

• Abstract 6292: Highly sensitive detection of circulating-tumor DNA in plasma using whole genome sequencing

  Cancer Research · 2025-04-21 · 1 citations

• Experiences from dual genome next-generation sequencing panel testing for mitochondrial disorders: a comprehensive molecular diagnosis

  Frontiers in Genetics · 2025-03-05 · 2 citations

• Clinical validation of RNA sequencing for Mendelian disorder diagnostics

  The American Journal of Human Genetics · 2025-03-04 · 24 citations

• P645: Reflex RNA sequencing for enhanced variant classification on ES/GS improves patient outcomes

  Genetics in Medicine Open · 2025-01-01

• Comparing the Diagnostic Yield of Germline Exome Versus Panel Sequencing in the Diverse Population of the Texas KidsCanSeq Pediatric Cancer Study

  JCO Precision Oncology · 2024-09-01 · 5 citations

• CffDNA screening for Niemann–pick disease, type C1: a case series

  Frontiers in Medicine · 2024-08-05 · 3 citations