Kristen M. Laricchia

Career Trajectory

Research Cluster Map

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

• Integrating 730,947 exome sequences with clinical literature improves gene discovery

  medRxiv · 2026-03-25 · 2 citations

• Author Correction: The effect of LRRK2 loss-of-function variants in humans

  UNC Libraries · 2025-05-14

• The effect of LRRK2 loss-of-function variants in humans

  UNC Libraries · 2025-05-14

• Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases

  Human Genetics and Genomics Advances · 2025-04-15 · 1 citations

• Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed casesPreprint

  medRxiv · 2024-12-26 · 1 citations

• Quantifying constraint in the human mitochondrial genome

  Nature · 2024-10-16 · 58 citations

• A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disorders

  Nature Communications · 2024-09-27 · 9 citations