Mark Chaisson

Career Trajectory

Research Cluster Map

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

• Defining a tandem repeat catalog and variation clusters for genome-wide analyses and population databases

  The American Journal of Human Genetics · 2026-04-22 · 2 citations

• Population differences of chromosome 22q11.2 duplication structure predispose differentially to microdeletion and inversion

  Nature Communications · 2026-04-18

• Author Correction: Genotyping sequence-resolved copy number variation using pangenomes reveals paralog-specific global diversity and expression divergence of duplicated genes

  Nature Genetics · 2026-02-16

• TRcompDB v2.0, a global reference of human tandem repeat composition and mutation rate from long-read assemblies

  Open MIND · 2026-01-23 · 1 citations

• Long-read sequencing identifies <i>FGF14</i> repeat expansions in Parkinson’s disease

  Brain · 2025-11-29 · 1 citations

• Structural and transduction patterns of human-specific polymorphic SVA insertions

  Mobile DNA · 2025-11-06 · 1 citations

• Genotyping sequence-resolved copy number variation using pangenomes reveals paralog-specific global diversity and expression divergence of duplicated genes

  Nature Genetics · 2025-10-17 · 1 citations

• Author Correction: Complex genetic variation in nearly complete human genomes

  Nature · 2025-08-26 · 2 citations

• Long-read sequencing identifies <i>FGF14</i> repeat expansions in Parkinson’s diseasePreprint

  medRxiv · 2025-08-19 · 2 citations

• Complex genetic variation in nearly complete human genomes

  Nature · 2025-07-23 · 80 citations

• Identification of <scp>GGC</scp> Repeat Expansions in <scp><i>ZFHX3</i></scp> among Chilean Movement Disorder Patients

  Movement Disorders · 2025-06-03 · 3 citations

• Identification of GGC Repeat Expansions in <i>ZFHX3</i> Among Chilean Movement Disorder PatientsPreprint

  medRxiv · 2025-03-19

• Long-read sequencing of hundreds of diverse brains provides insight into the impact of structural variation on gene expression and DNA methylationPreprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2024-12-18 · 16 citations

• An integrative TAD catalog in lymphoblastoid cell lines discloses the functional impact of deletions and insertions in human genomes

  Genome Research · 2024-12-01 · 2 citations

• Complex genetic variation in nearly complete human genomesPreprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2024-09-25 · 27 citations

• Genotyping sequence-resolved copy number variation using pangenomes reveals paralog-specific global diversity and expression divergence of duplicated genesPreprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2024-08-11 · 1 citations

• VISTA: an integrated framework for structural variant discovery

  Briefings in Bioinformatics · 2024-07-25 · 3 citations