Michael C. Zody

Career Trajectory

Research Cluster Map

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

• Comparison of variant callers using 60 532 multi-ancestry whole genome sequences

  UNC Libraries · 2026-06-09

• Lancet2: Improved and accelerated somatic variant calling with joint multi-sample local assembly graphs

  NAR Genomics and Bioinformatics · 2026-03-25

• Erratum for Yuan et al., “Case-control and genomic epidemiology characterization of SARS-CoV-2 breakthrough infections during Delta-to-Omicron transition”

  mBio · 2026-03-09

• Comparison of variant callers using 60 532 multi-ancestry whole genome sequences

  Briefings in Bioinformatics · 2026-03-01

• Structural Variants Associated with Sporadic Alzheimer's Disease Pathologies and Segregates in Caribbean Hispanics and Non‐Hispanic White Families

  Alzheimer s & Dementia · 2025-12-01

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

  Mobile DNA · 2025-11-06 · 1 citations

• FAVOR 2.0: A reengineered functional annotation of variants online resource for interpreting genomic variation

  Nucleic Acids Research · 2025-10-21 · 1 citations

• Stratifying ALS Patients by Mode of Inheritance Reveals Transcriptomic Signatures Specific to sALS and fALS

  International Journal of Molecular Sciences · 2025-09-22

• A rare genetic variant confers resistance to neurodegeneration across multiple neurological disorders by augmenting selective autophagy

  Neuron · 2025-09-13 · 5 citations

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

  Nature · 2025-08-26 · 2 citations

• Complex genetic variation in nearly complete human genomes

  Nature · 2025-07-23 · 80 citations

• Error-corrected flow-based sequencing at whole-genome scale and its application to circulating cell-free DNA profiling

  Nature Methods · 2025-04-11 · 15 citations

• Lancet2: Improved and accelerated somatic variant calling with joint multi-sample local assembly graphsPreprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2025-02-23 · 1 citations

• A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucoma

  UNC Libraries · 2025-02-01

• 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

• Beyond GWAS: Investigating Structural Variants and Their Segregation in Familial Alzheimer’s Disease

  Alzheimer s & Dementia · 2024-12-01

• High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation

  Genome Research · 2024-10-02 · 77 citations

• Complex genetic variation in nearly complete human genomesPreprint

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

• Semi-supervised machine learning method for predicting homogeneous ancestry groups to assess Hardy-Weinberg equilibrium in diverse whole-genome sequencing studies

  The American Journal of Human Genetics · 2024-09-12 · 6 citations

• Multi-omic analysis of Huntington’s disease reveals a compensatory astrocyte state

  Nature Communications · 2024-08-08 · 38 citations