Michael C. Zody

New York Genome Center — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

77h-index75.1kcitations214works15.82yr avg
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Research Topics

Genomics and Phylogenetic Studies(54), Chromosomal and Genetic Variations(32), Genomics and Rare Diseases(32), Genomic variations and chromosomal abnormalities(29), Cancer Genomics and Diagnostics(29)

Publications183 total

Structural Variants Associated with Sporadic Alzheimer's Disease Pathologies and Segregates in Caribbean Hispanics and Non‐Hispanic White Families
Alzheimer s & Dementia·2025Open Access
Structural and transduction patterns of human-specific polymorphic SVA insertions
Mobile DNA·2025Open Access
FAVOR 2.0: A reengineered functional annotation of variants online resource for interpreting genomic variation
Nucleic Acids Research·2025· 1 citedOpen Access
Stratifying ALS Patients by Mode of Inheritance Reveals Transcriptomic Signatures Specific to sALS and fALS
International Journal of Molecular Sciences·2025Open Access
A rare genetic variant confers resistance to neurodegeneration across multiple neurological disorders by augmenting selective autophagy
Neuron·2025· 4 citedOpen Access
Author Correction: Complex genetic variation in nearly complete human genomes
Nature·2025· 1 citedOpen Access
Complex genetic variation in nearly complete human genomes
Nature·2025· 43 citedOpen Access
Error-corrected flow-based sequencing at whole-genome scale and its application to circulating cell-free DNA profiling
Nature Methods·2025· 12 citedOpen Access
Lancet2: Improved and accelerated somatic variant calling with joint multi-sample local assembly graphs
2025· 1 citedOpen Access
A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucoma
UNC Libraries·2025Open Access
Beyond GWAS: Investigating Structural Variants and Their Segregation in Familial Alzheimer’s Disease
Alzheimer s & Dementia·2024Open Access
An integrative TAD catalog in lymphoblastoid cell lines discloses the functional impact of deletions and insertions in human genomes
Genome Research·2024· 1 citedOpen Access
High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation
Genome Research·2024· 62 citedOpen Access
Complex genetic variation in nearly complete human genomes
2024· 26 citedOpen Access
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· 5 citedOpen Access
Multi-omic analysis of Huntington’s disease reveals a compensatory astrocyte state
Nature Communications·2024· 26 citedOpen Access
Omics Approaches to Investigate the Pathogenesis of Suicide
Biological Psychiatry·2024· 6 citedOpen Access
Rare genetic variation in fibronectin 1 (FN1) protects against APOEε4 in Alzheimer’s disease
Acta Neuropathologica·2024· 46 citedOpen Access
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates
npj Genomic Medicine·2024· 22 citedOpen Access
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation
2024· 41 citedOpen Access
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Frequent Co-authors

Kerstin Lindblad‐Toh(13), Eric S. Lander(10), Evan Mauceli(9), Evan E. Eichler(9), Sante Gnerre(8), Chad Nusbaum(7), David B. Jaffe(7), Eric S. Lander(6), Mark J. Daly(6), Bruce W. Birren(5), Claire M. Wade(5), Manfred Grabherr(5), Ted Sharpe(5), Manuel Garber(5), Allison Regier(5), André Corvelo(5), Ira M. Hall(5), Jill P. Mesirov(4), Elaine R. Mardis(4), Michèle Clamp(4)