Michael A. Lodato

发表

Histone H3K27ac separates active from poised enhancers and predicts developmental state

R. Young, P. Sharp, R. Jaenisch, 2010, Proceedings of the National Academy of Sciences.

Aging and neurodegeneration are associated with increased mutations in single human neurons

Peter J. Park, Minseok Kwon, Thomas W. Chittenden, 2017 .

Predicting professional preferences for intuition‐based hiring

Scott Highhouse, Margaret E. Brooks, Michael A. Lodato, 2011 .

Aging and neurodegeneration are associated with increased mutations in single human neurons

Peter J. Park, Minseok Kwon, Thomas W. Chittenden, 2017, Science.

Somatic mutation in single human neurons tracks developmental and transcriptional history

Peter J. Park, Eunjung Lee, Thomas W. Chittenden, 2015, Science.

Sox2 co-occupies distal enhancer elements with cell-type-specific POU factors to specify cell identity in embryonic stem cells and neural precursor cells

Michael A. Lodato, 2012 .

Persistent DNA damage associated with ATM kinase deficiency promotes microglial dysfunction

E. Lee, Michael A. Lodato, Ailsa M. Jeffries, 2022, Nucleic acids research.

Analysis of somatic mutations in 131 human brains reveals aging-associated hypermutability

Sara B. Linker, Ryan E. Mills, J. V. Moran, 2022, Science.

Somatic mutations in single human cardiomyocytes reveal age-associated DNA damage and widespread oxidative genotoxicity

E. Lee, Michael A. Lodato, Junho Kim, 2022, Nature Aging.

The two faces of DNA oxidation in genomic and functional mosaicism during aging in human neurons

Michael A. Lodato, Jennifer S Ziegenfuss, Jennifer S. Ziegenfuss, 2022, Frontiers in Aging.

Prevalence and mechanisms of somatic deletions in single human neurons during normal aging and in DNA repair disorders

E. Lee, Michael A. Lodato, Junho Kim, 2022, Nature Communications.

APP gene copy number changes reflect exogenous contamination

C. Walsh, E. Lee, Michael A. Lodato, 2020, Nature.

Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements

Lovelace J. Luquette, C. Libert, C. Gawad, 2022, Nature Genetics.

Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network

Ryan E. Mills, J. V. Moran, Jennifer A. Erwin, 2017, Science.

H2AZ Is Enriched at Polycomb Complex Target Genes in ES Cells and Is Necessary for Lineage Commitment

R. Young, R. Jaenisch, J. Hanna, 2008, Cell.

A drug-inducible transgenic system for direct reprogramming of multiple somatic cell types

Marius Wernig, Rudolf Jaenisch, C. Lengner, 2008, Nature Biotechnology.

The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing

Sara B. Linker, Ryan E. Mills, J. V. Moran, 2021, Nature Neuroscience.

Genome aging: somatic mutation in the brain links age-related decline with disease and nominates pathogenic mechanisms.

C. Walsh, Michael A. Lodato, 2019, Human molecular genetics.

SOX2 Co-Occupies Distal Enhancer Elements with Distinct POU Factors in ESCs and NPCs to Specify Cell State

R. Jaenisch, E. Fraenkel, A. Cheng, 2013, PLoS genetics.

Linked-read analysis identifies mutations in single-cell DNA-sequencing data

Lovelace J. Luquette, Michael E. Coulter, C. Walsh, 2019, Nature Genetics.

Somatic genomic changes in single Alzheimer’s disease neurons

Derek H. Oakley, Lovelace J. Luquette, B. Hyman, 2022, Nature.

Reprogramming of Postnatal Neurons into Induced Pluripotent Stem Cells by Defined Factors

C. Lengner, R. Jaenisch, O. Kirak, 2011, Stem cells.

Single-nucleus transcriptomic analyses reveal microglial activation underlying cerebellar degeneration in Ataxia Telangiectasia

E. Lee, T. Yu, T. Chittenden, 2021 .

Editorial: Somatic mutations, genome mosaicism and aging

Michael A. Lodato, J. Vijg, 2023, Frontiers in Aging.

Evidence that APP gene copy number changes reflect recombinant vector contamination

C. Walsh, E. Lee, Michael A. Lodato, 2019, bioRxiv.

Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development

Sara B. Linker, Ryan E. Mills, Kiely N. James, 2023, Nature Genetics.

Functional integration of dopaminergic neurons directly converted from mouse fibroblasts.

C. Lengner, R. Jaenisch, L. Tsai, 2011, Cell stem cell.

Ultraspecific somatic SNV and indel detection in single neurons using primary template-directed amplification

Lovelace J. Luquette, C. Walsh, P. Park, 2021, bioRxiv.

Enhancing Soldier-Centered Learning with Emerging Training Technologies and Integrated Assessments

Randall D. Spain, Paul Cummings, Joanne Barnieu, 2013 .

Understanding the training needs of department chairs

Morell E. Mullins, J. Burnfield, Michael A. Lodato, 2005 .

PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimation

Michael E. Coulter, C. Walsh, P. Park, 2017, bioRxiv.

Going With Your Gut: An Investigation of Why Managers Prefer Intuitive Employee Selection

Michael A. Lodato, 2008 .

Local Hosts and Organizing Committee

Lovelace J. Luquette, C. Walsh, P. Park, 2015 .

SapT, a lanthionine‐containing peptide involved in aerial hyphae formation in the streptomycetes

Michael A. Lodato, F. Picart, J. Willey, 2005, Molecular microbiology.

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

Sara B. Linker, Evan Z. Macosko, Thomas G. Gilgenast, 2023, Cell genomics.

Control-independent mosaic single nucleotide variant detection with DeepMosaic

Ryan E. Mills, J. V. Moran, Michael E. Coulter, 2023, Nature Biotechnology.

ATM-deficiency-induced microglial activation promotes neurodegeneration in ataxia-telangiectasia

E. Lee, T. Yu, T. Chittenden, 2021, bioRxiv.

APP gene copy number changes reflect exogenous contamination

C. Walsh, E. Lee, Gwendolyn E. Kaeser, 2020, Nature.

Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortex

Michael A. Lodato, R. Hill, Yanmei Dou, 2023, bioRxiv.

Linked-read analysis identifies mutations in single-cell DNA-sequencing data

Minseok Kwon, Lovelace J Luquette, Isidro Cortés-Ciriano, 2019, Nature Genetics.

Linked-read analysis identifies mutations in single cell DNA sequencing data

Lovelace J. Luquette, Michael E. Coulter, C. Walsh, 2017, bioRxiv.