Tatsuhiko Naito

Psychiatry
1 Brookdale Plz
Brooklyn, NY 11212

Last Updated: 09/26/2026

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Found 49 publications

The New York Genome Center ALS Consortium resource integrates postmortem tissue transcriptomics and whole genome sequencing to empower biological discovery.

The New York Genome Center ALS Consortium resource integrates postmortem tissue transcriptomics and whole genome sequencing to empower biological discovery.

Journal: medRxiv : the preprint server for health sciences
Published: May 18, 2026

Publisher Correction: A meta-analysis of single-nucleus expression quantitative trait loci linking genetic risk to brain disorders.

Publisher Correction: A meta-analysis of single-nucleus expression quantitative trait loci linking genetic risk to brain disorders.

Journal: Nature genetics
Published: April 07, 2026

Mechanistic analysis of an IRF7-dependent pathway in virus-induced fibrosis in chronic lung allograft dysfunction.

Mechanistic analysis of an IRF7-dependent pathway in virus-induced fibrosis in chronic lung allograft dysfunction.

Journal: EBioMedicine
Published: November 08, 2025

Spatial transcriptomics reveals coordinated endothelial and epithelial activator protein-1 activation in chronic lung allograft dysfunction.

Spatial transcriptomics reveals coordinated endothelial and epithelial activator protein-1 activation in chronic lung allograft dysfunction.

Journal: The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation
Published: September 17, 2025

Polygenic scores for precision psychiatry: a study on the effect heterogeneity of antidepressants.

Polygenic scores for precision psychiatry: a study on the effect heterogeneity of antidepressants.

Journal: medRxiv : the preprint server for health sciences
Published: July 15, 2025

Mosaic chromosomal alterations in blood are associated with an increased risk of Alzheimer's disease.

Mosaic chromosomal alterations in blood are associated with an increased risk of Alzheimer's disease.

Journal: medRxiv : the preprint server for health sciences
Published: June 12, 2025

Elucidating genetic backgrounds of myasthenia gravis in Japanese by genome-wide association studies and multi-omics analyses of thymoma.

Elucidating genetic backgrounds of myasthenia gravis in Japanese by genome-wide association studies and multi-omics analyses of thymoma.

Journal: Nature communications
Published: May 28, 2025

Multiancestry genome-wide association and multiomics analyses elucidate spatiocellular features of multiple sclerosis genetics.

Multiancestry genome-wide association and multiomics analyses elucidate spatiocellular features of multiple sclerosis genetics.

Journal: Nature genetics
Published: May 07, 2025

SingleBrain: A Meta-Analysis of Single-Nucleus eQTLs Linking Genetic Risk to Brain Disorders.

SingleBrain: A Meta-Analysis of Single-Nucleus eQTLs Linking Genetic Risk to Brain Disorders.

Journal: medRxiv : the preprint server for health sciences
Published: March 17, 2025

A meta-analysis of single-nucleus expression quantitative trait loci linking genetic risk to brain disorders.

A meta-analysis of single-nucleus expression quantitative trait loci linking genetic risk to brain disorders.

Journal: Nature genetics
Published: March 13, 2025

Whole-genome sequencing reveals rare and structural variants contributing to psoriasis and identifies CERCAM as a risk gene.

Whole-genome sequencing reveals rare and structural variants contributing to psoriasis and identifies CERCAM as a risk gene.

Journal: Cell genomics
Published: February 01, 2025

Leveraging functional annotations to map rare variants associated with Alzheimer's disease with gruyere.

Leveraging functional annotations to map rare variants associated with Alzheimer's disease with gruyere.

Journal: medRxiv : the preprint server for health sciences
Published: December 16, 2024
Showing 1-12 of 49

Last Updated: 09/26/2026