Alex Tokolyi

Wellington Road
Clayton, VIC, Australia

Last Updated: 09/26/2026

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Found 22 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

Trans-eQTLs reveal the architecture of human gene regulatory networks.

Trans-eQTLs reveal the architecture of human gene regulatory networks.

Journal: medRxiv : the preprint server for health sciences

Published: April 29, 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

Mapping genetic effects on splicing in ten thousand post-mortem brain samples reveals novel mediators of neurological disease risk.

Mapping genetic effects on splicing in ten thousand post-mortem brain samples reveals novel mediators of neurological disease risk.

Journal: medRxiv : the preprint server for health sciences

Published: October 03, 2025

Integrating natural and engineered genetic variations to decode regulatory influence on blood traits.

Integrating natural and engineered genetic variations to decode regulatory influence on blood traits.

Journal: Cell reports

Published: March 21, 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

The common VTE-protective G haplotype of F5 increases factor V-short, TFPI function, and risk of bleeding.

The common VTE-protective G haplotype of F5 increases factor V-short, TFPI function, and risk of bleeding.

Journal: Blood advances

Published: July 10, 2024

Author Correction: Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort.

Author Correction: Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort.

Journal: Nature genetics

Published: February 29, 2024

Misexpression of inactive genes in whole blood is associated with nearby rare structural variants.

Misexpression of inactive genes in whole blood is associated with nearby rare structural variants.

Journal: American journal of human genetics

Published: January 12, 2024

Phenotypic complexities of rare heterozygous neurexin-1 deletions.

Phenotypic complexities of rare heterozygous neurexin-1 deletions.

Journal: Nature

Published: December 12, 2023

The contribution of genetic determinants of blood gene expression and splicing to molecular phenotypes and health outcomes.

The contribution of genetic determinants of blood gene expression and splicing to molecular phenotypes and health outcomes.

Journal: Nature genetics

Published: December 05, 2023

Showing 1-12 of 22

Last Updated: 09/26/2026