Nikolaos I. Panousis

Gunnels Wood Road
Stevenage, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 22 publications

An Alzheimer's disease-associated common regulatory variant in a PTK2B intron alters microglial function.

An Alzheimer's disease-associated common regulatory variant in a PTK2B intron alters microglial function.

Journal: iScience
Published: October 13, 2025

Cell-type-resolved genetic regulatory variation shapes inflammatory bowel disease risk.

Cell-type-resolved genetic regulatory variation shapes inflammatory bowel disease risk.

Journal: medRxiv : the preprint server for health sciences
Published: July 16, 2025

Cell-type-resolved genetic variation shapes inflammatory bowel disease risk.

Cell-type-resolved genetic variation shapes inflammatory bowel disease risk.

Journal: Nature
Published: June 24, 2025

Fine-mapping and molecular characterisation of primary sclerosing cholangitis genetic risk loci.

Fine-mapping and molecular characterisation of primary sclerosing cholangitis genetic risk loci.

Journal: Nature communications
Published: August 22, 2023

Gene expression QTL mapping in stimulated iPSC-derived macrophages provides insights into common complex diseases.

Gene expression QTL mapping in stimulated iPSC-derived macrophages provides insights into common complex diseases.

Journal: Nature communications
Published: July 25, 2023

Splicing QTL mapping in stimulated macrophages associates low-usage splice junctions with immune-mediated disease risk.

Splicing QTL mapping in stimulated macrophages associates low-usage splice junctions with immune-mediated disease risk.

Journal: Nature communications
Published: July 25, 2023

Identifying novel regulatory effects for clinically relevant genes through the study of the Greek population.

Identifying novel regulatory effects for clinically relevant genes through the study of the Greek population.

Journal: BMC genomics
Published: March 02, 2023

Multiallelic Copy Number Variation in ORM1 is Associated with Plasma Cell-Free DNA Levels as an Intermediate Phenotype for Venous Thromboembolism.

Multiallelic Copy Number Variation in ORM1 is Associated with Plasma Cell-Free DNA Levels as an Intermediate Phenotype for Venous Thromboembolism.

Journal: Thrombosis and haemostasis
Published: January 25, 2023

Integrated GWAS and Gene Expression Suggest ORM1 as a Potential Regulator of Plasma Levels of Cell-Free DNA and Thrombosis Risk.

Integrated GWAS and Gene Expression Suggest ORM1 as a Potential Regulator of Plasma Levels of Cell-Free DNA and Thrombosis Risk.

Journal: Thrombosis and haemostasis
Published: March 10, 2022

Mapping interindividual dynamics of innate immune response at single-cell resolution.

Mapping interindividual dynamics of innate immune response at single-cell resolution.

Journal: Nature genetics
Published: August 28, 2021

A map of transcriptional heterogeneity and regulatory variation in human microglia.

A map of transcriptional heterogeneity and regulatory variation in human microglia.

Journal: Nature genetics
Published: May 15, 2020

Extensive fragmentation and re-organization of transcription in Systemic Lupus Erythematosus.

Extensive fragmentation and re-organization of transcription in Systemic Lupus Erythematosus.

Journal: Scientific reports
Published: April 08, 2020
Showing 1-12 of 22

Last Updated: 09/26/2026