NERINE reveals rare variant associations in gene networks across phenotypes and implicates an SNCA-PRL-LRRK2 subnetwork in Parkinson’s disease

Read full text
Authors: Sumaiya Nazeen, Xinyuan Wang, Autumn R. Morrow, Ronya Strom, Elizabeth Ethier, Dylan Ritter, Alexander B.H. Henderson, Jalwa Afroz, Christopher S. Cassa, Nathan O. Stitziel, Rajat M. Gupta, Kelvin C. Luk
+3 more Lorenz Studer, Vikram Khurana, Shamil R. Sunyaev
Cited by: 1
References: 132

Abstract

Studying the genetic basis of human phenotypes involves two primary strategies. Model-system experiments generate interpretable gene networks but do not establish relevance to human disease. In contrast, statistical genetics identifies variant- and gene-level associations but cannot test mechanistic models. Here, we bridge these approaches by introducing NERINE, a hierarchical model-based rare variant association test that incorporates gene network topology while remaining robust to network inaccuracies. NERINE supports analysis of networks from established pathway databases and model-system screens. A comprehensive search across pathway databases reveals associations for breast cancer, cardiovascular diseases, and type 2 diabetes not detected by single-gene tests. Applied to experimental screen-derived networks in Parkinson's disease (PD), NERINE highlights autophagy-, vesicle-trafficking-, and protein-homeostasis-related gene modules. Genome-scale CRISPR interference (CRISPRi) screening in human neurons and NERINE converge on PRL, revealing an intraneuronal α-synuclein/prolactin stress response that may impact resilience to PD.

Fields of Study & Subjects

Genetic Associations and Epidemiology Bioinformatics and Genomic Networks Parkinson's Disease Mechanisms and Treatments

Publication details

Journal / source
Cell Genomics
Publisher
Elsevier BV
Volume
6
Issue
7
Pages
101284–101284
Publication date
22 June 2026
Language
EN