Gut microbiome at the crossroad of genetic variants and behavior disorders

L Cheng, H Wu, Z Chen, H Hao, X Zheng - Gut Microbes, 2023 - Taylor & Francis
Genetic variants are traditionally known to shape the susceptibility to neuropsychiatric
disorders. An increasing number of studies indicate that remodeling of the gut microbiome …

[HTML][HTML] The impact of rare protein coding genetic variation on adult cognitive function

CY Chen, R Tian, T Ge, M Lam, G Sanchez-Andrade… - Nature Genetics, 2023 - nature.com
Compelling evidence suggests that human cognitive function is strongly influenced by
genetics. Here, we conduct a large-scale exome study to examine whether rare protein …

[HTML][HTML] Genomic findings in schizophrenia and their implications

MJ Owen, SE Legge, E Rees, JTR Walters… - Molecular …, 2023 - nature.com
There has been substantial progress in understanding the genetics of schizophrenia over
the past 15 years. This has revealed a highly polygenic condition with the majority of the …

Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder

CM Nievergelt, AX Maihofer, EG Atkinson, CY Chen… - Nature Genetics, 2024 - nature.com
Post-traumatic stress disorder (PTSD) genetics are characterized by lower discoverability
than most other psychiatric disorders. The contribution to biological understanding from …

Multi-omics data integration methods and their applications in psychiatric disorders

A Sathyanarayanan, TT Mueller, MA Moni… - European …, 2023 - Elsevier
To study mental illness and health, in the past researchers have often broken down their
complexity into individual subsystems (eg, genomics, transcriptomics, proteomics, clinical …

[PDF][PDF] Joint analysis of GWAS and multi-omics QTL summary statistics reveals a large fraction of GWAS signals shared with molecular phenotypes

Y Wu, T Qi, NR Wray, PM Visscher, J Zeng, J Yang - Cell Genomics, 2023 - cell.com
Molecular quantitative trait loci (xQTLs) are often harnessed to prioritize genes or functional
elements underpinning variant-trait associations identified from genome-wide association …

Improving fine-mapping by modeling infinitesimal effects

R Cui, RA Elzur, M Kanai, JC Ulirsch, O Weissbrod… - Nature Genetics, 2024 - nature.com
Fine-mapping aims to identify causal genetic variants for phenotypes. Bayesian fine-
mapping algorithms (for example, SuSiE, FINEMAP, ABF and COJO-ABF) are widely used …

[HTML][HTML] Transcriptional linkage analysis with in vivo AAV-Perturb-seq

AJ Santinha, E Klingler, M Kuhn, R Farouni, S Lagler… - Nature, 2023 - nature.com
The ever-growing compendium of genetic variants associated with human pathologies
demands new methods to study genotype–phenotype relationships in complex tissues in a …

[HTML][HTML] Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease

J Lake, C Warly Solsberg, JJ Kim, J Acosta-Uribe… - Molecular …, 2023 - nature.com
Genome-wide association studies (GWAS) of Alzheimer's disease are predominantly carried
out in European ancestry individuals despite the known variation in genetic architecture and …

Rhinitis associated with asthma is distinct from rhinitis alone: The ARIA‐MeDALL hypothesis

J Bousquet, E Melén, T Haahtela, GH Koppelman… - Allergy, 2023 - Wiley Online Library
Asthma, rhinitis, and atopic dermatitis (AD) are interrelated clinical phenotypes that partly
overlap in the human interactome. The concept of “one‐airway‐one‐disease,” coined over …