Results 241 to 250 of about 283,327 (339)

Increased genomic predictive ability in mango using GWAS-preselected variants and fixed-effect SNPs. [PDF]

Front Plant Sci
Munyengwa N, Wilkinson MJ, Ortiz-Barrientos D, Dillon NL, Webb M, Ali A, Bally ISE, Myburg AA, Hardner CM.   +8 more
europepmc   +1 more source

CXCR4 involvement in neurodegenerative diseases [PDF]

, 2018
Karch, Celeste M., Wen, Natalie
core   +1 more source

Functional validation of GWAS gene candidates for abnormal liver function during zebrafish liver development

, 2013
Leah Y. Liu, Caroline S. Fox, Trista E. North, Wolfram Goessling   +3 more
openalex   +1 more source

Cloud‐Based GWAS Platform: An Innovative Solution for Efficient Acquisition and Analysis of Genomic Data

Med Research, EarlyView.
This graphical abstract illustrates the cloud‐based GWAS platform as a hub that integrates six major multiomics domains: phenomics, neuroscience, proteomics, microbiomics, metabolomics, and nutrigenomics. The platform unifies diverse data types—including clinical phenotypes, neuroimaging, plasma proteomics, microbiome profiles, metabolic biomarkers ...
Xiaohong Ke, Kailai Li, Aimin Jiang, Yasi Zhang, Qi Wang, Zhengrui Li, Jian Zhang, András Hajd, Wenjie Shi, Ulf Kahlert, Anqi Lin, Pengpeng Zhang, Peng Luo   +12 more
wiley   +1 more source

Cross-tissue transcriptome-wide association studies identify genetic susceptibility genes for prostate cancer. [PDF]

BMC Cancer
Hua J, Qian Y, Lu Y, Zhang Q, Que H, Zeng T, Li Q, Deng J, Xie J.   +8 more
europepmc   +1 more source

Genome-wide analysis of self-reported risk-taking behaviour and cross-disorder genetic correlations in the UK Biobank cohort [PDF]

, 2018
Bierut, Laura, et al,, Hartz, Sarah, Horton, Amy   +3 more
core   +1 more source

Characterization of the full site frequency spectrum of GWAS risk alleles in psychiatric disorders

, 2020
Dmytro Pravdyvets
openalex   +1 more source

MendelR: A One‐Stop R Toolkit for Mendelian Randomization Analysis

Med Research, EarlyView.
ABSTRACT MendelR is a fully automated R package specifically developed for Mendelian randomization (MR) studies, designed to address the technical challenges of causal inference in biomedical research. As a powerful causal inference method, Mendelian randomization can effectively reduce confounding bias in observational studies.
Xiaohong Ke, Kailai Li, Anqi Lin, Yasi Zhang, Peng Luo   +4 more
wiley   +1 more source

Genetic underpinnings and causal effects of brain structure and function on chronic pain intensity. [PDF]

Nat Commun
Wang X, Liu J, Wang X, Yang J, Le Y, Song Y, Su Q, Xiao X, Li Y, Qin W, Yu C, Wang P, Liang M.   +12 more
europepmc   +1 more source

Does COMT Play a Role in Parkinson's Disease Susceptibility across Diverse Ancestral Populations?

Movement Disorders, EarlyView.
Abstract Background The catechol‐O‐methyltransferase (COMT) gene is involved in brain catecholamine metabolism, but its association with Parkinson's disease (PD) risk remains unclear. Objective Our aim was to investigate the relationship between COMT genetic variants and PD risk across diverse ancestries.
Miguel Martín‐Bórnez, Nisar Shar, Mohamed Ahmed Nour, David Murphy, Inas Elsayed, Megha Shri Nanjundaswamy, Francisca Nwaokorie, Adedunni Olusanya, Nicole Kuznetsov, Sara Bandres‐Ciga, Alastair J. Noyce, Hirotaka Iwaki, Lietsel Jones, Pilar Gómez‐Garre, Pablo Mir, The Global Parkinson's Genetics Program (GP2), María Teresa Periñán   +16 more
wiley   +1 more source