日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Discovering genetic mechanisms underlying the co-occurrence of Parkinson's disease and non-motor traits

揭示帕金森病与非运动症状共存的遗传机制

Gokuladhas, Sreemol; Fadason, Tayaza; Farrow, Sophie; Cooper, Antony; O'Sullivan, Justin M

Links between melanoma germline risk loci, driver genes and comorbidities: insight from a tissue-specific multi-omic analysis

黑色素瘤种系风险位点、驱动基因与合并症之间的联系:来自组织特异性多组学分析的启示

Pudjihartono, Michael; Golovina, Evgeniia; Fadason, Tayaza; O'Sullivan, Justin M; Schierding, William

De novo identification of complex traits associated with asthma

从头识别与哮喘相关的复杂性状

Zaied, Roan E; Fadason, Tayaza; O'Sullivan, Justin M

Comorbidity genetic risk and pathways impact SARS-CoV-2 infection outcomes

合并症遗传风险和通路影响SARS-CoV-2感染结局

Jaros, Rachel K; Fadason, Tayaza; Cameron-Smith, David; Golovina, Evgeniia; O'Sullivan, Justin M

De novo discovery of traits co-occurring with chronic obstructive pulmonary disease

从头发现与慢性阻塞性肺病共存的特征

Golovina, Evgeniia; Fadason, Tayaza; Jaros, Rachel K; Kumar, Haribalan; John, Joyce; Burrowes, Kelly; Tawhai, Merryn; O'Sullivan, Justin M

Establishing gene regulatory networks from Parkinson's disease risk loci

从帕金森病风险位点建立基因调控网络

Farrow, Sophie L; Schierding, William; Gokuladhas, Sreemol; Golovina, Evgeniia; Fadason, Tayaza; Cooper, Antony A; O'Sullivan, Justin M

A Review of Feature Selection Methods for Machine Learning-Based Disease Risk Prediction

基于机器学习的疾病风险预测的特征选择方法综述

Pudjihartono, Nicholas; Fadason, Tayaza; Kempa-Liehr, Andreas W; O'Sullivan, Justin M

Unravelling the Shared Genetic Mechanisms Underlying 18 Autoimmune Diseases Using a Systems Approach

运用系统方法揭示18种自身免疫性疾病的共同遗传机制

Gokuladhas, Sreemol; Schierding, William; Golovina, Evgeniia; Fadason, Tayaza; O'Sullivan, Justin

Untangling the genetic link between type 1 and type 2 diabetes using functional genomics

利用功能基因组学揭开1型糖尿病和2型糖尿病之间的遗传联系

Nyaga, Denis M; Vickers, Mark H; Jefferies, Craig; Fadason, Tayaza; O'Sullivan, Justin M

Understanding the impact of SNPs associated with autism spectrum disorder on biological pathways in the human fetal and adult cortex

了解与自闭症谱系障碍相关的单核苷酸多态性对人类胎儿和成人大脑皮层生物通路的影响

Golovina, E; Fadason, T; Lints, T J; Walker, C; Vickers, M H; O'Sullivan, J M