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Matthew Zawistowski

University of Michigan
H指数:31
被引数:5,146
浏览量:0

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DNA methylation age acceleration mediates the relationship between systemic inflammation and cognitive impairment

DNA甲基化年龄加速在全身炎症与认知障碍之间的关系中起中介作用。

2025-12-040
OAAI
Expanding biobank pharmacogenomics through machine learning calls of structural variation

通过机器学习识别结构变异以拓展生物样本库的药物基因组学

2025-05-090
PRE
The role of genetically predicted serum iron levels on neurodegenerative and cardiovascular traits
2024-10-190
OAAI
The mediating role of systemic inflammation and moderating role of racialization in disparities in incident dementia
2024-07-130
OA
Relationship between alcohol consumption and dementia with Mendelian randomization approaches among older adults in the United States
2024-06-200
OA
Clinical associations with a polygenic predisposition to benign lower white blood cell counts

与良性低白细胞计数多基因易感性相关的临床特征

2024-04-220
OAAI
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants

通过多祖先全基因组发现187种新的风险变异来表征前列腺癌风险

2023-11-0928
OA
Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration

4,787个体的全基因组测序确定了年龄相关性黄斑变性中基于基因的罕见变异

2023-11-024
OA
A pilot genome-wide association study meta-analysis of gastroparesis

胃轻瘫的初步全基因组关联研究荟萃分析

2023-09-081
OAAI
The phenotype-genotype reference map: Improving biobank data science through replication

表型-基因型参考图: 通过复制改进生物库数据科学

2023-09-015
OAAI
Cardiometabolic disease and obesity patterns differentially predict acute kidney injury after total joint replacement: a retrospective analysis

心脏代谢疾病和肥胖模式差异预测全关节置换术后急性肾损伤: 一项回顾性分析

2023-07-011
PRE
The Michigan Genomics Initiative: A biobank linking genotypes and electronic clinical records in Michigan Medicine patients
2023-02-0135
OAAI
Fibromuscular Dysplasia and Abdominal Aortic Aneurysms Are Dimorphic Sex-Specific Diseases With Shared Complex Genetic Architecture

纤维肌性发育不良和腹主动脉瘤是具有共同复杂遗传结构的双态性特异性疾病

2022-12-018
OA
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease

全球生物银行荟萃分析倡议: 推动人类疾病的基因发现

2022-10-01126
OAAI
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases (vol 12, 6031, 2021)
2022-04-200
OAAI
GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer (vol 11, 3981, 2020)
2021-12-161
OAAI
Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders

对53,400例肠易激综合征患者的全基因组分析突出了情绪和焦虑障碍的共同遗传途径

2021-11-05129
OAAI
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases
2021-10-1535
OAAI
A survey of functional dyspepsia in 361,360 individuals: Phenotypic and genetic cross-disease analyses

361,360个体功能性消化不良的调查: 表型和遗传交叉疾病分析

2021-08-119
OAAI
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (Jan, 10.1038/s41380-020-01006-9, 2021)
2021-03-050
OAAI