arrow
P

Patrick Deelen

university medical center groningen
H指数:60
被引数:1.9万

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Human genetics implicates a BACH2–NRF2 axis in fetal haemoglobin activation

人类遗传学提示BACH2–NRF2轴在胎儿血红蛋白激活中的作用

Nature
IF48.5
2026-09-300
OAAI
Low-cost generation of clinical-grade , layperson-friendly pharmacogenetic passports using oligonucleotide arrays

使用寡核苷酸阵列低成本生成临床级、面向非专业人士的药物基因组学护照

2025-05-010
OAAI
Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases

脑表达数量性状基因座和网络分析揭示了脑相关疾病的下游效应和推定驱动因素

2023-02-2359
OAAI
KidneyNetwork: using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney disease
2023-02-207
OAAI
Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts
2023-01-0135
OAAI
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021)

肌萎缩性侧索硬化症的常见和罕见变异关联分析确定了15个具有不同遗传结构和神经元特异性生物学的风险位点 (第53卷,1636页,2021)

2022-01-311
OAAI
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

肌萎缩性侧索硬化症的常见和罕见变异关联分析确定了15个具有不同遗传结构和神经元特异性生物学的风险位点

2021-12-06235
OAAI
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

大规模顺式和反式eQTL分析确定了数千个调节血液基因表达的遗传基因座和多基因评分

2021-09-02736
OAAI
TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobility
2021-08-3020
OAAI
RNA-Sequencing Highlights Inflammation and Impaired Integrity of the Vascular Wall in Brain Arteriovenous Malformations
STROKE
IF8.9
2020-01-0125
OAAI
WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene
2019-12-1010
OAAI
Associations of autozygosity with a broad range of human phenotypes

自合性与广泛的人类表型的关联

2019-10-3172
OAAI
Immunochip meta-analysis in European and Argentinian populations identifies two novel genetic loci associated with celiac disease
2019-10-0718
OAAI
Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits
2019-07-24176
OAAI
Improving the diagnostic yield of exome-sequencing by predicting gene-phenotype associations using large-scale gene expression analysis
2019-06-2886
OAAI