S
Sisse Rye Ostrowski
H-index:72
Citation Count:2.0万
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Alzheimer’s disease genetics converges on microglial and neuronal dysregulation
阿尔茨海默病遗传学研究聚焦于小胶质细胞和神经元功能失调
Nature
IF48.5
A multimodal total-body dynamic [18F]FDG PET/CT/MRI dataset of 100 healthy humans
包含100名健康受试者的多模态全身动态[18F]FDG PET/CT/MRI数据集
Scientific Data
IF6.9
Genetic architecture of cytokine autoantibodies and associated risk of common diseases
细胞因子自身抗体遗传结构和相关常见疾病风险
Nature Communications
IF15.7
The genetic architecture of fibromyalgia across 2.5 million individuals
纤维肌痛的遗传结构:一项涉及250万个体的研究
Nature Medicine
IF50
Psychiatric genetic liability is associated with the severity of COVID-19 and other acute respiratory infections: an observational study across five Northern European countries
精神遗传易感性与中国肺炎和其他急性呼吸道感染的严重程度相关:一项跨越五个北欧国家的观察性研究
Genome Medicine
IF11.2
Genome-wide association analyses of borderline personality disorder identify 11 loci and highlight shared risk with mental and somatic disorders
边缘性人格障碍的全基因组关联分析鉴定了11个位点,并突出了与精神和躯体疾病的共享风险
Nature Genetics
IF29
Combining genome-wide polygenic scores with registry data for colorectal cancer risk-based screening
结合全基因组多基因评分与登记数据用于结直肠癌风险导向筛查
The Danish Lymphoid Cancer Research (DALY-CARE): Genetic Cohort Profile
丹麦淋巴瘤癌症研究(DALY-CARE):遗传队列简介
Genome-wide meta-analysis identifies genetic drivers of bile acid metabolism in intrahepatic cholestasis of pregnancy
全基因组荟萃分析确定妊娠期肝内胆汁淤积症胆汁酸代谢的遗传驱动因素
Nature Communications
IF15.7
Severe allergic and anaphylactic transfusion reactions in consecutive recipients from the same donor
连续接受同一供者输血后出现的严重过敏和过敏性休克反应
Haematologica
IF7.9
Genomic analyses implicate hormonal and metabolic dysregulation in polycystic ovary syndrome
基因组分析暗示多囊卵巢综合征中的激素和代谢失调
Nature Genetics
IF29
Fibrotic disease co-occurrence and associated risk of subsequent organ failure: a nationwide matched cohort study
纤维化疾病共病及后续器官衰竭相关风险的全国性匹配队列研究
Rheumatology
IF4.4
Central role of glycosylation processes in human genetic susceptibility to SARS-CoV-2 infections with Omicron variants
糖基化过程在人类对Omicron变体的SARS-CoV-2感染的遗传易感性中的核心作用
Nature Genetics
IF29
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
主动脉狭窄的基因组和转录组学分析可增强治疗靶点的发现和疾病预测
Nature Genetics
IF29

