T
Thomas Folkmann Hansen
H-index:92
Citation Count:6.3万
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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
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
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
A structural deletion in the 3′UTR of SLC11A2 is associated with altered iron status: Evidence from two large Danish cohorts
SLC11A2基因3′UTR区域的缺失与铁状态改变相关:来自两个大型丹麦队列的证据
Cohort profile: Copenhagen Hospital Biobank-chronic inflammatory disease—inflammatory bowel disease (CHB-CID:IBD) genetic cohort
队列概要:哥本哈根医院生物库—慢性炎症性疾病—炎症性肠病(CHB-CID:IBD)遗传队列
Associations between past infectious mononucleosis diagnosis and 47 inflammatory and vascular stress biomarkers
过去传染性单核细胞增多症诊断与47种炎症和血管应激生物标志物之间的关联
SCIENTIFIC REPORTS
IF3.9
Lost earnings among triptan non-responders in the general population of Denmark: a measure of disproportionate migraine-attributed burden and of unrecognised and unmet treatment need
丹麦普通人群中曲坦无应答者的收入损失:对不成比例的偏头痛相关负担以及未被识别和未满足的治疗需求的衡量
A genome-wide association meta-analysis links hidradenitis suppurativa to common and rare sequence variants causing disruption of the Notch and Wnt/β-catenin signaling pathways
全基因组关联荟萃分析将化脓性汗腺炎与导致Notch和Wnt/β-catenin信号通路中断的常见和罕见序列变异联系起来
Corroborating written history with ancient DNA: The case of the Well-man described in an Old Norse saga
用古代DNA佐证书面历史:关于《古诺尔斯萨迦》中描述的“韦尔曼”案例
ISCIENCE
IF4.1
Genome-wide association meta-analysis identifies five loci associated with postpartum hemorrhage
全基因组关联荟萃分析确定了与产后出血相关的五个基因座
NATURE GENETICS
IF31.8

