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D

Dirk S. Paul

Centre for Genomics Research
H指数:3
被引数:94

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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
Natural History and Clinicopathological Associations of TRPC6-Associated Podocytopathy
2024-10-010
PRE
Damaging mutations in liver X receptor-α are hepatotoxic and implicate cholesterol sensing in liver health

肝脏X受体-α 的破坏性突变具有肝毒性,并暗示肝脏健康中的胆固醇感应

2024-09-250
OAAI
Misexpression of inactive genes in whole blood is associated with nearby rare structural variants
2024-08-011
OAAI
Protein-truncating variants in BSN are associated with severe adult-onset obesity, type 2 diabetes and fatty liver disease

BSN中的蛋白质截断变体与严重的成人肥胖,2型糖尿病和脂肪肝疾病有关

2024-04-042
OAAI
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
2023-11-3017
OAAI
Rare variant associations with plasma protein levels in the UK Biobank

英国生物库中与血浆蛋白水平的罕见变异关联

Nature
IF48.5
2023-10-040
OAAI
Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets (vol 24, pg 1540, 2023)
2023-09-076
OAAI
Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets
2023-08-10207
OAAI
Human genetics uncovers MAP3K15 as an obesity-independent therapeutic target for diabetes
2022-11-1611
OAAI
Pharmacogenomic study of heart failure and candesartan response from the CHARM programme

CHARM计划对心力衰竭和坎地沙坦反应的药物基因组学研究

2022-06-232
OAAI
Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus (vol 13, 1222, 2022)

阐明原血管疾病位点遗传交叉疾病关联的机制 (第13卷,1222,2022)

2022-04-060
OAAI
Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus
2022-03-096
OAAI
Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci
2021-09-1033
OAAI
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (vol 52, pg 1314, 2020)

通过对130万个人的荟萃分析发现与血压调节相关的罕见变异 (第52卷,1314页,2020)

2021-03-161
OAAI
A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis
2021-02-03100
OAAI