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Muralidharan Sargurupremraj

university of texas health sciences center
H指数:31
被引数:8,788

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Proteogenomics in cerebrospinal fluid and plasma reveals new biological fingerprint of cerebral small vessel disease

脑脊液和血浆蛋白质组学揭示脑小血管病新的生物指纹

2025-11-200
OAAI
The brain neurovascular epigenome and its association with dementia

脑神经血管表观基因组及其与痴呆症的关系

Neuron
IF15
2025-10-300
OAAI
Polygenic score integrating neurodegenerative and vascular risk informs dementia risk stratification

多基因评分整合神经退行性和血管性风险,为痴呆风险分层提供信息

2025-03-050
OAAI
Genetic variants for head size share genes and pathways with cancer

头部大小的遗传变异与癌症共享基因和途径

2024-05-010
OAAI
Mendelian Randomization Applied to Neurology
2024-02-2712
OAAI
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

血管周围空间负荷的基因组学阐明脑小血管病的早期机制

2023-04-1733
OAAI
Stroke genetics informs drug discovery and risk prediction across ancestries
Nature
IF48.5
2022-09-300
OAAI
Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities
2022-08-0318
OAAI
Genomic Studies Across the Lifespan Point to Early Mechanisms Determining Subcortical Volumes
2022-06-014
OAAI
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate

脑小血管疾病极端情况的基因定位研究表明TRIM47是一个强有力的候选者

BRAIN
IF11.7
2022-05-0212
OAAI
Associations Between Brainstem Volume and Alzheimer's Disease Pathology in Middle-Aged Individuals of the Framingham Heart Study
2022-04-192
OA
Circulating Metabolome and White Matter Hyperintensities in Women and Men
2022-04-0520
OA
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors (vol 52, pg 1303, 2020)

颅内动脉瘤的全基因组关联研究确定了17个风险基因座和与临床风险因素的遗传重叠 (第52卷,1303页,2020)

2020-12-225
OAAI
Cerebral small vessel disease genomics and its implications across the lifespan

脑小血管疾病基因组学及其在整个生命周期中的意义

2020-12-08106
OAAI
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

颅内动脉瘤的全基因组关联研究确定了17个危险位点并与临床危险因素遗传重叠

2020-11-16172
OAAI