日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

An ACOT4 Multi-Nucleotide Variant Is Associated with Cardiovascular Risk in Norfolk Island and UK Biobank Cohorts

ACOT4多核苷酸变异与诺福克岛和英国生物银行队列中的心血管风险相关

期刊:Genes
影响因子:2.8
doi:10.3390/genes17020205
Meyjes-Brown, Jacob W I; Sutherland, Heidi G; Tran, Kim Ngan; Benton, Miles C; Lea, Rod A; Griffiths, Lyn R
发表日期：2026
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Heparan Sulfate Proteoglycans as Potential Markers for In Vitro Human Neural Lineage Specification.

硫酸乙酰肝素蛋白聚糖作为体外人类神经谱系分化的潜在标志物

期刊:Cells
影响因子:5.2
doi:10.3390/cells14151158
Yu Chieh, Nguyen Duy L B, Gyimesi Martina, Peall Ian W, Pham Son H, Griffiths Lyn R, Okolicsanyi Rachel K, Haupt Larisa M
神经科学
Human
发表日期：2025
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Therapeutic Potentials of the Seaweed-Derived Compounds for Alzheimer's Disease

海藻提取物在阿尔茨海默病治疗中的应用潜力

期刊:Molecules
影响因子:4.6
doi:10.3390/molecules30224456
Ward, Keanie; Cole, Michael H; Griffiths, Lyn R; Sutherland, Heidi G; Winberg, Pia; Meyer, Barbara J; Fernandez, Francesca
阿尔茨海默症
发表日期：2025
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Genome-wide association study identifies novel variants in olfactory, vitamin A, vitamin B, and cadherin pathways associated with learning and memory

全基因组关联研究发现嗅觉、维生素A、维生素B和钙黏蛋白通路中与学习和记忆相关的新变异

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-025-32828-8
Hopkins, Lloyd N; Avgan, Nesli; Sutherland, Heidi G; Fernandez, Francesca E; Knowles, Emma E M; Haupt, Larisa M; Blangero, John; Glahn, David C; Shum, David H K; Lea, Rod A; Griffiths, Lyn R
信号转导
发表日期：2025
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New composite phenotypes enhance chronic kidney disease classification and genetic associations

新的复合表型增强了慢性肾脏病的分类和遗传关联分析

期刊:PLoS Genetics
影响因子:3.7
doi:10.1371/journal.pgen.1011718
Tran, Kim Ngan; Sutherland, Heidi G; Mallett, Andrew J; Griffiths, Lyn R; Lea, Rodney A
发表日期：2025
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Shared genetic risk and causal associations between Post-traumatic stress disorder and migraine with antithrombotic agents and other medications

创伤后应激障碍与偏头痛的共同遗传风险和因果关系，以及抗血栓药物和其他药物的影响

期刊:Neurobiology of Stress
影响因子:3.6
doi:10.1016/j.ynstr.2024.100703
Bainomugisa, Charlotte K; Bruenig, Dagmar; Sutherland, Heidi G; Griffiths, Lyn R; Nyholt, Dale R; Mehta, Divya
偏头痛
创伤后应激障碍
心血管
神经科学
发表日期：2025
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Genetic Insights into Hemiplegic Migraine: Whole Exome Sequencing Highlights Vascular Pathway Involvement via Association Analysis

偏瘫型偏头痛的遗传学见解：全外显子组测序通过关联分析揭示血管通路参与

期刊:Genes
影响因子:2.8
doi:10.3390/genes16080895
Molaee, Zizi; Smith, Robert A; Maksemous, Neven; Griffiths, Lyn R
信号转导
偏头痛
神经科学
发表日期：2025
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The Spectrum of NOTCH3 Variants in an Australian CADASIL Cohort

澳大利亚 CADASIL 患者队列中 NOTCH3 变异谱

期刊:Genes
影响因子:2.8
doi:10.3390/genes16111353
Guyler, Solomon K; Tsai, Jasmine; Maksemous, Neven; Smith, Robert A; Sutherland, Heidi G; Harvey, Evelyn; Duggins, Andrew; Griffiths, Lyn R
NOTCH
OTC
ADAS
ADA
发表日期：2025
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Gene-Based Burden Testing of Rare Variants in Hemiplegic Migraine: A Computational Approach to Uncover the Genetic Architecture of a Rare Brain Disorder

基于基因的偏瘫型偏头痛罕见变异负担检测：一种揭示罕见脑部疾病遗传结构的计算方法

期刊:Genes
影响因子:2.8
doi:10.3390/genes16070807
Alfayyadh, Mohammed M; Maksemous, Neven; Sutherland, Heidi G; Lea, Rodney A; Griffiths, Lyn R
偏头痛
神经科学
发表日期：2025
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Pedigree-Based Estimation of Y-STR Mutation and Male Differentiation Rates: Application to Historical Remains Identification

基于谱系的Y-STR突变率和男性分化率估计：在历史遗骸鉴定中的应用

期刊:Genes
影响因子:2.8
doi:10.3390/genes16101211
Connell, Jasmine R; White, Toni; Zielke, Thais; Armstrong, Luke; Mitchell, Natasha; Griffiths, Lyn R
发表日期：2025
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