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

Characterizing Self-Reported Daily Diary Epistaxis Measures in Hereditary Hemorrhagic Telangiectasia

对遗传性出血性毛细血管扩张症患者自我报告的每日鼻出血日记测量结果进行特征分析

期刊:Laryngoscope Investigative Otolaryngology
影响因子:1.7
doi:10.1002/lio2.70354
Tarulli, C M; Ma, X; Bayoumi, A M; Patel, A; Vozoris, N T; Lee, J M; Faughnan, M E
发表日期：2026
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Engagement to Identify Health Priorities of People With Intellectual and/or Developmental Disability

参与确定智力及/或发育障碍人士的健康优先事项

期刊:Otjr-Occupation Participation and Health
影响因子:1.5
doi:10.1177/15394492251385448
Benevides, Teal W; Pham, Hoangmai H; Andresen, May-Lynn; Bahr, Madelyn R; Corey, Tim; Nicholson, Joanne; Faughnan, Kristen; Jaremski, Jennifer E; Langer, Carolyn; Siasoco, Vincent; Hernandez-Hons, Alexis; Shore, Stephen M
发育与干细胞
发表日期：2026
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Standardization of Terminology, Definitions, and Outcome Criteria for Bleeding in Hereditary Hemorrhagic Telangiectasia: International Consensus Report

遗传性出血性毛细血管扩张症出血术语、定义和结局标准标准化：国际共识报告

期刊:American Journal of Hematology
影响因子:9.9
doi:10.1002/ajh.70011
Al-Samkari, Hanny; Kasthuri, Raj S; Mager, Hans-Jurgen; Zhou, Jenny Y; Serra, Marcelo M; Samuelson-Bannow, Bethany T; Van Doren, Layla N; Piccirillo, Jay F; Clancy, Marianne S; McCrae, Keith R; Thomas, Sonia M; Riera-Mestre, Antoni; Pishko, Allyson M; Sewaralthahab, Sarah; Gossage, James R; Iyer, Vivek N; Hermans, Cedric; Hammill, Adrienne; Winship, Ingrid; Mei-Zahav, Meir; von Drygalski, Annette; Olitsky, Scott; Faughnan, Marie E
发表日期：2025
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Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis

遗传性出血性毛细血管扩张症动静脉畸形中的体细胞突变支持双等位基因二次打击突变的发病机制。

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2025.03.007
DeBose-Scarlett, Evon; Ressler, Andrew K; Gallione, Carol J; Cantis, Gonzalo Sapisochin; Friday, Cassi; Weinsheimer, Shantel; Schimmel, Katharina; Spiekerkoetter, Edda; Kim, Helen; Gossage, James R; Faughnan, Marie E; Marchuk, Douglas A
细胞生物学
发表日期：2025
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Recurrent somatic copy number alterations in resected cerebral cavernous malformations

切除的脑海绵状血管畸形中复发性体细胞拷贝数改变

期刊:Human Genomics
影响因子:4.3
doi:10.1186/s40246-025-00886-8
Ressler, Andrew K; Debose-Scarlett, Evon; Fuenzalida, Amanda; Lightle, Rhonda; Weinsheimer, Shantel; Faughnan, Marie E; Spiekerkoetter, Edda; Schimmel, Katharina; Lawton, Michael; Kim, Helen; Awad, Issam; Marchuk, Douglas A
细胞生物学
神经科学
发表日期：2025
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Health outcomes following COVID-19 infection and vaccination in hereditary hemorrhagic telangiectasia

遗传性出血性毛细血管扩张症患者感染新冠病毒和接种疫苗后的健康结果

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-025-03561-2
Tarulli, Christopher M; Ma, Xiayi; Chokar, Kamalprit; Vozoris, Nicholas T; Clancy, Marianne S; Faughnan, Marie E
炎症/感染
新冠
微生物学
发表日期：2025
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Assessing racial differences in North American hereditary hemorrhagic telangiectasia study recruitment and care

评估北美遗传性出血性毛细血管扩张症研究招募和护理中的种族差异

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-025-03883-1
Scott, Gabriella; Agundiz, Ashlee; Nelson, Jeffrey; Hetts, Steven; Clancy, Marianne; Kim, Helen; Faughnan, Marie E
发表日期：2025
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Common and distinct circulating microRNAs in four neurovascular disorders

四种神经血管疾病中常见和特有的循环microRNA

期刊:Biochemistry and Biophysics Reports
影响因子:2.2
doi:10.1016/j.bbrep.2025.102189
Koskimäki, Janne; Jhaveri, Aditya; Srinath, Abhinav; Bindal, Akash; Vera Cruz, Diana; Priyanka Yeradoddi, Geetha; Lightle, Rhonda; Lee, Justine; Stadnik, Agnieszka; Iqbal, Javed; Alcazar-Felix, Roberto; Hage, Stephanie; Romanos, Sharbel; Shenkar, Robert; Loeb, Jeffrey; Faughnan, Marie E; Weinsheimer, Shantel; Kim, Helen; Girard, Romuald; Awad, Issam A
发表日期：2025
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CDK6-mediated endothelial cell cycle acceleration drives arteriovenous malformations in hereditary hemorrhagic telangiectasia

CDK6介导的内皮细胞周期加速驱动遗传性出血性毛细血管扩张症中的动静脉畸形

期刊:Nature Cardiovascular Research
影响因子:9.4
doi:10.1038/s44161-024-00550-9
Sajeth Dinakaran # ，Sima Qutaina # ，Haitian Zhao ，Yuefeng Tang ，Zhimin Wang ，Santiago Ruiz ，Aya Nomura-Kitabayashi ，Christine N Metz ，Helen M Arthur ，Stryder M Meadows ，Lionel Blanc ，Marie E Faughnan ，Philippe Marambaud
内皮细胞
CDK6
细胞生物学
发表日期：2024
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Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis

遗传性出血性毛细血管扩张症动静脉畸形中的体细胞突变支持双等位基因二次打击突变的发病机制。

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2024.08.020
DeBose-Scarlett, Evon; Ressler, Andrew K; Gallione, Carol J; Sapisochin Cantis, Gonzalo; Friday, Cassi; Weinsheimer, Shantel; Schimmel, Katharina; Spiekerkoetter, Edda; Kim, Helen; Gossage, James R; Faughnan, Marie E; Marchuk, Douglas A
细胞生物学
发表日期：2024
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