Shared burden of ultra-rare genetic variants across a spectrum of motor neuron diseases.

IF 19.1 1区医学 Q1 NEUROSCIENCES

Translational Neurodegeneration Pub Date : 2025-10-29 DOI:10.1186/s40035-025-00516-2

Gang Wu, Wenan Chen, Joanne Wuu, Angita Jain, Jason Myers, Isabell Cordts, Evadnie Rampersaud, Jeannine M Heckmann, Melissa Nel, Volkan Granit, Jeffrey Statland, Andrea Swenson, John Ravits, Corey T McMillan, Lauren Elman, James Caress, Ted M Burns, Erik P Pioro, Jaya Trivedi, Jonathan Katz, Carlayne Jackson, Samuel Maiser, David Walk, Yuen So, Jacob L McCauley, Matthew C Baker, J Paul Taylor, Stephan Zuchner, Rosa Rademakers, Marka van Blitterswijk, Michael Benatar

引用次数: 0

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运动神经元疾病谱系中超罕见基因变异的共同负担。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Translational Neurodegeneration Neuroscience-Cognitive Neuroscience

CiteScore

19.50

自引率

0.80%

发文量

审稿时长

10 weeks

期刊介绍： Translational Neurodegeneration, an open-access, peer-reviewed journal, addresses all aspects of neurodegenerative diseases. It serves as a prominent platform for research, therapeutics, and education, fostering discussions and insights across basic, translational, and clinical research domains. Covering Parkinson's disease, Alzheimer's disease, and other neurodegenerative conditions, it welcomes contributions on epidemiology, pathogenesis, diagnosis, prevention, drug development, rehabilitation, and drug delivery. Scientists, clinicians, and physician-scientists are encouraged to share their work in this specialized journal tailored to their fields.