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YA

Yevgeniya Abramzon

National Human Genome Research Institute US

37
Publications
10,643
Citations
25
H-Index
25
i10-Index
6.0
2yr Mean Cite
-
Cite/Paper
Data combined from OpenAlex + Semantic Scholar. OA = OpenAlex S2 = Semantic Scholar
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Publication & Citation Trends

Publications

36 total

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study PDF

Elisa Majounie, Alan E. Renton, Kin Y. Mok, Elise G.P. Dopper, Adrian J. Waite et al. - The Lancet Neurology, 2012
Cited by 1,214 OpenAlex

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD PDF

Alan E. Renton, Elisa Majounie, Adrian J. Waite, Javier Simón‐Sánchez, Sara Rollinson et al. - Neuron, 2011
Cited by 4,430 OpenAlex

Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS PDF

Janel O. Johnson, Jessica Mandrioli, Michael Benatar, Yevgeniya Abramzon, Vivianna M. Van Deerlin et al. - Neuron, 2010
Cited by 1,223 OpenAlex

Research Topics

Amyotrophic Lateral Sclerosis Research (25) Neurological diseases and metabolism (15) Neurogenetic and Muscular Disorders Research (13) Genetic Neurodegenerative Diseases (5) Parkinson's Disease Mechanisms and Treatments (4)

Affiliations

Università Cattolica del Sacro Cuore
IT 2014 - 2014
National Institutes of Health
US 2021 - 2010
Sobell House
GB 2021 - 2016
National Human Genome Research Institute
US 2025 - 2025
National Institute on Aging
US 2021 - 2010

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