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Abramzon, Yevgeniya A.
73  results:
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1

Investigation of the genetic aetiology of Lewy body disease..:

Wu, Lesley Yue ; Real, Raquel ; Martinez-Carrasco, Alejandro...
Brain Communications.  6 (2024)  4 - p. , 2024
Link: https://doi.org/10.1093/..
 
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2

Identification of genetic risk loci and prioritization of g..:

Chia, Ruth ; Saez-Atienzar, Sara ; Murphy, Natalie...
Proceedings of the National Academy of Sciences.  119 (2022)  5 - p. , 2022
Link: https://doi.org/10.1073/..
 
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3

Genetic analysis of amyotrophic lateral sclerosis identifie..:

Saez-Atienzar, Sara ; Bandres-Ciga, Sara ; Langston, Rebekah G....
Science Advances.  7 (2021)  3 - p. , 2021
Link: https://doi.org/10.1126/..
 
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4

Pathogenic Huntingtin Repeat Expansions in Patients with Fr..:

Dewan, Ramita ; Chia, Ruth ; Ding, Jinhui...
Neuron.  109 (2021)  3 - p. 448-460.e4 , 2021
Link: https://doi.org/10.1016/..
 
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5

Genome sequencing analysis identifies new loci associated w..:

Chia, Ruth ; Sabir, Marya S. ; Bandres-Ciga, Sara...
Nature Genetics.  53 (2021)  3 - p. 294-303 , 2021
Link: https://doi.org/10.1038/..
 
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6

The Overlapping Genetics of Amyotrophic Lateral Sclerosis a..:

Abramzon, Yevgeniya A. ; Fratta, Pietro ; Traynor, Bryan J..
Frontiers in Neuroscience.  14 (2020)  - p. , 2020
Link: https://doi.org/10.3389/..
 
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7

Genetic analysis of neurodegenerative diseases in a patholo..:

Blauwendraat, Cornelis ; Pletnikova, Olga ; Geiger, Joshua T....
Neurobiology of Aging.  76 (2019)  - p. 214.e1-214.e9 , 2019
Link: https://doi.org/10.1016/..
 
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8

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene:

Nicolas, Aude ; Kenna, Kevin P. ; Renton, Alan E....
Neuron.  97 (2018)  6 - p. 1267-1288 , 2018
Link: https://doi.org/10.1016/..
 
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9

NeuroChip, an updated version of the NeuroX genotyping plat..:

Blauwendraat, Cornelis ; Faghri, Faraz ; Pihlstrom, Lasse...
Neurobiology of Aging.  57 (2017)  - p. 247.e9-247.e13 , 2017
Link: https://doi.org/10.1016/..
 
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10

Exome sequencing establishes a gelsolin mutation as the cau..:

Caress, James B. ; Johnson, Janel O. ; Abramzon, Yevgeniya A....
Muscle & Nerve.  56 (2017)  5 - p. 1001-1005 , 2017
Link: https://doi.org/10.1002/..
 
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11

Mutations in the Matrin 3 gene cause familial amyotrophic l..:

ITALSGEN ; Johnson, Janel O ; Pioro, Erik P...
Nature Neuroscience.  17 (2014)  5 - p. 664-666 , 2014
Link: https://doi.org/10.1038/..
 
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12

Frequency of the C9orf72 hexanucleotide repeat expansion in..:

Majounie, Elisa ; Renton, Alan E ; Mok, Kin...
The Lancet Neurology.  11 (2012)  4 - p. 323-330 , 2012
Link: https://doi.org/10.1016/..
 
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13

Exome sequencing reveals riboflavin transporter mutations a..:

Johnson, Janel O. ; Gibbs, J. Raphael ; Megarbane, Andre...
Brain.  135 (2012)  9 - p. 2875-2882 , 2012
Link: https://doi.org/10.1093/..
 
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14

Valosin-containing protein (VCP) mutations in sporadic amyo..:

Abramzon, Yevgeniya ; Johnson, Janel O. ; Scholz, Sonja W....
Neurobiology of Aging.  33 (2012)  9 - p. 2231.e1-2231.e6 , 2012
Link: https://doi.org/10.1016/..
 
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15

Large C9orf72 repeat expansions are not a common cause of P..:

Majounie, Elisa ; Abramzon, Yevgeniya ; Renton, Alan E....
Neurobiology of Aging.  33 (2012)  10 - p. 2527.e1-2527.e2 , 2012
Link: https://doi.org/10.1016/..
 
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