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Akçimen, Fulya
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1

Genome sequence analyses identify novel risk loci for multi..:

Chia, Ruth ; Ray, Anindita ; Shah, Zalak...
Neuron.  112 (2024)  13 - p. 2142-2156.e5 , 2024
Link: https://doi.org/10.1016/..
 
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2

Rare-variant and polygenic analyses of amyotrophic lateral ..:

Ross, Jay P. ; Akçimen, Fulya ; Liao, Calwing...
Genetics in Medicine.  26 (2024)  1 - p. 100967 , 2024
Link: https://doi.org/10.1016/..
 
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3

Investigating the Protective Role of the Mitochondrial 2158..:

Akçimen, Fulya ; van Midden, Vesna ; Akerman, S. Can...
Movement Disorders.  , 2024
Link: https://doi.org/10.1002/..
 
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4

Normal and pathogenic variation of RFC1 repeat expansions: ..:

Dominik, Natalia ; Magri, Stefania ; Currò, Riccardo...
Brain.  146 (2023)  12 - p. 5060-5069 , 2023
Link: https://doi.org/10.1093/..
 
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5

Amyotrophic lateral sclerosis: translating genetic discover..:

Akçimen, Fulya ; Lopez, Elia R. ; Landers, John E....
Nature Reviews Genetics.  24 (2023)  9 - p. 642-658 , 2023
Link: https://doi.org/10.1038/..
 
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6

Progress in the genetics of restless legs syndrome: the pat..:

Akçimen, Fulya ; Dion, Patrick A ; Rouleau, Guy A
Sleep.  45 (2022)  8 - p. , 2022
Link: https://doi.org/10.1093/..
 
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7

Transcriptome-wide association study reveals increased neur..:

Liao, Calwing ; Vuokila, Veikko ; Catoire, Hélène...
Communications Biology.  5 (2022)  1 - p. , 2022
Link: https://doi.org/10.1038/..
 
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8

The Complex Genetic Landscape of Hereditary Ataxias in Turk..:

Vural, Atay ; Şimşir, Gülşah ; Tekgül, Şeyma...
Movement Disorders.  36 (2021)  7 - p. 1676-1688 , 2021
Link: https://doi.org/10.1002/..
 
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9

Evidence for Non‐Mendelian Inheritance in Spastic Paraplegi..:

Estiar, Mehrdad A. ; Yu, Eric ; Haj Salem, Ikhlass...
Movement Disorders.  36 (2021)  7 - p. 1664-1675 , 2021
Link: https://doi.org/10.1002/..
 
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10

Diagnostic Yield of Whole Exome Sequencing for Adults with ..:

da Graça, Felipe Franco ; Peluzzo, Thiago M. ; Bonadia, Luciana Cardoso...
The Cerebellum.  21 (2021)  1 - p. 49-54 , 2021
Link: https://doi.org/10.1007/..
 
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11

Multiomics Analyses Identify Genes and Pathways Relevant to..:

Liao, Calwing ; Sarayloo, Faezeh ; Rochefort, Daniel...
Movement Disorders.  35 (2020)  7 - p. 1153-1162 , 2020
Link: https://doi.org/10.1002/..
 
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12

Genome-wide association study identifies genetic factors th..:

Akçimen, Fulya ; Martins, Sandra ; Liao, Calwing...
Aging.  12 (2020)  6 - p. 4742-4756 , 2020
Link: https://doi.org/10.18632..
 
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13

Phenotypic and genotypic features of patients diagnosed wit..:

Kotan, Dilcan ; Özözen Ayas, Zeynep ; Tunca, Ceren...
Acta Neurologica Belgica.  120 (2020)  6 - p. 1411-1418 , 2020
Link: https://doi.org/10.1007/..
 
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14

Transcriptomic Changes Resulting From STK32B Overexpression..:

Liao, Calwing ; Sarayloo, Faezeh ; Vuokila, Veikko...
Frontiers in Genetics.  11 (2020)  - p. , 2020
Link: https://doi.org/10.3389/..
 
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15

SKOR1 has a transcriptional regulatory role on genes involv..:

Sarayloo, Faezeh ; Spiegelman, Dan ; Rochefort, Daniel...
European Journal of Human Genetics.  28 (2020)  11 - p. 1520-1528 , 2020
Link: https://doi.org/10.1038/..
 
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