Suchergebnisse - "Akçimen, Fulya"

PubPharm (55)

1

Questioning the association of the STMN2 dinucleotide repeat with ALS

enthalten in: bioRxiv.org | 2024

von Ross, J. | Akcimen, F. | Liao, C. | +6

2

Rare-variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genome

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2024

von Ross, J. | Akçimen, F. | Liao, C. | +9

3

Genomic analysis identifies risk factors in restless legs syndrome

enthalten in: bioRxiv.org | 2023

von Akçimen, F. | Chia, R. | Saez-Atienzar, S. | +9

4

Genomic analysis identifies risk factors in restless legs syndrome

enthalten in: medRxiv : the preprint server for health sciences | 2023

von Akçimen, F. | Chia, R. | Saez-Atienzar, S. | +9

5

Normal and pathogenic variation of RFC1 repeat expansions : implications for clinical diagnosis

enthalten in: Brain : a journal of neurology | 2023

von Dominik, N. | Magri, S. | Currò, R. | +116

ErratumIn: Brain. 2024 Feb 1;147(2):e23. - PMID 38181422

6

Amyotrophic lateral sclerosis : translating genetic discoveries into therapies

enthalten in: Nature reviews. Genetics | 2023

von Akçimen, F. | Lopez, E. | Landers, J. | +4

7

Rare and common variant analyses of amyotrophic lateral sclerosis in the French-Canadian genome

enthalten in: bioRxiv.org | 2022

von Ross, J. | Akçimen, F. | Liao, C. | +9

8

Questioning the Association of the STMN2 Dinucleotide Repeat With Amyotrophic Lateral Sclerosis

enthalten in: Neurology. Genetics | 2022

von Ross, J. | Akçimen, F. | Liao, C. | +6

9

Progress in the genetics of restless legs syndrome : the path ahead in the era of whole-genome sequencing

enthalten in: Sleep | 2022

von Akçimen, F. | Dion, P. | Rouleau, G.

CommentOn: Sleep. 2022 Aug 11;45(8):. - PMID 35486972

10

Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette's syndrome

enthalten in: Communications biology | 2022

von Liao, C. | Vuokila, V. | Catoire, H. | +6

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