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List of works by Fulya Akçimen

A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID

scientific article published on 17 August 2019

Clinical and molecular characterization and response to acitretin in three families with Sjögren-Larsson syndrome

scientific article published on 27 April 2018

Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project

scientific article published on 07 November 2020

Genetic and epidemiological characterization of restless legs syndrome in Québec

scientific article published on 30 October 2019

Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression

scientific article published on 14 November 2019

Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database

scientific article published on 24 June 2020

SKOR1 has a transcriptional regulatory role on genes involved in pathways related to restless legs syndrome

scientific article published on 22 June 2020

Transcriptome-wide association study for restless legs syndrome identifies new susceptibility genes

scientific article published on 10 July 2020

Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes

scientific article published on 01 October 2019

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