Fulya Akçimen

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

Calwing Liao, Alexandre D. Laporte, Dan Spiegelman et al. · Nature Communications · 2019 · 112 citations · Full text

Investigation of the RFC1 Repeat Expansion in a Canadian and a Brazilian Ataxia Cohort: Identification of Novel Conformations

Fulya Akçimen, Jay P. Ross, Cynthia V. Bourassa et al. · Frontiers in Genetics · 2019 · 74 citations · Full text

Normal and pathogenic variation of <i>RFC1</i> repeat expansions: implications for clinical diagnosis

Natalia Dominik, Stefania Magri, Riccardo Curró et al. · Brain · 2023 · 66 citations · Full text

Disease Progression, Immunodeficiencies, Genetics +21

Genome sequence analyses identify novel risk loci for multiple system atrophy

Ruth Chia, Anindita Ray, Zalak Shah et al. · Neuron · 2024 · 34 citations · Full text

Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients

Konstantinos Mitropoulos, Eleni Merkouri Papadima, Georgia Xiromerisiou et al. · Human Genomics · 2017 · 26 citations · Full text