Fulya Akcimen (Seçil Vural, Fulya Akçimen)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 21

Top Topics

Dna Methylation

Amyotrophic Lateral Sclerosis

Genome Wide Association

Top Venues

medRxiv : the preprint server for health sciences

Annals of neurology

Movement disorders : official journal of the Movement Disorder Society

Communications biology

This page only lists publications with an associated author ORCID identifier.

Publications

Fulya Akcimen, Ruth Chia, Sara Saez-Atienzar, Paola Ruffo, Memoona Rasheed, Jay P Ross, Calwing Liao, Anindita Ray, Patrick A Dion, Sonja W Scholz, Guy A Rouleau, Bryan J Traynor
Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome. Annals of neurology (2024)
Fulya Akcimen, Ruth Chia, Sara Saez-Atienzar, Paola Ruffo, Memoona Rasheed, Jay P Ross, Calwing Liao, Anindita Ray, Patrick A Dion, Sonja W Scholz, Guy A Rouleau, Bryan J Traynor
Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome. Annals of neurology (2024)
Fulya Akcimen, Vesna Marija van Midden, S Can Akerman, Mary B Makarious, null null, Jeffrey D Rothstein, Zih-Hua Fang, Sara Bandres-Ciga
Investigating the Protective Role of the Mitochondrial 2158 T > C Variant in Parkinson's Disease. Movement disorders : official journal of the Movement Disorder Society (2024)
Fulya Akcimen, Elia R Lopez, John E Landers, Avindra Nath, Adriano Chiò, Ruth Chia, Bryan J Traynor
Amyotrophic lateral sclerosis: translating genetic discoveries into therapies. Nature reviews. Genetics (2023)
Natalia Dominik, Stefania Magri, Riccardo Currò, Elena Abati, Stefano Facchini, Marinella Corbetta, Hannah MacPherson, Daniela Di Bella, Elisa Sarto, Igor Stevanovski, Sanjog R Chintalaphani, Fulya Akcimen, Arianna Manini, Elisa Vegezzi, Ilaria Quartesan, Kylie-Ann Montgomery, Valentina Pirota, Emmanuele Crespan, Cecilia Perini, Glenda Paola Grupelli, Pedro José Tomaselli, Wilson Marques, null null, Joseph Shaw, James Polke, Ettore Salsano, Silvia Fenu, Davide Pareyson, Chiara Pisciotta, George K Tofaris, Andrea H Nemeth, John Ealing, Aleksandar Radunovic, Seamus Kearney, Kishore R Kumar, Steve Vucic, Marina Kennerson, Mary M Reilly, Henry Houlden, Ira W Deveson, Arianna Tucci, Franco Taroni, Andreas Cortese
Normal and pathogenic variation of RFC1 repeat expansions: implications for clinical diagnosis. Brain : a journal of neurology (2023)
Fulya Akcimen, Ruth Chia, Sara Saez-Atienzar, Paola Ruffo, Memoona Rasheed, Jay P Ross, Calwing Liao, Anindita Ray, Patrick A Dion, Sonja W Scholz, Guy A Rouleau, Bryan J Traynor
Genomic analysis identifies risk factors in restless legs syndrome. medRxiv : the preprint server for health sciences (2023)
Fulya Akcimen, Ruth Chia, Sara Saez-Atienzar, Paola Ruffo, Memoona Rasheed, Jay P Ross, Calwing Liao, Anindita Ray, Patrick A Dion, Sonja W Scholz, Guy A Rouleau, Bryan J Traynor
Genomic analysis identifies risk factors in restless legs syndrome. medRxiv : the preprint server for health sciences (2023)
Fulya Akcimen, Ruth Chia, Sara Saez-Atienzar, Paola Ruffo, Memoona Rasheed, Jay P Ross, Calwing Liao, Anindita Ray, Patrick A Dion, Sonja W Scholz, Guy A Rouleau, Bryan J Traynor
Genomic analysis identifies risk factors in restless legs syndrome. medRxiv : the preprint server for health sciences (2023)
Fulya Akcimen, Ruth Chia, Sara Saez-Atienzar, Paola Ruffo, Memoona Rasheed, Jay P Ross, Calwing Liao, Anindita Ray, Patrick A Dion, Sonja W Scholz, Guy A Rouleau, Bryan J Traynor
Genomic analysis identifies risk factors in restless legs syndrome. medRxiv : the preprint server for health sciences (2023)
Fulya Akcimen, Ruth Chia, Sara Saez-Atienzar, Paola Ruffo, Memoona Rasheed, Jay P Ross, Calwing Liao, Anindita Ray, Patrick A Dion, Sonja W Scholz, Guy A Rouleau, Bryan J Traynor
Genomic analysis identifies risk factors in restless legs syndrome. medRxiv : the preprint server for health sciences (2023)
Jay P Ross, Fulya Akcimen, Calwing Liao, Dan Spiegelman, Ben Weisburd, Nicolas Dupré, Patrick A Dion, Guy A Rouleau, Sali M K Farhan
Questioning the Association of the STMN2 Dinucleotide Repeat With Amyotrophic Lateral Sclerosis. Neurology. Genetics 8 (4) (2022)
Calwing Liao, Veikko Vuokila, Hélène Catoire, Fulya Akcimen, Jay P Ross, Cynthia V Bourassa, Patrick A Dion, Inge A Meijer, Guy A Rouleau
Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette's syndrome. Communications biology 5 (1) (2022)
Fulya Akcimen, Patrick A Dion, Guy A Rouleau
Progress in the genetics of restless legs syndrome: the path ahead in the era of whole-genome sequencing. Sleep 45 (8) (2022)
Faezeh Sarayloo, Dan Spiegelman, Daniel Rochefort, Fulya Akcimen, Rachel De Barros Oliveira, Patrick A Dion, Guy A Rouleau
SKOR1 has a transcriptional regulatory role on genes involved in pathways related to restless legs syndrome. European journal of human genetics : EJHG 28 (11) (2020)
Fulya Akcimen, Jay P Ross, Calwing Liao, Dan Spiegelman, Patrick A Dion, Guy A Rouleau
Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project. Movement disorders : official journal of the Movement Disorder Society 36 (2) (2020)
Fulya Akcimen, Faezeh Sarayloo, Calwing Liao, Jay P Ross, Rachel De Barros Oliveira, Patrick A Dion, Guy A Rouleau
Transcriptome-wide association study for restless legs syndrome identifies new susceptibility genes. Communications biology 3 (1) (2020)
Ceren Tunca, Tuncay Şeker, Fulya Akcimen, Cemre Coşkun, Elif Bayraktar, Robin Palvadeau, Seyit Zor, Cemile Kocoglu, Ece Kartal, Nesli Ece Şen, Hamid Hamzeiy, Aslıhan Özoğuz Erimiş, Utku Norman, Oğuzhan Karakahya, Gülden Olgun, Tahsin Akgün, Hacer Durmuş, Erdi Şahin, Arman Çakar, Esra Başar Gürsoy, Gülsen Babacan Yıldız, Barış İşak, Kayıhan Uluç, Haşmet Hanağası, Başar Bilgiç, Nilda Turgut, Fikret Aysal, Mustafa Ertaş, Cavit Boz, Dilcan Kotan, Halil İdrisoğlu, Aysun Soysal, Nurten Uzun Adatepe, Mehmet Ali Akalın, Filiz Koç, Ersin Tan, Piraye Oflazer, Feza Deymeer, Öznur Taştan, A Ercüment Çiçek, Erşen Kavak, Yeşim Parman, Ayse Nazli Basak
Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database. Human mutation 41 (8) (2020)
Calwing Liao, Alexandre D Laporte, Dan Spiegelman, Fulya Akcimen, Ridha Joober, Patrick A Dion, Guy A Rouleau
Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes. Nature communications 10 (1) (2019)
Fulya Akcimen, Atay Vural, Hacer Durmuş, Arman Çakar, Henry Houlden, Yeşim G Parman, A Nazlı Başak
A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID. Journal of human genetics 64 (11) (2019)
Faezeh Sarayloo, Alexandre Dionne-Laporte, Helene Catoire, Daniel Rochefort, Gabrielle Houle, Jay P Ross, Fulya Akcimen, Rachel De Barros Oliveira, Gustavo Turecki, Patrick A Dion, Guy A Rouleau
Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression. PloS one 14 (11) (2019)
Fulya Akcimen, Atay Vural, Seçil Vural, Işın S Bağci, Ceren Tunca, Asli Gündoğdu Eken, Thomas Ruzicka, A Nazli Başak
Clinical and molecular characterization and response to acitretin in three families with Sjögren-Larsson syndrome. International journal of dermatology 57 (7) (2018)