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Suna and İnan Kıraç Foundation

Alternate names: Suna ve İnan Kıraç Vakfı, The Suna and İnan Kıraç Foundation
ROR: 01m07n183
OpenAlex ID: I4405270958
Genome-Wide Analyses Identify KIF5A as a Novel ALS Gene
2018 · Aude Nicolas, Kevin P. Kenna, et al. · Neuron · 697
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Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis
2018 · Wouter Van Rheenen, Sara L. Pulit, et al. · European Journal of Human Genetics · 179
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The genetic structure of the Turkish population reveals high levels of variation and admixture
2021 · M. Ece Kars, A. Nazlı Başak, et al. · Proceedings of the National Academy of Sciences · 116
The distinct genetic pattern of ALS in Turkey and novel mutations
2015 · Aslıhan Özoğuz, Özgün Uyan, et al. · Neurobiology of Aging · 110
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis
2021 · Janel O. Johnson, Ruth Chia, et al. · JAMA Neurology · 90
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Comprehensive Research on Past and Future Therapeutic Strategies Devoted to Treatment of Amyotrophic Lateral Sclerosis
2022 · Belgin Sever, Halilibrahim Ciftci, et al. · International Journal of Molecular Sciences · 82
Clinico‐Genetic, Imaging and Molecular Delineation of COQ8A ‐Ataxia: A Multicenter Study of 59 Patients
2020 · Andreas Traschütz, Tommaso Schirinzi, et al. · Annals of Neurology · 81
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Efficient Prevention of Neurodegenerative Diseases by Depletion of Starvation Response Factor Ataxin-2
2017 · Georg Auburger, Nesli-Ece Sen, et al. · Trends in Neurosciences · 69
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Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking
2021 · Leslie E Sanderson, Kristina Lanko, et al. · Brain · 53
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Human CRY1 variants associate with attention deficit/hyperactivity disorder
2020 · O. Emre Onat, M. Ece Kars, et al. · Journal of Clinical Investigation · 48
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Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease
2024 · Riccardo Currò, Natalia Dominik, et al. · Brain · 42
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Reconsidering the causality of TIA1 mutations in ALS
2017 · Rick A. van der Spek, Wouter van Rheenen, et al. · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · 38
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Search for SCA2 blood RNA biomarkers highlights Ataxin-2 as strong modifier of the mitochondrial factor PINK1 levels
2016 · Nesli Ece Sen, Jessica Drost, et al. · Neurobiology of Disease · 37
ERLIN1 mutations cause teenage-onset slowly progressive ALS in a large Turkish pedigree
2018 · Ceren Tunca, Fulya Akçimen, et al. · European Journal of Human Genetics · 36
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Elevated Global DNA Methylation Is Not Exclusive to Amyotrophic Lateral Sclerosis and Is Also Observed in Spinocerebellar Ataxia Types 1 and 2
2018 · Hamid Hamzeiy, Doruk Savaş, et al. · Neurodegenerative Diseases · 35
Cerebellar cognitive-affective syndrome preceding ataxia associated with complex extrapyramidal features in a Turkish SCA48 family
2019 · R. Palvadeau, Z. E. Kaya-Güleç, et al. · Neurogenetics · 33
The ARCA Registry: A Collaborative Global Platform for Advancing Trial Readiness in Autosomal Recessive Cerebellar Ataxias
2021 · Andreas Traschütz, Selina Reich, et al. · Frontiers in Neurology · 32
Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients
2017 · Konstantinos Mitropoulos, Eleni Merkouri Papadima, et al. · Human Genomics · 28
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Genome-Wide Copy Number Variation in Sporadic Amyotrophic Lateral Sclerosis in the Turkish Population: Deletion of EPHA3 Is a Possible Protective Factor
2013 · Özgün Uyan, Özgür Ömür, et al. · PLoS ONE · 28
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De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia
2022 · Liedewei Van de Vondel, Jonathan De Winter, et al. · Movement Disorders · 27
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis
2026 · Paul J. Hop, Maarten Kooyman, et al. · Nature Genetics · 25
Oligogenic structure of amyotrophic lateral sclerosis has genetic testing, counselling and therapeutic implications
2025 · Alfredo Iacoangeli, Allison A. Dilliott, et al. · Journal of Neurology Neurosurgery & Psychiatry · 25
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Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database
2020 · Ceren Tunca, Tuncay Şeker, et al. · Human Mutation · 23
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A biallelic mutation linksMYORGto autosomal-recessive primary familial brain calcification
2018 · Yalda Forouhideh, Kathrin Müller, et al. · Brain · 22
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Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families
2018 · Cemile Kocoglu, Asli Gundogdu, et al. · Neurology Genetics · 22
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Works count: 96
Citation count: 7,774
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