Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation M Kolmogorov, KJ Billingsley, M Mastoras, M Meredith, J Monlong, ... Nature Methods 20 (10), 1483-1492, 2023 | 68 | 2023 |
Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study M Rizig, S Bandres-Ciga, MB Makarious, OO Ojo, PW Crea, OV Abiodun, ... The Lancet Neurology 22 (11), 1015-1025, 2023 | 65 | 2023 |
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy CH Lin, PI Tsai, HY Lin, N Hattori, M Funayama, B Jeon, K Sato, K Abe, ... Brain 143 (11), 3352-3373, 2020 | 55 | 2020 |
Neuromelanin MRI is useful for monitoring motor complications in Parkinson’s and PARK2 disease T Hatano, A Okuzumi, K Kamagata, K Daida, D Taniguchi, M Hori, ... Journal of Neural Transmission 124 (4), 407-415, 2017 | 36 | 2017 |
The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism E Bressan, X Reed, V Bansal, E Hutchins, MM Cobb, MG Webb, E Alsop, ... Cell genomics 3 (3), 2023 | 26 | 2023 |
α‐Synuclein V15A variant in familial Parkinson's disease exhibits a weaker lipid‐binding property K Daida, S Shimonaka, K Shiba‐Fukushima, J Ogata, H Yoshino, ... Movement Disorders 37 (10), 2075-2085, 2022 | 23 | 2022 |
Genotype-phenotype correlation of Parkinson's disease with PRKN variants H Yoshino, Y Li, K Nishioka, K Daida, A Hayashida, Y Ishiguro, D Yamada, ... Neurobiology of Aging 114, 117-128, 2022 | 23 | 2022 |
The presence of cerebral microbleeds is associated with cognitive impairment in Parkinson's disease K Daida, R Tanaka, K Yamashiro, T Ogawa, G Oyama, K Nishioka, ... Journal of the Neurological Sciences 393, 39-44, 2018 | 23 | 2018 |
Cytomegalovirus-associated encephalomyelitis in an immunocompetent adult: a two-stage attack of direct viral and delayed immune-mediated invasions. case report K Daida, Y Ishiguro, H Eguchi, Y Machida, N Hattori, H Miwa BMC neurology 16, 1-6, 2016 | 23 | 2016 |
The identified clinical features of Parkinson's disease in homo-, heterozygous and digenic variants of PINK1 A Hayashida, Y Li, H Yoshino, K Daida, A Ikeda, K Ogaki, A Fuse, A Mori, ... Neurobiology of Aging 97, 146. e1-146. e13, 2021 | 22 | 2021 |
Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan Y Li, A Ikeda, H Yoshino, G Oyama, M Kitani, K Daida, A Hayashida, ... Journal of human genetics 65 (9), 771-781, 2020 | 22 | 2020 |
A novel mutation of CHCHD2 p. R8H in a sporadic case of Parkinson's disease A Ikeda, T Matsushima, K Daida, S Nakajima, S Conedera, Y Li, ... Parkinsonism & Related Disorders 34, 66-68, 2017 | 20 | 2017 |
Shared metabolic profile of caffeine in Parkinsonian disorders H Takeshige‐Amano, S Saiki, M Fujimaki, SI Ueno, Y Li, T Hatano, ... Movement Disorders 35 (8), 1438-1447, 2020 | 19 | 2020 |
Long‐Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease K Daida, M Funayama, KJ Billingsley, L Malik, A Miano‐Burkhardt, ... Movement Disorders 38 (12), 2249-2257, 2023 | 18 | 2023 |
PLA2G6 variants associated with the number of affected alleles in Parkinson’s disease in Japan K Daida, K Nishioka, Y Li, H Yoshino, T Shimada, N Dougu, Y Nakatsuji, ... Neurobiology of Aging 97, 147. e1-147. e9, 2021 | 18 | 2021 |
CSF1R mutation p. G589R and the distribution pattern of brain calcification K Daida, K Nishioka, Y Li, S Nakajima, R Tanaka, N Hattori Internal Medicine 56 (18), 2507-2512, 2017 | 18 | 2017 |
Clinical manifestations of Parkinson's disease harboring VPS35 retromer complex component p. D620N with long-term follow-up M Ishiguro, Y Li, H Yoshino, K Daida, Y Ishiguro, G Oyama, S Saiki, ... Parkinsonism & Related Disorders 84, 139-143, 2021 | 15 | 2021 |
Mutation analysis of LRP10 in Japanese patients with familial Parkinson's disease, progressive supranuclear palsy, and frontotemporal dementia K Daida, K Nishioka, Y Li, H Yoshino, A Kikuchi, T Hasegawa, ... Neurobiology of Aging 84, 235. e11-235. e16, 2019 | 14 | 2019 |
Genome-wide association identifies novel etiological insights associated with Parkinson’s disease in African and African Admixed Populations M Rizig, S Bandres-Ciga, MB Makarious, O Ojo, PW Crea, O Abiodun, ... medRxiv, 2023 | 13 | 2023 |
Pathological findings in a patient with alpha-synuclein p. A53T and familial Parkinson's disease K Nishioka, Y Hashizume, M Takanashi, K Daida, Y Li, H Yoshino, ... Parkinsonism & Related Disorders 81, 183-187, 2020 | 11 | 2020 |