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National Institutes of Health: Bethesda, US

2022-04-07 to present | Postdoctoral fellow (Laboratory of Neurogenetics)
Employment
Source: Self-asserted source
Kensuke Daida

Works (39)

The Utility of Long‐Read Sequencing in Diagnosing Early Onset Parkinson's Disease

Annals of Neurology
2024-12-19 | Journal article
Contributors: Kensuke Daida; Hiroyo Yoshino; Laksh Malik; Breeana Baker; Mayu Ishiguro; Rylee Genner; Kimberly Paquette; Yuanzhe Li; Kenya Nishioka; Satoshi Masuzugawa et al.
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Crossref

CNV-Finder: Streamlining Copy Number Variation Discovery

2024-11-23 | Preprint
Contributors: Nicole Kuznetsov; Kensuke Daida; Mary B. Makarious; Bashayer Al-Mubarak; Kajsa Atterling Brolin; Laksh Malik; Cedric Kouam; Breeana Baker; Miriam Ostrozovicova; Katherine M. Andersh et al.
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Crossref

Characterizing a complex CT-rich haplotype in intron 4 of SNCA using large-scale targeted amplicon long-read sequencing

npj Parkinson's Disease
2024-07-26 | Journal article
Contributors: Pilar Alvarez Jerez; Kensuke Daida; Francis P. Grenn; Laksh Malik; Abigail Miano-Burkhardt; Mary B. Makarious; Jinhui Ding; J. Raphael Gibbs; Anni Moore; Xylena Reed et al.
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Crossref

The Utility of Long-Read Sequencing in Diagnosing Genetic Autosomal Recessive Parkinson’s Disease: a genetic screening study

2024-06-15 | Preprint
Contributors: Kensuke Daida; Hiroyo Yoshino; Laksh Malik; Breeana Baker; Mayu Ishiguro; Rylee Genner; Kimberly Paquette; Yuanzhe Li; Kenya Nishioka; Satoshi Masuzugawa et al.
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Crossref

Profiling complex repeat expansions in RFC1 in Parkinson’s disease

npj Parkinson's Disease
2024-05-24 | Journal article
Contributors: Pilar Alvarez Jerez; Kensuke Daida; Abigail Miano-Burkhardt; Hirotaka Iwaki; Laksh Malik; Guillaume Cogan; Mary B. Makarious; Roisin Sullivan; Jana Vandrovcova; Jinhui Ding et al.
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Crossref

Long-read sequencing unravels the complexity of structural variants inPRKNin two individuals with early-onset Parkinson’s disease

2024-05-03 | Preprint
Contributors: Guillaume Cogan; Kensuke Daida; Kimberley J. Billingsley; Christelle Tesson; Sylvie Forlani; Ludmila Jornea; Lionel Arnaud; Laurene Tissier; Eric LeGuern; Andrew B. Singleton et al.
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Crossref

Efficacy and Safety of Elobixibat in Parkinson's Disease with Chronic Constipation: CONST‐PD Study

Movement Disorders Clinical Practice
2024-04 | Journal article
Contributors: Taku Hatano; Genko Oyama; Yasushi Shimo; Kotaro Ogaki; Noriko Nishikawa; Ryota Nakamura; Taiji Tsunemi; Takashi Ogawa; Hiroto Eguchi; Kensuke Daida et al.
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Crossref

The Role of Structural Variants in the Genetic Architecture of Parkinson’s Disease

International Journal of Molecular Sciences
2024-04 | Journal article | Author
Contributors: Abigail Miano-Burkhardt; Pilar Alvarez Jerez; Kensuke Daida; Sara Bandres Ciga; Kimberley J Billingsley
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Multidisciplinary Digital Publishing Institute
grade
Preferred source (of 2)‎

Long‐Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease

Movement Disorders
2023-12 | Journal article
Contributors: Kensuke Daida; Manabu Funayama; Kimberley J. Billingsley; Laksh Malik; Abigail Miano‐Burkhardt; Hampton L. Leonard; Mary B. Makarious; Hirotaka Iwaki; Jinhui Ding; J. Raphael Gibbs et al.
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Crossref

Long-read sequencing resolves a complex structural variant inPRKNParkinson’s disease

2023-08-21 | Preprint
Contributors: Kensuke Daida; Manabu Funayama; Kimberley J Billingsley; Laksh Malik; Abigail Miano-Burkhardt; Hampton L. Leonard; Mary B. Makarious; Hirotaka Iwaki; Jinhui Ding; J. Raphael Gibbs et al.
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Crossref

α‐Synuclein V15A Variant in Familial Parkinson's Disease Exhibits a Weaker Lipid‐Binding Property

Movement Disorders
2022-10 | Journal article
Contributors: Kensuke Daida; Shotaro Shimonaka; Kahori Shiba‐Fukushima; Jun Ogata; Hiroyo Yoshino; Ayami Okuzumi; Taku Hatano; Yumiko Motoi; Tomoki Hirunagi; Masahisa Katsuno et al.
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Crossref

Radiation-induced Brain Calcification Leads to L-dopa-resistant Parkinsonism and Cerebellar Ataxia.

Internal medicine (Tokyo, Japan)
2022-05 | Journal article
Contributors: Shimada T; Kamo R; Daida K; Nishioka K; Hattori N; Tsunemi T
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

A complex form of hereditary spastic paraplegia harboring a novel variant, p.W1515*, in the <i>SPG11</i> gene.

eNeurologicalSci
2022-01 | Journal article
Contributors: Daida K; Nishioka Y; Li Y; Yoshino H; Funayama M; Hattori N; Nishioka K
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Genotype-phenotype correlation of Parkinson's disease with PRKN variants.

Neurobiology of aging
2022-01 | Journal article
Contributors: Yoshino H; Li Y; Nishioka K; Daida K; Hayashida A; Ishiguro Y; Yamada D; Izawa N; Nishi K; Nishikawa N et al.
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Commentary: Progressive Encephalomyelitis with Rigidity and Myoclonus and Myasthenia Gravis Comorbid Status with Thymoma.

Movement disorders clinical practice
2021-08 | Journal article
Contributors: Balint B; Ogawa T; Ogaki K; Daida K; Nishimaki T; Ando M; Kawajiri S; Wada R; Noda K; Hattori N et al.
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Progressive Encephalomyelitis with Rigidity and Myoclonus and Myasthenia Gravis Comorbid Status with Thymoma.

Movement disorders clinical practice
2021-08 | Journal article
Contributors: Ogawa T; Ogaki K; Daida K; Nishimaki T; Ando M; Kawajiri S; Wada R; Noda K; Hattori N; Okuma Y
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Causal Connection Between Serum Levodopa Metabolic Profile and Medication in Parkinson’s Disease

2021-04 | Preprint
Contributors: Chukyo A; Fujimaki M; Kaga N; Taka H; Li Y; Ueno S; Takeshige-Amano H; Funayama M; Ishimaru T; Miyamoto K et al.
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Clinical manifestations of Parkinson's disease harboring VPS35 retromer complex component p.D620N with long-term follow-up

Parkinsonism & Related Disorders
2021-03 | Journal article
Contributors: Mayu Ishiguro; Yuanzhe Li; Hiroyo Yoshino; Kensuke Daida; Yuta Ishiguro; Genko Oyama; Shinji Saiki; Manabu Funayama; Nobutaka Hattori; Kenya Nishioka
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Crossref

Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy.

Brain : a journal of neurology
2020-12 | Journal article
Contributors: Lin CH; Tsai PI; Lin HY; Hattori N; Funayama M; Jeon B; Sato K; Abe K; Mukai Y; Takahashi Y et al.
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Pathological findings in a patient with alpha-synuclein p.A53T and familial Parkinson's disease.

Parkinsonism & related disorders
2020-11 | Journal article
Contributors: Nishioka K; Hashizume Y; Takanashi M; Daida K; Li Y; Yoshino H; Tambasco N; Prontera P; Hattori Y; Ueda A et al.
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Identification of Disease-Associated Variants by Targeted Gene Panel Resequencing in Parkinson's Disease.

Frontiers in neurology
2020-09 | Journal article
Contributors: Daida K; Funayama M; Li Y; Yoshino H; Hayashida A; Ikeda A; Ogaki K; Nishioka K; Hattori N
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

PLA2G6 variants associated with the number of affected alleles in Parkinson's disease in Japan.

Neurobiology of aging
2020-07 | Journal article
Contributors: Daida K; Nishioka K; Li Y; Yoshino H; Shimada T; Dougu N; Nakatsuji Y; Ohara S; Hashimoto T; Okiyama R et al.
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

The identified clinical features of Parkinson's disease in homo-, heterozygous and digenic variants of PINK1.

Neurobiology of aging
2020-07 | Journal article
Contributors: Hayashida A; Li Y; Yoshino H; Daida K; Ikeda A; Ogaki K; Fuse A; Mori A; Takanashi M; Nakahara T et al.
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

CD8+ T-cell encephalitis mimicking PRES in AIDS: a case report.

BMC neurology
2020-05 | Journal article
Contributors: Ishiguro M; Ueno Y; Ishiguro Y; Takanashi M; Murai K; Taieb G; Daida K; Suda A; Yokoyama K; Naito T et al.
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan.

Journal of human genetics
2020-05 | Journal article
Contributors: Li Y; Ikeda A; Yoshino H; Oyama G; Kitani M; Daida K; Hayashida A; Ogaki K; Yoshida K; Kimura T et al.
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Shared Metabolic Profile of Caffeine in Parkinsonian Disorders.

Movement disorders : official journal of the Movement Disorder Society
2020-05 | Journal article
Contributors: Takeshige-Amano H; Saiki S; Fujimaki M; Ueno SI; Li Y; Hatano T; Ishikawa KI; Oji Y; Mori A; Okuzumi A et al.
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Steroid-Responsive Parkinsonism Caused by Cerebral Amyloid Angiopathy-Related Inflammation.

Movement disorders clinical practice
2020-02 | Journal article
Contributors: Yamashita Y; Hatano T; Ogawa T; Daida K; Motoi Y; Hattori N
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Somnolence Preceded the Development of a Subthalamic Lesion in Neuromyelitis Optica Spectrum Disorder.

Internal medicine (Tokyo, Japan)
2019-10 | Journal article
Contributors: Daida K; Ogaki K; Hayashida A; Ando M; Yokoyama K; Noda K; Kanbayashi T; Hattori N; Okuma Y
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Mutation analysis of LRP10 in Japanese patients with familial Parkinson's disease, progressive supranuclear palsy, and frontotemporal dementia.

Neurobiology of aging
2019-09 | Journal article
Contributors: Daida K; Nishioka K; Li Y; Yoshino H; Kikuchi A; Hasegawa T; Funayama M; Hattori N
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

New-onset Refractory Status Epilepticus Involving the Limbic System, Spinal Cord, and Peripheral Nerves.

Internal medicine (Tokyo, Japan)
2019-09 | Journal article
Contributors: Daida K; Nishioka K; Takanashi M; Kobayashi M; Yoshikawa K; Kusunoki S; Yokoyama K; Hattori N
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Deep brain stimulation shows high efficacy in two patients with GCH1 variants.

Parkinsonism & related disorders
2019-06 | Journal article
Contributors: Daida K; Nishioka K; Shimo Y; Umemura A; Yoshino H; Hattori N
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Neuromelanin or DaT-SPECT: which is the better marker for discriminating advanced Parkinson's disease?

European journal of neurology
2019-06 | Journal article
Contributors: Okuzumi A; Hatano T; Kamagata K; Hori M; Mori A; Oji Y; Taniguchi D; Daida K; Shimo Y; Yanagisawa N et al.
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

The presence of cerebral microbleeds is associated with cognitive impairment in Parkinson's disease.

Journal of the neurological sciences
2018-08 | Journal article
Contributors: Daida K; Tanaka R; Yamashiro K; Ogawa T; Oyama G; Nishioka K; Shimo Y; Umemura A; Hattori N
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Bilateral Caudate Nucleus Infarctions Following Upper Gastrointestinal Bleeding.

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association
2018-05 | Journal article
Contributors: Daida K; Miyamoto N; Takagi H; Ueno Y; Yamashiro K; Tanaka R; Hattori N
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

CSF1R Mutation p.G589R and the Distribution Pattern of Brain Calcification.

Internal medicine (Tokyo, Japan)
2017-08 | Journal article
Contributors: Daida K; Nishioka K; Li Y; Nakajima S; Tanaka R; Hattori N
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Dystonia due to bilateral caudate hemorrhage associated with a COL4A1 mutation.

Parkinsonism & related disorders
2017-04 | Journal article
Contributors: Hatano T; Daida K; Hoshino Y; Li Y; Saitsu H; Matsumoto N; Hattori N
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Neuromelanin MRI is useful for monitoring motor complications in Parkinson's and PARK2 disease.

Journal of neural transmission (Vienna, Austria : 1996)
2017-02 | Journal article
Contributors: Hatano T; Okuzumi A; Kamagata K; Daida K; Taniguchi D; Hori M; Yoshino H; Aoki S; Hattori N
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Cytomegalovirus-associated encephalomyelitis in an immunocompetent adult: a two-stage attack of direct viral and delayed immune-mediated invasions. case report.

BMC neurology
2016-11 | Journal article
Contributors: Daida K; Ishiguro Y; Eguchi H; Machida Y; Hattori N; Miwa H
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

A novel mutation of CHCHD2 p.R8H in a sporadic case of Parkinson's disease.

Parkinsonism & related disorders
2016-10 | Journal article
Contributors: Ikeda A; Matsushima T; Daida K; Nakajima S; Conedera S; Li Y; Yoshino H; Oyama G; Funayama M; Nishioka K et al.
Source: Self-asserted source
Kensuke Daida via Europe PubMed Central

Peer review (1 review for 1 publication/grant)

Review activity for NPJ Parkinson's disease. (1)