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Mathias Toft

Showing results (101-110 of 129) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|December 25, 2025
Bivariate GSA-MiXeR: A Novel Tool for Functional Genomic Analyses Implicates Diverse Neural Cell Types for Psychiatric and Neurodegenerative DisordersNadine Parker, Julian Furher, Dat Nguyen, et al.
JAMA Neurology|July 25, 2018
Frequency of Loss of Function Variants in LRRK2 in Parkinson DiseaseCornelis Blauwendraat, Xylena Reed, Demis A Kia, et al.
Scientific Reports|May 9, 2019
GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association studyArvid Rongve, Aree Witoelar, Agustín Ruiz, et al.
Annals of Neurology|April 26, 2021
Investigation of Autosomal Genetic Sex Differences in Parkinson's DiseaseCornelis Blauwendraat, Hirotaka Iwaki, Mary B Makarious, et al.
Scientific Reports|October 18, 2019
Author Correction: GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association studyArvid Rongve, Aree Witoelar, Agustín Ruiz, et al.
NPJ Parkinson'S Disease|June 7, 2024
Genome-wide determinants of mortality and motor progression in Parkinson's diseaseManuela M X Tan, Michael A Lawton, Miriam I Pollard, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 9, 2019
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanismsCornelis Blauwendraat, Karl Heilbron, Costanza L Vallerga, et al.
Neurology. Genetics|August 13, 2019
Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohortsHirotaka Iwaki, Cornelis Blauwendraat, Hampton L Leonard, et al.
Annals of Neurology|January 25, 2020
Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt SynucleinopathiesLynne Krohn, Richard Y J Wu, Karl Heilbron, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 5, 2015
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's diseaseChristina M Lill, Aina Rengmark, Lasse Pihlstrøm, et al.
Pageof 13

Showing results (101-110 of 129) with videos related to

Sort By:
Pageof 13
Medrxiv : the Preprint Server for Health Sciences|December 25, 2025
Bivariate GSA-MiXeR: A Novel Tool for Functional Genomic Analyses Implicates Diverse Neural Cell Types for Psychiatric and Neurodegenerative DisordersNadine Parker, Julian Furher, Dat Nguyen, et al.
JAMA Neurology|July 25, 2018
Frequency of Loss of Function Variants in LRRK2 in Parkinson DiseaseCornelis Blauwendraat, Xylena Reed, Demis A Kia, et al.
Scientific Reports|May 9, 2019
GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association studyArvid Rongve, Aree Witoelar, Agustín Ruiz, et al.
Annals of Neurology|April 26, 2021
Investigation of Autosomal Genetic Sex Differences in Parkinson's DiseaseCornelis Blauwendraat, Hirotaka Iwaki, Mary B Makarious, et al.
Scientific Reports|October 18, 2019
Author Correction: GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association studyArvid Rongve, Aree Witoelar, Agustín Ruiz, et al.
NPJ Parkinson'S Disease|June 7, 2024
Genome-wide determinants of mortality and motor progression in Parkinson's diseaseManuela M X Tan, Michael A Lawton, Miriam I Pollard, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 9, 2019
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanismsCornelis Blauwendraat, Karl Heilbron, Costanza L Vallerga, et al.
Neurology. Genetics|August 13, 2019
Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohortsHirotaka Iwaki, Cornelis Blauwendraat, Hampton L Leonard, et al.
Annals of Neurology|January 25, 2020
Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt SynucleinopathiesLynne Krohn, Richard Y J Wu, Karl Heilbron, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 5, 2015
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's diseaseChristina M Lill, Aina Rengmark, Lasse Pihlstrøm, et al.
Pageof 13