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Iris E Jansen

Showing results (1-10 of 48) with videos related to

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Experimental Neurology|May 31, 2014
C9orf72; abnormal RNA expression is the keyPeter Heutink, Iris E Jansen, Emily M Lynes
Scientific Reports|February 7, 2023
Rare variant aggregation in 148,508 exomes identifies genes associated with proxy dementiaDouglas P Wightman, Jeanne E Savage, Christiaan A de Leeuw, et al.
Neurobiology of Aging|April 12, 2023
The genetic overlap between Alzheimer's disease, amyotrophic lateral sclerosis, Lewy body dementia, and Parkinson's diseaseDouglas P Wightman, Jeanne E Savage, Elleke Tissink, et al.
Neurobiology of Aging|May 30, 2015
EIF4G1 mutations do not cause Parkinson's diseaseNoah Nichols, Jose M Bras, Dena G Hernandez, et al.
Brain : a Journal of Neurology|November 16, 2017
Excessive burden of lysosomal storage disorder gene variants in Parkinson's diseaseLaurie A Robak, Iris E Jansen, Jeroen van Rooij, et al.
Behavior Genetics|September 28, 2013
A twin-sibling study on the relationship between exercise attitudes and exercise behaviorCharlotte Huppertz, Meike Bartels, Iris E Jansen, et al.
Diabetes|August 19, 2022
Disentangling Genetic Risks for Metabolic SyndromeEva S van Walree, Iris E Jansen, Nathaniel Y Bell, et al.
Neuro-Degenerative Diseases|October 21, 2016
Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal DementiaCarlo Wilke, Frank Gillardon, Christian Deuschle, et al.
Neurobiology of Aging|November 3, 2015
Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variantsCornelis Blauwendraat, Carlo Wilke, Iris E Jansen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2017
The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjectsCornelis Blauwendraat, Carlo Wilke, Javier Simón-Sánchez, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Experimental Neurology|May 31, 2014
C9orf72; abnormal RNA expression is the keyPeter Heutink, Iris E Jansen, Emily M Lynes
Scientific Reports|February 7, 2023
Rare variant aggregation in 148,508 exomes identifies genes associated with proxy dementiaDouglas P Wightman, Jeanne E Savage, Christiaan A de Leeuw, et al.
Neurobiology of Aging|April 12, 2023
The genetic overlap between Alzheimer's disease, amyotrophic lateral sclerosis, Lewy body dementia, and Parkinson's diseaseDouglas P Wightman, Jeanne E Savage, Elleke Tissink, et al.
Neurobiology of Aging|May 30, 2015
EIF4G1 mutations do not cause Parkinson's diseaseNoah Nichols, Jose M Bras, Dena G Hernandez, et al.
Brain : a Journal of Neurology|November 16, 2017
Excessive burden of lysosomal storage disorder gene variants in Parkinson's diseaseLaurie A Robak, Iris E Jansen, Jeroen van Rooij, et al.
Behavior Genetics|September 28, 2013
A twin-sibling study on the relationship between exercise attitudes and exercise behaviorCharlotte Huppertz, Meike Bartels, Iris E Jansen, et al.
Diabetes|August 19, 2022
Disentangling Genetic Risks for Metabolic SyndromeEva S van Walree, Iris E Jansen, Nathaniel Y Bell, et al.
Neuro-Degenerative Diseases|October 21, 2016
Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal DementiaCarlo Wilke, Frank Gillardon, Christian Deuschle, et al.
Neurobiology of Aging|November 3, 2015
Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variantsCornelis Blauwendraat, Carlo Wilke, Iris E Jansen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2017
The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjectsCornelis Blauwendraat, Carlo Wilke, Javier Simón-Sánchez, et al.
Pageof 5