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J Raphael

Showing results (331-340 of 488) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|December 18, 2016
ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodiesCornelis Blauwendraat, Mike A Nalls, Monica Federoff, et al.
Biorxiv : the Preprint Server for Biology|August 14, 2023
Divergent patterns of healthy aging across human brain regions at single-cell resolution reveal links to neurodegenerative diseaseMegan F Duffy, Jinhui Ding, Rebekah G Langston, et al.
Human Molecular Genetics|January 11, 2011
Distinct DNA methylation changes highly correlated with chronological age in the human brainDena G Hernandez, Michael A Nalls, J Raphael Gibbs, et al.
Plos One|September 16, 2016
Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia PatientsGamze Guven, Ebba Lohmann, Jose Bras, et al.
Plos Genetics|March 14, 2009
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical geneticsMichael A Nalls, Javier Simon-Sanchez, J Raphael Gibbs, et al.
Current Oncology (Toronto, Ont.)|July 26, 2024
Addressing the Rising Trend in Early-Age-Onset Cancers in CanadaPetra Wildgoose, Filomena Servidio-Italiano, Michael J Raphael, et al.
Annals of Neurology|August 28, 2018
A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson diseaseLasse Pihlstrøm, Cornelis Blauwendraat, Chiara Cappelletti, et al.
Journal of the National Cancer Institute|August 2, 2023
Mortality among patients with diffuse large B-cell lymphoma and mental disorders: a population-based studyInna Y Gong, Matthew C Cheung, Kelvin K W Chan, et al.
Neurology|June 8, 2012
Exome sequencing identifies a novel TRPV4 mutation in a CMT2C familyGuida Landouré, Jeremy M Sullivan, Janel O Johnson, et al.
The Lancet. Neurology|June 13, 2015
CHCHD2 and Parkinson's diseaseIris E Jansen, Jose M Bras, Suzanne Lesage, et al.
Pageof 49

Showing results (331-340 of 488) with videos related to

Sort By:
Pageof 49
Movement Disorders : Official Journal of the Movement Disorder Society|December 18, 2016
ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodiesCornelis Blauwendraat, Mike A Nalls, Monica Federoff, et al.
Biorxiv : the Preprint Server for Biology|August 14, 2023
Divergent patterns of healthy aging across human brain regions at single-cell resolution reveal links to neurodegenerative diseaseMegan F Duffy, Jinhui Ding, Rebekah G Langston, et al.
Human Molecular Genetics|January 11, 2011
Distinct DNA methylation changes highly correlated with chronological age in the human brainDena G Hernandez, Michael A Nalls, J Raphael Gibbs, et al.
Plos One|September 16, 2016
Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia PatientsGamze Guven, Ebba Lohmann, Jose Bras, et al.
Plos Genetics|March 14, 2009
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical geneticsMichael A Nalls, Javier Simon-Sanchez, J Raphael Gibbs, et al.
Current Oncology (Toronto, Ont.)|July 26, 2024
Addressing the Rising Trend in Early-Age-Onset Cancers in CanadaPetra Wildgoose, Filomena Servidio-Italiano, Michael J Raphael, et al.
Annals of Neurology|August 28, 2018
A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson diseaseLasse Pihlstrøm, Cornelis Blauwendraat, Chiara Cappelletti, et al.
Journal of the National Cancer Institute|August 2, 2023
Mortality among patients with diffuse large B-cell lymphoma and mental disorders: a population-based studyInna Y Gong, Matthew C Cheung, Kelvin K W Chan, et al.
Neurology|June 8, 2012
Exome sequencing identifies a novel TRPV4 mutation in a CMT2C familyGuida Landouré, Jeremy M Sullivan, Janel O Johnson, et al.
The Lancet. Neurology|June 13, 2015
CHCHD2 and Parkinson's diseaseIris E Jansen, Jose M Bras, Suzanne Lesage, et al.
Pageof 49