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J Raphael

Showing results (371-380 of 488) with videos related to

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The Lancet. Neurology|March 17, 2007
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of dataJennifer C Schymick, Sonja W Scholz, Hon-Chung Fung, et al.
Human Molecular Genetics|September 24, 2013
Genetic comorbidities in Parkinson's diseaseMike A Nalls, Mohamad Saad, Alastair J Noyce, et al.
Neurobiology of Disease|June 18, 2016
Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodiesJoshua T Geiger, Jinhui Ding, Barbara Crain, et al.
American Journal of Human Genetics|January 22, 2013
Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticityMonia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, et al.
Neuro-Degenerative Diseases|May 31, 2017
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African FamiliesMonia B Hammer, Jinhui Ding, Fanny Mochel, et al.
Nature Genetics|January 22, 2026
Genomic evolution of pancreatic cancer at single-cell resolutionHaochen Zhang, Palash Sashittal, Elias-Ramzey Karnoub, et al.
Neurobiology of Disease|March 22, 2012
Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brainDena G Hernandez, Mike A Nalls, Matthew Moore, et al.
Human Mutation|July 11, 2012
Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunitiesFlorian Mittag, Finja Büchel, Mohamad Saad, et al.
Brain Communications|August 28, 2025
Cerebellum mitochondrial DNA copy number is increased in Parkinson's diseaseTalia Beglarian, David R Tyrpak, J Raphael Gibbs, et al.
Nature Genetics|December 16, 2014
Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexesMark D M Leiserson, Fabio Vandin, Hsin-Ta Wu, et al.
Pageof 49

Showing results (371-380 of 488) with videos related to

Sort By:
Pageof 49
The Lancet. Neurology|March 17, 2007
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of dataJennifer C Schymick, Sonja W Scholz, Hon-Chung Fung, et al.
Human Molecular Genetics|September 24, 2013
Genetic comorbidities in Parkinson's diseaseMike A Nalls, Mohamad Saad, Alastair J Noyce, et al.
Neurobiology of Disease|June 18, 2016
Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodiesJoshua T Geiger, Jinhui Ding, Barbara Crain, et al.
American Journal of Human Genetics|January 22, 2013
Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticityMonia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, et al.
Neuro-Degenerative Diseases|May 31, 2017
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African FamiliesMonia B Hammer, Jinhui Ding, Fanny Mochel, et al.
Nature Genetics|January 22, 2026
Genomic evolution of pancreatic cancer at single-cell resolutionHaochen Zhang, Palash Sashittal, Elias-Ramzey Karnoub, et al.
Neurobiology of Disease|March 22, 2012
Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brainDena G Hernandez, Mike A Nalls, Matthew Moore, et al.
Human Mutation|July 11, 2012
Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunitiesFlorian Mittag, Finja Büchel, Mohamad Saad, et al.
Brain Communications|August 28, 2025
Cerebellum mitochondrial DNA copy number is increased in Parkinson's diseaseTalia Beglarian, David R Tyrpak, J Raphael Gibbs, et al.
Nature Genetics|December 16, 2014
Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexesMark D M Leiserson, Fabio Vandin, Hsin-Ta Wu, et al.
Pageof 49