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Alan Pittman

Showing results (31-40 of 55) with videos related to

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Annals of Neurology|February 21, 2013
Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystoniaJoshua Hersheson, Niccolo E Mencacci, Mary Davis, et al.
Neurobiology of Aging|September 4, 2013
Validation of next-generation sequencing technologies in genetic diagnosis of dementiaJohn Beck, Alan Pittman, Gary Adamson, et al.
Neurology|May 16, 2014
Novel CLN3 mutation causing autophagic vacuolar myopathyAndrea Cortese, Arianna Tucci, Giovanni Piccolo, et al.
Annals of Neurology|March 11, 2021
Mitochondrial DNA Analysis from Exome Sequencing Data Improves Diagnostic Yield in Neurological DiseasesOlivia V Poole, Chiara Pizzamiglio, David Murphy, et al.
Human Molecular Genetics|May 3, 2011
Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genesLuis G Carvajal-Carmona, Jean-Baptiste Cazier, Angela M Jones, et al.
Annals of Neurology|August 2, 2018
Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotypeEdwin Jabbari, John Woodside, Manuela M X Tan, et al.
Circulation. Genomic and Precision Medicine|February 3, 2022
Rare Variation in Drug Metabolism and Long QT Genes and the Genetic Susceptibility to Acquired Long QT SyndromeBelinda Gray, Alban-Elouen Baruteau, Albert A Antolin, et al.
Brain : a Journal of Neurology|May 25, 2016
Genetic and phenotypic characterization of complex hereditary spastic paraplegiaEleanna Kara, Arianna Tucci, Claudia Manzoni, et al.
Nature Genetics|December 18, 2007
Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer riskEmma Jaeger, Emily Webb, Kimberley Howarth, et al.
Neurobiology of Aging|September 3, 2014
Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansionPietro Fratta, James M Polke, Jia Newcombe, et al.
Pageof 6

Showing results (31-40 of 55) with videos related to

Sort By:
Pageof 6
Annals of Neurology|February 21, 2013
Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystoniaJoshua Hersheson, Niccolo E Mencacci, Mary Davis, et al.
Neurobiology of Aging|September 4, 2013
Validation of next-generation sequencing technologies in genetic diagnosis of dementiaJohn Beck, Alan Pittman, Gary Adamson, et al.
Neurology|May 16, 2014
Novel CLN3 mutation causing autophagic vacuolar myopathyAndrea Cortese, Arianna Tucci, Giovanni Piccolo, et al.
Annals of Neurology|March 11, 2021
Mitochondrial DNA Analysis from Exome Sequencing Data Improves Diagnostic Yield in Neurological DiseasesOlivia V Poole, Chiara Pizzamiglio, David Murphy, et al.
Human Molecular Genetics|May 3, 2011
Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genesLuis G Carvajal-Carmona, Jean-Baptiste Cazier, Angela M Jones, et al.
Annals of Neurology|August 2, 2018
Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotypeEdwin Jabbari, John Woodside, Manuela M X Tan, et al.
Circulation. Genomic and Precision Medicine|February 3, 2022
Rare Variation in Drug Metabolism and Long QT Genes and the Genetic Susceptibility to Acquired Long QT SyndromeBelinda Gray, Alban-Elouen Baruteau, Albert A Antolin, et al.
Brain : a Journal of Neurology|May 25, 2016
Genetic and phenotypic characterization of complex hereditary spastic paraplegiaEleanna Kara, Arianna Tucci, Claudia Manzoni, et al.
Nature Genetics|December 18, 2007
Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer riskEmma Jaeger, Emily Webb, Kimberley Howarth, et al.
Neurobiology of Aging|September 3, 2014
Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansionPietro Fratta, James M Polke, Jia Newcombe, et al.
Pageof 6