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Peter De Rijk

Showing results (31-40 of 48) with videos related to

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Frontiers in Nutrition|June 12, 2023
Mitochondrial DNA methylation in metabolic associated fatty liver diseaseArchibold Mposhi, Fabian Cortés-Mancera, Janette Heegsma, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 23, 2012
Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?Maarten J Van Den Bossche, Mandy Johnstone, Mojca Strazisar, et al.
Molecular Neuropsychiatry|May 31, 2016
Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental IllnessMandy Johnstone, Alan Maclean, Lien Heyrman, et al.
Plos One|August 20, 2011
Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish populationLotte N Moens, Peter De Rijk, Joke Reumers, et al.
Bioinformatics (Oxford, England)|September 10, 2024
Scywalker: scalable end-to-end data analysis workflow for long-read single-cell transcriptome sequencingPeter De Rijk, Tijs Watzeels, Fahri Küçükali, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 11, 2012
Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disordersMaarten J Van Den Bossche, Mojca Strazisar, Stephan De Bruyne, et al.
Human Molecular Genetics|January 15, 2010
SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesiclesDries Castermans, Karolien Volders, An Crepel, et al.
Brain Communications|November 8, 2021
Dissection of <i>TAF1</i> neuronal splicing and implications for neurodegeneration in X-linked dystonia-parkinsonismSimona Capponi, Nadja Stöffler, Ellen B Penney, et al.
Frontiers in Cell and Developmental Biology|May 10, 2021
Long-Read Sequencing to Unravel Complex Structural Variants of <i>CEP78</i> Leading to Cone-Rod Dystrophy and Hearing LossGiulia Ascari, Nanna D Rendtorff, Marieke De Bruyne, et al.
Nature Genetics|December 15, 2010
Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel diseaseYukihide Momozawa, Myriam Mni, Kayo Nakamura, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Frontiers in Nutrition|June 12, 2023
Mitochondrial DNA methylation in metabolic associated fatty liver diseaseArchibold Mposhi, Fabian Cortés-Mancera, Janette Heegsma, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 23, 2012
Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?Maarten J Van Den Bossche, Mandy Johnstone, Mojca Strazisar, et al.
Molecular Neuropsychiatry|May 31, 2016
Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental IllnessMandy Johnstone, Alan Maclean, Lien Heyrman, et al.
Plos One|August 20, 2011
Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish populationLotte N Moens, Peter De Rijk, Joke Reumers, et al.
Bioinformatics (Oxford, England)|September 10, 2024
Scywalker: scalable end-to-end data analysis workflow for long-read single-cell transcriptome sequencingPeter De Rijk, Tijs Watzeels, Fahri Küçükali, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 11, 2012
Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disordersMaarten J Van Den Bossche, Mojca Strazisar, Stephan De Bruyne, et al.
Human Molecular Genetics|January 15, 2010
SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesiclesDries Castermans, Karolien Volders, An Crepel, et al.
Brain Communications|November 8, 2021
Dissection of <i>TAF1</i> neuronal splicing and implications for neurodegeneration in X-linked dystonia-parkinsonismSimona Capponi, Nadja Stöffler, Ellen B Penney, et al.
Frontiers in Cell and Developmental Biology|May 10, 2021
Long-Read Sequencing to Unravel Complex Structural Variants of <i>CEP78</i> Leading to Cone-Rod Dystrophy and Hearing LossGiulia Ascari, Nanna D Rendtorff, Marieke De Bruyne, et al.
Nature Genetics|December 15, 2010
Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel diseaseYukihide Momozawa, Myriam Mni, Kayo Nakamura, et al.
Pageof 5