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Peter De Rijk

Showing results (21-30 of 48) with videos related to

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Neurobiology of Disease|May 9, 2014
CMT-associated mutations in glycyl- and tyrosyl-tRNA synthetases exhibit similar pattern of toxicity and share common genetic modifiers in DrosophilaBiljana Ermanoska, William W Motley, Ricardo Leitão-Gonçalves, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 19, 2013
Identification of rare copy number variants in high burden schizophrenia familiesMaarten J Van Den Bossche, Mojca Strazisar, Sophia Cammaerts, et al.
Neuropsychobiology|September 6, 2012
Less cognitive and neurological deficits in schizophrenia patients carrying risk variant in ZNF804AMaarten J A Van Den Bossche, Lise Docx, Manuel Morrens, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 23, 2015
Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencingDaliya Kancheva, Derek Atkinson, Peter De Rijk, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 17, 2008
Detailed analysis of the serotonin transporter gene (SLC6A4) shows no association with bipolar disorder in the Northern Swedish populationMaaike Alaerts, Shana Ceulemans, Diego Forero, et al.
Archives of General Psychiatry|August 5, 2009
Support for NRG1 as a susceptibility factor for schizophrenia in a northern Swedish isolated populationMaaike Alaerts, Shana Ceulemans, Diego Forero, et al.
Nature Biotechnology|December 20, 2011
Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencingJoke Reumers, Peter De Rijk, Hui Zhao, et al.
Molecular Nutrition & Food Research|November 22, 2025
The Nutrigenomic Effect of Mela Rosa Marchigiana Callus Extract on Cellular Senescence: Insight From a Preliminary In Vitro StudyChiara Rucci, Enrica Sordini, Giuseppe Persico, et al.
European Journal of Human Genetics : EJHG|March 20, 2019
De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genesNirmal Vadgama, Alan Pittman, Michael Simpson, et al.
American Journal of Human Genetics|September 22, 2005
Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sampleRosa Rademakers, Marc Cruts, Kristel Sleegers, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Neurobiology of Disease|May 9, 2014
CMT-associated mutations in glycyl- and tyrosyl-tRNA synthetases exhibit similar pattern of toxicity and share common genetic modifiers in DrosophilaBiljana Ermanoska, William W Motley, Ricardo Leitão-Gonçalves, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 19, 2013
Identification of rare copy number variants in high burden schizophrenia familiesMaarten J Van Den Bossche, Mojca Strazisar, Sophia Cammaerts, et al.
Neuropsychobiology|September 6, 2012
Less cognitive and neurological deficits in schizophrenia patients carrying risk variant in ZNF804AMaarten J A Van Den Bossche, Lise Docx, Manuel Morrens, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 23, 2015
Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencingDaliya Kancheva, Derek Atkinson, Peter De Rijk, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 17, 2008
Detailed analysis of the serotonin transporter gene (SLC6A4) shows no association with bipolar disorder in the Northern Swedish populationMaaike Alaerts, Shana Ceulemans, Diego Forero, et al.
Archives of General Psychiatry|August 5, 2009
Support for NRG1 as a susceptibility factor for schizophrenia in a northern Swedish isolated populationMaaike Alaerts, Shana Ceulemans, Diego Forero, et al.
Nature Biotechnology|December 20, 2011
Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencingJoke Reumers, Peter De Rijk, Hui Zhao, et al.
Molecular Nutrition & Food Research|November 22, 2025
The Nutrigenomic Effect of Mela Rosa Marchigiana Callus Extract on Cellular Senescence: Insight From a Preliminary In Vitro StudyChiara Rucci, Enrica Sordini, Giuseppe Persico, et al.
European Journal of Human Genetics : EJHG|March 20, 2019
De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genesNirmal Vadgama, Alan Pittman, Michael Simpson, et al.
American Journal of Human Genetics|September 22, 2005
Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sampleRosa Rademakers, Marc Cruts, Kristel Sleegers, et al.
Pageof 5