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Dirk Goossens

Showing results (21-30 of 41) with videos related to

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Environmental Pollution (Barking, Essex : 1987)|November 14, 2022
Microplastic appraisal of soil, water, ditch sediment and airborne dust: The case of agricultural systemsEsperanza Huerta Lwanga, Ilse van Roshum, Davi R Munhoz, et al.
Oncotarget|October 30, 2016
Performance of multiplicom's BRCA MASTR Dx kit on the detection of BRCA1 and BRCA2 mutations in fresh frozen ovarian and breast tumor samplesCindy Badoer, Céline Garrec, Dirk Goossens, 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.
Human Mutation|May 1, 2009
Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian populationKaren Nuytemans, Bram Meeus, David Crosiers, et al.
Human Molecular Genetics|November 16, 2007
Strong evidence that GNB1L is associated with schizophreniaNigel M Williams, Beate Glaser, Nadine Norton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 15, 2012
Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystoniaJessie Theuns, David Crosiers, Luc Debaene, et al.
Brain : a Journal of Neurology|August 8, 2007
A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorderVeerle Bogaerts, Sebastiaan Engelborghs, Samir Kumar-Singh, 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.
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.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Environmental Pollution (Barking, Essex : 1987)|November 14, 2022
Microplastic appraisal of soil, water, ditch sediment and airborne dust: The case of agricultural systemsEsperanza Huerta Lwanga, Ilse van Roshum, Davi R Munhoz, et al.
Oncotarget|October 30, 2016
Performance of multiplicom's BRCA MASTR Dx kit on the detection of BRCA1 and BRCA2 mutations in fresh frozen ovarian and breast tumor samplesCindy Badoer, Céline Garrec, Dirk Goossens, 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.
Human Mutation|May 1, 2009
Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian populationKaren Nuytemans, Bram Meeus, David Crosiers, et al.
Human Molecular Genetics|November 16, 2007
Strong evidence that GNB1L is associated with schizophreniaNigel M Williams, Beate Glaser, Nadine Norton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 15, 2012
Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystoniaJessie Theuns, David Crosiers, Luc Debaene, et al.
Brain : a Journal of Neurology|August 8, 2007
A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorderVeerle Bogaerts, Sebastiaan Engelborghs, Samir Kumar-Singh, 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.
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.
Pageof 5