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Jurgen Del-Favero

Affiliations: 
Universitaire Instelling Antwerpen (Belgium) 
Area:
Molecular Biology, Genetics
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"Jurgen Del-Favero"
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Parents

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Children

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Dirk Goossens grad student 2001 Universitaire Instelling Antwerpen (Belgium)
Sandra M. Villafuerte grad student 2001 Universitaire Instelling Antwerpen (Belgium)
Diego A Forero grad student 2006-2009 University of Antwerp (GenetiTree)

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Publications

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Szatkiewicz J, Crowley JJ, Adolfsson AN, et al. (2019) The genomics of major psychiatric disorders in a large pedigree from Northern Sweden. Translational Psychiatry. 9: 60
Dries DR, Zhu Y, Brooks MM, et al. (2016) Loss of Nicastrin from Oligodendrocytes Results in Hypomyelination and Schizophrenia with Compulsive Behavior. The Journal of Biological Chemistry
Forero DA, Herteleer L, De Zutter S, et al. (2016) A network of synaptic genes associated with schizophrenia and bipolar disorder. Schizophrenia Research
Johnstone M, Maclean A, Heyrman L, et al. (2015) Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness. Molecular Neuropsychiatry. 1: 175-190
Strazisar M, Cammaerts S, van der Ven K, et al. (2015) MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene sets. Molecular Psychiatry. 20: 472-81
Van Den Bossche MJ, Strazisar M, Cammaerts S, et al. (2013) Identification of rare copy number variants in high burden schizophrenia families. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 273-82
Theuns J, Crosiers D, Debaene L, et al. (2012) Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystonia. Movement Disorders : Official Journal of the Movement Disorder Society. 27: 1451-6
Van Den Bossche MJ, Docx L, Morrens M, et al. (2012) Less cognitive and neurological deficits in schizophrenia patients carrying risk variant in ZNF804A. Neuropsychobiology. 66: 158-66
Van Den Bossche MJ, Johnstone M, Strazisar M, et al. (2012) Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not? American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 812-22
Van Den Bossche MJ, Strazisar M, De Bruyne S, et al. (2012) Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 465-75
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