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» Authors » Sonia De Zutter

Sonia De Zutter

Explore the profile of Sonia De Zutter including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 13
Citations 160
Followers 0
Related Specialties
Psychiatry
Neurology
Genetics
Top 10 Co-Authors
Jurgen Del-Favero
Rolf Adolfsson
Karl-Fredrik Norrback
An-Sofie Lenaerts
Lien Heyrman
Peter De Rijk
Lars-Goran Nilsson
Dirk Goossens
Maaike Alaerts
Shana Ceulemans
Published In
Am J Med Genet B Neuropsychiatr Genet
Psychiatr Genet
Arch Gen Psychiatry
Neuron
Schizophr Res
Affiliations
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Recent Articles
1.
A network of synaptic genes associated with schizophrenia and bipolar disorder
Forero D, Herteleer L, De Zutter S, Norrback K, Nilsson L, Adolfsson R, et al.
Schizophr Res . 2016 Feb; 172(1-3):68-74. PMID: 26899345
Identification of novel candidate genes for schizophrenia (SZ) and bipolar disorder (BP), two psychiatric disorders with large epidemiological impacts, is a key research area in neurosciences and psychiatric genetics. Previous...
2.
Identification of rare copy number variants in high burden schizophrenia families
Van Den Bossche M, Strazisar M, Cammaerts S, Liekens A, Vandeweyer G, Depreeuw V, et al.
Am J Med Genet B Neuropsychiatr Genet . 2013 Mar; 162B(3):273-82. PMID: 23505263
Over the last years, genome-wide studies consistently showed an increased burden of rare copy number variants (CNVs) in schizophrenia patients, supporting the "common disease, rare variant" hypothesis in at least...
3.
Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?
Van Den Bossche M, Johnstone M, Strazisar M, Pickard B, Goossens D, Lenaerts A, et al.
Am J Med Genet B Neuropsychiatr Genet . 2012 Aug; 159B(7):812-22. PMID: 22911887
From a number of genome-wide association studies it was shown that de novo and/or rare copy number variants (CNVs) are found at an increased frequency in neuropsychiatric diseases. In this...
4.
Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disorders
Van Den Bossche M, Strazisar M, De Bruyne S, Bervoets C, Lenaerts A, De Zutter S, et al.
Am J Med Genet B Neuropsychiatr Genet . 2012 Apr; 159B(4):465-75. PMID: 22488967
The GWAS-based association of CACNA1C with bipolar disorder (BPD) is one of the strongest genetic findings to date. CACNA1C belongs to the family of CACN genes encoding voltage-dependent calcium channels...
5.
Evidence for the involvement of the glucocorticoid receptor gene in bipolar disorder in an isolated northern Swedish population
Ceulemans S, De Zutter S, Heyrman L, Norrback K, Nordin A, Nilsson L, et al.
Bipolar Disord . 2011 Nov; 13(7-8):614-23. PMID: 22085474
Objectives: Dysfunction of the hypothalamus-pituitary-adrenal (HPA) axis is one of the most consistent findings in the pathophysiology of mood disorders. The potential role of genes related to HPA axis function...
6.
Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population
Moens L, De Rijk P, Reumers J, Van Den Bossche M, Glassee W, De Zutter S, et al.
PLoS One . 2011 Aug; 6(8):e23450. PMID: 21853134
In recent years, DISC1 has emerged as one of the most credible and best supported candidate genes for schizophrenia and related neuropsychiatric disorders. Furthermore, increasing evidence--both genetic and functional--indicates that...
7.
PCM1 and schizophrenia: a replication study in the Northern Swedish population
Moens L, Ceulemans S, Alaerts M, Van Den Bossche M, Lenaerts A, De Zutter S, et al.
Am J Med Genet B Neuropsychiatr Genet . 2010 May; 153B(6):1240-3. PMID: 20468070
Previous studies implicated centrosomal dysfunction as a source of various neuropsychiatric disorders, including schizophrenia (SZ). Two recent reports [Gurling et al., 2006; Datta et al., 2008. Mol Psychiatry] described an...
8.
Support for NRG1 as a susceptibility factor for schizophrenia in a northern Swedish isolated population
Alaerts M, Ceulemans S, Forero D, Moens L, De Zutter S, Heyrman L, et al.
Arch Gen Psychiatry . 2009 Aug; 66(8):828-37. PMID: 19652122
Context: Neuregulin 1 (NRG1), a growth factor involved in neurodevelopment, myelination, neurotransmitter receptor expression, and synaptic plasticity, first joined the list of candidate genes for schizophrenia when a 7-marker haplotype...
9.
Detailed analysis of the serotonin transporter gene (SLC6A4) shows no association with bipolar disorder in the Northern Swedish population
Alaerts M, Ceulemans S, Forero D, Moens L, De Zutter S, Heyrman L, et al.
Am J Med Genet B Neuropsychiatr Genet . 2008 Sep; 150B(4):585-92. PMID: 18792946
Through active reuptake of serotonin into presynaptic neurons, the serotonin transporter (5-HTT) plays an important role in regulating serotonin concentrations in the brain, and it is the site of binding...
10.
Lack of association of an insertion/deletion polymorphism in the G protein-coupled receptor 50 with bipolar disorder in a Northern Swedish population
Alaerts M, Venken T, Lenaerts A, De Zutter S, Norrback K, Adolfsson R, et al.
Psychiatr Genet . 2006 Nov; 16(6):235-6. PMID: 17106423
GPR50 is a G protein-coupled receptor, located on Xq28 and related to the melatonin receptor family. It is suggested as a functional and positional candidate gene for bipolar disorder (BP)....