Dirk Goossens, Ph.D.

Affiliations: 
2001 Universitaire Instelling Antwerpen (Belgium) 
Area:
Molecular Biology, Genetics
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"Dirk Goossens"

Parents

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Jurgen Del-Favero grad student 2001 Universitaire Instelling Antwerpen (Belgium)
 (Cloning of candidate genes for bipolar disorder starting from expanded trinucleotide repeats.)

Collaborators

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Diego A Forero collaborator 2006-2009 University of Antwerp (GenetiTree)
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Publications

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Boulet G, Barel DV, Rotthier A, et al. (2017) Accurate and precise targeted NGS with BRCA MASTR Plus Dx for BRCA1 and BRCA2 mutation detection in formalin-fixed paraffin-embedded tumor tissue-derived DNA. Journal of Clinical Oncology. 35
Badoer C, Garrec C, Goossens D, et al. (2016) Performance of multiplicom's BRCA MASTR Dx kit on the detection of BRCA1 and BRCA2 mutations in fresh frozen ovarian and breast tumor samples. Oncotarget
Marques C, Bettens K, Goossens D, et al. (2016) Detection of NRAS, KRAS and BRAF mutations in FFPE derived DNA with a novel targeted resequencing-based diagnostics assay Annals of Oncology. 27: vi405
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
Zimoń M, Battaloğlu E, Parman Y, et al. (2015) Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approach. Neurogenetics. 16: 33-42
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, 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
Kruse LV, Nyegaard M, Christensen U, et al. (2012) A genome-wide search for linkage to allergic rhinitis in Danish sib-pair families. European Journal of Human Genetics : Ejhg. 20: 965-72
Pickard BS, Van Den Bossche MJ, Malloy MP, et al. (2012) Multiplex amplicon quantification screening the ABCA13 gene for copy number variation in schizophrenia and bipolar disorder. Psychiatric Genetics. 22: 269-70
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