Year |
Citation |
Score |
2018 |
Vermeulen T, Lemey L, Van Diermen L, Schrijvers D, Madani Y, Sabbe B, Van Den Bossche MJA, van der Mast RC, Østergaard SD. Clinical validation of the Psychotic Depression Assessment Scale (PDAS) against independent global severity ratings in older adults. Acta Neuropsychiatrica. 1-6. PMID 29501075 DOI: 10.1017/Neu.2018.2 |
0.399 |
|
2014 |
Docx L, Sabbe B, Fransen E, Bervoets C, Hulstijn W, Van Den Bossche MJ, Vermeylen S, Temmerman A, Morsel A, Morrens M. Longitudinal evaluation of the psychomotor syndrome in schizophrenia. The Journal of Neuropsychiatry and Clinical Neurosciences. 26: 359-68. PMID 26037858 DOI: 10.1176/Appi.Neuropsych.13020027 |
0.664 |
|
2014 |
Bervoets C, Docx L, Sabbe B, Vermeylen S, Van Den Bossche MJ, Morsel A, Morrens M. The nature of the relationship of psychomotor slowing with negative symptomatology in schizophrenia. Cognitive Neuropsychiatry. 19: 36-46. PMID 23725330 DOI: 10.1080/13546805.2013.779578 |
0.622 |
|
2014 |
Docx L, Sabbe B, Fransen E, Bervoets C, Hulstijn W, Van Den Bossche MJA, Vermeylen S, Temmerman A, Morsel A, Morrens M. Longitudinal evaluation of the psychomotor syndrome in schizophrenia Journal of Neuropsychiatry and Clinical Neurosciences. 26: 359-368. |
0.634 |
|
2013 |
Van Den Bossche MJ, Strazisar M, Cammaerts S, Liekens AM, Vandeweyer G, Depreeuw V, Mattheijssens M, Lenaerts AS, De Zutter S, De Rijk P, Sabbe B, Del-Favero J. 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. PMID 23505263 DOI: 10.1002/Ajmg.B.32146 |
0.574 |
|
2012 |
Van Den Bossche MJ, Docx L, Morrens M, Cammaerts S, Strazisar M, Bervoets C, Smolders S, Depreeuw V, Lenaerts AS, De Rijk P, Del-Favero J, Sabbe BG. Less cognitive and neurological deficits in schizophrenia patients carrying risk variant in ZNF804A. Neuropsychobiology. 66: 158-66. PMID 22948380 DOI: 10.1159/000339731 |
0.642 |
|
2012 |
Van Den Bossche MJ, Johnstone M, Strazisar M, Pickard BS, Goossens D, Lenaerts AS, De Zutter S, Nordin A, Norrback KF, Mendlewicz J, Souery D, De Rijk P, Sabbe BG, Adolfsson R, Blackwood D, et al. 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. PMID 22911887 DOI: 10.1002/Ajmg.B.32088 |
0.527 |
|
2012 |
Van Den Bossche MJ, Strazisar M, De Bruyne S, Bervoets C, Lenaerts AS, De Zutter S, Nordin A, Norrback KF, Goossens D, De Rijk P, Green EK, Grozeva D, Mendlewicz J, Craddock N, Sabbe BG, et al. 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. PMID 22488967 DOI: 10.1002/Ajmg.B.32053 |
0.53 |
|
2012 |
Van Den Bossche MJ, Van Wallendael KL, Strazisar M, Sabbe B, Del-Favero J. Co-occurrence of Marfan syndrome and schizophrenia: what can be learned? European Journal of Medical Genetics. 55: 252-5. PMID 22406088 DOI: 10.1016/J.Ejmg.2012.02.005 |
0.606 |
|
2012 |
Pickard BS, Van Den Bossche MJ, Malloy MP, Johnstone M, Lenaerts AS, Nordin A, Goossens D, St Clair D, Muir WJ, Nilsson LG, Sabbe B, Adolfsson R, Blackwood DH, Del-Favero J. Multiplex amplicon quantification screening the ABCA13 gene for copy number variation in schizophrenia and bipolar disorder. Psychiatric Genetics. 22: 269-70. PMID 22392056 DOI: 10.1097/Ypg.0B013E32835185B3 |
0.573 |
|
2012 |
Reumers J, De Rijk P, Zhao H, Liekens A, Smeets D, Cleary J, Van Loo P, Van Den Bossche M, Catthoor K, Sabbe B, Despierre E, Vergote I, Hilbush B, Lambrechts D, Del-Favero J. Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing. Nature Biotechnology. 30: 61-8. PMID 22178994 DOI: 10.1038/Nbt.2053 |
0.37 |
|
2011 |
Moens LN, De Rijk P, Reumers J, Van den Bossche MJ, Glassee W, De Zutter S, Lenaerts AS, Nordin A, Nilsson LG, Medina Castello I, Norrback KF, Goossens D, Van Steen K, Adolfsson R, Del-Favero J. Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population. Plos One. 6: e23450. PMID 21853134 DOI: 10.1371/Journal.Pone.0023450 |
0.456 |
|
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