Jurgen Del-Favero - Publications

Affiliations: 
Universitaire Instelling Antwerpen (Belgium) 
Area:
Molecular Biology, Genetics

76 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Szatkiewicz J, Crowley JJ, Adolfsson AN, Åberg KA, Alaerts M, Genovese G, McCarroll S, Del-Favero J, Adolfsson R, Sullivan PF. The genomics of major psychiatric disorders in a large pedigree from Northern Sweden. Translational Psychiatry. 9: 60. PMID 30718465 DOI: 10.1038/s41398-019-0414-9  0.32
2016 Dries DR, Zhu Y, Brooks MM, Forero DA, Adachi M, Cenik B, West JM, Han YH, Yu C, Arbella J, Nordin A, Adolfsson R, Del-Favero J, Lu QR, Callaerts P, et al. Loss of Nicastrin from Oligodendrocytes Results in Hypomyelination and Schizophrenia with Compulsive Behavior. The Journal of Biological Chemistry. PMID 27008863 DOI: 10.1074/jbc.M116.715078  0.48
2016 Forero DA, Herteleer L, De Zutter S, Norrback KF, Nilsson LG, Adolfsson R, Callaerts P, Del-Favero J. A network of synaptic genes associated with schizophrenia and bipolar disorder. Schizophrenia Research. PMID 26899345 DOI: 10.1016/j.schres.2016.02.012  0.48
2015 Johnstone M, Maclean A, Heyrman L, Lenaerts AS, Nordin A, Nilsson LG, De Rijk P, Goossens D, Adolfsson R, St Clair DM, Hall J, Lawrie SM, McIntosh AM, Del-Favero J, Blackwood DH, et al. Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness. Molecular Neuropsychiatry. 1: 175-190. PMID 27239468 DOI: 10.1159/000438788  0.44
2015 Strazisar M, Cammaerts S, van der Ven K, Forero DA, Lenaerts AS, Nordin A, Almeida-Souza L, Genovese G, Timmerman V, Liekens A, De Rijk P, Adolfsson R, Callaerts P, Del-Favero J. MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene sets. Molecular Psychiatry. 20: 472-81. PMID 24888363 DOI: 10.1038/mp.2014.53  0.48
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  0.48
2012 Theuns J, Crosiers D, Debaene L, Nuytemans K, Meeus B, Sleegers K, Goossens D, Corsmit E, Elinck E, Peeters K, Mattheijssens M, Pickut B, Del-Favero J, Engelborghs S, De Deyn PP, et al. Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystonia. Movement Disorders : Official Journal of the Movement Disorder Society. 27: 1451-6. PMID 22976901 DOI: 10.1002/mds.25147  0.48
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  0.48
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, ... Del-Favero J, 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  0.48
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, ... ... Del-Favero J, 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  0.48
2012 Kruse LV, Nyegaard M, Christensen U, Møller-Larsen S, Haagerup A, Deleuran M, Hansen LG, Venø SK, Goossens D, Del-Favero J, Børglum AD. A genome-wide search for linkage to allergic rhinitis in Danish sib-pair families. European Journal of Human Genetics : Ejhg. 20: 965-72. PMID 22419170 DOI: 10.1038/ejhg.2012.46  0.48
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  0.48
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  0.48
2012 Ceulemans S, van der Ven K, Del-Favero J. Targeted screening and validation of copy number variations. Methods in Molecular Biology (Clifton, N.J.). 838: 311-28. PMID 22228019 DOI: 10.1007/978-1-61779-507-7_15  0.48
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  0.48
2012 Wikgren M, Maripuu M, Karlsson T, Nordfjäll K, Bergdahl J, Hultdin J, Del-Favero J, Roos G, Nilsson LG, Adolfsson R, Norrback KF. Short telomeres in depression and the general population are associated with a hypocortisolemic state. Biological Psychiatry. 71: 294-300. PMID 22055018 DOI: 10.1016/j.biopsych.2011.09.015  0.48
2011 Ceulemans S, De Zutter S, Heyrman L, Norrback KF, Nordin A, Nilsson LG, Adolfsson R, Del-Favero J, Claes S. Evidence for the involvement of the glucocorticoid receptor gene in bipolar disorder in an isolated northern Swedish population. Bipolar Disorders. 13: 614-23. PMID 22085474 DOI: 10.1111/j.1399-5618.2011.00960.x  0.48
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  0.48
2011 Liekens AM, De Knijf J, Daelemans W, Goethals B, De Rijk P, Del-Favero J. BioGraph: unsupervised biomedical knowledge discovery via automated hypothesis generation. Genome Biology. 12: R57. PMID 21696594 DOI: 10.1186/gb-2011-12-6-r57  0.48
2011 Karling P, Danielsson Å, Wikgren M, Söderström I, Del-Favero J, Adolfsson R, Norrback KF. The relationship between the val158met catechol-O-methyltransferase (COMT) polymorphism and irritable bowel syndrome. Plos One. 6: e18035. PMID 21437260 DOI: 10.1371/journal.pone.0018035  0.32
2011 Van Schijndel JE, Van Zweeden M, Van Loo KM, Djurovic S, Andreassen OA, Hansen T, Werge T, Nyegaard M, Sørensen KM, Nordentoft M, Mortensen PB, Mors O, Børglum AD, Del-Favero J, Norrback KF, et al. Dual association of a TRKA polymorphism with schizophrenia. Psychiatric Genetics. 21: 125-31. PMID 21317683 DOI: 10.1097/YPG.0b013e3283437194  0.32
2011 Momozawa Y, Mni M, Nakamura K, Coppieters W, Almer S, Amininejad L, Cleynen I, Colombel JF, de Rijk P, Dewit O, Finkel Y, Gassull MA, Goossens D, Laukens D, Lémann M, ... ... Del-Favero J, et al. Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease. Nature Genetics. 43: 43-7. PMID 21151126 DOI: 10.1038/ng.733  0.44
2011 De Knijf J, Liekens A, Daelemans W, De Rijk P, Del-Favero J, Goethals B. BioGraph: Knowledge discovery and exploration in the Biomedical domain Proceedings - Ieee International Conference On Data Mining, Icdm. 1223-1226. DOI: 10.1109/ICDMW.2011.39  0.48
2010 Baets J, Deconinck T, Smets K, Goossens D, Van den Bergh P, Dahan K, Schmedding E, Santens P, Rasic VM, Van Damme P, Robberecht W, De Meirleir L, Michielsens B, Del-Favero J, Jordanova A, et al. Mutations in SACS cause atypical and late-onset forms of ARSACS. Neurology. 75: 1181-8. PMID 20876471 DOI: 10.1212/WNL.0b013e3181f4d86c  0.48
2010 Deprez L, Weckhuysen S, Holmgren P, Suls A, Van Dyck T, Goossens D, Del-Favero J, Jansen A, Verhaert K, Lagae L, Jordanova A, Van Coster R, Yendle S, Berkovic SF, Scheffer I, et al. Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations. Neurology. 75: 1159-65. PMID 20876469 DOI: 10.1212/WNL.0b013e3181f4d7bf  0.44
2010 Forero DA, van der Ven K, Callaerts P, Del-Favero J. miRNA genes and the brain: implications for psychiatric disorders. Human Mutation. 31: 1195-204. PMID 20725930 DOI: 10.1002/humu.21344  0.48
2010 van West D, Del-Favero J, Deboutte D, Van Broeckhoven C, Claes S. Associations between common arginine vasopressin 1b receptor and glucocorticoid receptor gene variants and HPA axis responses to psychosocial stress in a child psychiatric population. Psychiatry Research. 179: 64-8. PMID 20472303 DOI: 10.1016/j.psychres.2009.04.002  0.48
2010 Moens LN, Ceulemans S, Alaerts M, Van Den Bossche MJ, Lenaerts AS, De Zutter S, Norrback KF, Adolfsson R, Del-Favero J. PCM1 and schizophrenia: a replication study in the Northern Swedish population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 1240-3. PMID 20468070 DOI: 10.1002/ajmg.b.31088  0.48
2010 Castermans D, Volders K, Crepel A, Backx L, De Vos R, Freson K, Meulemans S, Vermeesch JR, Schrander-Stumpel CT, De Rijk P, Del-Favero J, Van Geet C, Van De Ven WJ, Steyaert JG, Devriendt K, et al. SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles. Human Molecular Genetics. 19: 1368-78. PMID 20071347 DOI: 10.1093/hmg/ddq013  0.48
2009 van West D, Del-Favero J, Deboutte D, Van Broeckhoven C, Claes S. Arginine vasopressin receptor gene-based single-nucleotide polymorphism analysis in attention deficit hyperactivity disorder. Psychiatric Genetics. 19: 102-3. PMID 19668115 DOI: 10.1097/YPG.0b013e32832a0b2b  0.48
2009 Alaerts M, Ceulemans S, Forero D, Moens LN, De Zutter S, Heyrman L, Lenaerts AS, Norrback KF, De Rijk P, Nilsson LG, Goossens D, Adolfsson R, Del-Favero J. Support for NRG1 as a susceptibility factor for schizophrenia in a northern Swedish isolated population. Archives of General Psychiatry. 66: 828-37. PMID 19652122 DOI: 10.1001/archgenpsychiatry.2009.82  0.48
2009 Nuytemans K, Meeus B, Crosiers D, Brouwers N, Goossens D, Engelborghs S, Pals P, Pickut B, Van den Broeck M, Corsmit E, Cras P, De Deyn PP, Del-Favero J, Van Broeckhoven C, Theuns J. Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population. Human Mutation. 30: 1054-61. PMID 19405094 DOI: 10.1002/humu.21007  0.48
2009 Goossens D, Moens LN, Nelis E, Lenaerts AS, Glassee W, Kalbe A, Frey B, Kopal G, De Jonghe P, De Rijk P, Del-Favero J. Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing. Human Mutation. 30: 472-6. PMID 19058222 DOI: 10.1002/humu.20873  0.44
2009 Alaerts M, Ceulemans S, Forero D, Moens LN, De Zutter S, Heyrman L, Lenaerts AS, Norrback KF, Goossens D, De Rijk P, Nilsson LG, Adolfsson R, Del-Favero J. Detailed analysis of the serotonin transporter gene (SLC6A4) shows no association with bipolar disorder in the Northern Swedish population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 585-92. PMID 18792946 DOI: 10.1002/ajmg.b.30853  0.48
2009 Gijselinck I, Sleegers K, Engelborghs S, Robberecht W, Martin JJ, Vandenberghe R, Sciot R, Dermaut B, Goossens D, van der Zee J, De Pooter T, Del-Favero J, Santens P, De Jonghe P, De Deyn PP, et al. Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS. Neurobiology of Aging. 30: 1329-31. PMID 18068872 DOI: 10.1016/j.neurobiolaging.2007.11.002  0.48
2008 Aulchenko YS, Hoppenbrouwers IA, Ramagopalan SV, Broer L, Jafari N, Hillert J, Link J, Lundström W, Greiner E, Dessa Sadovnick A, Goossens D, Van Broeckhoven C, Del-Favero J, Ebers GC, Oostra BA, et al. Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis. Nature Genetics. 40: 1402-3. PMID 18997785 DOI: 10.1038/ng.251  0.48
2008 Suls A, Dedeken P, Goffin K, Van Esch H, Dupont P, Cassiman D, Kempfle J, Wuttke TV, Weber Y, Lerche H, Afawi Z, Vandenberghe W, Korczyn AD, Berkovic SF, Ekstein D, ... ... Del-Favero J, et al. Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1. Brain : a Journal of Neurology. 131: 1831-44. PMID 18577546 DOI: 10.1093/brain/awn113  0.48
2008 Venken T, Alaerts M, Souery D, Goossens D, Sluijs S, Navon R, Van Broeckhoven C, Mendlewicz J, Del-Favero J, Claes S. Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families. Molecular Psychiatry. 13: 442-50. PMID 17579605 DOI: 10.1038/sj.mp.4002039  0.48
2007 Moens LN, Soetaert A, van der Ven K, Del-Favero J, De Coen WM. Use of suppression subtractive hybridization PCR for the development of cDNA arrays for the detection of endocrine disruption in carp (Cyprinus carpio). Comparative Biochemistry and Physiology. Part D, Genomics & Proteomics. 2: 18-33. PMID 20483275 DOI: 10.1016/j.cbd.2006.10.004  0.48
2007 Weckx S, De Rijk P, Glassee W, Van Broeckhoven C, Del-Favero J. SNPbox: web-based high-throughput primer design with an eye for repetitive sequences. Methods in Molecular Biology (Clifton, N.J.). 402: 179-200. PMID 17951796  0.44
2007 Sutrala SR, Goossens D, Williams NM, Heyrman L, Adolfsson R, Norton N, Buckland PR, Del-Favero J. Gene copy number variation in schizophrenia. Schizophrenia Research. 96: 93-9. PMID 17826036 DOI: 10.1016/j.schres.2007.07.029  0.48
2007 Van Den Eede F, Venken T, Van Den Bogaert A, Del-Favero J, Norrback KF, Nilsson LG, Adolfsson R, Van Broeckhoven C, Claes SJ. Single nucleotide polymorphism analysis of corticotropin-releasing factor-binding protein gene in bipolar disorder. Psychiatric Genetics. 17: 304-7. PMID 17728670 DOI: 10.1097/YPG.0b013e328133f342  0.32
2007 Van Den Eede F, Venken T, Del-Favero J, Norrback KF, Souery D, Nilsson LG, Van den Bossche B, Hulstijn W, Sabbe BG, Cosyns P, Mendlewicz J, Adolfsson R, Van Broeckhoven C, Claes SJ. Single nucleotide polymorphism analysis of corticotropin-releasing factor-binding protein gene in recurrent major depressive disorder. Psychiatry Research. 153: 17-25. PMID 17599466 DOI: 10.1016/j.psychres.2006.12.018  0.48
2007 Deprez L, Peeters K, Van Paesschen W, Claeys KG, Claes LR, Suls A, Audenaert D, Van Dyck T, Goossens D, Del-Favero J, De Jonghe P. Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9q. Neurology. 68: 1995-2002. PMID 17460155 DOI: 10.1212/01.wnl.0000262764.78511.17  0.44
2007 Moens LN, Smolders R, van der Ven K, van Remortel P, Del-Favero J, De Coen WM. Effluent impact assessment using microarray-based analysis in common carp: a systems toxicology approach. Chemosphere. 67: 2293-304. PMID 17267021 DOI: 10.1016/j.chemosphere.2006.09.092  0.48
2006 Alaerts M, Venken T, Lenaerts AS, De Zutter S, Norrback KF, Adolfsson R, Del-Favero J. Lack of association of an insertion/deletion polymorphism in the G protein-coupled receptor 50 with bipolar disorder in a Northern Swedish population. Psychiatric Genetics. 16: 235-6. PMID 17106423 DOI: 10.1097/01.ypg.0000242193.28526.b3  0.32
2006 Van Den Bogaert A, Sleegers K, De Zutter S, Heyrman L, Norrback KF, Adolfsson R, Van Broeckhoven C, Del-Favero J. Association of brain-specific tryptophan hydroxylase, TPH2, with unipolar and bipolar disorder in a Northern Swedish, isolated population. Archives of General Psychiatry. 63: 1103-10. PMID 17015812 DOI: 10.1001/archpsyc.63.10.1103  0.32
2006 Van Den Bogaert A, Sleegers K, De Zutter S, Heyrman L, Norrback KF, Adolfsson R, Van Broeckhoven C, Del-Favero J. No allelic association or interaction of three known functional polymorphisms with bipolar disorder in a northern Swedish isolated population. Psychiatric Genetics. 16: 209-12. PMID 16969276 DOI: 10.1097/01.ypg.0000218623.03752.e4  0.32
2006 Suls A, Claeys KG, Goossens D, Harding B, Van Luijk R, Scheers S, Deprez L, Audenaert D, Van Dyck T, Beeckmans S, Smouts I, Ceulemans B, Lagae L, Buyse G, Barisic N, ... ... Del-Favero J, et al. Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients. Human Mutation. 27: 914-20. PMID 16865694 DOI: 10.1002/humu.20350  0.44
2006 Moens LN, van der Ven K, Van Remortel P, Del-Favero J, De Coen WM. Expression profiling of endocrine-disrupting compounds using a customized Cyprinus carpio cDNA microarray. Toxicological Sciences : An Official Journal of the Society of Toxicology. 93: 298-310. PMID 16835292 DOI: 10.1093/toxsci/kfl057  0.48
2006 Dikeos DG, Papadimitriou GN, Souery D, Del-Favero J, Massat I, Blackwood D, Cichon S, Daskalopoulou E, Ivezic S, Kaneva R, Karadima G, Lorenzi C, Milanova V, Muir W, Nöthen M, et al. Lack of genetic association between the phospholipase A2 gene and bipolar mood disorder in a European multicentre case-control study. Psychiatric Genetics. 16: 169-71. PMID 16829784 DOI: 10.1097/01.ypg.0000218615.19892.86  0.48
2006 Venken T, Alaerts M, Adolfsson R, Broeckhoven CV, Del-Favero J. No association of the trace amine-associated receptor 6 with bipolar disorder in a northern Swedish population Psychiatric Genetics. 16: 1-2. PMID 16395122 DOI: 10.1097/01.ypg.0000180682.18665.a6  0.48
2006 Deprez L, Claes LR, Claeys KG, Audenaert D, Van Dyck T, Goossens D, Van Paesschen W, Del-Favero J, Van Broeckhoven C, De Jonghe P. Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation. Human Genetics. 118: 618-25. PMID 16273391 DOI: 10.1007/s00439-005-0077-x  0.44
2006 van West D, Van Den Eede F, Del-Favero J, Souery D, Norrback KF, Van Duijn C, Sluijs S, Adolfsson R, Mendlewicz J, Deboutte D, Van Broeckhoven C, Claes S. Glucocorticoid receptor gene-based SNP analysis in patients with recurrent major depression. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 31: 620-7. PMID 16192984 DOI: 10.1038/sj.npp.1300898  0.48
2005 Van Den Bogaert A, De Zutter S, Heyrman L, Mendlewicz J, Adolfsson R, Van Broeckhoven C, Del-Favero J. Response to Zhang et al (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major Depression. Neuron 45, 11-16. Neuron. 48: 704; author reply 70. PMID 16337903 DOI: 10.1016/j.neuron.2005.11.017  0.32
2005 Rademakers R, Melquist S, Cruts M, Theuns J, Del-Favero J, Poorkaj P, Baker M, Sleegers K, Crook R, De Pooter T, Bel Kacem S, Adamson J, Van den Bossche D, Van den Broeck M, Gass J, et al. High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy. Human Molecular Genetics. 14: 3281-92. PMID 16195395 DOI: 10.1093/hmg/ddi361  0.48
2005 Kuhlenbäumer G, Hannibal MC, Nelis E, Schirmacher A, Verpoorten N, Meuleman J, Watts GD, De Vriendt E, Young P, Stögbauer F, Halfter H, Irobi J, Goossens D, Del-Favero J, Betz BG, et al. Mutations in SEPT9 cause hereditary neuralgic amyotrophy. Nature Genetics. 37: 1044-6. PMID 16186812 DOI: 10.1038/ng1649  0.48
2005 Rademakers R, Cruts M, Sleegers K, Dermaut B, Theuns J, Aulchenko Y, Weckx S, De Pooter T, Van den Broeck M, Corsmit E, De Rijk P, Del-Favero J, van Swieten J, van Duijn CM, Van Broeckhoven C. Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample. American Journal of Human Genetics. 77: 643-52. PMID 16175510 DOI: 10.1086/491749  0.48
2005 Cruts M, Rademakers R, Gijselinck I, van der Zee J, Dermaut B, de Pooter T, de Rijk P, Del-Favero J, van Broeckhoven C. Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region. Human Molecular Genetics. 14: 1753-62. PMID 15888485 DOI: 10.1093/hmg/ddi182  0.48
2005 Weckx S, Del-Favero J, Rademakers R, Claes L, Cruts M, De Jonghe P, Van Broeckhoven C, De Rijk P. novoSNP, a novel computational tool for sequence variation discovery. Genome Research. 15: 436-42. PMID 15741513 DOI: 10.1101/gr.2754005  0.44
2005 Venken T, Claes S, Sluijs S, Paterson AD, van Duijn C, Adolfsson R, Del-Favero J, Van Broeckhoven C. Genomewide scan for affective disorder susceptibility Loci in families of a northern Swedish isolated population. American Journal of Human Genetics. 76: 237-48. PMID 15614721 DOI: 10.1086/427836  0.48
2005 Massat I, Souery D, Del-Favero J, Nothen M, Blackwood D, Muir W, Kaneva R, Serretti A, Lorenzi C, Rietschel M, Milanova V, Papadimitriou GN, Dikeos D, Van Broekhoven C, Mendlewicz J. Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study. Molecular Psychiatry. 10: 598-605. PMID 15583702 DOI: 10.1038/sj.mp.4001615  0.48
2004 Mendlewicz J, Souery D, Del-Favero J, Massat I, Lindblad K, Engström C, Van den Bossche D, Adolfsson R, Schalling M, Van Broeckhoven C. Expanded RED products and loci containing CAG/CTG repeats on chromosome 17 (ERDA1) and chromosome 18 (CTG18.1) in trans-generational pairs with bipolar affective disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 128: 71-5. PMID 15211635 DOI: 10.1002/ajmg.b.20006  0.32
2004 van West D, Del-Favero J, Aulchenko Y, Oswald P, Souery D, Forsgren T, Sluijs S, Bel-Kacem S, Adolfsson R, Mendlewicz J, Van Duijn C, Deboutte D, Van Broeckhoven C, Claes S. A major SNP haplotype of the arginine vasopressin 1B receptor protects against recurrent major depression. Molecular Psychiatry. 9: 287-92. PMID 15094789 DOI: 10.1038/sj.mp.4001420  0.48
2003 Claes S, Villafuerte S, Forsgren T, Sluijs S, Del-Favero J, Adolfsson R, Van Broeckhoven C. The corticotropin-releasing hormone binding protein is associated with major depression in a population from Northern Sweden. Biological Psychiatry. 54: 867-72. PMID 14573312  0.32
2003 Lambrechts D, Storkebaum E, Morimoto M, Del-Favero J, Desmet F, Marklund SL, Wyns S, Thijs V, Andersson J, van Marion I, Al-Chalabi A, Bornes S, Musson R, Hansen V, Beckman L, et al. VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death. Nature Genetics. 34: 383-94. PMID 12847526 DOI: 10.1038/ng1211  0.48
2003 Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberger JI, Craddock N, DePaulo JR, Baron M, Gershon ES, Ekholm J, Cichon S, Turecki G, Claes S, Kelsoe JR, ... ... Del-Favero J, et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. American Journal of Human Genetics. 73: 49-62. PMID 12802785 DOI: 10.1086/376547  0.48
2003 Claes L, Ceulemans B, Audenaert D, Smets K, Löfgren A, Del-Favero J, Ala-Mello S, Basel-Vanagaite L, Plecko B, Raskin S, Thiry P, Wolf NI, Van Broeckhoven C, De Jonghe P. De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy. Human Mutation. 21: 615-21. PMID 12754708 DOI: 10.1002/humu.10217  0.48
2002 Del-Favero J, Gestel SV, Børglum AD, Muir W, Ewald H, Mors O, Ivezic S, Oruc L, Adolfsson R, Blackwood D, Kruse T, Mendlewicz J, Schalling M, Van Broeckhoven C. European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder. European Journal of Human Genetics : Ejhg. 10: 276-80. PMID 12032737 DOI: 10.1038/sj.ejhg.5200803  0.48
2002 Villafuerte SM, Del-Favero J, Adolfsson R, Souery D, Massat I, Mendlewicz J, Van Broeckhoven C, Claes S. Gene-based SNP genetic association study of the corticotropin-releasing hormone receptor-2 (CRHR2) in major depression. American Journal of Medical Genetics. 114: 222-6. PMID 11857585 DOI: 10.1002/ajmg.10179  0.32
2002 Massat I, Souery D, Del-Favero J, Van Gestel S, Serretti A, Macciardi F, Smeraldi E, Kaneva R, Adolfsson R, Nylander PO, Blackwood D, Muir W, Papadimitriou GN, Dikeos D, Oruc L, et al. Positive association of dopamine D2 receptor polymorphism with bipolar affective disorder in a European Multicenter Association Study of affective disorders. American Journal of Medical Genetics. 114: 177-85. PMID 11857579 DOI: 10.1002/ajmg.10118  0.32
2002 Goossens D, Del-Favero J, Van Broeckhoven C. Trinucleotide repeat expansions: do they contribute to bipolar disorder? Brain Research Bulletin. 56: 243-57. PMID 11719258 DOI: 10.1016/S0361-9230(01)00657-8  0.32
2001 Theuns J, Feuk L, Dermaut B, Del-Favero J, Roks G, Van den Bossche D, Corsmit E, Van den Broeck M, van Duijn CM, Cruts M, Brookes AJ, Van Broeckhoven C. The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease. Human Genetics. 108: 552-3. PMID 11499683 DOI: 10.1007/s004390100508  0.48
2000 Theuns J, Del-Favero J, Dermaut B, van Duijn CM, Backhovens H, Van den Broeck MV, Serneels S, Corsmit E, Van Broeckhoven CV, Cruts M. Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression. Human Molecular Genetics. 9: 325-31. PMID 10655540 DOI: 10.1093/HMG/9.3.325  0.48
1999 Wang SY, Cruts M, Del-Favero J, Zhang Y, Tissir F, Potier MC, Patterson D, Nizetic D, Bosch A, Chen H, Bennett L, Estivill X, Kessling A, Antonarakis SE, van Broeckhoven C. A high-resolution physical map of human chromosome 21p using yeast artificial chromosomes. Genome Research. 9: 1059-73. PMID 10568746 DOI: 10.1101/gr.9.11.1059  0.48
1994 Del-Favero J, Vauterin M, Weyens G, Edwards KE, Jacobs M. Construction and characterisation of a yeast artificial chromosome library containing five haploid sugarbeet (Beta vulgaris L.) genome equivalents. Tag. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik. 88: 449-53. PMID 24186033 DOI: 10.1007/BF00223659  0.48
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