| Year |
Citation |
Score |
| 2019 |
Stahl EA, Breen G, Forstner AJ, McQuillin A, Ripke S, Trubetskoy V, Mattheisen M, Wang Y, Coleman JRI, Gaspar HA, de Leeuw CA, Steinberg S, Pavlides JMW, Trzaskowski M, Byrne EM, ... ... Del-Favero J, et al. Genome-wide association study identifies 30 loci associated with bipolar disorder. Nature Genetics. PMID 31043756 DOI: 10.1038/S41588-019-0397-8 |
0.419 |
|
| 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 |
0.387 |
|
| 2019 |
Crowley J, Mudgal P, Adolfsson AN, Åberg K, Alaerts M, Genovese G, McCarroll S, Del-Favero J, Adolfsson R, Sullivan P. The genomics of bipolar and schizophrenic disorders in a large pedigree from a northern Swedish isolate European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.217 |
0.352 |
|
| 2017 |
Boulet G, Barel DV, Rotthier A, Goossens D, Del-Favero J. 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. DOI: 10.1200/Jco.2017.35.15_Suppl.E23116 |
0.579 |
|
| 2016 |
Hestand MS, Nowakowska BA, Vergaelen E, Van Houdt J, Dehaspe L, Suhl JA, Del-Favero J, Mortier G, Zackai E, Swillen A, Devriendt K, Gur RE, McDonald-McGinn DM, Warren ST, Emanuel BS, et al. A catalog of hemizygous variation in 127 22q11 deletion patients. Human Genome Variation. 3: 15065. PMID 27274857 DOI: 10.1038/Hgv.2015.65 |
0.448 |
|
| 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 |
0.728 |
|
| 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 |
0.766 |
|
| 2016 |
Marques C, Bettens K, Goossens D, Heyrman L, Heusdens C, Kupers S, Berwouts S, Van Barel D, Rotthier A, Del-Favero J. Detection of NRAS, KRAS and BRAF mutations in FFPE derived DNA with a novel targeted resequencing-based diagnostics assay Annals of Oncology. 27: vi405. DOI: 10.1093/Annonc/Mdw380.16 |
0.582 |
|
| 2016 |
Herteleer L, Zwarts L, Hens K, Forero D, Del-Favero J, Callaerts P. Mood stabilizing drugs regulate transcription of immune, neuronal and metabolic pathway genes in Drosophila Psychopharmacology. 1-12. DOI: 10.1007/S00213-016-4223-Z |
0.704 |
|
| 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 |
0.658 |
|
| 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 |
0.726 |
|
| 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 |
0.392 |
|
| 2013 |
Ancín I, Cabranes JA, Vázquez-Álvarez B, Santos JL, Sánchez-Morla E, Alaerts M, Del-Favero J, Barabash A. NR4A2: effects of an "orphan" receptor on sustained attention in a schizophrenic population. Schizophrenia Bulletin. 39: 555-63. PMID 22294735 DOI: 10.1093/Schbul/Sbr176 |
0.332 |
|
| 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 |
0.618 |
|
| 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 |
0.327 |
|
| 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 |
0.685 |
|
| 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 |
0.678 |
|
| 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 |
0.654 |
|
| 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 |
0.338 |
|
| 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 |
0.652 |
|
| 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 |
0.363 |
|
| 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 |
0.428 |
|
| 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 |
0.685 |
|
| 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 |
0.32 |
|
| 2011 |
Claes S, Myint AM, Domschke K, Del-Favero J, Entrich K, Engelborghs S, De Deyn P, Mueller N, Baune B, Rothermundt M. The kynurenine pathway in major depression: haplotype analysis of three related functional candidate genes. Psychiatry Research. 188: 355-60. PMID 21492941 DOI: 10.1016/J.Psychres.2011.03.012 |
0.323 |
|
| 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 |
0.39 |
|
| 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 |
0.623 |
|
| 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 |
0.621 |
|
| 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 |
0.616 |
|
| 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 |
0.72 |
|
| 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 |
0.314 |
|
| 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 |
0.358 |
|
| 2010 |
Kumps C, Van Roy N, Heyrman L, Goossens D, Del-Favero J, Noguera R, Vandesompele J, Speleman F, De Preter K. Multiplex Amplicon Quantification (MAQ), a fast and efficient method for the simultaneous detection of copy number alterations in neuroblastoma. Bmc Genomics. 11: 298. PMID 20459859 DOI: 10.1186/1471-2164-11-298 |
0.611 |
|
| 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 |
0.399 |
|
| 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 |
0.322 |
|
| 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 |
0.749 |
|
| 2009 |
Alaerts M, Del-Favero J. Searching genetic risk factors for schizophrenia and bipolar disorder: learn from the past and back to the future. Human Mutation. 30: 1139-52. PMID 19626716 DOI: 10.1002/Humu.21042 |
0.429 |
|
| 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 |
0.632 |
|
| 2009 |
Matimba A, Del-Favero J, Van Broeckhoven C, Masimirembwa C. Novel variants of major drug-metabolising enzyme genes in diverse African populations and their predicted functional effects. Human Genomics. 3: 169-90. PMID 19164093 DOI: 10.1186/1479-7364-3-2-169 |
0.356 |
|
| 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 |
0.628 |
|
| 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 |
0.763 |
|
| 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 |
0.628 |
|
| 2009 |
van West D, Del-Favero J, Deboutte D, Van Broeckhoven C, Claes S. P.7.b.005 Arginine vasopressin receptor gene-based single nucleotide polymorphism (SNP) analysis in ADHD European Neuropsychopharmacology. 19: S686. DOI: 10.1016/S0924-977X(09)71109-5 |
0.305 |
|
| 2009 |
Claes S, van West D, Del-Favero J, Deboutte D. Stress Responsivity in Childhood and Adulthood: Role of the Glucocorticoid Receptor Gene European Psychiatry. 24: 1-1. DOI: 10.1016/S0924-9338(09)70537-1 |
0.349 |
|
| 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 |
0.608 |
|
| 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 |
0.614 |
|
| 2008 |
Gijselinck I, van der Zee J, Engelborghs S, Goossens D, Peeters K, Mattheijssens M, Corsmit E, Del-Favero J, De Deyn PP, Van Broeckhoven C, Cruts M. Progranulin locus deletion in frontotemporal dementia. Human Mutation. 29: 53-8. PMID 18157829 DOI: 10.1002/Humu.20651 |
0.663 |
|
| 2008 |
López-León S, Janssens ACJW, Ladd AMG, Del-Favero J, Claes S, Oostra BA, Duijn CMv. Meta-analyses of genetic studies on major depressive disorder. Molecular Psychiatry. 13: 772-785. PMID 17938638 DOI: 10.1038/Sj.Mp.4002088 |
0.389 |
|
| 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 |
0.655 |
|
| 2008 |
Forero D, Lambertz I, Alaerts M, Ceulemans S, De Zutter S, Heyrman L, Norrback K, Goossens D, Marine J, Adolfsson R, Callaerts P, Del-Favero J. miRNA DYSFUNCTION IN SCHIZOPHRENIA: GENETIC AND FUNCTIONAL EVIDENCE Schizophrenia Research. 102: 185-186. DOI: 10.1016/S0920-9964(08)70564-4 |
0.761 |
|
| 2008 |
Del-Favero J, Ceulemans S, Alaerts M, Forero D, Heyrman L, Glassee W, Moens L, De Rijk P, Goossens D. MAQ, A NOVEL METHOD FOR PCR BASED, HIGH-THROUGHPUT COPY NUMBER VARIATION ANALYSIS APPLIED TO THE 22q11 DELETION SYNDROME Schizophrenia Research. 102: 185. DOI: 10.1016/S0920-9964(08)70562-0 |
0.721 |
|
| 2008 |
Alaerts M, Forero D, Ceulemans S, De Zutter S, Norrback K, Goossens D, De Rijk P, Adolfsson R, Del-Favero J. IDENTIFYINGGENES FOR SCHIZOPHRENIA IN A LARGE PEDIGREE FROMA NORTHERN SWEDISH ISOLATED POPULATION Schizophrenia Research. 102: 181. DOI: 10.1016/S0920-9964(08)70552-8 |
0.705 |
|
| 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 |
0.33 |
|
| 2007 |
Rijk PD, Del-Favero J. novoSNP3: variant detection and sequence annotation in resequencing projects. Methods in Molecular Biology (Clifton, N.J.). 396: 331-44. PMID 18025702 DOI: 10.1007/978-1-59745-515-2_21 |
0.322 |
|
| 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 |
0.652 |
|
| 2007 |
Massat I, Lerer B, Souery D, Blackwood D, Muir W, Kaneva R, Nöthen MM, Oruc L, Papadimitriou GN, Dikeos D, Serretti A, Bellivier F, Golmard JL, Milanova V, Del-Favero J, et al. HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study. Molecular Psychiatry. 12: 797-798. PMID 17767148 DOI: 10.1038/Sj.Mp.4002018 |
0.349 |
|
| 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 |
0.416 |
|
| 2007 |
Bogaerts V, Engelborghs S, Kumar-Singh S, Goossens D, Pickut B, van der Zee J, Sleegers K, Peeters K, Martin JJ, Del-Favero J, Gasser T, Dickson DW, Wszolek ZK, De Deyn PP, Theuns J, et al. A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder. Brain : a Journal of Neurology. 130: 2277-91. PMID 17681982 DOI: 10.1093/Brain/Awm167 |
0.667 |
|
| 2007 |
Venken T, Del-Favero J. Chasing genes for mood disorders and schizophrenia in genetically isolated populations. Human Mutation. 28: 1156-70. PMID 17659644 DOI: 10.1002/Humu.20582 |
0.423 |
|
| 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 |
0.386 |
|
| 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 |
0.608 |
|
| 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 |
0.365 |
|
| 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 |
0.323 |
|
| 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 |
0.425 |
|
| 2006 |
Sleegers K, Brouwers N, Gijselinck I, Theuns J, Goossens D, Wauters J, Del-Favero J, Cruts M, van Duijn CM, Van Broeckhoven C. APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy. Brain : a Journal of Neurology. 129: 2977-83. PMID 16921174 DOI: 10.1093/Brain/Awl203 |
0.632 |
|
| 2006 |
Van Den Bogaert A, Del-Favero J, Van Broeckhoven C. Major affective disorders and schizophrenia: a common molecular signature? Human Mutation. 27: 833-53. PMID 16917879 DOI: 10.1002/Humu.20369 |
0.404 |
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| 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 |
0.655 |
|
| 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 |
0.403 |
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| 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 |
0.315 |
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| 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 |
0.645 |
|
| 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 |
0.397 |
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| 2006 |
Cruts M, Rademakers R, Sleegers K, Theuns J, Rijk PD, Pooter TD, Bossche DVD, Del-Favero J, Broeckhoven CV. P3-162: Increased variability of the tau gene MAPT due to genomic instability Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.1430 |
0.306 |
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| 2006 |
Sleegers K, Brouwers N, Gijselinck I, Theuns J, Goossens D, Del-Favero J, Cruts M, Duijn CMv, Broeckhoven CV. O2-02-08 Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.118 |
0.533 |
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| 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 |
0.349 |
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| 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 |
0.334 |
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| 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 |
0.641 |
|
| 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 |
0.4 |
|
| 2005 |
Oswald P, Del-Favero J, Massat I, Souery D, Claes S, Van Broeckhoven C, Mendlewicz J. No implication of brain-derived neurotrophic factor (BDNF) gene in unipolar affective disorder: evidence from Belgian first and replication patient-control studies. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. 15: 491-5. PMID 16139165 DOI: 10.1016/J.Euroneuro.2005.01.001 |
0.353 |
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| 2005 |
Mendlewicz J, Oswald P, Claes S, Massat I, Souery D, Van Broeckhoven C, Del-Favero J. Patient-control association study of substance P-related genes in unipolar and bipolar affective disorders. The International Journal of Neuropsychopharmacology / Official Scientific Journal of the Collegium Internationale Neuropsychopharmacologicum (Cinp). 8: 505-13. PMID 15927090 DOI: 10.1017/S1461145705005444 |
0.375 |
|
| 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 |
0.408 |
|
| 2005 |
Audenaert D, Claes L, Claeys KG, Deprez L, Dyck TV, Goossens D, Del-Favero J, Paesschen WV, Broeckhoven CV, Jonghe PD. A novel susceptibility locus at 2p24 for generalised epilepsy with febrile seizures plus Journal of Medical Genetics. 42: 947-952. PMID 15827091 DOI: 10.1136/Jmg.2005.031393 |
0.624 |
|
| 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 |
0.362 |
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| 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 |
0.392 |
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| 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 |
0.413 |
|
| 2005 |
Weckx S, De Rijk P, Van Broeckhoven C, Del-Favero J. SNPbox: a modular software package for large-scale primer design. Bioinformatics (Oxford, England). 21: 385-7. PMID 15347573 DOI: 10.1093/Bioinformatics/Bti006 |
0.319 |
|
| 2004 |
Claes L, Audenaert D, Deprez L, Paesschen WV, Depondt C, Goossens D, Del-Favero J, Broeckhoven CV, Jonghe PD. Novel locus on chromosome 12q22–q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizures Journal of Medical Genetics. 41: 710-714. PMID 15342703 DOI: 10.1136/Jmg.2004.019257 |
0.625 |
|
| 2004 |
Oswald P, Del-Favero J, Massat I, Souery D, Claes S, Van Broeckhoven C, Mendlewicz J. Non-replication of the brain-derived neurotrophic factor (BDNF) association in bipolar affective disorder: a Belgian patient-control study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 129: 34-5. PMID 15274036 DOI: 10.1002/Ajmg.B.30056 |
0.325 |
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| 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 |
0.378 |
|
| 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 |
0.364 |
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| 2004 |
Mendlewicz J, Massat I, Souery D, Del-Favero J, Oruc L, Nöthen MM, Blackwood D, Muir W, Battersby S, Lerer B, Segman RH, Kaneva R, Serretti A, Lilli R, Lorenzi C, et al. Serotonin transporter 5HTTLPR polymorphism and affective disorders: no evidence of association in a large European multicenter study. European Journal of Human Genetics : Ejhg. 12: 377-82. PMID 14735161 DOI: 10.1038/Sj.Ejhg.5201149 |
0.421 |
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| 2004 |
Oswald P, Del-Favero J, Massat I, Souery D, Claes S, Van Broeckhoven C, Mendlewicz J. P.1.06 Brain-derived neurotrophic factor (BDNF) gene in unipolar affective disorder: a Belgian patient-control association study European Neuropsychopharmacology. 14: S7. DOI: 10.1016/S0924-977X(04)90007-7 |
0.349 |
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| 2004 |
van Weep D, Del-Favero J, Souery D, Norrback K, van Duijn C, Sluijs S, Adolfsson R, Mendlewicz J, Deboutteb D, van Broecldaoven C, Claes S. P.1.051 A gene based SNP map analysis of the glucocorticoid receptor gene shows no evidence for association with major depression European Neuropsychopharmacology. 14: S195. DOI: 10.1016/S0924-977X(04)80140-8 |
0.338 |
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| 2003 |
Papadimitriou GN, Dikeos DG, Souery D, Del-Favero J, Massat I, Avramopoulos D, Blairy S, Cichon S, Ivezic S, Kaneva R, Karadima G, Lilli R, Milanova V, Nöthen M, Oruc L, et al. Genetic association between the phospholipase A2 gene and unipolar affective disorder: a multicentre case-control study. Psychiatric Genetics. 13: 211-20. PMID 14639048 DOI: 10.1097/00041444-200312000-00004 |
0.455 |
|
| 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 DOI: 10.1016/S0006-3223(03)00425-6 |
0.694 |
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| 2003 |
Van Agtmael T, Forrest SM, Del-Favero J, Van Broeckhoven C, Williamson R. Parametric and nonparametric genome scan analyses for human handedness. European Journal of Human Genetics : Ejhg. 11: 779-83. PMID 14512968 DOI: 10.1038/Sj.Ejhg.5201048 |
0.336 |
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| 2003 |
Oswald P, Souery D, Massat I, Del-Favero J, Linotte S, Papadimitriou G, Dikeos D, Kaneva R, Milanova V, Oruc L, Ivezic S, Serretti A, Lilli R, Van Broeckhoven C, Mendlewicz J. Lack of association between the 5HT2A receptor polymorphism (T102C) and unipolar affective disorder in a multicentric European study. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. 13: 365-8. PMID 12957335 DOI: 10.1016/S0924-977X(03)00041-5 |
0.367 |
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| 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 |
0.41 |
|
| 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 |
0.344 |
|
| 2003 |
Goossens D, Van Gestel S, Claes S, De Rijk P, Souery D, Massat I, Van den Bossche D, Backhovens H, Mendlewicz J, Van Broeckhoven C, Del-Favero J. A novel CpG-associated brain-expressed candidate gene for chromosome 18q-linked bipolar disorder. Molecular Psychiatry. 8: 83-9. PMID 12556911 DOI: 10.1038/Sj.Mp.4001190 |
0.671 |
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| 2003 |
Oswald P, Souery D, Del-Favero J, Van Broeckhoven C, Mendlewicz J. P.1.231 The brain-derived neurotrophic factor (BDNF) in bipolar affective disorder: A case-control association study European Neuropsychopharmacology. 13: S273. DOI: 10.1016/S0924-977X(03)91941-9 |
0.309 |
|
| 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 |
0.406 |
|
| 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 |
0.741 |
|
| 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 |
0.415 |
|
| 2002 |
Massat I, Souery D, Del-Favero J, Oruc L, Noethen MM, Blackwood D, Thomson M, Muir W, Papadimitriou GN, Dikeos DG, Kaneva R, Serretti A, Lilli R, Smeraldi E, Jakovljevic M, et al. Excess of allele1 for alpha3 subunit GABA receptor gene (GABRA3) in bipolar patients: a multicentric association study. Molecular Psychiatry. 7: 201-7. PMID 11840313 DOI: 10.1038/Sj.Mp.4000953 |
0.381 |
|
| 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 |
0.652 |
|
| 2002 |
Claes S, Del-Favero J, Souery D, Mendlewicz J, Adolfsson R, Broeckhoven CV. Association between major depressive disorder and a specific haplotype of the CRH binding protein gene European Psychiatry. 17: 145. DOI: 10.1016/S0924-9338(02)80633-2 |
0.337 |
|
| 2001 |
Massat I, Souery D, Del-Favero J, Oruc L, Jakovljevic M, Folnegovic V, Adolfsson R, Kaneva R, Papadimitriou G, Dikeos D, Jazin E, Milanova V, Broeckhoven CV, Mendlewicz J. Lack of association between GABRA3 and unipolar affective disorder: a multicentre study. The International Journal of Neuropsychopharmacology. 4: 273-278. PMID 11602034 DOI: 10.1017/S1461145701002449 |
0.393 |
|
| 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 |
0.354 |
|
| 2001 |
Claes L, Del-Favero J, Ceulemans B, Lagae L, Van Broeckhoven C, De Jonghe P. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy. American Journal of Human Genetics. 68: 1327-32. PMID 11359211 DOI: 10.1086/320609 |
0.319 |
|
| 2001 |
Souery D, Gestel SV, Massat I, Blairy S, Adolfsson R, Blackwood D, Del-Favero J, Dikeos D, Jakovljevic M, Kaneva R, Lattuada E, Lerer B, Lilli R, Milanova V, Muir W, et al. Tryptophan hydroxylase polymorphism and suicidality in unipolar and bipolar affective disorders: a multicenter association study. Biological Psychiatry. 49: 405-409. PMID 11274651 DOI: 10.1016/S0006-3223(00)01043-X |
0.377 |
|
| 2000 |
Goossens D, Villafuerte S, Tissir F, Van Gestel S, Claes S, Souery D, Massat I, Van den Bossche D, Van Zand K, Mendlewicz J, Van Broeckhoven C, Del-Favero J. No evidence for the involvement of CAG/CTG repeats from within 18q21.33-q23 in bipolar disorder. European Journal of Human Genetics : Ejhg. 8: 385-8. PMID 10854100 DOI: 10.1038/Sj.Ejhg.5200469 |
0.789 |
|
| 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 |
0.395 |
|
| 2000 |
Claes S, Patterson A, Del-Favero J, Van Gestel S, Mendlewicz J, Macciardi F. FC05.05 A genome-wide scan in 10 multiplex families with bipolar disorder European Psychiatry. 15: 255s-255s. DOI: 10.1016/S0924-9338(00)94093-8 |
0.351 |
|
| 1999 |
Mauger C, Del-Favero J, Ceuterick C, Lübke U, Broeckhoven Cv, Martin J. Identification and localization of ataxin-7 in brain and retina of a patient with cerebellar ataxia type II using anti-peptide antibody. Molecular Brain Research. 74: 35-43. PMID 10640674 DOI: 10.1016/S0169-328X(99)00256-9 |
0.324 |
|
| 1999 |
Kuhlenbäumer G, Schirmacher A, Meuleman J, Tissir F, Del-Favero J, Stögbauer F, Young P, Ringelstein B, Van Broeckhoven C, Timmerman V. A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes Genomics. 62: 242-250. PMID 10610718 DOI: 10.1006/Geno.1999.5991 |
0.363 |
|
| 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 |
0.31 |
|
| 1999 |
Verheyen GR, Del-Favero J, Mendlewicz J, Lindblad K, Van Zand K, Aalbregtse M, Schalling M, Souery D, Van Broeckhoven C. Molecular interpretation of expanded RED products in bipolar disorder by CAG/CTG repeats located at chromosomes 17q and 18q. Neurobiology of Disease. 6: 424-32. PMID 10527808 DOI: 10.1006/Nbdi.1999.0258 |
0.424 |
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| 1999 |
Martin J, Van Regemorter N, Del-Favero J, Löfgren A, Van Broeckhoven C. Spinocerebellar ataxia type 7 (SCA7) - correlations between phenotype and genotype in one large Belgian family. Journal of the Neurological Sciences. 168: 37-46. PMID 10500272 DOI: 10.1016/S0022-510X(99)00176-8 |
0.363 |
|
| 1999 |
Verheyen GR, Villafuerte SM, Del-Favero J, Souery D, Mendlewicz J, Van Broeckhoven C, Raeymaekers P. Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorder. European Journal of Human Genetics : Ejhg. 7: 427-34. PMID 10352933 DOI: 10.1038/Sj.Ejhg.5200318 |
0.755 |
|
| 1999 |
Del-Favero J, Goossens D, Van den Bossche D, Van Broeckhoven C. YAC fragmentation with repetitive and single-copy sequences: detailed physical mapping of the presenilin 1 gene on chromosome 14. Gene. 229: 193-201. PMID 10095119 DOI: 10.1016/S0378-1119(99)00023-2 |
0.615 |
|
| 1999 |
Theuns J, Cruts M, Del-Favero J, Goossens D, Dauwerse H, Wehnert A, den Dunnen JT, Van Broeckhoven C. Determination of the genomic organization of human presenilin 1 by fiber-FISH analysis and restriction mapping of cloned DNA. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 10: 410-4. PMID 10087304 DOI: 10.1007/S003359901013 |
0.573 |
|
| 1999 |
Michalík A, Del-Favero J, Mauger C, Löfgren A, Van Broeckhoven C. Genomic organisation of the spinocerebellar ataxia type 7 (SCA7) gene responsible for autosomal dominant cerebellar ataxia with retinal degeneration Human Genetics. 105: 410-417. DOI: 10.1007/S004390051123 |
0.402 |
|
| 1999 |
Del-Favero J, Goossens D, De Jonghe P, Benson K, Michalik A, Van den Bossche D, Horwitz M, Van Broeckhoven C. Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentation Human Genetics. 105: 217-225. DOI: 10.1007/S004390051092 |
0.66 |
|
| 1998 |
Marfany G, Del-Favero J, Valero R, De Jonghe C, Woodrow S, Hendriks L, Van Broeckhoven C, Gonzàlez-Duarte R. Identification of a Drosophila presenilin homologue: evidence of alternatively spliced forms. Journal of Neurogenetics. 12: 41-54. PMID 9666900 DOI: 10.3109/01677069809108554 |
0.359 |
|
| 1998 |
Del-Favero J, Krols L, Michalik A, Theuns J, Löfgren A, Goossens D, Wehnert A, Van den Bossche D, Van Zand K, Backhovens H, van Regenmorter N, Martin JJ, Van Broeckhoven C. Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion. Human Molecular Genetics. 7: 177-86. PMID 9425224 DOI: 10.1093/Hmg/7.2.177 |
0.666 |
|
| 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 |
0.303 |
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