| Year |
Citation |
Score |
| 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 |
0.554 |
|
| 2016 |
Badoer C, Garrec C, Goossens D, Ellison G, Mills J, Dzial M, El Housni H, Berwouts S, Concolino P, Guibert-Le Guevellou V, Delnatte C, Del Favero J, Capoluongo E, Bézieau S. 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. PMID 27793035 DOI: 10.18632/Oncotarget.12877 |
0.348 |
|
| 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 |
0.563 |
|
| 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 |
0.616 |
|
| 2015 |
Zimoń M, Battaloğlu E, Parman Y, Erdem S, Baets J, De Vriendt E, Atkinson D, Almeida-Souza L, Deconinck T, Ozes B, Goossens D, Cirak S, Van Damme P, Shboul M, Voit T, et al. Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approach. Neurogenetics. 16: 33-42. PMID 25231362 DOI: 10.1007/S10048-014-0422-0 |
0.431 |
|
| 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 |
0.597 |
|
| 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 |
0.654 |
|
| 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 |
0.641 |
|
| 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 |
0.632 |
|
| 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 |
0.617 |
|
| 2012 |
Izzi B, de Zegher F, Francois I, del Favero J, Goossens D, Wittevrongel C, Thys C, Van Geet C, Freson K. No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity. Journal of Human Genetics. 57: 277-9. PMID 22277900 DOI: 10.1038/Jhg.2012.1 |
0.389 |
|
| 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 |
0.657 |
|
| 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, 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 |
0.587 |
|
| 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 |
0.6 |
|
| 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 |
0.598 |
|
| 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 |
0.587 |
|
| 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 |
0.767 |
|
| 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 |
0.607 |
|
| 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 |
0.606 |
|
| 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 |
0.775 |
|
| 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 |
0.595 |
|
| 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 |
0.565 |
|
| 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, ... ... Goossens D, 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 |
0.596 |
|
| 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 |
0.634 |
|
| 2008 |
Williams NM, Glaser B, Norton N, Williams H, Pierce T, Moskvina V, Monks S, Del Favero J, Goossens D, Rujescu D, Giegling I, Kirov G, Craddock N, Murphy KC, O'Donovan MC, et al. Strong evidence that GNB1L is associated with schizophrenia. Human Molecular Genetics. 17: 555-66. PMID 18003636 DOI: 10.1093/Hmg/Ddm330 |
0.413 |
|
| 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 |
0.636 |
|
| 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 |
0.736 |
|
| 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 |
0.757 |
|
| 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 |
0.741 |
|
| 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 |
0.626 |
|
| 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 |
0.652 |
|
| 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 |
0.587 |
|
| 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 |
0.605 |
|
| 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, 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 |
0.634 |
|
| 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 |
0.632 |
|
| 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 |
0.492 |
|
| 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 |
0.626 |
|
| 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 |
0.6 |
|
| 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 |
0.603 |
|
| 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 |
0.642 |
|
| 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 |
0.608 |
|
| 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 |
0.773 |
|
| 1999 |
Paterson AD, DeLisi L, Faraone SV, Gejman PV, Goossens D, Hovatta I, Kaufmann CA, Klauck SM, Kunugi H, Levinson DF, Mors O, Norton N, Smalley SL. Sixth World Congress of Psychiatric Genetics X Chromosome Workshop. American Journal of Medical Genetics. 88: 279-286. PMID 10374746 DOI: 10.1002/(Sici)1096-8628(19990618)88:3<279::Aid-Ajmg14>3.0.Co;2-B |
0.421 |
|
| 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 |
0.584 |
|
| 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 |
0.534 |
|
| 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 |
0.644 |
|
| 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 |
0.638 |
|
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