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Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies

dc.contributor.authorBECKER, Felicitas
dc.contributor.authorGardiner, Mark R.
dc.contributor.authorMARINI, Carla
dc.contributor.authorGUERRINI, Renzo
dc.contributor.authorLehesjoki, Anna-Elina
dc.contributor.authorSiren, Auli
dc.contributor.authorNABBOUT, Rima
dc.contributor.authorBAULAC, Stephanie
dc.contributor.authorLEGUERN, Eric
dc.contributor.authorSERRATOSA, Jose M.
dc.contributor.authorROSENOW, Felix
dc.contributor.authorFEUCHT, Martha
dc.contributor.authorUNTERBERGER, Iris
dc.contributor.authorCOVANIS, Athanasios
dc.contributor.authorSULS, Arvid
dc.contributor.authorWECKHUYSEN, Sarah
dc.contributor.authorKANEVA, Radka
dc.contributor.authorCaglayan, Hande
dc.contributor.authorTurkdogan, Dilsad
dc.contributor.authorHEMPELMANN, Anne
dc.contributor.authorSCHULZ, Herbert
dc.contributor.authorRUESCHENDORF, Franz
dc.contributor.authorTRUCKS, Holger
dc.contributor.authorNUERNBERG, Peter
dc.contributor.authorAVANZINI, Giuliano
dc.contributor.authorKoeleman, Bobby P. C.
dc.contributor.authorSANDER, Thomas
dc.contributor.authorOzbek, Ugur
dc.contributor.authorBaykan, BETÜL
dc.contributor.authorBebek, Nerses
dc.contributor.authorLEU, Costin
dc.contributor.authorde Kovel, Carolien G. F.
dc.contributor.authorZARA, Federico
dc.contributor.authorSTRIANO, Pasquale
dc.contributor.authorPEZZELLA, Marianna
dc.contributor.authorROBBIANO, Angela
dc.contributor.authorBIANCHI, Amedeo
dc.contributor.authorBISULLI, Francesca
dc.contributor.authorCOPPOLA, Antonietta
dc.contributor.authorGIALLONARDO, Anna Teresa
dc.contributor.authorBECCARIA, Francesca
dc.contributor.authorTrenite, Dorothee Kasteleijn-Nolst
dc.contributor.authorLINDHOUT, Dick
dc.contributor.authorGAUS, Verena
dc.contributor.authorSCHMITZ, Bettina
dc.contributor.authorJANZ, Dieter
dc.contributor.authorWEBER, Yvonne G.
dc.contributor.authorLERCHE, Holger
dc.contributor.authorKLEEFUSS-LIE, Ailing A.
dc.contributor.authorHALLMAN, Kerstin
dc.contributor.authorKUNZ, Wolfram S.
dc.contributor.authorELGER, Christian E.
dc.contributor.authorMUHLE, Hiltrud
dc.contributor.authorSTEPHANI, Ulrich
dc.contributor.authorMOLLER, Rikke S.
dc.contributor.authorHJALGRIM, Helle
dc.contributor.authorMullen, Saul
dc.contributor.authorScheffer, Ingrid E.
dc.contributor.authorBerkovic, Samuel F.
dc.contributor.authorEVERETT, Kate V.
dc.date.accessioned2021-03-03T17:39:46Z
dc.date.available2021-03-03T17:39:46Z
dc.date.issued2012
dc.identifier.citationLEU C., de Kovel C. G. F. , ZARA F., STRIANO P., PEZZELLA M., ROBBIANO A., BIANCHI A., BISULLI F., COPPOLA A., GIALLONARDO A. T. , et al., "Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies", EPILEPSIA, cilt.53, sa.2, ss.308-318, 2012
dc.identifier.issn0013-9580
dc.identifier.othervv_1032021
dc.identifier.otherav_4ace4715-b089-4b93-8c8b-59206df25365
dc.identifier.urihttp://hdl.handle.net/20.500.12627/53726
dc.identifier.urihttps://doi.org/10.1111/j.1528-1167.2011.03379.x
dc.description.abstractPurpose: Genetic generalized epilepsies (GGEs) have a lifetime prevalence of 0.3% with heritability estimates of 80%. A considerable proportion of families with siblings affected by GGEs presumably display an oligogenic inheritance. The present genome-wide linkage meta-analysis aimed to map: (1) susceptibility loci shared by a broad spectrum of GGEs, and (2) seizure typerelated genetic factors preferentially predisposing to either typical absence or myoclonic seizures, respectively.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp
dc.titleGenome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies
dc.typeMakale
dc.relation.journalEPILEPSIA
dc.contributor.departmentUniversity of Cologne , ,
dc.identifier.volume53
dc.identifier.issue2
dc.identifier.startpage308
dc.identifier.endpage318
dc.contributor.firstauthorID46632


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