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Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

EPICURE Consortium, EMINet Consortium, Steffens, Michael, Leu, Costin, Ruppert, Ann-Kathrin, Zara, Federico, Striano, Pasquale, Robbiano, Angela, Capovilla, Giuseppe, Tinuper, Paolo, Gambardella, Antonio, Bianchi, Amedeo, La Neve, Angela, Crichiutti, Giovanni, de Kovel, Carolien G.F., Kasteleijn-Nolst Trenité, Dorothee, de Haan, Gerrit-Jan, Lindhout, Dick, Gaus, Verena, Schmitz, Bettina, Janz, Dieter, Weber, Yvonne G., Becker, Felicitas, Lerche, Holger, Steinhoff, Bernhard J., Kleefuß-Lie, Ailing A., Kunz, Wolfram S., Surges, Rainer, Elger, Christian E., Muhle, Hiltrud, von Spiczak, Sarah, Ostertag, Philipp, Helbig, Ingo, Stephani, Ulrich, Møller, Rikke S., Hjalgrim, Helle, Dibbens, Leanne M., Bellows, Susannah, Oliver, Karen, Mullen, Saul, Scheffer, Ingrid E., Berkovic, Samuel F., Everett, Kate V., Gardiner, Mark R., Marini, Carla, Guerrini, Renzo, Lehesjoki, Anna-Elina, Siren, Auli, Guipponi, Michel, Malafosse, Alain, Thomas, Pierre, Nabbout, Rima, Baulac, Stephanie, Leguern, Eric, Guerrero, Rosa, Serratosa, Jose M., Reif, Philipp S., Rosenow, Felix, Mörzinger, Martina, Feucht, Martha, Zimprich, Fritz, Kapser, Claudia, Schankin, Christoph J., Suls, Arvid, Smets, Katrin, De Jonghe, Peter, Jordanova, Albena, Caglayan, Hande, Yapici, Zuhal, Yalcin, Destina A., Baykan, Betul, Bebek, Nerses, Ozbek, Ugur, Gieger, Christian, Wichmann, Heinz-Erich, Balschun, Tobias, Ellinghaus, David, Franke, Andre, Meesters, Christian, Becker, Tim, Wienker, Thomas F., Hempelmann, Anne, Schulz, Herbert, Rüschendorf, Franz, Leber, Markus, Pauck, Steffen M., Trucks, Holger, Toliat, Mohammad R., Nürnberg, Peter, Avanzini, Giuliano, Koeleman, Bobby P.C. and Sander, Thomas 2012, Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32, Human molecular genetics, vol. 21, no. 24, pp. 5359-5372, doi: 10.1093/hmg/dds373.

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Title Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32
Author(s) EPICURE Consortium
EMINet Consortium
Steffens, Michael
Leu, Costin
Ruppert, Ann-Kathrin
Zara, Federico
Striano, Pasquale
Robbiano, Angela
Capovilla, Giuseppe
Tinuper, Paolo
Gambardella, Antonio
Bianchi, Amedeo
La Neve, Angela
Crichiutti, Giovanni
de Kovel, Carolien G.F.
Kasteleijn-Nolst Trenité, Dorothee
de Haan, Gerrit-Jan
Lindhout, Dick
Gaus, Verena
Schmitz, Bettina
Janz, Dieter
Weber, Yvonne G.
Becker, Felicitas
Lerche, Holger
Steinhoff, Bernhard J.
Kleefuß-Lie, Ailing A.
Kunz, Wolfram S.
Surges, Rainer
Elger, Christian E.
Muhle, Hiltrud
von Spiczak, Sarah
Ostertag, Philipp
Helbig, Ingo
Stephani, Ulrich
Møller, Rikke S.
Hjalgrim, Helle
Dibbens, Leanne M.
Bellows, Susannah
Oliver, Karen
Mullen, Saul
Scheffer, Ingrid E.
Berkovic, Samuel F.
Everett, Kate V.
Gardiner, Mark R.
Marini, Carla
Guerrini, Renzo
Lehesjoki, Anna-Elina
Siren, Auli
Guipponi, Michel
Malafosse, Alain
Thomas, Pierre
Nabbout, Rima
Baulac, Stephanie
Leguern, Eric
Guerrero, Rosa
Serratosa, Jose M.
Reif, Philipp S.
Rosenow, Felix
Mörzinger, Martina
Feucht, Martha
Zimprich, Fritz
Kapser, Claudia
Schankin, Christoph J.
Suls, Arvid
Smets, Katrin
De Jonghe, Peter
Jordanova, Albena
Caglayan, Hande
Yapici, Zuhal
Yalcin, Destina A.
Baykan, Betul
Bebek, Nerses
Ozbek, Ugur
Gieger, Christian
Wichmann, Heinz-Erich
Balschun, Tobias
Ellinghaus, David
Franke, Andre
Meesters, Christian
Becker, Tim
Wienker, Thomas F.
Hempelmann, Anne
Schulz, Herbert
Rüschendorf, Franz
Leber, Markus
Pauck, Steffen M.
Trucks, Holger
Toliat, Mohammad R.
Nürnberg, Peter
Avanzini, Giuliano
Koeleman, Bobby P.C.
Sander, Thomas
Journal name Human molecular genetics
Volume number 21
Issue number 24
Start page 5359
End page 5372
Total pages 14
Publisher Oxford University Press
Place of publication Oxford, Eng.
Publication date 2012-12-15
ISSN 0964-6906
1460-2083
Keyword(s) Alleles
Epilepsy, Absence
Epilepsy, Generalized
Genetic Predisposition to Disease
Genome-Wide Association Study
Homeodomain Proteins
Humans
Myoclonic Epilepsy, Juvenile
NAV1.1 Voltage-Gated Sodium Channel
Protein-Serine-Threonine Kinases
Receptor, Muscarinic M3
Repressor Proteins
Zinc Finger E-box Binding Homeobox 2
EPICURE Consortium
EMINet Consortium
Science & Technology
Life Sciences & Biomedicine
Biochemistry & Molecular Biology
Genetics & Heredity
JUVENILE MYOCLONIC EPILEPSY
INDEPENDENT TESTS
SEIZURE TYPES
RISK
MECHANISMS
MUTATIONS
MICRODELETIONS
VISUALIZATION
ARCHITECTURE
REPLICATION
Language eng
DOI 10.1093/hmg/dds373
Field of Research 06 Biological Sciences
11 Medical And Health Sciences
HERDC Research category C1.1 Refereed article in a scholarly journal
Copyright notice ©2012, The Authors
Free to Read? Yes
Persistent URL http://hdl.handle.net/10536/DRO/DU:30110656

Document type: Journal Article
Collections: Faculty of Health
School of Psychology
Open Access Collection
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Every reasonable effort has been made to ensure that permission has been obtained for items included in DRO. If you believe that your rights have been infringed by this repository, please contact drosupport@deakin.edu.au.