Hakutulokset - Jörg Hansen
- Näytetään 1 - 4 yhteensä 4 tuloksesta
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1
Targeted next generation sequencing as a diagnostic tool in epileptic disorders Tekijä Johannes R. Lemke, Erik Riesch, Tim Scheurenbrand, Max Schubach, Christian Wilhelm, Isabelle Steiner, Jörg Hansen, Carolina Courage, Sabina Gallati, Sarah Bürki, Susi Strozzi, Barbara Goeggel Simonetti, Sebastian Grunt, Maja Steinlin, Michael Alber, Markus Wolff, Thomas Klopstock, Eva Christina Prott, Rüdiger Lorenz, Christiane Spaich, Sabine Rona, Maya Lakshminarasimhan, Judith F. Kroll, Thomas Dorn, Günter Krämer, Matthis Synofzik, Felicitas Becker, Yvonne G. Weber, Holger Lerche, Detlef Böhm, Saskia Biskup
Julkaistu 2012Artigo -
2
Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study Tekijä Dalia Kasperavičiūtė, Claudia B. Catarino, Erin L. Heinzen, Chantal Depondt, Gianpiero L. Cavalleri, Luís Otávio Sales Ferreira Caboclo, Sarah K. Tate, Jennifer Jamnadas-Khoda, Krishna Chinthapalli, Lisa M. Clayton, Kevin V. Shianna, Rodney A. Radtke, Mohamad A. Mikati, William Gallentine, Aatif M. Husain, Saud Alhusaini, David Leppert, Lefkos Middleton, Rachel A. Gibson, Michael R. Johnson, Paul M. Matthews, David A. Hosford, Kjell Heuser, Leslie Amos, Marcos Ortega, Dominik Zumsteg, Heinz Gregor Wieser, Bernhard J. Steinhoff, Günter Krämer, Jörg Hansen, Thomas Dorn, Anne-Mari Kantanen, Leif Gjerstad, Terhi Peuralinna, Dena Hernández, Kai Eriksson, Reetta Kälviäinen, Colin P. Doherty, Nicholas Wood, Massimo Pandolfo, John S. Duncan, Josemir W. Sander, Norman Delanty, David B. Goldstein, Sanjay M. Sisodiya
Julkaistu 2010Artigo -
3
Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes Tekijä Erin L. Heinzen, Rodney A. Radtke, Thomas Urban, Gianpiero L. Cavalleri, Chantal Depondt, Anna C. Need, Sophie Nicole, Paola Nicoletti, Dongliang Ge, Claudia B. Catarino, John S. Duncan, Dalia Kasperavičiūtė, Sarah K. Tate, Luís Otávio Sales Ferreira Caboclo, Josemir W. Sander, Lisa M. Clayton, Kristen N. Linney, Kevin V. Shianna, Curtis Gumbs, Jason P. Smith, Kenneth Cronin, Jessica M. Maia, Colin P. Doherty, Massimo Pandolfo, David Leppert, Lefkos Middleton, Rachel A. Gibson, Michael R. Johnson, Paul M. Matthews, David A. Hosford, Reetta Kälviäinen, Kai Eriksson, Anne-Mari Kantanen, Thomas Dorn, Jörg Hansen, Günter Krämer, Bernhard J. Steinhoff, Heinz Gregor Wieser, Dominik Zumsteg, Marcos Ortega, Nicholas Wood, Julie Huxley‐Jones, Mohamad A. Mikati, William Gallentine, Aatif M. Husain, Patrick G. Buckley, R.L. Stallings, Mihai V. Podgoreanu, Norman Delanty, Sanjay M. Sisodiya, David B. Goldstein
Julkaistu 2010Artigo -
4
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A Tekijä Dalia Kasperavičiūtė, Claudia B. Catarino, Mar Matarín, Costin Leu, Jan Nový, Anna Tostevin, Bárbara Leal, Ellen V.S. Hessel, Kerstin Hallmann, Michael S. Hildebrand, Hans‐Henrik M. Dahl, Mina Ryten, Daniah Trabzuni, Adaikalavan Ramasamy, Saud Alhusaini, Colin P. Doherty, Thomas Dorn, Jörg Hansen, Günter Krämer, Bernhard J. Steinhoff, Dominik Zumsteg, Susan Duncan, Reetta Kälviäinen, Kai Eriksson, Anne-Mari Kantanen, Massimo Pandolfo, U Gruber‐Sedlmayr, Kurt Schlachter, Eva M. Reinthaler, Elisabeth Stögmann, Fritz Zimprich, Emilie Théâtre, Colin Smith, Terence J. O’Brien, K. Meng Tan, Slavé Petrovski, Angela Robbiano, Roberta Paravidino, Federico Zara, Pasquale Striano, Michael R. Sperling, Russell J. Buono, Hákon Hákonarson, João Chaves, Paulo Costa, Berta Martins da Silva, António Martins da Silva, P.N.E. de Graan, Bobby P.C. Koeleman, Albert J. Becker, Susanne Schoch, Marec von Lehe, Philipp S. Reif, Felix Rosenow, Felicitas Becker, Yvonne G. Weber, Holger Lerche, Karl Rössler, Michael Buchfelder, Hajo M. Hamer, Katja Kobow, Roland Coras, Ingmar Blümcke, Ingrid E. Scheffer, Samuel F. Berkovic, Michael E. Weale, Norman Delanty, Chantal Depondt, Gianpiero L. Cavalleri, Wolfram S. Kunz, Sanjay M. Sisodiya
Julkaistu 2013Revisão
Työkalut:
Liittyvät aiheet
Epilepsy
Medicine
Neuroscience
Biology
Gene
Genetics
Genotype
Phenotype
Psychology
Clinical neurology
Copy-number variation
Epilepsy syndromes
Genetic architecture
Genetic association
Genetic linkage
Genetic predisposition
Genetic variation
Genome
Genome-wide association study
Genotyping
Haploinsufficiency
Heritability
Hippocampal formation
Hippocampal sclerosis
Locus (genetics)
Missing heritability problem
Odds ratio
Pathology
Psychiatry
Single-nucleotide polymorphism