Dietary Fatty Acids Directly Impact Central Nervous System Autoimmunity via the Small Intestine
Haghikia, Aiden, Jörg, Stefanie, Duscha, Alexander, Berg, Johannes, Manzel, Arndt, Waschbisch, Anne, Hammer, Anna, Lee, De-Hyung, May, Caroline, Wilck, Nicola, Balogh, Andras, Ostermann, Annika I., Schebb, Nils Helge, Akkad, Denis A., Grohme, Diana A., Kleinewietfeld, Markus, Kempa, Stefan, Thöne, Jan, Demir, Seray, Müller, Dominik N., Gold, Ralf, Linker, Ralf A.
Published in Immunity (Cambridge, Mass.) (20.10.2015)
Published in Immunity (Cambridge, Mass.) (20.10.2015)
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Dietary Fatty Acids Directly Impact Central Nervous System Autoimmunity via the Small Intestine
Haghikia, Aiden, Jörg, Stefanie, Duscha, Alexander, Berg, Johannes, Manzel, Arndt, Waschbisch, Anne, Hammer, Anna, Lee, De-Hyung, May, Caroline, Wilck, Nicola, Balogh, Andras, Ostermann, Annika I., Schebb, Nils Helge, Akkad, Denis A., Grohme, Diana A., Kleinewietfeld, Markus, Kempa, Stefan, Thöne, Jan, Demir, Seray, Müller, Dominik N., Gold, Ralf, Linker, Ralf A.
Published in Immunity (Cambridge, Mass.) (19.04.2016)
Published in Immunity (Cambridge, Mass.) (19.04.2016)
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PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease
Taherzadeh-Fard, Elahe, Saft, Carsten, Akkad, Denis A, Wieczorek, Stefan, Haghikia, Aiden, Chan, Andrew, Epplen, Jörg T, Arning, Larissa
Published in Molecular neurodegeneration (19.05.2011)
Published in Molecular neurodegeneration (19.05.2011)
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Combinations of susceptibility genes are associated with higher risk for multiple sclerosis and imply disease course specificity
Akkad, Denis A, Olischewsky, Alexandra, Reiner, Franziska, Hellwig, Kerstin, Esser, Sarika, Epplen, Jörg T, Curk, Tomaz, Gold, Ralf, Haghikia, Aiden
Published in PloS one (26.05.2015)
Published in PloS one (26.05.2015)
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SOX9 duplication linked to intersex in deer
Kropatsch, Regina, Dekomien, Gabriele, Akkad, Denis A, Gerding, Wanda M, Petrasch-Parwez, Elisabeth, Young, Neil D, Altmüller, Janine, Nürnberg, Peter, Gasser, Robin B, Epplen, Jörg T
Published in PloS one (06.09.2013)
Published in PloS one (06.09.2013)
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mtDNA nt13708A variant increases the risk of multiple sclerosis
Yu, Xinhua, Koczan, Dirk, Sulonen, Anna-Maija, Akkad, Denis A, Kroner, Antje, Comabella, Manuel, Costa, Gianna, Corongiu, Daniela, Goertsches, Robert, Camina-Tato, Montserrat, Thiesen, Hans-Juergen, Nyland, Harald I, Mørk, Sverre J, Montalban, Xavier, Rieckmann, Peter, Marrosu, Maria G, Myhr, Kjell-Morten, Epplen, Joerg T, Saarela, Janna, Ibrahim, Saleh M
Published in PloS one (13.02.2008)
Published in PloS one (13.02.2008)
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Ccdc66 null mutation causes retinal degeneration and dysfunction
GERDING, Wanda M, SCHREIBER, Sabrina, RÜLICKE, Thomas, IBRAHIM, Saleh, EPPLEN, Jörg T, PETRASCH-PARWEZ, Elisabeth, SCHULTE-MIDDELMANN, Tobias, DE CASTRO MARQUES, Andreia, ATORF, Jenny, AKKAD, Denis A, DEKOMIEN, Gabriele, KREMERS, Jan, DERMIETZEL, Rolf, GAL, Andreas
Published in Human molecular genetics (15.09.2011)
Published in Human molecular genetics (15.09.2011)
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ASK1 and MAP2K6 as modifiers of age at onset in Huntington’s disease
Arning, Larissa, Monté, Didier, Hansen, Wiebke, Wieczorek, Stefan, Jagiello, Peter, Akkad, Denis A., Andrich, Jürgen, Kraus, Peter H., Saft, Carsten, Epplen, Jörg T.
Published in Journal of molecular medicine (Berlin, Germany) (01.04.2008)
Published in Journal of molecular medicine (Berlin, Germany) (01.04.2008)
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Genomic NGFB variation and multiple sclerosis in a case control study
Akkad, Denis A, Kruse, Niels, Arning, Larissa, Gold, Ralf, Epplen, Jörg T
Published in BMC medical genetics (08.12.2008)
Published in BMC medical genetics (08.12.2008)
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Exome Sequencing Reveals AGBL5 as Novel Candidate Gene and Additional Variants for Retinitis Pigmentosa in Five Turkish Families
Kastner, Simone, Thiemann, Ina-Janine, Dekomien, Gabriele, Petrasch-Parwez, Elisabeth, Schreiber, Sabrina, Akkad, Denis A, Gerding, Wanda M, Hoffjan, Sabine, Günes, Sezgin, Günes, Selçuk, Bagci, Hasan, Epplen, Jörg T
Published in Investigative ophthalmology & visual science (01.12.2015)
Published in Investigative ophthalmology & visual science (01.12.2015)
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A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis
Gu, Ben J, Field, Judith, Dutertre, Sébastien, Ou, Amber, Kilpatrick, Trevor J, Lechner-Scott, Jeannette, Scott, Rodney, Lea, Rodney, Taylor, Bruce V, Stankovich, Jim, Butzkueven, Helmut, Gresle, Melissa, Laws, Simon M, Petrou, Steven, Hoffjan, Sabine, Akkad, Denis A, Graham, Colin A, Hawkins, Stanley, Glaser, Anna, Bedri, Sahl Khalid, Hillert, Jan, Matute, Carlos, Antiguedad, Alfredo, Wiley, James S
Published in Human molecular genetics (01.10.2015)
Published in Human molecular genetics (01.10.2015)
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Left-Right Axis Differentiation and Functional Lateralization: a Haplotype in the Methyltransferase Encoding Gene SETDB2 Might Mediate Handedness in Healthy Adults
Ocklenburg, Sebastian, Arning, Larissa, Gerding, Wanda M., Hengstler, Jan G., Epplen, Jörg T., Güntürkün, Onur, Beste, Christian, Akkad, Denis A.
Published in Molecular neurobiology (01.11.2016)
Published in Molecular neurobiology (01.11.2016)
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Interferon-beta affects mitochondrial activity in CD4+ lymphocytes: Implications for mechanism of action in multiple sclerosis
Haghikia, Aiden, Faissner, Simon, Pappas, Derek, Pula, Bartosz, Akkad, Denis A, Arning, Larissa, Ruhrmann, Sabrina, Duscha, Alexander, Gold, Ralf, Baranzini, Sergio E, Malhotra, Sunny, Montalban, Xavier, Comabella, Manuel, Chan, Andrew
Published in Multiple sclerosis (01.09.2015)
Published in Multiple sclerosis (01.09.2015)
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Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk
Lill, Christina M, Schjeide, Brit-Maren M, Graetz, Christiane, Liu, Tian, Damotte, Vincent, Akkad, Denis A, Blaschke, Paul, Gerdes, Lisa-Ann, Kroner, Antje, Luessi, Felix, Cournu-Rebeix, Isabelle, Hoffjan, Sabine, Winkelmann, Alexander, Touze, Emmanuel, Pico, Fernando, Corcia, Philippe, Otaegui, David, Antigüedad, Alfredo, Alcina, Antonio, Comabella, Manuel, Montalban, Xavier, Olascoaga, Javier, Matesanz, Fuencisla, Dörner, Thomas, Li, Shu-Chen, Steinhagen-Thiessen, Elisabeth, Lindenberger, Ulman, Chan, Andrew, Rieckmann, Peter, Hartung, Hans-Peter, Aktas, Orhan, Lohse, Peter, Buttmann, Mathias, Kümpfel, Tania, Kubisch, Christian, Zettl, Uwe K, Epplen, Joerg T, Fontaine, Bertrand, Zipp, Frauke, Vandenbroeck, Koen, Bertram, Lars
Published in Journal of medical genetics (01.03.2013)
Published in Journal of medical genetics (01.03.2013)
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Multiple sclerosis risk loci correlate with cervical cord atrophy and may explain the course of disability
Akkad, Denis A., Bellenberg, Barbara, Esser, Sarika, Weiler, Florian, Epplen, Jörg T., Gold, Ralf, Lukas, Carsten, Haghikia, Aiden
Published in Neurogenetics (01.07.2015)
Published in Neurogenetics (01.07.2015)
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Multiple sclerosis in families: risk factors beyond known genetic polymorphisms
Akkad, Denis A., Lee, De-Hyung, Bruch, Kathrin, Haghikia, Aiden, Epplen, Jörg T., Hoffjan, Sabine, Linker, Ralf A.
Published in Neurogenetics (01.04.2016)
Published in Neurogenetics (01.04.2016)
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Assessment of microRNA-related SNP effects in the 3′ untranslated region of the IL22RA2 risk locus in multiple sclerosis
Lill, Christina M., Schilling, Marcel, Ansaloni, Sara, Schröder, Julia, Jaedicke, Marian, Luessi, Felix, Schjeide, Brit-Maren M., Mashychev, Andriy, Graetz, Christiane, Akkad, Denis A., Gerdes, Lisa-Ann, Kroner, Antje, Blaschke, Paul, Hoffjan, Sabine, Winkelmann, Alexander, Dörner, Thomas, Rieckmann, Peter, Steinhagen-Thiessen, Elisabeth, Lindenberger, Ulman, Chan, Andrew, Hartung, Hans-Peter, Aktas, Orhan, Lohse, Peter, Buttmann, Mathias, Kümpfel, Tania, Kubisch, Christian, Zettl, Uwe K., Epplen, Joerg T., Zipp, Frauke, Bertram, Lars
Published in Neurogenetics (01.05.2014)
Published in Neurogenetics (01.05.2014)
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