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Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects
Authors: Lill, C. M.; Liu, T.; Schjeide, B. M. M.; Roehr, J. T.; Akkad, D. A.; Damotte, V.; Alcina, A.; Ortiz, M. A.; Arroyo, R.; de Lapuente, A. L.; Blaschke, P.; Winkelmann, A.; Gerdes, L. A.; Luessi, F.; Fernadez, O.; Izquierdo, G.; Antiguedad, A.; Hoffjan, S.; Cournu-Rebeix, I.; Gromöller, S.; Faber, H.; Liebsch, M.; Meissner, E.; Chanvillard, C.; Touze, E.; Pico, F.; Corcia, P.; Dorner, T.; Steinhagen-Thiessen, E.; Baeckman, L.; Heekeren, H. R.; Li, S. C.; Lindenberger, U.; Chan, A.; Hartung, H. P.; Aktas, O.; Lohse, P.; Kümpfel, T.; Kubisch, C.; Epplen, J. T.; Zettl, U. K.; Fontaine, B.; Vandenbroeck, K.; Matesanz, F.; Urcelay, E.; Bertram, L.; Zipp, F.
Date of Publication (YYYY-MM-DD): 2012-09
Title of Journal: Journal of Medical Genetics
Volume: 49
Issue / Number: 9
Start Page: 558
End Page: 562
Document Type: Article
ID: 629807.0


Determination of the real effect of genes identified in GWAS: the example of IL2RA in multiple sclerosis
Authors: Babron, M. C.; Perdry, H.; Handel, A. E.; Ramagopalan, S. V.; Damotte, V.; Fontaine, B.; Müller-Myhsok, B.; Ebers, G. C.; Cerget-Darpoux, F.
Date of Publication (YYYY-MM-DD): 2012-03
Title of Journal: European Journal of Human Genetics
Volume: 20
Issue / Number: 3
Start Page: 321
End Page: 325
Document Type: Article
ID: 596921.0


Closing the case of APOE in multiple sclerosis : No association with disease risk in over 29 000 subjects
Authors: Lill, C. M.; Liu, T.; Schjeide, B.-M. M.; Roehr, J. T.; Akkad, D. A.; Damotte, V.; Alcina, A.; Ortiz, M. A.; Arroyo, R.; Lapuente, A. L. d.; Blaschke, P.; Winkelmann, A.; Gerdes, L.-A.; Luessi, F.; Fernadez, O.; Izquierdo, G.; Antigüedad, A.; Hoffjan, S.; Cournu-Rebeix, I.; Gromöller, S.; Faber, H.; Liebsch, M.; Meissner, E.; Chanvillard, C.; Touze, E.; Pico, F.; Corcia, P.; Consortium, A.; Dörner, T.; Steinhagen-Thiessen, Elisabeth; Bäckman, Lars; Heekeren, Hauke R.; Li, Shu-Chen; Lindenberger, Ulman; Chan, A.; Hartung, H.-P.; Aktas, O.; Lohse, P.; Kümpfel, T.; Kubisch, C.; Epplen, J. T.; Zettl, U. K.; Fontaine, B.; Vandenbroeck, K.; Matesanz, F.; Urcelay, E.; Bertram, Lars; Zipp, F.
Date of Publication (YYYY-MM-DD): 2012
Title of Journal: Journal of Medical Genetics
Volume: 49
Issue / Number: 9
Start Page: 558
End Page: 562
Document Type: Article
ID: 630152.0


Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1
Authors: Winkelmann, J.; Czamara, D.; Schormair, B.; Knauf, F.; Schulte, E. C.; Trenkwalder, C.; Dauvilliers, Y.; Polo, O.; Högl, B.; Berger, K.; Fuhs, A.; Gross, N.; Stiasny-Kolster, K.; Oertel, W.; Bachmann, C. G.; Paulus, W.; Xiong, L.; Montplaisir, J.; Rouleau, G. A.; Fietze, I.; Vavrova, J.; Kemlink, D.; Sonka, K.; Nevsimalova, S.; Lin, S. C.; Wszolek, Z.; Vilarino-Guell, C.; Farrer, M. J.; Gschliesser, V.; Frauscher, B.; Falkenstetter, T.; Poewe, W.; Allen, R. P.; Earley, C. J.; Ondo, W. G.; Le, W. D.; Spieler, D.; Kaffe, M.; Zimprich, A.; Kettunen, J.; Perola, M.; Silander, K.; Cournu-Rebeix, I.; Francavilla, M.; Fontenille, C.; Fontaine, B.; Vodicka, P.; Prokisch, H.; Lichtner, P.; Peppard, P.; Faraco, J.; Mignot, E.; Gieger, C.; Illig, T.; Wichmann, H. E.; Müller-Myhsok, B.; Meitinger, T.
Date of Publication (YYYY-MM-DD): 2011-07
Title of Journal: PLoS Genetics
Volume: 7
Issue / Number: 7
Sequence Number of Article: e1002171
Document Type: Article
ID: 571350.0


Tyrosine kinase 2 variant influences T lymphocyte polarization and multiple sclerosis susceptibility
Authors: Couturier, N.; Bucciarelli, F.; Nurtdinov, R. N.; Debouverie, M.; Lebrun-Frenay, C.; Defer, G.; Moreau, T.; Confavreux, C.; Vukusic, S.; Cournu-Rebeix, I.; Goertsches, R. H.; Zettl, U. K.; Comabella, M.; Montalban, X.; Rieckmann, P.; Weber, F.; Müller-Myhsok, B.; Edan, G.; Fontaine, B.; Mars, L. T.; Saoudi, A.; Oksenberg, J. R.; Clanet, M.; Liblau, R. S.; Brassat, D.
Date of Publication (YYYY-MM-DD): 2011-03
Title of Journal: Brain
Volume: 134
Start Page: 693
End Page: 703
Document Type: Article
ID: 562708.0


Brody syndrome represents a differential diagnosis for painless exercise −induced stiffness without electrical myotonia: detection of 10 cases associated with mutations in ATP2A1 gene
Authors: Sternberg, D.; Chevessier, Frédéric; Bassez, G.; Behin, A.; Echaniz−Laguna, J. A.; Eymard, Bruno; Franques, J.; Péréon, Y.; Vicart, S.; Fontaine, B.; Hantai, B.; Fournier, F.
(Start) Date of Event
(YYYY-MM-DD):
 2011-01-01
Name of Conference/Meeting: International congress of Myology
Document Type: Poster
ID: 566014.0


Brody syndrome represents a differential diagnosis for painless exercise −induced stiffness without electrical myotonia: detection of 10 cases associated with mutations in ATP2A1 gene
Authors: Sternberg, D.; Chevessier, Frédéric; Bassez, G.; Behin, A.; Echaniz−Laguna, J. A.; Eymard, Bruno; Franques, J.; Péréon, Y.; Vicart, S.; Fontaine, B.; Hantai, B.; Fournier, F.
(Start) Date of Event
(YYYY-MM-DD):
 2011-01-01
Name of Conference/Meeting: International congress of Myology
Document Type: Poster
ID: 566334.0


Brody syndrome represents a differential diagnosis for painless exercise −induced stiffness without electrical myotonia: detection of 10 cases associated with mutations in ATP2A1 gene
Authors: Sternberg, D.; Chevessier, Frédéric; Bassez, G.; Behin, A.; Echaniz−Laguna, J. A.; Eymard, Bruno; Franques, J.; Péréon, Y.; Vicart, S.; Fontaine, B.; Hantai, B.; Fournier, F.
(Start) Date of Event
(YYYY-MM-DD):
 2011-01-01
Name of Conference/Meeting: International congress of Myology
Document Type: Poster
ID: 566791.0


Brody syndrome represents a differential diagnosis for painless exercise −induced stiffness without electrical myotonia: detection of 10 cases associated with mutations in ATP2A1 gene
Authors: Sternberg, D.; Chevessier, Frédéric; Bassez, G.; Behin, A.; Echaniz−Laguna, J. A.; Eymard, Bruno; Franques, J.; Péréon, Y.; Vicart, S.; Fontaine, B.; Hantai, B.; Fournier, F.
(Start) Date of Event
(YYYY-MM-DD):
 2011-01-01
Name of Conference/Meeting: International congress of Myology
Document Type: Poster
ID: 569720.0


Brody syndrome represents a differential diagnosis for painless exercise −induced stiffness without electrical myotonia: detection of 10 cases associated with mutations in ATP2A1 gene
Authors: Sternberg, D.; Chevessier, Frédéric; Bassez, G.; Behin, A.; Echaniz−Laguna, J. A.; Eymard, Bruno; Franques, J.; Péréon, Y.; Vicart, S.; Fontaine, B.; Hantai, B.; Fournier, F.
(Start) Date of Event
(YYYY-MM-DD):
 2011-01-01
Name of Conference/Meeting: International congress of Myology
Document Type: Poster
ID: 597810.0