Publikationen von Brit-Maren Schjeide

Martin Bellander, Lars Bäckman, Tian Liu, Brit-Maren Schjeide, Lars Bertram, Florian Schmiedek, Ulman Lindenberger, and Martin Lövdén, "Lower Baseline Performance but Greater Plasticity of Working Memory for Carriers of the Val Allele of the COMT Val(158)Met Polymorphism.," Neuropsychology 29 (2), 247-54 (2015).

Martin Bellander, Lars Bäckman, Tian Liu, Brit-Maren Schjeide, Lars Bertram, Florian Schmiedek, Ulman Lindenberger, and Martin Lövdén, "Lower baseline performance but greater plasticity of working memory for carriers of the val allele of the COMT val158met polymorphism," Neuropsychology 29 (2), 247-254 (2015).

Julia Schröder, Sara Ansaloni, Marcel Schilling, Tian Liu, Josefine Radke, Marian Jädicke, Brit-Maren Schjeide, Andriy Mashychev, Christina Tegeler, Helena Radbruch, Goran Papenberg, Sandra Düzel, Ilja Demuth, Nina Bucholtz, Ulman Lindenberger, Shu-Chen Li, Elisabeth Steinhagen-Thiessen, Christina M. Lill, and Lars Bertram, "MicroRNA-138 is a potential regulator of memory performance in humans," Frontiers in Human Neuroscience 8, 8:501 (2014).

Christina M. Lill, Marcel Schilling, Sara Ansaloni, Julia Schröder, Marian Jaedicke, Felix Luessi, Brit-Maren Schjeide, Andriy Mashychev, Christiana Graetz, Denis A. Akkad, Lisa-Ann Gerdes, Antje Kroner, Paul Blaschke, Sabine Hoffjan, Alexander Winkelmann, Thomas Dörner, Peter Rieckmann, Elisabeth Steinhagen-Thiessen, Ulman Lindenberger, Andrew Chan, Hans-Peter Hartung, Orhan Aktas, Peter Lohse, Mathias Buttmann, Tania Kümpfel, Christian Kubisch, Uwe K. Zettl, Joerg T. Epplen, Frauke Zipp, and Lars Bertram, "Assessment of microRNA-related SNP effects in the 3' untranslated region of the IL22RA2 risk locus in multiple sclerosis," Neurogenetics 15 (2), 129-134 (2014).

G. Papenberg, S. C. Li, I. E. Nagel, W. Nietfeld, B. M. Schjeide, J. Schröder, L. Bertram, Hauke R. Heekeren, U. Lindenberger, and L. Bäckman, "Dopamine and glutamate receptor genes interactively influence episodic memory in old age," Neurobiology of Aging 35 (5), 1213.e3-1213.e8 (2014).

Christina Lill, Marcel Schilling, Sara Ansaloni, Julia Schröder, Marian Jaedicke, Felix Luessi, Brit-Maren Schjeide, Andriy Mashychev, Christiane Graetz, Denis Akkad, Lisa-Ann Gerdes, Antje Kroner, Paul Blaschke, Sabine Hoffjan, Alexander Winkelmann, Thomas Dörner, Peter Rieckmann, Elisabeth Steinhagen-Thiessen, Ulman Lindenberger, Andrew Chan, Hans-Peter Hartung, Orhan Aktas, Peter Lohse, Mathias Buttmann, Tania Kümpfel, Christian Kubisch, Uwe Zettl, Jörg T. Epplen, Frauke Zipp, and Lars Bertram, "Assessment of microRNA-related SNP effects in the 3' untranslated region of the IL22RA2 risk locus in multiple sclerosis," Neurogenetics 15 (2), 129-134 (2014).

C. Lill, M. Schilling, S. Ansaloni, J. Schröder, M. Jaedicke, F. Luessi, B. M. Schjeide, A. Mashychev, C. Graetz, D. A. Akkad, L. A. Gerdes, A. Kroner, P. Blaschke, S. Hoffjan, A. Winkelmann, T. Dorner, P. Rieckmann, E. Steinhagen-Thiessen, U. Lindenberger, A. Chan, H. P. Hartung, O. Aktas, P. Lohse, M. Buttmann, T. Kumpfel, C. Kubisch, U. K. Zettl, J. T. Epplen, F. Zipp, and L. Bertram, "Assessment of microRNA-related SNP effects in the 3' untranslated region of the IL22RA2 risk locus in multiple sclerosis," Neurogenetics 15 (2), 129-134 (2014).

C. M. Lill, B.-M. Schjeide, C. Graetz, T. Liu, V. Damotte, D. A. Akkad, P. Blaschke, L. A. Gerdes, A. Kroner, F. Luessi, I. Cournu-Rebeix, S. Hoffjan, A. Winkelmann, E. Touze, F. Pico, P. Corcia, D. Otaegui, A. Antiguedad, A. Alcina, M. Comabella, X. Montalban, J. Olascoaga, F. Matesanz, T. Dorner, S. C. Li, E. Steinhagen-Thiessen, U. Lindenberger, A. Chan, P. Rieckmann, H. P. Hartung, O. Aktas, P. Lohse, M. Buttmann, T. Kumpfel, C. Kubisch, U. K. Zettl, J. T. Epplen, B. Fontaine, F. Zipp, K. Vandenbroeck, and L. Bertram, "Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk," Journal of Medical Genetics (London) 50 (3), 140-143 (2013).

C. M. Lill, B. M. Schjeide, C. Graetz, M. Ban, A. Alcina, M. A. Ortiz, J. Perez, V. Damotte, D. Booth, A. L. de Lapuente, L. Broer, M. Schilling, D. A. Akkad, O. Aktas, I. Alloza, A. Antiguedad, R. Arroyo, P. Blaschke, M. Buttmann, A. Chan, A. Compston, I. Cournu-Rebeix, T. Dorner, J. T. Epplen, O. Fernandez, L. A. Gerdes, L. Guillot-Noel, H. P. Hartung, S. Hoffjan, G. Izquierdo, A. Kemppinen, A. Kroner, C. Kubisch, T. Kumpfel, S. C. Li, U. Lindenberger, P. Lohse, C. Lubetzki, F. Luessi, S. Malhotra, J. Mescheriakova, X. Montalban, C. Papeix, L. F. Paredes, P. Rieckmann, E. Steinhagen-Thiessen, A. Winkelmann, U. K. Zettl, R. Hintzen, K. Vandenbroeck, G. Stewart, B. Fontaine, M. Comabella, E. Urcelay, F. Matesanz, S. Sawcer, L. Bertram, F. Zipp, and Int Multiple Sclerosis Genetics, "MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis," Brain 136 (6), 1778-1782 (2013).

N. W. Schuck, C. F. Doeller, B.-M. Schjeide, J. Schröder, P. A. Frensch, L. Bertram, and S. C. Li, "Aging and KIBRA/WWC1 Genotype Affect Spatial Memory Processes in a Virtual Navigation Task," Hippocampus 23 (10), 919-930 (2013).

N. W. Schuck, P. A. Frensch, B. M. Schjeide, J. Schröder, L. Bertram, and S. C. Li, "Effects of aging and dopamine genotypes on the emergence of explicit memory during sequence learning," Neuropsychologia 51 (13), 2757-2769 (2013).

C. M. Lill, T. Liu, B. M. Schjeide, J. T. Roehr, D. A. Akkad, V. Damotte, A. Alcina, M. A. Ortiz, R. Arroyo, A. L. de Lapuente, P. Blaschke, A. Winkelmann, L. A. Gerdes, F. Luessi, O. Fernadez, G. Izquierdo, A. Antiguedad, S. Hoffjan, I. Cournu-Rebeix, S. Gromöller, H. Faber, M. Liebsch, E. Meissner, C. Chanvillard, E. Touze, F. Pico, P. Corcia, T. Dörner, E. Steinhagen-Thiessen, L. Baeckman, H. R. Heekeren, S. C. Li, U. Lindenberger, A. Chan, H. P. Hartung, O. Aktas, P. Lohse, T. Kumpfel, C. Kubisch, J. T. Epplen, U. K. Zettl, B. Fontaine, K. Vandenbroeck, F. Matesanz, E. Urcelay, L. Bertram, and F. Zipp, "Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects," Journal of Medical Genetics (London) 49 (9), 558-562 (2012).

Christina M. Lill, Christina Roehr, M. B. McQueen, F. K. Kavvoura, S. Bagade, Brit-Maren Schjeide, Leif Schjeide, Esther Meissner, Ute Zauft, N. C. Allen, Tian Liu, Marcel Schilling, K. J. Anderson, G. Beecham, D. Berg, J. M. Biernacka, A. Brice, A. L. DeStefano, C. B. Do, N. Eriksson, S. A. Factor, M. J. Farrer, T. Foroud, T. Gasser, T. Hamza, J. A. Hardy, P. Heutink, E. M. Hill-Burns, C. Klein, J. C. Latourelle, D. M. Maraganore, E. R. Martin, M. Martinez, R. H. Myers, M. A. Nalls, N. Pankratz, H. Payami, W. Satake, W. K. Scott, M. Sharma, A. B. Singleton, K. Stefansson, T. Toda, J. Y. Tung, J. Vance, N. W. Wood, C. P. Zabetian, P. Young, R. E. Tanzi, M. J. Khoury, F. Zipp, Hans Lehrach, J. P. A. Ioannidis, Lars Bertram, Genetic Epidemiology Parkinson's, IPDGC, Parkinson's Dis GWAS Consortium, and WTCCC2, "Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database," PLoS Genetics 8 (3), e1002548 (2012).

C. M. Lill, B. M. Schjeide, D. A. Akkad, P. Blaschke, A. Winkelmann, L. A. Gerdes, S. Hoffjan, F. Luessi, T. Dorner, S. C. Li, E. Steinhagen-Thiessen, U. Lindenberger, A. Chan, H. P. Hartung, O. Aktas, P. Lohse, T. Kumpfel, C. Kubisch, J. T. Epplen, U. K. Zettl, L. Bertram, and F. Zipp, "Independent replication of STAT3 association with multiple sclerosis risk in a large German case-control sample," Neurogenetics 13 (1), 83-6 (2012).

B. M. Schjeide, C. Schnack, J. C. Lambert, C. M. Lill, J. Kirchheiner, H. Tumani, M. Otto, R. E. Tanzi, H. Lehrach, P. Amouyel, C. A. von Arnim, and L. Bertram, "The role of clusterin, complement receptor 1, and phosphatidylinositol binding clathrin assembly protein in Alzheimer disease risk and cerebrospinal fluid biomarker levels," Archives of General Psychiatry 68 (2), 207-13 (2011).

C. M. Lill, B. M. Schjeide, J. T. Roehr, U. Zauft, N. C. Allen, F. Zipp, M. B. McQueen, F. K. Kavvoura, J. P. Ioannidis, M. J. Khoury, R. E. Tanzi, and L. Bertram, "Correspondence to Sand et al. “Critical Reappraisal of a Catechol-O-Methyltransferase Transversion Variant in Schizophrenia”," Biological Psychiatry 67 (7), e45-e48 (2010).

V. Giedraitis, A. Glaser, T. Sarajarvi, R. Brundin, M. D. Gunnarsson, B. M. Schjeide, R. E. Tanzi, S. Helisalmi, T. Pirttila, L. Kilander, L. Lannfelt, H. Soininen, L. Bertram, M. Ingelsson, and M. Hiltunen, "CALHM1 P86L polymorphism does not alter amyloid-beta or tau in cerebrospinal fluid," Neuroscience Letters 469 (2), 265-267 (2010).

J. C. Lambert, K. Sleegers, A. Gonzalez-Perez, M. Ingelsson, G. W. Beecham, M. Hiltunen, O. Combarros, M. J. Bullido, N. Brouwers, K. Bettens, C. Berr, F. Pasquier, F. Richard, S. T. Dekosky, D. Hannequin, J. L. Haines, G. Tognoni, N. Fievet, J. F. Dartigues, C. Tzourio, S. Engelborghs, B. Arosio, E. Coto, P. De Deyn, M. Del Zompo, I. Mateo, M. Boada, C. Antunez, J. Lopez-Arrieta, J. Epelbaum, B. M. Schjeide, A. Frank-Garcia, V. Giedraitis, S. Helisalmi, E. Porcellini, A. Pilotto, P. Forti, R. Ferri, M. Delepine, D. Zelenika, M. Lathrop, E. Scarpini, G. Siciliano, V. Solfrizzi, S. Sorbi, G. Spalletta, G. Ravaglia, F. Valdivieso, S. Vepsalainen, V. Alvarez, P. Bosco, M. Mancuso, F. Panza, B. Nacmias, P. Bossu, O. Hanon, P. Piccardi, G. Annoni, D. Mann, P. Marambaud, D. Seripa, D. Galimberti, R. E. Tanzi, L. Bertram, C. Lendon, L. Lannfelt, F. Licastro, D. Campion, M. A. Pericak-Vance, H. Soininen, C. Van Broeckhoven, A. Alperovitch, A. Ruiz, M. I. Kamboh, and P. Amouyel, "The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study," J Alzheimers Dis 22 (1), 247-255 (2010).

Christina M. Lill, Esther Meissner, Leif Schjeide, Brit Maren Schjeide, Maria Liebsch, Christina Roehr, Guy Rouleau, Orla Hardiman, Bryan Traynor, Leonard Van den Berg, Ammar Al-Chalabi, and Lars Bertram, "Comprehensive Research Synopsis and Systematic Meta-Analyses in ALS Genetics: The ALSGene Database (P01.095)", in Neurology, (Advanstar Communications [etc.], Cleveland, Ohio [etc.], 2012), Vol. 78.