Publikationen von L. Bertram

H. Hampel, S. Lista, S. J. Teipel, F. Garaci, R. Nistico, K. Blennow, H. Zetterberg, L. Bertram, C. Duyckaerts, H. Bakardjian, A. Drzezga, O. Colliot, S. Epelbaum, K. Broich, S. Lehericy, A. Brice, Z. S. Khachaturian, P. S. Aisen, and B. Dubois, "Perspective on future role of biological markers in clinical therapy trials of Alzheimer's disease: A long-range point of view beyond 2020," Biochemical Pharmacology 88 (4), 426-449 (2014).

Harald Hampel, Simone Listab, Stefan J. Teipelc, Francesco Garacie, Robert Nisticòg, Kaj Blennowi, Henrik Zetterbergi, Lars Bertram, Charles Duyckaertsl, Hovagim Bakardjianm, Alexander Drzezgao, Olivier Colliotp, Stéphane Epelbaumu, Karl Broich, Stéphane Lehéricy, Alexis Brice, Zaven S. Khachaturian, Paul S. Aisen , and Bruno Dubois , "Perspective on future role of biological markers in clinical therapy trials of Alzheimer's disease: a long-range point of view beyond 2020," Biochemical Pharmacology 88 (4), 426-449 (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).

Emmanouil I. Athanasiadis, Kyriaki Antonopoulou, Foteini Chatzinasiou, Christina M. Lill, Marilena M. Bourdakou, Argiris Sakellariou, Katerina Kypreou, Irene Stefanaki, Evangelos Evangelou, John P.A. Ioannidis, Lars Bertram, Alexander J. Stratigos, and George M. Spyrou, "A Web-based database of genetic association studies in cutaneous melanoma enhanced with network-driven data exploration tools," Database: The Journal of Biological Databases and Curation 2014, pii: bau101 (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).

I. Pichler, F. Del Greco, M. Gögele, C. M. Lill, L. Bertram, C. B. Do, N. Eriksson, T. Foroud, R. H. Myers, M. Nalls, M. F. Keller, B. Benyamin, J. B. Whitfield, P. P. Pramstaller, A. A. Hicks, J. R. Thompson, C. Minelli, PD GWAS Consortium, Int Parkinsons Dis Genomics Consor, Wellcome Trust Case Control Consor, and Genetics Iron Status Consortium, "Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study," PLoS Medicine 10 (6), e1001462-e1001462 (2013).

J. Viswanathan, A. Haapasalo, K. M. A. Kurkinen, T. Natunen, P. Makinen, L. Bertram, H. Soininen, R. E. Tanzi, and M. Hiltunen, "Ubiquilin-1 Modulates gamma-Secretase-Mediated epsilon-Site Cleavage in Neuronal Cells," Biochemistry 52 (22), 3899-3912 (2013).

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).

L. Bertram, A. R. Parrado, and R. E. Tanzi, "TREM2 and Neurodegenerative Disease," The New England Journal of Medicine: NEJM / Publ. by the Massachusetts Medical Society 369 (16), 1565-1565 (2013).

L. Broer, C. Lill, M. Schuur, N. Amin, C. Roehr, L. Bertram, J. P. A. Ioannidis, and C. M. van Duijn, "Distinguishing true from false positives in genomic studies: p values," European Journal of Epidemiology 28 (2), 131-138 (2013).

S. C. Li, G. Papenberg, I. E. Nagel, C. Preuschhof, J. Schröder, W. Nietfeld, L. Bertram, H. R. Heekeren, U. Lindenberger, and L. Backman, "Aging magnifies the effects of dopamine transporter and D2 receptor genes on backward serial memory," Neurobiology of Aging 34 (1), 358.e1-358.e10 (2013).

S. C. Li, S. Passow, W. Nietfeld, J. Schröder, Lars Bertram, H. R. Heekeren, and U. Lindenberger, "Dopamine modulates attentional control of auditory perception: DARPP-32 (PPP1R1B) genotype effects on behavior and cortical evoked potentials," Neuropsychologia 51 (8), 1649-1661 (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).

T. Natunen, A. R. Parrado, S. Helisalmi, J. P. Pursiheimo, T. Sarajarvi, P. Makinen, K. M. A. Kurkinen, K. Mullin, I. Alafuzoff, A. Haapasalo, L. Bertram, H. Soininen, R. E. Tanzi, and M. Hiltunen, "Elucidation of the BACE1 Regulating Factor GGA3 in Alzheimer's Disease," Journal of Alzheimer's Disease 37 (1), 217-232 (2013).

G. Papenberg, L. Bäckman, I. E. Nagel, W. Nietfeld, J. Schröder, L. Bertram, Hauke R. Heekeren, U. Lindenberger, and S. C. Li, "Dopaminergic Gene Polymorphisms Affect Long-term Forgetting in Old Age: Further Support for the Magnification Hypothesis," Journal of Cognitive Neuroscience 25 (4), 571-579 (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).

P. Gonzalez-Perez, Y. B. Lu, R. J. Chian, P. C. Sapp, R. E. Tanzi, L. Bertram, D. McKenna-Yasek, F. B. Gao, and R. H. Brown, "Association of UBQLN1 mutation with Brown-Vialetto-Van Laere syndrome but not typical ALS," Neurobiology of Disease 48 (3), 391-398 (2012).

M. Sharma, J. P. Ioannidis, J. O. Aasly, G. Annesi, A. Brice, L. Bertram, M. Bozi, M. Barcikowska, D. Crosiers, C. E. Clarke, M. F. Facheris, M. Farrer, G. Garraux, S. Gispert, G. Auburger, C. Vilarino-Guell, G. M. Hadjigeorgiou, A. A. Hicks, N. Hattori, B. S. Jeon, Z. Jamrozik, A. Krygowska-Wajs, S. Lesage, C. M. Lill, J. J. Lin, T. Lynch, P. Lichtner, A. E. Lang, C. Libioulle, M. Murata, V. Mok, B. Jasinska-Myga, G. D. Mellick, K. E. Morrison, T. Meitnger, A. Zimprich, G. Opala, P. P. Pramstaller, I. Pichler, S. S. Park, A. Quattrone, E. Rogaeva, O. A. Ross, L. Stefanis, J. D. Stockton, W. Satake, P. A. Silburn, T. M. Strom, J. Theuns, E. K. Tan, T. Toda, H. Tomiyama, R. J. Uitti, C. Van Broeckhoven, K. Wirdefeldt, Z. Wszolek, G. Xiromerisiou, H. S. Yomono, K. C. Yueh, Y. Zhao, T. Gasser, D. Maraganore, and R. Krüger, "A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants," Journal of Medical Genetics (London) 49 (11), 721-726 (2012).

Christina M. Lill and Lars Bertram, "Developing the "next generation" of genetic association databases for complex diseases," Human Mutation 33 (9), 1366-1372 (2012).