Publikationen von L. Bertram

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).

M. J. Sobrido, P. Cacheiro, A. Carracedo, and L. Bertram, "Databases for neurogenetics: Introduction, overview, and challenges," Human Mutation 33 (9), 1311-1314 (2012).

M. Sharma, J. P. Ioannidis, J. O. Aasly, G. Annesi, A. Brice, C. Van Broeckhoven, L. Bertram, M. Bozi, D. Crosiers, C. Clarke, M. Facheris, M. Farrer, G. Garraux, S. Gispert, G. Auburger, C. Vilarino-Guell, G. M. Hadjigeorgiou, A. A. Hicks, N. Hattori, B. Jeon, S. Lesage, C. M. Lill, J. J. Lin, T. Lynch, P. Lichtner, A. E. Lang, V. Mok, B. Jasinska-Myga, G. D. Mellick, K. E. Morrison, 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, J. Theuns, E. K. Tan, T. Toda, H. Tomiyama, R. J. Uitti, K. Wirdefeldt, Z. Wszolek, G. Xiromerisiou, K. C. Yueh, Y. Zhao, T. Gasser, D. Maraganore, and R. Krüger, "Large-scale replication and heterogeneity in Parkinson disease genetic loci," Neurology 79 (7), 659-667 (2012).

B. C. Wallace, K. Small, C. E. Brodley, J. Lau, C. H. Schmid, L. Bertram, C. M. Lill, J. T. Cohen, and T. A. Trikalinos, "Toward modernizing the systematic review pipeline in genetics: efficient updating via data mining," GENETICS IN MEDICINE 14 (7), 663-669 (2012).

B. V. Hooli, G. Mohapatra, M. Mattheisen, A. R. Parrado, J. T. Roehr, Y. Shen, J. F. Gusella, R. Moir, A. J. Saunders, C. Lange, R. E. Tanzi, and Lars Bertram, "Role of common and rare APP DNA sequence variants in Alzheimer disease," Neurology 78 (16), 1250-1257 (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).

E. Lebedeva, J. C. Stingl, D. R. Thal, E. Ghebremedhin, J. Strauss, E. Ozer, L. Bertram, B. von Einem, H. Tumani, M. Otto, M. W. Riepe, J. Hogel, A. C. Ludolph, and C. A. von Arnim, "Genetic variants in PSEN2 and correlation to CSF beta-amyloid42 levels in AD," Neurobiology of Aging 33 (1), 201 e9-18 (2012).

E. Lebedeva, J. C. Stingl, D. R. Thal, E. Ghebremedhin, J. Strauss, E. Ozer, L. Bertram, B. von Einem, H. Tumani, M. Otto, M. W. Riepe, J. Hogel, A. C. Ludolph, and von Arnim, "Genetic variants in PSEN2 and correlation to CSF beta-amyloid42 levels in AD," Neurobiology of Aging 33 (1), 201.e9-201.e18 (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).

S. Won, Q. Lu, L. Bertram, R. E. Tanzi, and C. Lange, "On the Meta-Analysis of Genome-Wide Association Studies: A Robust and Efficient Approach to Combine Population and Family-Based Studies," Human Heredity 73 (1), 35-46 (2012).

S. H. Won, Q. Lu, L. Bertram, R. E. Tanzi, and C. Lange, "On the Meta-Analysis of Genome-Wide Association Studies: A Robust and Efficient Approach to Combine population and Family-Based Studies," Human Heredity 73 (1), 35-46 (2012).

J. Viswanathan, A. Haapasalo, C. Böttcher, R. Miettinen, K. M. Kurkinen, A. Lu, A. Thomas, C. J. Maynard, D. Romano, B. T. Hyman, O. Berezovska, L. Bertram, H. Soininen, N. P. Dantuma, R. E. Tanzi, and M. Hiltunen, "Alzheimer's Disease-Associated Ubiquilin-1 Regulates Presenilin-1 Accumulation and Aggresome Formation.," Traffic 12 (3), 330-348 (2011).

L. Bertram, "Alzheimer's genetics in the GWAS era: a continuing story of 'replications and refutations'," Current Neurology and Neuroscience Reports 11 (3), 246-53 (2011).

L. Bertram and H. Hampel, "The role of genetics for biomarker development in neurodegeneration," Progress in Neurobiology 95 (4), 501-4 (2011).

F. Chatzinasiou, C. M. Lill, K. Kypreou, I. Stefanaki, V. Nicolaou, G. Spyrou, E. Evangelou, J. T. Roehr, E. Kodela, A. Katsambas, H. Tsao, J. P. Ioannidis, L. Bertram, and A. J. Stratigos, "Comprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma," Journal of the National Cancer Institute 103 (16), 1227-35 (2011).

A. Haapasalo, J. Viswanathan, K. M. Kurkinen, L. Bertram, H. Soininen, N. P. Dantuma, R. E. Tanzi, and M. Hiltunen, "Involvement of ubiquilin-1 transcript variants in protein degradation and accumulation," Communicative & Integrative Biology 4 (4), 428-32 (2011).

H. Hampel, D. Prvulovic, S. Teipel, F. Jessen, C. Luckhaus, L. Frolich, M. W. Riepe, R. Dodel, T. Leyhe, L. Bertram, W. Hoffmann, and F. Faltraco, "The future of Alzheimer's disease: the next 10 years," Progress in Neurobiology 95 (4), 718-28 (2011).

A. Haworth, L. Bertram, P. Carrera, J. L. Elson, C. D. Braastad, D. W. Cox, M. Cruts, J. T. den Dunnen, M. J. Farrer, J. K. Fink, S. A. Hamed, H. Houlden, D. R. Johnson, K. Nuytemans, F. Palau, D. L. Rayan, P. N. Robinson, A. Salas, B. Schule, M. G. Sweeney, M. O. Woods, J. Amigo, R. G. Cotton, and M. J. Sobrido, "Call for participation in the neurogenetics consortium within the Human Variome Project," Neurogenetics 12 (3), 169-73 (2011).

A. Haworth, L. Bertram, P. Carrera, J. L. Elson, C. D. Braastad, D. W. Cox, M. Cruts, J. T. den Dunnen, M. J. Farrer, J. K. Fink, S. A. Hamed, H. Houlden, D. R. Johnson, K. Nuytemans, F. Palau, D. L. Rayan, P. N. Robinson, A. Salas, B. Schule, M. G. Sweeney, M. O. Woods, J. Amigo, R. G. Cotton, and M. J. Sobrido, "Call for participation in the neurogenetics consortium within the Human Variome Project," Neurogenetics 12 (3), 169-73 (2011).

M. Hiltunen, L. Bertram, and A. J. Saunders, "Genetic risk factors: their function and comorbidities in Alzheimer's disease," International Journal of Alzheimer's Disease 2011, 925362 (2011).