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

Sharma, M.; Ioannidis, J. P.; Aasly, J. O.; Annesi, G.; Brice, A.; Bertram, L.; Bozi, M.; Barcikowska, M.; Crosiers, D.; Clarke, C. E. et al.; Facheris, M. F.; Farrer, M.; Garraux, G.; Gispert, S.; Auburger, G.; Vilarino-Guell, C.; Hadjigeorgiou, G. M.; Hicks, A. A.; Hattori, N.; Jeon, B. S.; Jamrozik, Z.; Krygowska-Wajs, A.; Lesage, S.; Lill, C. M.; Lin, J. J.; Lynch, T.; Lichtner, P.; Lang, A. E.; Libioulle, C.; Murata, M.; Mok, V.; Jasinska-Myga, B.; Mellick, G. D.; Morrison, K. E.; Meitnger, T.; Zimprich, A.; Opala, G.; Pramstaller, P. P.; Pichler, I.; Park, S. S.; Quattrone, A.; Rogaeva, E.; Ross, O. A.; Stefanis, L.; Stockton, J. D.; Satake, W.; Silburn, P. A.; Strom, T. M.; Theuns, J.; Tan, E. K.; Toda, T.; Tomiyama, H.; Uitti, R. J.; Van Broeckhoven, C.; Wirdefeldt, K.; Wszolek, Z.; Xiromerisiou, G.; Yomono, H. S.; Yueh, K. C.; Zhao, Y.; Gasser, T.; Maraganore, D.; Krüger, R.: 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), pp. 721 - 726 (2012)

Lill, C. M.; Bertram, L.: Developing the "next generation" of genetic association databases for complex diseases. Human Mutation 33 (9), pp. 1366 - 1372 (2012)

Lill, C. M.; Liu, T.; Schjeide, B. M.; Roehr, J. T.; Akkad, D. A.; Damotte, V.; Alcina, A.; Ortiz, M. A.; Arroyo, R.; de Lapuente, A. L. et al.; 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.; Dörner, T.; Steinhagen-Thiessen, E.; Baeckman, L.; Heekeren, H. R.; Li, S. C.; Lindenberger, U.; Chan, A.; Hartung, H. P.; Aktas, O.; Lohse, P.; Kumpfel, T.; Kubisch, C.; Epplen, J. T.; Zettl, U. K.; Fontaine, B.; Vandenbroeck, K.; Matesanz, F.; Urcelay, E.; Bertram, L.; Zipp, F.: 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), pp. 558 - 562 (2012)

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

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

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

Lill, C. M.; Zipp, F.: [The genetic profile of multiple sclerosis: risk genes and the "dark matter"]. Der Nervenarzt 83 (6), pp. 705 - 713 (2012)

Hooli, B. V.; Mohapatra, G.; Mattheisen, M.; Parrado, A. R.; Roehr, J. T.; Shen, Y.; Gusella, J. F.; Moir, R.; Saunders, A. J.; Lange, C. et al.; Tanzi, R. E.; Bertram, L.: Role of common and rare APP DNA sequence variants in Alzheimer disease. Neurology 78 (16), pp. 1250 - 1257 (2012)

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

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

Lebedeva, E.; Stingl, J. C.; Thal, D. R.; Ghebremedhin, E.; Strauss, J.; Ozer, E.; Bertram, L.; von Einem, B.; Tumani, H.; Otto, M. et al.; Riepe, M. W.; Hogel, J.; Ludolph, A. C.; von Arnim: Genetic variants in PSEN2 and correlation to CSF beta-amyloid42 levels in AD. Neurobiology of Aging 33 (1), pp. 201.e9 - 201.e18 (2012)

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

Won, S.; Lu, Q.; Bertram, L.; Tanzi, R. E.; Lange, C.: 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), pp. 35 - 46 (2012)

Won, S. H.; Lu, Q.; Bertram, L.; Tanzi, R. E.; Lange, C.: 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), pp. 35 - 46 (2012)

Bertram, L.; Tanzi, R. E.: The Genetics of Alzheimer's Disease. In: Progress in Molecular Biology and Translational Science: Molecular Biology of Neurodegenerative Diseases, Vol. 107, pp. 79 - 100. Elsevier (2012)

Lill, C. M.; Meissner, E.; Schjeide, L.; Schjeide, B. M.; Liebsch, M.; Roehr, C.; Rouleau, G.; Hardiman, O.; Traynor, B.; Van den Berg, L. et al.; Al-Chalabi, A.; Bertram, L.: Comprehensive Research Synopsis and Systematic Meta-Analyses in ALS Genetics: The ALSGene Database (P01.095). Neurology 78, (2012)

Arnaout, F.; Liu, T.; Heinig, M.; Steinhagen, E.; Bertram, L.; Demuth, I.: Assessment and Genetic Associations of the 2d:4d Finger-Length Ratio within the Berlin Aging Study Ii (Base-Ii). GSA Sixty-Fifth Annual Scientific Meeting: Charting New Frontiers in Aging, San Diego, CA (2012)