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Journal Article (80)

21.
Journal Article
Hampel, H.; Listab, S.; Teipelc, S. J.; Garacie, F.; Nisticòg, .; Blennowi, K.; Zetterbergi, H.; Bertram, L.; Duyckaertsl, .; Bakardjianm, H. et al.; Drzezgao, .; Colliotp, O.; Epelbaumu, S.; Broich, K.; Lehéricy, S.; Brice, A.; Khachaturian, Z. S.; Aisen , P. S.; Dubois , B.: 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), pp. 426 - 449 (2014)
22.
Journal Article
Hampel, H.; Lista, S.; Teipel, S. J.; Garaci, F.; Nistico, R.; Blennow, K.; Zetterberg, H.; Bertram, L.; Duyckaerts, C.; Bakardjian, H. et al.; Drzezga, A.; Colliot, O.; Epelbaum, S.; Broich, K.; Lehericy, S.; Brice, A.; Khachaturian, Z. S.; Aisen, P. S.; Dubois, B.: 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), pp. 426 - 449 (2014)
23.
Journal Article
Lill, C.; Schilling, M.; Ansaloni, S.; Schröder, J.; Jaedicke, M.; Luessi, F.; Schjeide, B.-M.; Mashychev, A.; Graetz, C.; Akkad, D. et al.; Gerdes, L.-A.; Kroner, A.; Blaschke, P.; Hoffjan, S.; Winkelmann, A.; Dörner, T.; Rieckmann, P.; Steinhagen-Thiessen, E.; Lindenberger, U.; Chan, A.; Hartung, H.-P.; Aktas, O.; Lohse, P.; Buttmann, M.; Kümpfel, T.; Kubisch, C.; Zettl, U.; Epplen, J. T.; Zipp, F.; Bertram, L.: Assessment of microRNA-related SNP effects in the 3' untranslated region of the IL22RA2 risk locus in multiple sclerosis. Neurogenetics 15 (2), pp. 129 - 134 (2014)
24.
Journal Article
Athanasiadis, E. I.; Antonopoulou, K.; Chatzinasiou, F.; Lill, C. M.; Bourdakou, M. M.; Sakellariou, A.; Kypreou, K.; Stefanaki, I.; Evangelou, E.; Ioannidis, J. P.A. et al.; Bertram, L.; Stratigos, A. J.; Spyrou, G. M.: 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)
25.
Journal Article
Lill, C.; Schilling, M.; Ansaloni, S.; Schröder, J.; Jaedicke, M.; Luessi, F.; Schjeide, B. M.; Mashychev, A.; Graetz, C.; Akkad, D. A. et al.; Gerdes, L. A.; Kroner, A.; Blaschke, P.; Hoffjan, S.; Winkelmann, A.; Dorner, T.; Rieckmann, P.; Steinhagen-Thiessen, E.; Lindenberger, U.; Chan, A.; Hartung, H. P.; Aktas, O.; Lohse, P.; Buttmann, M.; Kumpfel, T.; Kubisch, C.; Zettl, U. K.; Epplen, J. T.; Zipp, F.; Bertram, L.: Assessment of microRNA-related SNP effects in the 3' untranslated region of the IL22RA2 risk locus in multiple sclerosis. Neurogenetics 15 (2), pp. 129 - 134 (2014)
26.
Journal Article
Pichler, I.; Del Greco, F.; Gögele, M.; Lill, C. M.; Bertram, L.; Do, C. B.; Eriksson, N.; Foroud, T.; Myers, R. H.; Nalls, M. et al.; Keller, M. F.; Benyamin, B.; Whitfield, J. B.; Pramstaller, P. P.; Hicks, A. A.; Thompson, J. R.; Minelli, C.; Consortium, P. G.; Consor, I. P. D. G.; Consor, W. T. C. C.; Consortium, G. I. S.: Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study. PLoS Medicine 10 (6), p. e1001462 - e1001462 (2013)
27.
Journal Article
Viswanathan, J.; Haapasalo, A.; Kurkinen, K. M. A.; Natunen, T.; Makinen, P.; Bertram, L.; Soininen, H.; Tanzi, R. E.; Hiltunen, M.: Ubiquilin-1 Modulates gamma-Secretase-Mediated epsilon-Site Cleavage in Neuronal Cells. Biochemistry 52 (22), pp. 3899 - 3912 (2013)
28.
Journal Article
Lill, C. M.; Schjeide, B.-M.; Graetz, C.; Liu, T.; Damotte, V.; Akkad, D. A.; Blaschke, P.; Gerdes, L. A.; Kroner, A.; Luessi, F. et al.; Cournu-Rebeix, I.; Hoffjan, S.; Winkelmann, A.; Touze, E.; Pico, F.; Corcia, P.; Otaegui, D.; Antiguedad, A.; Alcina, A.; Comabella, M.; Montalban, X.; Olascoaga, J.; Matesanz, F.; Dorner, T.; Li, S. C.; Steinhagen-Thiessen, E.; Lindenberger, U.; Chan, A.; Rieckmann, P.; Hartung, H. P.; Aktas, O.; Lohse, P.; Buttmann, M.; Kumpfel, T.; Kubisch, C.; Zettl, U. K.; Epplen, J. T.; Fontaine, B.; Zipp, F.; Vandenbroeck, K.; Bertram, L.: Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk. Journal of Medical Genetics (London) 50 (3), pp. 140 - 143 (2013)
29.
Journal Article
Bertram, L.; Parrado, A. R.; Tanzi, R. E.: TREM2 and Neurodegenerative Disease. The New England Journal of Medicine: NEJM / Publ. by the Massachusetts Medical Society 369 (16), p. 1565 - 1565 (2013)
30.
Journal Article
Broer, L.; Lill, C.; Schuur, M.; Amin, N.; Roehr, C.; Bertram, L.; Ioannidis, J. P. A.; van Duijn, C. M.: Distinguishing true from false positives in genomic studies: p values. European Journal of Epidemiology 28 (2), pp. 131 - 138 (2013)
31.
Journal Article
Lill, C. M.; Schjeide, B. M.; Graetz, C.; Ban, M.; Alcina, A.; Ortiz, M. A.; Perez, J.; Damotte, V.; Booth, D.; de Lapuente, A. L. et al.; Broer, L.; Schilling, M.; Akkad, D. A.; Aktas, O.; Alloza, I.; Antiguedad, A.; Arroyo, R.; Blaschke, P.; Buttmann, M.; Chan, A.; Compston, A.; Cournu-Rebeix, I.; Dorner, T.; Epplen, J. T.; Fernandez, O.; Gerdes, L. A.; Guillot-Noel, L.; Hartung, H. P.; Hoffjan, S.; Izquierdo, G.; Kemppinen, A.; Kroner, A.; Kubisch, C.; Kumpfel, T.; Li, S. C.; Lindenberger, U.; Lohse, P.; Lubetzki, C.; Luessi, F.; Malhotra, S.; Mescheriakova, J.; Montalban, X.; Papeix, C.; Paredes, L. F.; Rieckmann, P.; Steinhagen-Thiessen, E.; Winkelmann, A.; Zettl, U. K.; Hintzen, R.; Vandenbroeck, K.; Stewart, G.; Fontaine, B.; Comabella, M.; Urcelay, E.; Matesanz, F.; Sawcer, S.; Bertram, L.; Zipp, F.; Genetics, I. M. S.: MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis. Brain 136 (6), pp. 1778 - 1782 (2013)
32.
Journal Article
Li, S. C.; Papenberg, G.; Nagel, I. E.; Preuschhof, C.; Schröder, J.; Nietfeld, W.; Bertram, L.; Heekeren, H. R.; Lindenberger, U.; Backman, L.: Aging magnifies the effects of dopamine transporter and D2 receptor genes on backward serial memory. Neurobiology of Aging 34 (1), pp. 358.e1 - 358.e10 (2013)
33.
Journal Article
Li, S. C.; Passow, S.; Nietfeld, W.; Schröder, J.; Bertram, L.; Heekeren, H. R.; Lindenberger, U.: Dopamine modulates attentional control of auditory perception: DARPP-32 (PPP1R1B) genotype effects on behavior and cortical evoked potentials. Neuropsychologia 51 (8), pp. 1649 - 1661 (2013)
34.
Journal Article
Natunen, T.; Parrado, A. R.; Helisalmi, S.; Pursiheimo, J. P.; Sarajarvi, T.; Makinen, P.; Kurkinen, K. M. A.; Mullin, K.; Alafuzoff, I.; Haapasalo, A. et al.; Bertram, L.; Soininen, H.; Tanzi, R. E.; Hiltunen, M.: Elucidation of the BACE1 Regulating Factor GGA3 in Alzheimer's Disease. Journal of Alzheimer's Disease 37 (1), pp. 217 - 232 (2013)
35.
Journal Article
Papenberg, G.; Bäckman, L.; Nagel, I. E.; Nietfeld, W.; Schröder, J.; Bertram, L.; Heekeren, H. R.; Lindenberger, U.; Li, S. C.: Dopaminergic Gene Polymorphisms Affect Long-term Forgetting in Old Age: Further Support for the Magnification Hypothesis. Journal of Cognitive Neuroscience 25 (4), pp. 571 - 579 (2013)
36.
Journal Article
Schuck, N. W.; Doeller, C. F.; Schjeide, B.-M.; Schröder, J.; Frensch, P. A.; Bertram, L.; Li, S. C.: Aging and KIBRA/WWC1 Genotype Affect Spatial Memory Processes in a Virtual Navigation Task. Hippocampus 23 (10), pp. 919 - 930 (2013)
37.
Journal Article
Schuck, N. W.; Frensch, P. A.; Schjeide, B. M.; Schröder, J.; Bertram, L.; Li, S. C.: Effects of aging and dopamine genotypes on the emergence of explicit memory during sequence learning. Neuropsychologia 51 (13), pp. 2757 - 2769 (2013)
38.
Journal Article
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)
39.
Journal Article
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)
40.
Journal Article
Lill, C. M.; Bertram, L.: Developing the "next generation" of genetic association databases for complex diseases. Human Mutation 33 (9), pp. 1366 - 1372 (2012)
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