Publikationen von C. M. Lill

M. A. Nalls, J. Bras, G. D. Hernandez, M. F. Keller, E. Majounie, A. E. Renton, M. Saad, I. Jansen, R. Guerreiro, S. Lubbe, V. Plagnol, R. Gibbs, C. Schulte, N. Pankratz, M. Sutherland, L. Bertram, C. M. Lill, A. L. DeStefano, T. Faroud, N. Eriksson, J. Y. Tung, C. Edsall, N. Nichols, J. Brooks, S. Arepalli, H. Pliner, C. Letson, P. Heutink, M. Martinez, T. Gasser, B. J. Traynor, N. Wood, J. Hardy, and A. B. Singleton, "NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases," Neurobiology of Aging 36 (3), 1605.e7-1605.e12 (2015).

Ismaïl Ahmed, Pei-Chen Lee, Christina M. Lill, Susan Searles Nielsen, Fanny Artaud, Lisa G. Gallagher, Marie-Anne Loriot, Claire Mulot, Magali Nacfer, Tian Liu, Joanna M. Biernacka, Sebastian Armasu, Kari Anderson, Federico M. Farin, Christina Funch Lassen, Johnni Hansen, Jørgen H. Olsen, Lars Bertram, Demetrius M. Maraganore, Harvey Checkoway, Beate Ritz, and Alexis Elbaz, "Lack of replication of the GRIN2A-by-coffee interaction in Parkinson disease," PLoS Genetics 10 (11), e1004788 (2014).

Mike A Nalls, Nathan Pankratz, Christina M. Lill, Chuong B Do, Dena G. Hernandez, Mohamad Saad, Anita L. DeStefano, Eleanna Kara, Jose Bras, Manu Sharma, Claudia Schulte, Margaux F. Keller, Sampath Arepalli, Christopher Letson, Connor Edsall, Hreinn Stefansson, Xinmin Liu, Hannah Pliner, Joseph H. Lee, Rong Cheng, M. Arfan Ikram, John P.A. Ioannidis, Georgios M. Hadjigeorgiou, Joshua C. Bis, Maria Martinez, Joel S. Perlmutter, Alison Goate, Karen Marder, Brian Fiske, Margaret Sutherland, Georgia Xiromerisiou, Richard H. Myers, Lorraine N Clark, Kari Stefansson, John A. Hardy, Peter Heutink, Honglei Chen, Nicholas W. Wood, Henry Houlden, Haydeh Payami, Alexis Brice, William K Scott, Thomas Gasser, Lars Bertram, Nicholas Eriksson, Tatiana Foroud, and Andrew B. Singleton, "Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease," Nature Genetics 46 (9), 989-993 (2014).

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).

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).

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. 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).

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).

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).

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. 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).

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