Publications of Tian Liu

Journal Article (23)

2015
Journal Article
Davies, G., Armstrong, N., Bis, J. C., Bressler, J., Chouraki, V., Giddaluru, S., Hofer, E., Ibrahim-Verbaas, C. A., Kirin, M., Lahti, J., van der Lee, S. J., Le Hellard, S., Liu, T., Marioni, R. E., Oldmeadow, C., Postmus, I., Smith, A. V., Smith, J. A., Thalamuthu, A., Thomson, R., Vitart, V., Wang, J., Yu, L., Zgaga, L., Zhao, W., Boxall, R., Harris, S. E., Hill, W. D., Liewald, D. C., Luciano, M., Adams, H., Ames, D., Amin, N., Amouyel, P., Assareh, A. A., Au, R., Becker, J. T., Beiser, A., Berr, C., Bertram, L., Boerwinkle, E., Buckley, B. M., Campbell, H., Corley, J., De Jager, P. L., Dufouil, C., Eriksson, J. G., Espeseth, T., Faul, J. D., Ford, I., Scotland, G., Gottesman, R. F., Griswold, M. E., Gudnason, V., Harris, T. B., Heiss, G., Hofman, A., Holliday, E. G., Huffman, J., Kardia, S. L. R., Kochan, N., Knopman, D. S., Kwok, J. B., Lambert, J.-C., Lee, T., Li, G., Li, S.-C., Loitfelder, M., Lopez, O. L., Lundervold, A. J., Lundqvist, A., Mather, K. A., Mirza, S. S., Nyberg, L., Oostra, B. A., Palotie, A., Papenberg, G., Pattie, A., Petrovic, K., Polasek, O., Psaty, B. M., Redmond, P., Reppermund, S., Rotter, J. I., Schmidt, H., Schuur, M., Schofield, P. W., Scott, R. J., Steen, V. M., Stott, D. J., van Swieten, J. C., Taylor, K. D., Trollor, J., Trompet, S., Uitterlinden, A. G., Weinstein, G., Widen, E., Windham, B. G., Jukema, J. W., Wright, A. F., Wright, M. J., Yang, Q., Amieva, H., Attia, J. R., Bennett, D. A., Brodaty, H., de Craen, A. J. M., Hayward, C., Ikram, M. A., Lindenberger, U., Nilsson, L.-G., Porteous, D. J., Raikkonen, K., Reinvang, I., Rudan, I., Sachdev, P. S., Schmidt, R., Schofield, P. R., Srikanth, V., Starr, J. M., Turner, S. T., Weir, D. R., Wilson, J. F., van Duijn, C., Launer, L., Fitzpatrick, A. L., Seshadri, S., Mosley, T. H., & Deary, I. J. (2015). Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949). Molecular Psychiatry, 20, 183–192. https://doi.org/10.1038/mp.2014.188
Journal Article
Domingo, A., Westenberger, A., Lee, L. V., Braenne, I., Liu, T., Vater, I., Rosales, R., Jamora, R. D., Pasco, P. M., Cutiongco-de la Paz, E. M., Freimann, K., Schmidt, T. G. P. M., Dressler, D., Kaiser, F. J., Bertram, L., Erdmann, J., Lohmann, K., & Klein, C. (2015). New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3). European Journal of Human Genetics, 23, 1334–1340. https://doi.org/10.1038/ejhg.2014.292
Journal Article
Lill, C. M., Rengmark, A., Pihlstrøm, L., Fogh, I., Shatunov, A., Sleimane, P. M., Wangh, L.-S., Liu, T., Lassen, C. F., Meissner, E., Alexopoulos, P., Calvo, A., Chiol, A., Dizdar, N., Faltraco, F., Forsgren, L., Kirchheiner, J., Kurz, A., Larsen, J. P., Liebsch, M., Linder, J., Morrison, K. E., Nissbrandt, H., Otto, M., Pahnke, J., Partch, A., Restagno, G., Rujescu, D., Schnack, C., Shaw, C. E., Shaw, P. J., Tumani, H., Tysnes, O.-B., Valladares, O., Silaniac, V., van den Berg, L. H., van Rheenen, W., Veldink, J. H., Lindenberger, U., Steinhagen-Thiessen, E., SLAGEN Consortium, Teipel, S., Perneczkyk, R., Hakonarson, H., Hampel, H., von Arnim, C. A. F., Olsen, J. H., Deerlin, V. M. V., Al-Chalab, A., Toft, M., Ritz, B., & Bertram, L. (2015). The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease. Alzheimer's & Dementia, 11(12), 1407–1416. https://doi.org/10.1016/j.jalz.2014.12.009
Journal Article
Schrewe, L., Lill, C. M., Liu, T., Salmen, A., Gerdes, L. A., Guillot-Noel, L., Akkad, D. A., Blaschke, P., Graetz, C., Hoffjan, S., Kroner, A., Demir, S., Bohme, A., Rieckmann, P., ElAli, A., Hagemann, N., Hermann, D. M., Cournu-Rebeix, I., Zipp, F., Kumpfel, T., Buttmann, M., Zettl, U. K., Fontaine, B., Bertram, L., Gold, R., & Chan, A. (2015). Investigation of sex-specific effects of apolipoprotein E on severity of EAE and MS. Journal of Neuroinflammation, 12(1), Article 234. https://doi.org/10.1186/s12974-015-0429-y
2014
Journal Article
Ahmed, I., Lee, P.-C., Lill, C. M., Nielsen, S. S., Artaud, F., Gallagher, L. G., Loriot, M.-A., Mulot, C., Nacfer, M., Liu, T., Biernacka, J. M., Armasu, S., Anderson, K., Farin, F. M., Lassen, C. F., Hansen, J., Olsen, J. H., Bertram, L., Maraganore, D. M., Checkoway, H., Ritz, B., & Elbaz, A. (2014). Lack of replication of the GRIN2A-by-coffee interaction in Parkinson disease. PLoS Genetics, 10(11), Article e1004788. https://doi.org/10.1371/journal.pgen.1004788
Journal Article
Ghisletta, P., Bäckman, L., Bertram, L., Brandmaier, A. M., Gerstorf, D., Liu, T., & Lindenberger, U. (2014). The Val/Met polymorphism of the Brain-Derived Neurotrophic Factor (BDNF) gene predicts decline in perceptual speed in older adults. Psychology and Aging, 29(2), 384–392. https://doi.org/10.1037/a0035201
Journal Article
Li, X., Sui, Y., Liu, T., Wang, J., Li, Y., Lin, Z., Hegarty, J., Koltun, W. A., Wang, Z., & Wu, R. (2014). A model for family-based case-control studies of genetic imprinting and epistasis. Briefings in Bioinformatics, 15(6), 1069–1079. https://doi.org/10.1093/bib/bbt050
Journal Article
Liu, T., Li, S.-C., Papenberg, G., Schröder, J., Roehr, J. T., Nietfeld, W., Lindenberger, U., & Bertram, L. (2014). No association between CTNNBL1 and episodic memory performance. Translational Psychiatry, 4, Article e454. https://doi.org/10.1038/tp.2014.93
Journal Article
Schröder, J., Ansaloni, S., Schilling, M., Liu, T., Radke, J., Jädicke, M., Schjeide, B.-M. M., Mashychev, A., Tegeler, C., Radbruch, H., Papenberg, G., Düzel, S., Demuth, I., Bucholtz, N., Lindenberger, U., Li, S.-C., Steinhagen-Thiessen, E., Lill, C. M., & Bertram, L. (2014). MicroRNA-138 is a potential regulator of memory performance in humans. Frontiers in Human Neuroscience, 8, Article 501. https://doi.org/10.3389/fnhum.2014.00501
2013
Journal Article
Lill, C. M., Schjeide, B.-M. M., Graetz, C., Liu, T., Damotte, V., Akkad, D. A., Blaschke, P., Gerdes, L.-A., Kroner, A., Luessi, F., Cournu-Rebeix, I., Hoffjan, S., Winkelmann, A., Touze, E., Pico, F., Corcia, P., Otaegui, D., Antigüedad, A., Alcina, A., Comabella, M., Montalban, X., Olascoaga, J., Matesanz, F., Dörner, T., Li, S.-C., Steinhagen-Thiessen, E., Lindenberger, U., Chan, A., Rieckmann, P., Hartung, H.-P., Aktas, O., Lohse, P., Buttmann, M., Kümpfel, T., Kubisch, C., Zettl, U. K., Epplen, J. T., Fontaine, B., Zipp, F., Vandenbroeck, K., & Bertram, L. (2013). Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk. Journal of Medical Genetics, 50(3), 140–143. https://doi.org/10.1136/jmedgenet-2012-101411
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