Publications of Till Andlauer

Comes, A.; Adorjan, K.; Andlauer, T.; Budde, M.; Degenhardt, F.; Forstner, A. J.; Gade, K.; Heilbronner, U.; Kalman, J.; Kondofersky, I. et al.; Papiol, S.; Senner, F.; Sivalingam, S.; Falkai, P.; Schulze, T.: THE ROLE OF ENVIRONMENTAL STRESS AND DNA METHYLATION IN THE LONGITUDINAL COURSE OF BIPOLAR DISORDER. In EUROPEAN NEUROPSYCHOPHARMACOLOGY, 29, pp. 1300 - 1301. 26th World Congress of Psychiatric Genetics (WCPG), Glasgow, SCOTLAND, October 11, 2018 - October 15, 2018. (2019)

Degenhardt, F.; Koller, A. C.; Kaurani, L.; Worf, K.; Degenhardt, F. C.; Klockmeier, K.; Andlauer, T.; Thiele, H.; McQuillin, A.; Rujescu, D. et al.; Rietschel, M.; Maier, W.; Schwab, S.; Reif, A.; Noethen, M. M.: EXOME-SEQUENCING IN DENSLY AFFECTED PEDIGREES IDENTIFIES NEW CANDIDATE GENES FOR SCHIZOPHRENIA. In EUROPEAN NEUROPSYCHOPHARMACOLOGY, 29, p. S1005 - S1005. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, October 13, 2017 - October 17, 2017. (2019)

Gade, K.; Papiol, S.; Heilbronner, U.; Budde, M.; Adorjan, K.; Anderson-Schmidt, H.; Kalman, J.; Aldinger, F.; Andlauer, T. F. M.; Schulze, T.: THE IMPACT OF BIPOLAR AND SCHIZOPHRENIA POLYGENIC RISK SCORES ON FAMILIAL FEATURES OF BIPOLAR DISORDER. In EUROPEAN NEUROPSYCHOPHARMACOLOGY, 29, p. S968 - S968. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, October 13, 2017 - October 17, 2017. (2019)

Heilbronner, U.; Andlauer, T.; Papiol, S.; Budde, M.; Strohmaier, J.; Streit, F.; Frank, J.; Amelang, M.; Sturmer, T.; Muller-Myhsok, B. et al.; Rietschel, M.; Schulze, T. G.: COMMON GENETIC VARIANTS ASSOCIATED WITH PERSONALITY DIMENSIONS IN THE HEIDELBERG COHORT STUDY OF THE ELDERLY (HeiDE): AN UPDATE. In EUROPEAN NEUROPSYCHOPHARMACOLOGY, 29, p. S928 - S928. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, October 13, 2017 - October 17, 2017. (2019)

Ostkamp, P.; Goerlich, D.; Andlauer, T.F.M.; Salmen, A.; Schulte-Mecklenbeck, A.; Pignolet, B.; Gonzalez-Escamilla, G.; Bucciarelli, F.; Breuer, J.; Antony, G. et al.; Schneider-Hohendorf, T.; Mykicki, N.; Dankowski, T.; Mueller-Myhsok, B.; Kuempfel, T.; Meuth, S. G.; Zipp, F.; Hohlfeld, R.; Brassat, D.; Gold, R.; Gross, C. C.; Groppa, S.; Loser, K.; Wiendl, H.; Schwab, N.: Influence of ultraviolet radiation and diminished-function melanocortin 1 receptor variants on multiple sclerosis disease severity in two large multicenter cohort studies. In MULTIPLE SCLEROSIS JOURNAL, 25, pp. 59 - 60. 35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS, Stockholm, SWEDEN, September 11, 2019 - September 13, 2019. (2019)

Schaupp, S.; Budde, M.; Kondofersky, I.; Papiol, S.; Heilbronner, U.; Gade, K.; Anderson-Schmidt, H.; Kalman, J.; Senner, F.; Andlauer, T. F. M. et al.; Rietschel, M.; Degenhardt, F.; Mueller, N.; Theis, F. J.; Schulze, T.: POLYGENIC RISK SCORE ANALYSIS OF TRAJECTORIES OF COGNITIVE PERFORMANCE IN PSYCHIATRIC PATIENTS. In EUROPEAN NEUROPSYCHOPHARMACOLOGY, 29, p. 1161 - 1161. 26th World Congress of Psychiatric Genetics (WCPG), Glasgow, SCOTLAND, October 11, 2018 - October 15, 2018. (2019)

Schulte, E.; Kondofersky, I.; Budde, M.; Adorjan, K.; Aldinger, F.; Anderson-Schmidt, H.; Andlauer, T. F. M.; Gade, K.; Heilbronner, U.; Kalman, J. et al.; Papiol, S.; Theis, F. J.; Falkai, P.; Mueller, N.; Schulze, T. G.: POLYGENIC BURDEN ANALYSIS OF LONGITUDINAL CLUSTERS OF PSYCHOPATHOLOGICAL FEATURES IN A CROSS-DIAGNOSTIC GROUP OF INDIVIDUALS WITH SEVERE MENTAL ILLNESS. In EUROPEAN NEUROPSYCHOPHARMACOLOGY, 29, pp. S995 - S996. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, October 13, 2017 - October 17, 2017. (2019)

Sivalingam, S.; Forstner, A.; Herms, S.; Maaser, A.; Koller, A.; Reinbold, C.; Fischer, S.; Andlauer, T.; Streit, F.; Frank, J. et al.; Dukal, H.; Witt, S.; Heilmann-Heimbach, S.; Ludwig, K.; Degenhardt, F.; Krug, A.; Dannlowski, U.; Kircher, T.; Cichon, S.; Rietschel, M.; Hoffmann, P.; Noethen, M.: Integrated analysis of genetic and epigenetic data of healthy individuals with different risk factors for affective disorders. In EUROPEAN JOURNAL OF HUMAN GENETICS, 27, pp. 286 - 287. 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, ITALY, June 16, 2018 - June 19, 2018. (2019)

Andlauer, T.F.M.; Koechert, K.; Muehlau, M.; Munger, K. L.; Fitzgerald, K. C.; Arnason, B. G. W.; Comi, G.; Cook, S.; Filippi, M.; Goodin, D. S. et al.; Hartung, H. -.; Jeffery, D. R.; Kappos, L.; Ascherio, A.; Hemmer, B.; Pohl, C.; Mueller-Myhsok, B.: Influence of 25(OH)D levels and genetic variants on disease severity in MS. In MULTIPLE SCLEROSIS JOURNAL, 22 (Supplement 3), P1599, pp. 842 - 843. 32nd Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS), London, ENGLAND, September 14, 2016 - September 17, 2016. (2016)

Andlauer, T.F.M.; Buck, D.; Hemmer, B.; Müller-Myhsok, B.: Genome-wide association analysis in a German multiple sclerosis cohort. In MULTIPLE SCLEROSIS JOURNAL, 21 (Supplement 11), P360, p. 144 - 144. 31st Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS), Barcelona, SPAIN, October 07, 2015 - October 10, 2015. Sage Publications Inc., London, EC1Y 1SP (2015)

Dankowski, T.; Buck, D.; Andlauer, T. F.; Antony, G.; Bayas, A.; Bechmann, L.; Berthele, A.; Bettecken, T.; Chan, A.; Franke, A. et al.; Gold, R.; Graetz, C.; Haas, J.; Hecker, M.; Herms, S.; Hohlfeld, R.; Infante-Duarte, C.; Joeckel, K. -.; Kieseier, B. C.; Knier, B.; Knop, M.; Lichtner, P.; Lieb, W.; Lill, C. M.; Limmroth, V.; Linker, R. A.; Loleit, V.; Meuth, S.; Moebus, S.; Müller-Myhsok, B.; Nischwitz, S.; Noethen, M. M.; Friedemann, P.; Pütz, B.; Ruck, T.; Salmen, A.; Stangel, M.; Stellmann, J. -.; Strauch, K.; Stuerner, K. H.; Tackenberg, B.; Bergh, F. T.; Tumani, H.; Waldenberger, M.; Weber, F.; Wiend, H.; Wildemann, B.; Zettl, U. K.; Ziemann, U.; Zipp, F.; Hemmer, B.; Ziegler, A.: Exome Array GWAS in 10,000 Germans Identifies Association between MUC22 and Multiple Sclerosis. In HUMAN HEREDITY, 79 (1), pp. 32 - 33. 43rd European Mathematical Genetics Meeting (EMGM), Brest, France, April 16, 2015 - April 17, 2015. Karger, Basel, CH (2015)

Andlauer, T.F.M.; andlauer, t; Link, J.; Buck, D.; Ryner, M.; Grummel, V.; Auer, M.; Hegen, H.; Gasperi, C.; Mueller-Myhsok, B. et al.; Jensen, P. E. H.; Sellebjerg, F. T.; Kockum, I.; Olsson, T.; Pallardy, M.; Spindeldreher, S.; Deisenhammer, F.; Fogdell-Hahn, A.; Hemmer, B.: Genetic factors influencing the development of binding and neutralizing antibodies against interferon beta treatment in multiple sclerosis patients. 34th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS), Berlin, GERMANY (2018)

Ostkamp, P.; Breuer, J.; Andlauer, T.; Antony, G.; Dankowsky, T.; Mykicki, N.; Loser, K.; Wiendl, H.; Schwab, N.: Cross-sectional and longitudinal analysis of clinical parameters in a large-scale, national, multicentric multiple sclerosis cohort and the influence of MC1R SNPs. 34th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS), Berlin, GERMANY (2018)

Muehlau, M.; Andlauer, T. F. M.; Hemmer, B.: HLA Genetic Risk Burden in Multiple Sclerosis, JAMA NEUROLOGY 73, pp. 1500 - 1501 (2016)