Publikationen von Bertram Muller-Myhsok

Abbondanza, F.; Gialluisi, A.; Moll, K.; Vreeker, A.; Cecil, C.; Muller-Myhsok, B.; Schulte-Korne, G.; Whitehouse, A.; Wang, C.; Pennell, C. et al.; De Jong, P. F.; Van Bergen, E.; Alrouh, H.; Boomsma, D.; Michaelson, J. J.; Casten, L.; Eising, E.; Malanchini, M.; Wigg, K.; Price, K.; Barr, C.; McBride, C.; Paracchini, S.: Large-scale genomic meta-analysis on math abilities in cohorts of 20,000 participants. In EUROPEAN JOURNAL OF HUMAN GENETICS, 31, S. 341 - 341. (2023)

Fu, X.; Mueller-Myhsok, B.; Puetz, B.: Identification of transdiagnostic HIV-related Cryptococcosis by machine learning. In HIV MEDICINE, 24, S. 467 - 468. (2023)

Fu, X.; Wu, L.; Puetz, B.; Muller-Myhsok, B.: Risk factor predictions for threeyear mortality among HIV-related patients with disseminated Cryptococcosis. In HIV MEDICINE, 24, S. 619 - 620. (2023)

Rietkerk, J.; Huang, L.; Appadurai, V.; Pons, V. T.; van Loo, H.; Garvert, L.; van der Auwera-Palitschka, S.; Adams, M.; Grabe, H. J.; Schork, A. et al.; Mueller-Myhsok, B.; Dahl, A.; Cai, N.: COORDINATED EPISTASIS REVEALS SYMPTOM-SPECIFIC POLYGENIC PATHWAY INTERACTIONS IN MAJOR DEPRESSIVE DISORDER. In EUROPEAN NEUROPSYCHOPHARMACOLOGY, 75, S. S64 - S64. World Congress of Psychiatric Genetics (WCPG), Montreal, CANADA, 10. Oktober 2023 - 14. Oktober 2023. (2023)

Panzenhagen, A.; Schmaal, L.; Czisch, M.; Mueller-Myhsok, B.; Samann, P.: BICLUSTERING ALGORITHM APPLIED TO STRUCTURAL MAGNETIC RESONANCE IMAGING IN MAJOR DEPRESSIVE DISORDER. In EUROPEAN NEUROPSYCHOPHARMACOLOGY, 63, S. E170 - E170. World Congress of Psychiatric Genetics (WCPG), Florence, ITALY, 13. September 2022 - 17. September 2022. (2022)

Pain, O.; Hodgson, K.; Trubetskoy, V.; Baune, B.; Biernacka, J.; Fabbri, C.; Lewis, G.; Li, Q.; Mueller-Myhsok, B.; Perroud, N. et al.; Serretti, A.; McIntosh, A.; Lewis, C.: Investigating the common genetic basis of antidepressant response. In European Neuropsychopharmacology, 29, S. S91 - S92. 27th World Congress of Psychiatric Genetics (WCPG), Los Angeles, CA, 26. Oktober 2019 - 31. Oktober 2019. Elsevier, Amsterdam (2019)

Filosi, M.; Mueller-Myhsok, B.; Muglia, P.; Domenici, E.: Blood-based autism spectrum disorder signatures from the Italian autism network collection. In European Neuropsychopharmacology, 29, S. S912 - S912. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, 13. Oktober 2017 - 17. Oktober 2017. Elsevier, Amsterdam (2019)

Andlauer, T.; Muhleisen, T.; Hoffstaedter, F.; Teumer, A.; Teuber, A.; Reinbold, C.; Herms, S.; Teismann, H.; Moebus, S.; Grabe, H. J. et al.; Noethen, M.; Amunts, K.; Eickhoff, S.; Mueller-Myhsok, B.; Cichon, S.: GENETIC FACTORS INFLUENCING THE COMMON NEUROBIOLOGICAL SUBSTRATE FOR MENTAL DISORDERS. In EUROPEAN NEUROPSYCHOPHARMACOLOGY, 29, S. S798 - S798. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, 13. Oktober 2017 - 17. Oktober 2017. (2019)

Arloth, J.; Eraslan, G.; Andlauer, T.; Gieger, C.; Gold, R.; Heilmann-Heimbach, S.; Kacprowski, T.; Meitinger, T.; Laudes, M.; Luessi, F. et al.; Mueller-Myhsok, B.; Nischwitz, S.; Peters, A.; Paul, F.; Rawal, R.; Strauch, K.; Wiendl, H.; Hemmer, B.; Theis, F.; Binder, E.; Mueller, N.: Identification of functionally relevant genetic variants associated with multiple sclerosis using deep learning. In MULTIPLE SCLEROSIS JOURNAL, 25, S. 906 - 907. 35th Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS) / 24th Annual Conference of Rehabilitation in MS, Stockholm, SWEDEN, 11. September 2019 - 13. September 2019. (2019)

Foo, J.; Trautmann, N.; Sticht, C.; Treutlein, J.; Frank, J.; Streit, F.; Witt, S.; Sirignano, L.; Chen, J.; Mueller-Myhsok, B. et al.; Meyer-Lindenberg, A.; Witt, C.; Gilles, M.; Deuschle, M.; Rietschel, M.: LONGITUDINAL TRANSCRIPTOME-WIDE GENE EXPRESSION ANALYSIS OF SLEEP DEPRIVATION TREATMENT INDICATES INVOLVEMENT OF CIRCADIAN GENES AND IMMUNE PATHWAYS. In EUROPEAN NEUROPSYCHOPHARMACOLOGY, 29, S. S136 - S136. 27th World Congress of Psychiatric Genetics (WCPG), Los Angeles, CA, 26. Oktober 2019 - 31. Oktober 2019. (2019)

Gampawar, P.; Saba, Y.; Werner, U.; Schmidt, R.; Mueller-Myhsok, B.; Schmidt, H.: Establishing high sensitivity and specificity for exome sequencing on Ion Proton. In EUROPEAN JOURNAL OF HUMAN GENETICS, 27, S. 1636 - 1636. 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, SWEDEN, 15. Juni 2019 - 18. Juni 2019. (2019)

Halldorsdottir, T.; Kurtoic, D.; Mueller-Myhsok, B.; Binder, E.; Blair, C.: Neurobiology of Self-Regulation: Longitudinal Influence of FKBP5 Intimate Partner Violence on Emotional and Cognitive Development in Childhood. In JOURNAL OF NEURAL TRANSMISSION, 126 (11), S. 1569 - 1570. International Congress of the World-Association-for-Stress-Related-and-Anxiety-Disorders (WASAD), Wurzburg, GERMANY, 03. Oktober 2019 - 05. Oktober 2019. (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, S. S928 - S928. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, 13. Oktober 2017 - 17. Oktober 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, S. 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, 11. September 2019 - 13. September 2019. (2019)

Pain, O.; Hodgson, K.; Trubetskoy, V.; Baune, B.; Biernacka, J.; Fabbri, C.; Lewis, G.; Li, Q.; Mueller-Myhsok, B.; Perroud, N. et al.; Serretti, A.; McIntosh, A.; Lewis, C.: INVESTIGATING THE COMMON GENETIC BASIS OF ANTIDEPRESSANT RESPONSE. In EUROPEAN NEUROPSYCHOPHARMACOLOGY, 29, S. S91 - S92. 27th World Congress of Psychiatric Genetics (WCPG), Los Angeles, CA, 26. Oktober 2019 - 31. Oktober 2019. (2019)

Tilch, E.; Zhao, C.; Salminen, A.; Antic, A.; Schormair, B.; Oexle, K.; Sampson, J. B.; Muller-Myhsok, B.; Winkelmann, J.: Explaining RLS families using risk SNPs from GWAS. In EUROPEAN JOURNAL OF HUMAN GENETICS, 27, S. 658 - 659. (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, S. 842 - 843. 32nd Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS), London, ENGLAND, 14. September 2016 - 17. September 2016. (2016)

Stalder, T.; Ising, M.; von Klitzing, K.; Sierau, S.; Michel, A.; Klein, A.; Andreas, A.; Keil, J.; Resch, L.; Müller-Myhsok, B. et al.; Uhr, M.; Gausche, R.; Manly, J. T.; Crowley, M. J.; Kirschbaum, C.; White, L. O.: Hair cortisol in maltreated children and adolescents: Importance of developmental period and maltreatment characteristics. In PSYCHONEUROENDOCRINOLOGY, 71 (S), S. 73 - 73. 46th Annual Conference of the International-Society-of-Psychoneuroendocrinology - Personalized Medicine in the Neurosciences - Genetics, Imaging, and Hormones, Miami, FL, 08. September 2016 - 11. September 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, S. 144 - 144. 31st Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis (ECTRIMS), Barcelona, SPAIN, 07. Oktober 2015 - 10. Oktober 2015. Sage Publications Inc., London, EC1Y 1SP (2015)

Buck, D.; Dankowski, T.; Bayas, A.; Gold, R.; Heesen, C.; Hohlfeld, R.; Kieseier, B. C.; Lieb, W.; Limmroth, V.; Linker, R. et al.; Mueller-Myhsok, B.; Noethen, M. M.; Paul, F.; Stangel, M.; Tackenberg, B.; Bergh, F. T.; Tumani, H.; Weber, F.; Wiendl, H.; Wildemann, B.; Zettl, U. K.; Ziemann, U.; Zipp, F.; Ziegler, A.; Hemmer, B.: Exome array GWAS in 10,000 Germans identifies association between MUC22 and multiple sclerosis. In EUROPEAN JOURNAL OF NEUROLOGY, 22 (SI) Supplement 1 Aufl., O1113, S. 29 - 29. 1st Congress of the European-Academy-of-Neurology, Berlin, GERMANY, 2015. Wiley-Blackwell, Hoboken, NJ 07030-5774, USA (2015)