Publications Bertram Müller-Myhsok

Journal Article (21)

1.
Journal Article
Gialluisi, A.; Andlauer, T. F. M.; Mirza-Schreiber, N.; Moll, K.; Becker, J.; Hoffmann, P.; Ludwig, K. U.; Czamara, D.; St Pourcain, B.; Honbolygo, F. et al.: Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. MOLECULAR PSYCHIATRY (2020)
2.
Journal Article
Glanville, K. P.; Coleman I, J. R.; Hanscombe, K. B.; Euesden, J.; Choi, S. W.; Purves, K. L.; Breen, G.; Air, T. M.; Andlauer, T. F. M.; Baune, B. T. et al.: Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression. BIOLOGICAL PSYCHIATRY 87 (5), pp. 419 - 430 (2020)
3.
Journal Article
Andlauer, T. F. M.; Link, J.; Martin, D.; Ryner, M.; Hermanrud, C.; Grummel, V.; Auer, M.; Hegen, H.; Aly, L.; Gasperi, C. et al.: Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. BMC MEDICINE 18 (1), 298 (2020)
4.
Journal Article
Arloth, J.; Eraslan, G.; Andlauer, T. F. M.; Martins, J.; Iurato, S.; Kuehnel, B.; Waldenberger, M.; Frank, J.; Gold, R.; Hemmer, B. et al.: DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning. PLOS COMPUTATIONAL BIOLOGY 16 (2), e1007616 (2020)
5.
Journal Article
Cai, N.; Revez, J. A.; Adams, M. J.; Andlauer, T. F. M.; Breen, G.; Byrne, E. M.; Clarke, T.-K.; Forstner, A. J.; Grabe, H. J.; Hamilton, S. P. et al.: Minimal phenotyping yields genome-wide association signals of low specificity for major depression. NATURE GENETICS 52 (4), pp. 437 - 447 (2020)
6.
Journal Article
Chaichoompu, K.; Abegaz, F.; Cavadas, B.; Fernandes, V.; Mueller-Myhsok, B.; Pereira, L.; Van Steen, K.: A different view on fine-scale population structure in Western African populations. SI 139 (1), pp. 45 - 59 (2020)
7.
Journal Article
Coleman, J. R. I.; Peyrot, W. J.; Purves, K. L.; Davis, K. A. S.; Rayner, C.; Choi, S. W.; Hubel, C.; Gaspar, H. A.; Kan, C.; Van der Auwera, S. et al.: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. MOLECULAR PSYCHIATRY 25 (7), pp. 1430 - 1446 (2020)
8.
Journal Article
Faber, H.; Kurtoic, D.; Krishnamoorthy, G.; Weber, P.; Puetz, B.; Mueller-Myhsok, B.; Weber, F.; Andlauer, T. F. M.: Gene Expression in Spontaneous Experimental Autoimmune Encephalomyelitis Is Linked to Human Multiple Sclerosis Risk Genes. FRONTIERS IN IMMUNOLOGY 11, 2165 (2020)
9.
Journal Article
Filosi, M.; Kam-Thong, T.; Essioux, L.; Muglia, P.; Trabetti, E.; Spooren, W.; Muller-Myhsok, B.; Domenic, E.: Transcriptome signatures from discordant sibling pairs reveal changes in peripheral blood immune cell composition in Autism Spectrum Disorder. TRANSLATIONAL PSYCHIATRY 10 (1), 106 (2020)
10.
Journal Article
Gola, D.; Erdmann, J.; Lall, K.; Magi, R.; Mueller-Myhsok, B.; Schunkert, H.; Konig, I. R.: Population Bias in Polygenic Risk Prediction Models for Coronary Artery Disease. CIRCULATION-GENOMIC AND PRECISION MEDICINE 13 (6), pp. 569 - 575 (2020)
11.
Journal Article
Gola, D.; Erdmann, J.; Mueller-Myhsok, B.; Schunkert, H.; Koenig, I.: Population Stratification in Polygenic Risk Prediction Models for Coronary Artery Disease. HUMAN HEREDITY 84 (4-5), pp. 209 - 210 (2020)
12.
Journal Article
Gola, D.; Erdmann, J.; Mueller-Myhsok, B.; Schunkert, H.; Koenig, I. R.: Polygenic risk scores outperform machine learning methods in predicting coronary artery disease status. GENETIC EPIDEMIOLOGY 44 (2), pp. 125 - 138 (2020)
13.
Journal Article
Grasby, K. L.; Jahanshad, N.; Painter, J. N.; Colodro-Conde, L.; Bralten, J.; Hibar, D. P.; Lind, P. A.; Pizzagalli, F.; Ching, C. R. K.; McMahon, M. A. B. et al.: The genetic architecture of the human cerebral cortex. SI 367 (6484), pp. 1340 - + (2020)
14.
Journal Article
Grimm, T.; Garshasbi, M.; Puettmann, L.; Chen, W.; Ullmann, R.; Muller-Myhsok, B.; Klopocki, E.; Herbst, L.; Haug, J.; Jensen, L. R. et al.: A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q. ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 48 (6), pp. 478 - 489 (2020)
15.
Journal Article
Hagenaars, S. P.; Coleman I, J. R.; Choi, S. W.; Gaspar, H.; Adams, M. J.; Howard, D. M.; Hodgson, K.; Traylor, M.; Air, T. M.; Andlauer, T. F. M. et al.: Genetic comorbidity between major depression and cardio-metabolic traits, stratified by age at onset of major depression. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 183 (6), pp. 309 - 330 (2020)
16.
Journal Article
Meller, T.; Schmitt, S.; Stein, F.; Brosch, K.; Grotegerd, D.; Dohm, K.; Meinert, S.; Andlauer, T. F. M.; Rietschel, M.; Mueller-Myhsok, B. et al.: IMPACT OF POLYGENIC AND POLY-ENVIRONMENTAL RISK FACTORS ON A PSYCHOSIS RISK PHENOTYPE EXPLAINED THROUGH BRAIN STRUCTURE. SCHIZOPHRENIA BULLETIN 46, pp. S35 - S36 (2020)
17.
Journal Article
Tilch, E.; Schormair, B.; Zhao, C.; Salminen, A.; Nikolic, A. A.; Holzknecht, E.; Hoegl, B.; Poewe, W.; Bachmann, C.; Paulus, W. et al.: Deep targeted-NGS identifies RLS genes by differential burden with low-frequency variants and differential target sequencing depth. EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), p. 415 - 415 (2020)
18.
Journal Article
Tilch, E.; Schormair, B.; Zhao, C.; Salminen V, A.; Nikolic, A. A.; Holzknecht, E.; Hoegl, B.; Poewe, W.; Bachmann, C. G.; Paulus, W. et al.: Identification of Restless Legs Syndrome Genes by Mutational Load Analysis. ANNALS OF NEUROLOGY 87 (2), pp. 184 - 193 (2020)
19.
Journal Article
Weeger, J.; Ising, M.; Mueller-Myhsok, B.; Uhr, M.; Schmidt, U.; Steiger, A.: Salivary cortisol response to psychosocial stress in the late evening depends on CRHR1 genotype. PSYCHONEUROENDOCRINOLOGY 116, 104685 (2020)
20.
Journal Article
Weeger, J.; Ising, M.; Mueller-Myhsok, B.; Uhr, M.; Schmidt, U.; Yassouridis, A.; Steiger, A.: Influence of CRHR1 genotype on sleep and cortisol of healthy volunteers after Trier Social Stress Test in the late evening. JOURNAL OF SLEEP RESEARCH 29, pp. 117 - 118 (2020)
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