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Kappelmann, Nils, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X and Kopf-Beck, Johannes
(2021) Adapting the randomised controlled trial (RCT) for precision medicine: introducing the nested-precision RCT (npRCT). TRIALS, 22 (1). 13-.


Bordes, Joeri, Miranda, Lucas, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X and Schmidt, Mathias V
(2023) Advancing social behavioral neuroscience by integrating ethology and comparative psychology methods through machine learning. NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 151. 105243-.


Direk, Nese, Williams, Stephanie, Smith, Jennifer A, Ripke, Stephan, Air, Tracy, Amare, Azmeraw T, Amin, Najaf, Baune, Bernhard T, Bennett, David A, Blackwood, Douglas HR
et al (show 92 more authors) (2017) An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype. BIOLOGICAL PSYCHIATRY, 82 (5). pp. 322-329.


de Jong, Simone, Abdalla Diniz, Mateus Jose, Saloma, Andiara, Gadelha, Ary, Santoro, Marcos L, Ota, Vanessa K, Noto, Cristiano, Curtis, Charlesg, Newhouse, Stephen J, Patel, Hamel
et al (show 362 more authors) (2018) Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. COMMUNICATIONS BIOLOGY, 1 (1). 163-.


Marini, Sandro, Crawford, Katherine, Morotti, Andrea, Lee, Myung J, Pezzini, Alessandro, Moomaw, Charles J, Flaherty, Matthew L, Montaner, Joan, Roquer, Jaume, Jimenez-Conde, Jordi
et al (show 243 more authors) (2019) Association of Apolipoprotein E With Intracerebral Hemorrhage Risk by Race/Ethnicity A Meta-analysis. JAMA NEUROLOGY, 76 (4). pp. 480-491.


Meller, Tina, Schmitt, Simon, Stein, Frederike, Brosch, Katharina, Mosebach, Johannes, Yueksel, Dilara, Zaremba, Dario, Grotegerd, Dominik, Dohm, Katharina, Meinert, Susanne
et al (show 18 more authors) (2019) Associations of schizophrenia risk genes <i>ZNF804A</i> and <i>CACNA1C</i> with schizotypy and modulation of attention in healthy subjects. SCHIZOPHRENIA RESEARCH, 208. pp. 67-75.


Pulit, Sara L, Weng, Lu-Chen, McArdle, Patrick F, Trinquart, Ludovic, Choi, Seung Hoan, Mitchell, Braxton D, Rosand, Jonathan, de Bakker, Paul IW, Benjamin, Emelia J, Ellinor, Patrick T
et al (show 351 more authors) (2018) Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes. NEUROLOGY-GENETICS, 4 (6). e293-.


Bordes, Joeri, Miranda, Lucas, Reinhardt, Maya, Narayan, Sowmya, Hartmann, Jakob, Newman, Emily L, Brix, Lea Maria, van Doeselaar, Lotte, Engelhardt, Clara, Dillmann, Larissa
et al (show 6 more authors) (2023) Automatically annotated motion tracking identifies a distinct social behavioral profile following chronic social defeat stress. NATURE COMMUNICATIONS, 14 (1). 4319-.


Andlauer, Till FM, Guzman-Parra, Jose, Streit, Fabian, Strohmaier, Jana, Gonzalez, Maria Jose, Gil Flores, Susana, Cabaleiro Fabeiro, Francisco J, del Rio Noriega, Francisco, Perez, Fermin Perez, Haro Gonzalez, Jesus
et al (show 20 more authors) (2021) Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders. MOLECULAR PSYCHIATRY, 26 (4). pp. 1286-1298.


Mercer, Louise, Cookson, Alex, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X and van Vuuren, Julie
(2023) Burnout and secondary traumatic stress in staff working with people with intellectual disabilities: The role of adverse childhood experiences, resilience and trauma-informed organisational climate. JOURNAL OF APPLIED RESEARCH IN INTELLECTUAL DISABILITIES, 36 (6). pp. 1297-1307.


Klein, Ana, Selter, Rebecca C, Hapfelmeier, Alexander, Berthele, Achim, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Pongratz, Viola, Gasperi, Christiane, Zimmer, Claus, Muehlau, Mark and Hemmer, Bernhard
(2019) CSF parameters associated with early MRI activity in patients with MS. NEUROLOGY-NEUROIMMUNOLOGY & NEUROINFLAMMATION, 6 (4). e573-.


Glanville, Kylie P, Coleman, Jonathan RI, Hanscombe, Ken B, Euesden, Jack, Choi, Shing Wan, Purves, Kirstin L, Breen, Gerome, Air, Tracy M, Andlauer, Till FM, Baune, Bernhard T
et al (show 197 more authors) (2020) Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression. BIOLOGICAL PSYCHIATRY, 87 (5). pp. 419-430.


White, Lars O, Ising, Marcus, von Klitzing, Kai, Sierau, Susan, Michel, Andrea, Klein, Annette M, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Uhr, Manfred, Crowley, Michael J, Kirschbaum, Clemens
et al (show 1 more authors) (2017) Commentary: The importance of exploring dose-dependent, subtype-specific, and age-related effects of maltreatment on the HPA axis and the mediating link to psychopathology. A response to Fisher (2017). JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY, 58 (9). pp. 1011-1013.


Xiao, Xiao, Wang, Lu, Wang, Chuang, Yuan, Ti-Fei, Zhou, Dongsheng, Zheng, Fanfan, Li, Lingyi, Grigoroiu-Serbanescu, Maria, Ikeda, Masashi, Iwata, Nakao
et al (show 27 more authors) (2017) Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders. TRANSLATIONAL PSYCHIATRY, 7 (12). 1273-.


Rost, Nicolas, Bruckl, Tanja M, Koutsouleris, Nikolaos, Binder, Elisabeth B and Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X
(2022) Creating sparser prediction models of treatment outcome in depression: a proof-of-concept study using simultaneous feature selection and hyperparameter tuning. BMC MEDICAL INFORMATICS AND DECISION MAKING, 22 (1). 181-.


Iurato, Stella, Carrillo-Roa, Tania, Arloth, Janine, Czamara, Darina, Diener-Hoelzl, Laura, Lange, Jennifer, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Binder, Elisabeth B and Erhardt, Angelika
(2017) DNA Methylation signatures in panic disorder. TRANSLATIONAL PSYCHIATRY, 7 (12). 1287-.


Moser, Sylvain, Martins, Jade, Czamara, Darina, Lange, Jennifer, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X and Erhardt, Angelika
(2022) DNA-methylation dynamics across short-term, exposure-containing CBT in patients with panic disorder. TRANSLATIONAL PSYCHIATRY, 12 (1). 46-.


Buck, Dorothea, Andlauer, Till FM, Igl, Wilmar, Wicklein, Eva-Maria, Muehlau, Mark, Weber, Frank, Koechert, Karl, Pohl, Christoph, Arnason, Barry, Comi, Giancarlo
et al (show 11 more authors) (2019) Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials. MULTIPLE SCLEROSIS JOURNAL, 25 (4). pp. 565-573.


Schmitt, Simon, Meller, Tina, Stein, Frederike, Brosch, Katharina, Ringwald, Kai, Pfarr, Julia-Katharina, Bordin, Clemens, Peusch, Nina, Steinstrater, Olaf, Grotegerd, Dominik
et al (show 17 more authors) (2022) Effects of polygenic risk for major mental disorders and cross-disorder on cortical complexity. PSYCHOLOGICAL MEDICINE, 52 (16). pp. 4127-4138.


Zannas, Anthony S, Jia, Meiwen, Hafner, Kathrin, Baumert, Jens, Wiechmann, Tobias, Pape, Julius C, Arloth, Janine, Koedel, Maik, Martinelli, Silvia, Roitman, Maria
et al (show 23 more authors) (2019) Epigenetic upregulation of FKBP5 by aging and stress contributes to NF-kappa B-driven inflammation and cardiovascular risk. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 116 (23). pp. 11370-11379.


Gampawar, Piyush, Saba, Yasaman, Werner, Ulrike, Schmidt, Reinhold, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X and Schmidt, Helena
(2019) Evaluation of the Performance of AmpliSeq and SureSelect Exome Sequencing Libraries for Ion Proton. FRONTIERS IN GENETICS, 10 (SEP). 856-.


Foo, Jerome C, Streit, Fabian, Frank, Josef, Witt, Stephanie H, Treutlein, Jens, Baune, Bernhard T, Moebus, Susanne, Joeckel, Karl-Heinz, Forstner, Andreas J, Noethen, Markus M
et al (show 195 more authors) (2019) Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 180 (1). pp. 35-45.


Polimanti, Renato, Peterson, Roseann E, Ong, Jue-Sheng, MacGregor, Stuart, Edwards, Alexis C, Clarke, Toni-Kim, Frank, Josef, Gerring, Zachary, Gillespie, Nathan A, Lind, Penelope A
et al (show 362 more authors) (2019) Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium. PSYCHOLOGICAL MEDICINE, 49 (7). pp. 1218-1226.


Walton, E, Hibar, D, Yilmaz, Z, Jahanshad, N, Cheung, J, Batury, V-L, Seitz, J, Bulik, CM, Thompson, PM, Ehrlich, Stefan
et al (show 500 more authors) (2019) Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa. MOLECULAR NEUROBIOLOGY, 56 (7). pp. 5146-5156.


Renzi, Chiara, Provencal, Nadine, Bassil, Katherine C, Evers, Kathinka, Kihlbom, Ulrik, Radford, Elizabeth J, Koupil, Ilona, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Hansson, Mats G and Rutten, Bart PF
(2018) From Epigenetic Associations to Biological and Psychosocial Explanations in Mental Health. NEUROEPIGENETICS AND MENTAL ILLNESS, 158. pp. 299-323.


Gergei, Ingrid, Zheng, Jie, Andlauer, Till FM, Brandenburg, Vincent, Mirza-Schreiber, Nazanin, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Kraemer, Bernhard K, Richard, Daniel, Falk, Louise, Moverare-Skrtic, Sofia
et al (show 5 more authors) (2022) GWAS meta-analysis followed by Mendelian randomization revealed potential control mechanisms for circulating alpha-Klotho levels. HUMAN MOLECULAR GENETICS, 31 (5). pp. 792-802.


Mullins, Niamh, Bigdeli, Tim B, Borglum, Anders D, Coleman, Jonathan RI, Demontis, Ditte, Mehta, Divya, Power, Robert A, Ripke, Stephan, Stahl, Eli A, Starnawska, Anna
et al (show 108 more authors) (2019) GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. American Journal of Psychiatry, 176 (8). pp. 651-660.


Faber, Hans, Kurtoic, Dunja, Krishnamoorthy, Gurumoorthy, Weber, Peter, Puetz, Benno, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Weber, Frank and Andlauer, Till FM
(2020) Gene Expression in Spontaneous Experimental Autoimmune Encephalomyelitis Is Linked to Human Multiple Sclerosis Risk Genes. FRONTIERS IN IMMUNOLOGY, 11. 2165-.


Muehleisen, Thomas W, Reinbold, Celine S, Forstner, Andreas J, Abramova, Lilia I, Alda, Martin, Babadjanova, Gulja, Bauer, Michael, Brennan, Paul, Chuchalin, Alexander, Cruceanu, Cristiana
et al (show 54 more authors) (2018) Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder. JOURNAL OF AFFECTIVE DISORDERS, 228. pp. 20-25.


Zhao, Huiying, Eising, Else, de Vries, Boukje, Vijfhuizen, Lisanne S, Anttila, Verneri, Winsvold, Bendik S, Kurth, Tobias, Stefansson, Hreinn, Kallela, Mikko, Malik, Rainer
et al (show 26 more authors) (2016) Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. CEPHALALGIA, 36 (7). pp. 648-657.


Treutlein, Jens, Frank, Josef, Streit, Fabian, Reinbold, Celine S, Juraeva, Dilafruz, Degenhardt, Franziska, Rietschel, Liz, Witt, Stephanie H, Forstner, Andreas J, Ridinger, Monika
et al (show 32 more authors) (2017) Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis. GENES, 8 (7). E183-.


Becker, Jessica, Czamara, Darina, Scerri, Tom S, Ramus, Franck, Csepe, Valeria, Talcott, Joel B, Stein, John, Morris, Andrew, Ludwig, Kerstin U, Hoffmann, Per
et al (show 31 more authors) (2014) Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. EUROPEAN JOURNAL OF HUMAN GENETICS, 22 (5). pp. 675-680.


Pang, Shichao, Yengo, Loic, Nelson, Christopher P, Bourier, Felix, Zeng, Lingyao, Li, Ling, Kessler, Thorsten, Erdmann, Jeanette, Maegi, Reedik, Laell, Kristi
et al (show 5 more authors) (2022) Genetic and modifiable risk factors combine multiplicatively in common disease. CLINICAL RESEARCH IN CARDIOLOGY, 112 (2). pp. 247-257.


Satizabal, Claudia L, Adams, Hieab HH, Hibar, Derrek P, White, Charles C, Knol, Maria J, Stein, Jason L, Scholz, Markus, Sargurupremraj, Muralidharan, Jahanshad, Neda, Roshchupkin, Gennady V
et al (show 279 more authors) (2019) Genetic architecture of subcortical brain structures in 38,851 individuals. NATURE GENETICS, 51 (11). 1624-+.


Hagenaars, Saskia P, Coleman, Jonathan RI, Choi, Shing Wan, Gaspar, Helena, Adams, Mark J, Howard, David M, Hodgson, Karen, Traylor, Matthew, Air, Tracy M, Andlauer, Till FM
et al (show 38 more authors) (2020) 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.


Andlauer, Till FM, Muehleisen, Thomas W, Hoffstaedter, Felix, Teumer, Alexander, Wittfeld, Katharina, Teuber, Anja, Reinbold, Celine S, Grotegerd, Dominik, Buelow, Robin, Caspers, Svenja
et al (show 18 more authors) (2021) Genetic factors influencing a neurobiological substrate for psychiatric disorders. TRANSLATIONAL PSYCHIATRY, 11 (1). 192-.


Kim-Hellmuth, Sarah, Bechheim, Matthias, Puetz, Benno, Mohammadi, Pejman, Nedelec, Yohann, Giangreco, Nicholas, Becker, Jessica, Kaiser, Vera, Fricker, Nadine, Beier, Esther
et al (show 9 more authors) (2017) Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations. NATURE COMMUNICATIONS, 8 (1). 266-.


Amin, Najaf, Allebrandt, Karla V, van der Spek, Ashley, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tonu, van Mill, Josine G, Mbarek, Hamdi
et al (show 64 more authors) (2016) Genetic variants in <i>RBFOX3</i> are associated with sleep latency. EUROPEAN JOURNAL OF HUMAN GENETICS, 24 (10). pp. 1488-1495.


Hahn, Tim, Winter, Nils R, Ernsting, Jan, Gruber, Marius, Mauritz, Marco J, Fisch, Lukas, Leenings, Ramona, Sarink, Kelvin, Blanke, Julian, Holstein, Vincent
et al (show 20 more authors) (2023) Genetic, individual, and familial risk correlates of brain network controllability in major depressive disorder. MOLECULAR PSYCHIATRY, 28 (3). pp. 1057-1063.


Zeng, Yanni, Navarro, Pau, Shirali, Masoud, Howard, David M, Adams, Mark J, Hall, Lynsey S, Clarke, Toni-Kim, Thomson, Pippa A, Smith, Blair H, Murray, Alison
et al (show 29 more authors) (2017) Genome-wide Regional Heritability Mapping Identifies a Locus Within the <i>TOX2</i> Gene Associated With Major Depressive Disorder. BIOLOGICAL PSYCHIATRY, 82 (5). pp. 312-321.


Wray, Naomi R, Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M, Abdellaoui, Abdel, Adams, Mark J, Agerbo, Esben, Air, Tracy M, Andlauer, Till MF
et al (show 208 more authors) (2018) Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. NATURE GENETICS, 50 (05). pp. 668-681.


Gialluisi, Alessandro, Andlauer, Till FM, Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U, Czamara, Darina, St Pourcain, Beate, Brandler, William
et al (show 35 more authors) (2019) Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. TRANSLATIONAL PSYCHIATRY, 9 (1). 77-.


Gialluisi, Alessandro, Andlauer, Till FM, Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U, Czamara, Darina, St Pourcain, Beate, Honbolygo, Ferenc
et al (show 39 more authors) (2021) Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. MOLECULAR PSYCHIATRY, 26 (7). pp. 3004-3017.


Arnau-Soler, Aleix, Macdonald-Dunlop, Erin, Adams, Mark J, Clarke, Toni-Kim, MacIntyre, Donald J, Milburn, Keith, Navrady, Lauren, Hayward, Caroline, McIntosh, Andrew M, Thomson, Pippa A
et al (show 195 more authors) (2019) Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland. TRANSLATIONAL PSYCHIATRY, 9 (1). 14-.


Coleman, Jonathan RI, Peyrot, Wouter J, Purves, Kirstin L, Davis, Katrina AS, Rayner, Christopher, Choi, Shing Wan, Hubel, Christopher, Gaspar, Helena A, Kan, Carol, Van der Auwera, Sandra
et al (show 215 more authors) (2020) Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. MOLECULAR PSYCHIATRY, 25 (7). pp. 1430-1446.


Schulz, Herbert, Ruppert, Ann-Kathrin, Herms, Stefan, Wolf, Christiane, Mirza-Schreiber, Nazanin, Stegle, Oliver, Czamara, Darina, Forstner, Andreas J, Sivalingam, Sugirthan, Schoch, Susanne
et al (show 11 more authors) (2017) Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus. NATURE COMMUNICATIONS, 8 (1). 1511-.


Lee, Phil H, Anttila, Verneri, Won, Hyejung, Feng, Yen-Chen A, Rosenthal, Jacob, Zhu, Zhaozhong, Tucker-Drob, Elliot M, Nivard, Michel G, Grotzinger, Andrew D, Posthuma, Danielle
et al (show 592 more authors) (2019) Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. CELL, 179 (7). 1469-+.


Stalder, Tobias, Ising, Marcus, von Klitzing, Kai, Sierau, Susan, Michel, Andrea, Klein, Annette, Andreas, Anna, Keil, Jan, Resch, Leonhard, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X
et al (show 6 more authors) (2016) Hair cortisol in maltreated children and adolescents: Importance of developmental period and maltreatment characteristics. PSYCHONEUROENDOCRINOLOGY, 71. p. 73.


Heilbronner, Urs, Papiol, Sergi, Budde, Monika, Andlauer, Till FM, Strohmaier, Jana, Streit, Fabian, Frank, Josef, Degenhardt, Franziska, Heilmann-Heimbach, Stefanie, Witt, Stephanie H
et al (show 8 more authors) (2021) "The Heidelberg Five" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 186 (2). pp. 77-89.


Kraemer, Robert MM, Moissl, Angela PP, Lorkowski, Stefan, Kraemer, Bernhard KK, Lehtimaeki, Terho, Mishra, Binisha HH, Mishra, Pashupati PP, Leipe, Jan, Maerz, Winfried, Kleber, Marcus EE
et al (show 2 more authors) (2023) High genetic risk for depression as an independent risk factor for mortality in patients referred for coronary angiography. FRONTIERS IN CARDIOVASCULAR MEDICINE, 10. 1125151-.


Price, Kaitlyn M, Wigg, Karen G, Eising, Else, Feng, Yu, Blokland, Kirsten, Wilkinson, Margaret, Kerr, Elizabeth N, Guger, Sharon L, Abbondanza, Filippo, Allegrini, Andrea G
et al (show 80 more authors) (2022) Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities. TRANSLATIONAL PSYCHIATRY, 12 (1). 495-.


Tilch, Erik, Schormair, Barbara, Zhao, Chen, Salminen, Aaro V, Nikolic, Ana Antic, Holzknecht, Evi, Hoegl, Birgit, Poewe, Werner, Bachmann, Cornelius G, Paulus, Walter
et al (show 12 more authors) (2020) Identification of Restless Legs Syndrome Genes by Mutational Load Analysis. ANNALS OF NEUROLOGY, 87 (2). pp. 184-193.


Chang, Hong, Li, Lingyi, Peng, Tao, Grigoroiu-Serbanescu, Maria, Bergen, Sarah E, Landen, Mikael, Hultman, Christina M, Forstner, Andreas J, Strohmaier, Jana, Hecker, Julian
et al (show 16 more authors) (2017) Identification of a Bipolar Disorder Vulnerable Gene <i>CHDH</i> at 3p21.1. MOLECULAR NEUROBIOLOGY, 54 (7). pp. 5166-5176.


Grove, Jakob, Ripke, Stephan, Als, Thomas D, Mattheisen, Manuel, Walters, Raymond K, Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A, Anney, Richard
et al (show 266 more authors) (2019) Identification of common genetic risk variants for autism spectrum disorder. NATURE GENETICS, 51 (3). 431-+.


Forstner, Andreas J, Hecker, Julian, Hofmann, Andrea, Maaser, Anna, Reinbold, Celine S, Muehleisen, Thomas W, Leber, Markus, Strohmaier, Jana, Degenhardt, Franziska, Treutlein, Jens
et al (show 59 more authors) (2017) Identification of shared risk loci and pathways for bipolar disorder and schizophrenia. PLOS ONE, 12 (2). e0171595-.


Pelin, Helena, Ising, Marcus, Stein, Frederike, Meinert, Susanne, Meller, Tina, Brosch, Katharina, Winter, Nils R, Krug, Axel, Leenings, Ramona, Lemke, Hannah
et al (show 20 more authors) (2021) Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning. NEUROPSYCHOPHARMACOLOGY, 46 (11). pp. 1895-1905.


Czamara, Darina, Eraslan, Goekcen, Page, Christian M, Lahti, Jari, Lahti-Pulkkinen, Marius, Hamalainen, Esa, Kajantie, Eero, Laivuori, Hannele, Villa, Pia M, Reynolds, Rebecca M
et al (show 219 more authors) (2019) Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. NATURE COMMUNICATIONS, 10 (1). 2548-.


Rivera, Margarita, Locke, Adam E, Corre, Tanguy, Czamara, Darina, Wolf, Christiane, Ching-Lopez, Ana, Milaneschi, Yuri, Kloiber, Stefan, Cohen-Woods, Sara, Rucker, James
et al (show 28 more authors) (2017) Interaction between the <i>FTO</i> gene, body mass index and depression: meta-analysis of 13701 individualst. BRITISH JOURNAL OF PSYCHIATRY, 211 (2). pp. 70-76.


Ringwald, Kai G, Meller, Tina, Schmitt, Simon, Andlauer, Till FM, Stein, Frederike, Brosch, Katharina, Pfarr, Julia-Katharina, Steinstraeter, Olaf, Meinert, Susanne, Lemke, Hannah
et al (show 16 more authors) (2021) Interaction of developmental factors and ordinary stressful life events on brain structure in adults. NEUROIMAGE-CLINICAL, 30. 102683-.


Zhou, Jiayan, Passero, Kristin, Palmiero, Nicole E, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Kleber, Marcus E, Maerz, Winfried and Hall, Molly A
(2020) Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. PLOS ONE, 15 (9). e0238304-.


Foo, Jerome C, Trautmann, Nina, Sticht, Carsten, Treutlein, Jens, Frank, Josef, Streit, Fabian, Witt, Stephanie H, De La Torre, Carolina, von Heydendorff, Steffen Conrad, Sirignano, Lea
et al (show 7 more authors) (2019) Longitudinal transcriptome-wide gene expression analysis of sleep deprivation treatment shows involvement of circadian genes and immune pathways. TRANSLATIONAL PSYCHIATRY, 9 (1). 343-.


Gupta, Juhi K ORCID: 0000-0002-8292-9846, Care, Angharad ORCID: 0000-0003-2131-0406, Goodfellow, Laura ORCID: 0000-0002-8111-5007, Alfirevic, Zarko, Lian, Lu-Yun, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Alfirevic, Ana ORCID: 0000-0002-2801-9817 and Phelan, Marie M
(2021) Metabolic profiling of maternal serum of women a high-risk of spontaneous preterm birth using NMR and MGWAS approach. BIOSCIENCE REPORTS, 41 (9). BSR20210759-.


Cai, Na, Revez, Joana A, Adams, Mark J, Andlauer, Till FM, Breen, Gerome, Byrne, Enda M, Clarke, Toni-Kim, Forstner, Andreas J, Grabe, Hans J, Hamilton, Steven P
et al (show 22 more authors) (2020) Minimal phenotyping yields genome-wide association signals of low specificity for major depression. NATURE GENETICS, 52 (4). 437-+.


Hall, Molly A, Wallace, John, Lucas, Anastasia M, Bradford, Yuki, Verma, Shefali S, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Passero, Kristin, Zhou, Jiayan, McGuigan, John, Jiang, Beibei
et al (show 11 more authors) (2021) Novel EDGE encoding method enhances ability to identify genetic interactions. PLOS GENETICS, 17 (6). e1009534-.


Hibar, Derrek P, Adams, Hieab HH, Jahanshad, Neda, Chauhan, Ganesh, Stein, Jason L, Hofer, Edith, Renteria, Miguel E, Bis, Joshua C, Arias-Vasquez, Alejandro, Ikram, M Kamran
et al (show 322 more authors) (2017) Novel genetic loci associated with hippocampal volume. NATURE COMMUNICATIONS, 8 (1). 13624-.


Passero, Kristin, He, Xi, Zhou, Jiayan, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Kleber, Marcus E, Maerz, Winfried and Hall, Molly A
(2020) Phenome-wide association studies on cardiovascular health and fatty acids considering phenotype quality control practices for epidemiological data. PACIFIC SYMPOSIUM ON BIOCOMPUTING 2020, 25 (2020). pp. 659-670.


Gola, Damian, Erdmann, Jeannette, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Schunkert, Heribert and Koenig, Inke R
(2020) Polygenic risk scores outperform machine learning methods in predicting coronary artery disease status. GENETIC EPIDEMIOLOGY, 44 (2). pp. 125-138.


White, Lars O, Ising, Marcus, von Klitzing, Kai, Sierau, Susan, Michel, Andrea, Klein, Annette M, Andreas, Anna, Keil, Jan, Quintero, Leonhard, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X
et al (show 6 more authors) (2017) Reduced hair cortisol after maltreatment mediates externalizing symptoms in middle childhood and adolescence. JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY, 58 (9). pp. 998-1007.


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This list was generated on Sat Apr 20 18:49:41 2024 BST.