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Number of items: 33.


Anttila, Verneri, Bulik-Sullivan, Brendan, Finucane, Hilary K, Walters, Raymond K, Bras, Jose, Duncan, Laramie, Escott-Price, Valentina, Falcone, Guido J, Gormley, Padhraig, Malik, Rainer
et al (show 561 more authors) (2018) Analysis of shared heritability in common disorders of the brain. SCIENCE, 360 (6395). 1313-+.


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-.


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.


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.


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.


Arloth, Janine, Eraslan, Gökcen, Andlauer, Till FM, Martins, Jade, Iurato, Stella, Kühnel, Brigitte, Waldenberger, Melanie, Frank, Josef, Gold, Ralf, Hemmer, Bernhard
et al (show 18 more authors) (2020) DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning. PLoS computational biology, 16 (2). e1007616-e1007616.


Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D, Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth
et al (show 137 more authors) (2022) Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics, 54 (11). pp. 1621-1629.


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.


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.


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.


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-.


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-.


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.


Eising, Else, Mirza-Schreiber, Nazanin, de Zeeuw, Eveline L, Wang, Carol A, Truong, Dongnhu T, Allegrini, Andrea G, Shapland, Chin Yang, Zhu, Gu, Wigg, Karen G, Gerritse, Margot L
et al (show 85 more authors) (2022) Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Proceedings of the National Academy of Sciences of the United States of America, 119 (35). e2202764119-e2202764119.


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.


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-+.


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.


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-.


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-+.


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-.


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-.


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-+.


Hahn, Tim, Jamalabadi, Hamidreza, Emden, Daniel, Goltermann, Janik, Ernsting, Jan, Winter, Nils R, Fisch, Lukas, Leenings, Ramona, Sarink, Kelvin, Holstein, Vincent
et al (show 24 more authors) (2021) A Network Control Theory Approach to Longitudinal Symptom Dynamics in Major Depressive Disorder. CoRR, abs/21.


Ostkamp, Patrick, Salmen, Anke, Pignolet, Beatrice, Goerlich, Dennis, Andlauer, Till FM, Schulte-Mecklenbeck, Andreas, Gonzalez-Escamilla, Gabriel, Bucciarelli, Florence, Gennero, Isabelle, Breuer, Johanna
et al (show 36 more authors) (2021) Sunlight exposure exerts immunomodulatory effects to reduce multiple sclerosis severity. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 118 (1). e2018457118-.


Paul, Riya, Andlauer, Till FM, Czamara, Darina, Hoehn, David, Lucae, Susanne, Puetz, Benno, Lewis, Cathryn M, Uher, Rudolf, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Ising, Marcus
et al (show 1 more authors) (2019) Treatment response classes in major depressive disorder identified by model-based clustering and validated by clinical prediction models. TRANSLATIONAL PSYCHIATRY, 9 (1). 187-.


Andlauer, Till FM, Link, Jenny, Martin, Dorothea, Ryner, Malin, Hermanrud, Christina, Grummel, Verena, Auer, Michael, Hegen, Harald, Aly, Lilian, Gasperi, Christiane
et al (show 11 more authors) (2020) Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. BMC MEDICINE, 18 (1). 298-.


Zeng, Lingyao, Moser, Sylvain, Mirza-Schreiber, Nazanin, Lamina, Claudia, Coassin, Stefan, Nelson, Christopher P, Annilo, Tarmo, Franzen, Oscar, Kleber, Marcus E, Mack, Salome
et al (show 25 more authors) (2022) <i>Cis</i>-epistasis at the <i>LPA</i> locus and risk of cardiovascular diseases. CARDIOVASCULAR RESEARCH, 118 (4). pp. 1088-1102.


van der Lee, Sven J ORCID: 0000-0003-1606-8643, Conway, Olivia J, Jansen, Iris, Carrasquillo, Minerva M, Kleineidam, Luca ORCID: 0009-0006-3309-6856, van den Akker, Erik, Hernández, Isabel, van Eijk, Kristel R, Stringa, Najada, Chen, Jason A
et al (show 98 more authors) (2019) A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity. Acta neuropathologica, 138 (2). pp. 237-250.

This list was generated on Sat Mar 23 12:29:18 2024 GMT.