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Items where Author is "Børglum, Anders D."

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Number of items: 4.

2021

Demontis, Ditte and Walters, Raymond K. and Rajagopal, Veera M. and Waldman, Irwin D. and Grove, Jakob and Als, Thomas D. and Dalsgaard, Søren and Ribasés, Marta and Bybjerg-Grauholm, Jonas and Bækvad-Hansen, Maria and Werge, Thomas and Nordentoft, Merete and Mors, Ole and Mortensen, Preben Bo and ADHD Working Group of the Psychiatric Genomics Consortium, and Cormand, Bru and Hougaard, David M. and Neale, Benjamin M. and Franke, Barbara and Faraone, Stephen V. and Børglum, Anders D.. (2021) Risk Variants and Polygenic Architecture of Disruptive Behavior Disorders in the Context of Attention-Deficit/Hyperactivity Disorder. Nature Communications, 12 (1). p. 1166.

2019

Demontis, Ditte and Walters, Raymond K. and Martin, Joanna and Mattheisen, Manuel and Als, Thomas D. and Agerbo, Esben and Baldursson, Gísli and Belliveau, Rich and Bybjerg-Grauholm, Jonas and Bækvad-Hansen, Marie and Cerrato, Felecia and Chambert, Kimberly and Churchhouse, Claire and Dumont, Ashley and Eriksson, Nicholas and Gandal, Michael and Goldstein, Jacqueline I. and Grasby, Katrina L. and Grove, Jakob and Gudmundsson, Olafur O. and Hansen, Christine S. and Hauberg, Mads Engel and Hollegaard, Mads V. and Howrigan, Daniel P. and Huang, Hailiang and Maller, Julian B. and Martin, Alicia R. and Martin, Nicholas G. and Moran, Jennifer and Pallesen, Jonatan and Palmer, Duncan S. and Pedersen, Carsten Bøcker and Pedersen, Marianne Giørtz and Poterba, Timothy and Poulsen, Jesper Buchhave and Ripke, Stephan and Robinson, Elise B. and Satterstrom, F. Kyle and Stefansson, Hreinn and Stevens, Christine and Turley, Patrick and Walters, G. Bragi and Won, Hyejung and Wright, Margaret J. and Adhd Working Group of the Psychiatric Genomics Consortium, and Early Lifecourse, and Genetic Epidemiology Consortium, and Andreassen, Ole A. and Asherson, Philip and Burton, Christie L. and Boomsma, Dorret I. and Cormand, Bru and Dalsgaard, Søren and Franke, Barbara and Gelernter, Joel and Geschwind, Daniel and Hakonarson, Hakon and Haavik, Jan and Kranzler, Henry R. and Kuntsi, Jonna and Langley, Kate and Lesch, Klaus-Peter and Middeldorp, Christel and Reif, Andreas and Rohde, Luis Augusto and Roussos, Panos and Schachar, Russell and Sklar, Pamela and Sonuga-Barke, Edmund J. S. and Sullivan, Patrick F. and Thapar, Anita and Tung, Joyce Y. and Waldman, Irwin D. and Medland, Sarah E. and Stefansson, Kari and Nordentoft, Merete and Hougaard, David M. and Werge, Thomas and Mors, Ole and Mortensen, Preben Bo and Daly, Mark J. and Faraone, Stephen V. and Børglum, Anders D. and Neale, Benjamin M.. (2019) Discovery of the First Genome-Wide Significant Risk Loci for Attention Deficit/Hyperactivity Disorder. Nature Genetics, 51 (1). pp. 63-75.

2018

Martin, Joanna and Walters, Raymond K. and Demontis, Ditte and Mattheisen, Manuel and Lee, S. Hong and Robinson, Elise and Brikell, Isabell and Ghirardi, Laura and Larsson, Henrik and Lichtenstein, Paul and Eriksson, Nicholas and Mountain View, California. and Psychiatric Genomics Consortium: Adhd Subgroup, and iPsych–Broad Adhd Workgroup, and Werge, Thomas and Mortensen, Preben Bo and Pedersen, Marianne Giørtz and Mors, Ole and Nordentoft, Merete and Hougaard, David M. and Bybjerg-Grauholm, Jonas and Wray, Naomi R. and Franke, Barbara and Faraone, Stephen V. and O'Donovan, Michael C. and Thapar, Anita and Børglum, Anders D. and Neale, Benjamin M.. (2018) A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder. Biological Psychiatry, 83 (12). pp. 1044-1053.

2015

Luo, Xiong-Jian and Mattheisen, Manuel and Li, Ming and Huang, Liang and Rietschel, Marcella and Børglum, Anders D. and Als, Thomas D. and van den Oord, Edwin J. and Aberg, Karolina A. and Mors, Ole and Mortensen, Preben Bo and Luo, Zhenwu and Degenhardt, Franziska and Cichon, Sven and Schulze, Thomas G. and Nöthen, Markus M. and iPSYCH-GEMS, SCZ working group and MooDS, SCZ Consortium and Su, Bing and Zhao, Zhongming and Gan, Lin and Yao, Yong-Gang. (2015) Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function. Schizophrenia Bulletin, 41 (6). pp. 1294-1308.

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