نتائج البحث - Jonatan Pallesen
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1
Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci حسب Anders D. Børglum, Ditte Demontis, Jakob Grove, Jonatan Pallesen, Mads V. Hollegaard, Carsten Bøcker Pedersen, Anne Hedemand, Manuel Mattheisen, André G. Uitterlinden, Mette Nyegaard, Torben Ørntoft, Carsten Wiuf, Michael Didriksen, Merete Nordentoft, Markus M. Nöthen, Marcella Rietschel, Roel A. Ophoff, Sven Cichon, Robert H. Yolken, David M. Hougaard, Preben Bo Mortensen, Ole Mors
منشور في 2013Artigo -
2
Genome-wide association study implicates CHRNA2 in cannabis use disorder حسب Ditte Demontis, Veera M. Rajagopal, Thorgeir E. Thorgeirsson, Thomas D. Als, Jakob Grove, Kalle Leppälä, Daníel F. Guðbjartsson, Jonatan Pallesen, Carsten Hjorthøj, Gunnar W. Reginsson, Þórarinn Tyrfingsson, Valgerður Rúnarsdóttir, Per Qvist, Jane Christensen, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Laura M. Huckins, Eli A. Stahl, Allan Timmermann, Esben Agerbo, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Merete Nordentoft, Mark J. Daly, Hreinn Stefánsson, Kāri Stefánsson, Mette Nyegaard, Anders D. Børglum
منشور في 2019Artigo -
3
Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity حسب Veera M. Rajagopal, Andrea Ganna, Jonathan R. I. Coleman, Andrea G. Allegrini, Georgios Voloudakis, Jakob Grove, Thomas D. Als, Henriette Thisted Horsdal, Liselotte Petersen, Vivek Appadurai, Andrew J. Schork, Alfonso Buil, Cynthia M. Bulik, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, David M. Hougaard, Ole Mors, Merete Nordentoft, Thomas Werge, Rich Belliveau, Caitlin E. Carey, Felecia Cerrato, Kimberly Chambert, Tracy Air, Mark J. Daly, Ashley Dumont, Jacqueline I. Goldstein, Christine Søholm Hansen, Daniel P. Howrigan, Hailiang Huang, Julian Maller, Alicia R. Martin, Joanna Martin, Manuel Mattheisen, Jennifer L. Moran, Benjamin M. Neale, Jonatan Pallesen, Duncan S. Palmer, Carsten Bcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Stephan Ripke, F. Kyle Satterstrom, Wesley K. Thompson, Patrick Turley, Raymond K. Walters, Preben Bo Mortensen, Gerome Breen, Panos Roussos, Robert Plomin, Esben Agerbo, Anders D. Børglum, Ditte Demontis
منشور في 2023Artigo -
4
Discovery of the first genome-wide significant risk loci for ADHD حسب Ditte Demontis, Raymond K. Walters, Joanna Martin, Manuel Mattheisen, Thomas D. Als, Esben Agerbo, Rich Belliveau, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Felecia Cerrato, Kimberly Chambert, Tracy Air, Ashley Dumont, Nicholas Eriksson, Michael J. Gandal, Jacqueline I. Goldstein, Jakob Grove, Christine Søholm Hansen, Mads E. Hauberg, Mads V. Hollegaard, Daniel P. Howrigan, Hailiang Huang, Julian Maller, Joanna Martin, Jennifer L. Moran, Jonatan Pallesen, Duncan S. Palmer, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Jesper Buchhave Poulsen, Stephan Ripke, Elise Robinson, Kyle F. Satterstrom, Christine Stevens, Patrick Turley, Hyejung Won, Ole A. Andreassen, Christie L. Burton, Dorret I. Boomsma, Bru Cormand, Søren Dalsgaard, Barbara Franke, Joel Gelernter, Daniel H. Geschwind, Hákon Hákonarson, Jan Haavik, Henry R. Kranzler, Jonna Kuntsi, K. Langley, Klaus‐Peter Lesch, Christel M. Middeldorp, Andreas Reif, Luís Augusto Rohde, Panos Roussos, Russell Schachar, Pamela Sklar, Edmund Sonuga‐Barke, Patrick F. Sullivan, Anita Thapar, Joyce Y. Tung, Irwin D. Waldman, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Mark J. Daly, Stephen V. Faraone, Anders D. Børglum, Benjamin M. Neale
منشور في 2017Pré-impressão -
5
Common risk variants identified in autism spectrum disorder حسب Jakob Grove, Stephan Ripke, Thomas D. Als, Manuel Mattheisen, Raymond K. Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A. Andreassen, Richard Anney, Rich Belliveau, Francesco Bettella, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, Marie Bækved-Hansen, Felecia Cerrato, Kimberly Chambert, Jane Christensen, Tracy Air, Karin Dellenvall, Ditte Demontis, Silvia De Rubeis, Bernie Devlin, Srdjan Djurovic, Ashle Dumont, Jacqueline I. Goldstein, Christine Søholm Hansen, Mads E. Hauberg, Mads V. Hollegaard, Sigrun Hope, Daniel P. Howrigan, Hailiang Huang, Christina M. Hultman, Lambertus Klei, Julian Maller, Joanna Martin, Alicia R. Martin, Jennifer L. Moran, Mette Nyegaard, Terje Nærland, Duncan S. Palmer, Aarno Palotie, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Jesper Buchhave Poulsen, Beaté St Pourcain, Per Qvist, Karola Rehnström, Avi Reichenberg, Jennifer Reichert, Elise Robinson, Kathryn Roeder, Panos Roussos, Evald Sæmundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Hreinn Stefánsson, Kāri Stefánsson, Stacy Steinberg, Christine Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Daniel H. Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum
منشور في 2017Pré-impressão -
6
Identification of common genetic risk variants for autism spectrum disorder حسب Jakob Grove, Stephan Ripke, Thomas D. Als, Manuel Mattheisen, Raymond K. Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A. Andreassen, Richard Anney, Swapnil Awashti, Rich Belliveau, Francesco Bettella, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Felecia Cerrato, Kimberly Chambert, Jane Christensen, Tracy Air, Karin Dellenvall, Ditte Demontis, Silvia De Rubeis, Bernie Devlin, Srdjan Djurovic, Ashley Dumont, Jacqueline I. Goldstein, Christine Søholm Hansen, Mads E. Hauberg, Mads V. Hollegaard, Sigrun Hope, Daniel P. Howrigan, Hailiang Huang, Christina M. Hultman, Lambertus Klei, Julian Maller, Joanna Martin, Alicia R. Martin, Jennifer L. Moran, Mette Nyegaard, Terje Nærland, Duncan S. Palmer, Aarno Palotie, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy dPoterba, Jesper Buchhave Poulsen, Beaté St Pourcain, Per Qvist, Karola Rehnström, Abraham Reichenberg, Jennifer Reichert, Elise Robinson, Kathryn Roeder, Panos Roussos, Evald Sæmundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Hreinn Stefánsson, Stacy Steinberg, Christine Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Kāri Stefánsson, Daniel H. Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum
منشور في 2019Artigo -
7
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder حسب Ditte Demontis, Raymond K. Walters, Joanna Martin, Manuel Mattheisen, Thomas D. Als, Esben Agerbo, Gísli Baldursson, Rich Belliveau, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Felecia Cerrato, Kimberly Chambert, Tracy Air, Ashley Dumont, Nicholas Eriksson, Michael J. Gandal, Jacqueline I. Goldstein, Katrina L. Grasby, Jakob Grove, Ólafur Ó. Guðmundsson, Christine Søholm Hansen, Mads E. Hauberg, Mads V. Hollegaard, Daniel P. Howrigan, Hailiang Huang, Julian Maller, Alicia R. Martin, Nicholas G. Martin, Jennifer L. Moran, Jonatan Pallesen, Duncan S. Palmer, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Jesper Buchhave Poulsen, Stephan Ripke, Elise Robinson, F. Kyle Satterstrom, Hreinn Stefánsson, Christine Stevens, Patrick Turley, G. Bragi Walters, Hyejung Won, Margaret J. Wright, Ole A. Andreassen, Philip Asherson, Christie L. Burton, Dorret I. Boomsma, Bru Cormand, Søren Dalsgaard, Barbara Franke, Joel Gelernter, Daniel H. Geschwind, Hákon Hákonarson, Jan Haavik, Henry R. Kranzler, Jonna Kuntsi, K. Langley, Klaus‐Peter Lesch, Christel M. Middeldorp, Andreas Reif, Luís Augusto Rohde, Panos Roussos, Russell Schachar, Pamela Sklar, Edmund Sonuga‐Barke, Patrick F. Sullivan, Anita Thapar, Joyce Y. Tung, Irwin D. Waldman, Sarah E. Medland, Kāri Stefánsson, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Mark J. Daly, Stephen V. Faraone, Anders D. Børglum, Benjamin M. Neale
منشور في 2018Revisão
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Genome-wide association study
Genotype
Psychology
Single-nucleotide polymorphism
Genetic association
Psychiatry
Association (psychology)
Genome
Psychotherapist
Attention deficit hyperactivity disorder
Autism
Autism spectrum disorder
Clinical psychology
Environmental health
Genetic architecture
Medicine
Phenotype
Population
Schizophrenia (object-oriented programming)
Behavioral medicine
Cannabis
Central nervous system
Computational biology
Copy-number variation
Creativity
Cytomegalovirus
Cytomegalovirus infection