Identification of common genetic risk variants for autism spectrum disorder

Unknown, Jakob Grove, Unknown, Unknown, Unknown, 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 H. Christensen, Claire Churchhouse, Karin Dellenvall, Ditte Demontis, Silvia De Rubeis, Bernie Devlin, Srdjan Djurovic, Ashley L. Dumont, Jacqueline I. Goldstein, Christine S. Hansen, Mads Engel 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, Beate St Pourcain, Per Qvist, Karola Rehnström, Abraham Reichenberg, Jennifer Reichert, Elise B. Robinson, Kathryn Roeder, Panos Roussos, Evald Saemundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Hreinn Stefansson, Stacy Steinberg, Christine R. Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Kari Stefansson, Daniel H. Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum

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DOI: 10.1038/s41588-019-0344-8
Published: 2019-02-25
Container: Nature Genetics
Publisher: Springer Science and Business Media LLC
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1038/s41588-019-0344-8,
title = {Identification of common genetic risk variants for autism spectrum disorder},
author = {Unknown and Jakob Grove and Unknown and Unknown and Unknown and Stephan Ripke and Thomas D. Als and Manuel Mattheisen and Raymond K. Walters and Hyejung Won and Jonatan Pallesen and Esben Agerbo and Ole A. Andreassen and Richard Anney and Swapnil Awashti and Rich Belliveau and Francesco Bettella and Joseph D. Buxbaum and Jonas Bybjerg-Grauholm and Marie Bækvad-Hansen and Felecia Cerrato and Kimberly Chambert and Jane H. Christensen and Claire Churchhouse and Karin Dellenvall and Ditte Demontis and Silvia De Rubeis and Bernie Devlin and Srdjan Djurovic and Ashley L. Dumont and Jacqueline I. Goldstein and Christine S. Hansen and Mads Engel Hauberg and Mads V. Hollegaard and Sigrun Hope and Daniel P. Howrigan and Hailiang Huang and Christina M. Hultman and Lambertus Klei and Julian Maller and Joanna Martin and Alicia R. Martin and Jennifer L. Moran and Mette Nyegaard and Terje Nærland and Duncan S. Palmer and Aarno Palotie and Carsten Bøcker Pedersen and Marianne Giørtz Pedersen and Timothy dPoterba and Jesper Buchhave Poulsen and Beate St Pourcain and Per Qvist and Karola Rehnström and Abraham Reichenberg and Jennifer Reichert and Elise B. Robinson and Kathryn Roeder and Panos Roussos and Evald Saemundsen and Sven Sandin and F. Kyle Satterstrom and George Davey Smith and Hreinn Stefansson and Stacy Steinberg and Christine R. Stevens and Patrick F. Sullivan and Patrick Turley and G. Bragi Walters and Xinyi Xu and Kari Stefansson and Daniel H. Geschwind and Merete Nordentoft and David M. Hougaard and Thomas Werge and Ole Mors and Preben Bo Mortensen and Benjamin M. Neale and Mark J. Daly and Anders D. Børglum},
year = {2019},
journal = {Nature Genetics},
doi = {10.1038/s41588-019-0344-8},
url = {https://doi.org/10.1038/s41588-019-0344-8}
}

RIS

TY  - JOUR
TI  - Identification of common genetic risk variants for autism spectrum disorder
AU  - Unknown
AU  - Jakob Grove
AU  - Unknown
AU  - Unknown
AU  - Unknown
AU  - Stephan Ripke
AU  - Thomas D. Als
AU  - Manuel Mattheisen
AU  - Raymond K. Walters
AU  - Hyejung Won
AU  - Jonatan Pallesen
AU  - Esben Agerbo
AU  - Ole A. Andreassen
AU  - Richard Anney
AU  - Swapnil Awashti
AU  - Rich Belliveau
AU  - Francesco Bettella
AU  - Joseph D. Buxbaum
AU  - Jonas Bybjerg-Grauholm
AU  - Marie Bækvad-Hansen
AU  - Felecia Cerrato
AU  - Kimberly Chambert
AU  - Jane H. Christensen
AU  - Claire Churchhouse
AU  - Karin Dellenvall
AU  - Ditte Demontis
AU  - Silvia De Rubeis
AU  - Bernie Devlin
AU  - Srdjan Djurovic
AU  - Ashley L. Dumont
AU  - Jacqueline I. Goldstein
AU  - Christine S. Hansen
AU  - Mads Engel Hauberg
AU  - Mads V. Hollegaard
AU  - Sigrun Hope
AU  - Daniel P. Howrigan
AU  - Hailiang Huang
AU  - Christina M. Hultman
AU  - Lambertus Klei
AU  - Julian Maller
AU  - Joanna Martin
AU  - Alicia R. Martin
AU  - Jennifer L. Moran
AU  - Mette Nyegaard
AU  - Terje Nærland
AU  - Duncan S. Palmer
AU  - Aarno Palotie
AU  - Carsten Bøcker Pedersen
AU  - Marianne Giørtz Pedersen
AU  - Timothy dPoterba
AU  - Jesper Buchhave Poulsen
AU  - Beate St Pourcain
AU  - Per Qvist
AU  - Karola Rehnström
AU  - Abraham Reichenberg
AU  - Jennifer Reichert
AU  - Elise B. Robinson
AU  - Kathryn Roeder
AU  - Panos Roussos
AU  - Evald Saemundsen
AU  - Sven Sandin
AU  - F. Kyle Satterstrom
AU  - George Davey Smith
AU  - Hreinn Stefansson
AU  - Stacy Steinberg
AU  - Christine R. Stevens
AU  - Patrick F. Sullivan
AU  - Patrick Turley
AU  - G. Bragi Walters
AU  - Xinyi Xu
AU  - Kari Stefansson
AU  - Daniel H. Geschwind
AU  - Merete Nordentoft
AU  - David M. Hougaard
AU  - Thomas Werge
AU  - Ole Mors
AU  - Preben Bo Mortensen
AU  - Benjamin M. Neale
AU  - Mark J. Daly
AU  - Anders D. Børglum
PY  - 2019
JO  - Nature Genetics
DO  - 10.1038/s41588-019-0344-8
UR  - https://doi.org/10.1038/s41588-019-0344-8
ER  -

APA

Unknown, Grove, J., Unknown, Unknown, Unknown, Ripke, S., Als, T. D., Mattheisen, M., Walters, R. K., Won, H., Pallesen, J., Agerbo, E., Andreassen, O. A., Anney, R., Awashti, S., Belliveau, R., Bettella, F., Buxbaum, J. D., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Cerrato, F., Chambert, K., Christensen, J. H., Churchhouse, C., Dellenvall, K., Demontis, D., Rubeis, S. D., Devlin, B., Djurovic, S., Dumont, A. L., Goldstein, J. I., Hansen, C. S., Hauberg, M. E., Hollegaard, M. V., Hope, S., Howrigan, D. P., Huang, H., Hultman, C. M., Klei, L., Maller, J., Martin, J., Martin, A. R., Moran, J. L., Nyegaard, M., Nærland, T., Palmer, D. S., Palotie, A., Pedersen, C. B., Pedersen, M. G., dPoterba, T., Poulsen, J. B., Pourcain, B. S., Qvist, P., Rehnström, K., Reichenberg, A., Reichert, J., Robinson, E. B., Roeder, K., Roussos, P., Saemundsen, E., Sandin, S., Satterstrom, F. K., Smith, G. D., Stefansson, H., Steinberg, S., Stevens, C. R., Sullivan, P. F., Turley, P., Walters, G. B., Xu, X., Stefansson, K., Geschwind, D. H., Nordentoft, M., Hougaard, D. M., Werge, T., Mors, O., Mortensen, P. B., Neale, B. M., Daly, M. J., & Børglum, A. D. (2019). Identification of common genetic risk variants for autism spectrum disorder. Nature Genetics. https://doi.org/10.1038/s41588-019-0344-8

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crossref · retrieved 2026-09-25T15:18:31.626Z