Correction: Common-variant associations with fragile X syndrome

The Original Article was published on 07 December 2018

Correction to: Molecular Psychiatry (2019) 24:338–344

https://doi.org/10.1038/s41380-018-0290-3 published online 07 December 2018

Following publication, the authors realised that ‘Stephanie N. Giamberardino’ was inadvertently omitted from the author list. The author list of this article should therefore be considered to be as follows:

James J. Crowley1, Jin Szatkiewicz1, Anna K. Kähler2, Paola Giusti-Rodriguez1, NaEshia Ancalade1, Jessica K. Booker3, Jennifer L. Carr3, Stephanie N. Giamberardino1, Greg E. Crawford4, Molly Losh5, Craig A. Stockmeier6, Annette K. Taylor7, Joseph Piven8,9, Patrick F. Sullivan1,2,8

1Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA

2Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden

3Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA

4Department of Pediatrics, Duke University, Durham, NC, USA

5Department of Communication Sciences, Northwestern University, Evanston, IL, USA

6University of Mississippi Medical Center, Jackson, MS, USA

7Kimball Genetics, Denver, CO, USA

8Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA

9Carolina Institute for Developmental Disabilities, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA

The authors would like to apologise for this error. This has not been corrected in the PDF or HTML of this article.

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Correspondence to Joseph Piven or Patrick F. Sullivan.

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Crowley, J.J., Szatkiewicz, J., Kähler, A.K. et al. Correction: Common-variant associations with fragile X syndrome. Mol Psychiatry 25, 3450 (2020). https://doi.org/10.1038/s41380-019-0526-x

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