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Correction: Common-variant associations with fragile X syndrome.

Molecular psychiatry

Crowley JJ, Szatkiewicz J, Kähler AK, Giusti-Rodriguez P, Ancalade N, Booker JK, Carr JL, Giamberardino SN, Crawford GE, Losh M, Stockmeier CA, Taylor AK, Piven J, Sullivan PF.
PMID: 31548576
Mol Psychiatry. 2020 Dec;25(12):3450. doi: 10.1038/s41380-019-0526-x.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Cite
Crowley JJ, Szatkiewicz J, Kähler AK, et al. Correction: Common-variant associations with fragile X syndrome. Mol Psychiatry. 2020;25(12):3450doi: 10.1038/s41380-019-0526-x.
Crowley, J. J., Szatkiewicz, J., Kähler, A. K., Giusti-Rodriguez, P., Ancalade, N., Booker, J. K., Carr, J. L., Giamberardino, S. N., Crawford, G. E., Losh, M., Stockmeier, C. A., Taylor, A. K., Piven, J., & Sullivan, P. F. (2020). Correction: Common-variant associations with fragile X syndrome. Molecular psychiatry, 25(12), 3450. https://doi.org/10.1038/s41380-019-0526-x
Crowley, James J, et al. "Correction: Common-variant associations with fragile X syndrome." Molecular psychiatry vol. 25,12 (2020): 3450. doi: https://doi.org/10.1038/s41380-019-0526-x
Crowley JJ, Szatkiewicz J, Kähler AK, Giusti-Rodriguez P, Ancalade N, Booker JK, Carr JL, Giamberardino SN, Crawford GE, Losh M, Stockmeier CA, Taylor AK, Piven J, Sullivan PF. Correction: Common-variant associations with fragile X syndrome. Mol Psychiatry. 2020 Dec;25(12):3450. doi: 10.1038/s41380-019-0526-x. PMID: 31548576.
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LEGAL AND ETHICAL IMPLICATIONS OF CRISPR APPLICATIONS IN PSYCHIATRY.

North Carolina law review

Foulkes AL, Soda T, Farrell M, Giusti-Rodríguez P, Lázaro-Muñoz G.
PMID: 31871365
North Carol Law Rev. 2019;97(5):1359-1398.

Gene-environment interactions play a key role in how psychiatric disorders manifest and develop. Psychiatric genetics researchers are making progress in identifying genomic correlates of many disorders. And recently, the field of genetics has given rise to a technology that...

Cite
Foulkes AL, Soda T, Farrell M, et al. LEGAL AND ETHICAL IMPLICATIONS OF CRISPR APPLICATIONS IN PSYCHIATRY. North Carol Law Rev. 2019;97(5):1359-1398
Foulkes, A. L., Soda, T., Farrell, M., Giusti-Rodríguez, P., & Lázaro-Muñoz, G. (2019). LEGAL AND ETHICAL IMPLICATIONS OF CRISPR APPLICATIONS IN PSYCHIATRY. North Carolina law review, 97(5), 1359-1398.
Foulkes, Alexandra L, et al. "LEGAL AND ETHICAL IMPLICATIONS OF CRISPR APPLICATIONS IN PSYCHIATRY." North Carolina law review vol. 97,5 (2019): 1359-1398.
Foulkes AL, Soda T, Farrell M, Giusti-Rodríguez P, Lázaro-Muñoz G. LEGAL AND ETHICAL IMPLICATIONS OF CRISPR APPLICATIONS IN PSYCHIATRY. North Carol Law Rev. 2019;97(5):1359-1398. PMID: 31871365; PMCID: PMC6927684.
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Bayesian modeling of skewed X inactivation in genetically diverse mice identifies a novel Xce allele associated with copy number changes.

Genetics

Sun KY, Oreper D, Schoenrock SA, McMullan R, Giusti-Rodríguez P, Zhabotynsky V, Miller DR, Tarantino LM, Pardo-Manuel de Villena F, Valdar W.
PMID: 33693696
Genetics. 2021 May 17;218(1). doi: 10.1093/genetics/iyab034.

Female mammals are functional mosaics of their parental X-linked gene expression due to X chromosome inactivation (XCI). This process inactivates one copy of the X chromosome in each cell during embryogenesis and that state is maintained clonally through mitosis....

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Sun KY, Oreper D, Schoenrock SA, et al. Bayesian modeling of skewed X inactivation in genetically diverse mice identifies a novel Xce allele associated with copy number changes. Genetics. 2021;218(1)doi: 10.1093/genetics/iyab034.
Sun, K. Y., Oreper, D., Schoenrock, S. A., McMullan, R., Giusti-Rodríguez, P., Zhabotynsky, V., Miller, D. R., Tarantino, L. M., Pardo-Manuel de Villena, F., & Valdar, W. (2021). Bayesian modeling of skewed X inactivation in genetically diverse mice identifies a novel Xce allele associated with copy number changes. Genetics, 218(1), . https://doi.org/10.1093/genetics/iyab034
Sun, Kathie Y, et al. "Bayesian modeling of skewed X inactivation in genetically diverse mice identifies a novel Xce allele associated with copy number changes." Genetics vol. 218,1 (2021). doi: https://doi.org/10.1093/genetics/iyab034
Sun KY, Oreper D, Schoenrock SA, McMullan R, Giusti-Rodríguez P, Zhabotynsky V, Miller DR, Tarantino LM, Pardo-Manuel de Villena F, Valdar W. Bayesian modeling of skewed X inactivation in genetically diverse mice identifies a novel Xce allele associated with copy number changes. Genetics. 2021 May 17;218(1). doi: 10.1093/genetics/iyab034. PMID: 33693696; PMCID: PMC8128399.
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Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia.

Nature communications

Halvorsen M, Huh R, Oskolkov N, Wen J, Netotea S, Giusti-Rodriguez P, Karlsson R, Bryois J, Nystedt B, Ameur A, Kähler AK, Ancalade N, Farrell M, Crowley JJ, Li Y, Magnusson PKE, Gyllensten U, Hultman CM, Sullivan PF, Szatkiewicz JP.
PMID: 34987162
Nat Commun. 2022 Jan 05;13(1):191. doi: 10.1038/s41467-021-27826-z.

No abstract available.

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Halvorsen M, Huh R, Oskolkov N, et al. Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia. Nat Commun. 2022;13(1):191doi: 10.1038/s41467-021-27826-z.
Halvorsen, M., Huh, R., Oskolkov, N., Wen, J., Netotea, S., Giusti-Rodriguez, P., Karlsson, R., Bryois, J., Nystedt, B., Ameur, A., Kähler, A. K., Ancalade, N., Farrell, M., Crowley, J. J., Li, Y., Magnusson, P. K. E., Gyllensten, U., Hultman, C. M., Sullivan, P. F., & Szatkiewicz, J. P. (2022). Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia. Nature communications, 13(1), 191. https://doi.org/10.1038/s41467-021-27826-z
Halvorsen, Matthew, et al. "Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia." Nature communications vol. 13,1 (2022): 191. doi: https://doi.org/10.1038/s41467-021-27826-z
Halvorsen M, Huh R, Oskolkov N, Wen J, Netotea S, Giusti-Rodriguez P, Karlsson R, Bryois J, Nystedt B, Ameur A, Kähler AK, Ancalade N, Farrell M, Crowley JJ, Li Y, Magnusson PKE, Gyllensten U, Hultman CM, Sullivan PF, Szatkiewicz JP. Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia. Nat Commun. 2022 Jan 05;13(1):191. doi: 10.1038/s41467-021-27826-z. PMID: 34987162.
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Showing 1 to 4 of 4 entries