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Catechol-o-methyl transferase (COMT) val158met polymorphism and adolescent cortical development in patients with childhood-onset schizophrenia, their non-psychotic siblings, and healthy controls.
Raznahan A, Greenstein D, Lee Y, Long R, Clasen L, Gochman P, Addington A, Giedd JN, Rapoport JL, Gogtay N. Raznahan A, et al. Among authors: long r. Neuroimage. 2011 Aug 15;57(4):1517-23. doi: 10.1016/j.neuroimage.2011.05.032. Epub 2011 May 15. Neuroimage. 2011. PMID: 21620981 Free PMC article.
Castellanos replies.
Castellanos F, Lau E, Tayebi N, Lee P, Long R, Giedd J, Sharp W, Marsh W, Walter J, Hamburger S, Ginns E, Rapoport J, Sidransky E. Castellanos F, et al. Among authors: long r. Mol Psychiatry. 1999 Sep;4(5):414. doi: 10.1038/sj.mp.4000597. Mol Psychiatry. 1999. PMID: 10523812 No abstract available.
A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders.
Addington AM, Gauthier J, Piton A, Hamdan FF, Raymond A, Gogtay N, Miller R, Tossell J, Bakalar J, Inoff-Germain G, Gochman P, Long R, Rapoport JL, Rouleau GA. Addington AM, et al. Among authors: long r. Mol Psychiatry. 2011 Mar;16(3):238-9. doi: 10.1038/mp.2010.59. Epub 2010 May 18. Mol Psychiatry. 2011. PMID: 20479756 Free PMC article. No abstract available.
Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability.
Nguyen LS, Jolly L, Shoubridge C, Chan WK, Huang L, Laumonnier F, Raynaud M, Hackett A, Field M, Rodriguez J, Srivastava AK, Lee Y, Long R, Addington AM, Rapoport JL, Suren S, Hahn CN, Gamble J, Wilkinson MF, Corbett MA, Gecz J. Nguyen LS, et al. Among authors: long r. Mol Psychiatry. 2012 Nov;17(11):1103-15. doi: 10.1038/mp.2011.163. Epub 2011 Dec 20. Mol Psychiatry. 2012. PMID: 22182939 Free PMC article.
2,446 results