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Page 1
Sex chromosome anomalies in childhood onset schizophrenia: an update.
Eckstrand K, Addington AM, Stromberg T, Merriman B, Miller R, Gochman P, Long R, Dutra A, Chen Z, Meltzer P, Nelson SF, Rapoport JL. Eckstrand K, et al. Among authors: long r. Mol Psychiatry. 2008 Oct;13(10):910-1. doi: 10.1038/mp.2008.67. Mol Psychiatry. 2008. PMID: 18800051 Free PMC article. 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.
HLA antigens in childhood onset schizophrenia.
Jacobsen LK, Mittleman BB, Kumra S, Lenane MC, Barracchini KC, Adams S, Simonis T, Lee PR, Long RT, Sharp W, Sidransky E, Ginns EI, Rapoport JL. Jacobsen LK, et al. Among authors: long rt. Psychiatry Res. 1998 May 8;78(3):123-32. doi: 10.1016/s0165-1781(98)00015-8. Psychiatry Res. 1998. PMID: 9657416 Free article.
Large CAG/CTG repeats are associated with childhood-onset schizophrenia.
Burgess CE, Lindblad K, Sidransky E, Yuan QP, Long RT, Breschel T, Ross CA, McInnis M, Lee P, Ginns EI, Lenane M, Kumra S, Jacobsen L, Rapoport JL, Schalling M. Burgess CE, et al. Among authors: long rt. Mol Psychiatry. 1998 Jul;3(4):321-7. doi: 10.1038/sj.mp.4000405. Mol Psychiatry. 1998. PMID: 9702740
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.
Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: identification of a BAC contig spanning the translocation breakpoint at 7q21.
Yan WL, Guan XY, Green ED, Nicolson R, Yap TK, Zhang J, Jacobsen LK, Krasnewich DM, Kumra S, Lenane MC, Gochman P, Damschroder-Williams PJ, Esterling LE, Long RT, Martin BM, Sidransky E, Rapoport JL, Ginns EI. Yan WL, et al. Among authors: long rt. Am J Med Genet. 2000 Dec 4;96(6):749-53. doi: 10.1002/1096-8628(20001204)96:6<749::aid-ajmg10>3.0.co;2-k. Am J Med Genet. 2000. PMID: 11121174
2,341 results