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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
Walsh T, McClellan JM, McCarthy SE, Addington AM, Pierce SB, Cooper GM, Nord AS, Kusenda M, Malhotra D, Bhandari A, Stray SM, Rippey CF, Roccanova P, Makarov V, Lakshmi B, Findling RL, Sikich L, Stromberg T, Merriman B, Gogtay N, Butler P, Eckstrand K, Noory L, Gochman P, Long R, Chen Z, Davis S, Baker C, Eichler EE, Meltzer PS, Nelson SF, Singleton AB, Lee MK, Rapoport JL, King MC, Sebat J. Walsh T, et al. Among authors: stromberg t. Science. 2008 Apr 25;320(5875):539-43. doi: 10.1126/science.1155174. Epub 2008 Mar 27. Science. 2008. PMID: 18369103
Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia.
Seal JL, Gornick MC, Gogtay N, Shaw P, Greenstein DK, Coffey M, Gochman PA, Stromberg T, Chen Z, Merriman B, Nelson SF, Brooks J, Arepalli S, Wavrant-De Vrièze F, Hardy J, Rapoport JL, Addington AM. Seal JL, et al. Among authors: stromberg t. J Med Genet. 2006 Nov;43(11):887-92. doi: 10.1136/jmg.2006.043380. Epub 2006 Jun 8. J Med Genet. 2006. PMID: 16763011 Free PMC article.
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: stromberg t. 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.
128 results