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Page 1
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: merriman b. 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: merriman b. 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: merriman b. 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.
High density SNP association study of a major autism linkage region on chromosome 17.
Stone JL, Merriman B, Cantor RM, Geschwind DH, Nelson SF. Stone JL, et al. Among authors: merriman b. Hum Mol Genet. 2007 Mar 15;16(6):704-15. doi: 10.1093/hmg/ddm015. Epub 2007 Mar 21. Hum Mol Genet. 2007. PMID: 17376794
In an attempt to comprehensively test for association of common variants to autism within the region on chromosome 17 defined in Stone et al. (Stone, J.L., Merriman, B., Cantor, R.M., Yonan, A.L., Gilliam, T.C., Geschwind, D.H. and Nelson, S.F. (2004) Evidence for s …
In an attempt to comprehensively test for association of common variants to autism within the region on chromosome 17 defined in Stone et al …
Local alignment of generalized k-base encoded DNA sequence.
Homer N, Nelson SF, Merriman B. Homer N, et al. Among authors: merriman b. BMC Bioinformatics. 2010 Jun 24;11:347. doi: 10.1186/1471-2105-11-347. BMC Bioinformatics. 2010. PMID: 20576157 Free PMC article.
Local alignment of two-base encoded DNA sequence.
Homer N, Merriman B, Nelson SF. Homer N, et al. Among authors: merriman b. BMC Bioinformatics. 2009 Jun 9;10:175. doi: 10.1186/1471-2105-10-175. BMC Bioinformatics. 2009. PMID: 19508732 Free PMC article.
83 results