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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.
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 …
Evidence for sex-specific risk alleles in autism spectrum disorder.
Stone JL, Merriman B, Cantor RM, Yonan AL, Gilliam TC, Geschwind DH, Nelson SF. Stone JL, et al. Among authors: merriman b. Am J Hum Genet. 2004 Dec;75(6):1117-23. doi: 10.1086/426034. Epub 2004 Oct 5. Am J Hum Genet. 2004. PMID: 15467983 Free PMC article.
Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia.
Rock MJ, Prenen J, Funari VA, Funari TL, Merriman B, Nelson SF, Lachman RS, Wilcox WR, Reyno S, Quadrelli R, Vaglio A, Owsianik G, Janssens A, Voets T, Ikegawa S, Nagai T, Rimoin DL, Nilius B, Cohn DH. Rock MJ, et al. Among authors: merriman b. Nat Genet. 2008 Aug;40(8):999-1003. doi: 10.1038/ng.166. Epub 2008 Jun 29. Nat Genet. 2008. PMID: 18587396 Free PMC article.
83 results