Preoperative hypoglycemia in a patient receiving insulin detemir. by Olson, R, Bethel, M, Lien, L

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1. by Francks, C, Fisher, S, Olson, R, Pennington, B, Smith, S, DeFries, J, Monaco, A

The crystal structure of CHIR-AB1: a primordial avian classical Fc receptor. by Arnon, T, Kaiser, J, West, A, Olson, R, Diskin, R, Viertlboeck, B, Göbel, T, Bjorkman, P

Optimizing Tip Diameter in Phacoemulsification of Varying Lens Sizes: An in vitro Study by Ramshekar A, Heczko J, Bernhisel A, Barlow Jnr W, Zaugg B, Olson R, Pettey J

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Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci. by Gayán, J, Willcutt, E, Fisher, S, Francks, C, Cardon, L, Olson, R, Pennington, B, Smith, S, Monaco, A, DeFries, J

Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder by Gayan, J, Willcutt, E, Fisher, S, Francks, C, Cardon, L, Olson, R, Pennington, B, Smith, S, Monaco, A, DeFries, J

Correction: identification of candidate genes for dyslexia susceptibility on chromosome 18. by Scerri, T, Paracchini, S, Morris, A, Macphie, I, Talcott, J, Stein, J, Smith, S, Pennington, B, Olson, R, Defries, J, Monaco, A, Richardson, A

Identification of biomarkers for differentiation of hypervirulent Klebsiella pneumoniae from classical K. pneumoniae by Russo, TA, Olson, R, Fang, C-T, Stoesser, N, Miller, M, Macdonald, U, Hutson, A, Barker, JH, La Hoz, RM, Johnson, JR

Bivariate linkage analyses for reading difficulties and rapid naming by Davis, C, Fisher, S, Francks, C, MacPhie, I, Gayan, J, Smith, S, Cardon, L, Pennington, B, Olson, R, Monaco, A, DeFries, J

Identification of candidate genes for dyslexia susceptibility on chromosome 18 by Richardson, A, Morris, A, Monaco, A, Pennington, B, MacPhie, I, DeFries, J, Stein, J, Talcott, J, Olson, R, Smith, S, Paracchini, S, Scerri, T

Identification of candidate genes for dyslexia susceptibility on chromosome 18. by Scerri, T, Paracchini, S, Morris, A, MacPhie, I, Talcott, J, Stein, J, Smith, S, Pennington, B, Olson, R, DeFries, J, Monaco, A, Richardson, A

The metagenomics RAST server – a public resource for the automatic phylogenetic and functional analysis of metagenomes by Stevens R, Rodriguez A, Paczian T, Kubal M, Glass EM, Olson R, D'Souza M, Paarmann D, Meyer F, Wilke A, Wilkening J, Edwards RA

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NIF capsule performance modeling by Weber S., Callahan D., Cerjan C., Edwards M., Haan S., Hicks D., Jones O., Kyrala G., Meezan N., Olson R., Robey H., Spears B., Springer P., Town R.

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A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. by Francks, C, Paracchini, S, Smith, S, Richardson, A, Scerri, T, Cardon, L, Marlow, A, MacPhie, I, Walter, J, Pennington, B, Fisher, S, Olson, R, DeFries, J, Stein, J, Monaco, A

Association mapping of the 6p23-21.3 QTL for reading disability by Francks, C, Paracchini, S, Smith, S, Richardson, A, Scerri, T, Cardon, L, Marlow, A, MacPhie, I, Walter, J, Pennington, B, Fisher, S, Olson, R, DeFries, J, Stein, J, Monaco, A

Towards an integrated model of the NIC layered implosions by Jones O., Callahan D., Cerjan C., Clark D., Edwards M.J., Glenzer S., Marinak M., Meezan N., Milovich J., Olson R., Patel M., Robey H., Sepke S., Spears B., Springer P., Weber S., Wilson D.

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Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. by Fisher, S, Francks, C, Marlow, A, MacPhie, I, Newbury, D, Cardon, L, Ishikawa-Brush, Y, Richardson, A, Talcott, J, Gayán, J, Olson, R, Pennington, B, Smith, S, DeFries, J, Stein, J, Monaco, A

Quantitative trait analysis of the entire genome in large samples of dyslexic sib-pairs from the UK and US. by Fisher, S, Francks, C, Marlow, A, MacPhie, I, Newbury, D, Cardon, L, Ishikawa-Brush, Y, Richardson, A, Talcott, J, Gayan, J, Olson, R, Pennington, B, Smith, S, DeFries, J, Stein, J, Monaco, A

Genome-wide screening for DNA variants associated with reading and language traits. by Gialluisi, A, Newbury, D, Wilcutt, E, Olson, R, DeFries, J, Brandler, WM, Pennington, B, Smith, S, Scerri, T, Simpson, N, Luciano, M, Evans, D, Bates, T, Stein, J, Talcott, J, Monaco, A, Paracchini, S, Francks, C, Fisher, SE

Ignition tuning for the National Ignition Campaign by Landen O., Edwards J., Haan S.W., Lindl J.D., Boehly T.R., Bradley D.K., Callahan D.A., Celliers P.M., Dewald E.L., Dixit S., Doeppner T., Eggert J., Farley D., Frenje J.A., Glenn S., Glenzer S.H., Hamza A., Hammel B.A., Haynam C., LaFortune K., Hicks D.G., Hoffman N., Izumi N., Jones O.S., Kilkenny J.D., Kline J.L., Kyrala G.A., Mackinnon A.J., Milovich J., Moody J., Meezan N., Michel P., Munro D.H., Olson R.E., Ralph J., Robey H.F., Nikroo A., Regan S.P., Spears B.K., Suter L.J., Thomas C.A., Town R., Wilson D.C., MacGowan B.J., Atherton L.J., Moses E.I.

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