Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibility von Buono, R.J, Lohoff, F.W, Sander, T, Sperling, M.R, O’Connor, M.J, Dlugos, D.J, Ryan, S.G, Golden, G.T, Zhao, H, Scattergood, T.M, Berrettini, W.H, Ferraro, T.N

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Alternative transcripts and evidence of imprinting of GNAL on 18p11.2 von CORRADI, J. P, RAVYN, V, ROBBINS, A. K, HAGAN, K. W, PETERS, M. F, BOSTWICK, R, BUONO, R. J, BERRETTINI, W. H, FURLONG, S. T

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Confirmation of multiple seizure susceptibility QTLs on chromosome 15 in C57BL/6J and DBA/2J inbred mice von Ferraro, T N, Smith, G G, Schwebel, C L, Doyle, G A, Ruiz, S E, Oleynick, J U, Lohoff, F W, Berrettini, W H, Buono, R J

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Analysis of candidate genes for morphine preference quantitative trait locus Mop2 von Doyle, G.A, Schwebel, C.L, Ruiz, S.E, Chou, A.D, Lai, A.T, Wang, M.-J, Smith, G.G, Buono, R.J, Berrettini, W.H, Ferraro, T.N

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Genetic influences on electrical seizure threshold von Ferraro, T.N, Golden, G.T, Snyder, R, Laibinis, M, Smith, G.G, Buono, R.J, Berrettini, W.H

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Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene von Ferraro, Thomas N, Golden, Gregory T, Smith, George G, Martin, James F, Lohoff, Falk W, Gieringer, Tracy A, Zamboni, Deborah, Schwebel, Candice L, Press, Danielle M, Kratzer, Stephanie O, Zhao, Hongyu, Berrettini, Wade H, Buono, Russell J

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Hypoxic Repression of Lactate Dehydrogenase-B in Retina von BUONO, RUSSELL J, LANG, ROBYN K

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Mapping loci for pentylenetetrazol-induced seizure susceptibility in mice von Ferraro, T N, Golden, G T, Smith, G G, St Jean, P, Schork, N J, Mulholland, N, Ballas, C, Schill, J, Buono, R J, Berrettini, W H

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Quantitative trait loci for electrical seizure threshold mapped in C57BLKS/J and C57BL/10SnJ mice von Ferraro, T. N., Smith, G. G., Ballard, D., Zhao, H., Schwebel, C. L., Gupta, A., Rappaport, E. F., Ruiz, S. E., Lohoff, F. W., Doyle, G. A., Berrettini, W. H., Buono, R. J.

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Lack of association between temporal lobe epilepsy and a novel polymorphism in the alpha 2 subunit gene (ATP1A2) of the sodium potassium transporting ATPase von Buono, R.J., Ferraro, T.N., O'Connor, M.J., Sperling, M.R., Abbey, M., Finanger, E., Lohoff, F., Mulholland, N., Berrettini, W.H.

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Defining the clinical role of pharmacogenetics in antiepileptic drug therapy von Dlugos, D J, Buono, R J, Ferraro, T N

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Mouse strain variation in maximal electroshock seizure threshold von Ferraro, Thomas N., Golden, Gregory T., Smith, George G., DeMuth, Denis, Buono, Russell J., Berrettini, Wade H.

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Lack of Association Between an Interleukin 1 Beta (IL‐1β) Gene Variation and Refractory Temporal Lobe Epilepsy von Buono, Russell J., Ferraro, Thomas N., O'Connor, Michael J., Sperling, Michael R., Ryan, Stephen G., Scattergood, Theresa, Mulholland, Nicole, Gilmore, Joan, Lohoff, Falk W., Berrettini, Wade H.

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Human G(olf) gene polymorphisms and vulnerability to bipolar disorder von Berrettini, W H, Vuoristo, J, Ferraro, T N, Buono, R J, Wildenauer, D, Ala-Kokko, L

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Quantitative Genetic Study of Maximal Electroshock Seizure Threshold in Mice: Evidence for a Major Seizure Susceptibility Locus on Distal Chromosome 1 von Ferraro, Thomas N., Golden, Gregory T., Smith, George G., Longman, Ryan L., Snyder, Robert L., DeMuth, Denis, Szpilzak, Ivanna, Mulholland, Nicole, Eng, Elaine, Lohoff, Falk W., Buono, Russell J., Berrettini, Wade H.

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Cloning of murine CDK9/PITALRE and its tissue-specific expression in development von Bagella, Luigi, MacLachlan, Timothy K., Buono, Russell J., Pisano, M. Michele, Giordano, Antonio, De Luca, Antonio

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Genotyping microsatellite polymorphisms by agarose gel electrophoresis with ethidium bromide staining: application to quantitative trait loci analysis of seizure susceptibility in... von Ferraro, T N, Schill, J F, Ballas, C, Mulholland, N, Golden, G T, Smith, G G, Buono, R J, Berrettini, W H

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Changes in expression and distribution of lactate dehydrogenase isoenzymes in the developing chick retina von Buono, Russell J., Sheffield, Joel B.

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Identification of five mouse μ-opioid receptor (MOR) gene ( Oprm1) splice variants containing a newly identified alternatively spliced exon von Doyle, Glenn A., Sheng, X. Rebecca, Lin, Sharon S.J., Press, Danielle M., Grice, Dorothy E., Buono, Russell J., Ferraro, Thomas N., Berrettini, Wade H.

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Identification of three mouse μ-opioid receptor (MOR) gene ( Oprm1) splice variants containing a newly identified alternatively spliced exon von Doyle, Glenn A., Rebecca Sheng, X., Lin, Sharon S.J., Press, Danielle M., Grice, Dorothy E., Buono, Russell J., Ferraro, Thomas N., Berrettini, Wade H.

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