Pharmacogenetics of Neonatal Opioid Toxicity Following Maternal Use of Codeine During Breastfeeding: A Case-Control Study von Madadi, P, Ross, CJD, Hayden, MR, Carleton, BC, Gaedigk, A, Leeder, JS, Koren, G

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Ethyl-EPA in Huntington disease : A double-blind, randomized, placebo-controlled trial von PURI, B. K, LEAVITT, B. R, MANKU, M, MURCK, H, HAYDEN, M. R, ROSS, C. A, ROSENBLATT, A, GREENAMYRE, J. T, HERSCH, S, VADDADI, K. S, SWORD, A, HORROBIN, D. F

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A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length von Langbehn, DR, Brinkman, RR, Falush, D, Paulsen, JS, Hayden, MR

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Human Mendelian pain disorders: a key to discovery and validation of novel analgesics von Goldberg, YP, Pimstone, SN, Namdari, R, Price, N, Cohen, C, Sherrington, RP, Hayden, MR

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Influence of lamotrigine on progression of early Huntington disease : A randomized clinical trial von KREMER, B, CLARK, C. M, HAYDEN, M. R, ALMQVIST, E. W, RAYMOND, L. A, GRAF, P, JACOVA, C, MEZEI, M, HARDY, M. A, SNOW, B, MARTIN, W

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What monozygotic twins discordant for phenotype illustrate about mechanisms influencing genetic forms of neurodegeneration von Ketelaar, ME, Hofstra, RMW, Hayden, MR

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Balance between synaptic versus extrasynaptic NMDA receptor activity influences inclusions and neurotoxicity of mutant huntingtin von Talantova, Maria, Kaul, Marcus, Yao, Dongdong, Xia, Peng, Ehrnhoefer, Dagmar E, Zaidi, Rameez, Lipton, Stuart A, Graham, Rona K, Tong, Gary, Zhang, Dongxian, Clemente, Arjay, Okamoto, Shu-ichi, Hayden, Michael R, Pouladi, Mahmoud A, Vincent Chen, H-S

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Deranged neuronal calcium signaling and Huntington disease von Bezprozvanny, Ilya, Hayden, Michael R.

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Replication of TPMT and ABCC3 Genetic Variants Highly Associated With Cisplatin-Induced Hearing Loss in Children von Pussegoda, K, Ross, C J, Visscher, H, Yazdanpanah, M, Brooks, B, Rassekh, S R, Zada, Y F, Dubé, M-P, Carleton, B C, Hayden, M R

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Personalized gene silencing therapeutics for Huntington disease von Kay, C., Skotte, N.H., Southwell, A.L., Hayden, M.R.

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Huntingtin interacts with REST/NRSF to modulate the transcription of NRSE-controlled neuronal genes von Cattaneo, Elena, Zuccato, Chiara, Tartari, Marzia, Crotti, Andrea, Goffredo, Donato, Valenza, Marta, Conti, Luciano, Cataudella, Tiziana, Leavitt, Blair R, Hayden, Michael R, Timmusk, Tõnis, Rigamonti, Dorotea

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Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines von Greenamyre, J. Timothy, Panov, Alexander V, Gutekunst, Claire-Anne, Leavitt, Blair R, Hayden, Michael R, Burke, James R, Strittmatter, Warren J

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Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis von Papanikolaou, George, Babakaiff, Ryan, Goldberg, Y Paul, Franchini, Patrick L, Dubé, Marie-Pierre, MacFarlane, Julie, Pape, Terry D, Radomski, Christopher C, Davidas, Owen, Risler, Jenni K, Nemeth, Elizabeta, Zaborowska, Catherine, Politou, Marianna, Lockitch, Gillian, Brissot, Pierre, Thompson, Jay, Ludwig, Erwin H, MacDonald, Marcia L E, Samuels, Mark E, Sakellaropoulos, Nikos, Ganz, Tomas, Hayden, Michael R, Andres, Lisa, Christakis, John

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Intestinal ABCA1 directly contributes to HDL biogenesis in vivo von Brunham, Liam R, Kruit, Janine K, Iqbal, Jahangir, Fievet, Catherine, Timmins, Jenelle M, Pape, Terry D, Coburn, Bryan A, Bissada, Nagat, Staels, Bart, Groen, Albert K, Hussain, M Mahmood, Parks, John S, Kuipers, Folkert, Hayden, Michael R

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Targeted inactivation of hepatic Abca1 causes profound hypoalphalipoproteinemia and kidney hypercatabolism of apoA-I von Timmins, Jenelle M, Lee, Ji-Young, Boudyguina, Elena, Kluckman, Kimberly D, Brunham, Liam R, Mulya, Anny, Gebre, Abraham K, Coutinho, Jonathan M, Colvin, Perry L, Smith, Thomas L, Hayden, Michael R, Maeda, Nobuyo, Parks, John S

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A common truncation variant of lipoprotein lipase (Ser447X) confers protection against coronary heart disease: the Framingham Offspring Study von Gagné, Se, Larson, Mg, Pimstone, Sn, Schaefer, Ej, Kastelein, Jjp, Wilson, Pwf, Ordovas, Jm, Hayden, Mr

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Predictive testing for Huntington disease: interpretation and significance of intermediate alleles von Semaka, A, Creighton, S, Warby, S, Hayden, MR

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Deficiency of ABCA1 Impairs Apolipoprotein E Metabolism in Brain von Hirsch-Reinshagen, Veronica, Zhou, Steven, Burgess, Braydon L., Bernier, Lise, McIsaac, Sean A., Chan, Jeniffer Y., Tansley, Gavin H., Cohn, Jeffrey S., Hayden, Michael R., Wellington, Cheryl L.

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Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia von Olivecrona, Gunilla, Ehrenborg, Ewa, Semb, Henrik, Makoveichuk, Elena, Lindberg, Anna, Hayden, Michael R., Gin, Peter, Davies, Brandon S.J., Weinstein, Michael M., Fong, Loren G., Beigneux, Anne P., Young, Stephen G., Olivecrona, Thomas, Hernell, Olle

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Increased Sensitivity to N-Methyl-D-Aspartate Receptor-Mediated Excitotoxicity in a Mouse Model of Huntington's Disease von Zeron, Melinda M, Hansson, Oskar, Chen, Nansheng, Wellington, Cheryl L, Leavitt, Blair R, Brundin, Patrik, Hayden, Michael R, Raymond, Lynn A

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