A CHRNA5 allele related to nicotine addiction and schizophrenia von Hong, L. E., Yang, X., Wonodi, I., Hodgkinson, C. A., Goldman, D., Stine, O. C., Stein, E. S., Thaker, G. K.

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DISC-1 Leu607Phe alleles differentially affect centrosomal PCM1 localization and neurotransmitter release von Eastwood, S L, Hodgkinson, C A, Harrison, P J

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A preliminary study suggests that nicotine and prefrontal dopamine affect cortico‐striatal areas in smokers with performance feedback von Lee, M. R., Gallen, C. L., Ross, T. J., Kurup, P., Salmeron, B. J., Hodgkinson, C. A., Goldman, D., Stein, E. A., Enoch, M. A.

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Methylomic profiling and replication implicates deregulation of PCSK9 in alcohol use disorder von Lohoff, F W, Sorcher, J L, Rosen, A D, Mauro, K L, Fanelli, R R, Momenan, R, Hodgkinson, C A, Vendruscolo, L F, Koob, G F, Schwandt, M, George, D T, Jones, I S, Holmes, A, Zhou, Z, Xu, M-J, Gao, B, Sun, H, Phillips, M J, Muench, C, Kaminsky, Z A

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The contribution of rare and common variants in 30 genes to risk nicotine dependence von Yang, J, Wang, S, Yang, Z, Hodgkinson, C A, Iarikova, P, Ma, J Z, Payne, T J, Goldman, D, Li, M D

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Association of genetic ancestry with striatal dopamine D2/D3 receptor availability von Wiers, C E, Towb, P C, Hodgkinson, C A, Shen, P-H, Freeman, C, Miller, G, Lindgren, E, Shokri-Kojori, E, Demiral, Ş B, Kim, S W, Tomasi, D, Sun, H, Wang, G-J, Goldman, D, Volkow, N D

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Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein von Hodgkinson, Colin A., Moore, Karen J., Nakayama, Atsuo, Steingrímsson, Eiríkur, Copeland, Neal G., Jenkins, Nancy A., Arnheiter, Heinz

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The glucagon-like peptide-1 receptor as a potential treatment target in alcohol use disorder: evidence from human genetic association studies and a mouse model of alcohol dependenc... von Suchankova, P, Yan, J, Schwandt, M L, Stangl, B L, Caparelli, E C, Momenan, R, Jerlhag, E, Engel, J A, Hodgkinson, C A, Egli, M, Lopez, M F, Becker, H C, Goldman, D, Heilig, M, Ramchandani, V A, Leggio, L

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microphthalmia, a critical factor in melanocyte development, defines a discrete transcription factor family von Hemesath, T J, Steingrímsson, E, McGill, G, Hansen, M J, Vaught, J, Hodgkinson, C A, Arnheiter, H, Copeland, N G, Jenkins, N A, Fisher, D E

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A novel form of autosomal recessive pure hereditary spastic paraplegia maps to chromosome 13q14 von HODGKINSON, C. A, BOHLEGA, S, ABU-AMERO, S. N, CUPLER, E, KAMBOURIS, M, MEYER, B. F, BHARUCHA, V. A

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Elucidating the relationship between DISC1, NDEL1 and NDE1 and the risk for schizophrenia: Evidence of epistasis and competitive binding von Burdick, Katherine E., Kamiya, Atsushi, Hodgkinson, Colin A., Lencz, Todd, DeRosse, Pamela, Ishizuka, Koko, Elashvili, Sarah, Arai, Hiroyuki, Goldman, David, Sawa, Akira, Malhotra, Anil K.

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Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences von Steingrímsson, Eiríkur, Moore, Karen J., Lamoreux, M. Lynn, Ferré-D'Amaré, Adrian R., Burley, Stephen K., Sanders Zimring, Debra C., Skow, Loren C., Hodgkinson, Colin A., Arnheiter, Heinz, Copeland, Neal G., Jenkins, Nancy A.

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Striatal dopamine release and genetic variation of the serotonin 2C receptor in humans von Mickey, Brian J, Sanford, Benjamin J, Love, Tiffany M, Shen, Pei-Hong, Hodgkinson, Colin A, Stohler, Christian S, Goldman, David, Zubieta, Jon-Kar

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Addictions Biology: Haplotype-Based Analysis for 130 Candidate Genes on a Single Array von Hodgkinson, Colin A., Yuan, Qiaoping, Xu, Ke, Shen, Pei-Hong, Heinz, Elizabeth, Lobos, Elizabeth A., Binder, Elizabeth B., Cubells, Joe, Ehlers, Cindy L., Gelernter, Joel, Mann, John, Riley, Brien, Roy, Alec, Tabakoff, Boris, Todd, Richard D., Zhou, Zhifeng, Goldman, David

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Defining the role of corticotropin releasing factor binding protein in alcohol consumption von Haass-Koffler, C L, Henry, A T, Melkus, G, Simms, J A, Naemmuddin, M, Nielsen, C K, Lasek, A W, Magill, M, Schwandt, M L, Momenan, R, Hodgkinson, C A, Bartlett, S E, Swift, R M, Bonci, A, Leggio, L

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BDNF polymorphism predicts general intelligence after penetrating traumatic brain injury von Rostami, Elham, Krueger, Frank, Zoubak, Serguei, Dal Monte, Olga, Raymont, Vanessa, Pardini, Matteo, Hodgkinson, Colin A, Goldman, David, Risling, Mårten, Grafman, Jordan

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Cloning of MITF, the human homolog of the mouse microphthalmia gene and assignment to chromosome 3p14.1-p12.3 von TACHIBANA, M, PEREZ-JURADO, L. A, NAKAYAMA, A, HODGKINSON, C. A, XU LI, SCHNEIDER, M, MIKI, T, FEX, J, FRANCKE, U, ARNHEITER, H

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Antiviral determinants of rat Mx GTPases map to the carboxy-terminal half von Johannes, L, Kambadur, R, Lee-Hellmich, H, Hodgkinson, C A, Arnheiter, H, Meier, E

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Melanocyte development in vivo and in neural crest cell cultures: crucial dependence on the Mitf basic-helix-loop-helix-zipper transcription factor von Opdecamp, K, Nakayama, A, Nguyen, M T, Hodgkinson, C A, Pavan, W J, Arnheiter, H

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Mutation at the anophthalmic white locus in Syrian hamsters : haploinsufficiency in the Mitf gene mimics human Waardenburg syndrome type 2 von HODGKINSON, C. A, NAKAYAMA, A, HUA LI, SWENSON, L.-B, OPDECAMP, K, ASHER, J. H, ARNHEITER, H, GLASER, T

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