Resultats de la cerca - Darvasi, A

Selective DNA Pooling for Determination of Linkage between a Molecular Marker and a Quantitative Trait Locus per Darvasi, A., Soller, M.

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Advanced Intercross Lines, an Experimental Population for Fine Genetic Mapping per Darvasi, A., Soller, M.

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Detecting Marker-Qtl Linkage and Estimating Qtl Gene Effect and Map Location Using a Saturated Genetic Map per Darvasi, A., Weinreb, A., Minke, V., Weller, J. I., Soller, M.

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Inheritance and Mapping of Compact (Cmpt), a New Mutation Causing Hypermuscularity in Mice per Varga, L., Szabo, G., Darvasi, A., Muller, G., Sass, M., Soller, M.

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Quantitative trait locus mapping in dairy cattle by means of selective milk DNA pooling using dinucleotide microsatellite markers: analysis of milk protein percentage. per Lipkin, E, Mosig, M O, Darvasi, A, Ezra, E, Shalom, A, Friedmann, A, Soller, M

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Genetic architecture of prostate cancer in the Ashkenazi Jewish population per Vijai, J, Kirchhoff, T, Gallagher, D, Hamel, N, Guha, S, Darvasi, A, Lencz, T, Foulkes, W D, Offit, K, Klein, R J

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The molecular basis of partial penetrance of splicing mutations in cystic fibrosis. per Rave-Harel, N, Kerem, E, Nissim-Rafinia, M, Madjar, I, Goshen, R, Augarten, A, Rahat, A, Hurwitz, A, Darvasi, A, Kerem, B

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High rate of disease-related copy number variations in childhood onset schizophrenia per Ahn, K, Gotay, N, Andersen, TM, Anvari, AA, Gochman, P, Lee, Y, Sanders, S, Guha, S, Darvasi, A, Glessner, JT, Hakonarson, H, Lencz, T, State, MW, Shugart, YY, Rapoport, JL

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Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2 (FGFR2) per O’Donovan, M.C., Norton, N., Williams, H., Peirce, T., Moskvina, V., Nikolov, I., Hamshere, M., Carroll, L., Georgieva, L., Dwyer, S, Holmans, P., Marchini, J. L., Spencer, C.C.A., Howie, B., Leung, H-T., Giegling, I., Hartmann, A.M., Möller, H.-J., Morris, D.W., Shi, Y., Feng, G., Hoffmann, P., Propping, P., Vasilescu, C., Maier, W., Rietschel, M., Zammit, S., Schumacher, J., Quinn, E.M., Schulze, T.G., Iwata, N., Ikeda, M., Darvasi, A., Shifman, S., He, L., Duan, J., Sanders, A.R., Levinson, D.F., Adolfsson, R., Ösby, U., Terenius, Lars, Jönsson, Erik G, Cichon, S., Nöthen, M. M., Gill, M., Corvin, A.P., Rujescu, D., Gejman, P.V., Kirov, G., Craddock, N., Williams, N.M., Owen, M.J.

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GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia per Chen, X, Lee, G, Maher, BS, Fanous, AH, Chen, J, Zhao, Z, Guo, A, van den Oord, E, Sullivan, PF, Shi, J, Levinson, DF, Gejman, PV, Sanders, A, Duan, J, Owen, MJ, Craddock, NJ, O’Donovan, MC, Blackman, J, Lewis, D, Kirov, GK, Qin, W, Schwab, S, Wildenauer, D, Chowdari, K, Nimgaonkar, V, Straub, RE, Weinberger, DR, O’Neill, FA, Walsh, D, Bronstein, M, Darvasi, A, Lencz, T, Malhotra, AK, Rujescu, D, Giegling, I, Werge, T, Hansen, T, Ingason, A, Nöethen, MM, Rietschel, M, Cichon, S, Djurovic, S, Andreassen, OA, Cantor, RM, Ophoff, R, Corvin, A, Morris, DW, Gill, M, Pato, CN, Pato, MT, Macedo, A, Gurling, HMD, McQuillin, A, Pimm, J, Hultman, C, Lichtenstein, P, Sklar, P, Purcell, SM, Scolnick, E, St Clair, D, Blackwood, DHR, Kendler, KS

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