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1مؤتمر
المؤلفون: Marmarelis, V.Z., Mitsis, G.D., Huecking, K., Bergman, R.N.
المصدر: Proceedings of the Second Joint 24th Annual Conference and the Annual Fall Meeting of the Biomedical Engineering Society] [Engineering in Medicine and Biology Joint EMBS-BMES conference Engineering in Medicine and Biology, 2002. 24th Annual Conference and the Annual Fall Meeting of the Biomedical Engineering Society EMBS/BMES Conference, 2002. Proceedings of the Second Joint. 1:224-225 vol.1 2002
Relation: Conference Proceedings. Second Joint EMBS-BMES Conference 2002 24th Annual International Conference of the Engineering in Medicine and Biology Society. Annual Fall Meeting of the Biomedical Engineering Society
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2مؤتمر
المؤلفون: Bergman, R.N., Kalaba, B.E.
المصدر: 1977 11th Asilomar Conference on Circuits, Systems and Computers, 1977. Conference Record. Circuits, Systems and Computers, 1977. Conference Record. 1977 11th Asilomar Conference on. :405-409 1977
Relation: 1977 11th Asilomar Conference on Circuits, Systems and Computers, 1977. Conference Record.
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3دورية أكاديمية
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تسجيل الدخول للوصول الكامل. -
4دورية أكاديمية
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5دورية أكاديمية
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6دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
7دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
8دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
9دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
10
المؤلفون: Voight, B.F., Raychaudhuri, S., Purcell, S., McCarroll, S.A., Segrè, A.V., Ardlie, K., Burtt, N.P., Crawford, G., Elliott, A.L., Green, T., Guiducci, C., Saxena, R., Daly, M.J., Florez, J.C., Altshuler, D., Meigs, J.B., Scott, L.J., Welch, R.P., Willer, C.J., Ganser, M., Jackson, A.U., Stringham, H.M., Abecasis, G.R., Boehnke, M., Steinthorsdottir, V., Thorleifsson, G., Kong, A., Walters, G.B., Thorsteinsdottir, U., Stefansson, K., Dina, C., Proença, C., Cauchi, S., Froguel, P., Zeggini, E., Bumpstead, S., Payne, F., Smith, N., Barroso, I., Ferreira, T., Elliott, K.S., Lindgren, C.M., Prokopenko, I., Rayner, N.W., Robertson, N.R., Morris, A.P., McCarthy, M.I., Huth, C., Grallert, H., Gieger, C., Klopp, N., Meitinger, T., Petersen, A.-K., Thorand, B., Wichmann, H.-E., Illig, T., Aulchenko, Y.S., Amin, N., Witteman, J., Hofman, A., Van Duijn, C.M., McCulloch, L.J., Bennett, A.J., Groves, C.J., Hassanali, N., Owen, K.R., Gloyn, A.L., Wu, G., Stein, L.D., Langenberg, C., Griffin, S., Wareham, N.J., Hoffmann, O.M., Hide, W.A., Dupuis, J., Qi, L., Kraft, P., Sun, Q., Hunter, D., Hu, F.B., Cornelis, M., VanDam, R., Van Hoek, M., Van Herpt, T., Sijbrands, E., Uitterlinden, A., Navarro, P., Balkau, B., Benediktsson, R., Sigurdsson, G., Blagieva, R., Boehm, B.O., Boerwinkle, E., Bonnycastle, L.L., Chines, P.S., Erdos, M.R., Morken, M.A., Narisu, N., Swift, A.J., Boström, K.B., Bravenboer, B., Charpentier, G., Couper, D.J., Doney, A.S.F., Morris, A.D., Palmer, C.N.A., Fox, C.S., Franklin, C.S., Rudan, I., Grarup, N., Hadjadj, S., Thomas Sparsø, [No Value], Campbell, H., Wilson, J.F., Hansen, T., Pedersen, O., Herder, C., Roden, M., Isomaa, B., Tuomi, T., Johnson, P.R.V., Jørgensen, T., Kao, W.H.L., Kuusisto, J., Laakso, M., Lauritzen, T., Li, M., Lieverse, A., Lyssenko, V., Nilsson, P., Groop, L., Marre, M., Midthjell, K., Platou, C., Hveem, K., Perry, J.R.B., Shields, B.M., Weedon, M.N., Frayling, T.M., Hattersley, A.T., Rathmann, W., Strassburger, K., Rocheleau, G., Sladek, R., Sampson, M.J., Shrader, P., Tichet, J., Bergman, R.N., Collins, F.S., Gyllensten, U., Hitman, G.A., Mohlke, K.L., Pramstaller, P.P., Tuomilehto, J., Walker, M., Watanabe, R.M., Pankow, J.S.
المساهمون: deCODE genetics, Sturlugata 8, 101 Reykjavík, Iceland. kong@decode.is
المصدر: Voight, B F, Raychaudhuri, S, Purcell, S, McCarroll, S A, Segrè, A V, Ardlie, K, Burtt, N P, Crawford, G, Elliott, A L, Green, T, Guiducci, C, Saxena, R, Daly, M J, Florez, J C, Altshuler, D, Meigs, J B, Scott, L J, Welch, R P, Willer, C J, Ganser, M, Jackson, A U, Stringham, H M, Abecasis, G R, Boehnke, M, Steinthorsdottir, V, Thorleifsson, G, Kong, A, Walters, G B, Thorsteinsdottir, U, Stefansson, K, Dina, C, Proença, C, Cauchi, S, Froguel, P, Zeggini, E, Bumpstead, S, Payne, F, Smith, N, Barroso, I, Ferreira, T, Elliott, K S, Lindgren, C M, Prokopenko, I, Rayner, N W, Robertson, N R, Morris, A P, McCarthy, M I, Huth, C, Grallert, H, Gieger, C, Klopp, N, Meitinger, T, Petersen, A-K, Thorand, B, Wichmann, H-E, Illig, T, Aulchenko, Y S, Amin, N, Witteman, J, Hofman, A, Van Duijn, C M, McCulloch, L J, Bennett, A J, Groves, C J, Hassanali, N, Owen, K R, Gloyn, A L, Wu, G, Stein, L D, Langenberg, C, Griffin, S, Wareham, N J, Hoffmann, O M, Hide, W A, Dupuis, J, Qi, L, Kraft, P, Sun, Q, Hunter, D, Hu, F B, Cornelis, M, VanDam, R, Van Hoek, M, Van Herpt, T, Sijbrands, E, Uitterlinden, A, Navarro, P, Balkau, B, Benediktsson, R, Sigurdsson, G, Blagieva, R, Boehm, B O, Boerwinkle, E, Bonnycastle, L L, Chines, P S, Erdos, M R, Morken, M A, Narisu, N, Swift, A J, Boström, K B, Bravenboer, B, Charpentier, G, Couper, D J, Doney, A S F, Morris, A D, Palmer, C N A, Fox, C S, Franklin, C S, Rudan, I, Grarup, N, Hadjadj, S, Thomas Sparsø, N V, Campbell, H, Wilson, J F, Hansen, T, Pedersen, O, Herder, C, Roden, M, Isomaa, B, Tuomi, T, Johnson, P R V, Jørgensen, T, Kao, W H L, Kuusisto, J, Laakso, M, Lauritzen, T, Li, M, Lieverse, A, Lyssenko, V, Nilsson, P, Groop, L, Marre, M, Midthjell, K, Platou, C, Hveem, K, Perry, J R B, Shields, B M, Weedon, M N, Frayling, T M, Hattersley, A T, Rathmann, W, Strassburger, K, Rocheleau, G, Sladek, R, Sampson, M J, Shrader, P, Tichet, J, Bergman, R N, Collins, F S, Gyllensten, U, Hitman, G A, Mohlke, K L, Pramstaller, P P, Tuomilehto, J, Walker, M, Watanabe, R M & Pankow, J S 2009, ' Parental origin of sequence variants associated with complex diseases ', Nature, vol. 462, no. 7275, pp. 868-874 . https://doi.org/10.1038/nature08625
Kong, A, Steinthorsdottir, V, Masson, G, Thorleifsson, G, Sulem, P, Besenbacher, S, Jonasdottir, A, Sigurdsson, A, Kristinsson, K T, Jonasdottir, A, Frigge, M L, Gylfason, A, Olason, P I, Gudjonsson, S A, Sverrisson, S, Stacey, S N, Sigurgeirsson, B, Benediktsdottir, K R, Sigurdsson, H, Jonsson, T, Benediktsson, R, Olafsson, J H, Johannsson, O T, Hreidarsson, A B, Sigurdsson, G, Ferguson-Smith, A C, Gudbjartsson, D F, Thorsteinsdottir, U, Stefansson, K, DIAGRAM Consortium & Lauritzen, T 2009, ' Parental origin of sequence variants associated with complex diseases ', Nature, vol. 462, no. 7275, pp. 868-74 . https://doi.org/10.1038/nature08625مصطلحات موضوعية: Male, CCCTC-Binding Factor, Iceland, Mothers, Breast Neoplasms, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Fathers, Genomic Imprinting, 03 medical and health sciences, 0302 clinical medicine, Polymorphism (computer science), Humans, SNP, Genetic Predisposition to Disease, Allele, Alleles, 030304 developmental biology, Genetics, 0303 health sciences, Binding Sites, Multidisciplinary, Genome, Human, Chromosomes, Human, Pair 11, Haplotype, DNA Methylation, Pedigree, Repressor Proteins, Diabetes Mellitus, Type 2, Haplotypes, Carcinoma, Basal Cell, DNA methylation, Female, Human genome, Genomic imprinting, Chromosomes, Human, Pair 7, 030217 neurology & neurosurgery
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