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1دورية أكاديمية
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2دورية أكاديمية
المؤلفون: Cichon, SAff1, ID4000864_cor1, Schmidt-Wolf, GAff1, Aff9, Schumacher, J, Müller, D J, Hürter, M, Schulze, T G, Albus, M, Borrmann-Hassenbach, M, Franzek, E, Lanczik, M, Fritze, J, Kreiner, R, Weigelt, B, Minges, J, Lichtermann, D, Lerer, B, Kanyas, K, Strauch, K, Windemuth, C, Baur, M P, Wienker, T F, Maier, W, Rietschel, M, Propping, P, Nöthen, M MAff1, Aff10
المصدر: Molecular Psychiatry. 6(3):342-349
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3دورية أكاديمية
المؤلفون: Windemuth, C, Schulz, H, Saar, K, Gennaro, E, Bianchi, A, Zara, F, Bulteau, C, Kaminska, A, Ville, D, Cieuta, C, Nabbout-Tarantino, R, Prud'homme, J.-F, Dulac, O, Bate, L, Gardiner, R.M, Lindhout, D, Wienker, T.F, Janz, D, Sander, T *
المصدر: In Epilepsy Research 2002 51(1):23-29
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المؤلفون: Hensen, P, Asadullah, K, Windemuth, C, Rüschendorf, F, Hüffmeier, U, Ständer, M, Schmitt-Egenolf, Marcus, Wienker, TF, Reis, A, Traupe, H
المصدر: British Journal of Dermatology. 149(2):381-385
مصطلحات موضوعية: complex diseases, cytokine, disease susceptibility, genetics, promoter polymorphism, psoriasis
وصف الملف: print
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المؤلفون: Hensen, P, Windemuth, C, Hüffmeier, U, Rüschendorf, F, Stadelmann, A, Hoppe, V, Fenneker, D, Ständer, M, Schmitt-Egenolf, Marcus, Wienker, TF, Traupe, H, Reis, A
المصدر: Experimental dermatology. 12(4):490-496
مصطلحات موضوعية: psoriasis, genetics, complex genetic diseases, disease susceptibility, microsatellites
وصف الملف: print
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المؤلفون: Schmitt-Egenolf, Marcus, Windemuth, C, Hennies, HC, Albis-Camps, M, von Engelhardt, B, Wienker, T, Reis, A, Traupe, H, Blasczyk, R
المصدر: Tissue Antigens. 57(5):440-446
مصطلحات موضوعية: hereditary diseases, genetics, disease-susceptibility, histocompatibility antigens, autoimmune disease, genetic markers
وصف الملف: print
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المؤلفون: Lee, YA, Rüschendorf, F, Windemuth, C, Schmitt-Egenolf, Marcus, Stadelmann, A, Nürnberg, G, Ständer, M, Wienker, TF, Reis, A, Traupe, H
المصدر: American Journal of Human Genetics. 67(4):1020-1024
مصطلحات موضوعية: linkage analysis, genetic dissection, complex traits, disease, identification, simulation, activation, models, map, hla
وصف الملف: print
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المؤلفون: Segurado, R., Detera-Wadleigh, S.D., Levinson, D.F., Lewis, C.M., Gill, M., Nurnberger, J.I., Craddock, N., DePaulo, J.R., Baron, M., Gershon, E.S., Ekholm, J., Cichon, S., Turecki, G., Claes, S., Kelsoe, J.R., Schofield, P.R., Badenhop, R.F., Morissette, J., Coon, H., Blackwood, D., McInnes, L.A., Foroud, T., Edenberg, H.J., Reich, T., Rice, J.P., Goate, A., McInnis, M.G., McMahon, F.J., Badner, J.A., Goldin, L.R., Bennett, P., Willour, V.L., Zandi, P.P., Liu, J., Gilliam, C., Juo, S.H., Berrettini, W.H., Yoshikawa, T., Peltonen, L., Lonnqvist, J., Nothen, M.M., Schumacher, J., Windemuth, C., Rietschel, M., Propping, P., Maier, W., Alda, M., Grof, P., Rouleau, G.A., Del-Favero, J., Van Broeckhoven, C., Mendlewicz, J., Adolfsson, R., Spence, M.A., Luebbert, H., Adams, L.J., Donald, J.A., Mitchell, P.B., Barden, N., Shink, E., Byerley, W., Muir, W., Visscher, P.M., Macgregor, S., Gurling, H., Kalsi, G., McQuillin, A., Escamilla, M.A., Reus, V.I., Leon, P., Freimer, N.B., Ewald, H., Kruse, T.A., Mors, O., Radhakrishna, U., Blouin, J.L., Antonarakis, S.E., Akarsu, N.
المصدر: Segurado, R, Detera-Wadleigh, S D, Levinson, D F, Lewis, C M, Gill, M, Nurnberger, J I, Craddock, N, DePaulo, J R, Baron, M, Gershon, E S, Ekholm, J, Cichon, S, Turecki, G, Claes, S, Kelsoe, J R, Schofield, P R, Badenhop, R F, Morissette, J, Coon, H, Blackwood, D, McInnes, L A, Foroud, T, Edenberg, H J, Reich, T, Rice, J P, Goate, A, McInnis, M G, McMahon, F J, Badner, J A, Goldin, L R, Bennett, P, Willour, V L, Zandi, P P, Liu, J, Gilliam, C, Juo, S H, Berrettini, W H, Yoshikawa, T, Peltonen, L, Lonnqvist, J, Nothen, M M, Schumacher, J, Windemuth, C, Rietschel, M, Propping, P, Maier, W, Alda, M, Grof, P, Rouleau, G A, Del-Favero, J, Van Broeckhoven, C, Mendlewicz, J, Adolfsson, R, Spence, M A, Luebbert, H, Adams, L J, Donald, J A, Mitchell, P B, Barden, N, Shink, E, Byerley, W, Muir, W, Visscher, P M, Macgregor, S, Gurling, H, Kalsi, G, McQuillin, A, Escamilla, M A, Reus, V I, Leon, P, Freimer, N B, Ewald, H, Kruse, T A, Mors, O, Radhakrishna, U, Blouin, J L, Antonarakis, S E & Akarsu, N 2003, ' Genome scan meta-analysis of schizophrenia and bipolar disorder, part III : Bipolar disorder ', American Journal of Human Genetics, vol. 73(1), pp. 49-62 .
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3062::77fdc3543bbec047f034e986725ffcda
https://portal.findresearcher.sdu.dk/da/publications/1ee73b00-6fd1-11db-81a9-000ea68e967b -
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المؤلفون: Sander, T., Windemuth, C., Schultz, H., Saar, K., Gennaro, E., Bianchi, A., Zara, F., Bulteau, C., Kaminska, A., Ville, D., Cieuta, C., Prud'homme, J.F., Dulac, O., Bate, L., Gardiner, R.M., Haan, G.J., Janssen, G.A.M.A.J., Witte, J., Halley, D.J.J., Lindhout, D., Wienker, T.F., Janz, D., The European Consortium on the Genetics of Idiopathic Generalized Epilepsy: participating clinicians: Kjeldsen M.J., Friis M.L.
المصدر: Sander, T, Windemuth, C, Schultz, H, Saar, K, Gennaro, E, Bianchi, A, Zara, F, Bulteau, C, Kaminska, A, Ville, D, Cieuta, C, Prud'homme, J F, Dulac, O, Bate, L, Gardiner, R M, Haan, G J, Janssen, G A M A J, Witte, J, Halley, D J J, Lindhout, D, Wienker, T F, Janz, D & The European Consortium on the Genetics of Idiopathic Generalized Epilepsy: participating clinicians: Kjeldsen M.J., Friis M.L. 2002, ' No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1 ', American Journal of Medical Genetics. Part A, vol. 114, no. 6, pp. 673-678 .
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3062::221e8f562d682c1e260882f3c10bd9aa
https://portal.findresearcher.sdu.dk/da/publications/81e1e300-a8af-11dc-9626-000ea68e967b -
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المؤلفون: Sander, T, Windemuth, C, Schulz, H, Saar, K, Gennaro, E, Bianchi, A, Zara, F, Bulteau, C, Kaminska, A, Ville, D, Cieuta, C, Prud'homme, J-F, Dulac, O, Bate, L, Gardiner, M, Haan, Janssen, GAMAJ, Witte, J, Halley, Dicky, Lindhout, D (Dick), Wienker, TF, Janz, D
المساهمون: Clinical Genetics
المصدر: American Journal of Medical Genetics, 114, 673-678. Wiley-Liss Inc.