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المؤلفون: Cichon, S^{Aff1, ID4000864_cor1}, Schmidt-Wolf, G^{Aff1, 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 M^{Aff1, Aff10}

المصدر: Molecular Psychiatry. 6(3):342-349

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

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

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-82437

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

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-82443

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

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-82444

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

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-82442

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

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

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.

URL الوصول: https://explore.openaire.eu/search/publication?articleId=narcis______::404047144477b7a49836631b2e85a346
https://pure.eur.nl/en/publications/814ab1d3-ef82-4324-aa2c-74456eb12c0c