المؤلفون: Segurado, R, Detera-Wadleigh, SD, Levinson, DF, Lewis, CM, Gill, M, Nurnberg, JI, Craddock, N, DePaulo, JR, Baron, M, Gershon, ES, Ekholm, J, Cichon, S, Turecki, G, Claes, S, Kelsoe, JR, Schofield, PR, Badenhop, RF, Morissette, J, Coon, H, Blackwood, D, McInnes, LA, Foroud, T, Edenberg, HJ, Reich, T, Rice, JP, Goate, A, McInnis, MG, McMahon, FJ, Badner, JA, Goldin, LR, Bennett, P, Willour, VL, Zandi, PP, Liu, JJ, Gilliam, C, Juo, SH, Berrettini, WH, Yoshikawa, T, Peltonen, L, Lonnqvist, J, Nothen, MM, Schumacher, J, Windemuth, C, Rietschel, M, Propping, P, Maier, W, Alda, M, Grof, P, Rouleau, GA, Del-Favero, J, Van Broeckhoven, C, Mendlewicz, J, Adolfsson, R, Spence, MA, Luebbert, H, Adams, LJ, Donald, JA, Mitchell, PB, Barden, N, Shink, E, Byerley, W, Muir, W, Visscher, PM, Macgregor, S, Gurling, H, Kalsi, G, McQuillin, A, Escamilla, MA, Reus, VI, Leon, P, Freimer, NB, Ewald, H, Kruse, TA, Mors, O, Radhakrishna, U, Blouin, JL, Antonarakis, SE, Akarsu, N

المساهمون: Tıbbi Genetik

مصطلحات موضوعية: Genetics & Heredity

وصف الملف: text/plain; application/pdf

العلاقة: American Journal Of Human Genetics; https://doi.org/10.1086/376547Test; http://hdl.handle.net/11655/16072Test; 73; 49; 62

الإتاحة: https://doi.org/10.1086/376547Test
http://hdl.handle.net/11655/16072Test

المؤلفون: Cichon, S, Foroud, T, McInnes, LA, Rouleau, GA, Grof, P, Blackwood, D, Coon, H, Morissette, J, Badenhop, RF, Schofield, PR, Rietschel, M, Kelsoe, JR, Claes, S, Turecki, G, Ekholm, J, Gershon, ES, Baron, M, DePaulo, JR, Craddock, N, Nurnberg, JI, Gill, M, Lewis, CM, Levinson, DF, Detera-Wadleigh, SD, Alda, M, Maier, W, Propping, P, Segurado, R, Del-Favero, J, Akarsu, N, Antonarakis, SE, Blouin, JL, Radhakrishna, U, Mors, O, Kruse, TA, Ewald, H, Freimer, NB, Leon, P, Reus, VI, Escamilla, MA, McQuillin, A, Kalsi, G, Gurling, H, Macgregor, S, Visscher, PM, Muir, W, Liu, JJ, Byerley, W, Shink, E, Barden, N, Mitchell, PB, Donald, JA, Zandi, PP, Gilliam, C, Juo, SH, Berrettini, WH, Yoshikawa, T, Peltonen, L, Willour, VL, Bennett, P, Lonnqvist, J, Nothen, MM, Schumacher, J, Windemuth, C, Goldin, LR, Adams, LJ, Badner, JA, McMahon, FJ, Luebbert, H, Spence, MA, Adolfsson, R, Mendlewicz, J, Van Broeckhoven, C, McInnis, MG, Goate, A, Rice, JP, Reich, T, Edenberg, HJ

العلاقة: 3c8ccfae-3d54-492b-873e-c0bb9c4a2301; https://avesis.hacettepe.edu.tr/publication/details/3c8ccfae-3d54-492b-873e-c0bb9c4a2301/oaiTest

الإتاحة: https://doi.org/10.1086/376547Test
https://avesis.hacettepe.edu.tr/publication/details/3c8ccfae-3d54-492b-873e-c0bb9c4a2301/oaiTest

المؤلفون: Cichon, S, Schmidt-Wolf, G, 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

المصدر: Molecular Psychiatry ; volume 6, issue 3, page 342-349 ; ISSN 1359-4184 1476-5578

مصطلحات موضوعية: Cellular and Molecular Neuroscience, Psychiatry and Mental health, Molecular Biology

الإتاحة: https://doi.org/10.1038/sj.mp.4000864Test
https://www.nature.com/articles/4000864.pdfTest
https://www.nature.com/articles/4000864Test

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

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

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

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

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

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

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

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

المؤلفون: Sander T., Windemuth C., Schulz H., Saar K., Gennaro E., Riggio C., Bianchi A., Zara F., Rudolf G., Picard F., Bulteau C., Kaminska A., Cieuta C., Prud'Homme J. -F., Dulac O., Bate L., Robinson R., Gardiner R. M., Covanis A., De Haan G. -J., Janssen G. A. M. A. J., Van Erp M. G., Boezeman E. H. J. F., Lindhout D., Heils A., Nurnberg P., Janz D.

المساهمون: Sander, T., Windemuth, C., Schulz, H., Saar, K., Gennaro, E., Riggio, C., Bianchi, A., Zara, F., Rudolf, G., Picard, F., Bulteau, C., Kaminska, A., Cieuta, C., Prud'Homme, J. -F., Dulac, O., Bate, L., Robinson, R., Gardiner, R. M., Covanis, A., De Haan, G. -J., Janssen, G. A. M. A. J., Van Erp, M. G., Boezeman, E. H. J. F., Lindhout, D., Heils, A., Nurnberg, P., Janz, D.

مصطلحات موضوعية: Chromosome 8, Genetic, Idiopathic generalized epilepsy, Linkage, Adult, Allele, Child, Dinucleotide Repeat, Epilepsy, Absence, Generalized, Tonic-Clonic, Europe, Female, Gene Frequency, Genetic Marker, Genetic Predisposition to Disease, Genotype, Human, Lod Score, Male, Models, Myoclonic Epilepsy, Juvenile, Phenotype, Polymorphism, Syndrome, Chromosome Mapping, Chromosomes, Pair 8

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/12581227; info:eu-repo/semantics/altIdentifier/wos/WOS:000180611600010; volume:44; firstpage:32; lastpage:39; numberofpages:8; journal:EPILEPSIA; https://hdl.handle.net/11567/1026631Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0037666057

الإتاحة: https://doi.org/10.1046/j.1528-1157.2003.51501.xTest
https://hdl.handle.net/11567/1026631Test

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 R. M., De Haan G. -J., Janssen G. A. M. A. J., Witte J., Halley D. J. J., Lindhout D., Wienker T. F., Janz D.

المساهمون: 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, R. M., De Haan, G. -J., Janssen, G. A. M. A. J., Witte, J., Halley, D. J. J., Lindhout, D., Wienker, T. F., Janz, D.

مصطلحات موضوعية: Chromosome 18, Genetic, Idiopathic generalized epilepsy, Linkage, Adolescent, Adult, Age of Onset, Child, Chromosome Mapping, Chromosomes, Human, Pair 18, Disease Susceptibility, Epilepsies, Myoclonic, Epilepsy, Generalized, Female, Genetic Linkage, Genetic Marker, Lod Score, Male, Microsatellite Repeat, Models, Nuclear Family, Polymorphism, Genetic Predisposition to Disease

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/12210286; info:eu-repo/semantics/altIdentifier/wos/WOS:000177185400016; volume:114; firstpage:673; lastpage:678; numberofpages:6; journal:AMERICAN JOURNAL OF MEDICAL GENETICS. PART B, NEUROPSYCHIATRIC GENETICS; https://hdl.handle.net/11567/1026644Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0037044006

الإتاحة: https://doi.org/10.1002/ajmg.10645Test
https://hdl.handle.net/11567/1026644Test

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.

المساهمون: 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.

مصطلحات موضوعية: Absence epilepsy, Chromosome 5, Genetic, Linkage, Replication

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000178697100004; volume:51; firstpage:23; lastpage:29; numberofpages:7; journal:EPILEPSY RESEARCH; https://hdl.handle.net/11567/1026635Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0036752268

الإتاحة: https://doi.org/10.1016/S0920-1211Test(02)00097-9
https://hdl.handle.net/11567/1026635Test