Association of Common Polymorphisms in the Nicotinic Acetylcholine Receptor Alpha4 Subunit Gene with an Electrophysiological Endophenotype in a Large Population-Based Sample
Mobascher, A, Diaz-Lacava, A, Wagner, M, Gallinat, J, Wienker, T F, Drichel, D, Becker, T, Steffens, M, Dahmen, N, Gründer, G, Thürauf, N, Kiefer, F, Kornhuber, J, Toliat, M R, Thiele, H, Nürnberg, P, Steinlein, O, Winterer, G
Published in PloS one (07.04.2016)
Published in PloS one (07.04.2016)
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Investigation of promoter variations in dendritic cell-specific ICAM3-grabbing non-integrin (DC-SIGN) (CD209) and their relevance for human cytomegalovirus reactivation and disease after allogeneic stem-cell transplantation
Mezger, M., Steffens, M., Semmler, C., Arlt, E.-M., Zimmer, M., Kristjanson, G.-I., Wienker, T.F., Toliat, M.R., Kessler, T., Einsele, H., Loeffler, J.
Published in Clinical microbiology and infection (01.03.2008)
Published in Clinical microbiology and infection (01.03.2008)
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German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2
Hoffmann, K, Mattheisen, M, Dahm, S, Nürnberg, P, Roe, C, Johnson, J, Cox, N. J, Wichmann, H. E, Wienker, T. F, Schulze, J, Schwarz, P. E, Lindner, T. H
Published in Diabetologia (01.07.2007)
Published in Diabetologia (01.07.2007)
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Evidence for susceptibility determinant(s) to psoriasis vulgaris in or near PTPN22 in German patients
Hüffmeier, U, Steffens, M, Burkhardt, H, Lascorz, J, Schürmeier-Horst, F, Ständer, M, Kelsch, R, Baumann, C, Küster, W, Mössner, R, Reich, K, Wienker, T F, Traupe, H, Reis, A
Published in Journal of medical genetics (01.06.2006)
Published in Journal of medical genetics (01.06.2006)
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Genome search for susceptibility loci of common idiopathic generalised epilepsies
SANDER, T, SCHULZ, H, VILLE, D, CIEUTA, C, PICARD, F, PRUD'HOMME, J.-F, BATE, L, SUNDQUIST, A, GARDINER, R. M, JANSSEN, G. A. M. A. J, DE HAAN, G.-J, KASTELEIJN-NOLST-TRENITE, D. G. A, SAAR, K, BADER, A, LINDHOUT, D, RIESS, O, WIENKER, T. F, JANZ, D, REIS, A, GENNARO, E, RIGGIO, M. C, BIANCHI, A, ZARA, F, LUNA, D, BULTEAU, C, KAMINSKA, A
Published in Human molecular genetics (12.06.2000)
Published in Human molecular genetics (12.06.2000)
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Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6
Sander, T, Bockenkamp, B, Hildmann, T, Blasczyk, R, Kretz, R, Wienker, T F, Volz, A, Schmitz, B, Beck-Mannagetta, G, Riess, O, Epplen, J T, Janz, D, Ziegler, A
Published in Neurology (01.09.1997)
Published in Neurology (01.09.1997)
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A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25-q26
CICHON, S, SCHMIDT-WOLF, G, FRITZE, J, KREINER, R, WEIGELT, B, MINGES, J, LICHTERMANN, D, LERER, B, KANYAS, K, STRAUCH, K, WINDEMUTH, C, BAUR, M. P, SCHUMACHER, J, WIENKER, T. F, MAIER, W, RIETSCHEL, M, PROPPING, P, NÖTHEN, M. M, MÜLLER, D. J, HÜRTER, M, SCHULZE, T. G, ALBUS, M, BORRMANN-HASSENBACH, M, FRANZEK, E, LANCZIK, M
Published in Molecular psychiatry (01.05.2001)
Published in Molecular psychiatry (01.05.2001)
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β-2 Adrenoceptor genetic variation is associated with genetic predisposition to essential hypertension: The Bergen Blood Pressure Study
Timmermann, Bernd, Mo, Rune, Luft, Friedrich C., Gerdts, Eva, Busjahn, Andreas, Omvik, Per, Li, Guo-Hua, Schuster, Herbert, Wienker, Thomas F., Hoehe, Margret R., Lund-Johansen, Per
Published in Kidney international (01.06.1998)
Published in Kidney international (01.06.1998)
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Conference Proceeding
Interleukin-10 promoter polymorphism IL10.G and familial early onset psoriasis
Hensen, P., Asadullah, K., Windemuth, C., Rüschendorf, F., Hüffmeier, U., Ständer, M., Schmitt-Egenolf, M., Wienker, T.F., Reis, A., Traupe, H.
Published in British journal of dermatology (1951) (01.08.2003)
Published in British journal of dermatology (1951) (01.08.2003)
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Association scan of the novel psoriasis susceptibility region on chromosome 19: evidence for both susceptible and protective loci
Hensen, P., Windemuth, C., Hüffmeier, U., Rüschendorf, F., Stadelmann, A., Hoppe, V., Fenneker, D., Ständer, M., Schmitt-Egenolf , M., Wienker, T. F., Traupe, H., Reis, A.
Published in Experimental dermatology (01.08.2003)
Published in Experimental dermatology (01.08.2003)
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Linkage of the Gene for the Triple A Syndrome to Chromosome 12q13 Near the Type II Keratin Gene Cluster
Weber, Angela, Wienker, Thomas F., Jung, Martin, Easton, Douglas, Dean, Heather J., Heinrichs, Claudine, Reis, Andre, Clark, Adrian J. L.
Published in Human molecular genetics (01.12.1996)
Published in Human molecular genetics (01.12.1996)
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Quantitative Analyses of SMN1 and SMN2 Based on Real-Time LightCycler PCR: Fast and Highly Reliable Carrier Testing and Prediction of Severity of Spinal Muscular Atrophy
Feldkötter, Markus, Schwarzer, Verena, Wirth, Radu, Wienker, Thomas F., Wirth, Brunhilde
Published in American journal of human genetics (01.02.2002)
Published in American journal of human genetics (01.02.2002)
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Investigation of a Family with Autosomal Dominant Dilated Cardiomyopathy Defines a Novel Locus on Chromosome 2q14-q22
Jung, Martin, Poepping, Imke, Perrot, Andreas, Ellmer, Annette E., Wienker, Thomas F., Dietz, Rainer, Reis, André, Osterziel, Karl Josef
Published in American journal of human genetics (01.10.1999)
Published in American journal of human genetics (01.10.1999)
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Pharmacogenetics of clozapine response
Schumacher, Johannes, Schulze, Thomas G, Wienker, Thomas F, Rietschel, Marcella, Nöthen, Markus M
Published in The Lancet (British edition) (05.08.2000)
Published in The Lancet (British edition) (05.08.2000)
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Diaphragmatic Spinal Muscular Atrophy with Respiratory Distress Is Heterogeneous, and One Form Is Linked to Chromosome 11q13-q21
Grohmann, Katja, Wienker, Thomas F., Saar, Kathrin, Rudnik-Schöneborn, Sabine, Stoltenburg-Didinger, Gisela, Rossi, Rainer, Novelli, Giuseppe, Nürnberg, Gudrun, Pfeufer, Arne, Wirth, Brunhilde, Reis, André, Zerres, Klaus, Hübner, Christoph
Published in American journal of human genetics (01.11.1999)
Published in American journal of human genetics (01.11.1999)
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Exclusion of the neuronal nicotinic acetylcholine receptor α7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locus
MEYER, J, ORTEGA, G, LESCH, K. P, SCHRAUT, K, NÜRNBERG, G, RÜSCHENDORF, F, SAAR, K, MÖSSNER, R, WIENKER, T. F, REIS, A, STÖBER, G
Published in Molecular psychiatry (01.02.2002)
Published in Molecular psychiatry (01.02.2002)
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The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21
SAAR, K, CHRZANOWSKA, K. H, STUMM, M, JUNG, M, NÜRNBERG, G, WIENKER, T. F, SEEMANOVA, E, WEGNER, R.-D, REIS, A, SPERLING, K
Published in American journal of human genetics (01.03.1997)
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Published in American journal of human genetics (01.03.1997)
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Limb Mammary Syndrome: A New Genetic Disorder with Mammary Hypoplasia, Ectrodactyly, and Other Hand/Foot Anomalies Maps to Human Chromosome 3q27
van Bokhoven, Hans, Jung, Martin, Smits, Arie P.T., van Beersum, Sylvia, Rüschendorf, Franz, van Steensel, Maurice, Veenstra, Monique, Tuerlings, Joep H.A.M., Mariman, Edwin C.M., Brunner, Han G., Wienker, Thomas F., Reis, Andre, Ropers, Hans-Hilger, Hamel, Ben C.J.
Published in American journal of human genetics (01.02.1999)
Published in American journal of human genetics (01.02.1999)
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Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12
Schuster, Herbert, Wienker, Thomas F, Bähring, Sylvia, Bilginturan, Nihat, Toka, Hakan R, Neitzel, Heidemarie, Jeschke, Eva, Toka, Okan, Gilbert, Dennis, Lowe, Adam, Ott, Jürg, Haller, Hermann, Luft, Friedrich C
Published in Nature genetics (01.05.1996)
Published in Nature genetics (01.05.1996)
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