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A 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.
Published in:
Diabetologia, 2007, v. 50, n. 7, p. 1418, doi. 10.1007/s00125-007-0658-4
By:
- Hoffmann, K.;
- Mattheisen, M.;
- Dahm, S.;
- Nürnberg, P.;
- Roe, C.;
- Johnson, J.;
- Cox, N.;
- Wichmann, H.;
- Wienker, T.;
- Schulze, J.;
- Schwarz, P.;
- Lindner, T.
Publication type:
Article
Association scan of the novel psoriasis susceptibility region on chromosome 19: evidence for both susceptible and protective loci.
Published in:
Experimental Dermatology, 2003, v. 12, n. 4, p. 490, doi. 10.1034/j.1600-0625.2003.00040.x
By:
- 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.
Publication type:
Article
Loss of constitutional heterozygosity on chromosome 11p in human ovarian cancer. Positive correlation with grade of differentiation.
Published in:
1993
By:
- Kiechle-Schwarz, Marion;
- Bauknecht, Thomas;
- Walz, Lioba;
- Pfleiderer, Albrecht;
- Wienker, Thomas;
- Kiechle-Schwarz, M;
- Bauknecht, T;
- Wienker, T;
- Walz, L;
- Pfleiderer, A
Publication type:
journal article
Families with autosomal dominant brachydactyly type E, short stature, and severe hypertension.
Published in:
1998
By:
- Toka, Hakan R.;
- Bähring, Sylvia;
- Chitayat, David;
- Melby, James C.;
- Whitehead, Richard;
- Jeschke, Eva;
- Wienker, Thomas F.;
- Toka, Okan;
- Schuster, Herbert;
- Luft, Friedrich C.;
- Toka, H R;
- Bähring, S;
- Chitayat, D;
- Melby, J C;
- Whitehead, R;
- Jeschke, E;
- Wienker, T F;
- Toka, O;
- Schuster, H;
- Luft, F C
Publication type:
journal article
Association of Common Polymorphisms in the Nicotinic Acetylcholine Receptor Alpha4 Subunit Gene with an Electrophysiological Endophenotype in a Large Population-Based Sample.
Published in:
PLoS ONE, 2016, v. 11, n. 4, p. 1, doi. 10.1371/journal.pone.0152984
By:
- 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.
Publication type:
Article
C6 LINKAGE STUDIES.
Published in:
International Journal of Immunogenetics, 1983, v. 10, n. 1, p. 61, doi. 10.1111/j.1744-313X.1983.tb01018.x
By:
- Bender, K.;
- Bissbort, S.;
- Mayerová, A.;
- Mauff, G.;
- Wienker, T. F.
Publication type:
Article
KCNQ4: a gene for age-related hearing impairment?
Published in:
Human Mutation, 2006, v. 27, n. 10, p. 1007, doi. 10.1002/humu.20375
By:
- Van Eyken, E.;
- Van Laer, L.;
- Fransen, E.;
- Topsakal, V.;
- Lemkens, N.;
- Laureys, W.;
- Nelissen, N.;
- Vandevelde, A.;
- Wienker, T.;
- Van De Heyning, P.;
- Van Camp, G.
Publication type:
Article
Y402H-Polymorphismus im Komplementfaktor H und altersabhängige Makuladegeneration (AMD).
Published in:
Der Ophthalmologe, 2005, v. 102, n. 11, p. 1029, doi. 10.1007/s00347-005-1270-y
By:
- Scholl, H.;
- Weber, B.;
- Nöthen, M.;
- Wienker, T.;
- Holz, F.
Publication type:
Article
Increased frequency of the CTLA-4 49 A/G polymorphism in patients with acquired haemophilia A compared to healthy controls.
Published in:
Haemophilia, 2008, v. 14, n. 2, p. 355, doi. 10.1111/j.1365-2516.2007.01618.x
By:
- Pavlova, A.;
- Diaz-Lacava, A.;
- Zeitler, H.;
- Satoguina, J.;
- Niemann, B.;
- Krause, M.;
- Scharrer, I.;
- Hoerauf, A.;
- Wienker, T.;
- Oldenburg, J.
Publication type:
Article
A neuronal nitric oxide synthase (NOS-I) haplotype associated with schizophrenia modifies prefrontal cortex function.
Published in:
Molecular Psychiatry, 2006, v. 11, n. 3, p. 286, doi. 10.1038/sj.mp.4001779
By:
- Reif, A.;
- Herterich, S.;
- Strobel, A.;
- Ehlis, A. -C.;
- Saur, D.;
- Jacob, C. P.;
- Wienker, T.;
- Töpner, T.;
- Fritzen, S.;
- Walter, U.;
- Schmitt, A.;
- Fallgatter, A. J.;
- Lesch, K. -P.
Publication type:
Article
Atopic eczema/dermatitis syndrome – a genetically complex disease. New advances in discovering the genetic contribution.
Published in:
Allergy, 2003, v. 58, n. 1, p. 5, doi. 10.1034/j.1398-9995.2003.02162.x
By:
- Klüken, H.;
- Wienker, T.;
- Bieber, T.
Publication type:
Article
The phenotypic spectrum related to the human epilepsy susceptibility gene 'EJM1'.
Published in:
Annals of Neurology, 1995, v. 38, n. 2, p. 210, doi. 10.1002/ana.410380213
By:
- Sander, T.;
- Hildmann, T.;
- Janz, D.;
- Wienker, T. F.;
- Neitzel, H.;
- Bianchi, A.;
- Bauer, G.;
- Sailer, U.;
- Berek, K.;
- Schmitz, B.;
- Beck-Mannagetta, G.
Publication type:
Article
Association and sibpair analysis for the HLA, Gm, Km, and insulin polymorphisms in multiplex IDDM families.
Published in:
Genetic Epidemiology, 1989, v. 6, n. 1, p. 107, doi. 10.1002/gepi.1370060120
By:
- Fimmers, R.;
- Neugebauer, M.;
- Dennert, J.;
- Wienker, T.;
- Baur, M. P.
Publication type:
Article
Interleukin-10 promoter polymorphism IL10.G and familial early onset psoriasis.
Published in:
British Journal of Dermatology, 2003, v. 149, n. 2, p. 381, doi. 10.1046/j.1365-2133.2003.05411.x
By:
- Hensen, P.;
- Asadullah, K.;
- Windemuth, C.;
- Rüschendorf, F.;
- Hüffmeier, U.;
- Ständer, M.;
- Schmitt-Egenolf, M.;
- Wienker, T. F.;
- Reis, A.;
- Traupe, H.
Publication type:
Article
A linkage study of malignant hyperthermia (MH).
Published in:
Clinical Genetics, 1990, v. 37, n. 3, p. 221, doi. 10.1111/j.1399-0004.1990.tb03506.x
By:
- Bender, K.;
- Senff, H.;
- Wienker, T. F.;
- Spiess-Kiefer, C.;
- Lehmann-Horn, F.
Publication type:
Article
Adrenoleukodystrophy (Siemerling-Creutzfeldt disease): Heterozygote with two clonal fibroblast populations.
Published in:
Clinical Genetics, 1977, v. 11, n. 2, p. 114, doi. 10.1111/j.1399-0004.1977.tb01287.x
By:
- Ropers, H.-H.;
- Zimmermann, J.;
- Wienker, T.
Publication type:
Article
Evolutionary conserved microsatellites in the promoter region of the 5-hydroxytryptamine receptor 2C gene (HTR2C) are not associated with bipolar disorder in females.
Published in:
Journal of Neural Transmission, 2002, v. 109, n. 5/6, p. 939, doi. 10.1007/s007020200077
By:
- Meyer, J.;
- Saam, W.;
- Mössner, R.;
- Cangir, Ö.;
- Ortega, G. R.;
- Tatschner, T.;
- Riederer, P.;
- Wienker, T. F.;
- Lesch, K. P.
Publication type:
Article

Found: 17