On the genetics of mandibular prognathism: analysis of large European noble families.

por Wolff, G, Wienker, T F, Sander, H
Publicado 1993

A BAM HI RFLP at the human tyrosine aminotransferase (TAT) gene locus at 16q.

por Wullich, B, Natt, E, Wienker, T F, Scherer, G
Publicado 1989

Evidence for preferential X-chromosome inactivation in a family with Fabry disease.

por Ropers, H H, Wienker, T F, Grimm, T, Schroetter, K, Bender, K
Publicado 1977

Reply to Ogino and Wilson

por Feldkötter, Markus, Schwarzer, Verena, Wirth, Radu, Wienker, Thomas F., Wirth, Brunhilde
Publicado 2002

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

por Feldkötter, Markus, Schwarzer, Verena, Wirth, Radu, Wienker, Thomas F., Wirth, Brunhilde
Publicado 2002

Linkage studies in a pedigree with Van der Woude syndrome.

por Wienker, T F, Hudek, G, Bissbort, S, Mayerová, A, Mauff, G, Bender, K
Publicado 1987

Clinical reinvestigation and linkage analysis in the family with Episkopi blindness (Norrie disease).

por Wolff, G, Mayerová, A, Wienker, T F, Atalianis, P, Ioannou, P, Warburg, M
Publicado 1992

Evaluating information content of SNPs for sample-tagging in re-sequencing projects

por Hu, Hao, Liu, Xiang, Jin, Wenfei, Hilger Ropers, H, Wienker, Thomas F
Publicado en Sci Rep (2015)

Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization.

por Strauch, K, Fimmers, R, Kurz, T, Deichmann, K A, Wienker, T F, Baur, M P
Publicado 2000

Linkage analysis of alcohol dependence using MOD scores

por Strauch, Konstantin, Fürst, Robert, Rüschendorf, Franz, Windemuth, Christine, Dietter, Johannes, Flaquer, Antonia, Baur, Max P, Wienker, Thomas F
Publicado 2005

New mutation to Huntington's disease.

por Wolff, G, Deuschl, G, Wienker, T F, Hummel, K, Bender, K, Lücking, C H, Schumacher, M, Hammer, J, Oepen, G
Publicado 1989

Investigation of a Family with Autosomal Dominant Dilated Cardiomyopathy Defines a Novel Locus on Chromosome 2q14-q22

por Jung, Martin, Poepping, Imke, Perrot, Andreas, Ellmer, Annette E., Wienker, Thomas F., Dietz, Rainer, Reis, André, Osterziel, Karl Josef
Publicado 1999

Deletion at 12p in a Japanese child with brachydactyly overlaps the assigned locus of brachydactyly with hypertension in a Turkish family.

por Bähring, S, Nagai, T, Toka, H R, Nitz, I, Toka, O, Aydin, A, Mühl, A, Wienker, T F, Schuster, H, Luft, F C
Publicado 1997

Klüver–Bucy syndrome associated with a recessive variant in HGSNAT in two siblings with Mucopolysaccharidosis type IIIC (Sanfilippo C)

por Hu, Hao, Hübner, Christoph, Lukacs, Zoltan, Musante, Luciana, Gill, Esther, Wienker, Thomas F, Ropers, Hans-Hilger, Knierim, Ellen, Schuelke, Markus
Publicado en Eur J Hum Genet (2017)

Previously reported new type of autosomal recessive primary microcephaly is caused by compound heterozygous ASPM gene mutations

por Hu, Hao, Suckow, Vanessa, Musante, Luciana, Roggenkamp, Viola, Kraemer, Nadine, Ropers, Hans-Hilger, Hübner, Christoph, Wienker, Thomas F, Kaindl, Angela M
Publicado 2014

Localization of a Gene for Syndactyly Type 1 to Chromosome 2q34-q36

por Bosse, Kristin, Betz, Regina C., Lee, Young-Ae, Wienker, Thomas F., Reis, André, Kleen, Heidi, Propping, Peter, Cichon, Sven, Nöthen, Markus M.
Publicado 2000

The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21.

por Saar, K, Chrzanowska, K H, Stumm, M, Jung, M, Nürnberg, G, Wienker, T F, Seemanová, E, Wegner, R D, Reis, A, Sperling, K
Publicado 1997

Genomewide Scan in German Families Reveals Evidence for a Novel Psoriasis-Susceptibility Locus on Chromosome 19p13

por Lee, Young-Ae, Rüschendorf, Franz, Windemuth, Christine, Schmitt-Egenolf, Marcus, Stadelmann, Antje, Nürnberg, Gudrun, Ständer, Markward, Wienker, Thomas F., Reis, André, Traupe, Heiko
Publicado 2000

Splitting Schizophrenia: Periodic Catatonia–Susceptibility Locus on Chromosome 15q15

por Stöber, Gerald, Saar, Kathrin, Rüschendorf, Franz, Meyer, Jobst, Nürnberg, Gudrun, Jatzke, Susanne, Franzek, Ernst, Reis, André, Lesch, Klaus-Peter, Wienker, Thomas F., Beckmann, Helmut
Publicado 2000

The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families

por Davarniya, Behzad, Hu, Hao, Kahrizi, Kimia, Musante, Luciana, Fattahi, Zohreh, Hosseini, Masoumeh, Maqsoud, Fariba, Farajollahi, Reza, Wienker, Thomas F., Ropers, H. Hilger, Najmabadi, Hossein
Publicado en PLoS One (2015)