Reply to Ogino and Wilson

di Feldkötter, Markus, Schwarzer, Verena, Wirth, Radu, Wienker, Thomas F., Wirth, Brunhilde
Pubblicazione 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

di Feldkötter, Markus, Schwarzer, Verena, Wirth, Radu, Wienker, Thomas F., Wirth, Brunhilde
Pubblicazione 2002

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

di Hu, Hao, Liu, Xiang, Jin, Wenfei, Hilger Ropers, H, Wienker, Thomas F
Pubblicato in Sci Rep (2015)

Linkage analysis of alcohol dependence using MOD scores

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

VarWatch—A stand-alone software tool for variant matching

di Fredrich, Broder, Schmöhl, Marcus, Junge, Olaf, Gundlach, Sven, Ellinghaus, David, Pfeufer, Arne, Bettecken, Thomas, Siddiqui, Roman, Franke, Andre, Wienker, Thomas F., Hoeppner, Marc P., Krawczak, Michael
Pubblicato in PLoS One (2019)

Diaphragmatic Spinal Muscular Atrophy with Respiratory Distress Is Heterogeneous, and One Form Is Linked to Chromosome 11q13-q21

di 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
Pubblicazione 1999

Polymorphisms in the Genes Encoding Chemokine Receptor 5, Interleukin-10, and Monocyte Chemoattractant Protein 1 Contribute to Cytomegalovirus Reactivation and Disease after Alloge...

di Loeffler, Juergen, Steffens, Michael, Arlt, Eva-Maria, Toliat, Mohammad-Reza, Mezger, Markus, Suk, Anita, Wienker, Thomas F., Hebart, Holger, Nürnberg, Peter, Boeckh, Michael, Ljungman, Per, Trenschel, Rudolf, Einsele, Hermann
Pubblicazione 2006

A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disability

di Larti, Farzaneh, Kahrizi, Kimia, Musante, Luciana, Hu, Hao, Papari, Elahe, Fattahi, Zohreh, Bazazzadegan, Niloofar, Liu, Zhe, Banan, Mehdi, Garshasbi, Masoud, Wienker, Thomas F, Ropers, H Hilger, Galjart, Niels, Najmabadi, Hossein
Pubblicato in Eur J Hum Genet (2015)

A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disability

di Larti, Farzaneh, Kahrizi, Kimia, Musante, Luciana, Hu, Hao, Papari, Elahe, Fattahi, Zohreh, Bazazzadegan, Niloofar, Liu, Zhe, Banan, Mehdi, Garshasbi, Masoud, Wienker, Thomas F, Hilger Ropers, H, Galjart, Niels, Najmabadi, Hossein
Pubblicato in Eur J Hum Genet (2015)

Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation

di Hartmann, Bianca, Wai, Timothy, Hu, Hao, MacVicar, Thomas, Musante, Luciana, Fischer-Zirnsak, Björn, Stenzel, Werner, Gräf, Ralph, van den Heuvel, Lambert, Ropers, Hans-Hilger, Wienker, Thomas F, Hübner, Christoph, Langer, Thomas, Kaindl, Angela M
Pubblicato in eLife (2016)

De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome

di Bainbridge, Matthew N, Hu, Hao, Muzny, Donna M, Musante, Luciana, Lupski, James R, Graham, Brett H, Chen, Wei, Gripp, Karen W, Jenny, Kim, Wienker, Thomas F, Yang, Yaping, Sutton, V Reid, Gibbs, Richard A, Ropers, H Hilger
Pubblicazione 2013

Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia

di Stanke, Frauke, Becker, Tim, Kumar, Vinod, Hedtfeld, Silke, Becker, Christian, Cuppens, Harry, Tamm, Stephanie, Yarden, Jennifer, Laabs, Ulrike, Siebert, Benny, Fernandez, Luis, Macek, Milan, Radojkovic, Dragica, Ballmann, Manfred, Greipel, Joachim, Cassiman, Jean-Jacques, Wienker, Thomas F, Tümmler, Burkhard
Pubblicazione 2010

The opioid peptides enkephalin and β-endorphin in alcohol dependence

di Racz, Ildiko, Schürmann, Britta, Karpushova, Anna, Reuter, Martin, Cichon, Sven, Montag, Christian, Fürst, Robert, Schütz, Christian, Franke, Petra E., Strohmaier, Jana, Wienker, Thomas F., Terenius, Lars, Ösby, Urban, Gunnar, Agneta, Maier, Wolfgang, Bilkei-Gorzó, Andras, Nöthen, Markus, Zimmer, Andreas
Pubblicazione 2008