Thomas F Wienker

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Artikel 29

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2017-04-28

Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation

Luis R Hernandez-Miranda, Nadine Kraemer, Olaf Ninnemann, Carmen Birchmeier, Thomas F Wienker, Freda D. Miller
2015-05-11

PDE3A mutations cause autosomal dominant hypertension with brachydactyly

Sigmar Stricker, Sylvia Bähring, Atakan Aydin, Stefan Mundlos, Jens Tank, Peter Krawitz, Philipp Maass, Friedrich C. Luft, Hermann Haller, Franz Rüschendorf, Lars-Olof Hattenbach, Anita Rauch, Hakan R Toka, Jens Jordan, Carsten Lindschau, Fatimunnisa Qadri, Astrid Mühl, Thomas F Wienker, Nihat Bilginturan, Enno Klussmann, Okan Toka
2014-12-18

Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study

Thomas Meitinger, Jean-Daniel Chiche, Emma E Davenport, Tom Parks, Anthony Gordon, Michael Steffens, Charles Mein, Julian C Knight, Mark Caulfield, Jordi Rello, Adrian V. S. Hill, Peter Lichtner, Thomas F Wienker, Katherine S Elliott
2013-09

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Geraldine Dawson, Marcella Rietschel, Tatiana Foroud, Margaret A. Pericak-Vance, Gonneke Willemsen, Jouke-Jan Hottenga, Thomas Werge, Soumya Raychaudhuri, Guy A. Rouleau, Bertram Müller-Myhsok, Aarno Palotie, Devin Absher, Sian Caesar, Katherine Gordon-Smith, Hans-Christoph Steinhausen, Tobias Banaschewski, Aribert Rothenberger, Hakon Hakonarson, Philip Asherson, Herbert Roeyers, Mark Lathrop, Josephine Elia, Marta Ribasés, Mònica Bayés, Josep Antoni Ramos-Quiroga, Ana Miranda, Andreas Reif, Lindsey Kent, Klaus-Peter Lesch, Joseph Biederman, Sven Cichon, Franziska Degenhardt, Peter Propping, Jana Strohmaier, Srdjan Djurovic, Florian Holsboer, Darina Czamara, Manuel Mattheisen, Manfred Uhr, Marcus Ising, Enda M Byrne, Nancy G. Buccola, Benjamin S Pickard, Donald J. MacIntyre, Michael Steffens, Verneri Anttila, Matthew C Keller, Stephan J. Sanders, Timothy W Yu, Tiffany A Greenwood, Detelina Grozeva, Louise Gallagher, Stéphane Jamain, Stefan Herms, Guiomar Oliveira, Michael R. Barnes, Sarah E Bergen, Steven P Hamilton, Richard Anney, Ellen M. Wijsman, James S. Sutcliffe, Douglas M. Ruderfer, Astrid M. Vicente, Anjali K. Henders, Thomas F. Hansen, Jennifer L. Moran, Andrew D. Paterson, Stanley Zammit, Caroline M Nievergelt, Keith Matthews, Derek W. Morris, Catalina Betancur, Bruno Etain, Gunnar Morken, Andrew McQuillin, Christel M Middeldorp, Bru Cormand, Jonna Kuntsi, Todd Lencz, Gary J. Donohoe, Ingrid Agartz, Aiden Corvin, Michael Goddard, Richard Bruggeman, George Kirov, Sarah E. Medland, Naomi R. Wray, Francis J. McMahon, Russell Schachar, Patrik K E Magnusson, Andrew McIntosh, Anthony Monaco, Peter Holmans, Anita Thapar, Ian W. Craig, Joseph Buxbaum, Inez Myin-Germeys, Howard J Edenberg, John I. Nurnberger, Richard P. Ebstein, Barbara Franke, Ole A. Andreassen, Michael Gill, Michael C O'Donovan, Myrna M. Weissman, Peter M. Visscher, Markus M Nöthen, Stephen Faraone, Nick Martin, Kathryn Roeder, Daniel Moreno-De-Luca, William B. Lawson, Gerome Breen, Cathryn Lewis, Eric M. Morrow, Chunyu Liu, Éric Fombonne, David Curtis, Lydia Krabbendam, Gerard Van Grootheest, Sean Ennis, Morten Mattingsdal, Frank Bellivier, Marion Leboyer, Danielle Posthuma, Grant W. Montgomery, Paul Lichtenstein, Donald W. Black, Dale R Nyholt, Thomas H Wassink, William Coryell, Fritz Poustka, Jan Buitelaar, Catherine Lord, Peter Szatmari, Daniel Geschwind, Ian B Hickie, Christa Lese Martin, Edwin H Cook, Stephen W. Scherer, Lambertus Klei, Joseph Piven, Brenda Penninx, Ingrid Melle, Michael Boehnke, Christina M. Hultman, Mikael Landén, Dorret Boomsma, Kenneth Kendler, Benjamin M. Neale, Huda Akil, Lena Backlund, Nicholas J Bass, Hilary Coon, Eco de Geus, Frank Dudbridge, Matthew Flickinger, Elliot S Gershon, Andrew C. Heath, Ian Jones, Jung-Ying Tzeng, Radhika Kandaswamy, Elaine M Kenny, Niklas Långström, David H. Ledbetter, Jun Z. Li, Wolfgang Maier, Steven A McCarroll, Patrick Mcgrath, Peter McGuffin, Valentina Escott-Price, Richard M. Myers, Roel Ophoff, Michael Owen, Dan Rujescu, Alan R. Sanders, Nicholas J Schork, Federica Tozzi, Jens Treutlein, Stephanie H Witt, Allan H Young, Mark Joseph Daly, Patrick F Sullivan, Jordan W Smoller, Yunjung Kim, Thomas G. Schulze, Jonathan L Haines, Pamela A F Madden, Michael C. Neale, Ina Giegling, Ann Olincy, René S. Kahn, Wiepke Cahn, Jeffrey Lieberman, C. Robert Cloninger, Christopher A. Walsh, Pamela Sklar, Stephan Ripke, Susan L Slager, Michael Bauer, Veronica J Vieland, Rita M. Cantor, Douglas Blackwood, Walter J Muir, David St Clair, Michele T Pato, Paul D Shilling, Phil H Lee, Scott D Gordon, Johannes H Smit, Elisabeth Binder, Thomas W Mühleisen, Nelson A. Freimer, Annette M Hartmann, Roy H Perlis, Bryan Mowry, Farooq Amin, Adebayo Anjorin, Dan E Arking, Judith A Badner, Agatino Battaglia, Wade H Berrettini, Thomas Bettecken, Cinnamon Bloss, René Breuer, Paul Cormican, Aravinda Chakravarti, Kimberly Chambert, Tanzeem Choudhury, Jennifer Crosbie, Michael L Cuccaro, Susmita Datta, Alysa E Doyle, Jubao Duan, Eftichia Duketis, Ayman Fanous, Christine Fraser, Robert Freedman, Christine M Freitag, Marion Friedl, Louise Frisén, Pablo V Gejman, Dorothy E Grice, Weihua Guan, Lieuwe de Haan, Joachim Hallmayer, Marian L Hamshere, Martin Hautzinger, Susanne Hoefels, Witte J Hoogendijk, Vanessa Hus Bal, Andrés Ingason, Sabine M Klauck, Bettina Konte, Ania Korszun, Robert Krasucki, Phoenix Kwan, Douglas F Levinson, Falk W Lohoff, Sandra K Loo, Susanne Lucae, Elena Maestrini, Paméla McMahon-Morin, Shrikant M Mane, Kevin A McGhee, James J McGough, Melvin McInnis, Rebecca McKinney, Alan Mclean, Jobst Meyer, Lefkos T Middleton, Vihra Milanova, Pierandrea Muglia, Michael Murtha, Vishwajit Nimgaonkar, Willem A Nolen, Evaristus A Nwulia, Colm O'Dushlaine, Robert D Oades, Urban Osby, Jeremy R Parr, Michele L Pergadia, Jonathan Pimm, James B Potash, Vinay Puri, Digby Quested, Karola Rehnström, Lizzy Rossin, Susan L Santangelo, Martin Schalling, William A Scheftner, Markus Ludwig Rupert Schwarz, Edward M Scolnick, Laura Scott, Stanley I Shyn, Jeremy Silverman, Susan Smalley, John Strauss, T. Scott Stroup, Szabocls Szelinger, Srinivasa Thirumalai, Alexandre A Todorov, Stanley J Watson, Thomas F Wienker, Arthur Jeremy Willsey, Peter P Zandi, Frans G Zitman, Bernie Devlin, John R Kelsoe, Nick Craddock, Shaun M Purcell, David A Collier, Gerard D Schellenberg, William M. McMahon, John B Vincent, James L. Kennedy, Edmund Sonuga-Barke
2013-07-01

Familial aggregation of pure tone hearing thresholds in an aging European population

Michael Steffens, Ilmari Pyykkö, Dafydd Stephens, Cor W. R. J. Cremers, Hannie Kremer, Elina Mäki-Torkko, Patrick L M Huygen, Lut Van Laer, Els Van Eyken, Jeroen R Huyghe, Ingeborg Dhooge, Eva Orzan, Markus H F Pfister, Agnete Parving, Martti Sorri, Vedat Topsakal, Jan-Jaap Hendrickx, Samuli Hannula, Kelly Demeester, Anke Tropitzsch, Amanda Bonaconsa, Joke Huyghe, Sylvia J Kunst, Amalia Diaz-Lacava, Thomas F Wienker, Paul Van de Heyning
2012-09-01

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

Ingo Ruczinski, Sven Cichon, Peter Propping, Manuel Mattheisen, Nikolaos Daratsianos, Stefan Herms, Per Hoffmann, Michele Rubini, Markus M Nöthen, Regine PM Steegers-Theunissen, Mary L. Marazita, Thomas F Wienker, Jeffrey C Murray, Terri H Beaty, Kerstin U Ludwig, Anne C Böhmer, Elisabeth Mangold, Margrieta A. Alblas, Nadine Kluck, Heiko Reutter, Carola Lauster, Bert Braumann, Alexander Hemprich, Simone Pötzsch, Bettina Blaumeiser, Franz-Josef Kramer, Sandra Barth
2012-09-04

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

Albena Jordanova, Peter De Jonghe, Franz Rüschendorf, Tobias Balschun, Christian Gieger, Ulrich Stephani, Hiltrud Muhle, Dorothée Kasteleijn-Nolst Trenité, Felix Rosenow, Dick Lindhout, Verena Gaus, Rainer Surges, Peter Nürnberg, Heinz Erich Wichmann, Holger Lerche, Pasquale Striano, Antonio Gambardella, Anna-Elina Lehesjoki, Sarah von Spiczak, Ann-Kathrin Ruppert, Martha Feucht, Fritz Zimprich, Carla Marini, David Ellinghaus, Claudia Kapser, Arvid Suls, Susannah T Bellows, Karen Oliver, Michael Steffens, Gerrit-Jan de Haan, Ingrid Scheffer, Wolfram S. Kunz, Federico Zara, Paolo Tinuper, Samuel Berkovic, Rikke S Møller, Andre Franke, Carolien G de Kovel, Christian E Elger, Thomas F Wienker, Mohammad Reza Toliat, EPICURE Consortium, EMINet Consortium, Bernhard Steinhoff, Michel Guipponi, Alain Malafosse, Christoph J Schankin, Bobby Koeleman, Leanne Dibbens, Saul A Mullen, Angela Robbiano, Dieter Janz, Ailing A Kleefuss-Lie, Stéphanie Baulac, Anne Hempelmann, Rima Nabbout, José M Serratosa, Philipp Reif
2012-03-26

Schizophrenia risk polymorphisms in the TCF4 gene interact with smoking in the modulation of auditory sensory gating

Michael Nothnagel, Peter Nürnberg, Jürgen Gallinat, Boris B Quednow, Holger Thiele, Thomas F Wienker, Mohammad Reza Toliat, Norbert Dahmen, Amalia Diaz-Lacava, Wolfgang Maier, Michael Wagner
2011-03-11

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

Marcella Rietschel, Sven Cichon, Kári Stefánsson, Hreinn Stefansson, Mark Lathrop, Heinz Erich Wichmann, Bertram Müller-Myhsok, Susanne Moebus, Andreas Reif, Peter Propping, Jana Strohmaier, Srdjan Djurovic, Maria Grigoroiu-Serbanescu, Manuel Mattheisen, Engilbert Sigurdsson, Fermin Mayoral, Michael Steffens, Aleksandr Tiganov, Carmen C Diaconu, Stefan Herms, Stéphane Jamain, Bruno Etain, Sarah E. Medland, Frank Bellivier, Marion Leboyer, Philip B. Mitchell, Peter R Schofield, Grant W. Montgomery, Michael C O'Donovan, Markus M Nöthen, Nick Martin, Chantal Henry, Ole A. Andreassen, Stefan Schreiber, Michael Bauer, Piotr M Czerski, Scott D Gordon, Thomas G. Schulze, Thomas F Wienker, Ómar Gústafsson, Marian L Hamshere, Stacy Steinberg, Nick Craddock, Thomas W Mühleisen, René Breuer, Susanne Lucae, Gulja Babadjanova, Lilia Abramova, Joanna Twarowska-Hauser, Britta Haenisch, Lutz Priebe, Christine Schmäl, Simon Heath, Markus Ludwig Rupert Schwarz, Jutta Kammerer-Ciernioch, Jean-Pierre Kahn, Fabio Riva, Jennifer Vollmer, Martin Hautzinger, Helmut Vedder, Johanna Sasse, Franziska Degenhardt
2010-10-01

An integrated genome research network for studying the genetics of alcohol addiction

Benedikt Brors, Markus M Nöthen, Wolfgang H Sommer, Marcella Rietschel, Jan M. Deussing, Alexander Sartorius, Roland Eils, Rolf Sprengel, Heinz Erich Wichmann, Wolfgang Wurst, Thomas F Wienker, Falk Kiefer, Norbert Dahmen, Peter Gebicke-Haerter, Rainer Spanagel
2010-07-31

Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression.

Michael Steffens, Peter Kirsch, Stefan Herms, Benedikt Brors, Andreas Meyer-Lindenberg, Markus M Nöthen, Bertram Müller-Myhsok, Daniela Mier, Manuel Mattheisen, Sven Cichon, Franziska Degenhardt, Marcella Rietschel, Karl-Heinz Jöckel, Heinz Erich Wichmann, Stefan Schreiber, Thomas G. Schulze, Thomas F Wienker, Dilafruz Juraeva, Britta Haenisch, Jens Treutlein, Jana Strohmaier, Susanne Lucae, René Breuer, Christine Schmäl, Thomas Bettecken, Susanne Hoefels, Susanne Erk, Elisabeth Binder, Knut Schnell, Christine Esslinger
2010

Feasible and Successful: Genome-Wide Interaction Analysis Involving All 1.9 × 1011 Pair-Wise Interaction Tests

Michael Steffens, Stefan Herms, Sven Cichon, Markus M Nöthen, Thomas F Wienker, Rolf Fimmers
2010-01

VEGF Gene Haplotypes Are Associated With Sarcoidosis

Stefan Herms, Sven Cichon, Markus M Nöthen, Thomas F Wienker, Anna Karpushova
2009-07-01

Genome-wide association study of alcohol dependence

Nico Dragano, Marcella Rietschel, Sven Cichon, Michael Steffens, Anbarasu Lourdusamy, Wolfgang H Sommer, Markus M Nöthen, Heinz Erich Wichmann, Patrick F. Sullivan, Stefan Schreiber, Rainald Moessner, Thomas F Wienker, Falk Kiefer, Jens Treutlein, Monika Ridinger, Norbert Wodarz, Norbert Dahmen, Kerstin U Ludwig, Fernando Leonardi-Essmann, Peter Gebicke-Haerter, Rainer Spanagel
2009-12-20

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

Thomas Meitinger, Sven Cichon, Peter Propping, Manuel Mattheisen, Melissa Ferrian, Michael Steffens, Per Hoffmann, Stefan Herms, Peter Mossey, Michele Rubini, Markus M Nöthen, Michael Krawczak, Susanne Moebus, Regine PM Steegers-Theunissen, Stefan Schreiber, Thomas F Wienker, Kerstin U Ludwig, Elisabeth Mangold, Nadine Kluck, Heiko Reutter, Carola Lauster, Bert Braumann, Alexander Hemprich, Simone Pötzsch, Bettina Blaumeiser, Franz-Josef Kramer, Stefanie Birnbaum, Carlotta Baluardo, Nilma Almeida de Assis, Sandra Barth
2009-03-08

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

Sven Cichon, Melissa Ferrian, Michael Steffens, Stefan Herms, Per Hoffmann, Peter Mossey, Michele Rubini, Markus M Nöthen, Peter Propping, Susanne Moebus, Regine PM Steegers-Theunissen, Thomas F Wienker, Kerstin U Ludwig, Elisabeth Mangold, Margrieta A. Alblas, Heiko Reutter, Carola Lauster, Bert Braumann, Alexander Hemprich, Simone Pötzsch, Franz-Josef Kramer, Stefanie Birnbaum, Carlotta Baluardo, Nilma Almeida de Assis, Sandra Barth
2008-06-10

Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter study

Angeles Espeso, Michael Steffens, Guy Van Camp, Paul Van de Heyning, Ilmari Pyykkö, Dafydd Stephens, Cor W. R. J. Cremers, Hannie Kremer, Elina Mäki-Torkko, Patrick L M Huygen, Lut Van Laer, Els Van Eyken, Jeroen R Huyghe, Ingeborg Dhooge, Eva Orzan, Markus H F Pfister, Agnete Parving, Martti Sorri, Vedat Topsakal, Jan-Jaap Hendrickx, Samuli Hannula, Kelly Demeester, Anke Tropitzsch, Amanda Bonaconsa, Katia Verbruggen, Joke Huyghe, Sylvia J Kunst, Minna Manninen, Amalia Diaz-Lacava, Thomas F Wienker
2008-06-17

Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypes

Thomas Meitinger, Michael Steffens, Peter Lichtner, Michael G Hennerici, Thomas F Wienker
2008-10-12

Susceptibility variants for male-pattern baldness on chromosome 20p11.

Sven Cichon, Sibylle Eigelshoven, Anne-Katrin Kortüm, Roman Reinartz, Axel M Hillmer, Michael Steffens, Stefan Herms, Grant W. Montgomery, Markus M Nöthen, Nick Martin, Dale R Nyholt, Peter Propping, Karl-Heinz Jöckel, Susanne Moebus, Raimund Erbel, Thomas F Wienker, Thomas W Mühleisen, Margrieta A. Alblas, Felix F Brockschmidt, Roland Kruse, Sandra Hanneken
2008-08-28

Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait

Angeles Espeso, Guy Van Camp, Paul Van de Heyning, Peter Nürnberg, Ilmari Pyykkö, Dafydd Stephens, Christian Becker, Cor W. R. J. Cremers, Hannie Kremer, Elina Mäki-Torkko, Lut Van Laer, Els Van Eyken, Jeroen R Huyghe, Eva Orzan, Markus H F Pfister, Agnete Parving, Martti Sorri, Vedat Topsakal, Jan-Jaap Hendrickx, Samuli Hannula, Kelly Demeester, Amanda Bonaconsa, Sylvia J Kunst, Minna Manninen, Thomas F Wienker, Manuela Baur
2008-06-27

The opioid peptides enkephalin and beta-endorphin in alcohol dependence

Sven Cichon, Markus M Nöthen, Thomas F Wienker, Anna Karpushova, Jana Strohmaier, Petra E Franke
2007-09-17

The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q.

Sven Cichon, Marcella Rietschel, Fermin Mayoral, Markus M Nöthen, Rami Abou Jamra, Peter Propping, Radka Kaneva, Thomas G. Schulze, Thomas F Wienker, Assen V Jablensky, Guillermo Orozco y Diaz, Vihra Milanova, Fabio Riva, Eudoxia Gay, Francisco Cabaleiro, Clara Krystal Pérez Fermin, Christian Kostov, Vesselin Chorbov, Amelia Nikolova-Hill, Vessela Stoyanova, George Onchev, Ivo Kremensky, Georg Auburger
2007-10-06

The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment.

Michael Steffens, Paul Van de Heyning, Angeles Espeso, Guy Van Camp, Ilmari Pyykkö, Dafydd Stephens, Cor W. R. J. Cremers, Hannie Kremer, Elina Mäki-Torkko, Patrick L M Huygen, Lut Van Laer, Els Van Eyken, Jeroen R Huyghe, Ingeborg Dhooge, Eva Orzan, Markus H F Pfister, Agnete Parving, Martti Sorri, Vedat Topsakal, Jan-Jaap Hendrickx, Samuli Hannula, Kelly Demeester, Amanda Bonaconsa, Katia Verbruggen, Joke Huyghe, Sylvia J Kunst, Minna Manninen, Amalia Diaz-Lacava, Thomas F Wienker, Manuela Baur
2007-10-01

The contribution of GJB2 (Connexin 26) 35delG to age-related hearing impairment and noise-induced hearing loss.

Michael Steffens, Angeles Espeso, Ilmari Pyykkö, Dafydd Stephens, Mariola Sliwinska-Kowalska, Cor W. R. J. Cremers, Hannie Kremer, Elina Mäki-Torkko, Patrick L M Huygen, Lut Van Laer, Els Van Eyken, Ingeborg Dhooge, Eva Orzan, Markus H F Pfister, Agnete Parving, Martti Sorri, Vedat Topsakal, Jan-Jaap Hendrickx, Samuli Hannula, Kelly Demeester, Amanda Bonaconsa, Katia Verbruggen, Joke Huyghe, Sylvia J Kunst, Thomas F Wienker, Manuela Baur, Paul Van de Heyning
2006-09-21

SNP-based analysis of genetic substructure in the German population.

Michael Steffens, Andreas Ziegler, Jochen Hampe, Thomas Meitinger, Kathryn Roeder, Inke R. König, Michael Krawczak, Thomas Illig, Peter Lichtner, Norman Klopp, Heinz Erich Wichmann, Claudia Lamina, Stefan Schreiber, Thomas Bettecken, Thomas F Wienker, Amke Caliebe, Mohammad Reza Toliat, Amalia Diaz-Lacava
2005-11-02

Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.

Marcella Rietschel, Sven Cichon, Peter Propping, Stephanie Ohlraun, Fermin Mayoral, Markus M Nöthen, Peter Nürnberg, Rami Abou Jamra, Konstantin Strauch, Radka Kaneva, Luba Kalaydjieva, Thomas G. Schulze, Thomas F Wienker, Assen V Jablensky, Christine Windemuth, Guillermo Orozco y Diaz, Vihra Milanova, Fabio Riva, Eudoxia Gay, Francisco Cabaleiro, Clara Krystal Pérez Fermin, Christian Kostov, Vesselin Chorbov, Amelia Nikolova-Hill, Vessela Stoyanova, George Onchev, Ivo Kremensky, Georg Auburger
2005-05-18

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia

Jochen Hampe, Sven Cichon, Peter Propping, Hans Christian Hennies, Axel M Hillmer, Markus M Nöthen, Rami Abou Jamra, Stefan Schreiber, Regina Christine Betz, Thomas G. Schulze, Thomas F Wienker, Yun Freudenberg-Hua, Felix F Brockschmidt, Roland Kruse, Bettina Blaumeiser, Sandra Hanneken, Thomas Ruzicka
2003-09-25

No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach.

Markus M Nöthen, Sven Cichon, Rami Abou Jamra, Peter Propping, Thomas F Wienker, Petra E Franke, Jürgen Deckert
1998-01

A cross-over medication trial for patients with autosomal-dominant hypertension with brachydactyly

Andreas Busjahn, Friedrich C. Luft, Hermann Haller, Hakan R Toka, Thomas F Wienker, Nihat Bilginturan, Okan Toka, Sylvia Bähring

Human - wd:Q87946469

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