نتائج البحث - Michael Steffens

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  1. 1
    INTERSNP: genome-wide interaction analysis guided by a priori information

    INTERSNP: genome-wide interaction analysis guided by a priori information حسب Christine Herold, Michael Steffens, Felix F. Brockschmidt, Max P. Baur, Tim Becker

    منشور في 2009
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  2. 2
    Medical education in pharmacogenomics—results from a survey on pharmacogenetic knowledge in healthcare professionals within the European pharmacogenomics clinical implementation project Ubiquitous Pharmacogenomics (U-PGx)

    Medical education in pharmacogenomics—results from a survey on pharmacogenetic knowledge in healthcare professionals within the European pharmacogenomics clinical implementation pr... حسب Katja S. Just, Michael Steffens, Jesse J. Swen, George P. Patrinos, Henk‐Jan Guchelaar, Julia Stingl

    منشور في 2017
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  3. 3
    Analysis of differential gene expression of PBMC for the in vitro detection of drug sensitization

    Analysis of differential gene expression of PBMC for the in vitro detection of drug sensitization حسب A Glässner, Michael Steffens, Amol Fatangare, Gerda Wurpts, Per Hoffmann, Philipp N Deck, Christine Krämer, Stefani Röseler, Albert Sickmann, Markus M. Nöthen, Amir S. Yazdi, Bernhardt Sachs

    منشور في 2025
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  4. 4
    Genome‐wide significant association between alcohol dependence and a variant in the <i>ADH</i> gene cluster

    Genome‐wide significant association between alcohol dependence and a variant in the <i>ADH</i> gene cluster حسب Josef Frank, Sven Cichon, Jens Treutlein, Monika Ridinger, Manuel Mattheisen, Per Hoffmann, Stefan Herms, Norbert Wodarz, Michael Soyka, Peter Zill, Wolfgang Maier, Rainald Mößner, Wolfgang Gäebel, Norbert Dahmen, Norbert Scherbaum, Christine Schmäl, Michael Steffens, Susanne Lucae, Marcus Ising, Bertram Müller‐Myhsok, Markus M. Nöthen, Karl Mann, Falk Kiefer, Marcella Rietschel

    منشور في 2011
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  5. 5
    Non‐genetic factors associated with ACE‐inhibitor and angiotensin receptor blocker‐induced angioedema

    Non‐genetic factors associated with ACE‐inhibitor and angiotensin receptor blocker‐induced angioedema حسب Diana Dubrall, Nora L. Branding, Carina M. Mathey, Anna M. Weber, Michael Steffens, Maike Below, Matthias Schmid, Bettina Wedi, D. Wieczorek, Philipp M. Amann, H. Löffler, Lukas Koch, Clemens Schöffl, Heinrich Dickel, Nomun Ganjuur, Thorsten Hornung, Timo Buhl, Emel Aygören‐Pürsün, Gerda Wurpts, Jens Greve, Markus M. Nöthen, Andreas J. Forstner, Bernhardt Sachs

    منشور في 2025
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  6. 6
    Genome-wide Association Study of Alcohol Dependence

    Genome-wide Association Study of Alcohol Dependence حسب Jens Treutlein, Sven Cichon, Monika Ridinger, Norbert Wodarz, Michael B. Soyka, Peter Zill, Wolfgang Maier, Rainald Moessner, Wolfgang Gäebel, Norbert Dahmen, Christoph Fehr, Norbert Scherbaum, Michael Steffens, Kerstin U. Ludwig, Josef Frank, H.-Erich Wichmann, Stefan Schreiber, Nico Dragano, Wolfgang H. Sommer, Fernando Leonardi‐Essmann, Anbarasu Lourdusamy, Peter J. Gebicke‐Haerter, Thomas F. Wienker, Patrick F. Sullivan, Markus M. Nöthen, Falk Kiefer, Rainer Spanagel, Karl Mann, Marcella Rietschel

    منشور في 2009
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  7. 7
    Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis

    Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis حسب Ulrike Hüffmeier, Steffen Uebe, Arif B. Ekici, John Bowes, Emiliano Giardina, Eleanor Korendowych, Kristina Juneblad, Maria Apel, Ross McManus, Pauline Ho, Ian N Bruce, Anthony W. Ryan, Frank Behrens, Jesús Lascorz, Beate Böhm, Heiko Traupe, Jörg Lohmann, Christian Gieger, Heinz‐Erich Wichmann, Christine Herold, Michael Steffens, Lars Klareskog, Thomas F. Wienker, Oliver FitzGerald, Gerd-Marie Alenius, Neil McHugh, Giuseppe Novelli, Harald Burkhardt, Anne Barton, André Reis

    منشور في 2010
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  8. 8
    Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment

    Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment حسب Els Van Eyken, Guy Van Camp, Erik Fransén, Vedat Topsakal, Jan Hendrickx, K. Demeester, Paul Van de Heyning, E Mäki‐Torkko, Samuli Hannula, Martti Sorri, Martin Jensen, Agnete Parving, Mikkel Bille, Manuela Baur, Markus Pfister, Amanda Bonaconsa, Manuela Mazzoli, Eva Orzan, Angeles Espeso, D. Stephens, K. Verbruggen, Joke Huyghe, Ingeborg Dhooge, P.L.M. Huygen, Hannie Kremer, Cor W. R. J. Cremers, Stefanie Kunst, M. Manninen, Ilmari Pyykkö, Amalia Diaz Lacava, Michael Steffens, T. F. Wienker, L. Van Laer

    منشور في 2007
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  9. 9
    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

    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-ba... حسب Erik Fransén, Vedat Topsakal, Jan Hendrickx, Lut Van Laer, Jeroen R. Huyghe, Els Van Eyken, Nele Lemkens, Samuli Hannula, Elina Mäki‐Torkko, Mona Jensen, Kelly Demeester, Anke Tropitzsch, Amanda Bonaconsa, Manuela Mazzoli, Angeles Espeso, Katia Verbruggen, Joke Huyghe, P.L.M. Huygen, Sylvia J. W. Kunst, Minna Manninen, Amalia Díaz‐Lacava, Michael Steffens, Thomas F. Wienker, Ilmari Pyykkö, Cor W. R. J. Cremers, Hannie Kremer, Ingeborg Dhooge, Dafydd Stephens, Eva Orzan, Markus Pfister, Michael Bille, Agnete Parving, Martti Sorri, Paul Van de Heyning, Guy Van Camp

    منشور في 2008
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  10. 10
    The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment

    The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment حسب Lut Van Laer, Els Van Eyken, Erik Fransén, Jeroen R. Huyghe, Vedat Topsakal, Jan Hendrickx, Samuli Hannula, Elina Mäki‐Torkko, Mona Jensen, Kelly Demeester, Manuela Baur, Amanda Bonaconsa, Manuela Mazzoli, Angeles Espeso, Katia Verbruggen, Joke Huyghe, P.L.M. Huygen, Sylvia J. W. Kunst, Minna Manninen, Annelies Konings, Amalia Díaz‐Lacava, Michael Steffens, Thomas F. Wienker, Ilmari Pyykkö, Cor W. R. J. Cremers, Hannie Kremer, Ingeborg Dhooge, Dafydd Stephens, Eva Orzan, Markus Pfister, Michael Bille, Agnete Parving, Martti Sorri, Paul Van de Heyning, Guy Van Camp

    منشور في 2007
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  11. 11
    Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

    Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate حسب Elisabeth Mangold, Kerstin U. Ludwig, Stefanie Birnbaum, Carlotta Baluardo, Melissa Ferrian, Stefan Herms, Heiko Reutter, Nilma Almeida de Assis, Taofik Al Chawa, Manuel Mattheisen, Michael Steffens, Sandra Barth, Nadine Kluck, Anna Paul, Jessica Becker, Carola Lauster, Gül Schmidt, Bert Braumann, Martin Scheer, Rudolf H. Reich, Alexander Hemprich, Simone Pötzsch, Bettina Blaumeiser, Susanne Moebus, Michael Krawczak, Stefan Schreiber, Thomas Meitinger, Hans-Erich Wichmann, Régine P.M. Steegers‐Theunissen, Franz-Josef Kramer, Sven Cichon, Peter Propping, Thomas F. Wienker, Michael Knapp, Michele Rubini, Peter Mossey, Per Hoffmann, Markus M. Nöthen

    منشور في 2009
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  12. 12
    Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study

    Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study حسب Anna Rautanen, Tara C. Mills, Anthony Gordon, Paula Hutton, Michael Steffens, Rosamond Nuamah, Jean‐Daniel Chiche, Tom Parks, S. Jonathan Chapman, Emma E. Davenport, Katherine S. Elliott, Julian Bion, Peter Lichtner, Thomas Meitinger, Thomas F. Wienker, Mark J. Caulfield, Charles A. Mein, Frank Bloos, Ilona Bobek, Paolo Cotogni, Vladimír Šrámek, Silver Sarapuu, Makbule Kobilay, V. Marco Ranieri, Jordi Rello, Gonzalo Sirgo, Yoram Weiss, Stefan Rußwurm, E. Marion Schneider, Konrad Reinhart, Paul Holloway, Julian C. Knight, Chris Garrard, James A. Russell, Keith R. Walley, Frank Stüber, Adrian V. S. Hill, Charles Hinds

    منشور في 2014
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  13. 13
    Genome-wide association study reveals genetic risk underlying Parkinson's disease

    Genome-wide association study reveals genetic risk underlying Parkinson's disease حسب Javier Simón‐Sánchez, Claudia Schulte, José Brás, Manu Sharma, J. Raphael Gibbs, Daniela Berg, Coro Paisán-Ruı́z, Peter Lichtner, Sonja W. Scholz, Dena Hernández, Rejko Krüger, Monica Federoff, Christine Klein, Alison Goate, Joel S. Perlmutter, Michael Bonin, Michael A. Nalls, Thomas Illig, Christian Gieger, Henry Houlden, Michael Steffens, Michael S. Okun, Brad A. Racette, Mark Cookson, Kelly D. Foote, Hubert H. Fernandez, Bryan J. Traynor, Stefan Schreiber, Sampath Arepalli, Ryan R. Zonozi, Katrina Gwinn, Marcel van der Brug, Grisel Lopez, Stephen J. Chanock, Arthur Schatzkin, Yikyung Park, Albert R. Hollenbeck, Jianjun Gao, Xuemei Huang, Nicholas Wood, Delia Lorenz, Günther Deuschl, Honglei Chen, Olaf Rieß, John Hardy, Andrew Singleton, Thomas Gasser

    منشور في 2009
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  14. 14
    Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies

    Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies حسب Carolien G. F. de Kovel, Holger Trucks, Katherine L. Helbig, Heather C. Mefford, Carl Baker, Costin Leu, Christian Kluck, Hiltrud Muhle, Sarah von Spiczak, P Ostertag, Tanja Obermeier, Ailing A. Kleefuß‐Lie, Kerstin Hallmann, Michael Steffens, Verena Gaus, Karl Martin Klein, Hajo M. Hamer, Felix Rosenow, Eva H. Brilstra, Dorothee Kasteleijn‐Nolst Trenité, Mariëlle E.M. Swinkels, Yvonne G. Weber, Iris Unterberger, Fritz Zimprich, L Urak, Martha Feucht, Karoline Fuchs, Rikke S. Møller, Helle Hjalgrim, Peter De Jonghe, Arvid Suls, I.-M. Ruckert, H.‐Erich Wichmann, André Franke, S. Schreiber, Peter Nürnberg, Christian E. Elger, Holger Lerche, Ulrich Stephani, Bobby P.C. Koeleman, Dick Lindhout, Evan E. Eichler, T. Sander

    منشور في 2009
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  15. 15
    Meta-analysis of ACE inhibitor–induced angioedema identifies novel risk locus

    Meta-analysis of ACE inhibitor–induced angioedema identifies novel risk locus حسب Carina M. Mathey, Carlo Maj, Niclas Eriksson, Kristi Krebs, Julia Westmeier, Friederike S. David, Maria Koromina, Annika B. Scheer, Nóra Szabó, Bettina Wedi, D. Wieczorek, Philipp M. Amann, H. Löffler, Lukas Koch, Clemens Schöffl, Heinrich Dickel, Nomun Ganjuur, Thorsten Hornung, Timo Buhl, Jens Greve, Gerda Wurpts, Emel Aygören‐Pürsün, Michael Steffens, Stefan Herms, Stefanie Heilmann‐Heimbach, Per Hoffmann, Börge Schmidt, Laven Mavarani, Trine Andresen, Signe Bek Sørensen, Vibeke Andersen, Ulla Vogel, Mikael Landén, Cynthia M. Bulik, Anette Bygum, Patrik K. E. Magnusson, Christian von Buchwald, Pär Hallberg, Sisse Rye Ostrowski, Erik Sørensen, Ole Birger Pedersen, Henrik Ullum, Christian Erikstrup, Henning Bundgaard, Lili Milani, Eva Rye Rasmussen, Mia Wadelius, Jonas Ghouse, Bernhardt Sachs, Markus M. Nöthen, Andreas J. Forstner

    منشور في 2024
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  16. 16
    Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder

    Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder حسب Sven Cichon, Thomas W. Mühleisen, Franziska Degenhardt, Manuel Mattheisen, Xavier Miró, Jana Strohmaier, Michael Steffens, Christian Meesters, Stefan Herms, Moritz Weingarten, Lutz Priebe, Britta Haenisch, Michael P. Alexander, Jennifer Vollmer, René Breuer, Christine Schmäl, Peter Teßmann, Susanne Moebus, H.‐Erich Wichmann, Stefan Schreiber, Bertram Müller‐Myhsok, Susanne Lucae, Stéphane Jamain, Marion Leboyer, Frank Bellivier, Bruno Étain, Chantal Henry, Jean‐Pierre Kahn, Simon Heath, Marian Hamshere, Michael O’Donovan, Michael J. Owen, Nick Craddock, Markus Schwarz, Helmut Vedder, Jutta Kammerer-Ciernioch, Andreas Reif, Johanna Sasse, Michael Bauer, Martin Hautzinger, A. Jordan Wright, Philip B. Mitchell, Peter R. Schofield, Grant W. Montgomery, Sarah E. Medland, Scott D. Gordon, Nicholas G. Martin, Ómar Gústafsson, Ole A. Andreassen, Srdjan Djurovic, Engilbert Sigurðsson, Stacy Steinberg, Hreinn Stefánsson, Kāri Stefánsson, Lejla Pojskić, L Oruc, Fabio Rivas, Fermín Mayoral, А. Г. Чучалин, Gulja Babadjanova, Tiganov As, Galina Pantelejeva, Л. И. Абрамова, Maria Grigoroiu‐Serbânescu, Carmen C. Diaconu, Piotr M. Czerski, Joanna Hauser, Andreas Zimmer, Mark Lathrop, Thomas G. Schulze, Thomas F. Wienker, Johannes Schumacher, Wolfgang Maier, Peter Propping, Marcella Rietschel, Markus M. Nöthen

    منشور في 2011
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  17. 17
    Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

    Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 حسب Michael Steffens, Costin Leu, Ann‐Kathrin Ruppert, Federico Zara, Pasquale Striano, Angela Robbiano, Giuseppe Capovilla, Paolo Tinuper, Antonio Gambardella, Amedeo Bianchi, Angela La Neve, Giovanni Crichiutti, Carolien G. F. de Kovel, Dorothee Kasteleijn‐Nolst Trenité, Gerrit‐Jan de Haan, Dick Lindhout, Verena Gaus, Bettina Schmitz, Diéter Janz, Yvonne G. Weber, Felicitas Becker, Holger Lerche, Bernhard J. Steinhoff, Ailing A. Kleefuß‐Lie, Wolfram S. Kunz, Rainer Surges, Christian E. Elger, Hiltrud Muhle, Sarah von Spiczak, P Ostertag, Ingo Helbig, Ulrich Stephani, Rikke S. Møller, Helle Hjalgrim, Leanne M. Dibbens, Susannah T. Bellows, Karen Oliver, Saul A. Mullen, Ingrid E. Scheffer, Samuel F. Berkovic, Kate V. Everett, M. R. Gardiner, Carla Marini, Renzo Guerrini, Anna‐Elina Lehesjoki, Auli Sirén, Michel Guipponi, Alain Malafosse, Pierre Thomas, Rima Nabbout, Stéphanie Baulac, Eric LeGuern, Rosa Guerrero, José M. Serratosa, Philipp S. Reif, Felix Rosenow, Martina Mörzinger, Martha Feucht, Fritz Zimprich, Claudia Kapser, Christoph J. Schankin, Arvid Suls, Kaat Smets, Peter De Jonghe, Albena Jordanova, Hande Çağlayan, Zühal Yapıcı, Demet Yalcin, Betül Baykan, Nerses Bebek, Uğur Özbek, Christian Gieger, H.‐Erich Wichmann, Tobias Balschun, David Ellinghaus, André Franke, Christian Meesters, Tim Becker, T. F. Wienker, Anne Hempelmann, Herbert Schulz, Franz Rüschendorf, Markus Leber, S. M. Pauck, Holger Trucks, Mohammad-Reza Toliat, Peter Nürnberg, G. Avanzini, Bobby P.C. Koeleman, T. Sander

    منشور في 2012
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  18. 18
    Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

    Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe حسب M. Rietschel, Manuel Mattheisen, F. Degenhardt, René S. Kahn, Don Linszen, Jim van Os, Durk Wiersma, Richard Bruggeman, Wiepke Cahn, Lieuwe de Haan, Lydia Krabbendam, Inez Myin‐Germeys, Thomas W. Mühleisen, Peter Kirsch, Christine Esslinger, Stefan Herms, Ditte Demontis, Michael Steffens, J Strohmaier, Britta Haenisch, René Breuer, Piotr M. Czerski, I Giegling, E Strengman, C Schmael, Ole Mors, Preben Bo Mortensen, D M Hougaard, Torben Ørntoft, Paweł Kapelski, Lutz Priebe, F B Basmanav, Andreas J. Forstner, Per Hoffmann, S Meier, J A. Nikitopoulos, Susanne Moebus, Michael P. Alexander, R Mössner, H-E Wichmann, S. Schreiber, Fernando Rivandeneira, A. Hofman, André G. Uitterlinden, T. F. Wienker, J Schumacher, J Hauser, W. Maier, R. M. Cantor, Susanne Erk, Thomas G. Schulze, Hreinn Stefánsson, Stacy Steinberg, Ómar Gústafsson, Engilbert Sigurðsson, Hannes Pétursson, Augustine Kong, Kāri Stefánsson, Olli Pietiläinen, Annamari Tuulio‐Henriksson, Tiina Paunio, Jouko Lönnqvist, Jaana Suvisaari, Leena Peltonen, Mirella Ruggeri, Sarah Tosato, Muriel Walshe, Robin Murray, David Collier, David St Clair, Thomas Hansen, Andrés Ingason, Klaus D. Jakobsen, Linh Viet Duong, Thomas Werge, Ingrid Melle, Ole A. Andreassen, Srdjan Djurovic, István Bitter, János Réthelyi, Л. И. Абрамова, В. Г. Каледа, В. Е. Голимбет, Erik G. Jönsson, Lars Terenius, Ingrid Agartz, Ruud van Winkel, Günter Kenis, Marc D. Binder, Jan H. Veldink, Carsten Wiuf, Michael Didriksen, Nick Craddock, Michael J. Owen, Michael O’Donovan, Anders D. Børglum, Dan Rujescu, Henrik Walter, Andreas Meyer‐Lindenberg, Markus M. Nöthen

    منشور في 2011
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  19. 19
    Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

    Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts حسب Tae‐Hwi Schwantes‐An, Juan Zhang, Li‐Shiun Chen, Sarah M. Hartz, Robert Culverhouse, Xiangning Chen, Hilary Coon, Josef Frank, Helen M. Kamens, Bettina Konte, Leena Kovanen, Antti Latvala, Lisa N. Legrand, Brion S. Maher, Whitney E. Melroy, Elliot C. Nelson, Mark W. Reid, Jason D. Robinson, Pei‐Hong Shen, Bao‐Zhu Yang, Judy A. Andrews, Paul Aveyard, Olga Beltcheva, Sandra A. Brown, Dale S. Cannon, Sven Cichon, Robin P. Corley, Norbert Dahmen, Louisa Degenhardt, Tatiana Foroud, Wolfgang Gäebel, Ina Giegling, Stephen J. Glatt, Richard A. Grucza, Jill Hardin, Annette M. Hartmann, Andrew C. Heath, Stefan Herms, Colin A. Hodgkinson, Per Hoffmann, Hyman Hops, David Huizinga, Marcus Ising, Eric O. Johnson, Elaine Johnstone, Radka Kaneva, Kenneth S. Kendler, Falk Kiefer, Henry R. Kranzler, Ken Krauter, Orna Levran, Susanne Lucae, Michael T. Lynskey, Wolfgang Maier, Karl Mann, Nicholas G. Martin, Manuel Mattheisen, Grant W. Montgomery, Bertram Müller‐Myhsok, Michael Murphy, Michael C. Neale, Momchil Nikolov, Denise Nishita, Markus M. Nöthen, John I. Nürnberger, Timo Partonen, Michele L. Pergadia, Maureen Reynolds, Monika Ridinger, Richard J. Rose, Noora Rouvinen-Lagerström, Norbert Scherbaum, Christine Schmäl, Michael Soyka, Michael C. Stallings, Michael Steffens, Jens Treutlein, Ming T. Tsuang, Tamara L. Wall, Norbert Wodarz, Vadim Yuferov, Peter Zill, Andrew W. Bergen, Jingchun Chen, Paul M. Cinciripini, Howard J. Edenberg, Marissa A. Ehringer, Robert E. Ferrell, Joel Gelernter, David Goldman, John K. Hewitt, Christian J. Hopfer, William G. Iacono, Jaakko Kaprio, Mary Jeanne Kreek, Ivo Kremensky, Pamela A. F. Madden, Matt McGue, Marcus R. Munafò, Robert A. Philibert

    منشور في 2015
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