検索結果 - Lewin Eisele

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  1. 1
    Epigenetic Silencing of the Circadian Clock Gene CRY1 is Associated with an Indolent Clinical Course in Chronic Lymphocytic Leukemia

    Epigenetic Silencing of the Circadian Clock Gene CRY1 is Associated with an Indolent Clinical Course in Chronic Lymphocytic Leukemia 著者: Maher Hanoun, Lewin Eisele, Masako Suzuki, John M. Greally, Andreas Hüttmann, Semra Aydin, René Scholtysik, Ludger Klein‐Hitpaß, Ulrich Dührsen, Jan Dürig

    出版事項 2012
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  2. 2
    Shift work and the incidence of prostate cancer: a 10-year follow-up of a German population-based cohort study

    Shift work and the incidence of prostate cancer: a 10-year follow-up of a German population-based cohort study 著者: Thomas Behrens, Sylvia Rabstein, Katharina Wichert, Raimund Erbel, Lewin Eisele, Marina Arendt, Nico Dragano, Thomas Brà ⁄ ning, Karl-Heinz Jöckel

    出版事項 2017
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  3. 3
    Aging of blood can be tracked by DNA methylation changes at just three CpG sites

    Aging of blood can be tracked by DNA methylation changes at just three CpG sites 著者: Carola I. Weidner, Qiong Lin, Carmen Koch, Lewin Eisele, Fabian Beier, Patrick Ziegler, Dirk Bauerschlag, Karl‐Heinz Jöckel, Raimund Erbel, Thomas W. Mühleisen, Martin Zenke, Tim H. Brümmendorf, Wolfgang Wagner

    出版事項 2014
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  4. 4
    Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin’s lymphoma

    Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin’s lymphoma 著者: Matthew Frampton, Miguel Inácio da Silva Filho, Peter Broderick, Hauke Thomsen, Asta Försti, Jayaram Vijayakrishnan, Rosie Cooke, Victor Enciso-Mora, Per Hoffmann, Markus M. Nöthen, Amy Lloyd, Amy Holroyd, Lewin Eisele, Karl-Heinz Jöckel, Sabine Ponader, Elke Pogge von Strandmann, Tracy Lightfoot, Eve Roman, Annette Lake, Dorothy Montgomery, Ruth F. Jarrett, Anthony J. Swerdlow, Andreas Engert, Kari Hemminki, Richard S. Houlston

    出版事項 2013
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  5. 5
    Common variation at 10p12.31 near MLLT10 influences meningioma risk

    Common variation at 10p12.31 near MLLT10 influences meningioma risk 著者: Sara E. Dobbins, Peter Broderick, Beatrice Melin, Maria Feychting, Christoffer Johansen, Ulrika Andersson, Thomas Brännström, Johannes Schramm, Bianca Olver, Amy Lloyd, P. Yussanne, Fay J. Hosking, Stefan Lönn, Anders Ahlbom, Roger Henriksson, Minouk J. Schoemaker, Sarah Hepworth, Per Hoffmann, Thomas W. Mühleisen, Markus M. Nöthen, Susanne Moebus, Lewin Eisele, Michael Kosteljanetz, Kenneth Muir, Anthony J. Swerdlow, Matthias Simon, Richard S. Houlston

    出版事項 2011
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  6. 6
    Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype

    Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype 著者: Gabriele Migliorini, Bettina Fiege, Fay J. Hosking, Yussanne Ma, Rajiv Kumar, Amy L. Sherborne, Miguel Inácio da Silva Filho, Jayaram Vijayakrishnan, Rolf Koehler, Hauke Thomsen, Julie Irving, James M. Allan, Tracy Lightfoot, Eve Roman, Sally E. Kinsey, Eamonn Sheridan, Pamela Thompson, Per Hoffmann, Markus M. Nöthen, Thomas W. Mühleisen, Lewin Eisele, Martin Zimmermann, Claus R. Bartram, Martin Schrappe, Mel Greaves, Martin Stanulla, Kari Hemminki, Richard S. Houlston

    出版事項 2013
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  7. 7
    The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma

    The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma 著者: Niels Weinhold, David C. Johnson, Daniel Chubb, Bowang Chen, Asta Försti, Fay J. Hosking, Peter Broderick, P. Yussanne, Sara E. Dobbins, Dirk Hose, Brian A. Walker, Faith E. Davies, Martin Kaiser, Ni L Li, Walter A. Gregory, Graham Jackson, Mathias Witzens‐Harig, Kai Neben, Per Hoffmann, Markus M. Nöthen, Thomas W. Mühleisen, Lewin Eisele, Fiona M. Ross, Anna Jauch, Hartmut Goldschmidt, Richard S. Houlston, Gareth J. Morgan, Kari Hemminki

    出版事項 2013
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  8. 8
    Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222

    Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222 著者: Victor Enciso-Mora, Fay J. Hosking, Anna Luisa Di Stefano, Diana Zélénika, Sanjay Shete, Peter Broderick, Ahmed Idbaïh, J-Y Delattre, Khê Hoang‐Xuan, Y. Marie, Marianne Labussière, Agustí Alentorn, Pietro Ciccarino, Marta Rossetto, Georgina Armstrong, Yanhong Liu, Konstantinos Gousias, J. Schramm, Ching C. Lau, Sarah Hepworth, Minouk J. Schoemaker, Konstantin Strauch, Martina Müller‐Nurasyid, S. Schreiber, Andreas G. Franke, Susanne Moebus, Lewin Eisele, Anthony J. Swerdlow, Matthias Simon, Melissa L. Bondy, Mark Lathrop, Marc Sanson, Richard S. Houlston

    出版事項 2013
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  9. 9
    Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk

    Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk 著者: Daniel Chubb, Niels Weinhold, Peter Broderick, Bowang Chen, David C. Johnson, Asta Försti, Jayaram Vijayakrishnan, Gabriele Migliorini, Sara E. Dobbins, Amy Holroyd, Dirk Hose, Brian A. Walker, Faith E. Davies, Walter A. Gregory, Graham Jackson, Julie Irving, Guy Pratt, Chris Fegan, James A. L. Fenton, Kai Neben, Per Hoffmann, Markus M. Nöthen, Thomas W. Mühleisen, Lewin Eisele, Fiona M. Ross, Christian Straka, Hermann Einsele, Christian Langer, Elisabeth Dörner, James M. Allan, Anna Jauch, Gareth J. Morgan, Kari Hemminki, Richard S. Houlston, Hartmut Goldschmidt

    出版事項 2013
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  10. 10
    Deciphering the 8q24.21 association for glioma

    Deciphering the 8q24.21 association for glioma 著者: Victor Enciso-Mora, Fay J. Hosking, Ben Kinnersley, Yufei Wang, Sanjay Shete, Diana Zélénika, Peter Broderick, Ahmed Idbaïh, Jean-Yves Delattre, Khê Hoang‐Xuan, Yannick Marie, Anna Luisa Di Stefano, Marianne Labussière, Sara E. Dobbins, Blandine Boisselier, Pietro Ciccarino, Marta Rossetto, Georgina Armstrong, Yanhong Liu, Konstantinos Gousias, Johannes Schramm, Ching C. Lau, Sarah Hepworth, Konstantin Strauch, Martina Müller‐Nurasyid, Stefan Schreiber, André Franke, Susanne Moebus, Lewin Eisele, Asta Försti, Kari Hemminki, Ian Tomlinson, Anthony J. Swerdlow, Mark Lathrop, Matthias Simon, Melissa L. Bondy, Marc Sanson, Richard S. Houlston

    出版事項 2013
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  11. 11
    Chromosome 7p11.2 (EGFR) variation influences glioma risk

    Chromosome 7p11.2 (EGFR) variation influences glioma risk 著者: Marc Sanson, Fay J. Hosking, Sanjay Shete, Diana Zélénika, Sara E. Dobbins, Yussanne Ma, Victor Enciso-Mora, Ahmed Idbaïh, Jean-Yves Delattre, Khê Hoang‐Xuan, Yannick Marie, Blandine Boisselier, Alain Carpentier, Xiao-Wei Wang, Anna Luisa Di Stefano, Marianne Labussière, Konstantinos Gousias, Johannes Schramm, Anne Boland, Doris Lechner, Marta Gut, Georgina Armstrong, Yanhong Liu, Robert Yu, Ching C. Lau, Maria Chiara Di Bernardo, Lindsay B. Robertson, Kenneth Muir, Sarah Hepworth, Anthony J. Swerdlow, Minouk J. Schoemaker, H.-Erich Wichmann, Martina Müller‐Nurasyid, Stefan Schreiber, André Franke, Susanne Moebus, Lewin Eisele, Asta Försti, Kari Hemminki, Mark Lathrop, Melissa L. Bondy, Richard S. Houlston, Matthias Simon

    出版事項 2011
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  12. 12
    Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

    Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci 著者: Kyle J. Gaulton, Teresa Ferreira, Yeji Lee, Anne Raimondo, Reedik Mägi, Michael E. Reschen, Anubha Mahajan, Adam E. Locke, Nigel W. Rayner, Neil Robertson, Robert A. Scott, Inga Prokopenko, Laura J. Scott, Todd Green, Thomas Sparsø, Dorothée Thuillier, Loïc Yengo, Harald Grallert, Simone Wahl, Mattias Frånberg, Rona J. Strawbridge, Hans A. Kestler, Himanshu Chheda, Lewin Eisele, Stefan Gustafsson, Valgerður Steinthórsdóttir, Guðmar Þorleifsson, Lu Qi, Lennart C. Karssen, Jin‐Moo Lee, Sara M. Willems, Man Li, Han Chen, Christian Fuchsberger, Phoenix Kwan, Clement Ma, Michael D. Linderman, Yingchang Lu, Soren K. Thomsen, Jana K. Rundle, Nicola L. Beer, Martijn van de Bunt, Anil Chalisey, Hyun Min Kang, Benjamin F. Voight, Gonçalo R. Abecasis, Peter Almgren, Damiano Baldassarre, Beverley Balkau, Rafn Benediktsson, Matthias Blüher, Heiner Boeing, Lori L. Bonnycastle, Erwin P. Böttinger, Noël P. Burtt, Jason Carey, G. Charpentier, Peter S. Chines, Marilyn C. Cornelis, David Couper, Andrew Crenshaw, Rob M. van Dam, Alex S. F. Doney, Mozhgan Dorkhan, Sarah Edkins, Johan G. Eriksson, Tõnu Esko, Elodie Eury, João Fadista, Jason Flannick, Pierre Fontanillas, Caroline S. Fox, Paul W. Franks, Karl Gertow, Christian Gieger, Bruna Gigante, Omri Gottesman, George Grant, Niels Grarup, Christopher J. Groves, Maija Hassinen, Henri Theil, Christian Herder, Oddgeir L. Holmen, Ástráður B. Hreiðarsson, Steve E. Humphries, Sarah Hunt, Anne Jackson, Anna Jonsson, Marit E. Jørgensen, Torben Jørgensen, Wen‐Hong L. Kao, Nicola D. Kerrison, Leena Kinnunen, Norman Klopp, Augustine Kong, Péter Kovács, Peter Kraft, Jasmina Kravić, Cordelia Langford

    出版事項 2015
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  13. 13
    Genome-wide association study identifies 74 loci associated with educational attainment

    Genome-wide association study identifies 74 loci associated with educational attainment 著者: Aysu Okbay, Jonathan Beauchamp, Mark Alan Fontana, James J. Lee, Tune H. Pers, Cornelius A. Rietveld, Patrick Turley, Guo‐Bo Chen, Valur Emilsson, S. Fleur W. Meddens, Sven Oskarsson, Joseph K. Pickrell, Kevin Thom, Pascal Timshel, Ronald de Vlaming, Abdel Abdellaoui, Tarunveer S. Ahluwalia, Jonas Bacelis, Clemens Baumbach, Gyða Björnsdóttir, J Brandsma, Maria Pina Concas, Jaime Derringer, Nicholas A. Furlotte, Tessel E. Galesloot, Giorgia Girotto, Richa Gupta, Leanne M. Hall, Sarah E. Harris, Edith Hofer, Momoko Horikoshi, Jennifer E. Huffman, Kadri Kaasik, Ioanna Panagiota Kalafati, Robert Karlsson, Augustine Kong, Jari Lahti, Sven J. van der Lee, C. deLeeuw, Penelope A. Lind, Karl‐Oskar Lindgren, Tian Liu, Massimo Mangino, Jonathan Marten, Evelin Mihailov, Michael B. Miller, Peter J. van der Most, Christopher Oldmeadow, Antony Payton, Natalia Pervjakova, Wouter J. Peyrot, Yong Qian, Olli Raitakari, Rico Rueedi, Erika Salvi, Börge Schmidt, Katharina E. Schraut, Jianxin Shi, Albert V. Smith, Raymond A. Poot, Beaté St Pourcain, Alexander Teumer, Gudmar Thorleifsson, Niek Verweij, Dragana Vuckovic, Juergen Wellmann, Harm-Jan Westra, Jingyun Yang, Wei Zhao, Zhihong Zhu, Behrooz Z. Alizadeh, Najaf Amin, Andrew Bakshi, Sebastian E. Baumeister, Ginevra Biino, Klaus Bønnelykke, Patricia A. Boyle, Harry Campbell, Francesco P. Cappuccio, Gail Davies, Jan-Emmanuel De Neve, Panos Deloukas, Ilja Demuth, Jun Ding, Peter Eibich, Lewin Eisele, Niina Eklund, David M. Evans, Jessica D. Faul, Mary F. Feitosa, Andreas J. Forstner, Ilaria Gandin, Bjarni Gunnarsson, Bjarni V. Halldórsson, Tamara B. Harris, Andrew C. Heath, Lynne J. Hocking, Elizabeth G. Holliday, Georg Homuth, Michael A. Horan

    出版事項 2016
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  14. 14
    An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

    An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans 著者: Robert A. Scott, Laura J. Scott, Reedik Mägi, Letizia Marullo, Kyle J. Gaulton, Marika Kaakinen, Natalia Pervjakova, Tune H. Pers, Andrew D. Johnson, John D. Eicher, Anne Jackson, Teresa Ferreira, Yeji Lee, Clement Ma, Valgerður Steinthórsdóttir, Guðmar Þorleifsson, Lu Qi, Natalie R. van Zuydam, Anubha Mahajan, Han Chen, Peter Almgren, Benjamin F. Voight, Harald Grallert, Martina Müller‐Nurasyid, Janina S. Ried, Nigel W. Rayner, Neil Robertson, Lennart C. Karssen, Jin‐Moo Lee, Sara M. Willems, Christian Fuchsberger, Phoenix Kwan, Tanya M. Teslovich, Pritam Chanda, Man Li, Yingchang Lu, Christian Dina, Dorothée Thuillier, Loïc Yengo, Longda Jiang, Thomas Sparsø, Hans A. Kestler, Himanshu Chheda, Lewin Eisele, Stefan Gustafsson, Mattias Frånberg, Rona J. Strawbridge, Rafn Benediktsson, Ástráður B. Hreiðarsson, Augustine Kong, Gunnar Sigurðsson, Nicola D. Kerrison, Jian’an Luan, Liming Liang, Thomas Meitinger, Michael Roden, Barbara Thorand, Tõnu Esko, Evelin Mihailov, Caroline S. Fox, Yongmei Liu, Denis Rybin, Bo Isomaa, Valeriya Lyssenko, Jaakko Tuomilehto, David Couper, James S. Pankow, Niels Grarup, Henri Theil, Marit E. Jørgensen, Torben Jørgensen, Allan Linneberg, Marilyn C. Cornelis, Rob M. van Dam, Sarah Hunt, Peter Kraft, Qi Sun, Sarah Edkins, Katharine R. Owen, John R. B. Perry, Andrew R. Wood, Eleftheria Zeggini, Juan Tajes-Fernandes, Gonçalo R. Abecasis, Lori L. Bonnycastle, Peter S. Chines, Heather M. Stringham, Heikki A. Koistinen, Leena Kinnunen, Bengt Sennblad, Hae‐Won Uh, Markus M. Nöthen, Sonali Pechlivanis, Damiano Baldassarre, Karl Gertow, Steve E. Humphries, Elena Tremoli, Norman Klopp, Julia Meyer, Gerald Steinbach

    出版事項 2017
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  15. 15
    Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

    Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization 著者: Dan E. Arking, Sara L. Pulit, Lia Crotti, Pim van der Harst, Patricia B. Munroe, Tamara T. Koopmann, Nona Sotoodehnia, Elizabeth J. Rossin, Michael P. Morley, Xinchen Wang, Andrew D. Johnson, Alicia Lundby, Daníel F. Guðbjartsson, Peter A. Noseworthy, Mark Eijgelsheim, Yuki Bradford, Kirill V. Tarasov, Marcus Dörr, Martina Müller‐Nurasyid, Annukka M. Lahtinen, Ilja M. Nolte, Albert V. Smith, Joshua C. Bis, Aaron Isaacs, Stephen Newhouse, Daniel S. Evans, Wendy S. Post, Daryl Waggott, Leo‐Pekka Lyytikäinen, Andrew A. Hicks, Lewin Eisele, David Ellinghaus, Caroline Hayward, Pau Navarro, Sheila Ulivi, Toshiko Tanaka, David J. Tester, Stéphanie Chatel, Stefan Gustafsson, Meena Kumari, Richard Morris, Åsa Torinsson Naluai, Sandosh Padmanabhan, Alexander Kluttig, Bernhard Strohmer, Andrie G. Panayiotou, María Torres, Michael Knoflach, Jaroslav A. Hubáček, Kamil Slowikowski, Soumya Raychaudhuri, Runjun D. Kumar, Tamara B. Harris, Lenore J. Launer, Alan R. Shuldiner, Álvaro Alonso, Joel S. Bader, Georg Ehret, Hailiang Huang, W.H. Linda Kao, James B. Strait, Peter W. Macfarlane, Matthew A. Brown, Mark J. Caulfield, Nilesh J. Samani, Florian Kronenberg, Johann Willeit, J. Gustav Smith, Karin Halina Greiser, Henriette E. Meyer zu Schwabedissen, Karl Werdan, Massimo Carella, Leopoldo Zelante, Susan R. Heckbert, Bruce M. Psaty, Jerome I. Rotter, Ivana Kolčić, Ozren Polašek, Alan F. Wright, Maura Griffin, Mark J. Daly, Davíð O. Arnar, Hilma Hólm, Unnur Þorsteinsdóttir, Joshua C. Denny, Dan M. Roden, Rebecca L. Zuvich, Valur Emilsson, Andrew Plump, Martin G. Larson, Christopher J. O’Donnell, Xiaoyan Yin, Marco Bobbo, Pio D’Adamo, Alfonso Iorio, Gianfranco Sinagra, Ángel Carracedo, Steven R. Cummings, Michael A. Nalls, Antti Jula

    出版事項 2014
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  16. 16
    Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

    Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation 著者: Ingrid E. Christophersen, Michiel Rienstra, Carolina Roselli, Xiaoyan Yin, Bastiaan Geelhoed, John Barnard, Honghuang Lin, Dan E. Arking, Albert V. Smith, Christine M. Albert, Mark Chaffin, Nathan R. Tucker, Molong Li, Derek Klarin, Nathan A. Bihlmeyer, Siew‐Kee Low, Peter Weeke, Martina Müller‐Nurasyid, J. G. Smith, Jennifer A. Brody, Maartje N. Niemeijer, Marcus Dörr, Stella Trompet, Jennifer E. Huffman, Stefan Gustafsson, Claudia Schurmann, Marcus E. Kleber, Leo‐Pekka Lyytikäinen, Ilkka Seppälä, Rainer Malik, Andréa R. V. R. Horimoto, Marco Pérez, Juha Sinisalo, Stefanie Aeschbacher, Sébastien Thériault, Jie Yao, Farid Radmanesh, Stefan Weiß, Alexander Teumer, Seung Hoan Choi, Lu‐Chen Weng, Sebastian Clauß, Rajat Deo, Daniel J. Rader, Svati H. Shah, Albert Y. Sun, Jemma C. Hopewell, Stéphanie Debette, Ganesh Chauhan, Qiong Yang, Bradford B. Worrall, Guillaume Paré, Yoichiro Kamatani, Yanick Hagemeijer, Niek Verweij, Joylene E. Siland, Michiaki Kubo, Jonathan D. Smith, David R. Van Wagoner, Joshua C. Bis, Siegfried Perz, Bruce M. Psaty, Paul M. Ridker, Jared W. Magnani, Tamara B. Harris, Lenore J. Launer, M. Benjamin Shoemaker, Sandosh Padmanabhan, Jeffrey Haessler, Traci M. Bartz, Mélanie Waldenberger, Peter Lichtner, Marina Arendt, José Eduardo Krieger, Mika Kähönen, Lorenz Risch, Alfredo José Mansur, Annette Peters, Blair H. Smith, Lars Lind, Stuart A. Scott, Yingchang Lu, Erwin B. Bottinger, Jussi Hernesniemi, Cecilia M. Lindgren, Jorge Wong, Jie Huang, Markku Eskola, Andrew P. Morris, Ian Ford, Alex P. Reiner, Graciela Delgado, Lin Y. Chen, Yii-Der Ida Chen, Roopinder K. Sandhu, Man Li, Eric Boerwinkle, Lewin Eisele, Lars Lannfelt, Natalia S. Rost

    出版事項 2017
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