Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Hauke Thomsen"'
Autor:
Alyssa Clay-Gilmour, Subhayan Chattopadhyay, Michelle A. T. Hildebrandt, Hauke Thomsen, Niels Weinhold, Pavel Vodicka, Ludmila Vodickova, Per Hoffmann, Markus M. Nöthen, Karl-Heinz Jöckel, Börge Schmidt, Christian Langer, Roman Hajek, Göran Hallmans, Ulrika Pettersson-Kymmer, Claes Ohlsson, Florentin Späth, Richard Houlston, Hartmut Goldschmidt, Elisabet E. Manasanch, Aaron Norman, Shaji Kumar, S. Vincent Rajkumar, Susan Slager, Asta Försti, Celine M. Vachon, Kari Hemminki
Publikováno v:
Blood Cancer Journal. 12
CA extern
Autor:
Tobias Möllers, Laura Perna, Bernd Holleczek, Hannah Stocker, Hauke Thomsen, Hermann Brenner, Dan Rujescu, Korbinian Weigl, Ben Schöttker
Publikováno v:
Molecular Psychiatry
The strongest genetic risk factor for Alzheimer’s disease (AD) is the ε4 allele of Apolipoprotein E (APOE) and recent genome-wide association meta-analyses have confirmed additional associated genetic loci with smaller effects. The aim of this stu
Autor:
Annette Juul Vangsted, van, Duin, M, David E. Neal, Peter Hoffmann, A Wolk, Robert J. Hamilton, Anthony J. Swerdlow, F. Wiklund, De, Ruyck, K, Paul A. Townsend, S. N. Thibodeau, Asta Försti, Esther M. John, Unnur Thorsteinsdottir, W Gregory, Niels Frost Andersen, Peter Broderick, A-K Wihlborg, Frank Claessens, Doug Easton, Kathryn L. Penney, Keith W. Muir, Jeri Kim, Jonathan S. Mitchell, Johanna Schleutker, G Cancel-Tassin, Barry S. Rosenstein, Jy Park, Hauke Thomsen, Rowan Kuiper, C West, H Gronberg, Mina Ali, CM Tangen, Obul Reddy Bandapalli, Ana Vega, Faith E. Davies, Rosalind A. Eeles, Daniel F. Gudbjartsson, Fredrick R. Schumacher, Janet L. Stanford, Paul D.P. Pharoah, Owen W. Stephens, Monique J. Roobol, Richard S. Houlston, Gudmar Thorleifsson, Christian Langer, Susan L. Neuhausen, S Chanock, G.G. Giles, Azad Razack, S Koutros, F Canzian, S Benlloch, H. Einsele, Kari Hemminki, KD Sorensen, Y-J Lu, K-T Khaw, Hareth Nahi, FC Hamdy, D Albanes, Christopher A. Haiman, Ellinor Johnsson, Amit Sud, Adam S. Kibel, Pieter Sonneveld, Florence Menegaux, Manolis Kogevinas, Nawaid Usmani, Annemiek Broyl, K. H. Jöckel, Jolanta Nickel, David W. Johnson, Aaa Olama, B.G. Nordestgaard, Amy Holroyd, Niels Weinhold, Cezary Cybulski, Sigurdur Y. Kristinsson, Radka Kaneva, Ruth C. Travis, Kari Stefansson, SI Berndt, Bowang Chen, Scott Kimber, Davor Lessel, Philip J. Law, M. M. Nöthen, Lisa A. Cannon-Albright, BE Henderson, Ni Li, Urban Gullberg, Uta Bertsch, S Weinstein, Nora Pashayan, Christiane Maier, H Brenner, Ingemar Turesson, Hardev Pandha, Thorunn Rafnar, Alison M. Dunning, Fiona M. Ross, Graham Jackson, David V. Conti, Sue A. Ingles, da, Silva, Filho, Mi, Jens Hillengass, Lisa F. Newcomb, Giulia Orlando, Brian A Walker, Teixeira, Björn Nilsson, Jenny L Donovan, Molly Went, U. H. Mellqvist, Chiara Campo, Zsofia Kote-Jarai, VL Stevens, Martin Kaiser, B-M Halvarsson, J Clements, Martin Hansson, Manuela Gago-Dominguez, EM Grindedal, Anders Waage, Julian Peto, L Mucci, Gareth J. Morgan, J Batra, H. Goldschmidt
Publikováno v:
Nature Communications
Nature Communications, Vol 10, Iss 1, Pp 1-3 (2019)
PRACTICAL Consortium & Townsend, P A 2019, ' Author Correction : Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma ', Nature Communications, vol. 10, no. 1, pp. 213 . https://doi.org/10.1038/s41467-018-08107-8
PRACTICAL consortium 2019, ' Author Correction : Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma ', Nature Communications, vol. 10, no. 1, 213 . https://doi.org/10.1038/s41467-018-08107-8
Nature Communications, Vol 10, Iss 1, Pp 1-3 (2019)
PRACTICAL Consortium & Townsend, P A 2019, ' Author Correction : Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma ', Nature Communications, vol. 10, no. 1, pp. 213 . https://doi.org/10.1038/s41467-018-08107-8
PRACTICAL consortium 2019, ' Author Correction : Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma ', Nature Communications, vol. 10, no. 1, 213 . https://doi.org/10.1038/s41467-018-08107-8
Genome-wide association studies (GWAS) have transformed our understanding of susceptibility to multiple myeloma (MM), but much of the heritability remains unexplained. We report a new GWAS, a meta-analysis with previous GWAS and a replication series,
Autor:
Markus M. Nöthen, Per Hoffmann, Hartmut Goldschmidt, Christian Langer, Sonali Pechlivanis, Börge Schmidt, Subhayan Chattopadhyay, Asta Försti, Karl-Heinz Jöckel, Arendt Marina, Hauke Thomsen, Niels Weinhold, Miguel Inacio da Silva Filho, Kari Hemminki
Publikováno v:
Molecular Medicine, Vol 24, Iss 1, Pp 1-13 (2018)
Molecular Medicine
Molecular Medicine
Background Recent identification of 10 germline variants predisposing to monoclonal gammopathy of undetermined significance (MGUS) explicates genetic dependency of this asymptomatic precursor condition with multiple myeloma (MM). Yet much of genetic
Publikováno v:
The European Physical Journal D. 72
We review recent progress in theory and simulation of strongly correlated classical plasmas, in general, and dusty plasmas, in particular. Using the one-component plasma (OCP) as a model, the structural properties of extended and finite correlated sy
Autor:
Richard S. Houlston, David W. Johnson, Faith E. Davies, Stig Lenhoff, Hauke Thomsen, Hartmut Goldschmidt, Christian Langer, Bhairavi Swaminathan, Rowan Kuiper, Markus M. Nöthen, Markus Hansson, Niels Weinhold, Annette Juul Vangsted, Marc Henrion, Kari Stefansson, Asta Försti, Mark van Duin, Jonathan S. Mitchell, Anna-Karin Wihlborg, Ulla Vogel, Mina Ali, Hermann Einsele, Chiara Campo, Kari Hemminki, Ingemar Turesson, Brian A Walker, Martin Kaiser, Per Hoffmann, Graham Jackson, Björn Nilsson, Fiona M. Ross, Bowang Chen, Jolanta Nickel, Ulf-Henrik Mellqvist, Gareth J. Morgan, Anders Waage, Oleg Lenive, Sigurur Y. Kristinsson, Urban Gullberg, Daniel F. Gudbjartsson, Thorunn Rafnar, Magnus Jöud, Miguel Inacio da Silva Filho, Pieter Sonneveld, W Gregory, Peter Broderick, Owen W. Stephens, Uta Bertsch, Annemiek Broyl, Jens Hillengass, Gudmar Thorleifsson, Hareth Nahi, Britt Marie Halvarsson, Gabriele Migliorini, Ellinor Johnsson, Unnur Thorsteinsdottir, Ni Li, Sven Nelander
Publikováno v:
Nature Communications
Nature Communications, Vol 7, Iss 1, Pp 1-9 (2016)
Nature Communications, 7. Nature Publishing Group
Nature Communications, Vol 7, Iss 1, Pp 1-9 (2016)
Nature Communications, 7. Nature Publishing Group
Multiple myeloma (MM) is a plasma cell malignancy with a significant heritable basis. Genome-wide association studies have transformed our understanding of MM predisposition, but individual studies have had limited power to discover risk loci. Here w