Resultats de la cerca - Jan Freudenberg

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  1. 1
    Mappability and read length

    Mappability and read length per Wentian Li, Jan Freudenberg

    Publicat 2014
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  2. 2
    Absolute pitch exhibits phenotypic and genetic overlap with synesthesia

    Absolute pitch exhibits phenotypic and genetic overlap with synesthesia per Peter K. Gregersen, Elena Kowalsky, Annette Lee, Simon Baron‐Cohen, Simon E. Fisher, Julian E. Asher, D.H. Ballard, Jan Freudenberg, Wentian Li

    Publicat 2013
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  3. 3
    Cannabinoid receptor type 2 gene is associated with human osteoporosis

    Cannabinoid receptor type 2 gene is associated with human osteoporosis per Meliha Karsak, Martine Cohen‐Solal, Jan Freudenberg, Agnès Ostertag, C. Morieux, Uwe Kornak, Julia Essig, Edda Erxlebe, Itai Bab, Christian Kubisch, Marie‐Christine de Vernejoul, Andreas Zimmer

    Publicat 2005
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  4. 4
    Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease

    Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease per S Metzger, Rong Jiang, Huu Phuc Nguyen, Austin Cape, Jürgen Tomiuk, Anne S. Soehn, Peter Propping, Yun Freudenberg‐Hua, Jan Freudenberg, Liang Tong, S.-H. Li, Xing Li, O. Riess

    Publicat 2008
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  5. 5
    Transancestral mapping of the MHC region in systemic lupus erythematosus identifies new independent and interacting loci at <i>MSH5, HLA-DPB1</i> and <i>HLA-G</i>

    Transancestral mapping of the MHC region in systemic lupus erythematosus identifies new independent and interacting loci at <i>MSH5, HLA-DPB1</i> and <i>HLA-G</i> per Michelle M. A. Fernando, Jan Freudenberg, Annette Lee, David Morris, Lora Boteva, Benjamin Rhodes, María Francisca González‐Escribano, Miguel Ángel López‐Nevot, Sandra Navarra, Peter K. Gregersen, Javier Martı́n, Timothy J. Vyse

    Publicat 2012
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  6. 6
    Disease variants in genomes of 44 centenarians

    Disease variants in genomes of 44 centenarians per Yun Freudenberg‐Hua, Jan Freudenberg, Vladimir Vacic, Avinash Abhyankar, Anne‐Katrin Emde, Danny Ben‐Avraham, Nir Barzilai, Dayna M. Oschwald, Erika Christen, Jeremy Koppel, Blaine Greenwald, Robert B. Darnell, Søren Germer, Gil Atzmon, Peter Davies

    Publicat 2014
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  7. 7
    Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis

    Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis per Soumya Raychaudhuri, Cynthia Sandor, Eli A. Stahl, Jan Freudenberg, Hye Soon Lee, Xiaoming Jia, Lars Alfredsson, Leonid Padyukov, Lars Klareskog, Jane Worthington, Katherine Siminovitch, Sang‐Cheol Bae, Robert M. Plenge, Peter K. Gregersen, Paul I. W. de Bakker

    Publicat 2012
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  8. 8
    The DTNBP1 (Dysbindin) Gene Contributes to Schizophrenia, Depending on Family History of the Disease

    The DTNBP1 (Dysbindin) Gene Contributes to Schizophrenia, Depending on Family History of the Disease per Ann Van Den Bogaert, Johannes Schumacher, Thomas G. Schulze, A Otte, Stephanie Ohlraun, S. S. Kovalenko, Tim Becker, Jan Freudenberg, Erik G. Jönsson, Marja Mattila‐Evenden, Göran C. Sedvall, Piotr M. Czerski, Paweł Kapelski, Joanna Hauser, Wolfgang Maier, Marcella Rietschel, Peter Propping, Markus M. Nöthen, Sven Cichon

    Publicat 2003
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  9. 9
    Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder

    Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder per Sven Cichon, Ingeborg Winge, Manuel Mattheisen, Alexander Georgi, Anna Karpushova, Jan Freudenberg, Yun Freudenberg‐Hua, G. Babadjanova, Ann Van Den Bogaert, Л. И. Абрамова, S. Kapiletti, P.M. Knappskog, Jeffrey A. McKinney, W. Maier, Rami Abou Jamra, T. G. Schulze, J Schumacher, Peter Propping, M. Rietschel, Jan Haavik, Markus M. Nöthen

    Publicat 2007
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  10. 10
    Use of a Multiethnic Approach to Identify Rheumatoid- Arthritis-Susceptibility Loci, 1p36 and 17q12

    Use of a Multiethnic Approach to Identify Rheumatoid- Arthritis-Susceptibility Loci, 1p36 and 17q12 per Fina Kurreeman, Eli A. Stahl, Yukinori Okada, Katherine P. Liao, Dorothée Diogo, Soumya Raychaudhuri, Jan Freudenberg, Yuta Kochi, Nikolaos A. Patsopoulos, Namrata Gupta, Cynthia Sandor, So‐Young Bang, Hye‐Soon Lee, Leonid Padyukov, Akari Suzuki, Kathy Siminovitch, Jane Worthington, Peter K. Gregersen, Laura B. Hughes, Richard J. Reynolds, S. Louis Bridges, Sang‐Cheol Bae, Kazuhiko Yamamoto, Robert M. Plenge

    Publicat 2012
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  11. 11
    Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia

    Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia per Axel M. Hillmer, S. Hanneken, Sibylle Ritzmann, Tim Becker, Jan Freudenberg, Felix F. Brockschmidt, Antònia Flaquer, Yun Freudenberg‐Hua, Rami Abou Jamra, Christine Metzen, Uwe Heyn, Nadine Schweiger, Regina C. Betz, Bettina Blaumeiser, Jochen Hampe, Stefan Schreiber, Thomas G. Schulze, Hans Christian Hennies, Johannes Schumacher, Peter Propping, Thomas Ruzicka, Sven Cichon, Thomas F. Wienker, Roland Kruse, Markus M. Nöthen

    Publicat 2005
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  12. 12
    CSK regulatory polymorphism is associated with systemic lupus erythematosus and influences B-cell signaling and activation

    CSK regulatory polymorphism is associated with systemic lupus erythematosus and influences B-cell signaling and activation per Nataly Manjarrez‐Orduño, Emiliano Marasco, Sharon A. Chung, Matthew S. Katz, Jenna F Kiridly, Kim R. Simpfendorfer, Jan Freudenberg, D.H. Ballard, Emil Nashi, Thomas J Hopkins, Deborah S. Cunninghame Graham, Annette T. Lee, Marieke J. H. Coenen, Barbara Franke, Dorine W. Swinkels, Robert Graham, Robert P. Kimberly, Patrick M. Gaffney, Timothy J. Vyse, Timothy W. Behrens, Lindsey A. Criswell, Betty Diamond, Peter K. Gregersen

    Publicat 2012
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  13. 13
    C9orf72 ablation causes immune dysregulation characterized by leukocyte expansion, autoantibody production and glomerulonephropathy in mice

    C9orf72 ablation causes immune dysregulation characterized by leukocyte expansion, autoantibody production and glomerulonephropathy in mice per Amanda Atanasio, Vilma Decman, Derek W. R. White, Meg Ferrell Ramos, Burcin Ikiz, Hoi-Ching Lee, Chia-Jen Siao, Susannah Brydges, Elizabeth LaRosa, Yu Bai, Wen Fury, Patricia Burfeind, Ralica Zamfirova, Gregg Warshaw, Jamie Orengo, A. Oyejide, Michael Fralish, Wojtek Auerbach, William Poueymirou, Jan Freudenberg, Guochun Gong, Brian Zambrowicz, David M. Valenzuela, George D. Yancopoulos, Andrew Murphy, Gavin Thurston, Ka‐Man Venus Lai

    Publicat 2016
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  14. 14
    Functionally defective germline variants of sialic acid acetylesterase in autoimmunity

    Functionally defective germline variants of sialic acid acetylesterase in autoimmunity per Ira Surolia, Stephan P. Pirnie, Vasant Chellappa, Kendra N. Taylor, Annaiah Cariappa, Jesse Moya, Haoyuan Liu, Daphne W. Bell, David R. Driscoll, Sven Diederichs, K Haider, Ilka Arun Netravali, Sheila Le, Roberto Elia, Ethan Dow, Annette Lee, Jan Freudenberg, Philip L. De Jager, Yves Chrétien, Ajit Varki, Marcy E. MacDonald, Tammy Gillis, Timothy W. Behrens, Donald B. Bloch, Deborah Collier, Joshua R. Korzenik, Daniel K. Podolsky, David A. Hafler, Mandakolathur R. Murali, Bruce E. Sands, John H. Stone, Peter K. Gregersen, Shiv Pillai

    Publicat 2010
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  15. 15
    Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

    Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications per Rosalie Sterenborg, Inga Steinbrenner, Yong Li, Melissa Bujnis, Tatsuhiko Naito, Eirini Marouli, Tessel E. Galesloot, Oladapo Babajide, Laura Andreasen, Arne Astrup, Bjørn Olav Åsvold, Stefania Bandinelli, Marian Beekman, John Beilby, Jette Bork‐Jensen, Thibaud Boutin, Jennifer A. Brody, Suzanne J. Brown, Ben Brumpton, Purdey J. Campbell, Anne Rentoumis Cappola, Graziano Ceresini, Layal Chaker, Daniel I. Chasman, Maria Pina Concas, Rodrigo Coutinho de Almeida, Simone Cross, Francesco Cucca, Ian J. Deary, Alisa D. Kjærgaard, Justin B. Echouffo‐Tcheugui, Christina Ellervik, Johan G. Eriksson, Luigi Ferrucci, Jan Freudenberg, Christian Fuchsberger, Christian Gieger, Franco Giulianini, Martin Gögele, Sarah E. Graham, Niels Grarup, Ivana Gunjača, Torben Hansen, Barbara N. Harding, Sarah E. Harris, Stig Haunsø, Caroline Hayward, Jennie Hui, Till Ittermann, J. Wouter Jukema, Eero Kajantie, Jørgen K. Kanters, Line Lund Kårhus, Lambertus A. Kiemeney, M. Kloppenburg, Brigitte Kühnel, Jari Lahti, Claudia Langenberg, Bruno Lapauw, Graham Leese, Shuo Li, David C. Liewald, Allan Linneberg, Jesus V. T. Lominchar, Jian’an Luan, Nicholas G. Martin, Antonela Matana, Marcel E. Meima, Thomas Meitinger, Ingrid Meulenbelt, Braxton D. Mitchell, Line T. Møllehave, Samia Mora, Silvia Naitza, Matthias Nauck, Romana T. Netea‐Maier, Raymond Noordam, Casia Nursyifa, Yukinori Okada, Stefano Onano, Areti Papadopoulou, Colin N. A. Palmer, Cristian Pattaro, Oluf Pedersen, Annette Peters, Maik Pietzner, Ozren Polašek, Peter P. Pramstaller, Bruce M. Psaty, Ante Punda, Debashree Ray, Paul Redmond, J. Brent Richards, Paul M. Ridker, Tom C. Russ, Kathleen A. Ryan, Morten S. Olesen, Ulla T. Schultheiß, Elizabeth Selvin, Moneeza K. Siddiqui

    Publicat 2024
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