Rezultati - Jan Freudenberg
- Showing 1 - 15 results of 15
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Mappability and read length od Wentian Li, Jan Freudenberg
Izdano 2014Revisão -
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Cannabinoid receptor type 2 gene is associated with human osteoporosis od 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
Izdano 2005Artigo -
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Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease od 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
Izdano 2008Artigo -
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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> od 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
Izdano 2012Artigo -
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Disease variants in genomes of 44 centenarians od 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
Izdano 2014Artigo -
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Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis od 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
Izdano 2012Artigo -
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The DTNBP1 (Dysbindin) Gene Contributes to Schizophrenia, Depending on Family History of the Disease od 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
Izdano 2003Artigo -
9
Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder od 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
Izdano 2007Artigo -
10
Use of a Multiethnic Approach to Identify Rheumatoid- Arthritis-Susceptibility Loci, 1p36 and 17q12 od 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
Izdano 2012Revisão -
11
Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia od 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
Izdano 2005Artigo -
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CSK regulatory polymorphism is associated with systemic lupus erythematosus and influences B-cell signaling and activation od 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
Izdano 2012Artigo -
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C9orf72 ablation causes immune dysregulation characterized by leukocyte expansion, autoantibody production and glomerulonephropathy in mice od 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
Izdano 2016Artigo -
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Functionally defective germline variants of sialic acid acetylesterase in autoimmunity od 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
Izdano 2010Artigo -
15
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications od 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
Izdano 2024Revisão
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Sorodne teme
Biology
Gene
Genetics
Medicine
Genotype
Single-nucleotide polymorphism
Allele
Internal medicine
Endocrinology
Haplotype
Immunology
Disease
Genetic association
Genome-wide association study
Immune system
Antibody
Antigen
Bonferroni correction
Computer science
Environmental health
Genetic variation
Genome
Hormone
Human leukocyte antigen
Major histocompatibility complex
Mathematics
Population
Receptor
SNP
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