Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Mitja Mitrovic"'
Autor:
Prithvi Raj, Ekta Rai, Ran Song, Shaheen Khan, Benjamin E Wakeland, Kasthuribai Viswanathan, Carlos Arana, Chaoying Liang, Bo Zhang, Igor Dozmorov, Ferdicia Carr-Johnson, Mitja Mitrovic, Graham B Wiley, Jennifer A Kelly, Bernard R Lauwerys, Nancy J Olsen, Chris Cotsapas, Christine K Garcia, Carol A Wise, John B Harley, Swapan K Nath, Judith A James, Chaim O Jacob, Betty P Tsao, Chandrashekhar Pasare, David R Karp, Quan Zhen Li, Patrick M Gaffney, Edward K Wakeland
Publikováno v:
eLife, Vol 5 (2016)
Targeted sequencing of sixteen SLE risk loci among 1349 Caucasian cases and controls produced a comprehensive dataset of the variations causing susceptibility to systemic lupus erythematosus (SLE). Two independent disease association signals in the H
Externí odkaz:
https://doaj.org/article/9cb126754a5c4c41a78ee8db59f27c5a
Autor:
Karin Fransen, Mitja Mitrovic, Cleo C van Diemen, B K Thelma, Ajit Sood, Andre Franke, Stefan Schreiber, Vandana Midha, Garima Juyal, Uros Potocnik, Jingyuan Fu, Ilja Nolte, Rinse K Weersma
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e45287 (2012)
Genome-wide association studies of two main forms of inflammatory bowel diseases (IBD), Crohn's disease (CD) and ulcerative colitis (UC), have identified 99 susceptibility loci, but these explain only 23% of the genetic risk. Part of the 'hidden heri
Externí odkaz:
https://doaj.org/article/73c3116577e543ff9e1c8c8f7808c996
Autor:
Jakob Christensen, Mitja Mitrovic, Chris Cotsapas, Jakob Grove, Line Skotte, Julie Werenberg Dreier, Kirstine J Christensen, Anders D. Børglum, Bjarke Feenstra
Publikováno v:
Christensen, K J, Dreier, J W, Skotte, L, Feenstra, B, Grove, J, Børglum, A, Mitrovic, M, Cotsapas, C & Christensen, J 2021, ' Birth characteristics and risk of febrile seizures ', Acta Neurologica Scandinavica, vol. 144, no. 1, pp. 51-57 . https://doi.org/10.1111/ane.13420
Acta Neurol Scand
Acta Neurol Scand
Objective: Febrile seizure is a common childhood disorder that affects 2–5% of all children, and is associated with later development of epilepsy and psychiatric disorders. This study determines how the incidence of febrile seizures correlates with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe085ae60a1550bb87f3cb0c36589f72
https://doi.org/10.1111/ane.13420
https://doi.org/10.1111/ane.13420
Autor:
Kirstine Juul Christensen, Julie W. Dreier, Line Skotte, Bjarke Feenstra, Jakob Grove, Anders D. Børglum, Mitja Mitrovic, Chris Cotsapas, Jakob Christensen
Publikováno v:
Neuroepidemiology
Christensen, K J, Dreier, J W, Skotte, L, Feenstra, B, Grove, J, Børglum, A D, Mitrovic, M, Cotsapas, C & Christensen, J 2022, ' Seasonal Variation and Risk of Febrile Seizures : A Danish Nationwide Cohort Study ', Neuroepidemiology, vol. 56, no. 2, pp. 138-145 . https://doi.org/10.1159/000522065
Christensen, K J, Dreier, J W, Skotte, L, Feenstra, B, Grove, J, Børglum, A D, Mitrovic, M, Cotsapas, C & Christensen, J 2022, ' Seasonal Variation and Risk of Febrile Seizures : A Danish Nationwide Cohort Study ', Neuroepidemiology, vol. 56, no. 2, pp. 138-145 . https://doi.org/10.1159/000522065
Introduction: Onset of febrile seizures varies with calendar season. However, it has not previously been assessed, how season of birth interacts with age and peak risk of febrile seizures, and whether season of birth correlates with the cumulative ri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2477c2b10159c0b5b878743748e8d55b
https://pubmed.ncbi.nlm.nih.gov/35051933
https://pubmed.ncbi.nlm.nih.gov/35051933
Autor:
Leonid Padyukov, R. R. Graham, Chris Cotsapas, Mitja Mitrovic, Sung Chun, Matthew R Lincoln, David A. Hafler, Patrick M. Gaffney, Connally N, Carl D. Langefeld, Heel Dv, Cisca Wijmenga, Christiane Gasperi, Sunayev, Iris Jonkers, Pierre-Paul Axisa, Sebo Withoff, Stephen S. Rich
Autoimmune and inflammatory diseases are polygenic disorders of the immune system. Many genomic loci harbor risk alleles for several diseases, but the limited resolution of genetic mapping prevents determining if the same allele is responsible, indic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7f7695945875875467cd6f77be1e447
https://doi.org/10.1101/2021.05.13.21257044
https://doi.org/10.1101/2021.05.13.21257044
Autor:
Marine de Marcken, Margarita Dominguez-Villar, Anne-Sophie Gautron, David A. Hafler, Alexandra Kitz, Mitja Mitrovic
Publikováno v:
EMBO reports. 20
Foxp3(+) regulatory T cells (Tregs) exhibit plasticity, which dictates their function. Secretion of the inflammatory cytokine IFNγ, together with the acquisition of a T helper 1 (Th1)-like effector phenotype as observed in cancer, infection, and aut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::084d8a1229da9400e3808bb88cc6f306
https://doi.org/10.15252/embr.201948624
https://doi.org/10.15252/embr.201948624
Autor:
Fredrik Karpe, Graeme Stewart, Jan Hillert, Elisabetta Mascia, Matt J. Neville, Verena Grummel, Jonathan L. Haines, Kate Fitzgerald, Bernhard Hemmer, Julia Y Mescheriakova, Benedicte A. Lie, Efthimios Luessi, Federica Esposito, Andreas Ziegler, Ioanna Konidari, Cristin McCabe, Keith R. Edwards, Roland Martin, Daniele Cusi, Elisabeth Gulowsen Celius, Cristina Agliardi, Anne Spurkland, Georgios M. Hadjigeorgiou, Lena Guillot-Noel, Antonios Bayas, Uwe K. Zettl, Kjell-Morten Myhr, Maria Ban, Rogier Q. Hintzen, Frauke Zipp, Mireia Sospedra, Till F. M. Andlauer, Adrian J. Ivinson, Mary F. Davis, Mark Lathrop, Daniela Galimberti, Pierre-Antoine Gourraud, Genevieve Lachance, Bruce A.C. Cree, Robin Lemmens, Ashley Beecham, Steffan D. Bos, Bruce V. Taylor, Maurizio Leone, Manuel Comabella, Maja Jagodic, Helle Bach Søndergaard, David A. Hafler, Ingrid Kockum, Nadia Barizzone, Ralf Gold, Tania Kümpfel, Per Soelberg Sørensen, Seema Kalra, An Goris, Philip Van Damme, Marie B. D'hooghe, Cathy Schaefer, Efthimios Dardiotis, Alastair Compston, Lotti Tajoori, Sandra D'Alfonso, Ilijas Jelcic, Stephen Sawcer, Brigitte Wildemann, Friedemann Paul, Lise Wegner Thoerner, Silvia Delgado, Tomas Olsson, Mitja Mitrovic, Hayrettin Tumani, Henrik Ullum, Lisa F. Barcellos, Xavier Montalban, Ellen Lathi, Finn Sellebjerg, Thomas Werge, Christina M. Lill, Pernilla Stridh, Paul I.W. de Bakker, Cornelia M. van Duijn, Jyoti Khadake, Jac Charlesworth, Melissa Sorosina, Christiane Gasperi, Stephen L. Hauser, Anne H. Cross, Isabelle Cournu-Rebeix, Nikolaos A. Patsopoulos, Fredrik Piehl, Lars Alfredsson, Bertrand Fontaine, Marieme Dembele, Margaret A. Pericak-Vance, Janna Saarela, Ulf Ziemann, Annette Bang Oturai, Stacy J. Caillier, Jorge R. Oksenberg, Bénédicte Dubois, Björn Tackenberg, Christoph Heesen, Jacob L. McCauley, Florian Then Bergh, Clemens Warnke, Sergio E. Baranzini, Peter A. Calabresi, Chris Cotsapas, Clive Hawkins, Martin Stangel, Hakon Hakonarson, Sandra Vukusik, Christiane Graetz, Heinz Wiendl, Howard L. Weiner, Laura Piccio, Giancarlo Comi, Ralf A. Linker, Luisa Bernardinelli, Cristoforo Comi, Filippo Martinelli-Boneschi, Hanne F. Harbo, Dorothea Buck, Clara P. Manrique, David R. Booth, Benjamin Knier, Philip L. De Jager, Viola Pongratz, Laura Ferrè, Vincent Damotte, Adam Santaniello, Theresa Dankowski, Pirro G. Hysi
Multiple sclerosis is a common, complex neurological disease, where almost 20% of risk heritability can be attributed to common genetic variants, including >230 identified by genome-wide association studies (Patsopoulos et al., 2017). Multiple strand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca312b659a481d06422bdfe2f8ceb857
Publikováno v:
Handbook of clinical neurology. 148
Multiple sclerosis is a potentially progressive, autoimmune neurologic disorder of the central nervous system, resulting from an autoimmune attack on central nervous system white matter. It is a leading cause of neurologic symptoms in young adults, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1162dc3230fe7e1956ce2c0815ea2f8f
https://pubmed.ncbi.nlm.nih.gov/29478610
https://pubmed.ncbi.nlm.nih.gov/29478610
Autor:
Ashley Beecham, David A. Hafler, Colombe J, Ublick K, Stephen Sawcer, Marcus C. S. Lee, Adam Santaniello, An Goris, Frank Seibold, Xavier Montalban, G. Comi, Christiane Gasperi, Sandra D'Alfonso, Federica Esposito, Laurent Peyrin-Biroulet, Frauke Zipp, Ioanna Konidari, Elisabeth Gulowsen Celius, Achim Berthele, Amoroso A, Rogier Q. Hintzen, Johan Van Limbergen, Marieme Dembele, Fredrik Karpe, Zhang W, Robbins A, Moiola L, Annette Bang Oturai, Cristin McCabe, Filippo Martinelli-Boneschi, M Lindén, Keith R Edwards, Hanne F. Harbo, Zuccalà M, Marc Lémann, Felix Luessi, Noriko Isobe, Nadia Barizzone, Renata D'Incà, Croft A, Ioannis S. Vlachos, Frohlich I, Martinelli, Daniela Galimberti, Efthimios Dardiotis, Lisa F. Barcellos, Brendan T. Keenan, Maja Jagodic, Ferdinando Clarelli, Bénédicte Dubois, Nicholas A. Kennedy, Lohith Madireddy, Grant W. Montgomery, Tommy Olsson, Phil De Jager, Lo A, Peter A. Calabresi, Brandes A, Chris Cotsapas, Bakker Pd, Steffan D. Bos, Christina M. Lill, Karban A, Thoerner Lw, Tojo James, Wong G, Harald Peeters, M.-M. Hoshi, Roberts R, Fredrik Piehl, Lars Alfredsson, Giorgos M. Hadjigeorgiou, Bertrand Fontaine, Melissa Sorosina, Benedetti M, Maria Ban, Jorge R. Oksenberg, Howard L. Weiner, Ingrid Kockum, Mireia Sospedra, Taylor Km, Henrik Ullum, Izaura Lima Bomfim, Stronati L, Molyneux P, Replogle J, Stacy J. Caillier, Zhang H, Till F. M. Andlauer, Margaret A. Pericak-Vance, Jan Hillert, Luisa Bernardinelli, Taibo Li, Helle Bach Søndergaard, Ilijas Jelcic, Nikolaos A. Patsopoulos, Silvia Delgado, Cathy Schaefer, Thomas Korn, Laura Piccio, Mark Mühlau, Deborah D. Proctor, B. Hemmer, Elizabeth M. Bradshaw, Hysi P, Megan C Neville, Mary F. Davis, Dorlan J. Kimbrough, Jyoti Khadake, Jean-Pierre Hugot, David Gomez-Cabrero, Murray L. Barclay, Anne H. Cross, Kasper Lage, Stephen L. Hauser, A Compston, Zimmer A, Ivinson A, Anne Spurkland, Jonas Halfvarson, Charles C. White, Biberacher, Zarzycki O, Kathryn C. Fitzgerald, Finn Sellebjerg, Ellis Patrick, Andrea Zauli, Bruce V. Taylor, Maurizio Leone, Genevieve Lachance, Marta Olah, B. Cree, Manuel Comabella, Arie Levine, Domizia Vecchio, Mathias Chamaillard, Mark Lathrop, Clara Guaschino, Roland Martin, Hanigan K, Pierre-Antoine F. D. Gourraud, Maria Cimpean, Jonathan L. Haines, Dorothea Buck, Marco Salvetti, Per Soelberg Sørensen, Noel Lg, Mitja Mitrovic, Graeme J. Stewart, Benjamin Knier, Ellen Lathi, Cottone M, Laura Ferrè, Winn P, Duijn Cv, Monica Milla, Tune H. Pers, I. Oikonomou, An D, David R. Booth, Rebeix Ic, Clara P. Manrique, Massey D, Evelyn Ng Sm, Törkvist L, Daniele Cusi, Shoostari P, Vatn Mh, Paola Cavalla, Silvia Santoro, Gossum Av, Seema Kalra, Paul Rutgeerts, Clive Hawkins, Sandra Vukusik, Khan Ma, Hakon Hakonarson, Paul Henderson, Christiane Graetz, Julia Y Mescheriakova, Jean-François Rahier, Panteliadis I, Cristina Agliardi, Grummel, Jacob L. McCauley, Amie Baker, Janna Saarela, Sergio E. Baranzini, J W Thorpe, Damotte
We assembled and analyzed genetic data of 47,351 multiple sclerosis (MS) subjects and 68,284 control subjects and establish a reference map of the genetic architecture of MS that includes 200 autosomal susceptibility variants outside the major histoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3025a23da11c9c135923e48b9b008b4b
http://hdl.handle.net/2318/1771606
http://hdl.handle.net/2318/1771606