Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk
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creator | Patsopoulos, Nikolaos A. Beecham, Ashley H. Goris, An Dubois, Bénédicte D’hooghe, Marie B. Van Damme, Philip Søndergaard, Helle Bach Sellebjerg, Finn Ullum, Henrik Thørner, Lise W. Werge, Thomas Damotte, Vincent Fontaine, Bertrand Lathrop, Mark Gourraud, Pierre-Antoine Pongratz, Viola Gasperi, Christiane Bayas, Antonios Heesen, Christoph Linker, Ralf Paul, Friedemann Stangel, Martin Tackenberg, Björn Bergh, Florian Then Wildemann, Brigitte Tumani, Hayrettin Gold, Ralf Grummel, Verena Knier, Benjamin Lill, Christina M. Dardiotis, Efthimios Agliardi, Cristina Barizzone, Nadia Mascia, Elisabetta Bernardinelli, Luisa Cusi, Daniele Ferrè, Laura Comi, Cristoforo Galimberti, Daniela Leone, Maurizio A. Mescheriakova, Julia Hintzen, Rogier van Duijn, Cornelia Teunissen, Charlotte E. Bos, Steffan D. Myhr, Kjell-Morten Celius, Elisabeth G. Lie, Benedicte A. Comabella, Manuel Montalban, Xavier Alfredsson, Lars Stridh, Pernilla Hillert, Jan Piehl, Fredrik Jelčić, Ilijas Martin, Roland Sospedra, Mireia Hawkins, Clive Hysi, Pirro Karpe, Fredrik Khadake, Jyoti Lachance, Genevieve Neville, Matthew Santaniello, Adam Caillier, Stacy J. Calabresi, Peter A. Cross, Anne Davis, Mary F. de Bakker, Paul I.W. Delgado, Silvia Dembele, Marieme Edwards, Keith Fitzgerald, Kathryn C. Hakonarson, Hakon Konidari, Ioanna Lathi, Ellen Manrique, Clara P. Pericak-Vance, Margaret A. Piccio, Laura Schaefer, Cathy McCabe, Cristin Hadjigeorgiou, Georgios Taylor, Bruce Tajouri, Lotti Charlesworth, Jac Booth, David R. Harbo, Hanne F. Ivinson, Adrian J. Hauser, Stephen L. Compston, Alastair Stewart, Graeme Zipp, Frauke Barcellos, Lisa F. Baranzini, Sergio E. Martinelli-Boneschi, Filippo Ziegler, Andreas McCauley, Jacob L. Sawcer, Stephen J. De Jager, Philip L. Kockum, Ingrid |
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doi_str_mv | 10.1016/j.cell.2020.01.002 |
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Piehl, Fredrik ; Jelčić, Ilijas ; Martin, Roland ; Sospedra, Mireia ; Hawkins, Clive ; Hysi, Pirro ; Karpe, Fredrik ; Khadake, Jyoti ; Lachance, Genevieve ; Neville, Matthew ; Santaniello, Adam ; Caillier, Stacy J. ; Calabresi, Peter A. ; Cross, Anne ; Davis, Mary F. ; de Bakker, Paul I.W. ; Delgado, Silvia ; Dembele, Marieme ; Edwards, Keith ; Fitzgerald, Kathryn C. ; Hakonarson, Hakon ; Konidari, Ioanna ; Lathi, Ellen ; Manrique, Clara P. ; Pericak-Vance, Margaret A. ; Piccio, Laura ; Schaefer, Cathy ; McCabe, Cristin ; Hadjigeorgiou, Georgios ; Taylor, Bruce ; Tajouri, Lotti ; Charlesworth, Jac ; Booth, David R. ; Harbo, Hanne F. ; Ivinson, Adrian J. ; Hauser, Stephen L. ; Compston, Alastair ; Stewart, Graeme ; Zipp, Frauke ; Barcellos, Lisa F. ; Baranzini, Sergio E. ; Martinelli-Boneschi, Filippo ; Ziegler, Andreas ; McCauley, Jacob L. ; Sawcer, Stephen J. ; De Jager, Philip L. ; Kockum, Ingrid ; International Multiple Sclerosis Genetics Consortium ; International Multiple Sclerosis Genetics Consortium. 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Manuel ; Montalban, Xavier ; Alfredsson, Lars ; Stridh, Pernilla ; Hillert, Jan ; Piehl, Fredrik ; Jelčić, Ilijas ; Martin, Roland ; Sospedra, Mireia ; Hawkins, Clive ; Hysi, Pirro ; Karpe, Fredrik ; Khadake, Jyoti ; Lachance, Genevieve ; Neville, Matthew ; Santaniello, Adam ; Caillier, Stacy J. ; Calabresi, Peter A. ; Cross, Anne ; Davis, Mary F. ; de Bakker, Paul I.W. ; Delgado, Silvia ; Dembele, Marieme ; Edwards, Keith ; Fitzgerald, Kathryn C. ; Hakonarson, Hakon ; Konidari, Ioanna ; Lathi, Ellen ; Manrique, Clara P. ; Pericak-Vance, Margaret A. ; Piccio, Laura ; Schaefer, Cathy ; McCabe, Cristin ; Hadjigeorgiou, Georgios ; Taylor, Bruce ; Tajouri, Lotti ; Charlesworth, Jac ; Booth, David R. ; Harbo, Hanne F. ; Ivinson, Adrian J. ; Hauser, Stephen L. ; Compston, Alastair ; Stewart, Graeme ; Zipp, Frauke ; Barcellos, Lisa F. ; Baranzini, Sergio E. ; Martinelli-Boneschi, Filippo ; Ziegler, Andreas ; McCauley, Jacob L. ; Sawcer, Stephen J. ; De Jager, Philip L. ; Kockum, 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Frauke</creatorcontrib><creatorcontrib>Barcellos, Lisa F.</creatorcontrib><creatorcontrib>Baranzini, Sergio E.</creatorcontrib><creatorcontrib>Martinelli-Boneschi, Filippo</creatorcontrib><creatorcontrib>Ziegler, Andreas</creatorcontrib><creatorcontrib>McCauley, Jacob L.</creatorcontrib><creatorcontrib>Sawcer, Stephen J.</creatorcontrib><creatorcontrib>De Jager, Philip L.</creatorcontrib><creatorcontrib>Kockum, Ingrid</creatorcontrib><creatorcontrib>International Multiple Sclerosis Genetics Consortium</creatorcontrib><creatorcontrib>International Multiple Sclerosis Genetics Consortium. Electronic address: chris.cotsapas@yale.edu</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Other</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Other full text</collection><jtitle>CELL</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Patsopoulos, Nikolaos A.</au><au>Beecham, Ashley H.</au><au>Goris, An</au><au>Dubois, Bénédicte</au><au>D’hooghe, Marie B.</au><au>Van Damme, Philip</au><au>Søndergaard, Helle Bach</au><au>Sellebjerg, Finn</au><au>Ullum, Henrik</au><au>Thørner, Lise W.</au><au>Werge, Thomas</au><au>Damotte, Vincent</au><au>Fontaine, Bertrand</au><au>Lathrop, Mark</au><au>Gourraud, Pierre-Antoine</au><au>Pongratz, Viola</au><au>Gasperi, Christiane</au><au>Bayas, Antonios</au><au>Heesen, Christoph</au><au>Linker, Ralf</au><au>Paul, Friedemann</au><au>Stangel, Martin</au><au>Tackenberg, Björn</au><au>Bergh, Florian Then</au><au>Wildemann, Brigitte</au><au>Tumani, Hayrettin</au><au>Gold, Ralf</au><au>Grummel, Verena</au><au>Knier, Benjamin</au><au>Lill, Christina M.</au><au>Dardiotis, Efthimios</au><au>Agliardi, Cristina</au><au>Barizzone, Nadia</au><au>Mascia, Elisabetta</au><au>Bernardinelli, Luisa</au><au>Cusi, Daniele</au><au>Ferrè, Laura</au><au>Comi, Cristoforo</au><au>Galimberti, Daniela</au><au>Leone, Maurizio A.</au><au>Mescheriakova, Julia</au><au>Hintzen, Rogier</au><au>van Duijn, Cornelia</au><au>Teunissen, Charlotte E.</au><au>Bos, Steffan D.</au><au>Myhr, Kjell-Morten</au><au>Celius, Elisabeth G.</au><au>Lie, Benedicte A.</au><au>Comabella, Manuel</au><au>Montalban, Xavier</au><au>Alfredsson, Lars</au><au>Stridh, Pernilla</au><au>Hillert, Jan</au><au>Piehl, Fredrik</au><au>Jelčić, Ilijas</au><au>Martin, Roland</au><au>Sospedra, Mireia</au><au>Hawkins, Clive</au><au>Hysi, Pirro</au><au>Karpe, Fredrik</au><au>Khadake, Jyoti</au><au>Lachance, Genevieve</au><au>Neville, Matthew</au><au>Santaniello, Adam</au><au>Caillier, Stacy J.</au><au>Calabresi, Peter A.</au><au>Cross, Anne</au><au>Davis, Mary F.</au><au>de Bakker, Paul I.W.</au><au>Delgado, Silvia</au><au>Dembele, Marieme</au><au>Edwards, Keith</au><au>Fitzgerald, Kathryn C.</au><au>Hakonarson, Hakon</au><au>Konidari, Ioanna</au><au>Lathi, Ellen</au><au>Manrique, Clara P.</au><au>Pericak-Vance, Margaret A.</au><au>Piccio, Laura</au><au>Schaefer, Cathy</au><au>McCabe, Cristin</au><au>Hadjigeorgiou, Georgios</au><au>Taylor, Bruce</au><au>Tajouri, Lotti</au><au>Charlesworth, Jac</au><au>Booth, David R.</au><au>Harbo, Hanne F.</au><au>Ivinson, Adrian J.</au><au>Hauser, Stephen L.</au><au>Compston, Alastair</au><au>Stewart, Graeme</au><au>Zipp, Frauke</au><au>Barcellos, Lisa F.</au><au>Baranzini, Sergio E.</au><au>Martinelli-Boneschi, Filippo</au><au>Ziegler, Andreas</au><au>McCauley, Jacob L.</au><au>Sawcer, Stephen J.</au><au>De Jager, Philip L.</au><au>Kockum, Ingrid</au><aucorp>International Multiple Sclerosis Genetics Consortium</aucorp><aucorp>International Multiple Sclerosis Genetics Consortium. 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fulltext | fulltext |
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source | Cell Press Free Archives; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; SWEPUB Freely available online; ScienceDirect Journals (5 years ago - present) |
title | Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk |
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