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1دورية أكاديمية
المؤلفون: International Multiple Sclerosis Genetics Consortium, Wellcome Trust Case Control Consortium 2, Sawcer, Stephen, Hellenthal, Garrett, Pirinen, Matti, Spencer, Chris CA, Patsopoulos, Nikolaos A, Moutsianas, Loukas, Dilthey, Alexander, Su, Zhan, Freeman, Colin, Hunt, Sarah E, Edkins, Sarah, Gray, Emma, Booth, David R, Potter, Simon C, Goris, An, Band, Gavin, Oturai, Annette Bang, Strange, Amy, Saarela, Janna, Bellenguez, Céline, Fontaine, Bertrand, Gillman, Matthew, Hemmer, Bernhard, Gwilliam, Rhian, Zipp, Frauke, Jayakumar, Alagurevathi, Martin, Roland, Leslie, Stephen, Hawkins, Stanley, Giannoulatou, Eleni, D'alfonso, Sandra, Blackburn, Hannah, Martinelli Boneschi, Filippo, Liddle, Jennifer, Harbo, Hanne F, Perez, Marc L, Spurkland, Anne, Waller, Matthew J, Mycko, Marcin P, Ricketts, Michelle, Comabella, Manuel, Hammond, Naomi, Kockum, Ingrid, McCann, Owen T, Ban, Maria, Whittaker, Pamela, Kemppinen, Anu, Weston, Paul, Hawkins, Clive, Widaa, Sara, Zajicek, John, Dronov, Serge, Robertson, Neil, Bumpstead, Suzannah J, Barcellos, Lisa F, Ravindrarajah, Rathi, Abraham, Roby, Alfredsson, Lars, Ardlie, Kristin, Aubin, Cristin, Baker, Amie, Baker, Katharine, Baranzini, Sergio E, Bergamaschi, Laura, Bergamaschi, Roberto, Bernstein, Allan, Berthele, Achim, Boggild, Mike, Bradfield, Jonathan P, Brassat, David, Broadley, Simon A, Buck, Dorothea, Butzkueven, Helmut, Capra, Ruggero, Carroll, William M, Cavalla, Paola, Celius, Elisabeth G, Cepok, Sabine, Chiavacci, Rosetta, Clerget-Darpoux, Françoise, Clysters, Katleen, Comi, Giancarlo, Cossburn, Mark, Cournu-Rebeix, Isabelle, Cox, Mathew B, Cozen, Wendy, Cree, Bruce AC, Cross, Anne H, Cusi, Daniele, Daly, Mark J, Davis, Emma, de Bakker, Paul IW, Debouverie, Marc, D'hooghe, Marie Beatrice, Dixon, Katherine, Dobosi, Rita, Dubois, Bénédicte, Ellinghaus, David
المصدر: Nature. 476(7359)
مصطلحات موضوعية: International Multiple Sclerosis Genetics Consortium, Wellcome Trust Case Control Consortium 2, T-Lymphocytes, Helper-Inducer, Humans, Multiple Sclerosis, Genetic Predisposition to Disease, HLA-A Antigens, HLA-DR Antigens, Sample Size, Cell Differentiation, Immunity, Cellular, Major Histocompatibility Complex, Polymorphism, Single Nucleotide, Alleles, Genome, Human, Europe, Genome-Wide Association Study, HLA-DRB1 Chains, Genetics, Neurosciences, Neurodegenerative, Clinical Research, Brain Disorders, Autoimmune Disease, Human Genome, 2.1 Biological and endogenous factors, Neurological, Inflammatory and immune system, General Science & Technology
الوصول الحر: https://escholarship.org/uc/item/5x17t6tzTest
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2دورية أكاديمية
المؤلفون: Sawcer, Stephen, Hellenthal, Garrett, Pirinen, Matti, Spencer, Chris CA, Patsopoulos, Nikolaos A, Moutsianas, Loukas, Dilthey, Alexander, Su, Zhan, Freeman, Colin, Hunt, Sarah E, Edkins, Sarah, Gray, Emma, Booth, David R, Potter, Simon C, Goris, An, Band, Gavin, Oturai, Annette Bang, Strange, Amy, Saarela, Janna, Bellenguez, Celine, Fontaine, Bertrand, Gillman, Matthew, Hemmer, Bernhard, Gwilliam, Rhian, Zipp, Frauke, Jayakumar, Alagurevathi, Martin, Roland, Leslie, Stephen, Hawkins, Stanley, Giannoulatou, Eleni, D'alfonso, Sandra, Blackburn, Hannah, Boneschi, Filippo Martinelli, Liddle, Jennifer, Harbo, Hanne F, Perez, Marc L, Spurkland, Anne, Waller, Matthew J, Mycko, Marcin P, Ricketts, Michelle, Comabella, Manuel, Hammond, Naomi, Kockum, Ingrid, McCann, Owen T, Ban, Maria, Whittaker, Pamela, Kemppinen, Anu, Weston, Paul, Hawkins, Clive, Widaa, Sara, Zajicek, John, Dronov, Serge, Robertson, Neil, Bumpstead, Suzannah J, Barcellos, Lisa F, Ravindrarajah, Rathi, Abraham, Roby, Alfredsson, Lars, Ardlie, Kristin, Aubin, Cristin, Baker, Amie, Baker, Katharine, Baranzini, Sergio E, Bergamaschi, Laura, Bergamaschi, Roberto, Bernstein, Allan, Berthele, Achim, Boggild, Mike, Bradfield, Jonathan P, Brassat, David, Broadley, Simon A, Buck, Dorothea, Butzkueven, Helmut, Capra, Ruggero, Carroll, William M, Cavalla, Paola, Celius, Elisabeth G, Cepok, Sabine, Chiavacci, Rosetta, Clerget-Darpoux, Francoise, Clysters, Katleen, Comi, Giancarlo, Cossburn, Mark, Cournu-Rebeix, Isabelle, Cox, Mathew B, Cozen, Wendy, Cree, Bruce AC, Cross, Anne H, Cusi, Daniele, Daly, Mark J, Davis, Emma, de Bakker, Paul IW, Debouverie, Marc, D'hooghe, Marie Beatrice, Dixon, Katherine, Dobosi, Rita, Dubois, Benedicte, Ellinghaus, David, Elovaara, Irina, Esposito, Federica
المصدر: Nature. 476(7359)
مصطلحات موضوعية: Neurosciences, Prevention, Multiple Sclerosis, Biotechnology, Autoimmune Disease, Genetics, Brain Disorders, Human Genome, Neurodegenerative, 2.1 Biological and endogenous factors, Aetiology, Neurological, Inflammatory and immune system, Alleles, Cell Differentiation, Europe, Genetic Predisposition to Disease, Genome, Human, Genome-Wide Association Study, HLA-A Antigens, HLA-DR Antigens, HLA-DRB1 Chains, Humans, Immunity, Cellular, Major Histocompatibility Complex, Polymorphism, Single Nucleotide, Sample Size, T-Lymphocytes, Helper-Inducer, International Multiple Sclerosis Genetics Consortium, Wellcome Trust Case Control Consortium 2, General Science & Technology
الوصول الحر: https://escholarship.org/uc/item/5x17t6tzTest
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3دورية أكاديمية
المؤلفون: Leone, Maurizio A., Barizzone, Nadia, Esposito, Federica, Lucenti, Ausiliatrice, Harbo, Hanne F., Goris, An, Kockum, Ingrid, Oturai, Annette Bang, Celius, Elisabeth Gulowsen, Mero, Inger L., Dubois, Bénédicte, Olsson, Tomas, Søndergaard, Helle Bach, Cusi, Daniele, Lupoli, Sara, Andreassen, Bettina Kulle, Barcellos, L., Booth, D., Comabella, M., Compston, A., D'Alfonso, Sandra, De Jager, P., Fontaine, B., Hafler, D., Haines, J., Hauser, S. L., Hawkins, C., Hemmer, B., Hillert, J., Ivinson, A., MARTIN, Rossella, Martinelli Boneschi, F., McCauley, J. L., Oksenberg, J., Oturai, A., Patsopoulos, N., Pericak-Vance, M., Saarela, J., Sawcer, S., Spurkland, A., Stewart, G., Zipp, F., Myhr, Kjell-Morten, Guerini, Franca R., Naldi, Paola, Galimberti, Daniela, Scarpini, Elio, Bergamaschi, Roberto, Di Sapio, Antonella, Caputo, Domenico, Rosso, Gabriella, Cordera, Susanna, Cavalla, Paola, Cavallo, Roberto, Benedetti, Maria D., Salvetti, Marco, Capra, Ruggero, Ghezzi, Angelo, Annovazzi, Pietro, Coniglio, Gabriella, Liberatore, Giuseppe, Rodegher, Mariaemma, Moiola, Lucia, Colombo, Bruno, Radaelli, Marta, Rossi, Paolo, Martinelli, Vittorio, Comi, Giancarlo, Martinelli-Boneschi, Filippo
المساهمون: Leone, Maurizio A., Barizzone, Nadia, Esposito, Federica, Lucenti, Ausiliatrice, Harbo, Hanne F., Goris, An, Kockum, Ingrid, Oturai, Annette Bang, Celius, Elisabeth Gulowsen, Mero, Inger L., Dubois, Bénédicte, Olsson, Toma, Søndergaard, Helle Bach, Cusi, Daniele, Lupoli, Sara, Andreassen, Bettina Kulle, Barcellos, L., Booth, D., Comabella, M., Compston, A., D'Alfonso, Sandra, De Jager, P., Fontaine, B., Hafler, D., Haines, J., Hauser, S. L., Hawkins, C., Hemmer, B., Hillert, J., Ivinson, A., Martin, Rossella, Martinelli Boneschi, F., Mccauley, J. L., Oksenberg, J., Oturai, A., Patsopoulos, N., Pericak-Vance, M., Saarela, J., Sawcer, S., Spurkland, A., Stewart, G., Zipp, F., Myhr, Kjell-Morten, Guerini, Franca R., Naldi, Paola, Galimberti, Daniela, Scarpini, Elio, Bergamaschi, Roberto, Di Sapio, Antonella, Caputo, Domenico, Rosso, Gabriella, Cordera, Susanna, Cavalla, Paola, Cavallo, Roberto, Benedetti, Maria D., Salvetti, Marco, Capra, Ruggero, Ghezzi, Angelo, Annovazzi, Pietro, Coniglio, Gabriella, Liberatore, Giuseppe, Rodegher, Mariaemma, Moiola, Lucia, Colombo, Bruno, Radaelli, Marta, Rossi, Paolo, Martinelli, Vittorio, Comi, Giancarlo, Martinelli-Boneschi, Filippo
مصطلحات موضوعية: adult, female, genetic marker, hla-drb1 chain, human, male, meta-analysis as topic, middle aged, multiple sclerosi, oligoclonal band, polymorphism, single nucleotide, young adult, genome-wide association study, biochemistry, genetics and molecular biology (all), agricultural and biological sciences (all)
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23785401; info:eu-repo/semantics/altIdentifier/wos/WOS:000321038800116; volume:8; issue:6; firstpage:1; lastpage:5; numberofpages:5; journal:PLOS ONE; http://hdl.handle.net/11573/1140155Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84879052306
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4دورية أكاديمية
المؤلفون: Mechelli, Rosella, Umeton, Renato, Policano, Claudia, Annibali, Viviana, Coarelli, Giulia, V.A.G. Ricigliano, Vittori, Danila, Fornasiero, Arianna, Buscarinu, Maria Chiara, Romano, Silvia, Salvetti, Marco, Ristori, Giovanni, Sawcer, Stephen, Hellenthal, Garrett, Pirinen, Matti, Spencer, Chris C. A., Patsopoulos, Nikolaos A., Moutsianas, Loukas, Dilthey, Alexander, Su, Zhan, Freeman, Colin, Hunt, Sarah E., Edkins, Sarah, Gray, Emma, Booth, David R., Potter, Simon C., Goris, An, Band, Gavin, Oturai, Annette Bang, Strange, Amy, Saarela, Janna, Bellenguez, Céline, Fontaine, Bertrand, Gillman, Matthew, Hemmer, Bernhard, Gwilliam, Rhian, Zipp, Frauke, Jayakumar, Alagurevathi, Martin, Roland, Leslie, Stephen, Hawkins, Stanley, Giannoulatou, Eleni, D'alfonso, Sandra, Blackburn, Hannah, B. Filippo Martinelli, Liddle, Jennifer, Harbo, Hanne F., Perez, Marc L., Spurkland, Anne, Waller, Matthew J., Mycko, Marcin P., Ricketts, Michelle, Comabella, Manuel, Hammond, Naomi, Kockum, Ingrid, McCann, Owen T., Ban, Maria, Whittaker, Pamela, Kemppinen, Anu, Weston, Paul, Hawkins, Clive, Widaa, Sara, Zajicek, John, Dronov, Serge, Robertson, Neil, Bumpstead, Suzannah J., Barcellos, Lisa F., Ravindrarajah, Rathi, Abraham, Roby, Alfredsson, Lars, Ardlie, Kristin, Aubin, Cristin, Baker, Amie, Baker, Katharine, Baranzini, Sergio E., Bergamaschi, Laura, Bergamaschi, Roberto, Bernstein, Allan, Berthele, Achim, Boggild, Mike, Bradfield, Jonathan P., Brassat, David, Broadley, Simon A., Buck, Dorothea, Butzkueven, Helmut, Capra, Ruggero, Carroll, William M., Cavalla, Paola, Celius, Elisabeth G., Cepok, Sabine, Chiavacci, Rosetta, Clerget-Darpoux, Françoise, Clysters, Katleen, G. Comi, Cossburn, Mark, Cournu-Rebeix, Isabelle, Cox, Mathew B., Cozen, Wendy, Cree, Bruce A. C., Cross, Anne H., D. Cusi, Daly, Mark J., Davis, Emma, de Bakker, Paul I. W., Debouverie, Marc, D'hooghe, Marie Beatrice, Dixon, Katherine, Dobosi, Rita, Dubois, Bénédicte, Ellinghaus, David, Elovaara, Irina, Esposito, Federica, Fontenille, Claire, Foote, Simon, Franke, Andre, D. Galimberti, Ghezzi, Angelo, Glessner, Joseph, Gomez, Refujia, Gout, Olivier, Graham, Colin, Grant, Struan F. A., F.R. Guerini, Hakonarson, Hakon, Hall, Per, Hamsten, Anders, Hartung, Hans-Peter, Heard, Rob N., Heath, Simon, Hobart, Jeremy, Hoshi, Muna, Infante-Duarte, Carmen, Ingram, Gillian, Ingram, Wendy, Islam, Talat, Jagodic, Maja, Kabesch, Michael, Kermode, Allan G., Kilpatrick, Trevor J., Kim, Cecilia, Klopp, Norman, Koivisto, Keijo, Larsson, Malin, Lathrop, Mark, Lechner-Scott, Jeannette S., Leone, Maurizio A., Leppä, Virpi, Liljedahl, Ulrika, Bomfim, Izaura Lima, Lincoln, Robin R., Link, Jenny, Liu, Jianjun, Lorentzen, Åslaug R., S. Lupoli, F. Macciardi, Mack, Thomas, Marriott, Mark, Martinelli, Vittorio, Mason, Deborah, McCauley, Jacob L., Mentch, Frank, Mero, Inger-Lise, Mihalova, Tania, Montalban, Xavier, Mottershead, John, Myhr, Kjell-Morten, Naldi, Paola, Ollier, William, Page, Alison, Palotie, Aarno, Pelletier, Jean, Piccio, Laura, Pickersgill, Trevor, Piehl, Fredrik, Pobywajlo, Susan, Quach, Hong L., Ramsay, Patricia P., Reunanen, Mauri, Reynolds, Richard, Rioux, John D., Rodegher, Mariaemma, Roesner, Sabine, Rubio, Justin P., Rückert, Ina-Maria, E. Salvi, Santaniello, Adam, Schaefer, Catherine A., Schreiber, Stefan, Schulze, Christian, Scott, Rodney J., Sellebjerg, Finn, Selmaj, Krzysztof W., Sexton, David, Shen, Ling, Simms-Acuna, Brigid, Skidmore, Sheila, Sleiman, Patrick M. A., Smestad, Cathrine, Sørensen, Per Soelberg, Søndergaard, Helle Bach, Stankovich, Jim, Strange, Richard C., Sulonen, Anna-Maija, Sundqvist, Emilie, Syvänen, Ann-Christine, Taddeo, Francesca, Taylor, Bruce, Blackwell, Jenefer M., Tienari, Pentti, Bramon, Elvira, Tourbah, Ayman, Brown, Matthew A., Tronczynska, Ewa, Casas, Juan P., Tubridy, Niall, Corvin, Aiden, Vickery, Jane, Jankowski, Janusz, Villoslada, Pablo, Markus, Hugh S., Wang, Kai, Mathew, Christopher G., Wason, James, Palmer, Colin N. A., Wichmann, H-Erich, Plomin, Robert, Willoughby, Ernest, Rautanen, Anna, Winkelmann, Juliane, Wittig, Michael, Trembath, Richard C., Yaouanq, Jacqueline, Viswanathan, Ananth C., Zhang, Haitao, Wood, Nicholas W., Zuvich, Rebecca, Deloukas, Panos, Langford, Cordelia, Duncanson, Audrey, Oksenberg, Jorge R., Pericak-Vance, Margaret A., Haines, Jonathan L., Olsson, Tomas, Hillert, Jan, Ivinson, Adrian J., De Jager, Philip L., Peltonen, Leena, Stewart, Graeme J., Hafler, David A., Hauser, Stephen L., McVean, Gil, Donnelly, Peter, Compston, Alastair
المساهمون: M. Rosella, U. Renato, P. Claudia, A. Viviana, C. Giulia, V.A.G. Ricigliano, V. Danila, F. Arianna, B. Maria Chiara, R. Silvia, S. Marco, R. Giovanni, S. Stephen, H. Garrett, P. Matti, S. Chris C. A., P. Nikolaos A., M. Louka, D. Alexander, S. Zhan, F. Colin, H. Sarah E., E. Sarah, G. Emma, B. David R., P. Simon C., G. An, B. Gavin, O. Annette Bang, S. Amy, S. Janna, B. Céline, F. Bertrand, G. Matthew, H. Bernhard, G. Rhian, Z. Frauke, J. Alagurevathi, M. Roland, L. Stephen, H. Stanley, G. Eleni, D. Sandra, B. Hannah, F. MARTINELLI BONESCHI, L. Jennifer, H. Hanne F., P. Marc L., S. Anne, W. Matthew J., M. Marcin P., R. Michelle, C. Manuel, H. Naomi, K. Ingrid, M. Owen T., B. Maria, W. Pamela, K. Anu, W. Paul, H. Clive, W. Sara, Z. John, D. Serge, R. Neil, B. Suzannah J., B. Lisa F., R. Rathi, A. Roby, A. Lar, A. Kristin, A. Cristin, B. Amie, B. Katharine, B. Sergio E., B. Laura, B. Roberto, B. Allan, B. Achim, B. Mike, B. Jonathan P., B. David, B. Simon A., B. Dorothea, B. Helmut, C. Ruggero, C. William M., C. Paola, C. Elisabeth G., C. Sabine, C. Rosetta, C. Françoise, C. Katleen, G. Comi, C. Mark, C. Isabelle, C. Mathew B., C. Wendy, C. Bruce A. C., C. Anne H.
مصطلحات موضوعية: Genome-Wide Association Study, Genotype, Human, Multiple Sclerosi, Protein Binding, Biochemistry, Genetics and Molecular Biology (all), Agricultural and Biological Sciences (all), Settore MED/26 - Neurologia
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23696811; info:eu-repo/semantics/altIdentifier/wos/WOS:000319081900025; volume:8; issue:5; firstpage:1; lastpage:9; numberofpages:9; journal:PLOS ONE; http://hdl.handle.net/2434/533526Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84877798701
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5دورية أكاديمية
المؤلفون: Goris, An, Pauwels, Ine, Gustavsen, Marte W., Van Son, Brechtje, Hilven, Kelly, Bos, Steffan D., Celius, Elisabeth Gulowsen, Berg Hansen, Pal, Aarseth, Jan, Myhr, Kjell Morten, Leone, Maurizio A., Boneschi, Filippo Martinelli, Sorosina, Melissa, Liberatore, Giuseppe, Kockum, Ingrid, Olsson, Tomas, Hillert, Jan, Alfredsson, Lars, Bedri, Sahl Khalid, Hemmer, Bernhard, Buck, Dorothea, Berthele, Achim, Knier, Benjamin, Biberacher, Viola, Van Pesch, Vincent, Sindi, Christian, Oturai, Annette Bang, Søndergaard, Helle Bach, Sellebjerg, Finn, Jensen, Poul Erik H., Comabella, Manuel, Montalban, Xavier, Pérez Boza, Jennifer, Malhotra, Sunny, Lechner Scott, Jeannette, Broadley, Simon, Slee, Mark, Taylor, Bruce, Kermode, Allan G., Gourraud, Pierre Antoine, Sawcer, Stephen J., Andreassen, Bettina Kullle, Dubois, Bénédicte, Harbo, Hanne F., D'ALFONSO, Sandra, BARIZZONE, NADIA
المساهمون: Goris, An, Pauwels, Ine, Gustavsen, Marte W., Van Son, Brechtje, Hilven, Kelly, Bos, Steffan D., Celius, Elisabeth Gulowsen, Berg Hansen, Pal, Aarseth, Jan, Myhr, Kjell Morten, D'Alfonso, Sandra, Barizzone, Nadia, Leone, Maurizio A., Boneschi, Filippo Martinelli, Sorosina, Melissa, Liberatore, Giuseppe, Kockum, Ingrid, Olsson, Toma, Hillert, Jan, Alfredsson, Lar, Bedri, Sahl Khalid, Hemmer, Bernhard, Buck, Dorothea, Berthele, Achim, Knier, Benjamin, Biberacher, Viola, Van Pesch, Vincent, Sindi, Christian, Oturai, Annette Bang, Søndergaard, Helle Bach, Sellebjerg, Finn, Jensen, Poul Erik H., Comabella, Manuel, Montalban, Xavier, Pérez Boza, Jennifer, Malhotra, Sunny, Lechner Scott, Jeannette, Broadley, Simon, Slee, Mark, Taylor, Bruce, Kermode, Allan G., Gourraud, Pierre Antoine, Sawcer, Stephen J., Andreassen, Bettina Kullle, Dubois, Bénédicte, Harbo, Hanne F.
مصطلحات موضوعية: CSF, Genetic, Immunoglobulin, Multiple sclerosi, Oligoclonal band, Adolescent, Adult, Aged, Child, Preschool, Europe, Female, Genetic Association Studie, Human, Immunoglobulin G, Major Histocompatibility Complex, Male, Middle Aged, Polymorphism, Single Nucleotide, Severity of Illness Index, Smad4 Protein, Tumor Suppressor Protein, Young Adult, Genetic Variation, Medicine (all), Arts and Humanities (miscellaneous), Neurology (clinical)
وصف الملف: STAMPA
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/25616667; info:eu-repo/semantics/altIdentifier/wos/WOS:000351510700020; volume:138; issue:3; firstpage:632; lastpage:643; numberofpages:12; journal:BRAIN; http://hdl.handle.net/11579/85249Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84930571293; http://brain.oxfordjournals.orgTest/
الإتاحة: https://doi.org/10.1093/brain/awu405Test
http://hdl.handle.net/11579/85249Test
http://brain.oxfordjournals.orgTest/ -
6دورية أكاديمية
المؤلفون: Taylor, Jenny C, Martin, Hilary C, Lise, Stefano, Broxholme, John, Cazier, Jean-Baptiste, Rimmer, Andy, Kanapin, Alexander, Lunter, Gerton, Fiddy, Simon, Allan, Chris, Aricescu, A Radu, Attar, Moustafa, Babbs, Christian, Becq, Jennifer, Beeson, David, Bento, Celeste, Bignell, Patricia, Blair, Edward, Buckle, Veronica J, Bull, Katherine, Cais, Ondrej, Cario, Holger, Chapel, Helen, Copley, Richard R, Cornall, Richard, Craft, Jude, Dahan, Karin, Davenport, Emma E, Dendrou, Calliope, Devuyst, Olivier, Fenwick, Aimée L, Flint, Jonathan, Fugger, Lars, Gilbert, Rodney D, Goriely, Anne, Green, Angie, Greger, Ingo H, Grocock, Russell, Gruszczyk, Anja V, Hastings, Robert, Hatton, Edouard, Higgs, Doug, Hill, Adrian, Holmes, Chris, Howard, Malcolm, Hughes, Linda, Humburg, Peter, Johnson, David, Karpe, Fredrik, Kingsbury, Zoya, Kini, Usha, Knight, Julian C, Krohn, Jonathan, Lamble, Sarah, Langman, Craig, Lonie, Lorne, Luck, Joshua, McCarthy, Davis, McGowan, Simon J, McMullin, Mary Frances, Miller, Kerry A, Murray, Lisa, Németh, Andrea H, Nesbit, M Andrew, Nutt, David, Ormondroyd, Elizabeth, Oturai, Annette Bang, Pagnamenta, Alistair, Patel, Smita Y, Percy, Melanie, Petousi, Nayia, Piazza, Paolo, Piret, Sian E, Polanco-Echeverry, Guadalupe, Popitsch, Niko, Powrie, Fiona, Pugh, Chris, Quek, Lynn, Robbins, Peter A, Robson, Kathryn, Russo, Alexandra, Sahgal, Natasha, van Schouwenburg, Pauline A, Schuh, Anna, Silverman, Earl, Simmons, Alison, Sørensen, Per Soelberg, Sweeney, Elizabeth, Taylor, John, Thakker, Rajesh V, Tomlinson, Ian, Trebes, Amy, Twigg, Stephen R F, Uhlig, Holm H, Vyas, Paresh, Vyse, Tim, Wall, Steven A, Watkins, Hugh, Whyte, Michael P, Witty, Lorna, Wright, Ben, Yau, Chris, Buck, David, Humphray, Sean, Ratcliffe, Peter J, Bell, John I, Wilkie, Andrew O M, Bentley, David, Donnelly, Peter, McVean, Gilean
المصدر: Taylor , J C , Martin , H C , Lise , S , Broxholme , J , Cazier , J-B , Rimmer , A , Kanapin , A , Lunter , G , Fiddy , S , Allan , C , Aricescu , A R , Attar , M , Babbs , C , Becq , J , Beeson , D , Bento , C , Bignell , P , Blair , E , Buckle , V J , Bull , K , Cais , O , Cario , H , Chapel , H , Copley , R ....
مصطلحات موضوعية: Base Sequence, DNA Mutational Analysis, Genetic Diseases, Inborn, Genome, Human, High-Throughput Nucleotide Sequencing, Humans, Molecular Diagnostic Techniques, Molecular Sequence Annotation, Polymorphism, Single Nucleotide, Sensitivity and Specificity, /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being, name=SDG 3 - Good Health and Well-being
الإتاحة: https://doi.org/10.1038/ng.3304Test
https://pure.qub.ac.uk/en/publications/a6f9d7f8-fe31-4ea4-93c0-f9abf218dbc9Test -
7دورية أكاديمية
المؤلفون: Mero, Inger-Lise, Gustavsen, Marte W., Sæther, Hanne S., FlÃ¥m, Siri T., Berg-Hansen, PÃ¥l, Søndergaard, Helle B., Jensen, Poul Erik H., Berge, Tone, Bjølgerud, Anja, Muggerud, Aslaug, Aarseth, Jan H., International Multiple Sclerosis Genetics Consortium, Myhr, Kjell-Morten, Celius, Elisabeth G., Sellebjerg, Finn, Hillert, Jan, Alfredsson, Lars, Olsson, Tomas, Oturai, Annette Bang, Kockum, Ingrid, Lie, Benedicte A., Andreassen, Bettina Kulle, Harbo, Hanne F. Collaborators: Barcellos L, Booth D, Comabella M, Compston A, D'Alfonso S, De Jager P, Fontaine B, Goris A, Hafler D, Haines J, Harbo HF, Hauser SL, Hawkins C, Hemmer B, Hillert J, Ivinson A, Kockum I, Martin R, F. Martinelli Boneschi, McCauley JL, Oksenberg J, Olsson T, Oturai A, Patsopoulos N, Pericak-Vance M, Saarela J, Sawcer S, Spurkland A, Stewart G, Zipp F.
المساهمون: M. Inger-Lise, G. Marte W., S. Hanne S., F. Siri T., B. Pã¥l, S. Helle B., J. Poul Erik H., B. Tone, B. Anja, M. Aslaug, A. Jan H., I. Multiple Sclerosis Genetics Consortium, M. Kjell-Morten, C. Elisabeth G., S. Finn, H. Jan, A. Lar, O. Toma, O. Annette Bang, K. Ingrid, L. Benedicte A., A. Bettina Kulle, Harbo, H.F. Collaborators: Barcellos L, B. D, C. M, C. A, D. S, D.J. P, F. B, G. A, H. D, H. J, H. Hf, H. Sl, H. C, H. B, I. A, K. I, M. R, F. Martinelli Boneschi, M. Jl, O. J, O. T, O. A, P. N, P. M, S. J, S. S, S. A, S. G, Z. F.
مصطلحات موضوعية: Adult, Allele, Case-Control Studie, Denmark, Female, Gene Frequency, Genotype, HLA-DRB1 Chain, Human, Male, Multiple Sclerosi, Norway, Oligoclonal Band, Polymorphism, Single Nucleotide, Sweden, Genome-Wide Association Study, Medicine (all), Biochemistry, Genetics and Molecular Biology (all), Agricultural and Biological Sciences (all), Settore MED/26 - Neurologia
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23472185; info:eu-repo/semantics/altIdentifier/wos/WOS:000315637900131; volume:8; issue:3; firstpage:e58352; journal:PLOS ONE; http://hdl.handle.net/2434/533492Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84874604770; http://www.plosone.org/article/fetchObjectAttachment.action?uri=info%3Adoi%2F10.1371%2Fjournal.pone.0058352&representation=PDFTest
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8دورية أكاديمية
المؤلفون: F. Martinelli-Boneschi, Esposito, Federica, Brambilla, Paola, Lindström, Eva, Lavorgna, Giovanni, Stankovich, Jim, Rodegher, Mariaemma, Capra, Ruggero, Ghezzi, Angelo, Coniglio, Gabriella, Colombo, Bruno, Sorosina, Melissa, Martinelli, Vittorio, Booth, David, Oturai, Annette Bang, Stewart, Graeme, Harbo, Hanne F., Kilpatrick, Trevor John, Hillert, Jan, Rubio, Justin P., Abderrahim, Hadi, Wojcik, Jerome, Comi, Giancarlo
المساهمون: F. Martinelli-Boneschi, F. Esposito, P. Brambilla, E. Lindstrã¶m, G. Lavorgna, J. Stankovich, M. Rodegher, R. Capra, A. Ghezzi, G. Coniglio, B. Colombo, M. Sorosina, V. Martinelli, D. Booth, A.B. Oturai, G. Stewart, H.F. Harbo, T.J. Kilpatrick, J. Hillert, J.P. Rubio, H. Abderrahim, J. Wojcik, G. Comi
مصطلحات موضوعية: association studies in genetic, genome-wide association study, multiple sclerosi, primary progressive, single nucleotide polymorphism, Chromosomes, Human, Pair 7, Female, Genetic Predisposition to Disease, Genotype, HLA Antigen, Linkage Disequilibrium, Male, Middle Aged, Multiple Sclerosis, Chronic Progressive, Polymorphism, Single Nucleotide, Neurology, Neurology (clinical), Settore MED/26 - Neurologia
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/22457343; info:eu-repo/semantics/altIdentifier/pmid/000309359000006; info:eu-repo/semantics/altIdentifier/wos/WOS:000309359000006; volume:18; issue:10; firstpage:1384; lastpage:1394; numberofpages:11; journal:MULTIPLE SCLEROSIS; http://hdl.handle.net/2434/533445Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84867011935