Allelic imbalance of multiple sclerosis susceptibility genes IKZF3 and IQGAP1 in human peripheral blood

por Keshari, Pankaj K., Harbo, Hanne F., Myhr, Kjell-Morten, Aarseth, Jan H., Bos, Steffan D., Berge, Tone
Publicado 2016

Assessing the Power of Exome Chips

por Page, Christian Magnus, Baranzini, Sergio E., Mevik, Bjørn-Helge, Bos, Steffan Daniel, Harbo, Hanne F., Andreassen, Bettina Kulle
Publicado 2015

No differential gene expression for CD4(+) T cells of MS patients and healthy controls

por Brorson, Ina S, Eriksson, Anna, Leikfoss, Ingvild S, Celius, Elisabeth G, Berg-Hansen, Pål, Barcellos, Lisa F, Berge, Tone, Harbo, Hanne F, Bos, Steffan D
Publicado 2019

GREM1, FRZB and DKK1 mRNA levels correlate with osteoarthritis and are regulated by osteoarthritis-associated factors

por Leijten, Jeroen CH, Bos, Steffan D, Landman, Ellie BM, Georgi, Nicole, Jahr, Holger, Meulenbelt, Ingrid, Post, Janine N, van Blitterswijk, Clemens A, Karperien, Marcel
Publicado 2013

Multiple Sclerosis Risk Allele in CLEC16A Acts as an Expression Quantitative Trait Locus for CLEC16A and SOCS1 in CD4+ T Cells

por Leikfoss, Ingvild S., Keshari, Pankaj K., Gustavsen, Marte W., Bjølgerud, Anja, Brorson, Ina S., Celius, Elisabeth G., Spurkland, Anne, Bos, Steffan D., Harbo, Hanne F., Berge, Tone
Publicado 2015

Quantitative proteomic analyses of CD4(+) and CD8(+) T cells reveal differentially expressed proteins in multiple sclerosis patients and healthy controls

por Berge, Tone, Eriksson, Anna, Brorson, Ina Skaara, Høgestøl, Einar August, Berg-Hansen, Pål, Døskeland, Anne, Mjaavatten, Olav, Bos, Steffan Daniel, Harbo, Hanne F., Berven, Frode
Publicado 2019

Quantitative proteomics reveals protein dysregulation during T cell activation in multiple sclerosis patients compared to healthy controls

por Cappelletti, Chiara, Eriksson, Anna, Brorson, Ina Skaara, Leikfoss, Ingvild S., Kråbøl, Oda, Høgestøl, Einar August, Vitelli, Valeria, Mjaavatten, Olav, Harbo, Hanne F., Berven, Frode, Bos, Steffan D., Berge, Tone
Publicado 2022

Genome-Wide DNA Methylation Profiles Indicate CD8+ T Cell Hypermethylation in Multiple Sclerosis

por Bos, Steffan D., Page, Christian M., Andreassen, Bettina K., Elboudwarej, Emon, Gustavsen, Marte W., Briggs, Farren, Quach, Hong, Leikfoss, Ingvild S., Bjølgerud, Anja, Berge, Tone, Harbo, Hanne F., Barcellos, Lisa F.
Publicado 2015

Genes Involved in the Osteoarthritis Process Identified through Genome Wide Expression Analysis in Articular Cartilage; the RAAK Study

por Ramos, Yolande F. M., den Hollander, Wouter, Bovée, Judith V. M. G., Bomer, Nils, van der Breggen, Ruud, Lakenberg, Nico, Keurentjes, J. Christiaan, Goeman, Jelle J., Slagboom, P. Eline, Nelissen, Rob G. H. H., Bos, Steffan D., Meulenbelt, Ingrid
Publicado 2014

Evaluation of Cell-Specific Epigenetic Age Acceleration in People With Multiple Sclerosis

por Maltby, Vicki, Xavier, Alexandre, Ewing, Ewoud, Campagna, Maria-Pia, Sampangi, Sandeep, Scott, Rodney J., Butzkueven, Helmut, Jokubaitis, Vilija, Kular, Lara, Bos, Steffan, Slee, Mark, van der Mei, Ingrid A., Taylor, Bruce V., Ponsonby, Anne-Louise, Jagodic, Maja, Lea, Rodney, Lechner-Scott, Jeannette
Publicado 2023

Identification and systematic annotation of tissue-specific differentially methylated regions using the Illumina 450k array

por Slieker, Roderick C, Bos, Steffan D, Goeman, Jelle J, Bovée, Judith VMG, Talens, Rudolf P, van der Breggen, Ruud, Suchiman, H Eka D, Lameijer, Eric-Wubbo, Putter, Hein, van den Akker, Erik B, Zhang, Yanju, Jukema, J Wouter, Slagboom, P Eline, Meulenbelt, Ingrid, Heijmans, Bastiaan T
Publicado 2013

Pregnancy does not modify the risk of MS in genetically susceptible women

por Adams, Cameron J., Wu, Sean L., Shao, Xiaorong, Bradshaw, Patrick T., Gonzales, Edlin, Smith, Jessica B., Xiang, Anny H., Bellesis, Kalliope H., Chinn, Terrence, Bos, Steffan D., Wendel-Haga, Marte, Olsson, Tomas, Kockum, Ingrid, Langer-Gould, Annette M., Schaefer, Catherine, Alfredsson, Lars, Barcellos, Lisa F.
Publicado 2020

Increased DNA methylation of SLFN12 in CD4(+) and CD8(+) T cells from multiple sclerosis patients

por Rhead, Brooke, Brorson, Ina S., Berge, Tone, Adams, Cameron, Quach, Hong, Moen, Stine Marit, Berg-Hansen, Pål, Celius, Elisabeth Gulowsen, Sangurdekar, Dipen P., Bronson, Paola G., Lea, Rodney A., Burnard, Sean, Maltby, Vicki E., Scott, Rodney J., Lechner-Scott, Jeannette, Harbo, Hanne F., Bos, Steffan D., Barcellos, Lisa F.
Publicado 2018

Brain disconnectome mapping derived from white matter lesions and serum neurofilament light levels in multiple sclerosis: A longitudinal multicenter study

por Rise, Henning H., Brune, Synne, Chien, Claudia, Berge, Tone, Bos, Steffan D., Andorrà, Magí, Valdeolivas, Irene Pulido, Beyer, Mona K., Sowa, Piotr, Scheel, Michael, Brandt, Alexander U., Asseyer, Susanna, Blennow, Kaj, Pedersen, Mads L., Zetterberg, Henrik, de Schotten, Michel Thiebaut, Cellerino, Maria, Uccelli, Antonio, Paul, Friedemann, Villoslada, Pablo, Harbo, Hanne F., Westlye, Lars T., Høgestøl, Einar A.
Publicado 2022

Serum neurofilament light chain concentration predicts disease worsening in multiple sclerosis

por Brune, Synne, Høgestøl, Einar A, de Rodez Benavent, Sigrid A, Berg-Hansen, Pål, Beyer, Mona K, Leikfoss, Ingvild Sørum, Bos, Steffan D, Sowa, Piotr, Brunborg, Cathrine, Andorra, Magi, Pulido Valdeolivas, Irene, Asseyer, Susanna, Brandt, Alexander, Chien, Claudia, Scheel, Michael, Blennow, Kaj, Zetterberg, Henrik, Kerlero de Rosbo, Nicole, Paul, Friedemann, Uccelli, Antonio, Villoslada, Pablo, Berge, Tone, Harbo, Hanne F
Publicado 2022

Underlying molecular mechanisms of DIO2 susceptibility in symptomatic osteoarthritis

por Bomer, Nils, den Hollander, Wouter, Ramos, Yolande F M, Bos, Steffan D, van der Breggen, Ruud, Lakenberg, Nico, Pepers, Barry A, van Eeden, Annelies E, Darvishan, Arash, Tobi, Elmar W, Duijnisveld, Bouke J, van den Akker, Erik B, Heijmans, Bastiaan T, van Roon-Mom, Willeke MC, Verbeek, Fons J, van Osch, Gerjo J V M, Nelissen, Rob G H H, Slagboom, P Eline, Meulenbelt, Ingrid
Publicado 2015

Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies

por George, Michaela F., Briggs, Farren B.S., Shao, Xiaorong, Gianfrancesco, Milena A., Kockum, Ingrid, Harbo, Hanne F., Celius, Elisabeth G., Bos, Steffan D., Hedström, Anna, Shen, Ling, Bernstein, Allan, Alfredsson, Lars, Hillert, Jan, Olsson, Tomas, Patsopoulos, Nikolaos A., De Jager, Philip L., Oturai, Annette B., Søndergaard, Helle B., Sellebjerg, Finn, Sorensen, Per S., Gomez, Refujia, Caillier, Stacy J., Cree, Bruce A.C., Oksenberg, Jorge R., Hauser, Stephen L., D'Alfonso, Sandra, Leone, Maurizio A., Boneschi, Filippo Martinelli, Sorosina, Melissa, van der Mei, Ingrid, Taylor, Bruce V., Zhou, Yuan, Schaefer, Catherine, Barcellos, Lisa F.
Publicado 2016

Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations

por Olafsson, Sigurgeir, Stridh, Pernilla, Bos, Steffan Daniël, Ingason, Andres, Euesden, Jack, Sulem, Patrick, Thorleifsson, Gudmar, Gustafsson, Omar, Johannesson, Ari, Geirsson, Arni J., Thorsson, Arni V., Sigurgeirsson, Bardur, Ludviksson, Bjorn Runar, Olafsson, Elias, Kristjansdottir, Helga, Jonasson, Jon G., Olafsson, Jon Hjaltalin, Orvar, Kjartan B., Benediktsson, Rafn, Bjarnason, Ragnar, Kristjansdottir, Sjofn, Gislason, Thorarinn, Valdimarsson, Trausti, Mikaelsdottir, Evgenia, Sigurdsson, Snaevar, Jonsson, Stefan, Rafnar, Thorunn, Aarsland, Dag, Djurovic, Srdjan, Fladby, Tormod, Knudsen, Gun Peggy, Celius, Elisabeth G., Myhr, Kjell-Morten, Grondal, Gerdur, Steinsson, Kristjan, Valdimarsson, Helgi, Bjornsson, Sigurdur, Bjornsdottir, Unnur S., Bjornsson, Einar S, Nilsson, Bjorn, Andreassen, Ole A., Alfredsson, Lars, Hillert, Jan, Kockum, Ingrid Skelton, Masson, Gisli, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Stefansson, Hreinn, Hjaltason, Haukur, Harbo, Hanne F., Olsson, Tomas, Jonsdottir, Ingileif, Stefansson, Kari
Publicado 2017

A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip

por Evangelou, Evangelos, Kerkhof, Hanneke J, Styrkarsdottir, Unnur, Ntzani, Evangelia E, Bos, Steffan D, Esko, Tonu, Evans, Daniel S, Metrustry, Sarah, Panoutsopoulou, Kalliope, Ramos, Yolande F M, Thorleifsson, Gudmar, Tsilidis, Konstantinos K, Arden, Nigel, Aslam, Nadim, Bellamy, Nicholas, Birrell, Fraser, Blanco, Francisco J, Carr, Andrew, Chapman, Kay, Day-Williams, Aaron G, Deloukas, Panos, Doherty, Michael, Engström, Gunnar, Helgadottir, Hafdis T, Hofman, Albert, Ingvarsson, Thorvaldur, Jonsson, Helgi, Keis, Aime, Keurentjes, J Christiaan, Kloppenburg, Margreet, Lind, Penelope A, McCaskie, Andrew, Martin, Nicholas G, Milani, Lili, Montgomery, Grant W, Nelissen, Rob G H H, Nevitt, Michael C, Nilsson, Peter M, Ollier, William ER, Parimi, Neeta, Rai, Ashok, Ralston, Stuart H, Reed, Mike R, Riancho, Jose A, Rivadeneira, Fernando, Rodriguez-Fontenla, Cristina, Southam, Lorraine, Thorsteinsdottir, Unnur, Tsezou, Aspasia, Wallis, Gillian A, Wilkinson, J Mark, Gonzalez, Antonio, Lane, Nancy E, Lohmander, L Stefan, Loughlin, John, Metspalu, Andres, Uitterlinden, Andre G, Jonsdottir, Ingileif, Stefansson, Kari, Slagboom, P Eline, Zeggini, Eleftheria, Meulenbelt, Ingrid, Ioannidis, John PA, Spector, Tim D, van Meurs, Joyce B J, Valdes, Ana M
Publicado 2014

A Meta-Analysis of Thyroid-Related Traits Reveals Novel Loci and Gender-Specific Differences in the Regulation of Thyroid Function

por Porcu, Eleonora, Medici, Marco, Pistis, Giorgio, Volpato, Claudia B., Wilson, Scott G., Cappola, Anne R., Bos, Steffan D., Deelen, Joris, den Heijer, Martin, Freathy, Rachel M., Lahti, Jari, Liu, Chunyu, Lopez, Lorna M., Nolte, Ilja M., O'Connell, Jeffrey R., Tanaka, Toshiko, Trompet, Stella, Arnold, Alice, Bandinelli, Stefania, Beekman, Marian, Böhringer, Stefan, Brown, Suzanne J., Buckley, Brendan M., Camaschella, Clara, de Craen, Anton J. M., Davies, Gail, de Visser, Marieke C. H., Ford, Ian, Forsen, Tom, Frayling, Timothy M., Fugazzola, Laura, Gögele, Martin, Hattersley, Andrew T., Hermus, Ad R., Hofman, Albert, Houwing-Duistermaat, Jeanine J., Jensen, Richard A., Kajantie, Eero, Kloppenburg, Margreet, Lim, Ee M., Masciullo, Corrado, Mariotti, Stefano, Minelli, Cosetta, Mitchell, Braxton D., Nagaraja, Ramaiah, Netea-Maier, Romana T., Palotie, Aarno, Persani, Luca, Piras, Maria G., Psaty, Bruce M., Räikkönen, Katri, Richards, J. Brent, Rivadeneira, Fernando, Sala, Cinzia, Sabra, Mona M., Sattar, Naveed, Shields, Beverley M., Soranzo, Nicole, Starr, John M., Stott, David J., Sweep, Fred C. G. J., Usala, Gianluca, van der Klauw, Melanie M., van Heemst, Diana, van Mullem, Alies, H.Vermeulen, Sita, Visser, W. Edward, Walsh, John P., Westendorp, Rudi G. J., Widen, Elisabeth, Zhai, Guangju, Cucca, Francesco, Deary, Ian J., Eriksson, Johan G., Ferrucci, Luigi, Fox, Caroline S., Jukema, J. Wouter, Kiemeney, Lambertus A., Pramstaller, Peter P., Schlessinger, David, Shuldiner, Alan R., Slagboom, Eline P., Uitterlinden, André G., Vaidya, Bijay, Visser, Theo J., Wolffenbuttel, Bruce H. R., Meulenbelt, Ingrid, Rotter, Jerome I., Spector, Tim D., Hicks, Andrew A., Toniolo, Daniela, Sanna, Serena, Peeters, Robin P., Naitza, Silvia
Publicado 2013