Genetic variants of CC chemokine genes in experimental autoimmune encephalomyelitis, multiple sclerosis and rheumatoid arthritis
Öckinger, J, Stridh, P, Beyeen, A D, Lundmark, F, Seddighzadeh, M, Oturai, A, Sørensen, P S, Lorentzen, Å R, Celius, E G, Leppä, V, Koivisto, K, Tienari, P J, Alfredsson, L, Padyukov, L, Hillert, J, Kockum, I, Jagodic, M, Olsson, T
Published in Genes and immunity (01.03.2010)
Published in Genes and immunity (01.03.2010)
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IL12A, MPHOSPH9 CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci
Esposito, F, Patsopoulos, NA, Cepok, S, Kockum, I, Leppa, V, Booth, DR, Heard, RN, Stewart, GJ, Cox, M, Scott, RJ, Lechner-Scott, J, Goris, A, Dobosi, R, Dubois, B, Rioux, JD, Oturai, AB, Sondergaard, HB, Sellebjerg, F, Sorensen, PS, Reunanen, M, Koivisto, K, Cournu-Rebeix, I, Fontaine, B, Winkelmann, J, Gieger, C, Infante-Duarte, C, Zipp, F, Bergamaschi, L, Leone, M, Bergamaschi, R, Cavalla, P, Lorentzen, AR, Mero, IL, Celius, EG, Harbo, HF, Spurkland, A, Comabella, M, Brynedal, B, Alfredsson, L, Bernardinelli, L, Robertson, NP, Hawkins, CP, Barcellos, LF, Beecham, G, Bush, W, Cree, BAC, Daly, MJ, Ivinson, AJ, Aubin, C, Compston, A, D'Alfonso, S, Haines, JL, Hauser, SL, Hemmer, B, Hillert, J, McCauley, JL, Oksenberg, J, Olsson, T, Palotie, A, Peltonen, L, Pericak-Vance, MA, Saarela, J, Sawcer, SJ, Stranger, B, Boneschi, FM, Comi, G, Hafler, DA, de Bakker, PIW, De Jager, PL
Published in Genes and immunity (01.07.2010)
Published in Genes and immunity (01.07.2010)
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Genotype-Phenotype Analysis across 130,422 Genetic Variants Identifies Rspo3 as the First Genome-Wide Significant Modifier Gene in Primary Sclerosing Cholangitis
Alberts, R, de Vries, E.M, Alexander, G, Alvaro, D, Bergquist, A, Beuers, U, Björnsson, E, Boberg, K.M, Bowlus, C.L, Chapman, R.W, Chazouilléres, O, Cheung, A, Dalekos, G, Eksteen, B, Eaton, J.E, Ellinghaus, D, Färkkilä, M, Festen, E.A, Floreani, A, Folseraas, T, Goode, E, Gotthardt, D.N, Hirschfield, G.M, van Hoek, B, Hohenester, S, Holm, K, Hov, J.R, Imhann, F, Invernizzi, P, Jiang, X, Juran, B.D, Lazaridis, K.N, Leppa, V, Liu, J.Z, Löfberg, J, Manns, M.P, Marschall, H.-U, Marzioni, M, Mason, A.L, Melum, E, Müller, T, Milkiewicz, P, Pares, A, Pelkonen, V, Pinzani, M, Rombouts, K, Rupp, C, Rushbrook, S.M, Rust, C, Sampaziotis, F, Sandford, R.N, Schramm, C, Schreiber, S, Schrumpf, E, Silverberg, M, Srivastava, B, Sterneck, M, Teufel, A, Tittmann, L, Vallier, L, Vila, A.V, de Vries, B.A, Weismüller, T.J, Wijmenga, C, Zachou, K, Franke, A, Anderson, C.A, Karlsen, T.H, Ponsioen, C.Y, Weersma, K
Published in JOURNAL OF HEPATOLOGY (2016)
Published in JOURNAL OF HEPATOLOGY (2016)
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Rigor and reproducibility in genetic research on eating disorders
Hübel, Christopher, Leppä, Virpi, Breen, Gerome, Bulik, Cynthia M.
Published in The International journal of eating disorders (01.07.2018)
Published in The International journal of eating disorders (01.07.2018)
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GENETIC RISK FOR SCHIZOPHRENIA MODIFIES EATING DISORDER CLINICAL PRESENTATIONS
Zhang, Ruyue, Kuja-Halkola, Ralf, Borg, Stina, Leppa, Virpi, Thornton, Laura, Bulik, Cynthia, Bergen, Sarah
Published in EUROPEAN NEUROPSYCHOPHARMACOLOGY (01.10.2022)
Published in EUROPEAN NEUROPSYCHOPHARMACOLOGY (01.10.2022)
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Study protocol of comprehensive risk evaluation for anorexia nervosa in twins (CREAT): a study of discordant monozygotic twins with anorexia nervosa
Seidel, Maria, Ehrlich, Stefan, Breithaupt, Lauren, Welch, Elisabeth, Wiklund, Camilla, Hübel, Christopher, Thornton, Laura M, Savva, Androula, Fundin, Bengt T, Pege, Jessica, Billger, Annelie, Abbaspour, Afrouz, Schaefer, Martin, Boehm, Ilka, Zvrskovec, Johan, Rosager, Emilie Vangsgaard, Hasselbalch, Katharina Collin, Leppä, Virpi, Sjögren, Magnus, Nergårdh, Ricard, Feusner, Jamie D, Ghaderi, Ata, Bulik, Cynthia M
Published in BMC psychiatry (14.10.2020)
Published in BMC psychiatry (14.10.2020)
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SAT-372 - Genotype-Phenotype Analysis across 130,422 Genetic Variants Identifies Rspo3 as the First Genome-Wide Significant Modifier Gene in Primary Sclerosing Cholangitis
Alberts, R., de Vries, E.M., Alexander, G., Alvaro, D., Bergquist, A., Beuers, U., Björnsson, E., Boberg, K.M., Bowlus, C.L., Chapman, R.W., Chazouilléres, O., Cheung, A., Dalekos, G., Eksteen, B., Eaton, J.E., Ellinghaus, D., Färkkilä, M., Festen, E.A., Floreani, A., Folseraas, T., Goode, E., Gotthardt, D.N., Hirschfield, G.M., van Hoek, B., Hohenester, S., Holm, K., Hov, J.R., Imhann, F., Invernizzi, P., Jiang, X., Juran, B.D., Lazaridis, K.N., Leppa, V., Liu, J.Z., Löfberg, J., Manns, M.P., Marschall, H.-U., Marzioni, M., Mason, A.L., Melum, E., Müller, T., Milkiewicz, P., Pares, A., Pelkonen, V., Pinzani, M., Rombouts, K., Rupp, C., Rushbrook, S.M., Rust, C., Sampaziotis, F., Sandford, R.N., Schramm, C., Schreiber, S., Schrumpf, E., Silverberg, M., Srivastava, B., Sterneck, M., Teufel, A., Tittmann, L., Vallier, L., Vila, A.V., de Vries, B.A., Weismüller, T.J., Wijmenga, C., Zachou, K., Franke, A., Anderson, C.A., Karlsen, T.H., Ponsioen, C.Y., Weersma, K.
Published in Journal of hepatology (2016)
Published in Journal of hepatology (2016)
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Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks
Ruzzo, Elizabeth K., Pérez-Cano, Laura, Jung, Jae-Yoon, Wang, Lee-kai, Kashef-Haghighi, Dorna, Hartl, Chris, Singh, Chanpreet, Xu, Jin, Hoekstra, Jackson N., Leventhal, Olivia, Leppä, Virpi M., Gandal, Michael J., Paskov, Kelley, Stockham, Nate, Polioudakis, Damon, Lowe, Jennifer K., Prober, David A., Geschwind, Daniel H., Wall, Dennis P.
Published in Cell (08.08.2019)
Published in Cell (08.08.2019)
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COPY NUMBER VARIATION ANALYSIS OF A FINNISH COHORT OF CRIMINAL OFFENDERS
Rautiainen, MR, Tiihonen, J, Leppa, V, Pietilinen, O, Lahti, J, Liuhanen, J, Repo-Tiihonen, E, Eriksson, J, Virkkunen, M, Palotie, A, Paunio, T
Published in EUROPEAN NEUROPSYCHOPHARMACOLOGY (2017)
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Published in EUROPEAN NEUROPSYCHOPHARMACOLOGY (2017)
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Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis
Booth, David R, Heard, Robert N, Stewart, Graeme J, Cox, Mathew, Scott, Rodney J, Lechner-Scott, Jeannette, Goris, An, Dobosi, Rita, Dubois, Bénédicte, Saarela, Janna, Leppä, Virpi, Peltonen, Leena, Pirttila, Tuula, Cournu-Rebeix, Isabelle, Fontaine, Bertrand, Bergamaschi, Laura, D'Alfonso, Sandra, Leone, Maurizio, Lorentzen, Aslaug R, Harbo, Hanne F, Celius, Elisabeth G, Spurkland, Anne, Link, Jenny, Kockum, Ingrid, Olsson, Tomas, Hillert, Jan, Ban, Maria, Baker, Amie, Kemppinen, Anu, Sawcer, Stephen, Compston, Alastair, Robertson, Neil P, De Jager, Philip L, Hafler, David A, Barcellos, Lisa F, Ivinson, Adrian J, McCauley, Jacob L, Pericak-Vance, Margaret A, Oksenberg, Jorge R, Hauser, Stephen L, Sexton, David, Haines, Jonathan
Published in Nature genetics (01.06.2010)
Published in Nature genetics (01.06.2010)
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The Anorexia Nervosa Genetics Initiative (ANGI): Overview and methods
Thornton, Laura M., Munn-Chernoff, Melissa A., Baker, Jessica H., Juréus, Anders, Parker, Richard, Henders, Anjali K., Larsen, Janne T., Petersen, Liselotte, Watson, Hunna J., Yilmaz, Zeynep, Kirk, Katherine M., Gordon, Scott, Leppä, Virpi M., Martin, Felicity C., Whiteman, David C., Olsen, Catherine M., Werge, Thomas M., Pedersen, Nancy L., Kaye, Walter, Bergen, Andrew W., Halmi, Katherine A., Strober, Michael, Kaplan, Allan S., Woodside, D. Blake, Mitchell, James, Johnson, Craig L., Brandt, Harry, Crawford, Steven, Horwood, L. John, Boden, Joseph M., Pearson, John F., Duncan, Laramie E., Grove, Jakob, Mattheisen, Manuel, Jordan, Jennifer, Kennedy, Martin A., Birgegård, Andreas, Lichtenstein, Paul, Norring, Claes, Wade, Tracey D., Montgomery, Grant W., Martin, Nicholas G., Landén, Mikael, Mortensen, Preben Bo, Sullivan, Patrick F., Bulik, Cynthia M.
Published in Contemporary clinical trials (01.11.2018)
Published in Contemporary clinical trials (01.11.2018)
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Genotype-phenotype analysis across 130 422 genetic variants identifies RSPO3 as the first genome-wide significant modifier gene in primary sclerosing cholangitis
Alberts, R, de Vries, EM, Alexander, G, Alvaro, D, Bergquist, A, Beuers, U, Bjornsson, E, Boberg, KM, Bowlus, CL, Chapman, RW, Chazouilleres, O, Cheung, A, Dalekos, G, Eksteen, B, Ellinghaus, D, Farkkila, M, Festen, EA, Floreani, A, Folseraas, T, Goode, E, Gotthardt, DN, Hirschfield, GM, van Hoek, B, Holm, K, Hohenester, S, Hov, JR, Imhann, F, Invernizzi, P, Jiang, X, Eaton, J, Juran, BD, Lazaridis, KN, Leppa, V, Liu, JZ, Lofberg, J, Manns, MP, Marschall, HU, Marzioni, M, Mason, AL, Melum, E, Milkiewicz, P, Muller, T, Pares, A, Rupp, C, Rushbrook, SM, Rust, C, Sampaziotis, F, Sandford, RN, Schramm, C, Schreiber, S, Schrumpf, E, Silverberg, M, Srivastava, B, Sterneck, M, Teufel, A, Tittmann, L, Vallier, L, Vila, AV, de Vries, B, Weismuller, TJ, Wijmenga, C, Zachou, K, Franke, A, Anderson, CA, Karlsen, TH, Ponsioen, CY, Weersma, RK
Published in JOURNAL OF CROHNS & COLITIS (2016)
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Published in JOURNAL OF CROHNS & COLITIS (2016)
Conference Proceeding