The FCRL3 -169T>C polymorphism is associated with rheumatoid arthritis and shows suggestive evidence of involvement with juvenile idiopathic arthritis in a Scandinavian panel of... von Eike, MC, Nordang, GBN, Karlsen, TH, Boberg, KM, Vatn, MH, Dahl-Jorgensen, K, Ronningen, KS, Joner, G, Flato, B, Bergquist, A

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Protection against anti–citrullinated protein antibody–positive rheumatoid arthritis is predominantly associated with HLA–DRB11301: A meta‐analysis of HLA–DRB1 associations with an... von van der Woude, Diane, Lie, Benedicte A., Lundström, Emeli, Balsa, Alejandro, Feitsma, Anouk L., Houwing‐Duistermaat, Jeanine J., Verduijn, Willem, Nordang, Gry B. N., Alfredsson, Lars, Klareskog, Lars, Pascual‐Salcedo, Dora, Gonzalez‐Gay, Miguel A., Lopez‐Nevot, Miguel A., Valero, Fernando, Roep, Bart O., Huizinga, Tom W. J., Kvien, Tore K., Martín, Javier, Padyukov, Leonid, de Vries, René R. P., Toes, René E. M.

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Implication of Heterozygous Variants in Genes of the Leptin-Melanocortin Pathway in Severe Obesity von Courbage, Sophie, Poitou, Christine, Le Beyec-Le Bihan, Johanne, Karsenty, Alexandra, Lemale, Julie, Pelloux, Véronique, Lacorte, Jean-Marc, Carel, Jean-Claude, Lecomte, Nathalie, Storey, Caroline, De Filippo, Gianpaolo, Coupaye, Muriel, Oppert, Jean-Michel, Tounian, Patrick, Clément, Karine, Dubern, Béatrice

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Efficacy and safety of setmelanotide, an MC4R agonist, in individuals with severe obesity due to LEPR or POMC deficiency: single-arm, open-label, multicentre, phase 3 trials von Clément, Karine, van den Akker, Erica, Argente, Jesús, Bahm, Allison, Chung, Wendy K, Connors, Hillori, De Waele, Kathleen, Farooqi, I Sadaf, Gonneau-Lejeune, Julie, Gordon, Gregory, Kohlsdorf, Katja, Poitou, Christine, Puder, Lia, Swain, James, Stewart, Murray, Yuan, Guojun, Wabitsch, Martin, Kühnen, Peter, Pigeon-Kherchiche, Patricia, Flaus-Furmaniuk, Anna, Bald, Martin, Denzer, Christian, von Schnurbein, Julia, Abawi, Ozair, Blume-Peytavi, Ulrike, Krabusch, Philipp, Mai, Knut, Schnabel, Dirk, Wiegand, Susanna, Flück, Christa E, Schulz, Esther, Voss, Egbert, Bratina, Natasa, Weiss, Katja, Martos-Moreno, Gabriel Á, Danset, Alban, Gougis, Paul, Dubern, Béatrice, Clément, Karine, van den Akker, Erica L.T., Argente, Jesús, Bahm, Allison L, Chung, Wendy K, Connors, Hillori S, De Waele, Kathleen, Farooqi, Ismaa Sadaf, Gonneau-Lejeune, Julie, Gordon, Gregory A, Poitou, Christine, Puder, Lia, Swain, James M, Stewart, Murray W, Yuan, Goujun, Wabitsch, Martin, Kühnen, Peter

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Association between the interleukin (IL)-17A rs2275913 polymorphism and rheumatoid arthritis susceptibility: a meta-analysis and trial sequential analysis von Chen, Ping, Li, Yuhao, Li, Liangliang, Zhang, Guixin, Zhang, Feng, Tang, Yan, Zhou, Li, Yang, Yi, Li, Jing

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Prohormone convertase 1/3 deficiency causes obesity due to impaired proinsulin processing von Meier, Daniel T., Rachid, Leila, Wiedemann, Sophia J., Traub, Shuyang, Trimigliozzi, Kelly, Stawiski, Marc, Sauteur, Loïc, Winter, Denise V., Le Foll, Christelle, Brégère, Catherine, Guzman, Raphael, Odermatt, Alex, Böni-Schnetzler, Marianne, Donath, Marc Y.

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IL-17A, IL-17RC polymorphisms and IL17 plasma levels in Tunisian patients with rheumatoid arthritis von Dhaouadi, Tarak, Chahbi, Mayssa, Haouami, Youssra, Sfar, Imen, Abdelmoula, Leila, Ben Abdallah, Taieb, Gorgi, Yousr

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Associations between circulating IL-17 levels and rheumatoid arthritis and between IL-17 gene polymorphisms and disease susceptibility: a meta-analysis von Lee, Young Ho, Bae, Sang-Cheol

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Association of interleukin-17F (rs763780) single nucleotide polymorphism with multiple sclerosis and optic neuritis von Salah, Shereen, Sadeq, Yousra I., Mosaad, Youssef M., Elmenshawi, Ibrahim E. H., Tawhid, Ziyad M. E.

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IL-17F Gene rs763780 and IL-17A rs2275913 Polymorphisms in Patients with Periodontitis von Mazurek-Mochol, Małgorzata, Kozak, Małgorzata, Malinowski, Damian, Safranow, Krzysztof, Pawlik, Andrzej

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Are genetic variations in IL‐21–IL‐23R–IL‐17A cytokine axis involved in a pathogenic pathway of rheumatoid arthritis? Bayesian hierarchical meta‐analysis von Mohammadi, Fatemeh Sadat, Aslani, Saeed, Mostafaei, Shayan, Jamshidi, Ahmadreza, Riahi, Parisa, Mahmoudi, Mahdi

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IL17A and IL17F gene polymorphisms in patients with rheumatoid arthritis von Pawlik, Andrzej, Kotrych, Daniel, Malinowski, Damian, Dziedziejko, Violetta, Czerewaty, Michal, Safranow, Krzysztof

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Association between Interleukin-17F 7488A/G and 7383A/G polymorphisms and susceptibility to juvenile idiopathic arthritis von Abd Almonaem, Eman Rateb, Shaheen, Ashraf Mohamed, Abdelrahman, Amira M. N., Hassan, Waleed A., Daay El Khair, Noha Mohamed, Abdel Haie, Omima Mohamed

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Association of IL17A and IL17F genes with Rheumatoid Arthritis disease and the impact of genetic polymorphisms on response to treatment von Marwa, Ouled Salah, Kalthoum, Tizaoui, Wajih, Kaabachi, Kamel, Hamzaoui

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Gene polymorphisms of an interleukin‐23 receptor associated with susceptibility to rheumatoid arthritis in the Western Chinese Han population von Ren, Ruyu, Tan, Huiling, Wang, Xuean, Wang, Li, Yang, Bin

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A genetic variant in the IL-17 promoter is functionally associated with acute graft-versus-host disease after unrelated bone marrow transplantation von Espinoza, J Luis, Takami, Akiyoshi, Nakata, Katsuya, Onizuka, Makoto, Kawase, Takakazu, Akiyama, Hideki, Miyamura, Koichi, Morishima, Yasuo, Fukuda, Takahiro, Kodera, Yoshihisa, Nakao, Shinji

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Identification of systemic biomarkers and potential drug targets for age-related macular degeneration von Lei, Shizhen, Hu, Mang, Wei, Zhongtao

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IL-17, IL-21 and IL-22 polymorphisms in rheumatoid arthritis: A systematic review and meta-analysis von Agonia, Inês, Couras, Juliana, Cunha, Anita, Andrade, Alda João, Macedo, Juliana, Sousa-Pinto, Bernardo

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Genetic Obesity and Bariatric Surgery Outcome in 1014 Patients with Morbid Obesity von Cooiman, M.I., Kleinendorst, L., Aarts, E.O., Janssen, I.M.C., van Amstel, H.K. Ploos, Blakemore, A.I., Hazebroek, E.J., Meijers-Heijboer, H.J., van der Zwaag, B., Berends, F.J., van Haelst, M.M.

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GLP-1 Receptor Agonist Treatment in Morbid Obesity and Type 2 Diabetes Due to Pathogenic Homozygous Melanocortin-4 Receptor Mutation: A Case Report von Iepsen, Eva W., Have, Christian T., Veedfald, Simon, Madsbad, Sten, Holst, Jens J., Grarup, Niels, Pedersen, Oluf, Brandslund, Ivan, Holm, Jens-Christian, Hansen, Torben, Torekov, Signe S.

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