Multidrug resistance 1 gene in inflammatory bowel disease： A meta-analysis von Annese, V, Valvano, M-R, Palmieri, O, Latiano, A, Bossa, F, Andriulli, A

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Sequential evaluation of thiopurine methyltransferase, inosine triphosphate pyrophosphatase, and HPRT1 genes polymorphisms to explain thiopurines' toxicity and efficacy von PALMIERI, O., LATIANO, A., BOSSA, F., VECCHI, M., D’INCÀ, R., GUAGNOZZI, D., TONELLI, F., CUCCHIARA, S., VALVANO, M. R., LATIANO, T., ANDRIULLI, A., ANNESE, V.

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Exploring the Neandertal legacy of pancreatic ductal adenocarcinoma risk in Eurasians von Gentiluomo, Manuel, Piccardi, M., Bertoncini, S., Costello, E., Morelli, L., Landi, S., Milanetto, A., Schöttker, B., Di Franco, G., Ermini, S., Scarpa, A., Izbicki, J., Pezzilli, R., Uzunoglu, F., Talar-Wojnarowska, R., Goetz, M., Lawlor, R., Aoki, M., Bueno-de-Mesquita, B., Busch, O., Chammas, R., Tavano, F., van Laarhoven, H., Cavestro, G., Stocker, H., Bazzocchi, F., Pasquali, C., Chen, X., Puzzono, M., Ponz de Leon Pisani, R., Sperti, C., Lovecek, M., Erőss, B., Basso, D., Kupcinskas, J., Vanagas, T., Janciauskas, D., Poskiene, L., Tacelli, M., Duchonova, B. Mohelnikova, Perri, F., Latiano, A., Mambrini, A., Maiello, E., Hegyi, P., Szentesi, A., Bunduc, S., Hussein, T., Arcidiacono, P., Boggi, U., Hackert, T., Soucek, P., Lucchesi, M., Ginocchi, L., Gazouli, M., Zerbi, A., Roth, S., Jamroziak, K., Carrara, S., Hlavac, V., Oliverius, M., Neoptolemos, J., Theodoropoulos, G., van Eijck, C., Dannemann, M., Canzian, F., Tofanelli, S., Campa, D.

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Polymorphic variants involved in methylation regulation: a new strategy to discover risk loci for pancreatic ductal adenocarcinoma von Corradi, Chiara, Lencioni, G., Gentiluomo, M., Latiano, A., Kiudelis, G., van Eijck, C., Marta, K., Lawlor, R., Tavano, F., Boggi, U., Dijk, F., Cavestro, G., Vermeulen, R., Hackert, T., Petrone, M., Uzunoglu, F., Archibugi, L., Izbicki, J., Mesquita, B. Bueno-de, Morelli, L., Zerbi, A., Stocker, H., Talar-Wojnarowska, R., Di Franco, G., Hegyi, P., Sperti, C., Carrara, S., Capurso, G., Gazouli, M., Brenner, H., Bunduc, S., Busch, O., Landi, S., Perri, F., Oliverius, M., Goetz, M., Scognamiglio, P., Mambrini, A., Arcidiacono, P., Kreivenaite, E., Kupcinskas, J., Hussein, T., Ermini, S., Milanetto, A., Vodicka, P., Kiudelis, V., Hlavac, V., Soucek, P., Theodoropoulos, G., Basso, D., Aoki, M., Pezzilli, R., Pasquali, C., Chammas, R., Testoni, S., Mohelníková-Duchoňová, B., Lucchesi, M., Neoptolemos, J., Canzian, F., Campa, D.

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Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis von Goyette, P, Lefebvre, C, Ng, A, Brant, S R, Cho, J H, Duerr, R H, Silverberg, M S, Taylor, K D, Latiano, A, Aumais, G, Deslandres, C, Jobin, G, Annese, V, Daly, M J, Xavier, R J, Rioux, J D

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Glucocorticoid resistance in Crohn's disease and ulcerative colitis: an association study investigating GR and FKBP5 gene polymorphisms von Maltese, P, Palma, L, Sfara, C, de Rocco, P, Latiano, A, Palmieri, O, Corritore, G, Annese, V, Magnani, M

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Role of CARD15, DLG5 and OCTN genes polymorphisms in children with inflammatory bowel diseases von Cucchiara, S, Latiano, A, Palmieri, O, Staiano, A M, D'Incà, R, Guariso, G, Vieni, G, Rutigliano, V, Borrelli, O, Valvano, M R, Annese, V

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Association of genetic variants affecting microRNAs and pancreatic cancer risk von Lu, Y., Corradi, C., Gentiluomo, M., Theodoropoulos, G.E., Roth, S., Maiello, E., Morelli, L., L.Archibugi, Izbicki, J.R., Sarlós, P., Kiudelis, V., Oliverius, M., López de Maturana, E., Aoki, M.N., Vashist, Y., van Eijck, C.H.J., Gazouli, M., Talar-Wojnarowska, R., Mambrini, A., Pezzilli, R., Bueno-de-Mesquita, B., Hegyi, P., Souček, P., Neoptolemos, J., Di Franco, G., Sperti, C., Kauffmann, E.F., Hlaváč, V., Uzunoğlu, F.G., Ermini, S., Małecka-Panas, E., Lucchesi, M., Vanella, G., Dijk, F., Mohelníková-Duchoňová, B., Bambi, F., Petrone, M.C., Jamroziak, K., Guo, F., Kolarova, K., Capretti, G., Milanetto, A.C., Ginocchi, L., Loveček, M., Puzzono, M., van Laarhoven, H.W.M., Carrara, S., Ivanauskas, A., Papiris, K., Basso, D., Arcidiacono, P.G., Izbéki, F., Chammas, R., Vodicka, P., Hackert, T., Pasquali, C., Piredda, M.L., Costello-Goldring, E., Cavestro, G.M., Szentesi, A., Tavano, F., Włodarczyk, B., Brenner, H., Kreivenaite, E., Gao, X., Bunduc, S., Schneider, M.A., Latiano, A., Gioffreda, D., Testoni, S.G.G., Malats, N., Kupcinskas, J., Lawlor, R.T., Capurso, G., Campa, D., Canzian, F.

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Whole Exome Sequencing of very early onset ulcerative colitis patients identifies new variants in candidate genes von Palmieri, O, Aloi, M, Prudente, S, Mazza, T, Stronati, L, Corritore, G, Latiano, T, Bossa, F, Andriulli, A, Cucchiara, S, Latiano, A

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Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders von Eijsbouts, Chris, Zheng, Tenghao, Kennedy, Nicholas A., Bonfiglio, Ferdinando, Anderson, Carl A., Moutsianas, Loukas, Holliday, Joanne, Shi, Jingchunzi, Shringarpure, Suyash, Voda, Alexandru-Ioan, Farrugia, Gianrico, Franke, Andre, Hübenthal, Matthias, Abecasis, Gonçalo, Zawistowski, Matthew, Skogholt, Anne Heidi, Ness-Jensen, Eivind, Hveem, Kristian, Esko, Tõnu, Teder-Laving, Maris, Zhernakova, Alexandra, Camilleri, Michael, Boeckxstaens, Guy, Whorwell, Peter J., Spiller, Robin, McVean, Gil, D’Amato, Mauro, Jostins, Luke, Parkes, Miles

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Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study von Cleynen, Isabelle, PhD, Boucher, Gabrielle, MSc, Jostins, Luke, PhD, Schumm, L Philip, MA, Zeissig, Sebastian, PhD, Ahmad, Tariq, PhD, Andersen, Vibeke, Prof, Andrews, Jane M, Prof, Annese, Vito, MD, Brand, Stephan, Prof, Brant, Steven R, MD, Cho, Judy H, Prof, Daly, Mark J, Prof, Dubinsky, Marla, MD, Duerr, Richard H, Prof, Ferguson, Lynnette R, Prof, Franke, Andre, Prof, Gearry, Richard B, Prof, Goyette, Philippe, PhD, Hakonarson, Hakon, Prof, Halfvarson, Jonas, MD, Hov, Johannes R, PhD, Huang, Hailang, PhD, Kennedy, Nicholas A, PhD, Kupcinskas, Limas, Prof, Lawrance, Ian C, Prof, Lee, James C, PhD, Satsangi, Jack, Prof, Schreiber, Stephan, Prof, Théâtre, Emilie, PhD, van der Meulen-de Jong, Andrea E, MD, Weersma, Rinse K, Prof, Wilson, David C, Prof, Parkes, Miles, PhD, Vermeire, Severine, Prof, Rioux, John D, Prof, Mansfield, John, MD, Silverberg, Mark S, PhD, Radford-Smith, Graham, PhD, McGovern, Dermot P B, Prof, Barrett, Jeffrey C, Dr, Lees, Charlie W, Dr

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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs von Lee, S Hong, Ripke, Stephan, Neale, Benjamin M, Faraone, Stephen V, Purcell, Shaun M, Perlis, Roy H, Mowry, Bryan J, Thapar, Anita, Goddard, Michael E, Witte, John S, Absher, Devin, Agartz, Ingrid, Akil, Huda, Amin, Farooq, Andreassen, Ole A, Anjorin, Adebayo, Anney, Richard, Anttila, Verneri, Arking, Dan E, Asherson, Philip, Azevedo, Maria H, Backlund, Lena, Badner, Judith A, Bailey, Anthony J, Banaschewski, Tobias, Barchas, Jack D, Barnes, Michael R, Barrett, Thomas B, Bass, Nicholas, Battaglia, Agatino, Bauer, Michael, Bayés, Mònica, Bellivier, Frank, Bergen, Sarah E, Berrettini, Wade, Betancur, Catalina, Bettecken, Thomas, Biederman, Joseph, Binder, Elisabeth B, Black, Donald W, Blackwood, Douglas H R, Bloss, Cinnamon S, Boehnke, Michael, Boomsma, Dorret I, Breen, Gerome, Breuer, René, Bruggeman, Richard, Cormican, Paul, Buccola, Nancy G, Buitelaar, Jan K, Bunney, William E, Buxbaum, Joseph D, Byerley, William F, Byrne, Enda M, Caesar, Sian, Cahn, Wiepke, Cantor, Rita M, Casas, Miguel, Chakravarti, Aravinda, Chambert, Kimberly, Choudhury, Khalid, Cichon, Sven, Cloninger, C Robert, Collier, David A, Cook, Edwin H, Coon, Hilary, Cormand, Bru, Corvin, Aiden, Coryell, William H, Craig, David W, Craig, Ian W, Crosbie, Jennifer, Cuccaro, Michael L, Curtis, David, Czamara, Darina, Datta, Susmita, Dawson, Geraldine, Day, Richard, De Geus, Eco J, Degenhardt, Franziska, Djurovic, Srdjan, Donohoe, Gary J, Doyle, Alysa E, Duan, Jubao, Dudbridge, Frank, Duketis, Eftichia, Ebstein, Richard P, Edenberg, Howard J, Elia, Josephine, Ennis, Sean, Etain, Bruno, Fanous, Ayman, Farmer, Anne E, Ferrier, I Nicol, Flickinger, Matthew, Fombonne, Eric, Foroud, Tatiana, Frank, Josef, Franke, Barbara, Fraser, Christine

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Multidrug resistance 1 gene polymorphisms are not associated with inflammatory bowel disease and response to therapy in Italian patients von PALMIERI, O., LATIANO, A., VALVANO, R., D'INCÀ, R., VECCHI, M., STURNIOLO, G. C., SAIBENI, S., BOSSA, F., LATIANO, T., DEVOTO, M., ANDRIULLI, A., ANNESE, V.

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Increased intestinal permeability and NOD2 variants in familial and sporadic Crohn's disease von D'INCÀ, R., ANNESE, V., DI LEO, V., LATIANO, A., QUAINO, V., ABAZIA, C., VETTORATO, M. G., STURNIOLO, G. C.

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Genetic architecture of the inflammatory bowel diseases across East Asian and European ancestries von Liu, Zhanju, Liu, Ruize, Gao, Han, Jung, Seulgi, Gao, Xiang, Sun, Ruicong, Liu, Xiaoming, Kim, Yongjae, Lee, Ho-Su, Kawai, Yosuke, Nagasaki, Masao, Umeno, Junji, Tokunaga, Katsushi, Kinouchi, Yoshitaka, Masamune, Atsushi, Shi, Wenzhao, Shen, Chengguo, Guo, Zhenglin, Yuan, Kai, Zhu, Shu, Li, Dalin, Liu, Jianjun, Ge, Tian, Cho, Judy, Daly, Mark J., McGovern, Dermot P. B., Ye, Byong Duk, Song, Kyuyoung, Kakuta, Yoichi, Li, Mingsong, Huang, Hailiang

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IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes von Momozawa, Yukihide, Dmitrieva, Julia, Théâtre, Emilie, Deffontaine, Valérie, Rahmouni, Souad, Charloteaux, Benoît, Crins, François, Docampo, Elisa, Elansary, Mahmoud, Gori, Ann-Stephan, Lecut, Christelle, Mariman, Rob, Mni, Myriam, Oury, Cécile, Altukhov, Ilya, Alexeev, Dmitry, Aulchenko, Yuri, Amininejad, Leila, Bouma, Gerd, Hoentjen, Frank, Löwenberg, Mark, Oldenburg, Bas, Pierik, Marieke J., vander Meulen-de Jong, Andrea E., Janneke van der Woude, C., Visschedijk, Marijn C., Lathrop, Mark, Hugot, Jean-Pierre, Weersma, Rinse K., De Vos, Martine, Franchimont, Denis, Vermeire, Severine, Kubo, Michiaki, Louis, Edouard, Georges, Michel

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Heterogeneity of KRAS, NRAS, BRAF and PIK3CA mutations in metastatic colorectal cancer and potential effects on therapy in the CAPRI GOIM trial von Normanno, N., Rachiglio, A.M., Lambiase, M., Martinelli, E., Fenizia, F., Esposito, C., Roma, C., Troiani, T., Rizzi, D., Tatangelo, F., Botti, G., Maiello, E., Colucci, G., Ciardiello, F., Giuliani, F., Simone, G., Febbraro, A., Tommaselli, E., Cinieri, S., Criscuolo, M., Perrino, A., Rinaldi, A., Bordonaro, R., Manusia, M., Romito, S., Bufo, P., Cartenì, G., Biglietto, M., Nappi, O., Cardarelli, A., Montesarchio, E., Micheli, P., Nasti, G., Chicchinelli, N., Iannaccone, A., Russo, A., Cabibi, D., Giaccone, P., Barone, C., Rindi, G., Tonini, G., Onetti Muda, A., Perrone, G., Latiano, T., Graziano, P., Pisconti, S., Sebastio, A.

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Mapping the human genetic architecture of COVID-19 von Niemi, Mari E. K., Karjalainen, Juha, Daly, Mark, Ganna, Andrea, Mehtonen, Juha, Cordioli, Mattia, Kaunisto, Mari, Pigazzini, Sara, Donner, Kati, Kivinen, Katja, Palotie, Aarno, Daly, Mark J., Liao, Rachel G., Kanai, Masahiro, Veerapen, Kumar, Minica, Camelia, Trankiem, Amy, Balaconis, Mary K., Nguyen, Huy, Solomonson, Matthew, Francioli, Laurent, Wang, Qingbo, Green, Robert C., Bryant, Sam, Finucane, Hilary, Martin, Alicia R., Zhou, Wei, Nkambule, Lindokuhle, Karczewski, Konrad J., Atkinson, Elizabeth G., Tsuo, Kristin, Baya, Nikolas, Turley, Patrick, Gupta, Rahul, Walters, Raymond K., Palmer, Duncan S., Sarma, Gopal, Cheng, Nathan, Lu, Wenhan, Churchhouse, Claire, Goldstein, Jacqueline, King, Daniel, Seed, Cotton, Neale, Benjamin M., Satterstrom, F. Kyle, Pathak, Gita A., Wendt, Frank R., Polimanti, Renato, Andrews, Shea J., Sloofman, Laura, Sealfon, Stuart C., Fernandez-Cadenas, Israel, Schulte, Eva C., Protzer, Ulrike, Striano, Pasquale, Coviello, Domenico A., Zara, Federico, Salpietro, Vincenzo, Iacomino, Michele, Scudieri, Paolo, Bocciardi, Renata, Minetti, Carlo, Vari, Maria Stella, Madia, Francesca, Marouli, Eirini, Kanoni, Stavroula, Moutsianas, Loukas, Karim, Mohd Anisul, Ghoussaini, Maya, Schwartzentruber, Jeremy, Dunham, Ian, Savage, Jeanne, Posthuma, Danielle, Tissink, Elleke, Uffelmann, Emil, Butler-Laporte, Guillaume, Richards, J. Brent, Nakanishi, Tomoko, Morrison, David R., Forgetta, Vincenzo, Ghosh, Biswarup, Laurent, Laetitia, Henry, Danielle, Abdullah, Tala, Adeleye, Olumide, Mamlouk, Noor, Kimchi, Nofar, Afrasiabi, Zaman, Rezk, Nardin, Vulesevic, Branka, Bouab, Meriem, Guzman, Charlotte, Petitjean, Louis, Tselios, Chris, Xue, Xiaoqing, Afilalo, Jonathan, Adra, Darin, Kim, Han-Na, Okada, Yukinori, Byun, Jinyoung

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Variants of OCTN1–2 cation transporter genes are associated with both Crohn's disease and ulcerative colitis von PALMIERI, O., LATIANO, A., VALVANO, R., D'INCÀ, R., VECCHI, M., STURNIOLO, G. C., SAIBENI, S., PEYVANDI, F., BOSSA, F., ZAGARIA, C., ANDRIULLI, A., DEVOTO, M., ANNESE, V.

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The association of MYO9B gene in Italian patients with inflammatory bowel diseases von LATIANO, A., PALMIERI, O., VALVANO, M. R., D’INCÀ, R., CAPRILLI, R., CUCCHIARA, S., STURNIOLO, G. C., BOSSA, F., ANDRIULLI, A., ANNESE, V.

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