Phenotype frequencies of autosomal minor histocompatibility antigens display significant differences among populations von Spierings, Eric, Hendriks, Matthijs, Absi, Léna, Canossi, Angelica, Chhaya, Sonal, Crowley, John, Dolstra, Harry, Eliaou, Jean-François, Ellis, Tom, Enczmann, Jürgen, Fasano, Maria E, Gervais, Thibaut, Gorodezky, Clara, Kircher, Brigitte, Laurin, David, Leffell, Mary S, Loiseau, Pascale, Malkki, Mari, Markiewicz, Miroslaw, Martinetti, Miryam, Maruya, Etsuko, Mehra, Narinder, Oguz, Fatma, Oudshoorn, Machteld, Pereira, Noemi, Rani, Rajni, Sergeant, Ruhena, Thomson, Jackie, Tran, Thuong Hien, Turpeinen, Hannu, Yang, Kuo-Liang, Zunec, Renata, Carrington, Mary, de Knijff, Peter, Goulmy, Els

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Vitamin D receptor (VDR) gene SNPs influence VDR expression and modulate protection from multiple sclerosis in HLA-DRB115-positive individuals von Agliardi, Cristina, Guerini, Franca R., Saresella, Marina, Caputo, Domenico, Leone, Maurizio A., Zanzottera, Milena, Bolognesi, Elisabetta, Marventano, Ivana, Barizzone, Nadia, Fasano, Maria E., Al-Daghri, Nasser, Clerici, Mario

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Cytokines and chronic rejection: A study in kidney transplant long-term survivors von UBOLDI DE CAPEI, Mariafederica, DAMETTO, Ennia, FASANO, Maria E, MESSINA, Maria, PRATICO, Loredana, RENDINE, Sabina, SEGOLONI, Giuseppe, CURTONI, Emilio S

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HLA Genotyping: Methods for the Identification of the HLA-DQ2,-DQ8 Heterodimers Implicated in Celiac Disease (CD) Susceptibility von Fasano, Maria Edvige, Dametto, Ennia, D’Alfonso, Sandra

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Vitamin D receptor (VDR) gene SNPs influence VDR expression and modulate protection from multiple sclerosis in HLA-DRB1 15-positive individuals von Agliardi, Cristina, Guerini, Franca R, Saresella, Marina, Caputo, Domenico, Leone, Maurizio A, Zanzottera, Milena, Bolognesi, Elisabetta, Marventano, Ivana, Barizzone, Nadia, Fasano, Maria E, Al-Daghri, Nasser, Clerici, Mario

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A practical approach to HLA-DR genomic typing by heteroduplex analysis and a selective cleavage at position 86 von El-Borai, Mohamed H., D'Alfonso, Sandra, Mazzola, Gina, Fasano, Maria E.

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Introduction of Gluten, HLA Status, and the Risk of Celiac Disease in Children von Lionetti, Elena, Castellaneta, Stefania, Francavilla, Ruggiero, Pulvirenti, Alfredo, Tonutti, Elio, Amarri, Sergio, Barbato, Maria, Barbera, Cristiana, Barera, Graziano, Bellantoni, Antonella, Castellano, Emanuela, Guariso, Graziella, Limongelli, Maria Giovanna, Pellegrino, Salvatore, Polloni, Carlo, Ughi, Claudio, Zuin, Giovanna, Fasano, Alessio, Catassi, Carlo

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First detection of “Candidatus Rickettsia wissemanii” in Ornithodoros hasei (Schulze, 1935) (Acari: Argasidae) from Argentina von Colombo, Valeria C., Montani, Maria E., Pavé, Romina, Antoniazzi, Leandro R., Gamboa, Marcelo D., Fasano, Agustín A., Félix, Maria L., Nava, Santiago, Venzal, José M.

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Novel role of zonulin in the pathophysiology of gastro-duodenal transit: a clinical and translational study von Martinez, Enid E., Lan, Jinggang, Konno, Takumi, Miranda-Ribera, Alba, Fiorentino, Maria, Mehta, Nilesh M., Fasano, Alessio

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Massively parallel base editing to map variant effects in human hematopoiesis von Martin-Rufino, Jorge D., Castano, Nicole, Pang, Michael, Grody, Emanuelle I., Joubran, Samantha, Caulier, Alexis, Wahlster, Lara, Li, Tongqing, Qiu, Xiaojie, Riera-Escandell, Anna Maria, Newby, Gregory A., Al’Khafaji, Aziz, Chaudhary, Santosh, Black, Susan, Weng, Chen, Munson, Glen, Liu, David R., Wlodarski, Marcin W., Sims, Kacie, Oakley, Jamie H., Fasano, Ross M., Xavier, Ramnik J., Lander, Eric S., Klein, Daryl E., Sankaran, Vijay G.

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Genome-wide Analyses Identify KIF5A as a Novel ALS Gene von Kenna, Kevin P., Chia, Ruth, Dominov, Janice A., Nalls, Mike A., van Vugt, Joke J.F.A., Simone, Isabella, Caredda, Carla, Milia, Antonio, Floris, Gianluca, Caponnetto, Claudia, Mandich, Paola, Mora, Gabriele, Sideri, Riccardo, Penco, Silvana, Mandrioli, Jessica, Trojsi, Francesca, Ticca, Anna, Ortu, Enzo, Pugliatti, Maura, Benigni, Michele, Brunetti, Maura, Marrali, Giuseppe, Riva, Nilo, Conforti, Francesca L., Messina, Sonia, D’Alfonso, Sandra, Baloh, Robert H., Penny, Michelle, Moreno, Cristiane de Araujo Martins, Chung, Wendy K., Cirulli, Elizabeth T., Harris, Tim, Krueger, Brian J., Lasseigne, Brittany N., McKenna-Yasek, Diane, Myers, Richard M., Pulst, Stefan M., Raphael, Alya R., Rouleau, Guy A., Sapp, Peter C., Waite, Lindsay L., Wang, Quanli, Ostrow, Lyle W., Baas, Frank, Zaitlen, Noah, Hornstein, Eran, Patsopoulos, Nikolaos A., Kaye, Julia, Wyman, Stacia, LeNail, Alexander, Baxi, Emily, LeNail, Alex, Benatar, Michael, Hussain, Sumaira, Swenson, Andrea, Jackson, Carlayne, So, Yuen, Wuu, Joanne, Silani, Vincenzo, Fogh, Isabella, Cereda, Cristina, Ceroni, Mauro, Mazzini, Letizia, Maderna, Luca, Sorarù, Gianni, Bernard, Emilien, Laaksovirta, Hannu, McKenna-Yasek, Diane, Asress, Seneshaw, Al-Sarraj, Safa, Scholz, Sonja W., MacGowan, Daniel J.L., Kirby, Janine, Pioro, Erik P., Pamphlett, Roger, Dunckley, Travis L., Troncoso, Juan C., Moisse, Matthieu, Drory, Vivian E., Turner, Martin R., Blair, Ian P., de Carvalho, Mamede, Hide, Winston, Glass, Jonathan, Mill, Jonathan, Newhouse, Stephen, Pulit, Sara, Robberecht, Wim, Shaw, Pamela, van den Berg, Leonard, Williams, Kelly L., Zatz, Mayana, Rothstein, Jeffrey D., Simmons, Zachary, Van Damme, Philip, Sabatelli, Mario, Trojanowski, John Q., Brown, Robert H., Veldink, Jan H., Tienari, Pentti

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Human coagulation factor X and CD5 antigen-like are potential new members of the zonulin family proteins von Konno, Takumi, Martinez, Enid E., Ji, Jian, Miranda-Ribera, Alba, Fiorentino, Maria R., Fasano, Alessio

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Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis von Noyce, Alastair J., Hemani, Gibran, Mora, Gabriele, Bartolomei, Ilaria, Benigni, Michele, Borghero, Giuseppe, Brunetti, Maura, Calvo, Andrea, Cammarosano, Stefania, Cannas, Antonino, Caponnetto, Claudia, Casale, Federico, Cavallaro, Sebastiano, Chiò, Adriano, Colletti, Tiziana, Conforti, Francesca L., Conte, Amelia, Corrado, Lucia, Costantino, Emanuela, D'Alfonso, Sandra, Femiano, Cinzia, Ferrarese, Carlo, Fini, Nicola, Floris, Gianluca, Grassano, Maurizio, Lattante, Serena, Logroscino, Giancarlo, Loi, Daniela, Mancardi, Gianluigi, Mandich, Paola, Manera, Umberto, Marinou, Kalliopi, Marrali, Giuseppe, Marrosu, Maria Giovanna, Mazzini, Letizia, Melis, Maurizio, Messina, Sonia, Mora, Gabriele, Occhineri, Patrizia, Origone, Paola, Pani, Carla, Petrucci, Antonio, Pirisi, Angelo, Restagno, Gabriella, Ricci, Claudia, Riva, Nilo, Sabatelli, Mario, Santarelli, Marialuisa, Spataro, Rossella, Tanel, Raffaella, Tremolizzo, Lucio, Volanti, Paolo, Zollino, Marcella, Arepalli, Sampath, Bowser, Robert, Broach, James, Camu, William, Chia, Ruth, Chiò, Adriano, Ding, Jinhui, Dunckley, Travis L., Eicher, John D., Faghri, Faraz, Feldman, Eva, Fratta, Pietro, Geiger, Joshua T., Gerhard, Glenn, Hardy, John, Harms, Matthew B., Heiman‐Patterson, Terry D., Kamel, Freya, MacGowan, Daniel J.L., Maragakis, Nicholas J., Murphy, Natalie A., Myllykangas, Liisa, Nalls, Mike A., Nicolas, Aude, Orrell, Richard W., Pamphlett, Roger, Pickering‐Brown, Stuart, Pioro, Erik, Pliner, Hannah A., Pulst, Stefan M., Ravits, John M., Rothstein, Jeffrey D., Salvi, Erika, Sendtner, Michael, Simmons, Zachary, Stone, David C., Sulkava, Raimo, Troncoso, Juan C., Van Damme, Philip, Van Deerlin, Vivianna M., Van Den Bosch, Ludo, Zinman, Lorne, Tienari, Pentti J., Stone, David J., Nalls, Mike A., Singleton, Andrew B., Traynor, Bryan J.

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In vivo diffusion MRI of the human heart using a 300 mT/m gradient system von Afzali, Maryam, Mueller, Lars, Coveney, Sam, Fasano, Fabrizio, Evans, Christopher John, Engel, Maria, Szczepankiewicz, Filip, Teh, Irvin, Dall'Armellina, Erica, Jones, Derek K, Schneider, Jürgen E

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Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study von Tromp, Tycho R, Hartgers, Merel L, Hovingh, G Kees, Soran, Handrean, Freiberger, Tomas, Bertolini, Stefano, Harada-Shiba, Mariko, Cuchel, Marina, Tromp, Tycho R., Hartgers, Merel L., Vallejo-Vaz, Antonio J., Soran, Handrean, Bertolini, Stefano A., Pang, Jing, Watts, Gerald F., Stulnig, Thomas M., Descamps, Olivier S., Rymen, Daisy, Witters, Peter, Brunham, Liam R., Genest, Jacques, Ruel, Isabelle, Wang, Luya, Reiner, Željko, Ceska, Richard, Dvorakova, Jana, Dlouhy, Lubomir, Horak, Pavel, Soska, Vladimir, Tichy, Lukas, Urbanek, Robin, Vaverkova, Helena, Vrablik, Michal, Zemek, Stanislav, Reda, Ashraf, Béliard, Sophie, Bruckert, Eric, Elisaf, Moses S., Cohen, Hofit, Elis, Avishay, Hussein, Osama, Setia, Nitika, Verma, Ishwar C., Alareedh, Mohammed D., Rhadi, Sabah H., Shaghee, Foaad K., Arca, Marcello, Averna, Maurizio, Bucci, Marco, Buonuomo, Paola S., Calabrò, Paolo, Casula, Manuela, Cefalù, Angelo B., D'Addato, Sergio, Di Costanzo, Alessia, Fasano, Tommaso, Gazzotti, Marta, Rabacchi, Claudio, Ripoli, Carlo, Sbrana, Francesco, Tarugi, Patrizia, Trenti, Chiara, Hori, Mika, Ayesh, Mahmoud H., Azar, Sami T., Bitar, Fadi F., Madriz, Ramón, Cupido, Arjen J., Reijman, M. Doortje, Roeters-van Lennep, Jeanine E., Wiegman, Albert, Zuurbier, Linda, Sadiq, Fouzia, Chlebus, Krzysztof, Susekov, Andrey V., Charng, Min-Ji, Aktan, Melih, Altunkeser, Bulent B., Demircioglu, Sinan, Kose, Melis, Ilhan, Osman, Kayikcioglu, Meral, Kuku, Irfan, Kurtoglu, Erdal, Okutan, Harika, Ozcebe, Osman I., Pekkolay, Zafer, Yenercag, Mustafa, Yilmaz Yasar, Hamiyet, Lyons, Alexander R.M., Nguyen, Christina, Alieva, Rano, Shek, Aleksandr, Do, Doan-Loi, Kim, Ngoc-Thanh, Le, Hong-An, Truong, Thanh-Huong, Blom, Dirk J., Raal, Frederick J., Cuchel, Marina

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Virological response to entecavir is associated with a better clinical outcome in chronic hepatitis B patients with cirrhosis von Zoutendijk, Roeland, Reijnders, Jurrien GP, Zoulim, Fabien, Brown, Ashley, Mutimer, David J, Deterding, Katja, Hofmann, Wolf Peter, Petersen, Joerg, Fasano, Massimo, Buti, Maria, Berg, Thomas, Hansen, Bettina E, Sonneveld, Milan J, Wedemeyer, Heiner, Janssen, Harry L A

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UCP1‐dependent brown adipose activation accelerates cardiac metabolic remodeling and reduces initial hypertrophic and fibrotic responses to pathological stress von Challa, Azariyas A., Vidal, Pablo, Maurya, Santosh K., Maurya, Chandan K., Baer, Lisa A., Wang, Yang, James, Natasha Maria, Pardeshi, Parth J., Fasano, Matthew, Carley, Andrew N., Stanford, Kristin I., Lewandowski, E. Douglas

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Methylotroph Infections and Chronic Granulomatous Disease von Falcone, E Liana, Petts, Jennifer R, Fasano, Mary Beth, Ford, Bradley, Nauseef, William M, Neves, João Farela, Simões, Maria João, Tierce, 4th, Millard L, de la Morena, M Teresa, Greenberg, David E, Zerbe, Christa S, Zelazny, Adrian M, Holland, Steven M

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Steps on the Path to Clinical Translation: A workshop by the British and Irish Chapter of the ISMRM von Hubbard Cristinacce, Penny L., Markus, Julia E., Punwani, Shonit, Mills, Rebecca, Lopez, Maria Yanez, Grech‐Sollars, Matthew, Fasano, Fabrizio, Waterton, John C., Thrippleton, Michael J., Hall, Matt G., O'Connor, James P. B., Francis, Susan T., Statton, Ben, Murphy, Kevin, So, Po‐Wah, Hyare, Harpreet

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The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder von Kumble, Smitha, Levy, Amanda M., Punetha, Jaya, Gao, Hua, Ah Mew, Nicholas, Anyane‐Yeboa, Kwame, Benke, Paul J., Berger, Sara M., Bjerglund, Lise, Campos‐Xavier, Belinda, Ciliberto, Michael, Cohen, Julie S., Comi, Anne M., Curry, Cynthia, Damaj, Lena, Denommé‐Pichon, Anne‐Sophie, Emrick, Lisa, Faivre, Laurence, Fasano, Mary Beth, Fiévet, Alice, Finkel, Richard S., García‐Miñaúr, Sixto, Gerard, Amanda, Gomez‐Puertas, Paulino, Guillen Sacoto, Maria J., Hoffman, Trevor L., Howard, Lillian, Iglesias, Alejandro D., Izumi, Kosuke, Larson, Austin, Leiber, Anja, Lozano, Reymundo, Marcos‐Alcalde, Iñigo, Mintz, Cassie S., Mullegama, Sureni V., Møller, Rikke S., Odent, Sylvie, Oppermann, Henry, Ostergaard, Elsebet, Pacio‐Míguez, Marta, Palomares‐Bralo, Maria, Parikh, Sumit, Paulson, Anna M., Platzer, Konrad, Posey, Jennifer E., Potocki, Lorraine, Revah‐Politi, Anya, Rio, Marlene, Ritter, Alyssa L., Robinson, Scott, Rosenfeld, Jill A., Santos‐Simarro, Fernando, Sousa, Sérgio B., Wéber, Mathys, Xie, Yili, Chung, Wendy K., Brown, Natasha J., Tümer, Zeynep

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