PIGG defines the Emm blood group system by Lane, William J., Aeschlimann, Judith, Vege, Sunitha, Lomas-Francis, Christine, Burgos, Anna, Mah, Helen H., Halls, Justin B. L., Baeck, Peter, Ligthart, Peter C., Veldhuisen, Barbera, Shah, Ripal J., Joshi, Sanmukh R., Westhoff, Connie M.

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Three novel Er blood group system alleles and insights from protein modeling by Lane, William J., Vege, Sunitha, Mah, Helen H., Ochoa‐Garay, Gorka, Lomas‐Francis, Christine, Westhoff, Connie M.

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Automated typing of red blood cell and platelet antigens from whole exome sequences by Lane, William J., Vege, Sunitha, Mah, Helen H., Lomas‐Francis, Christine, Aguad, Maria, Smeland‐Wagman, Robin, Koch, Christopher, Killian, Jacqueline M., Gardner, Cubby L., De Castro, Mauricio, Lebo, Matthew S., Kaufman, Richard M., Green, Robert C., Westhoff, Connie M.

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ABO Genotyping finds more A2 to B kidney transplant opportunities than lectin-based subtyping by Joseph, Abigail, Murray, Cody J., Novikov, Natasha D., Velliquette, Randall W., Vege, Sunitha, Halls, Justin B.L., Mah, Helen H., Dellagatta, Jamie L., Comeau, Edward, Aguad, Maria, Kaufman, Richard M., Olsson, Martin L., Guleria, Indira, Stowell, Sean R., Milford, Edgar L., Hult, Annika K., Yeung, Melissa Y., Westhoff, Connie M., Murphey, Cathi L., Lane, William J.

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Overcoming the challenges of interpreting complex and uncommon RH alleles from whole genomes by Halls, Justin B.L., Vege, Sunitha, Simmons, Daimon P., Aeschlimann, Judith, Bujiriri, Baderha, Mah, Helen H., Lebo, Matthew S., Vijay Kumar, Prathik K., Westhoff, Connie M., Lane, William J.

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Multiple GYPB gene deletions associated with the U− phenotype in those of African ancestry by Lane, William J., Gleadall, Nicholas S., Aeschlimann, Judith, Vege, Sunitha, Sanchis‐Juan, Alba, Stephens, Jonathan, Sullivan, Jensyn Cone, Mah, Helen H., Aguad, Maria, Smeland‐Wagman, Robin, Lebo, Matthew S., Vijay Kumar, Prathik K., Kaufman, Richard M., Green, Robert C., Ouwehand, Willem H., Westhoff, Connie M.

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A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xga by Lane, William J., Aguad, Maria, Smeland‐Wagman, Robin, Vege, Sunitha, Mah, Helen H., Joseph, Abigail, Blout, Carrie L., Nguyen, Tiffany T., Lebo, Matthew S., Sidhu, Manpreet, Lomas‐Francis, Christine, Kaufman, Richard M., Green, Robert C., Westhoff, Connie M., Bates, David W., Blout, Carrie, Christensen, Kurt D., Cirino, Allison L., Green, Robert C., Ho, Carolyn Y., Krier, Joel B., Lane, William J., Lehmann, Lisa S., MacRae, Calum A., Morton, Cynthia C., Perry, Denise L., Seidman, Christine E., Sunyaev, Shamil R., Vassy, Jason L., Schonman, Erica, Nguyen, Tiffany, Steffens, Eleanor, Betting, Wendi Nicole, Aronson, Samuel J., Ceyhan‐Birsoy, Ozge, Lebo, Matthew S., Machini, Kalotina, McLaughlin, Heather M., Azzariti, Danielle R., Rehm, Heidi L., Tsai, Ellen A., Blumenthal‐Barby, Jennifer, Feuerman, Lindsay Z., McGuire, Amy L., Lee, Kaitlyn, Robinson, Jill O., Slashinski, Melody J., Diamond, Pamela M., Davis, Kelly, Ubel, Peter A., Kraft, Peter, Scott Roberts, J., Garber, Judy E., Hambuch, Tina, Murray, Michael F., Kohane, Isaac, Kong, Sek Won

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55-P: Donor Specific Antibodies (DSA) – Complement Binding or Not? The Impact on Kidney Regraft Outcomes by Wood, Isabelle G, Mohsin, Nabil, Guleria, Indira, Mah, Helen H, Milford, Edgar L

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P106 LinkSēq for ABO, a molecular based typing solution for the ABO blood group by Lane, William J., Novikov, Natasha, Mah, Helen H., Rodriguez, Joshua M., MacAskill, Peter C., Viard, Thierry, Russnak, Roland, Yuen, Vivian, Haddad, Rania, Kim, Isaac, Li, Raymond, Antovich, Zachary

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P162 Utilizing ABO Genotyping to avoid missed opportunities in kidney transplantation by Lane, William J., Joseph, Abigail, Novikov, Natasha D., Murray, Cody J., Mah, Helen H., Rodriguez, Joshua M., Vege, Sunitha, Baronas, Jane, DellaGatta, Jamie L., Westhoff, Connie M., Olsson, Martin L., Guleria, Indira, Milford, Edgar L., Hult, Annika K., Yeung, Melissa Y., Murphey, Cathi L.

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ABO Genotyping finds more A 2 to B kidney transplant opportunities than lectin-based subtyping by Joseph, Abigail, Murray, Cody J, Novikov, Natasha D, Velliquette, Randall W, Vege, Sunitha, Halls, Justin B L, Mah, Helen H, Dellagatta, Jamie L, Comeau, Edward, Aguad, Maria, Kaufman, Richard M, Olsson, Martin L, Guleria, Indira, Stowell, Sean R, Milford, Edgar L, Hult, Annika K, Yeung, Melissa Y, Westhoff, Connie M, Murphey, Cathi L, Lane, William J

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2010 McDonald criteria for diagnosing pediatric multiple sclerosis by Sadaka, Yair, Verhey, Leonard H., Shroff, Manohar M., Branson, Helen M., Arnold, Douglas L., Narayanan, Sridar, Sled, John G., Bar-Or, Amit, Sadovnick, A. Dessa, McGowan, Melissa, Marrie, Ruth Ann, Banwell, Brenda

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Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency by Le Voyer, Tom, Gervais, Adrian, Rosain, Jérémie, Rinchai, Darawan, Hancioglu, Gonca, Ghillani-Dalbin, Pascale, Charuel, Jean-Luc, Philippot, Quentin, Gueye, Mame Sokhna, Maglorius Renkilaraj, Majistor Raj Luxman, Ogishi, Masato, Soudée, Camille, Migaud, Mélanie, Rozenberg, Flore, Momenilandi, Mana, Delmonte, Ottavia M, Müller, Gabriele, Keller, Baerbel, Franco Gallego, William Alexander, Rubin, Tamar, Emiroglu, Melike, Parvaneh, Nima, Aranda-Guillen, Maribel, Berrios, David I, Vong, Linda, Katelaris, Constance H, Mustillo, Peter, Raedler, Johannes, Bohlen, Jonathan, Winter, Sarah, McLean, Catriona, Guffroy, Aurélien, DeRisi, Joseph L, Yu, David, Miller, Corey, Feng, Yi, Béziat, Vivien, Bustamante, Jacinta, Pan-Hammarström, Qiang, Holland, Steve M, Bosticardo, Marita, Kenney, Heather, Slade, Charlotte A, Boztuğ, Kaan, Mahlaoui, Nizar, Abraham, Roshini S, Lougaris, Vassilios, Hauck, Fabian, Sediva, Anna, Atschekzei, Faranaz, Poli, M Cecilia, Slatter, Mary A, Palterer, Boaz, Suan, Daniel, Wong, Melanie, Kane, Alisa, Ma, Cindy, Grombiříková, Hana, Dalal, Ilan, Aladjidi, Nathalie, Hie, Miguel, Lazaro, Estibaliz, Franco, Jose, Keles, Sevgi, Malphettes, Marion, Pasquet, Marlene, Maccari, Maria Elena, Meinhardt, Andrea, Shahrooei, Mohammad, Goodnow, Christopher C, Gray, Paul E, Belot, Alexandre, Kuehn, Hye Sun, Rosenzweig, Sergio D, Miyara, Makoto, Licciardi, Francesco, Servettaz, Amélie, Le Guenno, Guillaume, Herrmann, Vera-Maria, Sarrot-Reynauld, Françoise, Schuetz, Catharina, Cunningham-Rundles, Charlotte, Tangye, Stuart G, Sobacchi, Cristina, Grimbacher, Bodo, Fieschi, Claire, Berteloot, Laureline, Trouillet Assant, Sophie, Neven, Benedicte, Abel, Laurent, Cobat, Aurélie, Jouanguy, Emmanuelle, Kampe, Olle, Bastard, Paul, Roifman, Chaim M, Landegren, Nils, Notarangelo, Luigi D, Anderson, Mark S, Casanova, Jean-Laurent, Puel, Anne

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New genotypes of Liao ning virus (LNV) in Australia exhibit an insect-specific phenotype by Prow, Natalie A, Mah, Marcus G, Deerain, Joshua M, Warrilow, David, Colmant, Agathe M G, O'Brien, Caitlin A, Harrison, Jessica J, McLean, Breeanna J, Hewlett, Elise K, Piyasena, Thisun B H, Hall-Mendelin, Sonja, van den Hurk, Andrew F, Watterson, Daniel, Huang, Bixing, Schulz, Benjamin L, Webb, Cameron E, Johansen, Cheryl A, Chow, Weng K, Hobson-Peters, Jody, Cazier, Chris, Coffey, Lark L, Faddy, Helen M, Suhrbier, Andreas, Bielefeldt-Ohmann, Helle, Hall, Roy A

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Differences in Clinical Features and Comorbid Burden between HLA-C∗06:02 Carrier Groups in >9,000 People with Psoriasis by Douroudis, Konstantinos, Ramessur, Ravi, Barbosa, Ines A., Baudry, David, Duckworth, Michael, Angit, Caroline, Capon, Francesca, Curtis, Charles J., Di Meglio, Paola, Goulding, Jonathan M.R., Griffiths, Christopher E.M., Lee, Sang Hyuck, Mahil, Satveer K., Parslew, Richard, Reynolds, Nick J., Shipman, Alexa R., Warren, Richard B., Yiu, Zenas Z.N., Simpson, Michael A., Dand, Nick, Smith, Catherine H., Evans, Ian, Murphy, Ruth, McPherson, Tess, Kleyn, Elise, Laws, Philip, Rashid, Amir, Alabas, Oras, Morrison, Simon, Ahmed, Shehnaz, Pearson, Eleanor, Richards, Josh, Mackenzie, Teena, Kirby, Brian, Burden, David, Lawson, Linda, McElhone, Kathleen, Ormerod, Anthony, Owen, Caroline, Ali, Mahmud, Anstey, Alex, Antony, Fiona, Archer, Charles, August, Suzanna, Balasubramaniam, Periasamy, Baxter, Kay, Bonsall, Alexandra, Brown, Victoria, Burova, Katya, Butt, Aamir, Cliff, Sandeep, Costache, Mihaela, Darne, Sharmela, Davies, Emily, DeGiovanni, Claudia, Desai, Trupti, DeSilva, Bernadette, Diba, Victoria, Domanne, Eva, Fahy, Caoimhe, Ferguson, Leila, Gkini, Maria-Angeliki, Godwin, Alison, Hammonds, Fiona, Johnson, Sarah, Joseph, Teresa, Kalavala, Manju, Khorshid, Mohsen, Labinoti, Liberta, Lawson, Nicole, Layton, Alison, Lees, Tara, Levell, Nick, Lyon, Calum, McBride, Sandy, McCormack, Sally, McKenna, Kevin, Mellor, Serap, Popli, Urvi, Perera, Gay, Ponnambath, Nabil, Ramsay, Helen, Ranasinghe, Aruni, Reeken, Saskia, Rose, Rebecca, Rotarescu, Rada, Salvary, Ingrid, Sands, Kathy, Sinha, Tapati, Stefanescu, Simina, Sundararaj, Kavitha, Taylor, Michelle, Topliffe, Joanne, Verdolini, Roberto, Wachsmuth, Rachel, Wade, Martin, Walsh, Sarah, Walton, Shernaz, Wilcox, Louise, Wright, Andrew

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Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism influences the association of the methylome with maternal anxiety and neonatal brain volumes by Chen, Li, Pan, Hong, Tuan, Ta Anh, Teh, Ai Ling, MacIsaac, Julia L., Mah, Sarah M., McEwen, Lisa M., Li, Yue, Chen, Helen, Broekman, Birit F. P., Buschdorf, Jan Paul, Chong, Yap Seng, Kwek, Kenneth, Saw, Seang Mei, Gluckman, Peter D., Fortier, Marielle V., Rifkin-Graboi, Anne, Kobor, Michael S., Qiu, Anqi, Meaney, Michael J., Holbrook, Joanna D.

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Developing standardized corticosteroid treatment for Duchenne muscular dystrophy by Guglieri, Michela, Bushby, Kate, McDermott, Michael P, Hart, Kimberly A, Tawil, Rabi, Martens, William B, Herr, Barbara E, McColl, Elaine, Wilkinson, Jennifer, Kirschner, Janbernd, King, Wendy M, Eagle, Michele, Brown, Mary W, Willis, Tracey, Hirtz, Deborah, Shieh, Perry B, Straub, Volker, Childs, Anne-Marie, Ciafaloni, Emma, Butterfield, Russell J, Horrocks, Iain, Spinty, Stefan, Flanigan, Kevin M, Kuntz, Nancy L, Baranello, Giovanni, Roper, Helen, Morrison, Leslie, Mah, Jean K, Manzur, Adnan Y, McDonald, Craig M, Schara, Ulrike, von der Hagen, Maja, Barohn, Richard J, Campbell, Craig, Darras, Basil T, Finkel, Richard S, Vita, Giuseppe, Hughes, Imelda, Mongini, Tiziana, Pegoraro, Elena, Wicklund, Matthew, Wilichowski, Ekkehard, Bryan Burnette, W, Howard, James F, McMillan, Hugh J, Thangarajh, Mathula, Griggs, Robert C

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Correction to Identification of Quinoline-Based RIP2 Kinase Inhibitors with an Improved Therapeutic Index to the hERG Ion Channel by Haile, Pamela A., Casillas, Linda N., Bury, Michael J., Mehlmann, John F., Singhaus, Robert, Charnley, Adam K., Hughes, Terry V., DeMartino, Michael P., Wang, Gren Z., Romano, Joseph J., Dong, Xiaoyang, Plotnikov, Nikolay V., Lakdawala, Ami S., Duraiswami, Chaya, Convery, Maire A., Votta, Bartholomew J., Lipshutz, David B., Desai, Biva M., Swift, Barbara, Capriotti, Carol A., Berger, Scott B., Mahajan, Mukesh K., Reilly, Michael A., Rivera, Elizabeth J., Sun, Helen H., Nagilla, Rakesh, LePage, Carol, Ouellette, Michael T., Totoritis, Rachel D., Donovan, Brian T., Brown, Barry S., Chaudhary, Khuram W., Gough, Peter J., Bertin, John, Marquis, Robert W.

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Successful living donor kidney transplantation across HLA and ABO incompatibilities by Magee, Colm C., Mah, Helen, Tinckam, Kathryn, Wood, Isabelle, Ji, Fang, Powelson, John

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Separation of Acids, Bases, and Neutral Compounds by Fujita, Megumi, Mah, Helen M, Sgarbi, Paulo W. M, Lall, Manjinder S, Ly, Tai Wei, Browne, Lois M

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