The HO-1/CO system regulates mitochondrial-capillary density relationships in human skeletal muscle by Pecorella, Shelly R H, Potter, Jennifer V F, Cherry, Anne D, Peacher, Dionne F, Welty-Wolf, Karen E, Moon, Richard E, Piantadosi, Claude A, Suliman, Hagir B

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Sildenafil: Possible Prophylaxis against Swimming-induced Pulmonary Edema by MARTINA, STEFANIE D, FREIBERGER, JOHN J, PEACHER, DIONNE F, NATOLI, MICHAEL J, SCHINAZI, ERIC A, KERNAGIS, DAWN N, POTTER, JENNIFER V F, OTTENI, CLAIRE E, MOON, RICHARD E

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Last Word on Viewpoint: Why do some patients stop breathing after taking narcotics? Ventilatory chemosensitivity as a predictor of opioid-induced respiratory depression by Potter, Jennifer V F, Moon, Richard E

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Commentaries on Viewpoint: Why do some patients stop breathing after taking narcotics? Ventilatory chemosensitivity as a predictor of opioid-induced respiratory depression by Potter, Jennifer V F, Moon, Richard E

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Neurobiological markers of exercise-related brain plasticity in older adults by Voss, Michelle W, Erickson, Kirk I, Prakash, Ruchika Shaurya, Chaddock, Laura, Kim, Jennifer S, Alves, Heloisa, Szabo, Amanda, Phillips, Siobhan M, Wójcicki, Thomas R, Mailey, Emily L, Olson, Erin A, Gothe, Neha, Vieira-Potter, Victoria J, Martin, Stephen A, Pence, Brandt D, Cook, Marc D, Woods, Jeffrey A, McAuley, Edward, Kramer, Arthur F

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The adult galactosemic phenotype by Waisbren, Susan E., Potter, Nancy L., Gordon, Catherine M., Green, Robert C., Greenstein, Patricia, Gubbels, Cynthia S., Rubio-Gozalbo, Estela, Schomer, Donald, Welt, Corrine, Anastasoaie, Vera, D’Anna, Kali, Gentile, Jennifer, Guo, Chao-Yu, Hecht, Leah, Jackson, Roberta, Jansma, Bernadette M., Li, Yijun, Lip, Va, Miller, David T., Murray, Michael, Power, Leslie, Quinn, Nicolle, Rohr, Frances, Shen, Yiping, Skinder-Meredith, Amy, Timmers, Inge, Tunick, Rachel, Wessel, Ann, Wu, Bai-Lin, Levy, Harvey, Elsas, Louis, Berry, Gerard T.

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CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 by Rees, Elliott, Walters, James T R, Chambert, Kimberly D, O'Dushlaine, Colm, Szatkiewicz, Jin, Richards, Alexander L, Georgieva, Lyudmila, Mahoney-Davies, Gerwyn, Legge, Sophie E, Moran, Jennifer L, Genovese, Giulio, Levinson, Douglas, Morris, Derek W, Cormican, Paul, Kendler, Kenneth S, O'Neill, Francis A, Riley, Brien, Gill, Michael, Corvin, Aiden, Sklar, Pamela, Hultman, Christina, Pato, Carlos, Pato, Michele, Sullivan, Patrick F, Gejman, Pablo V, McCarroll, Steven A, O'Donovan, Michael C, Owen, Michael J, Kirov, George

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Alternative donor transplantation for severe aplastic anemia: a comparative study of the SAAWP EBMT by Montoro, Juan, Eikema, Dirk-Jan, Tuffnell, Joe, Potter, Victoria, Kalwak, Krzysztof, Halkes, Constantijn J. M., Kulagin, Alexander, Collin, Matthew, Wynn, Robert F., Robinson, Stephen, Nicholson, Emma, Sengeloev, Henrik, Clay, Jennifer, Halahleh, Khalid, Skorobogatova, Elena, Sanz, Jaime, Passweg, Jakob, Mielke, Stephan, Ryhänen, Samppa, Carpenter, Ben, Gedde-Dahl, Tobias, Tholouli, Eleni, Fanin, Renato, Lewalle, Philippe, Kulasekararaj, Austin, Risitano, Antonio, Peffault de Latour, Régis

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Common variant at 16p11.2 conferring risk of psychosis by Steinberg, Stacy, de Jong, S, Mattheisen, M, Demontis, D, Jamain, S, Papiol, S, Vassos, E, Giegling, I, Breuer, R, Fraser, G, Melle, Ingrid, Djurovic, Srdjan, Agartz, Ingrid, Suvisaari, J, Lonnqvist, J, Paunio, T, Hansen, T, Ingason, A, Pirinen, M, Strengman, E, Orntoft, T, Didriksen, M, Hollegaard, MV, Nordentoft, M, Abramova, L, Arrojo, M, Sanjuan, J, Arango, C, Etain, B, Bellivier, F, Meary, A, Schurhoff, F, Szoke, A, Ribolsi, M, Magni, V, Siracusano, A, Sperling, S, Rossner, M, Christiansen, C, Kiemeney, LA, Veldink, J, Curran, S, Bolton, P, Staal, W, Rehnstrom, K, Kilpinen, H, Freitag, CM, Meyer, J, Magnusson, P, Saemundsen, E, Martsenkovska, I, Paketchieva, K, Durmishi, N, Naneishvili, N, Mikeladze, N, Surguladze, S, Farmer, A, Mitchell, PB, Wright, A, Fullerton, JM, Montgomery, GW, Martin, NG, van Winkel, R, Kenis, G, De Hert, M, Rethelyi, JM, Bitter, I, Terenius, L, Jonsson, EG, Bakker, S, van Os, J, Jablensky, A, Bramon, E, Powell, J, Murray, R, Corvin, A, Gill, M, Morris, D, O'Neill, FA, Riley, B, Owen, MJ, O'Donovan, MC, Kong, A, Ehrenreich, H, Carracedo, A, Golimbet, V, Andreassen, Ole Andreas, Mors, O, Mortensen, PB, Werge, T, Nothen, MM, Cichon, S, Ruggeri, M, Tosato, S, Palotie, A, St Clair, D, Rujescu, D, Collier, DA, Stefansson, H, Stefánsson, Kári

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Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process by Springelkamp, Henriët., Höhn, René, Mishra, Aniket, Hysi, Pirro G., Khor, Chiea-Chuen, Loomis, Stephanie J., Bailey, Jessica N. Cooke, Gibson, Jane, Thorleifsson, Gudmar, Janssen, Sarah F., Luo, Xiaoyan, Ramdas, Wishal D., Vithana, Eranga, Nongpiur, Monisha E., Montgomery, Grant W., Xu, Liang, Mountain, Jenny E., Gharahkhani, Puya, Lu, Yi, Amin, Najaf, Karssen, Lennart C., Sim, Kar-Seng, van Leeuwen, Elisabeth M., Iglesias, Adriana I., Verhoeven, Virginie J. M., Hauser, Michael A., Loon, Seng-Chee, Despriet, Dominiek D. G., Nag, Abhishek, Venturini, Cristina, Sanfilippo, Paul G., Schillert, Arne, Kang, Jae H., Landers, John, Jonasson, Fridbert, Cree, Angela J., van Koolwijk, Leonieke M. E., Rivadeneira, Fernando, Souzeau, Emmanuelle, Jonsson, Vesteinn, Menon, Geeta, Weinreb, Robert N., de Jong, Paulus T. V. M., Oostra, Ben A., Uitterlinden, André G., Hofman, Albert, Ennis, Sarah, Thorsteinsdottir, Unnur, Burdon, Kathryn P., Spector, Timothy D., Mirshahi, Alireza, Saw, Seang-Mei, Vingerling, Johannes R., Teo, Yik-Ying, Haines, Jonathan L., Wolfs, Roger C. W., Lemij, Hans G., Tai, E-Shyong, Jansonius, Nomdo M., Jonas, Jost B., Cheng, Ching-Yu, Aung, Tin, Viswanathan, Ananth C., Klaver, Caroline C. W., Craig, Jamie E., Macgregor, Stuart, Mackey, David A., Lotery, Andrew J., Stefansson, Kari, Bergen, Arthur A. B., Young, Terri L., Wiggs, Janey L., Pfeiffer, Norbert, Wong, Tien-Yin, Pasquale, Louis R., Hewitt, Alex W., van Duijn, Cornelia M., Hammond, Christopher J.

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Transplant Outcomes in Patients with Ph+ Chronic Myeloid Leukemia: Haploidentical Donors Compared to Matched Sibling Donors and Matched/Mismatched Unrelated Donors: A Retrospective... by Onida, Francesco, Junran, Ge, Koster, Linda, Hamladji, Rose-Marie, Byrne, Jennifer, Potter, Victoria, Aljurf, Mahmoud, Robin, Marie, Halaburda, Kazimierz, Passweg, Jakob R., Salmenniemi, Urpu, Sengeloev, Henrik, Apperley, Jane F, Clark, Andrew, Reményi, Péter, Morozova, Elena V., Craddock, Charles, Lenhoff, Stig, Ganser, Arnold, Wu, Ka Lung, Perez Martinez, Antonio, Hayden, Patrick John, Gras, Luuk, Chalandon, Yves, Yakoub-Agha, Ibrahim

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A genome-wide association study of anorexia nervosa by Reichborn-Kjennerud, Ted, Knudsen, Gun Peggy, Andreassen, Ole Andreas, Espeseth, Thomas, Lundervold, Astri, Reinvang, Ivar, Steen, Vidar Martin, Le Hellard, Stephanie, Mattingsdal, Morten, Boraske, V, Franklin, CS, Floyd, James A. B, Thornton, Laura M, Huckins, L. M, Southam, L, Rayner, NW, Tachmazidou, I, Klump, KL, Treasure, Jim, Lewis, C. M, Schmidt, U, Tozzi, F, Kiezebrink, K, Hebebrand, J, Gorwood, P, Adan, R. A. H, Kas, M. J. H, Favaro, A, Santonastaso, P, Fernández-Aranda, Fernando, Gratacòs, Mònica, Rybakowski, Finn, Dmitrzak-Weglarz, M, Kaprio, J, Keski-Rahkonen, A, Raevuori, A, Van Furth, E. F, Slof-Op 't Landt, M. C. T, Hudson, JI, Monteleone, P, Kaplan, AS, Karwautz, A, Hakonarson, H, Berrettini, W. H, Guo, Y, Li, D, Schork, NJ, Komaki, G, Ando, T, Inoko, H

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Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia by Kendler, Kenneth S., Walters, James, Blackwell, Jenefer M., Bramon, Elvira, Markus, Hugh S., Rautanen, Anna, Freeman, Colin, Hopkins, Lucinda, Edkins, Sarah, Bumpstead, Suzannah J., Dronov, Serge, Gillman, Matthew, Gray, Emma, Liddle, Jennifer, Potter, Simon C., Weston, Paul, Ripke, Stephan, Farh, Kai‐How, Holmans, Peter A., Lee, Phil, Huang, Hailiang, Bacanu, Silviu A., Belliveau, Richard A., Bene, Judit, Bigdeli, Tim B., Bruggeman, Richard, Cahn, Wiepke, Carrera, Noa, Cheung, Eric F. C., Cohen, David, Craddock, Nick, Davis, Kenneth L., Dinan, Timothy, Drapeau, Elodie, Dudbridge, Frank, Durmishi, Naser, Eichhammer, Peter, Farrell, Martilias S., Franke, Lude, Freimer, Nelson B., Friedman, Joseph I., Fromer, Menachem, Gratten, Jacob, Haroutunian, Vahram, Hartmann, Annette M., Henskens, Frans A., Hofman, Andrea, Hollegaard, Mads V., Joa, Inge, Keller, Matthew C., Klovins, Janis, Konte, Bettina, Kucinskiene, Zita Ausrele, Laurent, Claudine, Loughland, Carmel M., Mallet, Jacques, Mattheisen, Manuel, McCarley, Robert W., McDonald, Colm, Meier, Sandra, Meijer, Carin J., Metspalu, Andres, Milani, Lili, Milanova, Vihra, Mokrab, Younes, Myin‐Germeys, Inez, Nenadic, Igor, Nikitina‐Zake, Liene, O'Callaghan, Eadbhard, O'Neill, F. Anthony, Paunio, Tiina, Pejovic‐Milovancevic, Milica, Perkins, Diana O., Pietiläinen, Olli, Quested, Digby, Reichenberg, Abraham, Salomaa, Veikko, Scolnick, Edward M., Silagadze, Teimuraz, So, Hon‐Cheong, Spencer, Chris C. A., Suvisaari, Jaana, Szatkiewicz, Jin P., Thirumalai, Srinivas, Tosato, Sarah, Waddington, John, Wang, Qiang, Williams, Nigel M., Witt, Stephanie H., Wormley, Brandon K., Zheng, Xuebin, Zimprich, Fritz, Wray, Naomi R., Buxbaum, Joseph D., Jablensky, Assen V., Knight, Jo, Levinson, Douglas F., Malhotra, Anil K., Weinberger, Daniel R., Werge, Thomas

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Genetic loci for retinal arteriolar microcirculation by Sim, Xueling, Jensen, Richard A, Ikram, M Kamran, Cotch, Mary Frances, Li, Xiaohui, MacGregor, Stuart, Xie, Jing, Smith, Albert Vernon, Boerwinkle, Eric, Mitchell, Paul, Klein, Ronald, Klein, Barbara E K, Glazer, Nicole L, Lumley, Thomas, McKnight, Barbara, Psaty, Bruce M, de Jong, Paulus T V M, Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, Andre G, van Duijn, Cornelia M, Aspelund, Thor, Eiriksdottir, Gudny, Harris, Tamara B, Jonasson, Fridbert, Launer, Lenore J, Attia, John, Baird, Paul N, Harrap, Stephen, Holliday, Elizabeth G, Inouye, Michael, Rochtchina, Elena, Scott, Rodney J, Viswanathan, Ananth, Li, Guo, Smith, Nicholas L, Wiggins, Kerri L, Kuo, Jane Z, Taylor, Kent D, Hewitt, Alex W, Martin, Nicholas G, Montgomery, Grant W, Sun, Cong, Young, Terri L, Mackey, David A, van Zuydam, Natalie R, Doney, Alex S F, Palmer, Colin N A, Morris, Andrew D, Rotter, Jerome I, Tai, E Shyong, Gudnason, Vilmundur, Vingerling, Johannes R, Siscovick, David S, Wang, Jie Jin, Wong, Tien Y

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eQuality: a Process Model to Develop an Integrated, Comprehensive Medical Education Curriculum for LGBT, Gender Nonconforming, and DSD Health by Holthouser, Amy, Sawning, Susan, Leslie, Katie F., Faye Jones, V., Steinbock, Stacie, Noonan, Emily J., Martin, Leslee J., Weingartner, Laura A., Potter, Jennifer, Davis, John, Eckstrand, Kristen L., Ann Shaw, M.

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A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis by Mechelli, Rosella, Umeton, Renato, Policano, Claudia, Annibali, Viviana, Coarelli, Giulia, Ricigliano, Vito A G, Vittori, Danila, Fornasiero, Arianna, Buscarinu, Maria Chiara, Romano, Silvia, Salvetti, Marco, Ristori, Giovanni

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A case for expanding carrier testing to include actionable X‐linked disorders by Rope, Alan F., Kauffman, Tia L., Himes, Pat, Amendola, Laura M., Punj, Sumit, Akkari, Yassmine, Potter, Amiee, Davis, James V., Schneider, Jennifer L., Reiss, Jacob A., Gilmore, Mari J., McMullen, Carmit K., Nickerson, Deborah A., Richards, C. Sue, Jarvik, Gail P., Wilfond, Benjamin S., Goddard, Katrina A. B.

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A case for expanding carrier testing to include actionable X-linked disorders by Rope, Alan F, Kauffman, Tia L, Himes, Pat, Amendola, Laura M, Punj, Sumit, Akkari, Yassmine, Potter, Amiee, Davis, James V, Schneider, Jennifer L, Reiss, Jacob A, Gilmore, Mari J, McMullen, Carmit K, Nickerson, Deborah A, Richards, C Sue, Jarvik, Gail P, Wilfond, Benjamin S, Goddard, Katrina A B

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