Review Article: Apoptosis in the Kidney von Davis, Myrtle A., Ryan, Dara H.

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Apoptosis in the kidney von DAVIS, M. A, RYAN, D. H

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Rare coding variation provides insight into the genetic architecture and phenotypic context of autism von Fu, Jack M., Satterstrom, F. Kyle, Peng, Minshi, Brand, Harrison, Collins, Ryan L., Dong, Shan, Wamsley, Brie, Klei, Lambertus, Wang, Lily, Hao, Stephanie P., Stevens, Christine R., Cusick, Caroline, Babadi, Mehrtash, Banks, Eric, Collins, Brett, Dodge, Sheila, Gabriel, Stacey B., Gauthier, Laura, Lee, Samuel K., Liang, Lindsay, Ljungdahl, Alicia, Mahjani, Behrang, Sloofman, Laura, Smirnov, Andrey N., Barbosa, Mafalda, Betancur, Catalina, Brusco, Alfredo, Chung, Brian H. Y., Cook, Edwin H., Cuccaro, Michael L., Domenici, Enrico, Ferrero, Giovanni Battista, Gargus, J. Jay, Herman, Gail E., Hertz-Picciotto, Irva, Maciel, Patricia, Manoach, Dara S., Passos-Bueno, Maria Rita, Persico, Antonio M., Renieri, Alessandra, Sutcliffe, James S., Tassone, Flora, Trabetti, Elisabetta, Campos, Gabriele, Cardaropoli, Simona, Carli, Diana, Chan, Marcus C. Y., Fallerini, Chiara, Giorgio, Elisa, Girardi, Ana Cristina, Hansen-Kiss, Emily, Lee, So Lun, Lintas, Carla, Ludena, Yunin, Nguyen, Rachel, Pavinato, Lisa, Pericak-Vance, Margaret, Pessah, Isaac N., Schmidt, Rebecca J., Smith, Moyra, Costa, Claudia I. S., Trajkova, Slavica, Wang, Jaqueline Y. T., Yu, Mullin H. C., Cutler, David J., De Rubeis, Silvia, Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J., Talkowski, Michael E.

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Radiation and systemic immunotherapy for metastatic uveal melanoma: a clinical retrospective review von Tran, Danielle H, Shanley, Ryan, Giubellino, Alessio, Tang, Peter H, Koozekanani, Dara D, Yuan, Jianling, Dusenbery, Kathryn, Domingo-Musibay, Evidio

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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism von Satterstrom, F. Kyle, Breen, Michael S., Grove, Jakob, Klei, Lambertus, Xu, Xinyi, Norman, Utku, Brand, Harrison, Schwartz, Grace, Barbosa, Mafalda, Bybjerg-Grauholm, Jonas, Carracedo, Angel, Chiocchetti, Andreas G., Chung, Brian H.Y., Coon, Hilary, Cuccaro, Michael L., Dalla Bernardina, Bernardo, Domenici, Enrico, Dong, Shan, Freitag, Christine M., González-Peñas, Javier, Guter, Stephen, He, Xin, Herman, Gail E., Hertz-Picciotto, Irva, Hougaard, David M., Ionita-Laza, Iuliana, Jacob, Suma, Jamison, Jesslyn, Jugessur, Astanand, Kolevzon, Alexander, Kushima, Itaru, Lee, So Lun, Lehtimäki, Terho, Lim, Elaine T., Lipkin, W. Ian, Lopergolo, Diego, Lopes, Fátima, Ludena, Yunin, Maciel, Patricia, Meiri, Gal, Menashe, Idan, Miller, Judith, Montenegro, Eduarda M.S., Muglia, Pierandrea, Nordentoft, Merete, Ozaki, Norio, Palotie, Aarno, Parellada, Mara, Passos-Bueno, Maria Rita, Persico, Antonio M., Pessah, Isaac, Puura, Kaija, Renieri, Alessandra, Riberi, Evelise, Robinson, Elise B., Samocha, Kaitlin E., Sandin, Sven, Santangelo, Susan L., Schellenberg, Gerry, Scherer, Stephen W., Schmitt, Lauren, Silva, Isabela M.W., Singh, Tarjinder, Siper, Paige M., Soares, Gabriela, Susser, Ezra, Szatmari, Peter, Tang, Lara, Tassone, Flora, Teufel, Karoline, Trelles, Maria del Pilar, Werge, Thomas, Werling, Donna M., Wigdor, Emilie M., Yu, Mullin H.C., Zachi, Elaine, Agerbo, Esben, Als, Thomas Damm, Bækvad-Hansen, Marie, Belliveau, Rich, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Maller, Julian, Mattheisen, Manuel, Moran, Jennifer, Pallesen, Jonatan, Poulsen, Jesper Buchhave, Ripke, Stephan, Gallagher, Louise, Gill, Michael, Zwick, Michael E., State, Matthew W., Daly, Mark J., Buxbaum, Joseph D.

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Resequencing Candidate Genes Implicates Rare Variants in Asthma Susceptibility von Torgerson, Dara G., Capurso, Daniel, Mathias, Rasika A., Graves, Penelope E., Hernandez, Ryan D., Beaty, Terri H., Bleecker, Eugene R., Raby, Benjamin A., Meyers, Deborah A., Barnes, Kathleen C., Weiss, Scott T., Martinez, Fernando D., Nicolae, Dan L., Ober, Carole

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Population Genetics of Rare Variants and Complex Diseases von Maher, M. Cyrus, Uricchio, Lawrence H., Torgerson, Dara G., Hernandez, Ryan D.

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An admixture mapping meta-analysis implicates genetic variation at 18q21 with asthma susceptibility in Latinos von Gignoux, Christopher R., Torgerson, Dara G., Pino-Yanes, Maria, Uricchio, Lawrence H., Galanter, Joshua, Roth, Lindsey A., Eng, Celeste, Hu, Donglei, Nguyen, Elizabeth A., Huntsman, Scott, Mathias, Rasika A., Kumar, Rajesh, Rodriguez-Santana, Jose, Thakur, Neeta, Oh, Sam S., McGarry, Meghan, Moreno-Estrada, Andres, Sandoval, Karla, Winkler, Cheryl A., Seibold, Max A., Padhukasahasram, Badri, Conti, David V., Farber, Harold J., Avila, Pedro, Brigino-Buenaventura, Emerita, Lenoir, Michael, Meade, Kelley, Serebrisky, Denise, Borrell, Luisa N., Rodriguez-Cintron, William, Thyne, Shannon, Joubert, Bonnie R., Romieu, Isabelle, Levin, Albert M., Sienra-Monge, Juan-Jose, del Rio-Navarro, Blanca Estela, Gan, Weiniu, Raby, Benjamin A., Weiss, Scott T., Bleecker, Eugene, Meyers, Deborah A., Martinez, Fernando J., Gauderman, W. James, Gilliland, Frank, London, Stephanie J., Bustamante, Carlos D., Nicolae, Dan L., Ober, Carole, Sen, Saunak, Barnes, Kathleen, Williams, L. Keoki, Hernandez, Ryan D., Burchard, Esteban G.

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A genome-wide association study of bronchodilator response in Latinos implicates rare variants von Drake, Katherine A., PhD, Torgerson, Dara G., PhD, Gignoux, Christopher R., MS, Galanter, Joshua M., MD, Roth, Lindsey A., MA, Huntsman, Scott, MS, Eng, Celeste, BS, Oh, Sam S., PhD, Yee, Sook Wah, PhD, Lin, Lawrence, BS, Bustamante, Carlos D., PhD, Moreno-Estrada, Andrés, MD, Sandoval, Karla, PhD, Davis, Adam, MA, MPH, Borrell, Luisa N., DDS, PhD, Farber, Harold J., MD, MSPH, Kumar, Rajesh, MD, Avila, Pedro C., MD, Brigino-Buenaventura, Emerita, MD, Chapela, Rocio, MD, Ford, Jean G., MD, LeNoir, Michael A., MD, Lurmann, Fred, MS, Meade, Kelley, MD, Serebrisky, Denise, MD, Thyne, Shannon, MD, Rodríguez-Cintrón, William, MD, Sen, Saunak, PhD, Rodríguez-Santana, José R., MD, Hernandez, Ryan D., PhD, Giacomini, Kathleen M., PhD, Burchard, Esteban G., MD, MPH

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Real-World, Patient-Reported and Clinic Data from Individuals with Type 1 Diabetes Using the MiniMed 670G Hybrid Closed-Loop System von DuBose, Stephanie N., Bauza, Colleen, Verdejo, Alandra, Beck, Roy W., Bergenstal, Richard M., Sherr, Jennifer

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Surgical management of acute appendicitis during the European COVID-19 second wave: safe and effective von Forssten, Maximilian Peter, Kaplan, Lewis J., Tolonen, Matti, Martinez-Casas, Isidro, Cao, Yang, Walsh, Thomas N., Bass, Gary Alan, Mohseni, Shahin

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Identifying tagging SNPs for African specific genetic variation from the African Diaspora Genome von Johnston, Henry Richard, Hu, Yi-Juan, Gao, Jingjing, O’Connor, Timothy D., Abecasis, Gonçalo R., Wojcik, Genevieve L, Gignoux, Christopher R., Gourraud, Pierre-Antoine, Lizee, Antoine, Hansen, Mark, Genuario, Rob, Bullis, Dave, Lawley, Cindy, Kenny, Eimear E., Bustamante, Carlos, Beaty, Terri H., Mathias, Rasika A., Barnes, Kathleen C., Qin, Zhaohui S.

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Genetic variation in CRHR1 is associated with short-term respiratory response to corticosteroids in preterm infants at risk for bronchopulmonary dysplasia von Lewis, Tamorah, Truog, William, Norberg, Mike, Ballard, Philip L., Torgerson, Dara

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Peripheral neuropathy in a family with Sandhoff disease and SH3TC2 deficiency von Grunseich, Christopher, Schindler, Alice B., Chen, Ke-lian, Bakar, Dara, Mankodi, Ami, Traslavina, Ryan, Ray-Chaudhury, Abhik, Lehky, Tanya J., Baker, Eva H., Maragakis, Nicholas J., Tifft, Cynthia J., Fischbeck, Kenneth H.

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Tissue Oxygenation Changes After Transfusion and Outcomes in Preterm Infants: A Secondary Near-Infrared Spectroscopy Study of the Transfusion of Prematures Randomized Clinical Tria... von Chock, Valerie Y, Kirpalani, Haresh, Bell, Edward F, Tan, Sylvia, Hintz, Susan R, Ball, M Bethany, Smith, Emily, Das, Abhik, Loggins, Yvonne C, Sood, Beena G, Chalak, Lina F, Wyckoff, Myra H, Kicklighter, Stephen D, Kennedy, Kathleen A, Patel, Ravi M, Carlo, Waldemar A, Johnson, Karen J, Watterberg, Kristi L, Sánchez, Pablo J, Laptook, Abbot R, Seabrook, Ruth B, Cotten, C Michael, Mancini, Toni, Sokol, Gregory M, Ohls, Robin K, Hibbs, Anna Maria, Poindexter, Brenda B, Reynolds, Anne Marie, DeMauro, Sara B, Chawla, Sanjay, Baserga, Mariana, Walsh, Michele C, Higgins, Rosemary D, Van Meurs, Krisa P

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Modelling Perception with Artificial Neural Networks von Tosh, Colin R, Ruxton, Graeme D

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Population Genetics of Rare Variants and Complex Diseases von Maher, M Cyrus, Uricchio, Lawrence H, Torgerson, Dara G, Hernandez, Ryan D

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Calibration monitoring for sensor calibration interval extension: Identifying technical gaps von Coble, J., Ramuhalli, P., Meyer, R., Hashemian, H., Shumaker, B., Cummins, D.

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Supplemental Material for Kockel et al., 2019 von Kockel, Lutz, Griffin, Catherine, Ahmed, Yaseen, Fidelak, Lauren, Rajan, Arjun, Gould, Ethan P., Haigney, Myles, Ralston, Benjamin, Tercek, Rex J., Galligani, Lara, Rao, Sagar, Huq, Lutfi, Hersh K. Bhargava, Dooner, Ailis C., Lemmerman, Emily G., Malusa, Ruby F., Nguyen, Tran H., Chung, Julie S., Gregory, Sara M., Kiyomasa M. Kuwana, Regenold, Jonathan T., Wei, Alexander, Ashton, Jake, Dickinson, Patrick, Martel, Kate, Cai, Connie, Chen, Carissa, Price, Stephen, Qiao, Jeffrey, Shepley, David, Zhang, Joanna, Chalasani, Meghana, Nguyen, Khanh, Aalto, August, ByungJun Kim, Tazawa-Goodchild, Erik, Sherwood, Amanda, Rahman, Ahmad, Sum Ying Celeste Wu, Lotzkar, Joel, Michaels, Serena, Aristotle, Hillary, Clark, Antigone, Gasper, Grace, Xiang, Evan, Schlör, Frieda Luna, Lu, Melissa, Haering, Kate, Friberg, Julia, Kuwana, Alyssa, Lee, Jonathan, Liu, Alan, Norton, Emma, Hamad, Leena, Lee, Clara, Okeremi, Dara, DiTullio, Harry, Dumoulin, Kat, Chi, Sun Yu Gordon, Derossi, Grayson S., Horowitch, Rose E., Issa, Elias C., Le, Dan T., Morales, Bryce C., Ayush Noori, Shao, Justin, Cho, Sophia, Hoang, Mai N., Johnson, Ian M., Lee, Katherine C., Lee, Maria, Madamidola, Elizabeth A., Schmitt, Katrina E., Byan, Gabriel, Taeyoung Park, Chen, Jonathan, Monovoukas, Alexi, Kang, Madison J., McGowan, Tanner, Walewski, Joseph J., Simon, Brennan, Zu, Sophia J., Miller, Gregory P., Fitzpatrick, Kate B., Lantz, Nicole, Fox, Elizabeth, Collette, Jeanette, Kurtz, Richard, Duncan, Chris, Palmer, Ryan, Rotondo, Cheryl, Janicki, Eric, Townley Chisholm, Rankin, Anne, Sangbin Park, Kim, Seung K.

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Peripheral neuropathy in a family with Sandhoff disease and SH3TC2 deficiency von Grunseich, Christopher, Schindler, Alice B, Chen, Ke-Lian, Bakar, Dara, Mankodi, Ami, Traslavina, Ryan, Ray-Chaudhury, Abhik, Lehky, Tanya J, Baker, Eva H, Maragakis, Nicholas J, Tifft, Cynthia J, Fischbeck, Kenneth H

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