Elucidating cortical neurovascular involvement in Huntington's disease using human brain tissue microarrays von Tan, Adelie Y.S., Martinez, Lance C.M.G., Murray, Helen C., Mehrabi, Nasim F., Tippett, Lynette J., Turner, Clinton P., Curtis, Maurice A., Faull, Richard L.M., Dragunow, Mike, Singh-Bains, Malvindar K.

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A European consensus statement on the use of four‐factor prothrombin complex concentrate for cardiac and non‐cardiac surgical patients von Erdoes, G., Koster, A., Ortmann, E., Meesters, M. I., Bolliger, D., Baryshnikova, E., Martinez Lopez De Arroyabe, B., Ahmed, A., Lance, M. D., Ranucci, M., von Heymann, C., Agarwal, S., Ravn, H. B.

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Recurrent emergence of SARS-CoV-2 spike deletion H69/V70 and its role in the Alpha variant B.1.1.7 von Curran, Martin D., Roy, Sunando, Shaaban, Sharif, de Cesare, Mariateresa, Stark, Richard, Palmer, Steve, Jeffries, Aaron R., da Silva Filipe, Ana, Davis, Thomas, Collins, Jennifer, Williams, Thomas, Haldenby, Sam T., Cook, Kate, Davies, Robert, Kay, Sally, Poplawski, Radoslaw, Reynolds, Nicola, Moll, Robin J., Thornton, Alicia, Gatica-Wilcox, Bree, Louka, Stavroula F., Kraemer, Moritz U.G., Freeman, Timothy M., Abudahab, Khalil, Menegazzo, Mirko, Mason, Jenifer, Holmes, Alison, Curran, Tanya, Mookerjee, Siddharth, Munn, Robert, Davies, Alisha, Smith, Nikki, Cormie, Claire, Lo, Stephanie, Auckland, Cressida, Mollett, Guy, Harper, Katherine L., Bonner, Stephen, Padgett, Debra, Burton-Fanning, Shirelle, Bedford, Luke, Coupland, Lindsay, Wright, Victoria, Ball, Jonathan, Boswell, Tim, Duckworth, Nichola, Williams, Rebecca, Cogger, Benjamin J., Farr, Ben W., Thurston, Scott A.J., Bronner, Iraad F., Aigrain, Louise, Gallagher, Michael D., Miah, Shahjahan, Ramsay, Mary, Schaefer, Ulf, Manesis, Nikos, Allara, Elias, Nichols, Jenna, Vamos, Edith E., Hughes, Margaret, Wilson, Harry D., Wilson, Rebekah E., Thompson, Thomas, O’Brien, Sarah, Rudder, Steven, McCluggage, Kathryn, Bonfield, James, Liddle, Jennifier, Rowe, Will, Bevan, Paul, Clark, Richard, Cutts, Tim, Densem, Aiden, Dodd, David, Griffiths, Coline, Kay, Keely, Lensing, Stefanie, Lewis-Wade, Amanah, Mamun, Irfan, Martin, Matt, McClintock, Jo, Nathwani, Claire, Nicholson, Jon, Patel, Gaurang, Petersen, Arabella, Reynolds, Joe, Rudd, Luke, Sadri, Ramin, Sizer, Dale, Soria, Carmen Diaz, Sousa, Catarina, Squares, Janet, Stickland, Tim, Still, Ian, Symons, Edward, Uphill, James, Van, Philip Jansen, Voak, Paul, Corti, Davide

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Genetic mechanisms of critical illness in COVID-19 von Pairo-Castineira, Erola, Clohisey, Sara, Klaric, Lucija, Bretherick, Andrew D., Rawlik, Konrad, Pasko, Dorota, Walker, Susan, Parkinson, Nick, Fourman, Max Head, Russell, Clark D., Furniss, James, Richmond, Anne, Gountouna, Elvina, Wrobel, Nicola, Harrison, David, Wang, Bo, Wu, Yang, Meynert, Alison, Griffiths, Fiona, Oosthuyzen, Wilna, Kousathanas, Athanasios, Moutsianas, Loukas, Yang, Zhijian, Zhai, Ranran, Zheng, Chenqing, Grimes, Graeme, Beale, Rupert, Millar, Jonathan, Shih, Barbara, Keating, Sean, Zechner, Marie, Haley, Chris, Porteous, David J., Hayward, Caroline, Yang, Jian, Knight, Julian, Summers, Charlotte, Shankar-Hari, Manu, Klenerman, Paul, Turtle, Lance, Ho, Antonia, Moore, Shona C., Hinds, Charles, Horby, Peter, Nichol, Alistair, Maslove, David, Ling, Lowell, McAuley, Danny, Montgomery, Hugh, Walsh, Timothy, Pereira, Alexandre C., Renieri, Alessandra, Shen, Xia, Ponting, Chris P., Fawkes, Angie, Tenesa, Albert, Caulfield, Mark, Scott, Richard, Rowan, Kathy, Murphy, Lee, Openshaw, Peter J. M., Semple, Malcolm G., Law, Andrew, Vitart, Veronique, Wilson, James F., Baillie, J. Kenneth

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Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts von Frésard, Laure, Smail, Craig, Ferraro, Nicole M., Teran, Nicole A., Li, Xin, Smith, Kevin S., Bonner, Devon, Kernohan, Kristin D., Marwaha, Shruti, Zappala, Zachary, Balliu, Brunilda, Davis, Joe R., Liu, Boxiang, Prybol, Cameron J., Kohler, Jennefer N., Zastrow, Diane B., Reuter, Chloe M., Fisk, Dianna G., Grove, Megan E., Davidson, Jean M., Hartley, Taila, Joshi, Ruchi, Strober, Benjamin J., Utiramerur, Sowmithri, Lind, Lars, Ingelsson, Erik, Battle, Alexis, Bejerano, Gill, Bernstein, Jonathan A., Ashley, Euan A., Boycott, Kym M., Merker, Jason D., Wheeler, Matthew T., Montgomery, Stephen B.

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Posterior Shoulder Instability, Part I—Diagnosis, Nonoperative Management, and Labral Repair for Posterior Shoulder Instability—An International Expert Delphi Consensus Statement... von Hurley, Eoghan T., Aman, Zachary S., Doyle, Tom R., Levin, Jay M., Jazrawi, Laith M., Garrigues, Grant E., Namdari, Surena, Hsu, Jason E., Klifto, Christopher S., Anakwenze, Oke, Dickens, Jonathan F., Athwal, George S., Bishop, Julie Y., Boache-Adjei, Yaw, Bradley, Kendall E., Brophy, Robert H., Calvo, Emilio, Camp, Christopher L., Cassidy, Tristan, Chalmers, Peter N., Cordasco, Frank A., Danilkowicz, Richard M., Dekker, Travis A., Delaney, Ruth A., Denard, Patrick J., Duralde, Xavier A., Erickson, Brandon J., Ernstbrunner, Lukas, Frangiamore, Salvatore J., Freehill, Michael T., Goltz, Daniel E., Griffith, Timothy B., Heuberer, Philipp R., Hoy, Greg, Hoyt, Benjamin W., Imhoff, Andreas B., Itoi, Eiji, Kilcoyne, Kelly G., Laedermann, Alexandre, Lau, Brian C., Leclere, Lance E., Levine, William N., Martinez-Catalan, Natalia, Matache, Bogdan A., McCarty, Eric C., Menendez, Mariano E., Millett, Peter J., Mirzayan, Raffy, Moroder, Philipp, Mullett, Hannan, Neyton, Lionel, Nicholson, Gregory P., O'Brien, Michael J., Owens, Brett D., Parada, Stephen A., Parnes, Nata, Pasqualini, Ignacio, Pauzenberger, Leo, Provencher, Matthew T., Frank, Rachel M., Ranalletta, Maximiliano, Rodeo, Scott A., Rossi, Luciano A., Sanchez-Sotelo, Joaquin, Scanaliato, John P., Lassiter, Tally, Taylor, Dean C., Toth, Alison P., Trasolini, Nicholas A., Wagner, Eric R., Waterman, Brian R., Whelan, Daniel B., Wickman, John R., Wittstein, Jocelyn R., Wong, Ivan

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Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain von Erger, Florian, Settas, Nikolaos, London, Edra, Torti, Erin, Nelson, Stanley F., Acosta, Maria T., Adams, David R., Balasubramanyam, Ashok, Baldridge, Dustin, Bale, Jim, Bamshad, Michael, Bayrak-Toydemir, Pinar, Beck, Anita, Bennett, Jimmy, Bernstein, Jonathan A., Blue, Elizabeth, Bohnsack, John, Bonnenmann, Carsten, Boyd, Brenna, Brokamp, Elly, Burke, Elizabeth A., Byrd, William E., Carrasquillo, Olveen, Chanprasert, Sirisak, Chao, Hsiao-Tuan, Coggins, Matthew, Cole, F. Sessions, Crouse, Andrew B., Cunningham, Michael, D’Souza, Precilla, Dai, Hongzheng, Dipple, Katrina, Doherty, Daniel, Earl, Dawn, Eckstein, David J., Eng, Christine M., Ferreira, Carlos, Glass, Ian, Gochuico, Bernadette, Goldman, Alica M., Goldstein, David B., Hassey, Kelly, Hom, Jason, Huang, Yong, Jarvik, Gail P., Jarvik, Jeffrey, Krasnewich, Donna M., LaMoure, Grace L., Lalani, Seema R., Lanpher, Brendan C., Latham, Lea, Liu, Pengfei, Liu, Xue Zhong, Macnamara, Ellen F., Malicdan, May Christine V., Manolio, Teri A., Maravilla, Kenneth, Marom, Ronit, Martin, Beth A., Marwaha, Shruti, McCormack, Colleen E., McGee, Elisabeth, Might, Matthew, Nakano-Okuno, Mariko, Nath, Avi, Nicholas, Sarah K., Novacic, Donna, Orengo, James P., Pallais, J. Carl, Palmer, Christina G.S., Parker, Neil H., Posey, Jennifer E., Quinlan, Aaron, Reuter, Chloe M., Robertson, Amy K., Ruzhnikov, Maura, Samson, Susan L., Saporta, Mario, Schaechter, Judy, Signer, Rebecca H., Smith, Kevin S., Ben Solomon, Stoler, Joan M., Sullivan, Jennifer A., Sullivan, Kathleen, Sun, Angela, Tabor, Holly K., Tucker, Brianna M., Vanderver, Adeline, Wallace, Stephanie, Wangler, Michael F., Ward, Patricia A., Whitlock, Jordan, Wolfe, Lynne A., Woods, Jeremy D., Zastrow, Diane B., Grange, Dorothy K., Willaert, Rebecca, Theiß, Susanne, Stocco, Amber

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Posterior Shoulder Instability, Part II—Glenoid Bone Grafting, Glenoid Osteotomy, and Rehabilitation/Return to Play—An International Expert Delphi Consensus Statement von Hurley, Eoghan T., Aman, Zachary S., Doyle, Tom R., Levin, Jay M., Matache, Bogdan A., Chalmers, Peter N., Waterman, Brian R., Erickson, Brandon J., Klifto, Christopher S., Anakwenze, Oke A., Dickens, Jonathan F., Athwal, George S., Bishop, Julie Y., Boache-Adjei, Yaw, Bradley, Kendall E., Brophy, Robert H., Calvo, Emilio, Camp, Christopher L., Cassidy, Tristan, Cordasco, Frank A., Danilkowicz, Richard M., Dekker, Travis A., Delaney, Ruth A., Denard, Patrick J., Duralde, Xavier A., Ernstbrunner, Lukas, Frangiamore, Salvatore J., Freehill, Michael T., Garrigues, Grant E., Goltz, Daniel E., Griffith, Timothy B., Heuberer, Philipp R., Hoy, Greg, Hoyt, Benjamin W., Hsu, Jason E., Imhoff, Andreas B., Itoi, Eiji, Jazrawi, Laith M., Kilcoyne, Kelly G., Laedermann, Alexandre, Lau, Brian C., Leclere, Lance E., Levine, William N., Martinez-Catalan, Natalia, McCarty, Eric C., Menendez, Mariano E., Millett, Peter J., Mirzayan, Raffy, Moroder, Philipp, Mullett, Hannan, Namdari, Surena, Neyton, Lionel, Nicholson, Gregory P., O'Brien, Michael J., Owens, Brett D., Parada, Stephen A., Parnes, Nata, Pasqualini, Ignacio, Pauzenberger, Leo, Provencher, Matthew T., Frank, Rachel M., Ranalletta, Maximiliano, Rodeo, Scott A., Rossi, Luciano A., Sanchez-Sotelo, Joaquin, Scanaliato, John P., Lassiter, Tally, Taylor, Dean C., Toth, Alison P., Trasolini, Nicholas A., Wagner, Eric R., Whelan, Daniel B., Wickman, John R., Wittstein, Jocelyn R., Wong, Ivan

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Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants von Liu, Hongbo, Abedini, Amin, Ha, Eunji, Ma, Ziyuan, Sheng, Xin, Dumoulin, Bernhard, Qiu, Chengxiang, Aranyi, Tamas, Li, Shen, Dittrich, Nicole, Chen, Hua-Chang, Tao, Ran, Tarng, Der-Cherng, Hsieh, Feng-Jen, Chen, Shih-Ann, Yang, Shun-Fa, Lee, Mei-Yueh, Kwok, Pui-Yan, Wu, Jer-Yuarn, Chen, Chien-Hsiun, Khan, Atlas, Limdi, Nita A, Wei, Wei-Qi, Walunas, Theresa L, Karlson, Elizabeth W, Kenny, Eimear E, Luo, Yuan, Kottyan, Leah, Connolly, John J, Jarvik, Gail P, Weng, Chunhua, Shang, Ning, Cole, Joanne B, Mercader, Josep M, Mandla, Ravi, Majarian, Timothy D, Florez, Jose C, Haas, Mary E, Lotta, Luca A, Drivas, Theodore G, Vy, Ha My T, Nadkarni, Girish N, Wiley, Laura K, Wilson, Melissa P, Gignoux, Christopher R, Rasheed, Humaira, Thomas, Laurent F, Åsvold, Bjørn Olav, Brumpton, Ben M, Hallan, Stein I, Hveem, Kristian, Zheng, Jie, Hellwege, Jacklyn N, Zawistowski, Matthew, Zöllner, Sebastian, Franceschini, Nora, Hu, Hailong, Zhou, Jianfu, Kiryluk, Krzysztof, Ritchie, Marylyn D, Palmer, Matthew, Edwards, Todd L, Voight, Benjamin F, Hung, Adriana M, Susztak, Katalin

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Genomic epidemiology of SARS-CoV-2 in a university outbreak setting and implications for public health planning von Nickbakhsh, Sema, Hughes, Joseph, Christofidis, Nicolaos, Griffiths, Emily, Shaaban, Sharif, Enright, Jessica, Smollett, Katherine, Nomikou, Kyriaki, Palmalux, Natasha, Tong, Lily, Carmichael, Stephen, Sreenu, Vattipally B., Orton, Richard, Goldstein, Emily J., Tomb, Rachael M., Templeton, Kate, Gunson, Rory N., da Silva Filipe, Ana, Milosevic, Catriona, Thomson, Emma, Robertson, David L., Holden, Matthew T. G., Illingworth, Christopher J. R., Smith-Palmer, Alison

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SARS-CoV-2 lineage dynamics in England from September to November 2021: high diversity of Delta sub-lineages and increased transmissibility of AY.4.2 von Eales, Oliver, Page, Andrew J, de Oliveira Martins, Leonardo, Wang, Haowei, Bodinier, Barbara, Haw, David, Jonnerby, Jakob, Atchison, Christina, Ashby, Deborah, Barclay, Wendy, Taylor, Graham, Cooke, Graham, Ward, Helen, Darzi, Ara, Riley, Steven, Chadeau-Hyam, Marc, Donnelly, Christl A, Elliott, Paul

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Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases von Krier, Joel B., Züchner, Stephan, Huang, Alden, Bastarache, Lisa, Bican, Anna, Liu, Pengfei, Adam, Margaret, Alejandro, Mercedes E., Alvey, Justin, Azamian, Mahshid S., Bademci, Guney, Baker, Eva, Balasubramanyam, Ashok, Bale, Jim, Beck, Anita, Bennett, Jimmy, Berry, Gerard T., Bican, Anna, Bohnsack, John, Bonner, Devon, Boyd, Brenna, Brown, Gabrielle, Burrage, Lindsay C., Butte, Manish J., Coakley, Terra R., Cobban, Laurel A., Cogan, Joy D., Cole, F. Sessions, Cunningham, Michael, Dorrani, Naghmeh, Doss, Argenia L., Douine, Emilie D., Eng, Christine M., Falk, Marni, Ferreira, Carlos, Findley, Laurie C., Fogel, Brent L., Forghani, Irman, Gahl, William A., Glass, Ian, Godfrey, Rena A., Hanchard, Neil A., Hing, Anne, Huryn, Laryssa, Isasi, Rosario, Kiley, Dana, Korrick, Susan, Krakow, Deborah, Lalani, Seema R., LeBlanc, Kimberly, Liu, Xue Zhong, MacDowall, John, MacRae, Calum A., Mamounas, Laura A., Maravilla, Kenneth, Markello, Thomas C., Martin, Beth A., Martin, Martin G., Marwaha, Shruti, McCauley, Jacob, Merritt, J. Lawrence, Might, Matthew, Moretti, Paolo, Murdock, David R., Nakano-Okuno, Mariko, Nickerson, Deborah, Oglesbee, Devin, Pace, Laura, Pallais, J. Carl, Papp, Jeanette C., Phillips, John A., Power, Bradley, Pusey, Barbara N., Raja, Archana N., Renteria, Genecee, Rosenwasser, Natalie, Rossignol, Francis, Ruzhnikov, Maura, Sampson, Jacinda B., Schedl, Timothy, Shin, Jimann, Smith, Edward C., Sun, Angela, Sutton, Shirley, Sweetser, David A., Sybert, Virginia, Toro, Camilo, Tucker, Brianna M., Velinder, Matt, Viskochil, Dave, Wambach, Jennifer, Wang, Lee-kai, Ward, Patricia A., Wener, Mark, Westerfield, Monte, Whitlock, Jordan, Woods, Jeremy D., Yamamoto, Shinya, Yang, John, Zein, Wadih

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Author Correction: GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19 von Pairo-Castineira, Erola, Rawlik, Konrad, Bretherick, Andrew D., Qi, Ting, Wu, Yang, Nassiri, Isar, McConkey, Glenn A., Zechner, Marie, Klaric, Lucija, Griffiths, Fiona, Oosthuyzen, Wilna, Kousathanas, Athanasios, Richmond, Anne, Millar, Jonathan, Russell, Clark D., Malinauskas, Tomas, Thwaites, Ryan, Morrice, Kirstie, Keating, Sean, Maslove, David, Nichol, Alistair, Semple, Malcolm G., Knight, Julian, Shankar-Hari, Manu, Summers, Charlotte, Hinds, Charles, Horby, Peter, Ling, Lowell, McAuley, Danny, Montgomery, Hugh, Openshaw, Peter J. M., Begg, Colin, Walsh, Timothy, Tenesa, Albert, Flores, Carlos, Riancho, José A., Rojas-Martinez, Augusto, Lapunzina, Pablo, Yang, Jian, Ponting, Chris P., Wilson, James F., Vitart, Veronique, Abedalthagafi, Malak, Luchessi, Andre D., Parra, Esteban J., Cruz, Raquel, Carracedo, Angel, Fawkes, Angie, Murphy, Lee, Rowan, Kathy, Pereira, Alexandre C., Law, Andy, Fairfax, Benjamin, Hendry, Sara Clohisey, Baillie, J. Kenneth

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Expression quantitative trait locus fine mapping of the 17q12–21 asthma locus in African American children: a genetic association and gene expression study von McKennan, Chris G, Bacharier, Leonard B, Hartert, Tina, Johnson, Christine C, Kattan, Meyer, Lemanske, Robert F, Lynch, Susan V, O'Connor, George T, Wegienka, Ganesa, Zoratti, Edward M, Levin, Albert M, Akkerman, Nonna, Aubuchon, Mary Ann, Barone, Charles, Becker, Patrice, Bednarek, Alyssa, Bendixsen, Casper G., Biagini Myers, Jocelyn M., Bobbitt, Kevin, Bochkov, Yury, Bourgeois, Karen, Brockman-Schneider, Rebecca, Burkle, Jeffrey W., Campbell, Janice, Cassidy-Bushrow, Andrea, Chappell, James D., Chasman, Deborah, Connolly, Alexandra, Cootauco, Michelle, Crisafi, Gina, Cruikshank, William, Davidson, Brent, Dixon, Samara, Donnerbauer, Erin, Dresen, Amy, Durrange, Janet, Erickson, Heidi, Ezell, Jerel, Filardo-Collins, Roxanne, Finazzo, Salvatore, Frome, Wayne, Gammell, Rebecca, Gangnon, Ronald E., Gebretsadik, Tebeb, Gibson, Heike, Halonen, Marilyn, Hartert, Tina V., Herbstman, Julie, Hoepner, Lori, Jones, Amelia, Keidel, Kristina, Keifer, Matthew C., Khurana Hershey, Gurgit K., Kim, Haejin, Koerkenmeier, Clint, Lemanske, Jr, Robert F., Liu, Xinhua, Lopez, Silvia, Lothrop, Nathan, Lynch, Susan, Mann, Erik, McCauley, Katherine, McKennon, Chris G., Meece, Jennifer, Miller, Rachel L., Mitchell, Herman, Morgan, Wayne, Nicolae, Daniel, O'Connor, George, O'Toole, Sharon, Pappas, Tressa, Perera, Frederica, Pierce, Marcela, Renneberg, Megan, Riley, Kylie, Roberg, Kathy, Sadovsky, Yoel, Schwartz, Joel, Seroogy, Christine M., Shilts, Meghan H., Sorkness, Ronald, Sperling, Rhoda, Stern, Debra A., Stoffel, Brandy, Strauchman Boyer, Cathey, Tang, Zhengzheng, Tisler, Christopher, Togias, Alkis, Turi, Kedir, Tuzova, Marina, Vrtis, Rose, Wang, Lena, Williams, L. Keoki, Wood, Robert A., Woodcroft, Kimberley, Wright, Rosalind, Zanobetti, Antonella, Zhang, Shirley, Zook, Patricia, Zoratti, Edward M.

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Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders von Gracia-Diaz, Carolina, Zhou, Yijing, Yang, Qian, Maroofian, Reza, Espana-Bonilla, Paula, Lee, Chul-Hwan, Zhang, Shuo, Padilla, Natàlia, Fueyo, Raquel, Waxman, Elisa A., Lei, Sunyimeng, Otrimski, Garrett, Li, Dong, Sheppard, Sarah E., Mark, Paul, Harr, Margaret H., Hakonarson, Hakon, Rodan, Lance, Jackson, Adam, Vasudevan, Pradeep, Powel, Corrina, Mohammed, Shehla, Maddirevula, Sateesh, Alzaidan, Hamad, Faqeih, Eissa A., Efthymiou, Stephanie, Turchetti, Valentina, Rahman, Fatima, Maqbool, Shazia, Salpietro, Vincenzo, Ibrahim, Shahnaz H., di Rosa, Gabriella, Houlden, Henry, Alharbi, Maha Nasser, Al-Sannaa, Nouriya Abbas, Bauer, Peter, Zifarelli, Giovanni, Estaras, Conchi, Hurst, Anna C. E., Thompson, Michelle L., Chassevent, Anna, Smith-Hicks, Constance L., de la Cruz, Xavier, Holtz, Alexander M., Elloumi, Houda Zghal, Hajianpour, M J, Rieubland, Claudine, Braun, Dominique, Banka, Siddharth, French, Deborah L., Heller, Elizabeth A., Saade, Murielle, Song, Hongjun, Ming, Guo-li, Alkuraya, Fowzan S., Agrawal, Pankaj B., Reinberg, Danny, Bhoj, Elizabeth J., Martínez-Balbás, Marian A., Akizu, Naiara

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First Detection of Two Near‐Earth Asteroids With a Southern Hemisphere Planetary Radar System von Benson, Craig, Reynolds, John, Stacy, N. J. S., Benner, Lance A. M., Edwards, P. G., Baines, Graham, Boyce, Russell, Giorgini, Jon D., Jao, Joseph S., Martinez, George, Slade, Martin A., Teitelbaum, Lawrence P., Anabtawi, Aseel, Kahan, Daniel, Oudrhiri, Kamal, Philips, C. J., Stevens, J. B., Kruzins, Ed, Lazio, T. Joseph W.

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Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases von Pena, Loren D M, Jiang, Yong-Hui, Schoch, Kelly, Spillmann, Rebecca C, Walley, Nicole, Stong, Nicholas, Rapisardo Horn, Sarah, Sullivan, Jennifer A, McConkie-Rosell, Allyn, Kansagra, Sujay, Smith, Edward C, El-Dairi, Mays, Bellet, Jane, Keels, Martha Ann, Jasien, Joan, Kranz, Peter G, Noel, Richard, Nagaraj, Shashi K, Lark, Robert K, Wechsler, Daniel S G, del Gaudio, Daniela, Leung, Marco L, Hendon, Laura G, Parker, Collette C, Jones, Kelly L, Goldstein, David B, Shashi, Vandana

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One is the loneliest number: genotypic matchmaking using the electronic health record von Koziura, Mary E., Phillips, John A., Peterson, Josh F., Newman, John H., Bastarache, Lisa, Bacino, Carlos A., Balasubramanyam, Ashok, Clark, Gary D., Dhar, Shweta U., Jamal, Fariha, Lalani, Seema R., Lewis, Richard A., Orengo, James P., Vogel, Tiphanie P., Wangler, Michael F., Goldstein, David B., Cope, Heidi, Jiang, Yong-hui, Spillmann, Rebecca C., Tan, Queenie K.-G., Walley, Nicole M., Fieg, Elizabeth L., Korrick, Susan, Krier, Joel B., Maas, Richard L., Pallais, J. Carl, Rodan, Lance H., Silverman, Edwin K., Esteves, Cecilia, Kelley, Emily G., Kohane, Isaac S., Bick, David P., Birch, Camille L., Boone, Braden E., Levy, Shawn E., Worthey, Elizabeth A., Oglesbee, Devin, Forghani, Irman, Grajewski, Alana, Isasi, Rosario, McCauley, Jacob, Sacco, Ralph, Thorson, Willa, Colley, Heather A., Krasnewich, Donna M., Mamounas, Laura A., Rowley, Robb K., Tamburro, Cecelia P., Bonnenmann, Carsten, Estwick, Tyra, Ferreira, Carlos, Godfrey, Rena A., Groden, Catherine A., Maduro, Valerie V., Novacic, Donna, Pusey, Barbara N., Sharma, Prashant, Toro, Camilo, Wahl, Colleen E., Yu, Guoyun, Baker, Eva, Adams, David R., Malicdan, May Christine V., Yang, John, Koeller, David M., Kyle, Jennifer E., Webb-Robertson, Bobbie-Jo M., Bernstein, Jonathan A., Bonner, Devon, Fernandez, Liliana, Huang, Yong, Kohler, Jennefer N., Majcherska, Marta M., Reuter, Chloe M., Sampson, Jacinda B., Wheeler, Matthew T., Zastrow, Diane B., Zhao, Chunli, Fresard, Laure, Bejerano, Gill, Butte, Manish J., Dell’Angelica, Esteban C., Dorrani, Naghmeh, Krakow, Deborah, Lee, Hane, Loo, Sandra K., Martin, Martin G., Woods, Jeremy D., Yoon, Amanda J., Botto, Lorenzo, Andrews, Ashley, Carey, John, Quinlan, Aaron, Bayrak-Toydemir, Pinar, Postlethwait, John H., Shakachite, Lisa, Wambach, Jennifer, Wegner, Daniel, Baldridge, Dustin, Solnica-Krezel, Lilianna

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Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids von Ferdinandusse, Sacha, McWalter, Kirsty, te Brinke, Heleen, IJlst, Lodewijk, Mooijer, Petra M., Ruiter, Jos P. N., van Lint, Alida E. M., Pras-Raves, Mia, Wever, Eric, Millan, Francisca, Guillen Sacoto, Maria J., Begtrup, Amber, Tarnopolsky, Mark, Brady, Lauren, Ladda, Roger L., Sell, Susan L., Nowak, Catherine B., Douglas, Jessica, Tian, Cuixia, Ulm, Elizabeth, Perlman, Seth, Drack, Arlene V., Chong, Karen, Martin, Nicole, Brault, Jennifer, Brokamp, Elly, Toro, Camilo, Gahl, William A., Macnamara, Ellen F., Wolfe, Lynne, Waisfisz, Quinten, Zwijnenburg, Petra J. G., Ziegler, Alban, Barth, Magalie, Smith, Rosemarie, Ellingwood, Sara, Gaebler-Spira, Deborah, Bakhtiari, Somayeh, Kruer, Michael C., van Kampen, Antoine H. C., Wanders, Ronald J. A., Waterham, Hans R., Cassiman, David, Vaz, Frédéric M.

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DYRK1A pathogenic variants in two patients with syndromic intellectual disability and a review of the literature von Macnamara, Ellen F., D'Souza, Precilla, Vezina, Gilbert, Tifft, Cynthia J., Adams, David R., Azamian, Mahshid S., Baldridge, Dustin, Bayrak‐Toydemir, Pinar, Beck, Anita, Berry, Gerard T., Bican, Anna, Bohnsack, John, Boyd, Brenna, Briere, Lauren C., Burke, Elizabeth A., Burrage, Lindsay C., Byrd, William E., Carey, John, Craigen, William J., Cunningham, Michael, Dayal, Jyoti G., Deardorff, Matthew, Doherty, Daniel, Dorrani, Naghmeh, Douine, Emilie D., Earl, Dawn, Eckstein, David J., Emrick, Lisa T., Ferreira, Carlos, Fieg, Elizabeth L., Forghani, Irman, Fresard, Laure, Gahl, William A., Glass, Ian, Goldman, Alica M., Goldstein, David B., Groden, Catherine A., Hassey, Kelly, Horike‐Pyne, Martha, Huang, Alden, Huang, Yong, Jarvik, Gail P., Jarvik, Jeffrey, Johnston, Jean M., Kohane, Isaac S., Krakow, Deborah, Kravets, Elijah, Korrick, Susan, Koziura, Mary, Krier, Joel B., Lalani, Seema R., Lam, Christina, Lanpher, Brendan C., Lincoln, Sharyn A., Loo, Sandra K., Loscalzo, Joseph, MacRae, Calum A., Malicdan, May Christine V., Mamounas, Laura A., Markello, Thomas C., Martin, Martin G., McCormack, Colleen E., McGee, Elisabeth, Merritt, J. Lawrence, Might, Matthew, Mulvihill, John J., Nelson, Stan F., Nicholas, Sarah K., Orengo, James P., Pace, Laura, Pak, Stephen, Pusey, Barbara N., Quinlan, Aaron, Raskind, Wendy, Sacco, Ralph, Saporta, Mario, Ron Scott, C., Schaechter, Judy, Schoch, Kelly, Sharma, Prashant, Shin, Jimann, Sillari, Catherine H., Sisco, Kathy, Smith, Kevin S., Stoler, Joan M., Stong, Nicholas, Tamburro, Cecelia P., Tekin, Mustafa, Tifft, Cynthia J., Toro, Camilo, Tucker, Brianna M., Vogel, Tiphanie P., Wambach, Jennifer, Wang, Lee‐kai, Wegner, Daniel, Wenger, Tara, Wesseling Perry, Katherine, Westerfield, Monte, Wolfe, Lynne A., Zuchner, Stephan

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