Vehicle line-locking brake system and method von Lamb Roger Allen

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VEHICLE LINE-LOCKING BRAKE SYSTEM AND METHOD von LAMB ROGER ALLEN

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High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletion... von Ballif, Blake C., Rosenfeld, Jill A., Traylor, Ryan, Theisen, Aaron, Bader, Patricia I., Ladda, Roger L., Sell, Susan L., Steinraths, Michelle, Surti, Urvashi, McGuire, Marianne, Williams, Shelley, Farrell, Sandra A., Filiano, James, Schnur, Rhonda E., Coffey, Lauren B., Tervo, Raymond C., Stroud, Tracy, Marble, Michael, Netzloff, Michael, Hanson, Kristen, Aylsworth, Arthur S., Bamforth, J. S., Babu, Deepti, Niyazov, Dmitriy M., Ravnan, J. Britt, Schultz, Roger A., Lamb, Allen N., Torchia, Beth S., Bejjani, Bassem A., Shaffer, Lisa G.

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Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems von Sahoo, Trilochan, Theisen, Aaron, Rosenfeld, Jill A, Lamb, Allen N, Ravnan, J Britt, Schultz, Roger A, Torchia, Beth S, Neill, Nicholas, Casci, Ian, Bejjani, Bassem A, Shaffer, Lisa G

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MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways von Paciorkowski, Alex R., Traylor, Ryan N., Rosenfeld, Jill A., Hoover, Jacqueline M., Harris, Catharine J., Winter, Susan, Lacassie, Yves, Bialer, Martin, Lamb, Allen N., Schultz, Roger A., Berry-Kravis, Elizabeth, Porter, Brenda E., Falk, Marni, Venkat, Anu, Vanzo, Rena J., Cohen, Julie S., Fatemi, Ali, Dobyns, William B., Shaffer, Lisa G., Ballif, Blake C., Marsh, Eric D.

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Effectiveness of a national quality improvement programme to improve survival after emergency abdominal surgery (EPOCH): a stepped-wedge cluster-randomised trial von Stephens, Tim, Kahan, Brennan, Brett, Stephen, Ackland, Gareth, Everingham, Kirsty, Abraham, Ajit, Gillies, Michael, Anderson, Iain, Drake, Sharon, Girling, Alan, Faiz, Omar, Blunt, Mark, Cabreros, Leilani, Obideyi, Ayodele, Brodbeck, Andreas, Gay, Mike, Pushpa, Nathan, Noble, Paul, Van De Velde, Niko, Singh, Satish, Gerstina, Nabua, Kuldip, Rai, Murray, Therese, Aryal, Kamal, Moncaster, Gareth, Abercrombie, John, Wells, John, Natarajan, Nat, Doughan, Samer, Mackinnon, John, Lawton, Greg, Watson, Mark, Stacey, Brenda, Fletcher, Steve, Prestwich, Stewart, Sharma, Abhiram, Hill, Oliver, Rose, Alastair, Narula, Harjeet, Buckley, Sarah, Dowling, Susan, Robin, Nicole, Januszewska, Marta, Bodger, Phoebe, Abbott, Tom, Full, Jens, Rehman, Almas, Mohr, Otto, Mateo, Dolores, Machesney, Michael, Borgeaud, Nathan, Harwood, Elizabeth, Moonesinghe, Ramani, Rafi, Amir, McNelis, Una, Roy, Alistair, Rimmer, Catherine, Monkhouse, Diane, Bhowmick, Arnab, Mcmullan, Sean, Doyle, Donna, Patel, Panna, Stergios, Tezas, Coldwell, Chris, Bronder, Christine, Stotz, Martin, Sugavanam, Anita, Tan, Melanie, Vashisht, Shubha, Vaganov, Sergei, Liasis, Lampros, Husain, Tariq, Baxter, Linden, Wilson, Chris, Williams, Dewi, Taylor, Lynn, Dickinson, Natalie, Gibson, Simon, Tan, Kerwei, Stevenson, Richard, Carey, Kate, Razouk, Khaled, Girgis, Amira, Somasekar, Krishnamurthy, Morgan-Jones, Tom, Martin, Michael, Watters, Malcolm, Sunthareswaran, Rame, Bell, Louise, Nash, Guy, Christie, Iain, Patrick, Abigail, Hanousek, Jan, Paddle, Jonathan, Pickford, Alison, Tucker, Olga, Leno, Emma, Colley, Julie, Wollaston, Julie, Singh, Jagdeep

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Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features von Lamb, Allen N., Rosenfeld, Jill A., Neill, Nicholas J., Talkowski, Michael E., Blumenthal, Ian, Girirajan, Santhosh, Keelean-Fuller, Debra, Fan, Zheng, Pouncey, Jill, Stevens, Cathy, Mackay-Loder, Loren, Terespolsky, Deborah, Bader, Patricia I., Rosenbaum, Kenneth, Vallee, Stephanie E., Moeschler, John B., Ladda, Roger, Sell, Susan, Martin, Judith, Ryan, Shawnia, Jones, Marilyn C., Moran, Rocio, Shealy, Amy, Madan-Khetarpal, Suneeta, McConnell, Juliann, Surti, Urvashi, Delahaye, Andrée, Heron-Longe, Bénédicte, Pipiras, Eva, Benzacken, Brigitte, Passemard, Sandrine, Verloes, Alain, Isidor, Bertrand, Le Caignec, Cedric, Glew, Gwen M., Opheim, Kent E., Descartes, Maria, Eichler, Evan E., Morton, Cynthia C., Gusella, James F., Schultz, Roger A., Ballif, Blake C., Shaffer, Lisa G.

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Lopinavir-ritonavir and hydroxychloroquine for critically ill patients with COVID-19: REMAP-CAP randomized controlled trial von Arabi, Yaseen M., Gordon, Anthony C., Derde, Lennie P. G., Nichol, Alistair D., Murthy, Srinivas, Beidh, Farah Al, Annane, Djillali, Swaidan, Lolowa Al, Beane, Abi, Beasley, Richard, Berry, Lindsay R., Bhimani, Zahra, Bonten, Marc J. M., Bradbury, Charlotte A., Brunkhorst, Frank M., Buxton, Meredith, Buzgau, Adrian, Cheng, Allen, De Jong, Menno, Detry, Michelle A., Duffy, Eamon J., Estcourt, Lise J., Fitzgerald, Mark, Fowler, Rob, Girard, Timothy D., Goligher, Ewan C., Goossens, Herman, Haniffa, Rashan, Higgins, Alisa M., Hills, Thomas E., Horvat, Christopher M., Huang, David T., King, Andrew J., Lamontagne, Francois, Lawler, Patrick R., Lewis, Roger, Linstrum, Kelsey, Litton, Edward, Lorenzi, Elizabeth, Malakouti, Salim, McAuley, Daniel F., McGlothlin, Anna, Mcguinness, Shay, McVerry, Bryan J., Montgomery, Stephanie K., Morpeth, Susan C., Mouncey, Paul R., Orr, Katrina, Parke, Rachael, Parker, Jane C., Patanwala, Asad E., Rowan, Kathryn M., Santos, Marlene S., Saunders, Christina T., Seymour, Christopher W., Shankar-Hari, Manu, Tong, Steven Y. C., Turgeon, Alexis F., Turner, Anne M., Van de Veerdonk, Frank Leo, Zarychanski, Ryan, Green, Cameron, Berry, Scott, Marshall, John C., McArthur, Colin, Angus, Derek C., Webb, Steven A.

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Transition metal cation separations with a resorcinarene-based amino acid stationary phase von Li, Na, Allen, Lee J, Harrison, Roger G, Lamb, John D

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Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH von Neill, Nicholas J, Ballif, Blake C, Lamb, Allen N, Parikh, Sumit, Ravnan, J Britt, Schultz, Roger A, Torchia, Beth S, Rosenfeld, Jill A, Shaffer, Lisa G

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OP041: Implementation of 2019 ACMG technical standards for the interpretation and reporting of constitutional CNVs: Experiences from an academic reference laboratory von Zhao, Jian, Zoe, Lewis, Reich, Daniel, Chapin, Alexander, Clayton, Adam, Clyde, Benjamin, Cox, Julie, Fulmer, Makenzie, Hong, Bo, Lamb, Allen, Mani, Coumarane, Pizzo, Lucilla, Quigley, Denise, Rushton, Patricia, Schultz, Roger, Tidwell, Timothy, Wen, Ting, Mendoza, Cinthya Zepeda, Andersen, Erica

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Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes von Rosenfeld, Jill A, Traylor, Ryan N, Schaefer, G Bradley, McPherson, Elizabeth W, Ballif, Blake C, Klopocki, Eva, Mundlos, Stefan, Shaffer, Lisa G, Aylsworth, Arthur S

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Deletions and duplications of developmental pathway genes in 5q31 contribute to abnormal phenotypes von Rosenfeld, Jill A., Drautz, Joanne Milisa, Clericuzio, Carol L., Cushing, Tom, Raskin, Salmo, Martin, Judith, Tervo, Raymond C., Pitarque, Jose A., Nowak, Dorota M., Karolak, Justyna A., Lamb, Allen N., Schultz, Roger A., Ballif, Blake C., Bejjani, Bassem A., Gajecka, Marzena, Shaffer, Lisa G.

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Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders von Rosenfeld, Jill A., Ballif, Blake C., Torchia, Beth S., Sahoo, Trilochan, Ravnan, J. Britt, Schultz, Roger, Lamb, Allen, Bejjani, Bassem A., Shaffer, Lisa G.

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44. Reevaluation of copy number variant (CNV) classifications in the clinical laboratory setting: challenges, insights, and experiences with a laboratory-initiated process von Quigley, Denise I, Lewis, Zoe K, Tidwell, Timothy, Clayton, Adam, Chandler, Brandon, Cox, Julie L, Hong, Bo, Lamb, Allen N, Mowery-Rushton, Patricia, Schultz, Roger, Toydemir, Reha, Xu, Xinjie, Andersen, Erica F

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The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes von Shaffer, Lisa G., Coppinger, Justine, Morton, S. Annie, Alliman, Sarah, Burleson, Jessica, Traylor, Ryan, Walker, Cathryn, Byerly, Steve, Lamb, Allen N., Schultz, Roger, Ravnan, J. Britt, Kashork, Catherine D., Torchia, Beth S., Sulpizio, Scott, Sundin, Kyle, Schermer, Mack, Adler, Karl, Dallaire, Stephanie, Ballif, Blake C.

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BioEarth: Envisioning and developing a new regional earth system model to inform natural and agricultural resource management von Adam, Jennifer C., Stephens, Jennie C., Chung, Serena H., Brady, Michael P., Evans, R. David, Kruger, Chad E., Lamb, Brian K., Liu, Mingliang, Stöckle, Claudio O., Vaughan, Joseph K., Rajagopalan, Kirti, Harrison, John A., Tague, Christina L., Kalyanaraman, Ananth, Chen, Yong, Guenther, Alex, Leung, Fok-Yan, Leung, L. Ruby, Perleberg, Andrew B., Yoder, Jonathan, Allen, Elizabeth, Anderson, Sarah, Chandrasekharan, Bhagyam, Malek, Keyvan, Mullis, Tristan, Miller, Cody, Nergui, Tsengel, Poinsatte, Justin, Reyes, Julian, Zhu, Jun, Choate, Janet S., Jiang, Xiaoyan, Nelson, Roger, Yoon, Jin-Ho, Yorgey, Georgine G., Johnson, Kristen, Chinnayakanahalli, Kiran J., Hamlet, Alan F., Nijssen, Bart, Walden, Von

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Ring 22 duplication/deletion mosaicism: clinical, cytogenetic, and molecular characterisation von Frizzley, Jill K, Stephan, Mark J, Lamb, Allen N, Jonas, Patricia P, Hinson, Roger M, Moffitt, Donald R, Shkolny, Dana L, McDermid, Heather E

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