Domain-specific visual languages for specifying and generating data mapping systems von Grundy, J.C., Hosking, J.G., Amor, R.W., Mugridge, W.B., Li, Y.

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ICAtect-II: a framework for the integration of building design tools: Product Modeling von AMOR, R. W, HOSKING, J. G, MUGRIDGE, W. B

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Support for collaborative, integrated software development von Grundy, J.C., Mugridge, W.B., Hosking, J.G., Amor, R.W.

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Seasonal home ranges and habitat selection of three elk (Cervus elaphus) herds in North Dakota von Amor, Jacqueline M, Newman, Robert, Jensen, William F, Rundquist, Bradley C, Walter, W David, Boulanger, Jason R

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A detailed map of Higgs boson interactions by the ATLAS experiment ten years after the discovery von Aad, G., Leopold, Alexander, Lundberg, Olof, Lund-Jensen, Bengt, Ohm, Christian, Ripellino, Giulia, Shaheen, Rabia, Shope, David R., Strandberg, Jonas, Zwalinski, L., et al

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Convergent Transcription at Intragenic Super-Enhancers Targets AID-Initiated Genomic Instability von Meng, Fei-Long, Du, Zhou, Federation, Alexander, Hu, Jiazhi, Wang, Qiao, Kieffer-Kwon, Kyong-Rim, Meyers, Robin M., Amor, Corina, Wasserman, Caitlyn R., Neuberg, Donna, Casellas, Rafael, Nussenzweig, Michel C., Bradner, James E., Liu, X. Shirley, Alt, Frederick W.

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Structure–function analysis of the SHOC2–MRAS–PP1C holophosphatase complex von Kwon, Jason J., Hajian, Behnoush, Bian, Yuemin, Young, Lucy C., Amor, Alvaro J., Fuller, James R., Fraley, Cara V., Sykes, Abbey M., So, Jonathan, Pan, Joshua, Baker, Laura, Lee, Sun Joo, Wheeler, Douglas B., Mayhew, David L., Persky, Nicole S., Yang, Xiaoping, Root, David E., Barsotti, Anthony M., Stamford, Andrew W., Perry, Charles K., Burgin, Alex, McCormick, Frank, Lemke, Christopher T., Hahn, William C., Aguirre, Andrew J.

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A French community-based intervention for parents of French-Canadian children with behavior problems: The EQUIPE program von Ben Amor, L., Lachal, J., Menard, M.-L., Pelletier, W., Mac Dermott, V., Ben Amor, R., Sanchez, I., Lapointe, L., Bouchard, P., Rousseau, B., Ricard, N.

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Translocator protein is a marker of activated microglia in rodent models but not human neurodegenerative diseases von Nutma, Erik, Fancy, Nurun, Weinert, Maria, Tsartsalis, Stergios, Marzin, Manuel C., Muirhead, Robert C. J., Falk, Irene, Breur, Marjolein, de Bruin, Joy, Hollaus, David, Pieterman, Robin, Anink, Jasper, Story, David, Chandran, Siddharthan, Tang, Jiabin, Trolese, Maria C., Saito, Takashi, Saido, Takaomi C., Wiltshire, Katharine H., Beltran-Lobo, Paula, Phillips, Alexandra, Antel, Jack, Healy, Luke, Dorion, Marie-France, Galloway, Dylan A., Benoit, Rochelle Y., Amossé, Quentin, Ceyzériat, Kelly, Badina, Aurélien M., Kövari, Enikö, Bendotti, Caterina, Aronica, Eleonora, Radulescu, Carola I., Wong, Jia Hui, Barron, Anna M., Smith, Amy M., Barnes, Samuel J., Hampton, David W., van der Valk, Paul, Jacobson, Steven, Howell, Owain W., Baker, David, Kipp, Markus, Kaddatz, Hannes, Tournier, Benjamin B., Millet, Philippe, Matthews, Paul M., Moore, Craig S., Amor, Sandra, Owen, David R.

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Jet energy scale measurements and their systematic uncertainties in proton-proton collisions at s =13 TeV with the ATLAS detector von Onofre, A., Castro, Nuno Filipe Silva Fernandes, ATLAS Collaboration

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Inhibition of Upf2-Dependent Nonsense-Mediated Decay Leads to Behavioral and Neurophysiological Abnormalities by Activating the Immune Response von Johnson, Jennifer L., Stoica, Loredana, Liu, Yuwei, Zhu, Ping Jun, Bhattacharya, Abhisek, Buffington, Shelly A., Huq, Redwan, Eissa, N. Tony, Larsson, Ola, Porse, Bo T., Domingo, Deepti, Nawaz, Urwah, Carroll, Renee, Jolly, Lachlan, Scerri, Tom S., Kim, Hyung-Goo, Brignell, Amanda, Coleman, Matthew J., Braden, Ruth, Kini, Usha, Jackson, Victoria, Baxter, Anne, Bahlo, Melanie, Scheffer, Ingrid E., Amor, David J., Hildebrand, Michael S., Bonnen, Penelope E., Beeton, Christine, Gecz, Jozef, Morgan, Angela T., Costa-Mattioli, Mauro

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Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogene... von Bruno, D L, Ganesamoorthy, D, Schoumans, J, Bankier, A, Coman, D, Delatycki, M, Gardner, R J M, Hunter, M, James, P A, Kannu, P, McGillivray, G, Pachter, N, Peters, H, Rieubland, C, Savarirayan, R, Scheffer, I E, Sheffield, L, Tan, T, White, S M, Yeung, A, Bowman, Z, Ngo, C, Choy, K W, Cacheux, V, Wong, L, Amor, D J, Slater, H R

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Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial disease von Amarasekera, Sumudu S C, Hock, Daniella H, Lake, Nicole J, Calvo, Sarah E, Grønborg, Sabine W, Krzesinski, Emma I, Amor, David J, Fahey, Michael C, Simons, Cas, Wibrand, Flemming, Mootha, Vamsi K, Lek, Monkol, Lunke, Sebastian, Stark, Zornitza, Østergaard, Elsebet, Christodoulou, John, Thorburn, David R, Stroud, David A, Compton, Alison G

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Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants von Pizzo, Lucilla, Jensen, Matthew, Polyak, Andrew, Rosenfeld, Jill A., Mannik, Katrin, Krishnan, Arjun, McCready, Elizabeth, Pichon, Olivier, Le Caignec, Cedric, Van Dijck, Anke, Pope, Kate, Voorhoeve, Els, Yoon, Jieun, Stankiewicz, Paweł, Cheung, Sau Wai, Pazuchanics, Damian, Huber, Emily, Kumar, Vijay, Kember, Rachel L., Mari, Francesca, Curró, Aurora, Castiglia, Lucia, Galesi, Ornella, Avola, Emanuela, Mattina, Teresa, Fichera, Marco, Mandarà, Luana, Vincent, Marie, Nizon, Mathilde, Mercier, Sandra, Bénéteau, Claire, Blesson, Sophie, Martin-Coignard, Dominique, Mosca-Boidron, Anne-Laure, Caberg, Jean-Hubert, Bucan, Maja, Zeesman, Susan, Nowaczyk, Małgorzata J. M., Lefebvre, Mathilde, Faivre, Laurence, Callier, Patrick, Skinner, Cindy, Keren, Boris, Perrine, Charles, Prontera, Paolo, Marle, Nathalie, Renieri, Alessandra, Reymond, Alexandre, Kooy, R. Frank, Isidor, Bertrand, Schwartz, Charles, Romano, Corrado, Sistermans, Erik, Amor, David J., Andrieux, Joris, Girirajan, Santhosh

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Germline Loss-of-Function Mutations in EPHB4 Cause a Second Form of Capillary Malformation-Arteriovenous Malformation (CM-AVM2) Deregulating RAS-MAPK Signaling von Amyere, Mustapha, Revencu, Nicole, Helaers, Raphaël, Pairet, Eleonore, Baselga, Eulalia, Cordisco, Maria, Chung, Wendy, Dubois, Josée, Lacour, Jean-Philippe, Martorell, Loreto, Mazereeuw-Hautier, Juliette, Pyeritz, Reed E, Amor, David J, Bisdorff, Annouk, Blei, Francine, Bombei, Hannah, Dompmartin, Anne, Brooks, David, Dupont, Juliette, González-Enseñat, Maria Antonia, Frieden, Ilona, Gérard, Marion, Kvarnung, Malin, Hanson-Kahn, Andrea Kwan, Hudgins, Louanne, Léauté-Labrèze, Christine, McCuaig, Catherine, Metry, Denise, Parent, Philippe, Paul, Carle, Petit, Florence, Phan, Alice, Quere, Isabelle, Salhi, Aicha, Turner, Anne, Vabres, Pierre, Vicente, Asuncion, Wargon, Orli, Watanabe, Shoji, Weibel, Lisa, Wilson, Ashley, Willing, Marcia, Mulliken, John B, Boon, Laurence M, Vikkula, Miikka

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Functional correlation of genome‐wide DNA methylation profiles in genetic neurodevelopmental disorders von Levy, Michael A., Relator, Raissa, McConkey, Haley, Pranckeviciene, Erinija, Kerkhof, Jennifer, Barat‐Houari, Mouna, Bargiacchi, Sara, Biamino, Elisa, Palomares Bralo, María, Cappuccio, Gerarda, Ciolfi, Andrea, Clarke, Angus, DuPont, Barbara R., Elting, Mariet W., Faivre, Laurence, Fee, Timothy, Ferilli, Marco, Fletcher, Robin S., Cherick, Florian, Foroutan, Aidin, Friez, Michael J., Gervasini, Cristina, Haghshenas, Sadegheh, Hilton, Benjamin A., Jenkins, Zandra, Kaur, Simranpreet, Lewis, Suzanne, Louie, Raymond J., Maitz, Silvia, Milani, Donatella, Morgan, Angela T., Oegema, Renske, Østergaard, Elsebet, Pallares, Nathalie R., Piccione, Maria, Plomp, Astrid S., Poulton, Cathryn, Reilly, Jack, Rius, Rocio, Robertson, Stephen, Rooney, Kathleen, Rousseau, Justine, Santen, Gijs W. E., Santos‐Simarro, Fernando, Schijns, Josephine, Squeo, Gabriella M., John, Miya St, Thauvin‐Robinet, Christel, Traficante, Giovanna, Sluijs, Pleuntje J., Vergano, Samantha A., Vos, Niels, Walden, Kellie K., Azmanov, Dimitar, Balci, Tugce B., Banka, Siddharth, Gecz, Jozef, Henneman, Peter, Lee, Jennifer A., Mannens, Marcel M. A. M., Roscioli, Tony, Siu, Victoria, Amor, David J., Baynam, Gareth, Bend, Eric G., Boycott, Kym, Brunetti‐Pierri, Nicola, Campeau, Philippe M., Campion, Dominique, Christodoulou, John, Dyment, David, Esber, Natacha, Fahrner, Jill A., Fleming, Mark D., Genevieve, David, Heron, Delphine, Husson, Thomas, Kernohan, Kristin D., McNeill, Alisdair, Menke, Leonie A., Merla, Giuseppe, Prontera, Paolo, Rockman‐Greenberg, Cheryl, Schwartz, Charles, Skinner, Steven A., Stevenson, Roger E., Vincent, Marie, Vitobello, Antonio, Tartaglia, Marco, Alders, Marielle, Tedder, Matthew L., Sadikovic, Bekim

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De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency von McFarland, Robert, Kirby, Denise M., Fowler, Kerry J., Ohtake, Akira, Ryan, Michael T., Amor, David J., Fletcher, Janice M., Dixon, Joanne W., Collins, Felicity A., Turnbull, Douglass M., Taylor, Robert W., Thorburn, David R.

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Search for Heavy Higgs Bosons A /H Decaying to a Top Quark Pair in pp Collisions at s =8 TeV with the ATLAS Detector von Aaboud, M, Aad, G, Abbott, B., Abdinov, O, Abeloos, B, Abidi, S. H., Åkesson, Torsten, Bocchetta, Simona, Doglioni, Caterina, Hedberg, Vincent, Jarlskog, Göran, Kalderon, Charles, Kellermann, Edgar, Lytken, Else, Mankinen, Katja, Mjörnmark, Ulf, Pöttgen, Ruth, Poulsen, Trine, Smirnova, Oxana, Viazlo, Oleksandr

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Somatic Tissue Engineering in Mouse Models Reveals an Actionable Role for WNT Pathway Alterations in Prostate Cancer Metastasis von Leibold, Josef, Ruscetti, Marcus, Cao, Zhen, Ho, Yu-Jui, Baslan, Timour, Zou, Min, Abida, Wassim, Feucht, Judith, Han, Teng, Barriga, Francisco M, Tsanov, Kaloyan M, Zamechek, Leah, Kulick, Amanda, Amor, Corina, Tian, Sha, Rybczyk, Katarzyna, Salgado, Nelson R, Sánchez-Rivera, Francisco J, Watson, Philip A, de Stanchina, Elisa, Wilkinson, John E, Dow, Lukas E, Abate-Shen, Cory, Sawyers, Charles L, Lowe, Scott W

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Search for squarks and gluinos in final states with jets and missing transverse momentum using 36 fb-1 of s =13 TeV pp collision data with the ATLAS detector von Onofre, A., Castro, Nuno Filipe, ATLAS Collaboration

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