IBM FlashSystem 9100 Architecture, Performance, and Implementation von Andrew Greenfield, Jon Herd, Corne Lottering, Tony Pacheco, Jagadeesh Papaiah, Thomas Ploski, Stephen Solewin, Jon Tate, Leandro Torolho, Alexander Watson

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Augmenting relational databases via database structure graph von Ploski, Thomas, Hoff, Roland

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AUGMENTING RELATIONAL DATABASES VIA DATABASE STRUCTURE GRAPH von Ploski, Thomas, Hoff, Roland

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METHODS AND APPARATUS FOR LOCATING A DEFECTIVE COMPONENT IN A DATA PROCESSING SYSTEM DURING SYSTEM STARTUP von PLOSKI, THOMAS F, LIM, MICHAEL Y, AHRENS, GEORGE H, RANDALL, DAVID L, RIBBENTROP, DANIEL J., SR, DAWKINS, GEORGE J

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Method and apparatus for locating and displaying a defective component in a data processing system during a system startup using location and progress codes associated with the com... von Ahrens, George Henry, Dawkins, George John, Lim, Michael Youhour, Ploski, Thomas Francis, Randall, David Lee, Ribbentrop, Sr., Daniel John

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Method and apparatus for locating and displaying a defective component in a data processing system during a system startup using location and progress codes associated with the com... von AHRENS GEORGE HENRY, LIM MICHAEL YOUHOUR, PLOSKI THOMAS FRANCIS, RANDALL DAVID LEE, DAWKINS GEORGE JOHN, RIBBENTROP, SR. DANIEL JOHN

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METHODS AND APPARATUS FOR LOCATING A DEFECTIVE COMPONENT IN A DATA PROCESSING SYSTEM DURING SYSTEM STARTUP von PLOSKI, THOMAS F, LIM, MICHAEL Y, AHRENS, GEORGE H, RANDALL, DAVID L, RIBBENTROP, DANIEL J., SR, DAWKINS, GEORGE J

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Hippocampus-driven feed-forward inhibition of the prefrontal cortex mediates relapse of extinguished fear von Marek, Roger, Jin, Jingji, Goode, Travis D., Giustino, Thomas F., Wang, Qian, Acca, Gillian M., Holehonnur, Roopashri, Ploski, Jonathan E., Fitzgerald, Paul J., Lynagh, Timothy, Lynch, Joseph W., Maren, Stephen, Sah, Pankaj

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NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early Childhood von Kremer, Laura S., Danhauser, Katharina, Herebian, Diran, Petkovic Ramadža, Danijela, Piekutowska-Abramczuk, Dorota, Seibt, Annette, Müller-Felber, Wolfgang, Haack, Tobias B., Płoski, Rafał, Lohmeier, Klaus, Schneider, Dominik, Klee, Dirk, Rokicki, Dariusz, Mayatepek, Ertan, Strom, Tim M., Meitinger, Thomas, Klopstock, Thomas, Pronicka, Ewa, Mayr, Johannes A., Baric, Ivo, Distelmaier, Felix, Prokisch, Holger

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De novo stop-loss variants in CLDN11 cause hypomyelinating leukodystrophy von Riedhammer, Korbinian M, Stockler, Sylvia, Ploski, Rafal, Wenzel, Maren, Adis-Dutschmann, Burkhard, Ahting, Uwe, Alhaddad, Bader, Blaschek, Astrid, Haack, Tobias B, Kopajtich, Robert, Lee, Jessica, Murcia Pienkowski, Victor, Pollak, Agnieszka, Szymanska, Krystyna, Tarailo-Graovac, Maja, van der Lee, Robin, van Karnebeek, Clara D, Meitinger, Thomas, Krägeloh-Mann, Ingeborg, Vill, Katharina

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peopling of Europe and the cautionary tale of Y chromosome lineage R-M269 von Busby, George B. J, Brisighelli, Francesca, Sánchez-Diz, Paula, Ramos-Luis, Eva, Martinez-Cadenas, Conrado, Thomas, Mark G, Bradley, Daniel G, Gusmão, Leonor, Winney, Bruce, Bodmer, Walter, Vennemann, Marielle, Coia, Valentina, Scarnicci, Francesca, Tofanelli, Sergio, Vona, Giuseppe, Ploski, Rafal, Vecchiotti, Carla, Zemunik, Tatijana, Rudan, Igor, Karachanak, Sena, Toncheva, Draga, Anagnostou, Paolo, Ferri, Gianmarco, Rapone, Cesare, Hervig, Tor, Moen, Torolf, Wilson, James F, Capelli, Cristian

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Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations von Domínguez, Fernando, Cuenca, Sofía, Bilińska, Zofia, Toro, Rocío, Villard, Eric, Barriales-Villa, Roberto, Ochoa, Juan Pablo, Asselbergs, Folkert, Sammani, Arjan, Franaszczyk, Maria, Akhtar, Mohammed, Coronado-Albi, Maria José, Rangel-Sousa, Diego, Rodriguez-Palomares, Jose F., Jiménez-Jáimez, Juan, Garcia-Pinilla, José Manuel, Ripoll-Vera, Tomás, Mogollón-Jiménez, Maria Victoria, Fontalba-Romero, Ana, Garcia-Medina, Dolores, Palomino-Doza, Julian, de Gonzalo-Calvo, David, Cicerchia, Marcos, Salazar-Mendiguchia, Joel, Salas, Clara, Pankuweit, Sabine, Hey, Thomas Morris, Mogensen, Jens, Barton, Paul J., Charron, Philippe, Elliott, Perry, Garcia-Pavia, Pablo, Eiskjær, Hans, Barriales, Roberto, Fernández Fernández, Xusto, Cicerchia, Marcos, Monserrat, Lorenzo, Ochoa, Juan Pablo, Salazar-Mendiguchia, Joel, Mogollón, Maria Victoria, Ripoll, Tomás, Charron, Philippe, Richard, Pascale, Villard, Eric, Palomino Doza, Julian, Fontalba, Ana, Alonso-Pulpón, Luis, Cobo-Marcos, Marta, Domínguez, Fernando, Garcia-Pavia, Pablo, Gómez-Bueno, Manuel, González-López, Esther, Hernández-Hernández, Aitor, Hernández-Pérez, Francisco José, López-Sainz, Ángela, Restrepo-Córdoba, Alejandra, Segovia-Cubero, Javier, Toro, Rocio, de Gonzalo-Calvo, David, Rosa Longobardo, Félix, Limeres, Javier, Rodriguez-Palomares, Jose F., Garcia-Pinilla, Jose Manuel, López-Garrido, Miguel A., Jiménez-Jaimez, Juan, Garcia-Medina, Dolores, Rangel Sousa, Diego, Peña, Maria Luisa, Mogensen, Jens, Morris-Hey, Thomas, Barton, Paul J., Cook, Stuart A., Midwinter, William, Roberts, Angharad M., Ware, James S., Walsh, Roddy, Akhtar, Mohammed, Elliott, Perry M., Rocha-Lopes, Luis, Savvatis, Konstantinos, Syrris, Petros, Michalak, Ewa, Ploski, Rafal, Sobieszczanska-Malek, Malgorzata, Bilińska, Zofia, Pankuweit, Sabine, Asselbergs, Folkert, Baas, Annette, Dooijes, Dennis, Sammani, Arjan

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Tyrosine kinase inhibitor–induced defects in DNA repair sensitize FLT3(ITD)-positive leukemia cells to PARP1 inhibitors von Maifrede, Silvia, Nieborowska-Skorska, Margaret, Sullivan-Reed, Katherine, Dasgupta, Yashodhara, Podszywalow-Bartnicka, Paulina, Le, Bac Viet, Solecka, Martyna, Lian, Zhaorui, Belyaeva, Elizaveta A., Nersesyan, Alina, Machnicki, Marcin M., Toma, Monika, Chatain, Nicolas, Rydzanicz, Malgorzata, Zhao, Huaqing, Jelinek, Jaroslav, Piwocka, Katarzyna, Sliwinski, Tomasz, Stoklosa, Tomasz, Ploski, Rafal, Fischer, Thomas, Sykes, Stephen M., Koschmieder, Steffen, Bullinger, Lars, Valent, Peter, Wasik, Mariusz A., Huang, Jian, Skorski, Tomasz

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Author Correction: Hippocampus-driven feed-forward inhibition of the prefrontal cortex mediates relapse of extinguished fear von Marek, Roger, Jin, Jingji, Goode, Travis D., Giustino, Thomas F., Wang, Qian, Acca, Gillian M., Holehonnur, Roopashri, Ploski, Jonathan E., Fitzgerald, Paul J., Lynagh, Timothy, Lynch, Joseph W., Maren, Stephen, Sah, Pankaj

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De novo stop-loss variants in CLDN11 cause hypomyelinating leukodystrophy von Riedhammer, Korbinian M., Stockler, Sylvia, Ploski, Rafal, Wenzel, Maren, Adis-Dutschmann, Burkhard, Ahting, Uwe, Alhaddad, Bader, Blaschek, Astrid, Haack, Tobias B., Kopajtich, Robert, Lee, Jessica, Pienkowski, Victor Murcia, Pollak, Agnieszka, Szymanska, Krystyna, Tarailo-Graovac, Maja, van der Lee, Robin, van Karnebeek, Clara D., Meitinger, Thomas, Kraegeloh-Mann, Ingeborg, Vill, Katharina

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CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder von Wortmann, Saskia B., Ziętkiewicz, Szymon, Kousi, Maria, Szklarczyk, Radek, Haack, Tobias B., Gersting, Søren W., Muntau, Ania C., Rakovic, Aleksandar, Renkema, G. Herma, Rodenburg, Richard J., Strom, Tim M., Meitinger, Thomas, Rubio-Gozalbo, M. Estela, Chrusciel, Elzbieta, Distelmaier, Felix, Golzio, Christelle, Jansen, Joop H., van Karnebeek, Clara, Lillquist, Yolanda, Lücke, Thomas, Õunap, Katrin, Zordania, Riina, Yaplito-Lee, Joy, van Bokhoven, Hans, Spelbrink, Johannes N., Vaz, Frédéric M., Pras-Raves, Mia, Ploski, Rafal, Pronicka, Ewa, Klein, Christine, Willemsen, Michel A.A.P., de Brouwer, Arjan P.M., Prokisch, Holger, Katsanis, Nicholas, Wevers, Ron A.

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De novo stop-loss variants in CLDN11 cause hypomyelinating leukodystrophy (vol 144, pg 411, 2020) von Riedhammer, Korbinian M., Stockler, Sylvia, Ploski, Rafal, Wenzel, Maren, Adis-Dutschmann, Burkhard, Ahting, Uwe, Alhaddad, Bader, Blaschek, Astrid, Haack, Tobias B., Kopajtich, Robert, Lee, Jessica, Pienkowski, Victor Murcia, Pollak, Agnieszka, Szymanska, Krystyna, Tarailo-Graovac, Maja, van der Lee, Robin, van Karnebeek, Clara D., Meitinger, Thomas, Krageloh-Mann, Ingeborg, Vill, Katharina

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Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal Neuropathy von Danhauser, Katharina, Alhaddad, Bader, Makowski, Christine, Piekutowska-Abramczuk, Dorota, Syrbe, Steffen, Gomez-Ospina, Natalia, Manning, Melanie A., Kostera-Pruszczyk, Anna, Krahn-Peper, Claudia, Berutti, Riccardo, Kovács-Nagy, Reka, Gusic, Mirjana, Graf, Elisabeth, Laugwitz, Lucia, Röblitz, Michaela, Wroblewski, Andreas, Hartmann, Hans, Das, Anibh M., Bültmann, Eva, Fang, Fang, Xu, Manting, Schatz, Ulrich A., Karall, Daniela, Zellner, Herta, Haberlandt, Edda, Feichtinger, René G., Mayr, Johannes A., Meitinger, Thomas, Prokisch, Holger, Strom, Tim M., Płoski, Rafał, Hoffmann, Georg F., Pronicki, Maciej, Bonnen, Penelope E., Morlot, Susanne, Haack, Tobias B.

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De novo stop-loss variants in CLDN11 cause hypomyelinating leukodystrophy (vol 144, pg 411, 2020) von Riedhammer, Korbinian M., Stockler, Sylvia, Ploski, Rafal, Wenzel, Maren, Adis-Dutschmann, Burkhard, Ahting, Uwe, Alhaddad, Bader, Blaschek, Astrid, Haack, Tobias B., Kopajtich, Robert, Lee, Jessica, Pienkowski, Victor Murcia, Pollak, Agnieszka, Szymanska, Krystyna, Tarailo-Graovac, Maja, van der Lee, Robin, van Karnebeek, Clara D., Meitinger, Thomas, Krageloh-Mann, Ingeborg, Vill, Katharina

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Stankiewicz-Isidor syndrome: expanding the clinical and molecular phenotype von Isidor, Bertrand, Ebstein, Frédéric, Hurst, Anna, Vincent, Marie, Bader, Ingrid, Rudy, Natasha L., Cogne, Benjamin, Mayr, Johannes, Brehm, Anja, Bupp, Caleb, Warren, Kathryn, Bacino, Carlos A., Gerard, Amanda, Ranells, Judith D., Metcalfe, Kay A., van Bever, Yolande, Jiang, Yong-Hui, Mendelssohn, Bryce A., Cope, Heidi, Rosenfeld, Jill A., Blackburn, Patrick R., Goodenberger, McKinsey L., Kearney, Hutton M., Kennedy, Joanna, Scurr, Ingrid, Szczaluba, Krzysztof, Ploski, Rafal, de Saint Martin, Anne, Alembik, Yves, Piton, Amélie, Bruel, Ange-Line, Thauvin-Robinet, Christel, Strong, Alanna, Diderich, Karin E.M., Bourgeois, Dominique, Dahan, Karin, Vignard, Virginie, Bonneau, Dominique, Colin, Estelle, Barth, Magalie, Camby, Caroline, Baujat, Geneviève, Briceño, Ignacio, Gómez, Alberto, Deb, Wallid, Conrad, Solène, Besnard, Thomas, Bézieau, Stéphane, Krüger, Elke, Küry, Sébastien, Stankiewicz, PaweƗ

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