Hybrid Analog And Digital System For The Analysis Of Action Potentials von MCGILLIVRAY, RICHARD, WALD, ROBERT W.

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A Versatile Trigger Circuit For Biological Signals von McGILLIVRAY, RICHARD, WALD, ROBERT W.

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A Microprocessor-Based Electrophysiologic Stimulator Controller von McGILLIVRAY, RICHARD, WALD, ROBERT W., CHAI, MAURICE W. M.

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Continuous On-Line Beat-to-Beat Analysis of AV Conduction Time von WAXMAN, MENASHE B., WALD, ROBERT W., MCGILLIVRAY, RICHARD, CAMERON, DOUGLAS A., SHARMA, ARJUN D., HUERTA, FELIX

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Le génitif pluriel dans le dialecte moderne de Cypre von Dawkins, Richard McGillivray

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"Partner", "Caregiver", or "Co-Survivor"-Might the Label We Give the Partners of Cancer Patients Affect the Health Outcome of the Patients and Their Partners? von McGillivray, Hannah M K, Piccolo, Elisabetta E L, Wassersug, Richard J

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Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3 von Sim, Joe C., Scerri, Thomas, Fanjul-Fernández, Miriam, Riseley, Jessica R., Gillies, Greta, Pope, Kate, van Roozendaal, Hanna, Heng, Julian I., Mandelstam, Simone A., McGillivray, George, MacGregor, Duncan, Kannan, Lakshminarayanan, Maixner, Wirginia, Harvey, A. Simon, Amor, David J., Delatycki, Martin B., Crino, Peter B., Bahlo, Melanie, Lockhart, Paul J., Leventer, Richard J.

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Pan-cancer analysis of whole genomes von Campbell, Peter J, Getz, Gad, Korbel, Jan O, Stuart, Joshua M, Jennings, Jennifer L, Stein, Lincoln D, Perry, Marc D

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A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders von Stark, Zornitza, Tan, Tiong Y., Chong, Belinda, Brett, Gemma R., Yap, Patrick, Walsh, Maie, Yeung, Alison, Peters, Heidi, Mordaunt, Dylan, Cowie, Shannon, Amor, David J., Savarirayan, Ravi, McGillivray, George, Downie, Lilian, Ekert, Paul G., Theda, Christiane, James, Paul A., Yaplito-Lee, Joy, Ryan, Monique M., Leventer, Richard J., Creed, Emma, Macciocca, Ivan, Bell, Katrina M., Oshlack, Alicia, Sadedin, Simon, Georgeson, Peter, Anderson, Charlotte, Thorne, Natalie, Gaff, Clara, White, Susan M.

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Deep Brain Stimulation of the Subthalamic Nucleus in Parkinson’s Disease: A Meta-Analysis of Mood Effects von Cartmill, Tomas, Skvarc, David, Bittar, Richard, McGillivray, Jane, Berk, Michael, Byrne, Linda K.

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Phenomenology of hoarding in children with comorbid attention-deficit/hyperactivity disorder (ADHD): The perceptions of parents von Lynch, Fiona A, Moulding, Richard, McGillivray, Jane A

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A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns von Jiao, Wei, Atwal, Gurnit, Polak, Paz, Karlic, Rosa, Cuppen, Edwin, Danyi, Alexandra, de Ridder, Jeroen, van Herpen, Carla, Lolkema, Martijn P., Steeghs, Neeltje, Getz, Gad, Morris, Quaid D., Stein, Lincoln D.

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Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene von CONTI, Valerio, CARABALONA, Aurelie, WATRIN, Françoise, LISE, Stefano, PAGNAMENTA, Alistair T, TAYLOR, Jenny C, KINI, Usha, CLAYTON-SMITH, Jill, NOVARA, Francesca, ZUFFARDI, Orsetta, DOBYNS, William B, SCHEFFER, Ingrid E, PALLESI-POCACHARD, Emilie, ROBERTSON, Stephen P, BERKOVIC, Samuel F, REPRESA, Alfonso, KEAYS, David A, CARDOSO, Carlos, GUERRINI, Renzo, PARRINI, Elena, LEVENTER, Richard J, BUHLER, Emmanuelle, MCGILLIVRAY, George, MICHEL, François J, STRIANO, Pasquale, MEI, Davide

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Integrative pathway enrichment analysis of multivariate omics data von Paczkowska, Marta, Barenboim, Jonathan, Sintupisut, Nardnisa, Fox, Natalie S., Zhu, Helen, Abd-Rabbo, Diala, Mee, Miles W., Boutros, Paul C., Reimand, Jüri

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Reducing the exome search space for mendelian diseases using genetic linkage analysis of exome genotypes von Smith, Katherine R, Bromhead, Catherine J, Hildebrand, Michael S, Shearer, A Eliot, Lockhart, Paul J, Najmabadi, Hossein, Leventer, Richard J, McGillivray, George, Amor, David J, Smith, Richard J, Bahlo, Melanie

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Genetic heterogeneity of polymicrogyria: study of 123 patients using deep sequencing von Stutterd, Chloe A, Brock, Stefanie, Stouffs, Katrien, Fanjul-Fernandez, Miriam, Lockhart, Paul J, McGillivray, George, Mandelstam, Simone, Pope, Kate, Delatycki, Martin B, Jansen, Anna, Leventer, Richard J

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Genomic footprints of activated telomere maintenance mechanisms in cancer von Sieverling, Lina, Hong, Chen, Koser, Sandra D., Ginsbach, Philip, Kleinheinz, Kortine, Hutter, Barbara, Braun, Delia M., Cortés-Ciriano, Isidro, Xi, Ruibin, Kabbe, Rolf, Park, Peter J., Eils, Roland, Schlesner, Matthias, Brors, Benedikt, Rippe, Karsten, Jones, David T. W., Feuerbach, Lars

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Pathway and network analysis of more than 2500 whole cancer genomes von Reyna, Matthew A., Haan, David, Paczkowska, Marta, Verbeke, Lieven P. C., Vazquez, Miguel, Kahraman, Abdullah, Pulido-Tamayo, Sergio, Barenboim, Jonathan, Wadi, Lina, Dhingra, Priyanka, Shrestha, Raunak, Getz, Gad, Lawrence, Michael S., Pedersen, Jakob Skou, Rubin, Mark A., Wheeler, David A., Brunak, Søren, Izarzugaza, Jose M. G., Khurana, Ekta, Marchal, Kathleen, von Mering, Christian, Sahinalp, S. Cenk, Valencia, Alfonso, Reimand, Jüri, Stuart, Joshua M., Raphael, Benjamin J.

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Increased premotor cortex activation in high functioning autism during action observation von Perkins, Tom J, Bittar, Richard G, McGillivray, Jane A, Cox, Ivanna I, Stokes, Mark A

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Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth von Todd, Emily J, Yau, Kyle S, Ong, Royston, Slee, Jennie, McGillivray, George, Barnett, Christopher P, Haliloglu, Goknur, Talim, Beril, Akcoren, Zuhal, Kariminejad, Ariana, Cairns, Anita, Clarke, Nigel F, Freckmann, Mary-Louise, Romero, Norma B, Williams, Denise, Sewry, Caroline A, Colley, Alison, Ryan, Monique M, Kiraly-Borri, Cathy, Sivadorai, Padma, Allcock, Richard J N, Beeson, David, Maxwell, Susan, Davis, Mark R, Laing, Nigel G, Ravenscroft, Gianina

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