Sökresultat - "Ellis, Colin A."

A new framework for comparing financial stability risks

Ellis, Colin., Speaker

Zero-Shot Extraction of Seizure Outcomes from Clinical Notes Using Generative Pretrained Transformers

Ojemann, William K. S.^{Aff1, Aff2}, Xie, Kevin^{Aff1, Aff2}, Liu, Kevin^{Aff2, Aff3}, Chang, Ellie^{Aff1, Aff2}, Roth, Dan, Litt, Brian^{Aff1, Aff2, Aff4}, Ellis, Colin A.^{Aff2, Aff4, IDs41666025001985_cor1}

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Should investors rely on central bank asset purchases to backstop markets?

Ellis, Colin., Speaker

Protocol for a type 3 hybrid implementation cluster randomized clinical trial to evaluate the effect of patient and clinician nudges to advance the use of genomic medicine across a diverse health system

Raper, Anna C., Weathers, Benita L., Drivas, Theodore G., Ellis, Colin A., Kripke, Colleen Morse, Oyer, Randall A., Owens, Anjali T., Verma, Anurag, Wileyto, Paul E., Wollack, Colin C., Zhou, Wenting, Ritchie, Marylyn D.^{Aff4, Aff6}, Schnoll, Robert A.^{Aff6, Aff7}, Nathanson, Katherine L.^{Aff1, Aff6, IDs13012024013855_cor14}

Variants in BSN, encoding the presynaptic protein Bassoon, result in a distinct neurodevelopmental disorder with a broad phenotypic range

Guzman, Stacy G. ^{1, 2}, Ruggiero, Sarah M. ^{2, 3, 4, 5}, Ganesan, Shiva ^{2, 3, 4, 5}, Ellis, Colin A. ^{2, 4, 5, 6}, Harrison, Alicia G. ^{2, 3, 4, 5}, Sullivan, Katie R. ^{2, 3, 4, 5}, Stark, Zornitza ^{7, 8, 9}, Brown, Natasha J. ^{7, 8, 9}, Kana, Sajel L. ¹⁰, Tuttle, Anabelle ¹¹, Tenorio, Jair ^{12, 13}, Lapunzina, Pablo ^{12, 13}, Nevado, Julián ^{12, 13, 14}, McDonald, Marie T. ¹⁵, Jensen, Courtney ¹⁶, Wheeler, Patricia G. ¹⁷, Stange, Lila ¹⁷, Morrison, Jennifer ¹⁷, Keren, Boris ¹⁸, Heide, Solveig ¹⁹, Keating, Meg W. ²⁰, Butler, Kameryn M. ²⁰, Lyons, Mike A. ^{20, 21}, Jain, Shailly ²², Yeganeh, Mehdi ²³, Thompson, Michelle L. ²⁴, Schroeder, Molly ^{24, 25}, Nguyen, Hoanh ^{24, 25}, Granadillo, Jorge ²⁵, Johnston, Kari M. ²⁶, Murali, Chaya N. ²⁶, Bosanko, Katie ²⁷, Burrow, T. Andrew ²⁷, Morgan, Syreeta ²⁸, Watson, Deborah J. ^{28, 29}, Hakonarson, Hakon ^{28, 29}, Helbig, Ingo ^{1, 2, 3, 4, 5, 6, ∗}

Genome-wide association meta-analyses of drug-resistant epilepsy

Amadori, Elisabetta, Andrade, Danielle M., Annesi, Grazia, Balagura, Ganna, Balestrini, Simona, Barba, Carmen, Barboza, Karen, Baumgartner, Tobias H., Baykan, Betül, Bebek, Nerses, Becker, Felicitas, Bennett, Caitlin A., Berkovic, Samuel F., Beydoun, Ahmad, Bisulli, Francesca, Borggräfe, Ingo, Bosselmann, Christian, Busch, Robyn M., Canafoglia, Laura, Castellotti, Barbara, Chou, I-Jun, Chung, Seo-Kyung, Cotsapas, Chris, Devinsky, Orrin, Dlugos, Dennis J., Doccini, Viola, Doherty, Colin P., Ellis, Colin A., El-Naggar, Hany, Evans, Meghan, Ferraro, Thomas N., Fitzgerald, Mark, Fortunato, Francesco, French, Jacqueline A., Freri, Elena, Gagliardi, Monica, Gambardella, Antonio, Goldman, Alica, Granata, Tiziana, Gupta, Namrata, Haas, Kevin, Hirose, Shinichi, Hoeper, Olivia, Hung, Po-Chen, Johnson, Michael R., Khoueiry-Zgheib, Nathalie, Khoury, Jean, Klein, Karl Martin, Knake, Susanne, Koupparis, Andreas, Kousiappa, Ioanna, Krause, Roland, Kunz, Wolfram S., Kuzniecky, Ruben I., Kwan, Patrick, Labate, Angelo, Lacey, Austin, Lal, Dennis, Lauxmann, Stephan, Lawthom, Charlotte, Lerche, Holger, Leu, Costin, Lewis-Smith, David, Liao, Calwing, Lin, Chih-Hsiang, Lin, Kuang-Lin, Linnankivi, Tarja, Lowenstein, Daniel H., Lui, Colin H.T., Madia, Francesca, Magri, Stefania, Maillard, Louis, Manna, Lorella, Marques, Paula, Mayer, Thomas, McGraw, Christopher M., Meador, Kimford J., Mei, Davide, Minardi, Raffaella, Mostacci, Barbara, Muccioli, Lorenzo, Müller-Schlüter, Karen, Nasreddine, Wassim, Neale, Benjamin M., Neubauer, Bernd A., Papacostas, Savvas S., Parrini, Elena, Pendziwiat, Manuela, Petrovski, Slavé, Pickrell, William O., Powell, Robert H.W., Ragona, Francesca, Rees, Mark I., Rheims, Sylvain, Riva, Antonella, Rosenow, Felix, Ryvlin, Philippe, Sadleir, Lynette G., Salman, Barış, Salmon, Andrea, Sammarra, Ilaria, Scala, Marcello, Scheffer, Ingrid E., Schubert-Bast, Susanne, Schulze-Bonhage, Andreas, Shiedley, Beth R., Sisodiya, Sanjay M., Sperling, Michael R., Steinhoff, Bernhard J., Stephani, Ulrich, Striano, Pasquale, Strzelczyk, Adam, Surges, Rainer, Suzuki, Toshimitsu, Talarico, Mariagrazia, Taneja, Randip S., Tanteles, George A., Tsai, Meng-Han, Tumiene, Birute, Turkdogan, Dilsad, Valton, Luc, van Baalen, Andreas, Vetro, Annalisa, von Wrede, Randi, Wagner, Ryan G., Weber, Yvonne G., Weckhuysen, Sarah, Widdess-Walsh, Peter, Wiebe, Samuel, Wolking, Stefan, Yamakawa, Kazuhiro, Yapıcı, Zuhal, Zahnert, Felix, Zara, Federico, Zizovic, Milena, Zsurka, Gábor, Ali, Quratulain Zulfiqar, Auce, Pauls, Avbersek, Andreja, Balling, Rudi, Berghuis, Bianca, Borghei, Mojgansadat, Brodie, Martin J., Campbell, Ellen, Cavalleri, Gianpiero L., Chinthapalli, Krishna, Coppola, Antonietta, Craig, John, Delanty, Norman, Demurtas, Rita, Depondt, Chantal, Francis, Ben, Gudmundsson, Lárus J., Heggeli, Kristin, Hengsbach, Christian, Hutton, Jane L., Ingason, Andrés, Jorgensen, Andrea, Klein, Karl M., Koeleman, Bobby P.C., Krenn, Martin, Langley, Sarah R., Marson, Anthony G., McCormack, Mark, Møller, Rikke S., Morris, Andrew, Muhle, Hiltrud, Nikanorova, Marina, O'Brien, Terence J., Petrovski, Slave, Rau, Sarah, Rener-Primec, Zvonka, Sander, Josemir W., Sargsyan, Narek, Schneider, Reinhard, Sills, Graeme J., Speed, Doug, Srivastava, Prashant K., Stefansson, Hreinn, Stefánsson, Kári, Todaro, Marian, Willis, Joseph, Zimprich, Fritz, Stevelink, Remi ^{e, f}, Custodio, Helena Martins ^{b, d}, Chen, Siwei ^{g, h}, Jonsson, Lina ^k, Unnsteinsdóttir, Unnur ^l, Jorgensen, Andrea L. ^m, Craig, John J. ^q, Hassanin, Emadeldin ^u, Omidvar, Maryam Erfanian ^v, Stefansson, Kari ^{l, ah}, May, Patrick ^u

Genetic testing in adults with neurologic disorders: indications, approach, and clinical impacts

Dratch, Laynie, Azage, Meron, Baldwin, Aaron, Johnson, Kelsey, Paul, Rachel A., Bardakjian, Tanya M.^{Aff1, Aff2}, Michon, Sara-Claude, Amado, Defne A., Baer, Michael, Deik, Andres F., Elman, Lauren B., Gonzalez-Alegre, Pedro^{Aff1, Aff3}, Guo, Michael H., Hamedani, Ali G., Irwin, David J., Lasker, Aaron, Orthmann-Murphy, Jennifer, Quinn, Colin, Tropea, Thomas F., Scherer, Steven S., Ellis, Colin A.^{Aff1, IDs00415023120586_cor21}

Investigating the effect of polygenic background on epilepsy phenotype in ‘monogenic’ families

Afawi, Zaid, Amrom, Dina, Andermann, Eva, Bautista, Jocelyn F., Bellows, Susannah T., Bluvstein, Judith, Cascino, Gregory D., Chung, Seo-Kyung, Cossette, Patrick, Curtis, Sarah W., Delanty, Norman, Devinsky, Orrin, Dlugos, Dennis, Epstein, Michael P., Freyer, Catharine, Gravel, Micheline, Harris, Rebekah V., Heinzen, Erin L., Henry, Olivia J., Kirsch, Heidi E., Knowlton, Robert C., Kossoff, Eric H., Loeb, Rebecca, Lowenstein, Daniel H., Marson, Anthony G., Mefford, Heather C., Motika, Paul V., O'Brien, Terence J., Ottman, Ruth, Paolicchi, Juliann M., Petrovski, Slave, Pickrell, William O., Rees, Mark I., Sadleir, Lynette G., Shih, Jerry J., Singh, Rani K., Smith, Michael C., Smith, Philip E.M., Thomas, Rhys H., Weisenberg, Judith, Widdess-Walsh, Peter, Winawer, Melodie R., Oliver, Karen L., Scheffer, Ingrid E., Ellis, Colin A., Grinton, Bronwyn E., Berkovic, Samuel F., Bahlo, Melanie

Clinical characteristics and surgical outcomes of epilepsy associated with temporal encephalocele: A systematic review

Zhou, Daniel J., Woodson-Smith, Sarah, Emmert, Brian E., Kornspun, Alana, Larocque, Joshua, Kulick-Soper, Catherine V., Qiu, Maylene K., Ellis, Colin A., Gugger, James J., Conrad, Erin C., Waldman, Genna, Ganguly, Taneeta, Sinha, Saurabh R., Davis, Kathryn A., Stein, Joel M., Liu, Grant T., Gelfand, Michael, Raghupathi, Ramya

How should risk professionals think about the rise in corporate indebtedness?

Ellis, Colin., Speaker

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10 Signs of a Toxic Boss — and How to Protect Yourself.

Ellis, Colin D.

Alcohol for seizure induction in the epilepsy monitoring unit

Emmert, Brian E. ^{a, ⁎}, Xie, Kevin ^{b, c}, Conrad, Erin C. ^{a, b, c}, Ghosn, Nina J. ^{b, c}, Bauman, Kristie ^a, Korzun, Jacob ^a, Kulick-Soper, Catherine V. ^a, Naveed, Omer ^a, Hartmann, Nicole ^a, LaRocque, Joshua J. ^a, Mindy Ganguly, Taneeta ^a, Gugger, James J. ^{a, c}, Raghupathi, Ramya ^a, Gelfand, Michael A. ^a, Davis, Kathryn A. ^{a, c}, Sinha, Saurabh R. ^a, Litt, Brian ^{a, b, c}, Shinohara, Russell T. ^{d, e}, Ellis, Colin A. ^a

Semantic Similarity Analysis Reveals Robust Gene-Disease Relationships in Developmental and Epileptic Encephalopathies

Galer, Peter D, Ganesan, Shiva, Lewis-Smith, David, McKeown, Sarah E, Pendziwiat, Manuela, Helbig, Katherine L, Ellis, Colin A, Rademacher, Annika, Smith, Lacey, Poduri, Annapurna, Seiffert, Simone, von Spiczak, Sarah, Muhle, Hiltrud, van Baalen, Andreas, Group, NCEE Study, Investigators, EPGP, Consortium, EuroEPINOMICS-RES, Network, Genomics Research and Innovation, Thomas, Rhys H, Krause, Roland, Weber, Yvonne, Helbig, Ingo

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Reinforcing or Disrupting Gender Affirmation: The Impact of Cancer on Transgender Embodiment and Identity

Ussher, Jane M.^{Aff1, IDs10508023025309_cor1}, Power, Rosalie, Allison, Kimberley, Sperring, Samantha, Parton, Chloe, Perz, Janette, Davies, Cristyn^{Aff3, Aff4}, Cook, Teddy, Hawkey, Alexandra J., Robinson, Kerry H., Hickey, Martha, Anazodo, Antoinette, Ellis, Colin

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De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus

Galosi, Serena, Edani, Ban H, Martinelli, Simone, Hansikova, Hana, Eklund, Erik A, Caputi, Caterina, Masuelli, Laura, Corsten-Janssen, Nicole, Srour, Myriam, Oegema, Renske, Bosch, Daniëlle G M, Ellis, Colin A, Amlie-Wolf, Louise, Accogli, Andrea, Atallah, Isis, Averdunk, Luisa, Barañano, Kristin W, Bei, Roberto, Bagnasco, Irene, Brusco, Alfredo, Demarest, Scott, Alaix, Anne-Sophie, Di Bonaventura, Carlo, Distelmaier, Felix, Elmslie, Frances, Gan-Or, Ziv, Good, Jean-Marc, Gripp, Karen, Kamsteeg, Erik-Jan, Macnamara, Ellen, Marcelis, Carlo, Mercier, Noëlle, Peeden, Joseph, Pizzi, Simone, Pannone, Luca, Shinawi, Marwan, Toro, Camilo, Verbeek, Nienke E, Venkateswaran, Sunita, Wheeler, Patricia G, Zdrazilova, Lucie, Zhang, Rong, Zorzi, Giovanna, Guerrini, Renzo, Sessa, William C, Lefeber, Dirk, Tartaglia, Marco, Hamdan, Fadi F, Grabińska, Kariona A, Leuzzi, Vincenzo

Lund University, Faculty of Medicine, Department of Clinical Sciences, Lund, Section V, Paediatrics (Lund), Lunds universitet, Medicinska fakulteten, Institutionen för kliniska vetenskaper, Lund, Sektion V, Pediatrik, Lund, Originator, Lund University, Faculty of Medicine, Department of Clinical Sciences, Lund, Section IV, Epilepsy Center, Lunds universitet, Medicinska fakulteten, Institutionen för kliniska vetenskaper, Lund, Sektion IV, Epilepsicentrum, Originator