065 - MAGGIC Score and Seattle Heart Failure Model are Less Reliable in Heart Failure with Preserved Ejection Fraction and Nonischemic Cardiomyopathy von Gopalakrishnan, Prabhakaran, Webner, C., Marzlin, K., Ponniah, S.R., Bardakjian, R., Cuadra, R., Manoharan, P., Podugu, R., Duffy, B., Nagajothi, Nagapradeep

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MAGGIC Score and Seattle Heart Failure Model are Less Reliable in Heart Failure with Preserved Ejection Fraction and Nonischemic Cardiomyopathy von Gopalakrishnan, Prabhakaran, Webner, C., Marzlin, K., Ponniah, S.R., Bardakjian, R., Cuadra, R., Manoharan, P., Podugu, R., Duffy, B., Nagajothi, Nagapradeep

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256-Channel Neural Recording and Delta Compression Microsystem With 3D Electrodes von Aziz, J.N.Y., Abdelhalim, K., Shulyzki, R., Genov, R., Bardakjian, B.L., Derchansky, M., Serletis, D., Carlen, P.L.

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Rescue of behavioral and EEG deficits in male and female Mecp2-deficient mice by delayed Mecp2 gene reactivation von Lang, Min, Wither, Robert G, Colic, Sinisa, Wu, Chiping, Monnier, Philippe P, Bardakjian, Berj L, Zhang, Liang, Eubanks, James H

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Pannexin-1 Deficiency Decreases Epileptic Activity in Mice von Aquilino, Mark S, Whyte-Fagundes, Paige, Lukewich, Mark K, Zhang, Liang, Bardakjian, Berj L, Zoidl, Georg R, Carlen, Peter L

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The molecular basis of spinocerebellar ataxia type 48 caused by a de novo mutation in the ubiquitin ligase CHIP von Umano, A., Fang, K., Qu, Z., Scaglione, J.B., Altinok, S., Treadway, C.J., Wick, E.T., Paulakonis, E., Karunanayake, C., Chou, S., Bardakjian, T.M., Gonzalez-Alegre, P., Page, R.C., Schisler, J.C., Brown, N.G., Yan, D., Scaglione, K.M.

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OTX2 microphthalmia syndrome: four novel mutations and delineation of a phenotype von Schilter, KF, Schneider, A, Bardakjian, T, Soucy, J-F, Tyler, RC, Reis, LM, Semina, EV

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Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice von Rainger, Joe, van Beusekom, Ellen, Ramsay, Jacqueline K, McKie, Lisa, Al-Gazali, Lihadh, Pallotta, Rosanna, Saponari, Anita, Branney, Peter, Fisher, Malcolm, Morrison, Harris, Bicknell, Louise, Gautier, Philippe, Perry, Paul, Sokhi, Kishan, Sexton, David, Bardakjian, Tanya M, Schneider, Adele S, Elcioglu, Nursel, Ozkinay, Ferda, Koenig, Rainer, Mégarbané, Andre, Semerci, C Nur, Khan, Ayesha, Zafar, Saemah, Hennekam, Raoul, Sousa, Sérgio B, Ramos, Lina, Garavelli, Livia, Furga, Andrea Superti, Wischmeijer, Anita, Jackson, Ian J, Gillessen-Kaesbach, Gabriele, Brunner, Han G, Wieczorek, Dagmar, van Bokhoven, Hans, FitzPatrick, David R

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Exome sequencing in 32 patients with anophthalmia/microphthalmia and developmental eye defects von Slavotinek, A.M., Garcia, S.T., Chandratillake, G., Bardakjian, T., Ullah, E., Wu, D., Umeda, K., Lao, R., Tang, P.L.-F., Wan, E., Madireddy, L., Lyalina, S., Mendelsohn, B.A., Dugan, S., Tirch, J., Tischler, R., Harris, J., Clark, M.J., Chervitz, S., Patwardhan, A., West, J.M., Ursell, P., de Alba Campomanes, A., Schneider, A., Kwok, P.-y., Baranzini, S., Chen, R.O.

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Temporal trends and yield of clinical diagnostic genetic testing in adult neurology von Guo, Michael H., Bardakjian, Tanya M., Brzozowski, Morgan R., Scherer, Steven S., Quinn, Colin, Elman, Lauren, Orthmann‐Murphy, Jennifer, Tropea, Thomas F., Ellis, Colin A., Gonzalez‐Alegre, Pedro

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The ClinGen Epilepsy Gene Curation Expert Panel—Bridging the divide between clinical domain knowledge and formal gene curation criteria von Helbig, Ingo, Riggs, Erin Rooney, Barry, Carrie‐Anne, Klein, Karl Martin, Dyment, David, Thaxton, Courtney, Sadikovic, Bekim, Sands, Tristan T., Wagnon, Jacy L., Liaquat, Khalida, Cilio, Maria Roberta, Mirzaa, Ghayda, Park, Kristen, Axeen, Erika, Butler, Elizabeth, Bardakjian, Tanya M., Striano, Pasquale, Poduri, Annapurna, Siegert, Rebecca K., Grant, Andrew R., Helbig, Katherine L., Mefford, Heather C.

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Bidirectional multisite seizure propagation in the intact isolated hippocampus: The multifocality of the seizure “focus” von Derchansky, M., Rokni, D., Rick, J.T., Wennberg, R., Bardakjian, B.L., Zhang, L., Yarom, Y., Carlen, P.L.

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A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same family von Ng, WY, Pasutto, F, Bardakjian, TM, Wilson, MJ, Watson, G, Schneider, A, Mackey, DA, Grigg, JR, Zenker, M, Jamieson, RV

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Increased High‐frequency Oscillations Precede in vitro Low‐Mg2+ Seizures von Khosravani, Houman, Pinnegar, C. Robert, Mitchell, J. Ross, Bardakjian, Berj L., Federico, Paolo, Carlen, Peter L.

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Requisite Role of Kv1.5 Channels in Coronary Metabolic Dilation von Ohanyan, Vahagn, Yin, Liya, Bardakjian, Raffi, Kolz, Christopher, Enrick, Molly, Hakobyan, Tatevik, Kmetz, John, Bratz, Ian, Luli, Jordan, Nagane, Masaki, Khan, Nadeem, Hou, Huagang, Kuppusamy, Periannan, Graham, Jacqueline, Fu, Frances Kwan, Janota, Danielle, Oyewumi, Moses O, Logan, Suzanna, Lindner, Jonathan R, Chilian, William M

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A Novel SPAST/SPG4 Splice-Site Variant in a Family with Dominant Hereditary Spastic Paraplegia von Gonzalez-Alegre, Pedro, Winder, Thomas L., Ozmore, Jillian R., Robbins, Nathaniel M., Bardakjian, Tanya M.

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Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice von Rainger, Joe, van Beusekom, Ellen, Ramsay, Jacqueline K, McKie, Lisa, Al-Gazali, Lihadh, Pallotta, Rosanna, Saponari, Anita, Branney, Peter, Fisher, Malcolm, Morrison, Harris, Bicknell, Louise, Gautier, Philippe, Perry, Paul, Sokhi, Kishan, Sexton, David, Bardakjian, Tanya M, Schneider, Adele S, Elcioglu, Nursel, Ozkinay, Ferda, Koenig, Rainer, Mégarbané, Andre, Semerci, C Nur, Khan, Ayesha, Zafar, Saemah, Hennekam, Raoul, Sousa, Sérgio B, Ramos, Lina, Garavelli, Livia, Furga, Andrea Superti, Wischmeijer, Anita, Jackson, Ian J, Gillessen-Kaesbach, Gabriele, Brunner, Han G, Wieczorek, Dagmar, van Bokhoven, Hans, Fitzpatrick, David R

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Brain-Silicon Interface for High-Resolution in vitro Neural Recording von Aziz, J.N.Y., Genov, R., Bardakjian, B.L., Derchansky, M., Carlen, P.L.

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Biallelic AOPEP Loss‐of‐Function Variants Cause Progressive Dystonia with Prominent Limb Involvement von Zech, Michael, Kumar, Kishore R., Reining, Sophie, Reunert, Janine, Tchan, Michel, Riley, Lisa G., Drew, Alexander P., Adam, Robert J., Berutti, Riccardo, Biskup, Saskia, Derive, Nicolas, Bakhtiari, Somayeh, Jin, Sheng Chih, Kruer, Michael C., Bardakjian, Tanya, Gonzalez‐Alegre, Pedro, Keller Sarmiento, Ignacio J., Mencacci, Niccolo E., Lubbe, Steven J., Kurian, Manju A., Clot, Fabienne, Méneret, Aurélie, Sainte Agathe, Jean‐Madeleine, Fung, Victor S.C., Vidailhet, Marie, Baumann, Matthias, Marquardt, Thorsten, Winkelmann, Juliane, Boesch, Sylvia

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The commercial genetic testing landscape for Parkinson's disease von Cook, Lola, Schulze, Jeanine, Verbrugge, Jennifer, Beck, James C., Marder, Karen S., Saunders-Pullman, Rachel, Klein, Christine, Naito, Anna, Alcalay, Roy N., Brice, Alexis, Kumeh, Amasi, West, Andrew B., Singleton, Andrew, Naito, Anna, Schüle, Birgitt, Fiske, Brian, Gabbert, Carolin, Marras, Connie, Blauwendraat, Cornelis, Thaxton, Courtney, Alessi, Dario, Craig, David, Fon, Edward A., Forbes, Emily, Valente, Enza Maria, Sammler, Esther, Chao, Gill, Riboldi, Giulietta, Elloumi, Houda Zghal, Mata, Ignacio, Beck, James C., Fong, Jamie C., Corvol, Jean-Christophe, Schulze, Jeanine, Verbrugge, Jennifer, Shulman, Joshua, Peterschmitt, Judith, Marder, Karen, Lohmann, Katja, Nudelman, Kelly, Lange, Lara, Cook, Lola, Cookson, Mark R., Nance, Martha, Farrer, Matthew, Grigorian, Melina, Schwarzschild, Michael A., Mencacci, Niccolo, Ross, Owen, Mistry, Pramod, Hodges, Priscila, Blake, Rachel, Saunders-Pullman, Rachel, Alcalay, Roy N., Sardi, S. Pablo, Farhan, Sali, Strom, Samuel, Padmanabhan, Shalini, Mohan, Shruthi, Longerich, Simonne, Schneider, Susanne, Lesage, Suzanne, Bardakjian, Tanya, Foroud, Tatiana, Courtin, Thomas, Tropea, Thomas, Liu, Yunlong, Gan-Or, Ziv, Shalash, Ali S., Hall, Anne, Thaler, Avner, Sue, Carolyn M., Mascalzoni, Deborah, Raymond, Deborah, Gatto, Emilia Mabel, Pal, Gian D., König, Inke, Novakovic, Ivana, Merello, Marcelo, Salari, Mehri, Mencacci, Niccolo Emanuele, Hattori, Nobutaka, Suchowersky, Oksana, Bardien, Soraya, Chung, Sun Ju, Simuni, Tatyana, Lynch, Timothy, Bonifati, Vincenzo

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