Magnetic resonance imaging in infections of the brain: findings in tuberculosis, listeriosis, toxoplasmosis, subacute sclerosing panencephalitis, and multiple sclerosis von JUST, M, HIGER, H.-P, KRAMER, G, GOLLA, G, BETTING, O, HOLPER, H, PFANNENSTIEL, P

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Computational methods of EEG signals analysis for Alzheimer’s disease classification von Vicchietti, Mário L., Ramos, Fernando M., Betting, Luiz E., Campanharo, Andriana S. L. O.

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Quantile graphs for EEG-based diagnosis of Alzheimer’s disease von Pineda, Aruane M, Ramos, Fernando M, Betting, Luiz Eduardo, Campanharo, Andriana S. L. O

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Barriers to patient recruitment in a poststroke neurorehabilitation multicenter trial in Brazil von Silva, T R da, Luvizutto, G J, Martins, L G, Costa, R D M da, Souza, J T de, Winckler, F C, Sartor, L C A, Modolo, G P, Ferreira, N C, Rodrigues, J C S, Kanda, R G, Fogaroli, M O, Borges, G F, Rizzatti, G R S, Ribeiro, P W, Pires, D S, Favoretto, D B, Aguiar, L R, Bazan, S G Z, Betting, L E G, Antunes, L C O, Nunes, H R C, Pereira, V M, Edwards, T G S, Pontes-Neto, O, Conforto, A B, Bazan, R

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Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project von Ceyhan-Birsoy, Ozge, Murry, Jaclyn B., Machini, Kalotina, Lebo, Matthew S., Yu, Timothy W., Fayer, Shawn, Genetti, Casie A., Schwartz, Talia S., Agrawal, Pankaj B., Parad, Richard B., Holm, Ingrid A., McGuire, Amy L., Green, Robert C., Rehm, Heidi L., Beggs, Alan H., Agrawal, Pankaj B., Beggs, Alan H., Betting, Wendi N., Ceyhan-Birsoy, Ozge, Christensen, Kurt D., Dukhovny, Dmitry, Fayer, Shawn, Frankel, Leslie A., Genetti, Casie A., Graham, Chet, Green, Robert C., Guiterrez, Amanda M., Harden, Maegan, Holm, Ingrid A., Krier, Joel B., Lebo, Matthew S., Levy, Harvey L., Lu, Xingquan, Machini, Kalotina, McGuire, Amy L., Murry, Jaclyn B., Naik, Medha, Nguyen, Tiffany T., Parad, Richard B., Peoples, Hayley A., Pereira, Stacey, Petersen, Devan, Ramamurthy, Uma, Ramanathan, Vivek, Rehm, Heidi L., Roberts, Amy, Robinson, Jill O., Roumiantsev, Serguei, Schwartz, Talia S., Truong, Tina K., VanNoy, Grace E., Waisbren, Susan E., Yu, Timothy W.

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Parental interest in genomic sequencing of newborns: enrollment experience from the BabySeq Project von Genetti, Casie A., Schwartz, Talia S., Robinson, Jill O., VanNoy, Grace E., Petersen, Devan, Pereira, Stacey, Fayer, Shawn, Peoples, Hayley A., Agrawal, Pankaj B., Betting, Wendi N., Holm, Ingrid A., McGuire, Amy L., Waisbren, Susan E., Yu, Timothy W., Green, Robert C., Beggs, Alan H., Parad, Richard B.

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Discordant results between conventional newborn screening and genomic sequencing in the BabySeq Project von Wojcik, Monica H., Zhang, Tian, Ceyhan-Birsoy, Ozge, Genetti, Casie A., Lebo, Matthew S., Yu, Timothy W., Parad, Richard B., Holm, Ingrid A., Rehm, Heidi L., Beggs, Alan H., Green, Robert C., Agrawal, Pankaj B., Agrawal, Pankaj B., Betting, Wendi N., Christensen, Kurt D., Dukhovny, Dmitry, Fayer, Shawn, Frankel, Leslie A., Graham, Chet, Guiterrez, Amanda M., Harden, Maegan, Krier, Joel B., Levy, Harvey L., Lu, Xingquan, Machini, Kalotina, McGuire, Amy L., Murry, Jaclyn B., Naik, Medha, Nguyen, Tiffany T., Peoples, Hayley A., Pereira, Stacey, Petersen, Devan, Ramamurthy, Uma, Ramanathan, Vivek, Roberts, Amy, Robinson, Jill O., Roumiantsev, Serguei, Schwartz, Talia S., Truong, Tina K., VanNoy, Grace E., Waisbren, Susan E.

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Analysis of Interictal Epileptiform Discharges in Mesial Temporal Lobe Epilepsy Using Quantitative EEG and Neuroimaging von Fujisao, Elaine Keiko, Alves, Karen Fernanda, Rezende, Thais O P, Betting, Luiz Eduardo

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Revisiting the clinical impact of variants in EFHC1 in patients with different phenotypes of genetic generalized epilepsy von Gonsales, Marina C., Ribeiro, Patrícia A.O., Betting, Luiz E., Alvim, Marina K.M., Guerreiro, Carlos M., Yasuda, Clarissa L., Gitaí, Daniel L.G., Cendes, Fernando, Lopes-Cendes, Iscia

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Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project von Pereira, Stacey, Robinson, Jill Oliver, Gutierrez, Amanda M, Petersen, Devan K, Hsu, Rebecca L, Lee, Caroline H, Schwartz, Talia S, Holm, Ingrid A, Beggs, Alan H, Green, Robert C, McGuire, Amy L

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The BabySeq project: implementing genomic sequencing in newborns von Holm, Ingrid A, Agrawal, Pankaj B, Ceyhan-Birsoy, Ozge, Christensen, Kurt D, Fayer, Shawn, Frankel, Leslie A, Genetti, Casie A, Krier, Joel B, LaMay, Rebecca C, Levy, Harvey L, McGuire, Amy L, Parad, Richard B, Park, Peter J, Pereira, Stacey, Rehm, Heidi L, Schwartz, Talia S, Waisbren, Susan E, Yu, Timothy W, Green, Robert C, Beggs, Alan H

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Returning a Genomic Result for an Adult-Onset Condition to the Parents of a Newborn: Insights From the BabySeq Project von Holm, Ingrid A, McGuire, Amy, Pereira, Stacey, Rehm, Heidi, Green, Robert C, Beggs, Alan H

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Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study von Lane, William J, Westhoff, Connie M, Gleadall, Nicholas S, Aguad, Maria, Smeland-Wagman, Robin, Vege, Sunitha, Simmons, Daimon P, Mah, Helen H, Lebo, Matthew S, Walter, Klaudia, Soranzo, Nicole, Di Angelantonio, Emanuele, Danesh, John, Roberts, David J, Watkins, Nick A, Ouwehand, Willem H, Butterworth, Adam S, Kaufman, Richard M, Rehm, Heidi L, Silberstein, Leslie E, Green, Robert C, Bates, David W., Blout, Carrie, Christensen, Kurt D., Cirino, Allison L., Ho, Carolyn Y., Krier, Joel B., Lehmann, Lisa S., MacRae, Calum A., Morton, Cynthia C., Perry, Denise L., Seidman, Christine E., Sunyaev, Shamil R., Vassy, Jason L., Schonman, Erica, Nguyen, Tiffany, Steffens, Eleanor, Betting, Wendi Nicole, Aronson, Samuel J., Ceyhan-Birsoy, Ozge, Machini, Kalotina, McLaughlin, Heather M., Azzariti, Danielle R., Tsai, Ellen A., Blumenthal-Barby, Jennifer, Feuerman, Lindsay Z., McGuire, Amy L., Lee, Kaitlyn, Robinson, Jill O., Slashinski, Melody J., Diamond, Pamela M., Davis, Kelly, Ubel, Peter A., Kraft, Peter, Roberts, J. Scott, Garber, Judy E., Hambuch, Tina, Murray, Michael F., Kohane, Isaac, Kong, Sek Won

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Short-term costs of integrating whole-genome sequencing into primary care and cardiology settings: a pilot randomized trial von Christensen, Kurt D., Vassy, Jason L., Phillips, Kathryn A., Blout, Carrie L., Azzariti, Danielle R., Lu, Christine Y., Robinson, Jill O., Lee, Kaitlyn, Douglas, Michael P., Yeh, Jennifer M., Machini, Kalotina, Stout, Natasha K., Rehm, Heidi L., McGuire, Amy L., Green, Robert C., Dukhovny, Dmitry

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Challenging the Current Recommendations for Carrier Testing in Children von VanNoy, Grace E, Genetti, Casie A, McGuire, Amy L, Green, Robert C, Beggs, Alan H, Holm, Ingrid A

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A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xg a von Lane, William J, Aguad, Maria, Smeland-Wagman, Robin, Vege, Sunitha, Mah, Helen H, Joseph, Abigail, Blout, Carrie L, Nguyen, Tiffany T, Lebo, Matthew S, Sidhu, Manpreet, Lomas-Francis, Christine, Kaufman, Richard M, Green, Robert C, Westhoff, Connie M

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A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xga von Lane, William J., Aguad, Maria, Smeland‐Wagman, Robin, Vege, Sunitha, Mah, Helen H., Joseph, Abigail, Blout, Carrie L., Nguyen, Tiffany T., Lebo, Matthew S., Sidhu, Manpreet, Lomas‐Francis, Christine, Kaufman, Richard M., Green, Robert C., Westhoff, Connie M., Bates, David W., Blout, Carrie, Christensen, Kurt D., Cirino, Allison L., Green, Robert C., Ho, Carolyn Y., Krier, Joel B., Lane, William J., Lehmann, Lisa S., MacRae, Calum A., Morton, Cynthia C., Perry, Denise L., Seidman, Christine E., Sunyaev, Shamil R., Vassy, Jason L., Schonman, Erica, Nguyen, Tiffany, Steffens, Eleanor, Betting, Wendi Nicole, Aronson, Samuel J., Ceyhan‐Birsoy, Ozge, Lebo, Matthew S., Machini, Kalotina, McLaughlin, Heather M., Azzariti, Danielle R., Rehm, Heidi L., Tsai, Ellen A., Blumenthal‐Barby, Jennifer, Feuerman, Lindsay Z., McGuire, Amy L., Lee, Kaitlyn, Robinson, Jill O., Slashinski, Melody J., Diamond, Pamela M., Davis, Kelly, Ubel, Peter A., Kraft, Peter, Scott Roberts, J., Garber, Judy E., Hambuch, Tina, Murray, Michael F., Kohane, Isaac, Kong, Sek Won

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Automatic Identification of Interictal Epileptiform Discharges with the Use of Complex Networks von Tomanik, Gustavo H., Betting, Luiz E., Campanharo, Andriana S. L. O.

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Reconciling newborn screening and a novel splice variant in BTD associated with partial biotinidase deficiency: a BabySeq Project case report von Murry, Jaclyn B, Machini, Kalotina, Ceyhan-Birsoy, Ozge, Kritzer, Amy, Krier, Joel B, Lebo, Matthew S, Fayer, Shawn, Genetti, Casie A, VanNoy, Grace E, Yu, Timothy W, Agrawal, Pankaj B, Parad, Richard B, Holm, Ingrid A, McGuire, Amy L, Green, Robert C, Beggs, Alan H, Rehm, Heidi L

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Use of Complex Networks for the Automatic Detection and the Diagnosis of Alzheimer's Disease von Pineda, Aruane Mello, Ramos, Fernando M., Betting, Luiz Eduardo, Campanharo, Andriana S. L. O.

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