Somatic variants in diverse genes leads to a spectrum of focal cortical malformations von Lai, Dulcie, Gade, Meethila, Yang, Edward, Koh, Hyun Yong, Lu, Jinfeng, Walley, Nicole M, Buckley, Anne F, Sands, Tristan T, Akman, Cigdem I, Mikati, Mohamad A, McKhann, Guy M, Goldman, James E, Canoll, Peter, Alexander, Allyson L, Park, Kristen L, Von Allmen, Gretchen K, Rodziyevska, Olga, Bhattacharjee, Meenakshi B, Lidov, Hart G W, Vogel, Hannes, Grant, Gerald A, Porter, Brenda E, Poduri, Annapurna H, Crino, Peter B, Heinzen, Erin L

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The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures von Burgess, Rosemary, Wang, Shuyu, McTague, Amy, Boysen, Katja E., Yang, Xiaoling, Zeng, Qi, Myers, Kenneth A., Rochtus, Anne, Trivisano, Marina, Gill, Deepak, Sadleir, Lynette G., Specchio, Nicola, Guerrini, Renzo, Marini, Carla, Zhang, Yue‐Hua, Mefford, Heather C., Kurian, Manju A., Poduri, Annapurna H., Scheffer, Ingrid E.

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Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy von Winawer, Melodie R., Griffin, Nicole G., Samanamud, Jorge, Baugh, Evan H., Rathakrishnan, Dinesh, Ramalingam, Senthilmurugan, Zagzag, David, Schevon, Catherine A., Dugan, Patricia, Hegde, Manu, Sheth, Sameer A., McKhann, Guy M., Doyle, Werner K., Grant, Gerald A., Porter, Brenda E., Mikati, Mohamad A., Muh, Carrie R., Malone, Colin D., Bergin, Ann Marie R., Peters, Jurriaan M., McBrian, Danielle K., Pack, Alison M., Akman, Cigdem I., LaCoursiere, Christopher M., Keever, Katherine M., Madsen, Joseph R., Yang, Edward, Lidov, Hart G. W., Shain, Catherine, Allen, Andrew S., Canoll, Peter D., Crino, Peter B., Poduri, Annapurna H., Heinzen, Erin L.

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Genetic Determinants of Sudden Unexpected Death in Pediatrics von Koh, Hyun Yong, Haghighi, Alireza, Keywan, Christine, Alexandrescu, Sanda, Plews-Ogan, Erin, Haas, Elisabeth A., Brownstein, Catherine A., Vargas, Sara O., Haynes, Robin L., Berry, Gerard T., Holm, Ingrid A., Poduri, Annapurna H., Goldstein, Richard D.

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De novo missense variants in HDAC3 leading to epigenetic machinery dysfunction are associated with a variable neurodevelopmental disorder von Yoon, Jihoon G., Lim, Seong-Kyun, Seo, Hoseok, Lee, Seungbok, Cho, Jaeso, Kim, Soo Yeon, Koh, Hyun Yong, Poduri, Annapurna H., Ramakumaran, Vijayalakshmi, Vasudevan, Pradeep, de Groot, Martijn J., Ko, Jung Min, Han, Dohyun, Chae, Jong-Hee, Lee, Chul-Hwan

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SCN1A variants associated with sudden infant death syndrome von Brownstein, Catherine A., Goldstein, Richard D., Thompson, Christopher H., Haynes, Robin L., Giles, Emma, Sheidley, Beth, Bainbridge, Matthew, Haas, Elisabeth A., Mena, Othon J., Lucas, Jonathan, Schaber, Bethann, Holm, Ingrid A., George, Alfred L., Kinney, Hannah C., Poduri, Annapurna H.

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Zebrafish models of candidate human epilepsy-associated genes provide evidence of hyperexcitability von LaCoursiere, Christopher Mark, Ullmann, Jeremy F.P., Koh, Hyun Yong, Turner, Laura, Baker, Cristina M., Robens, Barbara, Shao, Wanqing, Rotenberg, Alexander, McGraw, Christopher M., Poduri, Annapurna H.

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The fundamental need for unifying phenotypes in sudden unexpected pediatric deaths von Wojcik, Monica H, Poduri, Annapurna H, Holm, Ingrid A, MacRae, Calum A, Goldstein, Richard D

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Hippocampal Formation Maldevelopment and Sudden Unexpected Death across the Pediatric Age Spectrum von Kinney, Hannah C., Poduri, Annapurna H., Cryan, Jane B., Haynes, Robin L., Teot, Lisa, Sleeper, Lynn A., Holm, Ingrid A., Berry, Gerald T., Prabhu, Sanjay P., Warfield, Simon K., Brownstein, Catherine, Abram, Harry S., Kruer, Michael, Kemp, Walter L., Hargitai, Beata, Gastrang, Joanne, Mena, Othon J., Haas, Elisabeth A., Dastjerdi, Roya, Armstrong, Dawna D., Goldstein, Richard D.

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Genetic Factors Underlying Sudden Infant Death Syndrome von Keywan, Christine, Poduri, Annapurna H, Goldstein, Richard D, Holm, Ingrid A

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The role of sodium channels in sudden unexpected death in pediatrics von Rochtus, Anne M., Goldstein, Richard D., Holm, Ingrid A., Brownstein, Catherine A., Pérez‐Palma, Eduardo, Haynes, Robin, Lal, Dennis, Poduri, Annapurna H.

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Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age von Brownstein, Catherine A., Douard, Elise, Haynes, Robin L., Koh, Hyun Yong, Haghighi, Alireza, Keywan, Christine, Martin, Bree, Alexandrescu, Sanda, Haas, Elisabeth A., Vargas, Sara O., Wojcik, Monica H., Jacquemont, Sébastien, Poduri, Annapurna H., Goldstein, Richard D., Holm, Ingrid A.

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Utility of Exome Sequencing for Diagnosis in Unexplained Pediatric-Onset Epilepsy von Koh, Hyun Yong, Smith, Lacey, Wiltrout, Kimberly N, Podury, Archana, Chourasia, Nitish, D'Gama, Alissa M, Park, Meredith, Knight, Devon, Sexton, Emma L, Koh, Julia J, Oby, Brandon, Pinsky, Rebecca, Shao, Diane D, French, Courtney E, Shao, Wanqing, Rockowitz, Shira, Sliz, Piotr, Zhang, Bo, Mahida, Sonal, Moufawad El Achkar, Christelle, Yuskaitis, Christopher J, Olson, Heather E, Sheidley, Beth Rosen, Poduri, Annapurna H

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Mutations in NRXN1 and NRXN2 in a patient with early-onset epileptic encephalopathy and respiratory depression von Rochtus, Anne M, Trowbridge, Sara, Goldstein, Richard D, Sheidley, Beth Rosen, Prabhu, Sanjay P, Haynes, Robin, Kinney, Hannah C, Poduri, Annapurna H

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Writer Dependent Offline Signature Verification Based on Cluster-Specific Classifier von H, Annapurna, K S, Manjunatha, D S, Guru

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The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures

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The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures von Burgess, Rosemary, Wang, Shuyu, McTague, Amy, Boysen, Katja E, Yang, Xiaoling, Zeng, Qi, Myers, Kenneth A, Rochtus, Anne, Trivisano, Marina, Gill, Deepak, Sadleir, Lynette G, Specchio, Nicola, Guerrini, Renzo, Marini, Carla, Zhang, Yue-Hua, Mefford, Heather C, Kurian, Manju A, Poduri, Annapurna H, Scheffer, Ingrid E

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MTKD: An Algorithm for Multi-Tier Key Distribution for Securing Group Communication in WSN von H S, Annapurna, Siddappa, M.

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A Survey on Security Techniques in Group Communication for Wireless Sensor Networks von Annapurna, H S, Siddappa, M

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Interval-Valued Writer-Dependent Global Features for Off-line Signature Verification von Manjunatha, K. S., Guru, D. S., Annapurna, H.

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