Satellite inventory of Minnesota forest resources von Bauer, Marvin E., Burk, Thomas E., Ek, Alan R., Coppin, Pol R., Lime, Stephen D., Walsh, Terese A., Walters, David K., Befort, William, Heinzen, David F.

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Genome-wide mRNA expression correlates of viral control in CD4+ T-cells from HIV-1-infected individuals von Rotger, Margalida, Dang, Kristen K, Fellay, Jacques, Heinzen, Erin L, Feng, Sheng, Descombes, Patrick, Shianna, Kevin V, Ge, Dongliang, Günthard, Huldrych F, Goldstein, David B, Telenti, Amalio

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Mutations of the Sonic Hedgehog Pathway Underlie Hypothalamic Hamartoma with Gelastic Epilepsy von Hildebrand, Michael S., Griffin, Nicole G., Damiano, John A., Cops, Elisa J., Burgess, Rosemary, Ozturk, Ezgi, Jones, Nigel C., Leventer, Richard J., Freeman, Jeremy L., Harvey, A. Simon, Sadleir, Lynette G., Scheffer, Ingrid E., Major, Heather, Darbro, Benjamin W., Allen, Andrew S., Goldstein, David B., Kerrigan, John F., Berkovic, Samuel F., Heinzen, Erin L.

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De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies von Myers, Candace T., McMahon, Jacinta M., Schneider, Amy L., Petrovski, Slavé, Allen, Andrew S., Carvill, Gemma L., Zemel, Matthew, Saykally, Julia E., LaCroix, Amy J., Heinzen, Erin L., Hollingsworth, Georgina, Nikanorova, Marina, Corbett, Mark, Gecz, Jozef, Coman, David, Freeman, Jeremy, Calvert, Sophie, Gill, Deepak, Carney, Patrick, Lerman-Sagie, Tally, Sampaio, Hugo, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E., Epstein, Michael P., Glauser, Tracy, Johnson, Michael R., Kuzniecky, Ruben, Marson, Anthony G., O’Brien, Terence J., Ottman, Ruth, Petrou, Stephen, Poduri, Annapurna, Pickrell, William O., Chung, Seo-Kyung, Rees, Mark I., Sherr, Elliott, Sadleir, Lynette G., Goldstein, David B., Lowenstein, Daniel H., Møller, Rikke S., Berkovic, Samuel F., Scheffer, Ingrid E., Mefford, Heather C.

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The characterization of twenty sequenced human genomes von Pelak, Kimberly, Shianna, Kevin V, Ge, Dongliang, Maia, Jessica M, Zhu, Mingfu, Smith, Jason P, Cirulli, Elizabeth T, Fellay, Jacques, Dickson, Samuel P, Gumbs, Curtis E, Heinzen, Erin L, Need, Anna C, Ruzzo, Elizabeth K, Singh, Abanish, Campbell, C Ryan, Hong, Linda K, Lornsen, Katharina A, McKenzie, Alexander M, Sobreira, Nara L M, Hoover-Fong, Julie E, Milner, Joshua D, Ottman, Ruth, Haynes, Barton F, Goedert, James J, Goldstein, David B

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Rare Genetic Variation and Outcome of Surgery for Mesial Temporal Lobe Epilepsy von Perucca, Piero, Stanley, Kate, Harris, Natasha, McIntosh, Anne M., Asadi‐Pooya, Ali A., Mikati, Mohamad A., Andrade, Danielle M., Dugan, Patricia, Depondt, Chantal, Choi, Hyunmi, Heinzen, Erin L., Cavalleri, Gianpiero L., Buono, Russell J., Devinsky, Orrin, Sperling, Michael R., Berkovic, Samuel F., Delanty, Norman, Goldstein, David B., O'Brien, Terence J., Andrade, Danielle, Sen, Arjune, Bazil, Carl W., Boland, Michael, Cavalleri, Gianpiero, Choi, Hyunmi, Colombo, Sophie, Costello, Daniel, Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, Doherty, Colin Patrick, Dugan, Patricia, Frankel, Wayne, Goldstein, David, Heinzen, Erin, Johnson, Michael, Kwan, Patrick, Marson, Tony, McCormack, Mark, Mikati, Mohamad, O'Brien, Terry, Ottman, Ruth, Pandolfo, Massimo, Perucca, Piero, Petrovski, Slave, Radtke, Rodney, Rees, Mark, Sadoway, Tara, Valley, Nicole, Walley, Nicole, Wood, Nicholas, Zuberi, Sameer

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A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations von Zhu, Xiaolin, Padmanabhan, Raghavendra, Copeland, Brett, Bridgers, Joshua, Ren, Zhong, Kamalakaran, Sitharthan, O'Driscoll-Collins, Ailbhe, Berkovic, Samuel F, Scheffer, Ingrid E, Poduri, Annapurna, Mei, Davide, Guerrini, Renzo, Lowenstein, Daniel H, Allen, Andrew S, Heinzen, Erin L, Goldstein, David B

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Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributions von Green, Timothy E, Motelow, Joshua E, Bennett, Mark F, Ye, Zimeng, Bennett, Caitlin A, Griffin, Nicole G, Damiano, John A, Leventer, Richard J, Freeman, Jeremy L, Harvey, A Simon, Lockhart, Paul J, Sadleir, Lynette G, Boys, Amber, Scheffer, Ingrid E, Major, Heather, Darbro, Benjamin W, Bahlo, Melanie, Goldstein, David B, Kerrigan, John F, Heinzen, Erin L, Berkovic, Samuel F, Hildebrand, Michael S

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A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam von Campbell, Ciarán, McCormack, Mark, Patel, Sonn, Stapleton, Caragh, Bobbili, Dheeraj, Krause, Roland, Depondt, Chantal, Sills, Graeme J., Koeleman, Bobby P., Striano, Pasquale, Zara, Federico, Sander, Josemir W., Lerche, Holger, Kunz, Wolfram S., Stefansson, Kari, Stefansson, Hreinn, Doherty, Colin P., Heinzen, Erin L., Scheffer, Ingrid E., Goldstein, David B., O'Brien, Terence, Cotter, David, Berkovic, Samuel F., Sisodiya, Sanjay M., Delanty, Norman, Cavalleri, Gianpiero L.

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Complete Genome Sequence of the Q-Fever Pathogen Coxiella burnetii von Seshadri, Rekha, Paulsen, Ian T., Eisen, Jonathan A., Read, Timothy D., Nelson, Karen E., Nelson, William C., Ward, Naomi L., Tettelin, Hervé, Davidsen, Tanja M., Beanan, Maureen J., Deboy, Robert T., Daugherty, Sean C., Brinkac, Lauren M., Madupu, Ramana, Dodson, Robert J., Khouri, Hoda M., Lee, Kathy H., Carty, Heather A., Scanlan, David, Heinzen, Robert A., Thompson, Herbert A., Samuel, James E., Fraser, Claire M., Heidelberg, John F.

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A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB von Need, Anna C., Attix, Deborah K., McEvoy, Jill M., Cirulli, Elizabeth T., Linney, Kristen L., Hunt, Priscilla, Ge, Dongliang, Heinzen, Erin L., Maia, Jessica M., Shianna, Kevin V., Weale, Michael E., Cherkas, Lynn F., Clement, Gail, Spector, Tim D., Gibson, Greg, Goldstein, David B.

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Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies von Abou-Khalil, Bassel, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Balding, David J., Bast, Thomas, Baum, Larry, Becker, Albert J., Becker, Felicitas, Berghuis, Bianca, Berkovic, Samuel F., Boysen, Katja E., Bradfield, Jonathan P., Brody, Lawrence C., Buono, Russell J., Campbell, Ellen, Cascino, Gregory D., Catarino, Claudia B., Cavalleri, Gianpiero L., Cherny, Stacey S., Chinthapalli, Krishna, Coffey, Alison J., Compston, Alastair, Coppola, Antonietta, Cossette, Patrick, Craig, John J., de Haan, Gerrit-Jan, De Jonghe, Peter, de Kovel, Carolien G. F., Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, Dlugos, Dennis J., Doherty, Colin P., Elger, Christian E., Eriksson, Johan G., Ferraro, Thomas N., Feucht, Martha, Francis, Ben, Franke, Andre, French, Jacqueline A., Freytag, Saskia, Gaus, Verena, Geller, Eric B., Gieger, Christian, Glauser, Tracy, Glynn, Simon, Goldstein, David B., Gui, Hongsheng, Guo, Youling, Haas, Kevin F., Hakonarson, Hakon, Hallmann, Kerstin, Haut, Sheryl, Heinzen, Erin L., Helbig, Ingo, Hengsbach, Christian, Hjalgrim, Helle, Iacomino, Michele, Ingason, Andrés, Jamnadas-Khoda, Jennifer, Johnson, Michael R., Kälviäinen, Reetta, Kantanen, Anne-Mari, Kasperavičiūte, Dalia, Kasteleijn-Nolst Trenite, Dorothee, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Krause, Roland, Krenn, Martin, Kunz, Wolfram S., Kuzniecky, Ruben, Kwan, Patrick, Lal, Dennis, Lau, Yu-Lung, Lehesjoki, Anna-Elina, Lerche, Holger, Leu, Costin, Lieb, Wolfgang, Lindhout, Dick, Lo, Warren D., Lopes-Cendes, Iscia, Lowenstein, Daniel H., Malovini, Alberto, Marson, Anthony G., Mayer, Thomas, McCormack, Mark, Mills, James L., Mirza, Nasir, Moerzinger, Martina, Møller, Rikke S., Molloy, Anne M., Muhle, Hiltrud, Newton, Mark, Ng, Ping-Wing, Nöthen, Markus M., Nürnberg, Peter, O’Brien, Terence J., Oliver, Karen L.

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Somatic variants as a cause of drug‐resistant epilepsy including mesial temporal lobe epilepsy with hippocampal sclerosis von Carton, Robert J., Doyle, Michael G., Kearney, Hugh, Steward, Charles A., Lench, Nicholas J., Rogers, Anthony, Heinzen, Erin L., McDonald, Seamus, Fay, Joanna, Lacey, Austin, Beausang, Alan, Cryan, Jane, Brett, Francesca, El‐Naggar, Hany, Widdess‐Walsh, Peter, Costello, Daniel, Kilbride, Ronan, Doherty, Colin P., Sweeney, Kieron J., O'Brien, Donncha F., Henshall, David C., Delanty, Norman, Cavalleri, Gianpiero L., Benson, Katherine A.

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De Novo Mutations in PPP3CA Cause Severe Neurodevelopmental Disease with Seizures von Myers, Candace T., Stong, Nicholas, Mountier, Emily I., Helbig, Katherine L., Freytag, Saskia, Sullivan, Joseph E., Ben Zeev, Bruria, Nissenkorn, Andreea, Tzadok, Michal, Heimer, Gali, Shinde, Deepali N., Rezazadeh, Arezoo, Regan, Brigid M., Oliver, Karen L., Ernst, Michelle E., Lippa, Natalie C., Mulhern, Maureen S., Ren, Zhong, Poduri, Annapurna, Andrade, Danielle M., Bird, Lynne M., Bahlo, Melanie, Berkovic, Samuel F., Lowenstein, Daniel H., Scheffer, Ingrid E., Sadleir, Lynette G., Goldstein, David B., Mefford, Heather C., Heinzen, Erin L.

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Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery von Oliver, Karen L., Ellis, Colin A., Scheffer, Ingrid E., Ganesan, Shiva, Leu, Costin, Sadleir, Lynette G., Heinzen, Erin L., Mefford, Heather C., Bass, Andrew J., Curtis, Sarah W., Harris, Rebekah V., Whiteman, David C., Helbig, Ingo, Ottman, Ruth, Epstein, Michael P., Bahlo, Melanie, Berkovic, Samuel F.

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The Genetics of Neuropsychiatric Diseases: Looking In and Beyond the Exome von Heinzen, Erin L, Neale, Benjamin M, Traynelis, Stephen F, Allen, Andrew S, Goldstein, David B

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Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies von Anon

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Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects von Niestroj, Lisa-Marie, Perez-Palma, Eduardo, Howrigan, Daniel P, Zhou, Yadi, Cheng, Feixiong, Saarentaus, Elmo, Nürnberg, Peter, Stevelink, Remi, Daly, Mark J, Palotie, Aarno, Lal, Dennis

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The Epilepsy Genetics Initiative: Systematic reanalysis of diagnostic exomes increases yield von Berkovic, Samuel F., Goldstein, David B., Heinzen, Erin L., Laughlin, Brandon L., Lowenstein, Daniel H., Lubbers, Laura, Stewart, Randall, Whittemore, Vicky, Angione, Kaitlin, Bazil, Carl W., Bier, Louise, Bluvstein, Judith, Brimble, Elise, Campbell, Colleen, Cavalleri, Gianpiero, Chambers, Chelsea, Choi, Hyunmi, Cilio, Maria Roberta, Ciliberto, Michael, Cornes, Susannah, Delanty, Norman, Demarest, Scott, Devinsky, Orrin, Dlugos, Dennis, Dubbs, Holly, Dugan, Patricia, Ernst, Michelle E., Gibbons, Melissa, Goodkin, Howard P., Helbig, Ingo, Jansen, Laura, Johnson, Kaleas, Joshi, Charuta, Lippa, Natalie C., Marsh, Eric, Martinez, Alejandro, Millichap, John, Mulhern, Maureen S., Numis, Adam, Park, Kristen, Pippucci, Tommaso, Poduri, Annapurna, Porter, Brenda, Regan, Brigid, Sands, Tristan T., Scheffer, Ingrid E., Schreiber, John M., Sheidley, Beth, Singhal, Nilika, Smith, Lacey, Sullivan, Joseph, Taylor, Alan, Tolete, Patricia, Afgani, Tahseen M., Aggarwal, Vimla, Burgess, Rosemary, Dixon‐Salazar, Tracy, Hemati, Parisa, Milder, Julie, Petrovski, Slavé, Revah‐Politi, Anya, Stong, Nicholas

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A roadmap for precision medicine in the epilepsies von Anon

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