Structural variation and its potential impact on genome instability: Novel discoveries in the EGFR landscape by long-read sequencing von Cook, George W., Benton, Michael G., Akerley, Wallace, Mayhew, George F., Moehlenkamp, Cynthia, Raterman, Denise, Burgess, Daniel L., Rowell, William J., Lambert, Christine, Eng, Kevin, Gu, Jenny, Baybayan, Primo, Fussell, John T., Herboldl, Heath D., O'Shea, John M., Varghese, Thomas K., Emerson, Lyska L.

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Genetic Perturbation of the Maize Methylome von Li, Qing, Eichten, Steven R., Hermanson, Peter J., Zaunbrecher, Virginia M., Song, Jawon, Wendt, Jennifer, Rosenbaum, Heidi, Madzima, Thelma F., Sloan, Amy E., Huang, Ji, Burgess, Daniel L., Richmond, Todd A., McGinnis, Karen M., Meeley, Robert B., Danilevskaya, Olga N., Vaughn, Matthew W., Kaeppler, Shawn M., Jeddeloh, Jeffrey A., Springer, Nathan M.

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Alu element in the RNA binding motif protein, X-linked 2 (RBMX2) gene found to be linked to bipolar disorder von Laine, Pia, Rowell, William J., Paulin, Lars, Kujawa, Steve, Raterman, Denise, Mayhew, George, Wendt, Jennifer, Burgess, Daniel L., Partonen, Timo, Paunio, Tiina, Auvinen, Petri, Ekholm, Jenny M.

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Genomic targets for high-resolution inference of kinship, ancestry and disease susceptibility in orang-utans (genus: Pongo) von Banes, Graham L., Fountain, Emily D., Karklus, Alyssa, Huang, Hao-Ming, Jang-Liaw, Nian-Hong, Burgess, Daniel L., Wendt, Jennifer, Moehlenkamp, Cynthia, Mayhew, George F.

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LINE-1 Mediated Insertion into Poc1a (Protein of Centriole 1 A) Causes Growth Insufficiency and Male Infertility in Mice von Geister, Krista A, Brinkmeier, Michelle L, Cheung, Leonard Y, Wendt, Jennifer, Oatley, Melissa J, Burgess, Daniel L, Kozloff, Kenneth M, Cavalcoli, James D, Oatley, Jon M, Camper, Sally A

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Tracking Cancer Evolution Reveals Constrained Routes to Metastases: TRACERx Renal von Turajlic, Samra, Xu, Hang, Litchfield, Kevin, Rowan, Andrew, Chambers, Tim, Lopez, Jose I., Nicol, David, O’Brien, Tim, Larkin, James, Horswell, Stuart, Stares, Mark, Au, Lewis, Jamal-Hanjani, Mariam, Challacombe, Ben, Chandra, Ashish, Hazell, Steve, Eichler-Jonsson, Claudia, Soultati, Aspasia, Chowdhury, Simon, Rudman, Sarah, Lynch, Joanna, Fernando, Archana, Stamp, Gordon, Nye, Emma, Jabbar, Faiz, Spain, Lavinia, Lall, Sharanpreet, Guarch, Rosa, Falzon, Mary, Proctor, Ian, Pickering, Lisa, Gore, Martin, Watkins, Thomas B.K., Ward, Sophia, Stewart, Aengus, DiNatale, Renzo, Becerra, Maria F., Reznik, Ed, Hsieh, James J., Richmond, Todd A., Mayhew, George F., Hill, Samantha M., McNally, Catherine D., Jones, Carol, Rosenbaum, Heidi, Stanislaw, Stacey, Burgess, Daniel L., Alexander, Nelson R., Swanton, Charles

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Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10 von Ashizawa, Tetsuo, Matsuura, Tohru, Yamagata, Takanori, Burgess, Daniel L, Rasmussen, Astrid, Grewal, Raji P, Watase, Kei, Khajavi, Mehrdad, McCall, Alanna E, Davis, Caleb F, Zu, Lan, Achari, Madhureeta, Pulst, Stefan M, Alonso, Elisa, Noebels, Jeffrey L, Nelson, David L, Zoghbi, Huda Y

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Mutations in High-Voltage-Activated Calcium Channel Genes Stimulate Low-Voltage-Activated Currents in Mouse Thalamic Relay Neurons von Zhang, Yi, Mori, Mayra, Burgess, Daniel L, Noebels, Jeffrey L

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Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities von Bainbridge, Matthew N, Wang, Min, Wu, Yuanqing, Newsham, Irene, Muzny, Donna M, Jefferies, John L, Albert, Thomas J, Burgess, Daniel L, Gibbs, Richard A

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Targeted Bisulfite Sequencing Using the SeqCap Epi Enrichment System von Wendt, Jennifer, Rosenbaum, Heidi, Richmond, Todd A., Jeddeloh, Jeffrey A., Burgess, Daniel L.

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Whole exome capture in solution with 3 Gbp of data von Bainbridge, Matthew N, Wang, Min, Burgess, Daniel L, Kovar, Christie, Rodesch, Matthew J, D'Ascenzo, Mark, Kitzman, Jacob, Wu, Yuan-Qing, Newsham, Irene, Richmond, Todd A, Jeddeloh, Jeffrey A, Muzny, Donna, Albert, Thomas J, Gibbs, Richard A

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A Triplet Repeat Expansion Genetic Mouse Model of Infantile Spasms Syndrome, Arx(GCG)10+7, with Interneuronopathy, Spasms in Infancy, Persistent Seizures, and Adult Cognitive and B... von Price, Maureen G, Yoo, Jong W, Burgess, Daniel L, Deng, Fang, Hrachovy, Richard A, Frost, James D., Jr, Noebels, Jeffrey L

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Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functions von Meisler, Miriam H, Plummer, Nicholas W, Burgess, Daniel L, Buchner, David A, Sprunger, Leslie K

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Mutation of a new sodium channel gene, Scn8a , in the mouse mutant 'motor endplate disease' von Burgess, Daniel L, Kohrman, David C, Galt, James, Plummer, Nicholas W, Jones, Julie M, Spear, Brett, Meisler, Miriam H

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Loss of the Potassium Channel β‐Subunit Gene, KCNAB2, Is Associated with Epilepsy in Patients with 1p36 Deletion Syndrome von Heilstedt, Heidi A., Burgess, Daniel L., Anderson, Anne E., Chedrawi, Aziza, Tharp, Barry, Lee, Olivia, Kashork, Catherine D., Starkey, David E., Wu, Yuan‐Qing, Noebels, Jeffrey L., Shaffer, Lisa G., Shapira, Stuart K.

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Stargazin and Other Transmembrane AMPA Receptor Regulating Proteins Interact with Synaptic Scaffolding Protein MAGI-2 in Brain von Deng, Fang, Price, Maureen G, Davis, Caleb F, Mori, Mayra, Burgess, Daniel L

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Neonatal Epilepsy Syndromes and GEFS+: Mechanistic Considerations von Burgess, Daniel L.

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The α-Amino-3-hydroxyl-5-methyl-4-isoxazolepropionate Receptor Trafficking Regulator “Stargazin” Is Related to the Claudin Family of Proteins by Its Ability to Mediate Cell-Cell Ad... von Price, Maureen G., Davis, Caleb F., Deng, Fang, Burgess, Daniel L.

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Single gene defects in mice: the role of voltage-dependent calcium channels in absence models von Burgess, Daniel L., Noebels, Jeffrey L.

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Voltage-Dependent Calcium Channel Mutations in Neurological Disease von BURGESS, DANIEL L., NOEBELS, JEFFREY L.

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