Wrapping nodes in a drawing canvas von Hoyer, Crystal L, Dayen, Anna, Gerton, David M, Schorr, Janet L, Sherman, Scott A

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Wrapping nodes in a drawing canvas von DAYEN ANNA, SCHORR JANET L, HOYER CRYSTAL L, SHERMAN SCOTT A, GERTON DAVID M

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Wrapping nodes in a drawing canvas von DAYEN ANNA, SCHORR JANET L, HOYER CRYSTAL L, SHERMAN SCOTT A, GERTON DAVID M

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Integrative structure and functional anatomy of a nuclear pore complex von Kim, Seung Joong, Fernandez-Martinez, Javier, Nudelman, Ilona, Shi, Yi, Zhang, Wenzhu, Raveh, Barak, Herricks, Thurston, Slaughter, Brian D., Hogan, Joanna A., Upla, Paula, Chemmama, Ilan E., Pellarin, Riccardo, Echeverria, Ignacia, Shivaraju, Manjunatha, Chaudhury, Azraa S., Wang, Junjie, Williams, Rosemary, Unruh, Jay R., Greenberg, Charles H., Jacobs, Erica Y., Yu, Zhiheng, de la Cruz, M. Jason, Mironska, Roxana, Stokes, David L., Aitchison, John D., Jarrold, Martin F., Gerton, Jennifer L., Ludtke, Steven J., Akey, Christopher W., Chait, Brian T., Sali, Andrej, Rout, Michael P.

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The structure, function and evolution of a complete human chromosome 8 von Logsdon, Glennis A., Vollger, Mitchell R., Hsieh, PingHsun, Mao, Yafei, Liskovykh, Mikhail A., Koren, Sergey, Nurk, Sergey, Mercuri, Ludovica, Dishuck, Philip C., Rhie, Arang, de Lima, Leonardo G., Dvorkina, Tatiana, Porubsky, David, Harvey, William T., Mikheenko, Alla, Bzikadze, Andrey V., Kremitzki, Milinn, Graves-Lindsay, Tina A., Jain, Chirag, Hoekzema, Kendra, Murali, Shwetha C., Munson, Katherine M., Baker, Carl, Sorensen, Melanie, Lewis, Alexandra M., Surti, Urvashi, Gerton, Jennifer L., Larionov, Vladimir, Ventura, Mario, Miga, Karen H., Phillippy, Adam M., Eichler, Evan E.

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The variation and evolution of complete human centromeres von Logsdon, Glennis A., Rozanski, Allison N., Ryabov, Fedor, Potapova, Tamara, Shepelev, Valery A., Catacchio, Claudia R., Porubsky, David, Mao, Yafei, Yoo, DongAhn, Rautiainen, Mikko, Koren, Sergey, Nurk, Sergey, Lucas, Julian K., Hoekzema, Kendra, Munson, Katherine M., Gerton, Jennifer L., Phillippy, Adam M., Ventura, Mario, Alexandrov, Ivan A., Eichler, Evan E.

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Heterogeneous optoelectronic characteristics of Si micropillar arrays fabricated by metal-assisted chemical etching von Qian, Yang, Magginetti, David J., Jeon, Seokmin, Yoon, Yohan, Olsen, Tony L., Wang, Maoji, Gerton, Jordan M., Yoon, Heayoung P.

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The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes von Montgomery, Stephen B, Goode, David L, Kvikstad, Erika, Albers, Cornelis A, Zhang, Zhengdong D, Mu, Xinmeng Jasmine, Ananda, Guruprasad, Howie, Bryan, Karczewski, Konrad J, Smith, Kevin S, Anaya, Vanessa, Richardson, Rhea, Davis, Joe, MacArthur, Daniel G, Sidow, Arend, Duret, Laurent, Gerstein, Mark, Makova, Kateryna D, Marchini, Jonathan, McVean, Gil, Lunter, Gerton

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Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas von Palles, Claire, Cazier, Jean-Baptiste, Howarth, Kimberley M, Domingo, Enric, Jones, Angela M, Broderick, Peter, Kemp, Zoe, Spain, Sarah L, Guarino, Estrella, Salguero, Israel, Sherborne, Amy, Chubb, Daniel, Carvajal-Carmona, Luis G, Ma, Yusanne, Kaur, Kulvinder, Dobbins, Sara, Barclay, Ella, Gorman, Maggie, Martin, Lynn, Kovac, Michal B, Humphray, Sean, Lucassen, Anneke, Holmes, Christopher C, Bentley, David, Donnelly, Peter, Taylor, Jenny, Petridis, Christos, Roylance, Rebecca, Sawyer, Elinor J, Kerr, David J, Clark, Susan, Grimes, Jonathan, Kearsey, Stephen E, Thomas, Huw J W, McVean, Gilean, Houlston, Richard S, Tomlinson, Ian

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The bonobo genome compared with the chimpanzee and human genomes von Prüfer, Kay, Munch, Kasper, Hellmann, Ines, Akagi, Keiko, Miller, Jason R., Walenz, Brian, Koren, Sergey, Sutton, Granger, Kodira, Chinnappa, Winer, Roger, Knight, James R., Mullikin, James C., Meader, Stephen J., Ponting, Chris P., Lunter, Gerton, Higashino, Saneyuki, Hobolth, Asger, Dutheil, Julien, Karakoç, Emre, Alkan, Can, Sajjadian, Saba, Catacchio, Claudia Rita, Ventura, Mario, Marques-Bonet, Tomas, Eichler, Evan E., André, Claudine, Atencia, Rebeca, Mugisha, Lawrence, Junhold, Jörg, Patterson, Nick, Siebauer, Michael, Good, Jeffrey M., Fischer, Anne, Ptak, Susan E., Lachmann, Michael, Symer, David E., Mailund, Thomas, Schierup, Mikkel H., Andrés, Aida M., Kelso, Janet, Pääbo, Svante

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Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel von Delaneau, Olivier, Marchini, Jonathan

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Inaugurating High-Throughput Profiling of Extracellular Vesicles for Earlier Ovarian Cancer Detection von Jo, Ala, Green, Allen, Medina, Jamie E, Iyer, Sonia, Ohman, Anders W, McCarthy, Eric T, Reinhardt, Ferenc, Gerton, Thomas, Demehin, Daniel, Mishra, Ranjan, Kolin, David L, Zheng, Hui, Cheon, Jinwoo, Crum, Christopher P, Weinberg, Robert A, Rueda, Bo R, Castro, Cesar M, Dinulescu, Daniela M, Lee, Hakho

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Recessive mutations in SPTBN2 implicate β-III spectrin in both cognitive and motor development von Lise, Stefano, Clarkson, Yvonne, Perkins, Emma, Kwasniewska, Alexandra, Sadighi Akha, Elham, Schnekenberg, Ricardo Parolin, Suminaite, Daumante, Hope, Jilly, Baker, Ian, Gregory, Lorna, Green, Angie, Allan, Chris, Lamble, Sarah, Jayawant, Sandeep, Quaghebeur, Gerardine, Cader, M Zameel, Hughes, Sarah, Armstrong, Richard J E, Kanapin, Alexander, Rimmer, Andrew, Lunter, Gerton, Mathieson, Iain, Cazier, Jean-Baptiste, Buck, David, Taylor, Jenny C, Bentley, David, McVean, Gilean, Donnelly, Peter, Knight, Samantha J L, Jackson, Mandy, Ragoussis, Jiannis, Németh, Andrea H

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Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis von Sharma, Vikram P, Fenwick, Aimée L, Brockop, Mia S, McGowan, Simon J, Goos, Jacqueline A C, Hoogeboom, A Jeannette M, Brady, Angela F, Jeelani, Nu Owase, Lynch, Sally Ann, Mulliken, John B, Murray, Dylan J, Phipps, Julie M, Sweeney, Elizabeth, Tomkins, Susan E, Wilson, Louise C, Bennett, Sophia, Cornall, Richard J, Broxholme, John, Kanapin, Alexander, Johnson, David, Wall, Steven A, van der Spek, Peter J, Mathijssen, Irene M J, Maxson, Robert E, Twigg, Stephen R F, Wilkie, Andrew O M

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Development of a Patient-Derived 3D Immuno-Oncology Platform to Potentiate Immunotherapy Responses in Ascites-Derived Circulating Tumor Cells von Gerton, Thomas J, Green, Allen, Campisi, Marco, Chen, Minyue, Gjeci, Iliana, Mahadevan, Navin, Lee, Catherine A A, Mishra, Ranjan, Vo, Ha V, Haratani, Koji, Li, Ze-Hua, Hasselblatt, Kathleen T, Testino, Bryanna, Connor, Trevor, Lian, Christine G, Elias, Kevin M, Lizotte, Patrick, Ivanova, Elena V, Barbie, David A, Dinulescu, Daniela M

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Novel Type IV Secretion System Involved in Propagation of Genomic Islands von JUHAS, Mario, CROOK, Derrick W, DIMOPOULOU, Ioanna D, LUNTER, Gerton, HARDING, Rosalind M, FERGUSON, David J. P, HOOD, Derek W

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Whole-genome sequencing of bladder cancers reveals somatic CDKN1A mutations and clinicopathological associations with mutation burden von Cazier, J. -B., Rao, S. R., McLean, C. M., Walker, A. K., Wright, B. J., Jaeger, E. E. M., Kartsonaki, C., Marsden, L., Yau, C., Camps, C., Kaisaki, P., Taylor, J., Catto, J. W., Tomlinson, I. P. M., Kiltie, A. E., Hamdy, F. C.

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Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability von Twigg, Stephen R.F., Forecki, Jennifer, Goos, Jacqueline A.C., Richardson, Ivy C.A., Hoogeboom, A. Jeannette M., van den Ouweland, Ans M.W., Swagemakers, Sigrid M.A., Lequin, Maarten H., Van Antwerp, Daniel, McGowan, Simon J., Westbury, Isabelle, Miller, Kerry A., Wall, Steven A., van der Spek, Peter J., Mathijssen, Irene M.J., Pauws, Erwin, Merzdorf, Christa S., Wilkie, Andrew O.M.

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Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders von van Schouwenburg, Pauline A, Davenport, Emma E, Kienzler, Anne-Kathrin, Marwah, Ishita, Wright, Benjamin, Lucas, Mary, Malinauskas, Tomas, Martin, Hilary C, Lockstone, Helen E, Cazier, Jean-Baptiste, Chapel, Helen M, Knight, Julian C, Patel, Smita Y

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Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I von Babbs, C., Roberts, N. A., Sanchez-Pulido, L., McGowan, S. J., Ahmed, M. R., Brown, J. M., Sabry, M. A., Bentley, D. R., McVean, G. A., Donnelly, P., Gileadi, O., Ponting, C. P., Higgs, D. R., Buckle, V. J.

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