Patient-tailored approach in tertiary care expert centres using individual dynamic network analysis von Houtveen, J H, de Vroege, L, van Eck van der Sluijs, J F, Elfeddali, I, Videler, A C, Lunter, C H, Kop, W J, Geenen, R

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Maatwerk in hoogspecialistische ggz met individuele dynamische netwerkanalyse von Houtveen, J. H, de Vroege, L, van Eck van der Sluijs, J. F, Elfeddali, I, Videler, A. C, Lunter, C. H, Kop, W. J, Geenen, R

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Using genomic scars to select immunotherapy beneficiaries in advanced non-small cell lung cancer von Donker, H. C., van Es, B., Tamminga, M., Lunter, G. A., van Kempen, L. C. L. T., Schuuring, E., Hiltermann, T. J. N., Groen, H. J. M.

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Reliability of panel-based mutational signatures for immune-checkpoint-inhibition efficacy prediction in non-small cell lung cancer von Donker, H.C., Cuppens, K., Froyen, G., Groen, H.J.M., Hiltermann, T.J.N., Maes, B., Schuuring, E., Volders, P.-J., Lunter, G.A., van Es, B.

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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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Activated leukocyte cell adhesion molecule (ALCAM/CD166/MEMD), a novel actor in invasive growth, controls matrix metalloproteinase activity von LUNTER, Pim C, VAN KILSDONK, Jeroen W. J, VAN BECK, Hanneke, CORNELISSEN, Ine M. H. A, BERGERS, Mieke, WILLEMS, Peter H. G. M, VAN MUIJEN, Goos N. P, SWART, Guido W. M

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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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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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NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease von Schwerd, T, Bryant, R V, Pandey, S, Capitani, M, Meran, L, Cazier, J-B, Jung, J, Mondal, K, Parkes, M, Mathew, C G, Fiedler, K, McCarthy, D J, Sullivan, P B, Rodrigues, A, Travis, S P L, Moore, C, Sambrook, J, Ouwehand, W H, Roberts, D J, Danesh, J, Russell, R K, Wilson, D C, Kelsen, J R, Cornall, R, Denson, L A, Kugathasan, S, Knaus, U G, Serra, E G, Anderson, C A, Duerr, R H, McGovern, D PB, Cho, J, Powrie, F, Li, V SW, Muise, A M, Uhlig, H H

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Reliability of panel-based mutational signatures for immune-checkpoint-inhibition efficacy prediction in non-small cell lung cancer von Donker, H. C, Cuppens, K, Froyen, G, Groen, H. J. M, Hiltermann, T. J. N, Maes, B, Schuuring, E, Volders, Pieter-Jan, Lunter, G. A, van Es, B

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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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Erythrocytosis associated with a novel missense mutation in the BPGM gene von Petousi, Nayia, Copley, Richard R, Lappin, Terence R J, Haggan, Sally E, Bento, Celeste M, Cario, Holger, Percy, Melanie J, Ratcliffe, Peter J, Robbins, Peter A, McMullin, Mary Frances

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Recessive Mutations in SPTBN2 Implicate [beta]-III Spectrin in Both Cognitive and Motor Development von Lise, Stefano, Clarkson, Yvonne, Perkins, Emma, Kwasniewska, Alexandra, Akha, Elham Sadighi, 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 JE, Kanapin, Alexander, Rimmer, Andrew, Lunter, Gerton, Mathieson, Iain, Cazier, Jean-Baptiste, Buck, David, Taylor, Jenny C, Bentley, David, McVean, Gilean, Donnelly, Peter, Knight, Samantha JL, Jackson, Mandy, Ragoussis, Jiannis, Németh, Andrea H

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Multinomial belief networks for healthcare data von Donker, H. C, Neijzen, D, de Jong, J, Lunter, G. A

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The bonobo genome comparedwith 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, Karakoc, 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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Factors influencing success of clinical genome sequencing across a broad spectrum of disorders von Taylor, JC, Martin, HC, Lise, S, Broxholme, J, Cazier, J-B, Rimmer, A, Kanapin, A, Lunter, G, Fiddy, S, Allan, C, Aricescu, AR, Attar, M, Babbs, C, Becq, J, Beeson, D, Bento, C, Bignell, P, Blair, E, Buckle, VJ, Bull, K, Cario, H, Chapel, H, Copley, RR, Cornall, R, Craft, J, Dahan, K, Davenport, EE, Dendrou, C, Devuyst, O, Fenwick, AL, Flint, J, Fugger, L, Gilbert, RD, Goriely, A, Green, A, Greger, IH, Grocock, R, Gruszczyk, AV, Hastings, R, Higgs, D, Holmes, C, Howard, M, Hughes, L, Humburg, P, Johnson, D, Karpe, F, Kingsbury, Z, Kini, U, Knight, JC, Krohn, J, Lamble, S, Langman, C, Lonie, L, Luck, J, McCarthy, D, McGowan, SJ, McMullin, MF, Miller, KA, Murray, L, Nemeth, AH, Nesbit, MA, Nutt, D, Ormondroyd, E, Oturai, AB, Pagnamenta, A, Patel, SY, Percy, M, Petousi, N, Piazza, P, Piret, SE, Polanco-Echeverry, G, Powrie, F, Pugh, C, Quek, L, Robbins, PA, Robson, K, Russo, A, Schuh, A, Silverman, E, Simmons, A, Sorensen, PS, Sweeney, E, Taylor, J, Thakker, RV, Tomlinson, I, Trebes, A, Twigg, SRF, Vyas, P, Vyse, T, Watkins, H, Whyte, MP, Witty, L, Wright, B, Buck, D, Humphray, S, Ratcliffe, PJ, Bell, JI, Bentley, D, Donnelly, P, McVean, G

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Multinomial belief networks for healthcare data von Donker, H C, Neijzen, D, de Jong, J, Lunter, G A

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Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases von Pagnamenta, AT, Camps, C, Giacopuzzi, E, Taylor, JM, Hashim, M, Calpena, E, Kaisaki, PJ, Hashimoto, A, Yu, J, Sanders, E, Schwessinger, R, Hughes, JR, Lunter, G, Dreau, H, Ferla, M, Lange, L, Kesim, Y, Ragoussis, V, Vavoulis, DV, Allroggen, H, Ansorge, O, Babbs, C, Banka, S, Baños-Piñero, B, Beeson, D, Ben-Ami, T, Bennett, DL, Bento, C, Blair, E, Brasch-Andersen, C, Bull, KR, Cario, H, Cilliers, D, Conti, V, Davies, EG, Dhalla, F, Dacal, BD, Dong, Y, Dunford, JE, Guerrini, R, Harris, AL, Hartley, J, Hollander, G, Javaid, K, Kane, M, Kelly, D, Knight, SJL, Kreins, AY, Kvikstad, EM, Langman, CB, Lester, T, Lines, KE, Lord, SR, Lu, X, Mansour, S, Manzur, A, Maroofian, R, Marsden, B, Mason, J, McGowan, SJ, Mei, D, Mlcochova, H, Murakami, Y, Németh, AH, Okoli, S, Ormondroyd, E, Ousager, LB, Palace, J, Patel, SY, Pentony, MM, Pugh, C, Rad, A, Ramesh, A, Riva, SG, Roberts, I, Roy, N, Salminen, O, Schilling, KD, Scott, C, Sen, A, Smith, C, Stevenson, M, Thakker, RV, Twigg, SRF, Uhlig, HH, van Wijk, R, Vona, B, Wall, S, Wang, J, Watkins, H, Zak, J, Schuh, AH, Kini, U, Wilkie, AOM, Popitsch, N, Taylor, JC

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Intercenter reproducibility of binary typing for Staphylococcus aureus von van Leeuwen, Willem B., Snoeijers, Sandor, van der Werken-Libregts, Christel, Tuip, Anita, van der Zee, Anneke, Egberink, Diane, de Proost, Monique, Bik, Elisabeth, Lunter, Bjorn, Kluytmans, Jan, Gits, Etty, van Duyn, Inge, Heck, Max, van der Zwaluw, Kim, Wannet, Wim, Noordhoek, Gerda T., Mulder, Sije, Renders, Nicole, Boers, Miranda, Zaat, Sebastiaan, van der Riet, Daniëlle, Kooistra, Mirjam, Talens, Adriaan, Dijkshoorn, Lenie, van der Reyden, Tanny, Veenendaal, Dick, Bakker, Nancy, Cookson, Barry, Lynch, Alisson, Witte, Wolfgang, Cuny, Christa, Blanc, Dominique, Vernez, Isabelle, Hryniewicz, Waleria, Fiett, Janusz, Struelens, Marc, Deplano, Ariane, Landegent, Jim, Verbrugh, Henri A., van Belkum, Alex

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Additional file 3 of Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases von Pagnamenta, Alistair T., Camps, Carme, Giacopuzzi, Edoardo, Taylor, John M., Hashim, Mona, Calpena, Eduardo, Kaisaki, Pamela J., Hashimoto, Akiko, Yu, Jing, Sanders, Edward, Schwessinger, Ron, Hughes, Jim R., Lunter, Gerton, Dreau, Helene, Ferla, Matteo, Lange, Lukas, Kesim, Yesim, Ragoussis, Vassilis, Vavoulis, Dimitrios V., Allroggen, Holger, Ansorge, Olaf, Babbs, Christian, Banka, Siddharth, Baños-Piñero, Benito, Beeson, David, Ben-Ami, Tal, Bennett, David L., Bento, Celeste, Blair, Edward, Brasch-Andersen, Charlotte, Bull, Katherine R., Cario, Holger, Cilliers, Deirdre, Conti, Valerio, Davies, E. Graham, Dhalla, Fatima, Dacal, Beatriz Diez, Dong, Yin, Dunford, James E., Guerrini, Renzo, Harris, Adrian L., Hartley, Jane, Hollander, Georg, Javaid, Kassim, Kane, Maureen, Kelly, Deirdre, Kelly, Dominic, Knight, Samantha J. L., Kreins, Alexandra Y., Kvikstad, Erika M., Langman, Craig B., Lester, Tracy, Lines, Kate E., Lord, Simon R., Lu, Xin, Mansour, Sahar, Manzur, Adnan, Maroofian, Reza, Marsden, Brian, Mason, Joanne, McGowan, Simon J., Mei, Davide, Mlcochova, Hana, Murakami, Yoshiko, Németh, Andrea H., Okoli, Steven, Ormondroyd, Elizabeth, Ousager, Lilian Bomme, Palace, Jacqueline, Patel, Smita Y., Pentony, Melissa M., Pugh, Chris, Rad, Aboulfazl, Ramesh, Archana, Riva, Simone G., Roberts, Irene, Roy, Noémi, Salminen, Outi, Schilling, Kyleen D., Scott, Caroline, Sen, Arjune, Smith, Conrad, Stevenson, Mark, Thakker, Rajesh V., Twigg, Stephen R. F., Uhlig, Holm H., van Wijk, Richard, Vona, Barbara, Wall, Steven, Wang, Jing, Watkins, Hugh, Zak, Jaroslav, Schuh, Anna H., Kini, Usha, Wilkie, Andrew O. M., Popitsch, Niko, Taylor, Jenny C.

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