The AURORA initiative for metastatic breast cancer von Zardavas, D, Maetens, M, Irrthum, A, Goulioti, T, Engelen, K, Fumagalli, D, Salgado, R, Aftimos, P, Saini, K S, Sotiriou, C, Campbell, P, Dinh, P, von Minckwitz, G, Gelber, R D, Dowsett, M, Di Leo, A, Cameron, D, Baselga, J, Gnant, M, Goldhirsch, A, Norton, L, Piccart, M

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Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema von Mendola, A., Schlögel, M.J., Ghalamkarpour, A., Irrthum, A., Nguyen, H.L., Fastré, E., Bygum, A., van der Vleuten, C., Fagerberg, C., Baselga, E., Quere, I., Mulliken, J.B., Boon, L.M., Brouillard, P., Vikkula, M.

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First report of AURORA, the breast international group (BIG) molecular screening initiative for metastatic breast cancer (MBC) patients (pts) von Aftimos, P.G., Antunes De Melo e Oliveira, A.M., Hilbers, F., Venet, D., Vingiani, A., Nili Gal Yam, E., Martinez, J.L., Ndozeng, J., Irrthum, A., Piccart, M.

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Wisdom of crowds for robust gene network inference von Marbach, Daniel, Costello, James C, Küffner, Robert, Vega, Nicole M, Prill, Robert J, Camacho, Diogo M, Allison, Kyle R, Kellis, Manolis, Collins, James J, Stolovitzky, Gustavo

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Multiple mechanisms are implicated in the generation of 5q35 microdeletions in Sotos syndrome von Tatton-Brown, K, Douglas, J, Coleman, K, Baujat, G, Chandler, K, Clarke, A, Collins, A, Davies, S, Faravelli, F, Firth, H, Garrett, C, Hughes, H, Kerr, B, Liebelt, J, Reardon, W, Schaefer, G B, Splitt, M, Temple, I K, Waggoner, D, Weaver, D D, Wilson, L, Cole, T, Cormier-Daire, V, Irrthum, A, Rahman, N

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Partial NSD1 deletions cause 5% of Sotos syndrome and are readily identifiable by multiplex ligation dependent probe amplification von Douglas, J, Tatton-Brown, K, Coleman, K, Guerrero, S, Berg, J, Cole, T R P, FitzPatrick, D, Gillerot, Y, Hughes, H E, Pilz, D, Raymond, F L, Temple, I K, Irrthum, A, Schouten, J P, Rahman, N

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Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B von Méhes, Károly, Shannon, Nora, FitzPatrick, David, Reid, Sarah, Douglas, Jenny, Firth, Helen, Plaja, Alberto, Robin, Nathanial, Irrthum, Alexandre, Nash, Richard, Tolmie, John, Kidd, Alexa, Swansbury, John, Coleman, Kim, Hanks, Sandra, Rahman, Nazneen

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341MO Impact of aging on the genetic and transcriptional landscape of advanced breast cancer: an AURORA program (BIG 14-01) subanalysis von Zoppoli, G., Ravera, F., Santaniello, F., Ferrando, L., Venet, D., Seoane, J.A., Richard, F., Munzone, E., Hatse, S., Ballestrero, A., Crestani, T. Antoniolli, Adam, V.S., Irrthum, A., Aftimos, P.G., Zotano, A.L. Guerrero, Cameron, D.A., Piccart, M., Desmedt, C., Benelli, M., Wildiers, H.

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Mutations in the Transcription Factor Gene SOX18 Underlie Recessive and Dominant Forms of Hypotrichosis-Lymphedema-Telangiectasia von Irrthum, Alexandre, Devriendt, Koenraad, Chitayat, David, Matthijs, Gert, Glade, Conrad, Steijlen, Peter M., Fryns, Jean-Pierre, Van Steensel, Maurice A. M., Vikkula, Miikka

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Genotype-Phenotype Associations in Sotos Syndrome: An Analysis of 266 Individuals with NSD1 Aberrations von Tatton-Brown, Katrina, Douglas, Jenny, Coleman, Kim, Baujat, Geneviève, Cole, Trevor R.P., Das, Soma, Horn, Denise, Hughes, Helen E., Temple, I. Karen, Faravelli, Francesca, Waggoner, Darrel, Türkmen, Seval, Cormier-Daire, Valérie, Irrthum, Alexandre, Rahman, Nazneen

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152OFirst report of AURORA, the breast international group (BIG) molecular screening initiative for metastatic breast cancer (MBC) patients (pts) von Aftimos, P G, Antunes De Melo e Oliveira, A M, Hilbers, F, Venet, D, Vingiani, A, Nili Gal Yam, E, Martinez, J L, Ndozeng, J, Irrthum, A, Piccart, M

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Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase von Irrthum, Alexandre, Karkkainen, Marika J., Devriendt, Koen, Alitalo, Kari, Vikkula, Miikka

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The Breast International Group (BIG) AURORA pilot study for molecular screening in metastatic breast cancer (MBC) patients von Maetens, M., Irrthum, A., Loibl, S., Laes, J.F., Campbell, P., Aftimos, P., Thompson, A., Cortes Castan, J., Loi, S., Sotiriou, C.

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A Gene for Inherited Cutaneous Venous Anomalies (“Glomangiomas”) Localizes to Chromosome 1p21-22 von Boon, Laurence M., Brouillard, Pascal, Irrthum, Alexandre, Karttunen, Leena, Warman, Matthew L., Rudolph, Ross, Mulliken, John B., Olsen, Bjorn R., Vikkula, Miikka

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Myelin-derived lipids modulate macrophage activity by liver X receptor activation von Bogie, Jeroen F J, Timmermans, Silke, Huynh-Thu, Vân Anh, Irrthum, Alexandre, Smeets, Hubert J M, Gustafsson, Jan-Åke, Steffensen, Knut R, Mulder, Monique, Stinissen, Piet, Hellings, Niels, Hendriks, Jerome J A

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Linkage disequilibrium narrows locus for venous malformation with glomus cells (VMGLOM) to a single 1.48 Mbp YAC von Irrthum, A, Brouillard, P, Enjolras, O, Gibbs, N F, Eichenfield, L F, Olsen, B R, Mulliken, J B, Boon, L M, Vikkula, M

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Supplementary Material for: Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema von Mendola, A., Schlögel, M.J., Ghalamkarpour, A., Irrthum, A., Nguyen, H.L., Fastré, E., Bygum, A., Van Der Vleuten, C., Fagerberg, C., Baselga, E.

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Inferring regulatory networks from expression data using tree-based methods von Huynh-Thu, Vân Anh, Irrthum, Alexandre, Wehenkel, Louis, Geurts, Pierre

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Supervised learning with decision tree-based methods in computational and systems biology von Geurts, Pierre, Irrthum, Alexandre, Wehenkel, Louis

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MicroRNAs profiling in murine models of acute and chronic asthma: a relationship with mRNAs targets von Garbacki, Nancy, Di Valentin, Emmanuel, Huynh-Thu, Vân Anh, Geurts, Pierre, Irrthum, Alexandre, Crahay, Céline, Arnould, Thierry, Deroanne, Christophe, Piette, Jacques, Cataldo, Didier, Colige, Alain

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