Avdelningen för klinisk genetik

Organisation: avdelning

Fler filtreringsmöjligheter
  1. 2012
  2. Analysis of giant cell tumour of bone cells for Noonan syndrome/Cherubism-related mutations.

    Moskovszky, L., Idowu, B., Taylor, R., Fredrik Mertens, Athanasou, N. & Flanagan, A., 2012, I : Journal of Oral Pathology & Medicine.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. A Nonsynonymous Polymorphism in IRS1 Modifies Risk of Developing Breast and Ovarian Cancers in BRCA1 and Ovarian Cancer in BRCA2 Mutation Carriers

    Ding, Y. C., McGuffog, L., Healey, S., Friedman, E., Laitman, Y., Paluch-Shimon, S., Kaufman, B., Liljegren, A., Lindblom, A., Olsson, H., Kristoffersson, U., Stenmark-Askmalm, M., Melin, B., Domchek, S. M., Nathanson, K. L., Rebbeck, T. R., Jakubowska, A., Lubinski, J., Jaworska, K., Durda, K. & 141 andraGronwald, J., Huzarski, T., Cybulski, C., Byrski, T., Osorio, A., Ramony Cajal, T., Stavropoulou, A. V., Benitez, J., Hamann, U., Rookus, M., Aalfs, C. M., de Lange, J. L., Meijers-Heijboer, H. E. J., Oosterwijk, J. C., van Asperen, C. J., Garcia, E. B. G., Hoogerbrugge, N., Jager, A., van der Luijt, R. B., Easton, D. F., Peock, S., Frost, D., Ellis, S. D., Platte, R., Fineberg, E., Evans, D. G., Lalloo, F., Izatt, L., Eeles, R., Adlard, J., Davidson, R., Eccles, D., Cole, T., Cook, J., Brewer, C., Tischkowitz, M., Godwin, A. K., Pathak, H., Stoppa-Lyonnet, D., Sinilnikova, O. M., Mazoyer, S., Barjhoux, L., Leone, M., Gauthier-Villars, M., Caux-Moncoutier, V., de Pauw, A., Hardouin, A., Berthet, P., Dreyfus, H., Ferrer, S. F., Collonge-Rame, M-A., Sokolowska, J., Buys, S., Daly, M., Miron, A., Terry, M. B., Chung, W., John, E. M., Southey, M., Goldgar, D., Singer, C. F., Tea, M-K. M., Gschwantler-Kaulich, D., Fink-Retter, A., Hansen, T. V. O., Ejlertsen, B., Johannsson, O. T., Offit, K., Sarrel, K., Gaudet, M. M., Vijai, J., Robson, M., Piedmonte, M. R., Andrews, L., Cohn, D., DeMars, L. R., DiSilvestro, P., Rodriguez, G., Toland, A. E., Montagna, M., Agata, S., Imyanitov, E., Isaacs, C., Janavicius, R., Lazaro, C., Blanco, I., Ramus, S. J., Sucheston, L., Karlan, B. Y., Gross, J., Ganz, P. A., Beattie, M. S., Schmutzler, R. K., Wappenschmidt, B., Meindl, A., Arnold, N., Niederacher, D., Preisler-Adams, S., Gadzicki, D., Varon-Mateeva, R., Deissler, H., Gehrig, A., Sutter, C., Kast, K., Nevanlinna, H., Aittomaki, K., Simard, J., Spurdle, A. B., Beesley, J., Chen, X., Tomlinson, G. E., Weitzel, J., Garber, J. E., Olopade, O. I., Rubinstein, W. S., Tung, N., Blum, J. L., Narod, S. A., Brummel, S., Gillen, D. L., Lindor, N., Fredericksen, Z., Pankratz, V. S., Couch, F. J., Radice, P., Peterlongo, P., Greene, M. H., Loud, J. T., Mai, P. L., Andrulis, I. L., Glendon, G., Ozcelik, H., Gerdes, A-M., Thomassen, M., Jensen, U. B., Skytte, A-B., Caligo, M. A., Lee, A., Chenevix-Trench, G., Antoniou, A. C. & Neuhausen, S. L., 2012, I : Cancer Epidemiology Biomarkers & Prevention. 21, 8, s. 1362-1370

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  4. Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian Cancer

    Bolton, K. L., Chenevix-Trench, G., Goh, C., Sadetzki, S., Ramus, S. J., Karlan, B. Y., Lambrechts, D., Despierre, E., Barrowdale, D., McGuffog, L., Healey, S., Easton, D. F., Sinilnikova, O., Benitez, J., Garcia, M. J., Neuhausen, S., Gail, M. H., Hartge, P., Peock, S., Frost, D. & 55 andraEvans, G., Eeles, R., Godwin, A. K., Daly, M. B., Kwong, A., Ma, E. S. K., Lazaro, C., Blanco, I., Montagna, M., D'Andrea, E., Nicoletto, M. O., Johnatty, S. E., Krueger, S., Jensen, A., Hogdall, E., Goode, E. L., Fridley, B. L., Loud, J. T., Greene, M. H., Mai, P. L., Chetrit, A., Lubin, F., Hirsh-Yechezkel, G., Glendon, G., Andrulis, I. L., Toland, A. E., Senter, L., Gore, M. E., Gourley, C., Michie, C. O., Song, H., Tyrer, J., Whittemore, A. S., McGuire, V., Sieh, W., Ulf Kristoffersson, Håkan Olsson, Åke Borg, Levine, D. A., Steele, L., Beattie, M. S., Chan, S., Nussbaum, R. L., Moysich, K. B., Gross, J., Cass, I., Walsh, C., Li, A. J., Leuchter, R., Gordon, O., Garcia-Closas, M., Gayther, S. A., Chanock, S. J., Antoniou, A. C. & Pharoah, P. D. P., 2012, I : JAMA: the journal of the American Medical Association. 307, 4, s. 382-390

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. Biphasic, Hyperdiploid Breast Tumors in Children: A Distinct Entity?

    Charles Walther, David Gisselsson Nord, Magnusson, L., Nilsson, J., Grabau, D., Kullendorff, C-M., Karolin Hansén Nord & Fredrik Mertens, 2012, I : Journal of Pediatric Hematology/Oncology.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  6. Characterization of the chromosomal translocation t(10;17)(q22;p13) in clear cell sarcoma of kidney

    O'Meara, E., Stack, D., Lee, C-H., Garvin, A. J., Morris, T., Argani, P., Han, J. S., Jenny Karlsson, David Gisselsson Nord, Leuschner, I., Gessler, M., Graf, N., Fletcher, J. A. & O'Sullivan, M. J., 2012, I : Journal of Pathology. 227, 1, s. 72-80

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  7. Chromosome dynamics and genomic instablity in neuroblastoma. Three genomic pillars: MYCN amplification, numerical and structural changes.

    Lundberg, G., 2012, Faculty of Medicine, Lund University. 132 s.

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  8. Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.

    Couch, F. J., Gaudet, M. M., Antoniou, A. C., Ramus, S. J., Kuchenbaecker, K. B., Soucy, P., Beesley, J., Chen, X., Wang, X., Kirchhoff, T., McGuffog, L., Barrowdale, D., Lee, A., Healey, S., Sinilnikova, O. M., Andrulis, I. L., Ozcelik, H., Mulligan, A. M., Thomassen, M., Gerdes, A-M. & 170 andraJensen, U. B., Skytte, A-B., Kruse, T. A., Caligo, M. A., von Wachenfeldt, A., Barbany-Bustinza, G., Niklas Loman, Soller, M., Hans Ehrencrona, Karlsson, P., Nathanson, K. L., Rebbeck, T. R., Domchek, S. M., Jakubowska, A., Lubinski, J., Jaworska, K., Durda, K., Zlowocka, E., Huzarski, T., Byrski, T., Gronwald, J., Cybulski, C., Górski, B., Osorio, A., Durán, M., Tejada, M. I., Benitez, J., Hamann, U., Hogervorst, F. B. L., van Os, T. A., van Leeuwen, F. E., Meijers-Heijboer, H. E. J., Wijnen, J., Blok, M. J., Kets, M., Hooning, M. J., Oldenburg, R. A., Ausems, M. G. E. M., Peock, S., Frost, D., Ellis, S. D., Platte, R., Fineberg, E., Evans, D. G., Jacobs, C., Eeles, R. A., Adlard, J., Davidson, R., Eccles, D. M., Cole, T., Cook, J., Paterson, J., Brewer, C., Douglas, F., Hodgson, S. V., Morrison, P. J., Walker, L., Porteous, M. E., Kennedy, M. J., Side, L. E., Bove, B., Godwin, A. K., Stoppa-Lyonnet, D., Fassy-Colcombet, M., Castera, L., Cornelis, F., Mazoyer, S., Léoné, M., Boutry-Kryza, N., Bressac-de Paillerets, B., Caron, O., Pujol, P., Coupier, I., Delnatte, C., Akloul, L., Lynch, H. T., Snyder, C. L., Buys, S. S., Daly, M. B., Terry, M., Chung, W. K., John, E. M., Miron, A., Southey, M. C., Hopper, J. L., Goldgar, D. E., Singer, C. F., Rappaport, C., Tea, M-K. M., Fink-Retter, A., Hansen, T. V. O., Nielsen, F. C., Arason, A., Vijai, J., Shah, S., Sarrel, K., Robson, M. E., Piedmonte, M., Phillips, K., Basil, J., Rubinstein, W. S., Boggess, J., Wakeley, K., Ewart-Toland, A., Montagna, M., Agata, S., Imyanitov, E. N., Isaacs, C., Janavicius, R., Lazaro, C., Blanco, I., Feliubadalo, L., Brunet, J., Gayther, S. A., Pharoah, P. P. D., Odunsi, K. O., Karlan, B. Y., Walsh, C. S., Olah, E., Teo, S. H., Ganz, P. A., Beattie, M. S., van Rensburg, E. J., Dorfling, C. M., Diez, O., Kwong, A., Schmutzler, R. K., Wappenschmidt, B., Engel, C., Meindl, A., Ditsch, N., Arnold, N., Heidemann, S., Niederacher, D., Preisler-Adams, S., Gadzicki, D., Varon-Mateeva, R., Deissler, H., Gehrig, A., Sutter, C., Kast, K., Fiebig, B., Heinritz, W., Caldes, T., de la Hoya, M., Muranen, T. A., Nevanlinna, H., Tischkowitz, M. D., Spurdle, A. B., Neuhausen, S. L., Ding, Y. C., Lindor, N. M., Fredericksen, Z., Pankratz, V. S., Peterlongo, P., Manoukian, S., Peissel, B., Zaffaroni, D., Barile, M., Bernard, L., Viel, A., Giannini, G., Varesco, L., Radice, P., Greene, M. H., Mai, P. L., Easton, D. F., Chenevix-Trench, G., Offit, K. & Simard, J., 2012, I : Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 21, 4, s. 645-657

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  9. Copy Number Defects of G1-Cell Cycle Genes in Neuroblastoma are Frequent and Correlate with High Expression of E2F Target Genes and a Poor Prognosis

    Molenaar, J. J., Koster, J., Ebus, M. E., van Sluis, P., Westerhout, E. M., de Preter, K., David Gisselsson Nord, Ingrid Øra, Speleman, F., Caron, H. N. & Versteeg, R., 2012, I : Genes, Chromosomes and Cancer. 51, 1, s. 10-19

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  10. Distinct transcriptional control in major immunogenetic subsets of chronic lymphocytic leukemia exhibiting subset-biased global DNA methylation profiles

    Kanduri, M., Marincevic, M., Halldorsdottir, A. M., Mansouri, L., Junevik, K., Ntoufa, S., Kultima, H. G., Isaksson, A., Gunnar Juliusson, Andersson, P-O., Hans Ehrencrona, Stamatopoulos, K. & Rosenquist, R., 2012, I : Epigenetics. 7, 12, s. 1435-1442

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  11. Editorial: Genetics and Democracy

    Maria Hedlund, Hagen, N. & Ulf Kristoffersson, 2012, I : Journal of Community Genetics. 3, 2, s. 57-59

    Forskningsoutput: TidskriftsbidragLetter

  12. Food intake and meal pattern in IAPP knockout mice with and without infusion of exogenous IAPP

    Olsson, M., Herrington, M. K., Reidelberger, R. D., Permert, J., Samuel Gebre-Medhin & Arnelo, U., 2012, I : Scandinavian Journal of Gastroenterology. 47, 2, s. 191-196

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  13. FOSL1 as a candidate target gene for 11q12 rearrangements in desmoplastic fibroblastoma.

    Macchia, G., Trombetta, D., Möller, E., Fredrik Mertens, Storlazzi, C. T., Debiec-Rychter, M., Sciot, R. & Karolin Hansén Nord, 2012, I : Laboratory Investigation. 92, 5, s. 735-743

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  14. Friedreich ataxia in patients with FXN p.R165P point mutation.

    Ygland, E., Taroni, F., Gellera, C., Dunø, M., Johnels, P., Soller, M. & Andreas Puschmann, 2012, I : European Journal of Neurology. 19, suppl1, s. 727-727

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  15. Fusion of the AHRR and NCOA2 genes through a recurrent translocation t(5;8)(p15;q13) in soft tissue angiofibroma results in upregulation of aryl hydrocarbon receptor target genes.

    Jin, Y., Möller, E., Karolin Hansén Nord, Nils Mandahl, Fredrik Vult von Steyern, Domanski, H., Mariño-Enríquez, A., Magnusson, L., Nilsson, J., Sciot, R., Fletcher, C. D. M., Debiec-Rychter, M. & Fredrik Mertens, 2012, I : Genes, Chromosomes and Cancer. 51, 5, s. 510-520

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  16. Genetics and democracy-what is the issue?

    Hagen, N., Maria Hedlund, Susanne Lundin, Shai Mulinari & Ulf Kristoffersson, 2012, I : Journal of Community Genetics.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  17. High ERG gene expression is an unfavorable prognostic marker in pediatric acute myeloid leukemia Response

    Staffas, A., Kanduri, M., Hovland, R., Rosenquist, R., Ommen, H. B., Abrahamsson, J., Forestier, E., Jahnukainen, K., Jonsson, O. G., Zeller, B., Palle, J., Lonnerholm, G., Hasle, H., Hans Ehrencrona & Palmqvist, L., 2012, I : Blood. 119, 4, s. 1087-1088

    Forskningsoutput: TidskriftsbidragLetter

  18. High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome.

    Lundin, C., Lars Hjorth, Behrendtz, M., Nordgren, A., Palmqvist, L., Andersen, M. K., Biloglav, A., Forestier, E., Kajsa Paulsson & Bertil Johansson, 2012, I : Genes, Chromosomes and Cancer. 51, s. 196-206

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  19. Homozygous deletions of cadherin genes in chondrosarcoma-an array comparative genomic hybridization study

    Niini, T., Scheinin, I., Lahti, L., Savola, S., Fredrik Mertens, Hollmen, J., Bohling, T., Kivioja, A., Karolin Hansén Nord & Knuutila, S., 2012, I : Cancer genetics. 205, 11, s. 588-593

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  20. Homozygous deletions of CDKN2A are present in all dic(9;20)(p13.2;q11.2)-positive B-cell precursor acute lymphoblastic leukaemias and may be important for leukaemic transformation

    Zachariadis, V., Schoumans, J., Barbany, G., Heyman, M., Forestier, E., Bertil Johansson, Nordenskjold, M. & Nordgren, A., 2012, I : British Journal of Haematology. 159, 4, s. 488-491

    Forskningsoutput: TidskriftsbidragLetter

  21. Identification of a novel, recurrent HEY1-NCOA2 fusion in mesenchymal chondrosarcoma based on a genome-wide screen of exon-level expression data

    Wang, L., Motoi, T., Khanin, R., Olshen, A., Fredrik Mertens, Bridge, J., Dal Cin, P., Antonescu, C. R., Singer, S., Hameed, M., Bovee, J. V. M. G., Hogendoorn, P. C. W., Socci, N. & Ladanyi, M., 2012, I : Genes, Chromosomes and Cancer. 51, 2, s. 127-139

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  22. Increased incidence of childhood, prostate and breast cancers in relatives of childhood cancer patients.

    Magnusson, S., Thomas Wiebe, Ulf Kristoffersson, Helena Jernström & Håkan Olsson, 2012, I : Familial Cancer. 11, s. 145-155

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  23. Malignant fibrous histiocytoma and fibrosarcoma of bone: a re-assessment in the light of currently employed morphological, immunohistochemical and molecular approaches

    Romeo, S., Bovee, J. V. M. G., Kroon, H. M., Tirabosco, R., Natali, C., Zanatta, L., Sciot, R., Fredrik Mertens, Athanasou, N., Alberghini, M., Szuhai, K., Hogendoorn, P. C. W. & Tos, A. P. D., 2012, I : Virchows Archiv: an international journal of pathology. 461, 5, s. 561-570

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  24. Mantle cell lymphoma displays a homogenous methylation profile: A comparative analysis with chronic lymphocytic leukemia

    Halldorsdottir, A. M., Kanduri, M., Marincevic, M., Mansouri, L., Isaksson, A., Goransson, H., Axelsson, T., Agarwal, P., Jernberg-Wiklund, H., Stamatopoulos, K., Sander, B., Hans Ehrencrona & Rosenquist, R., 2012, I : American Journal of Hematology. 87, 4, s. 361-367

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  25. Molecular genetic characterization of the 11q13 breakpoint in a desmoplastic fibroma of bone

    Trombetta, D., Macchia, G., Nils Mandahl, Karolin Hansén Nord & Fredrik Mertens, 2012, I : Cancer genetics. 205, 7-8, s. 410-413

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  26. MUC4 Is a Sensitive and Extremely Useful Marker for Sclerosing Epithelioid Fibrosarcoma: Association With FUS Gene Rearrangement.

    Doyle, L. A., Wang, W-L., Dal Cin, P., Lopez-Terrada, D., Fredrik Mertens, Lazar, A. J. F., Fletcher, C. D. M. & Hornick, J. L., 2012, I : American Journal of Surgical Pathology. 36, 10, s. 1444-1451

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  27. Oncogenic activation of FOXR1 by 11q23 intrachromosomal deletion-fusions in neuroblastoma

    Santo, E. E., Ebus, M. E., Koster, J., Schulte, J. H., Lakeman, A., van Sluis, P., Vermeulen, J., David Gisselsson Nord, Ingrid Øra, Lindner, S., Buckley, P. G., Stallings, R. L., Vandesompele, J., Eggert, A., Caron, H. N., Versteeg, R. & Molenaar, J. J., 2012, I : Oncogene. 31, 12, s. 1571-1581

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  28. Overexpression of Aurora-A promotes laryngeal cancer progression by enhancing invasive ability and chromosomal instability

    Zhang, H., Chen, X., Jin, Y., Liu, B. & Zhou, L., 2012, I : European Archives of Oto-Rhino-Laryngology. 269, 2, s. 607-614

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  29. Recurrent Rearrangement of the PHF1 Gene in Ossifying Fibromyxoid Tumors.

    Samuel Gebre-Medhin, Karolin Hansén Nord, Möller, E., Nils Mandahl, Magnusson, L., Nilsson, J., Jo, V. Y., Fredrik Vult von Steyern, Brosjö, O., Larsson, O., Domanski, H., Sciot, R., Debiec-Rychter, M., Fletcher, C. D. M. & Fredrik Mertens, 2012, I : American Journal of Pathology. 181, 3, s. 1069-1077

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  30. Relation between smoking history and gene expression profiles in lung adenocarcinomas

    Johan Staaf, Göran B Jönsson, Mats Jönsson, Karlsson, A., Sofi Isaksson, Annette Salomonsson, Pettersson, H., Soller, M., Ewers, S-B., Johansson, L., Jönsson, P. & Maria Planck, 2012, I : BMC Medical Genomics. 5

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  31. Report from the European Myeloma Network on interphase FISH in multiple myeloma and related disorders

    Ross, F. M., Avet-Loiseau, H., Ameye, G., Gutierrez, N. C., Liebisch, P., O'Connor, S., Dalva, K., Fabris, S., Testi, A. M., Jarosova, M., Hodkinson, C., Collin, A., Kerndrup, G., Kuglik, P., Ladon, D., Bernasconi, P., Maes, B., Zemanova, Z., Michalova, K., Michau, L. & 10 andraNeben, K., Hermansen, N. E. U., Rack, K., Rocci, A., Protheroe, R., Chiecchio, L., Poirel, H. A., Sonneveld, P., Nyegaard, M. & Johnsen, H. E., 2012, I : Haematologica. 97, 8, s. 1272-1277

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  32. Retained heterodisomy is associated with high gene expression in hyperhaploid inflammatory leiomyosarcoma.

    Karolin Hansén Nord, Kajsa Paulsson, Veerla, S., Wejde, J., Brosjö, O., Nils Mandahl & Fredrik Mertens, 2012, I : Neoplasia. 14, 9, s. 807-812

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  33. Screening of Congenital Heart Disease Patients Using Multiplex Ligation-Dependent Probe Amplification: Early Diagnosis of Syndromic Patients

    Sorensen, K. M., El-Segaier, M., Eva Fernlund, Errami, A., Bouvagnet, P., Nehme, N., Steensberg, J., Hjortdal, V., Soller, M., Behjati, M., Werge, T., Kirchoff, M., Schouten, J., Tommerup, N., Andersen, P. S. & Larsen, L. A., 2012, I : American Journal of Medical Genetics. Part A. 158A, 4, s. 720-725

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  34. SIX1 protein expression selectively identifies blastemal elements in Wilms tumor.

    Sehic, D., Jenny Karlsson, Sandstedt, B. & David Gisselsson Nord, 2012, I : Pediatric Blood & Cancer. 59, 1, s. 62-68

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  35. Smooth muscle actin expression in primary bone tumours

    Hemingway, F., Kashima, T. G., Mahendra, G., Dhongre, A., Hogendoorn, P. C. W., Fredrik Mertens & Athanasou, N. A., 2012, I : Virchows Archiv: an international journal of pathology. 460, 5, s. 525-534

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  36. SNP array and FISH findings in two pleomorphic hyalinizing angiectatic tumors.

    Mohajeri, A., Kindblom, L-G., Sumathi, V. P., Brosjö, O., Magnusson, L., Nilsson, J., Karolin Hansén Nord & Fredrik Mertens, 2012, I : Cancer genetics. 205, 12, s. 673-6

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  37. The MDM2 SNP309 G allele is not preferentially amplified in bone and soft tissue tumors.

    Fredrik Mertens, Brosjö, O., Fredrik Vult von Steyern, Karolin Hansén Nord & Nils Mandahl, 2012, I : Cancer genetics. 205, 9, s. 470-473

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  38. The retinoblastoma gene undergoes rearrangements in BRCA1-deficient basal-like breast cancer.

    Jönsson, G. B., Staaf, J., Vallon-Christersson, J., Ringnér, M., Gruvberger, S., Saal, L., Holm, K., Hegardt, C., Arason, A., Fagerholm, R., Olsson, C., Grabau, D., Johnsson, E., Lövgren, K., Magnusson, L., Heikkilä, P., Agnarsson, B. A., Johannsson, O. T., Malmström, P., Fernö, M. & 5 andraHåkan Olsson, Niklas Loman, Nevanlinna, H., Barkardottir, R. B. & Åke Borg, 2012, I : Cancer Research. 72, 16, s. 4028-4036

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  39. Tumor-initiating cells in childhood neuroblastoma: Letter

    Sofie Mohlin, Alexander Pietras, Wigerup, C., Ingrid Øra, Andäng, M., Nilsson, K., Olofsson, T., David Gisselsson Nord & Sven Påhlman, 2012, I : Cancer Research. 72, 3, s. 821-822

    Forskningsoutput: TidskriftsbidragLetter

  40. Whole-exome sequencing of pediatric acute lymphoblastic leukemia.

    Henrik Lilljebjörn, Rissler, M., Lassen, C., Heldrup, J., Behrendtz, M., Felix Mitelman, Bertil Johansson & Thoas Fioretos, 2012, I : Leukemia. 26, s. 1602-1607

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  41. γ-Aminobutyric acid (GABA) signalling in human pancreatic islets is altered in type 2 diabetes.

    Taneera, J., Jin, Z., Jin, Y., Jabar Muhammed, S., Enming Zhang, Stefan Lang, S Albert Salehi, Korsgren, O., Erik Renström, Leif Groop & Birnir, B., 2012, I : Diabetologia. 55, 7, s. 1985-1994

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  42. 2011
  43. A large deletion identified in a Swedish family with type 1 VWD

    Johansson, A. M., Lanke, E., Torbjörn Säll, Lethagen, S. & Halldén, C., 2011, I : Thrombosis and Haemostasis. 105, 4, s. 733-734

    Forskningsoutput: TidskriftsbidragLetter

  44. Alternative lengthening of telomeres-An enhanced chromosomal instability in aggressive non-MYCN amplified and telomere elongated neuroblastomas.

    Lundberg, G., Sehic, D., Länsberg, J-K., Ingrid Øra, Attila Frigyesi, Castel, V., Navarro, S., Piqueras, M., Martinsson, T., Noguera, R. & David Gisselsson Nord, 2011, I : Genes, Chromosomes and Cancer. 50, 4, s. 250-262

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  45. Amplification of the G allele at SNP rs6983267 in 8q24 amplicons in myeloid malignancies as cause of the lack of MYC overexpression?

    Micale, L., Augello, B., Daniele, G., Macchia, G., L'Abbate, A., Muehlematter, D., Vandenberghe, P., Bertil Johansson, Cabrol, C., Sole, F., Dastugue, N., Slovak, M. L., Lillington, D., Raynaud, S., Lafage, M., Nacheva, E. D., Merla, G. & Storlazzi, C. T., 2011, I : Blood Cells, Molecules & Diseases. 47, 4, s. 259-261

    Forskningsoutput: TidskriftsbidragLetter

  46. Aneuploidy in cancer: Sudden or sequential?

    David Gisselsson Nord, 2011, I : Cell Cycle. 10, 3, s. 359-361

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  47. Bilateral Prophylactic Mastectomy in Swedish Women at High Risk of Breast Cancer: A National Survey.

    Arver, B., Isaksson, K., Atterhem, H., Baan, A., Bergkvist, L., Brandberg, Y., Hans Ehrencrona, Emanuelsson, M., Hellborg, H., Henriksson, K., Karlsson, P., Niklas Loman, Lundberg, J., Anita Ringberg, Askmalm, M. S., Wickman, M. & Sandelin, K., 2011, I : Annals of Surgery. 253, 6, s. 1147-1154

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  48. Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation

    Gilling, M., Lind-Thomsen, A., Mang, Y., Bak, M., Moller, M., Ullmann, R., Ulf Kristoffersson, Kalscheuer, V. M., Henriksen, K. F., Bugge, M., Tumer, Z. & Tommerup, N., 2011, I : European Journal of Medical Genetics. 54, 4, s. E383-E388

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  49. Clonal Evolution through Loss of Chromosomes and Subsequent Polyploidization in Chondrosarcoma.

    Linda Olsson, Kajsa Paulsson, Bovée, J. V. M. G. & Karolin Hansén Nord, 2011, I : PLoS ONE. 6, 9, e24977.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  50. Combination of pegylated IFN-alpha 2b with imatinib increases molecular response rates in patients with low- or intermediate-risk chronic myeloid leukemia

    Simonsson, B., Gedde-Dahl, T., Markevarn, B., Remes, K., Stentoft, J., Almqvist, A., Bjoreman, M., Flogegard, M., Koskenvesa, P., Lindblom, A., Malm, C., Mustjoki, S., Myhr-Eriksson, K., Ohm, L., Rasanen, A., Sinisalo, M., Sjalander, A., Stromberg, U., Bjerrum, O. W., Ehrencrona, H. & 8 andraGruber, F., Kairisto, V., Olsson, K., Sandin, F., Nagler, A., Nielsen, J. L., Hjorth-Hansen, H. & Porkka, K., 2011, I : Blood. 118, 12, s. 3228-3235

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  51. Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

    Mulligan, A. M., Couch, F. J., Barrowdale, D., Domchek, S. M., Eccles, D., Nevanlinna, H., Ramus, S. J., Robson, M., Sherman, M., Spurdle, A. B., Wappenschmidt, B., Lee, A., McGuffog, L., Healey, S., Sinilnikova, O. M., Janavicius, R., Hansen, T. V. O., Nielsen, F. C., Ejlertsen, B., Osorio, A. & 162 andraMunoz-Repeto, I., Duran, M., Godino, J., Pertesi, M., Benitez, J., Peterlongo, P., Manoukian, S., Peissel, B., Zaffaroni, D., Cattaneo, E., Bonanni, B., Viel, A., Pasini, B., Papi, L., Ottini, L., Savarese, A., Bernard, L., Radice, P., Hamann, U., Verheus, M., Meijers-Heijboer, H. E. J., Wijnen, J., Garcia, E. B. G., Nelen, M. R., Kets, C. M., Seynaeve, C., Tilanus-Linthorst, M. M. A., van der Luijt, R. B., van Os, T., Rookus, M., Frost, D., Jones, J. L., Evans, D. G., Lalloo, F., Eeles, R., Izatt, L., Adlard, J., Davidson, R., Cook, J., Donaldson, A., Dorkins, H., Gregory, H., Eason, J., Houghton, C., Barwell, J., Side, L. E., McCann, E., Murray, A., Peock, S., Godwin, A. K., Schmutzler, R. K., Rhiem, K., Engel, C., Meindl, A., Ruehl, I., Arnold, N., Niederacher, D., Sutter, C., Deissler, H., Gadzicki, D., Kast, K., Preisler-Adams, S., Varon-Mateeva, R., Schoenbuchner, I., Fiebig, B., Heinritz, W., Schaefer, D., Gevensleben, H., Caux-Moncoutier, V., Fassy-Colcombet, M., Cornelis, F., Mazoyer, S., Leone, M., Boutry-Kryza, N., Hardouin, A., Berthet, P., Muller, D., Fricker, J-P., Mortemousque, I., Pujol, P., Coupier, I., Lebrun, M., Kientz, C., Longy, M., Sevenet, N., Stoppa-Lyonnet, D., Isaacs, C., Caldes, T., de la Hoya, M., Heikkinen, T., Aittomaki, K., Blanco, I., Lazaro, C., Barkardottir, R. B., Soucy, P., Dumont, M., Simard, J., Montagna, M., Tognazzo, S., D'Andrea, E., Fox, S., Yan, M., Rebbeck, T., Olopade, O. I., Weitzel, J. N., Lynch, H. T., Ganz, P. A., Tomlinson, G. E., Wang, X., Fredericksen, Z., Pankratz, V. S., Lindor, N. M., Szabo, C., Offit, K., Sakr, R., Gaudet, M., Bhatia, J., Kauff, N., Singer, C. F., Tea, M-K., Gschwantler-Kaulich, D., Fink-Retter, A., Mai, P. L., Greene, M. H., Imyanitov, E., O'Malley, F. P., Ozcelik, H., Glendon, G., Toland, A. E., Gerdes, A-M., Thomassen, M., Kruse, T. A., Jensen, U. B., Skytte, A-B., Caligo, M. A., Soller, M., Henriksson, K., Wachenfeldt, V. A., Arver, B., Stenmark-Askmalm, M., Karlsson, P., Ding, Y. C., Neuhausen, S. L., Beattie, M., Pharoah, P. D. P., Moysich, K. B., Nathanson, K. L., Karlan, B. Y., Gross, J., John, E. M., Daly, M. B., Buys, S. M., Southey, M. C., Hopper, J. L., Terry, M. B., Chung, W., Miron, A. F., Goldgar, D., Chenevix-Trench, G., Easton, D. F., Andrulis, I. L. & Antoniou, A. C., 2011, I : Breast Cancer Research. 13, 6

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  52. CYTOGENETIC AND MOLECULAR GENETIC CHARACTERIZATION OF LIPOMAS

    Bartuma, H., 2011, Department of Clinical Genetics, Lund University. 166 s.

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  53. FUS-CREB3L2/L1-Positive Sarcomas Show a Specific Gene Expression Profile with Upregulation of CD24 and FOXL1.

    Möller, E., Hornick, J. L., Magnusson, L., Veerla, S., Domanski, H. & Fredrik Mertens, 2011, I : Clinical Cancer Research. 17, 9, s. 2646-2656

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  54. Fusion Gene Microarray Reveals Cancer Type-Specificity Among Fusion Genes

    Lovf, M., Thomassen, G. O. S., Bakken, A. C., Celestino, R., Thoas Fioretos, Lind, G. E., Lothe, R. A. & Skotheim, R. I., 2011, I : Genes, Chromosomes and Cancer. 50, 5, s. 348-357

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  55. Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion.

    Bartuma, H., Karolin Hansén Nord, Macchia, G., Isaksson, M., Nilsson, J., Domanski, H., Nils Mandahl & Fredrik Mertens, 2011, I : Genes, Chromosomes and Cancer. 50, s. 619-632

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  56. Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities Background Document to the ESHG recommendations on genetic testing and common disorders

    Becker, F., van El, C. G., Ibarreta, D., Zika, E., Hogarth, S., Borry, P., Cambon-Thomsen, A., Cassiman, J. J., Evers-Kiebooms, G., Hodgson, S., Janssens, A. C. J. W., Kaariainen, H., Krawczak, M., Kristoffersson, U., Lubinski, J., Patch, C., Penchaszadeh, V. B., Read, A., Rogowski, W., Sequeiros, J. & 6 andraTranebjaerg, L., van Langen, I. M., Wallace, H., Zimmern, R., Schmidtke, J. & Cornel, M. C., 2011, I : European Journal of Human Genetics. 19, S.1, s. S6-S44

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  57. Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers.

    Ramus, S. J., Kartsonaki, C., Gayther, S. A., Pharoah, P. D. P., Sinilnikova, O. M., Beesley, J., Chen, X., McGuffog, L., Healey, S., Couch, F. J., Wang, X., Fredericksen, Z., Peterlongo, P., Manoukian, S., Peissel, B., Zaffaroni, D., Roversi, G., Barile, M., Viel, A., Allavena, A. & 133 andraOttini, L., Papi, L., Gismondi, V., Capra, F., Radice, P., Greene, M. H., Mai, P. L., Andrulis, I. L., Glendon, G., Ozcelik, H., Thomassen, M., Gerdes, A-M., Kruse, T. A., Cruger, D., Jensen, U. B., Caligo, M. A., Håkan Olsson, Ulf Kristoffersson, Lindblom, A., Arver, B., Karlsson, P., Stenmark Askmalm, M., Åke Borg, Neuhausen, S. L., Ding, Y. C., Nathanson, K. L., Domchek, S. M., Jakubowska, A., Lubinski, J., Huzarski, T., Byrski, T., Gronwald, J., Górski, B., Cybulski, C., Debniak, T., Osorio, A., Durán, M., Tejada, M-I., Benítez, J., Hamann, U., Rookus, M. A., Verhoef, S., Tilanus-Linthorst, M. A., Vreeswijk, M. P., Bodmer, D., Ausems, M. G. E. M., van Os, T. A., Asperen, C. J., Blok, M. J., Meijers-Heijboer, H. E. J., Peock, S., Cook, M., Oliver, C., Frost, D., Dunning, A. M., Evans, D. G., Eeles, R., Pichert, G., Cole, T., Hodgson, S., Brewer, C., Morrison, P. J., Porteous, M., Kennedy, M. J., Rogers, M. T., Side, L. E., Donaldson, A., Gregory, H., Godwin, A., Stoppa-Lyonnet, D., Moncoutier, V., Castera, L., Mazoyer, S., Barjhoux, L., Bonadona, V., Leroux, D., Faivre, L., Lidereau, R., Nogues, C., Bignon, Y-J., Prieur, F., Collonge-Rame, M-A., Venat-Bouvet, L., Fert-Ferrer, S., Miron, A., Buys, S. S., Hopper, J. L., Daly, M. B., John, E. M., Terry, M. B., Goldgar, D., Hansen, T. V. O., Jønson, L., Ejlertsen, B., Agnarsson, B. A., Offit, K., Kirchhoff, T., Vijai, J., Dutra-Clarke, A. V. C., Przybylo, J. A., Montagna, M., Casella, C., Imyanitov, E. N., Janavicius, R., Blanco, I., Lázaro, C., Moysich, K. B., Karlan, B. Y., Gross, J., Beattie, M. S., Schmutzler, R., Wappenschmidt, B., Meindl, A., Ruehl, I., Fiebig, B., Sutter, C., Arnold, N., Deissler, H., Varon-Mateeva, R., Kast, K., Niederacher, D., Gadzicki, D., Caldes, T., de la Hoya, M., Nevanlinna, H., Aittomäki, K., Simard, J., Soucy, P., Spurdle, A. B., Holland, H., Chenevix-Trench, G., Easton, D. F. & Antoniou, A. C., 2011, I : Journal of the National Cancer Institute. 103, 2, s. 105-116

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  58. Genomic characterization of ETV6/RUNX1-positive acute lymphoblastic leukemia

    Henrik Lilljebjörn, 2011, Lund University. 61 s.

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  59. HMGA2 and MDM2 expression in lipomatous tumors with partial, low-level amplification of sequences from the long arm of chromosome 12.

    Nils Mandahl, Bartuma, H., Magnusson, L., Isaksson, M., Macchia, G. & Fredrik Mertens, 2011, I : Cancer genetics. 204, 10, s. 550-556

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  60. Identification of a Novel, Recurrent HEY1-NCOA2 Fusion in Mesenchymal Chondrosarcoma Based on a Genome-Wide Screen of Exon-Level Expression Data

    Wang, L., Motoi, T., Khanin, R., Socci, N., Olshen, A., Fredrik Mertens, Bridge, J., Dal Cin, P., Rushing, E. J., Fanburg-Smith, J., Antonescu, C., Hameed, M. & Ladanyi, M., 2011, I : Laboratory Investigation. 91, s. 23A

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  61. Impact of TP53 mutation and 17p deletion in mantle cell lymphoma

    Halldorsdottir, A. M., Lundin, A., Murray, F., Mansouri, L., Knuutila, S., Sundstrom, C., Laurell, A., Hans Ehrencrona, Sander, B. & Rosenquist, R., 2011, I : Leukemia. 25, 12, s. 1904-1908

    Forskningsoutput: TidskriftsbidragLetter

  62. Intratumor diversity and clonal evolution in cancer-a skeptical standpoint.

    David Gisselsson Nord, 2011, I : Advances in Cancer Research. 112, s. 1-9

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  63. Malignant Fibrous Histiocytoma and Fibrosarcoma of Bone in 2011: What's New?

    Romeo, S., Bovee, J. V. M. G., Carrareno, I., Tirabosco, R., Natali, C., Kroon, H. M., Zanatta, L., Sciot, R., Fredrik Mertens, Athanasou, N., Alberghini, M., Hogendoorn, P. C. W. & Dei Tos, A. P., 2011, I : Laboratory Investigation. 91, s. 20A

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  64. Mechanisms of Whole Chromosome Gains in Tumors - Many Answers to a Simple Question.

    David Gisselsson Nord, 2011, I : Cytogenetic and Genome Research. 133, s. 190-201

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  65. Mesenchymal stromal cells from primary osteosarcoma are non-malignant and strikingly similar to their bone marrow counterparts.

    Brune, J. C., Tormin, A., Maria C Johansson, Rissler, P., Brosjö, O., Löfvenberg, R., Fredrik Vult von Steyern, Fredrik Mertens, Anders Rydholm & Stefan Scheding, 2011, I : International Journal of Cancer. 129, s. 319-330

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  66. MUC4 Is a Highly Sensitive and Specific Marker for Low-grade Fibromyxoid Sarcoma.

    Doyle, L. A., Möller, E., Cin, P. D., Fletcher, C. D. M., Fredrik Mertens & Hornick, J. L., 2011, I : American Journal of Surgical Pathology. 35, s. 733-741

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  67. MUC4 Is a Highly Sensitive and Specific Marker for Low-Grade Fibromyxoid Sarcoma

    Doyle, L. A., Möller, E., Fredrik Mertens & Hornick, J. L., 2011, I : Laboratory Investigation. 91, s. 12A

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  68. Mutations in CEP57 cause mosaic variegated aneuploidy syndrome

    Snape, K., Hanks, S., Ruark, E., Barros-Nunez, P., Elliott, A., Murray, A., Lane, A. H., Shannon, N., Callier, P., Chitayat, D., Clayton-Smith, J., FitzPatrick, D. R., Gisselsson Nord, D., Jacquemont, S., Asakura-Hay, K., Micale, M. A., Tolmie, J., Turnpenny, P. D., Wright, M., Douglas, J. & 1 andraRahman, N., 2011, I : Nature Genetics. 43, 6, s. 527-529

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  69. Mutation Update for the PORCN Gene

    Lombardi, M. P., Bulk, S., Celli, J., Lampe, A., Gabbett, M. T., Ousager, L. B., van der Smagt, J. J., Soller, M., Stattin, E-L., Mannens, M. A. M. M., Smigiel, R. & Hennekam, R. C., 2011, I : Human Mutation. 32, 7, s. 723-728

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  70. Paediatric B-cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocols.

    Andersen, M. K., Autio, K., Barbany, G., Borgström, G., Cavelier, L., Golovleva, I., Heim, S., Heinonen, K., Hovland, R., Johannsson, J. H., Bertil Johansson, Kjeldsen, E., Nordgren, A., Palmqvist, L. & Forestier, E., 2011, I : British Journal of Haematology. 155, s. 235-243

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  71. Presence of FLT3-ITD and high BAALC expression are independent prognostic markers in childhood acute myeloid leukemia

    Staffas, A., Kanduri, M., Hovland, R., Rosenquist, R., Ommen, H. B., Abrahamsson, J., Forestier, E., Jahnukainen, K., Jonsson, O. G., Zeller, B., Palle, J., Lonnerholm, G., Hasle, H., Palmqvist, L. & Hans Ehrencrona, 2011, I : Blood. 118, 22, s. 5905-5913

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  72. Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study

    Presneau, N., Shalaby, A., Ye, H., Pillay, N., Halai, D., Idowu, B., Tirabosco, R., Whitwell, D., Jacques, T. S., Kindblom, L-G., Bruederlein, S., Moeller, P., Leithner, A., Liegl, B., Amary, F. M., Athanasou, N. N., Hogendoorn, P. C. W., Fredrik Mertens, Szuhai, K. & Flanagan, A. M., 2011, I : Journal of Pathology. 223, 3, s. 327-335

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  73. SMAD4 binds HOXA9 in the cytoplasm and protects primitive hematopoietic cells against nuclear activation by HOXA9 and leukemia transformation.

    Quere, R., Göran Karlsson, Hertwig, F., Rissler, M., Lindqvist, B., Thoas Fioretos, Vandenberghe, P., Slovak, M. L., Cammenga, J. & Stefan Karlsson, 2011, I : Blood. 117, s. 5918-5930

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  74. Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome

    Pansuriya, T. C., van Eijk, R., d'Adamo, P., van Ruler, M. A. J. H., Kuijjer, M. L., Oosting, J., Cleton-Jansen, A-M., van Oosterwijk, J. G., Verbeke, S. L. J., Meijer, D., van Wezel, T., Hansén Nord, K., Sangiorgi, L., Toker, B., Liegl-Atzwanger, B., San-Julian, M., Sciot, R., Limaye, N., Kindblom, L-G., Daugaard, S. & 7 andraGodfraind, C., Boon, L. M., Vikkula, M., Kurek, K. C., Szuhai, K., French, P. J. & Bovee, J. V. M. G., 2011, I : Nature Genetics. 43, 12, s. 1256-1261

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  75. The frequency and prognostic impact of dic(9;20)(p13.2;q11.2) in childhood B-cell precursor acute lymphoblastic leukemia: results from the NOPHO ALL-2000 trial

    Zachariadis, V., Gauffin, F., Kuchinskaya, E., Heyman, M., Schoumans, J., Blennow, E., Gustafsson, B., Barbany, G., Golovleva, I., Hans Ehrencrona, Cavelier, L., Palmqvist, L., Lonnerholm, G., Nordenskjold, M., Bertil Johansson, Forestier, E. & Nordgren, A., 2011, I : Leukemia. 25, 4, s. 622-628

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  76. The t(X;6) in subungual exostosis results in transcriptional deregulation of the gene for insulin receptor substrate 4.

    Fredrik Mertens, Möller, E., Nils Mandahl, Picci, P., Perez-Atayde, A. R., Samson, I., Sciot, R. & Debiec-Rychter, M., 2011, I : International Journal of Cancer. 128, s. 487-491

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  77. Translocation t(7;19)(q22;q13)-a recurrent chromosome aberration in pseudomyogenic hemangioendothelioma?

    Trombetta, D., Magnusson, L., Fredrik Vult von Steyern, Hornick, J. L., Fletcher, C. D. M. & Fredrik Mertens, 2011, I : Cancer genetics. 204, 4, s. 211-215

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  78. Tumor-Infiltrating Macrophages Are Associated with Metastasis Suppression in High-Grade Osteosarcoma: A Rationale for Treatment with Macrophage Activating Agents

    Buddingh, E. P., Kuijjer, M. L., Duim, R. A. J., Buerger, H., Agelopoulos, K., Myklebost, O., Serra, M., Fredrik Mertens, Hogendoom, P. C. W., Lankester, A. C. & Cleton-Jansen, A-M., 2011, I : Clinical Cancer Research. 17, 8, s. 2110-2119

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  79. Tumor-Infiltrating Macrophages Are Associated with Metastasis Suppression in High-Grade Osteosarcoma: A Rationale for Treatment with Macrophage-Activating Agents

    Buddingh, E. P., Kuijjer, M. L., Duim, R., Burger, H., Agelopoulos, K., Myklebost, O., Serra, M., Fredrik Mertens, Hogendoorn, P. C. W., Lankester, A. C. & Cleton-Jansen, A-M., 2011, I : Laboratory Investigation. 91, Feb 26 - Mar 4, 2011, s. 10A

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  80. Ultrasonographic findings in spontaneous miscarriage: relation to euploidy and aneuploidy

    Ljunger, E., Stavreus-Evers, A., Cnattingius, S., Ekbom, A., Lundin, C., Anneren, G. & Sundstrom-Poromaa, I., 2011, I : Fertility and Sterility. 95, 1, s. 221-224

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  81. 2010
  82. Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction

    Antoniou, A. C., Beesley, J., McGuffog, L., Sinilnikova, O. M., Healey, S., Neuhausen, S. L., Ding, Y. C., Rebbeck, T. R., Weitzel, J. N., Lynch, H. T., Isaacs, C., Ganz, P. A., Tomlinson, G., Olopade, O. I., Couch, F. J., Wang, X., Lindor, N. M., Pankratz, V. S., Radice, P., Manoukian, S. & 31 andraPeissel, B., Zaffaroni, D., Barile, M., Viel, A., Allavena, A., Dall'Olio, V., Peterlongo, P., Szabo, C. I., Zikan, M., Claes, K., Poppe, B., Foretova, L., Mai, P. L., Greene, M. H., Rennert, G., Lejbkowicz, F., Glendon, G., Ozcelik, H., Andrulis, I. L., Thomassen, M., Gerdes, A-M., Sunde, L., Cruger, D., Birk Jensen, U., Caligo, M., Friedman, E., Kaufman, B., Laitman, Y., Helena Jernström, Stenmark-Askmalm, M. & Ontario Cancer Genetics Network, 2010 dec 1, I : Cancer Research. 70, 23, s. 9742-54 13 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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  84. Benchmarks for Cystic Fibrosis carrier screening: A European consensus document

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  86. Comparison of high-frequency QRS components and ST-segment elevation to detect and quantify acute myocardial ischemia.

    Ringborn, M., Pettersson, J., Persson, E., Warren, S. G., Pyotr Platonov, Pahlm, O. & Wagner, G. S., 2010, I : Journal of Electrocardiology. 43, s. 113-120

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  87. Concomitant deletions of tumor suppressor genes MEN1 and AIP are essential for the pathogenesis of the brown fat tumor hibernoma.

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    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract