Avdelningen för klinisk genetik

Organisation: avdelning

Fler filtreringsmöjligheter
  1. 2013
  2. WHO Classification of Tumours of Soft Tissue and Bone: WHO Classification of Tumours, vol. 5

    WHO World Health Organization, Christopher Fletcher (red.), JA Bridge (red.), PCW Hogendoorn (red.) & Fredrik Mertens (red.), 2013, 4th uppl. World Health Organization. 468 s.

    Forskningsoutput: Bok/rapportAntologi (redaktör)

  3. Whole chromosome gain does not in itself confer cancer-like chromosomal instability.

    Anders Valind, Yuesheng Jin, Bo Baldetorp & David Gisselsson Nord, 2013, I : Proceedings of the National Academy of Sciences. 110, 52, s. 21119-21123

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  4. Whole-genome-amplified DNA as a source for mutational analysis underestimates the frequency of mutations in pediatric acute myeloid leukemia

    R. Rosenquist, Hans Ehrencrona, H. Hasle, J. Palle & M. Kanduri, 2013, I : Leukemia. 27, 2, s. 510-512

    Forskningsoutput: TidskriftsbidragLetter

  5. 2012
  6. Friedreich's ataxia in patients with FXN p.R165P point mutation

    E. Ygland, Franco Taroni, Cinzia Gellera, M Duno, P. Johnels, M. Soller & A. Puschmann, 2012 sep 1, I : European Journal of Neurology. 19, Suppl 1, s. 727 1 s.

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  7. Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

    Susan J Ramus, Antonis C Antoniou, Karoline B Kuchenbaecker, Penny Soucy, Jonathan Beesley, Xiaoqing Chen, Lesley McGuffog, Olga M Sinilnikova, Sue Healey, Daniel Barrowdale, Andrew Lee, Mads Thomassen, Anne-Marie Gerdes, Torben A Kruse, Uffe Birk Jensen, Anne-Bine Skytte, Maria A Caligo, Annelie Liljegren, Annika Lindblom, Håkan Olsson & 31 andra, Ulf Kristoffersson, Marie Stenmark-Askmalm, Beatrice Melin, Susan M Domchek, Katherine L Nathanson, Timothy R Rebbeck, Anna Jakubowska, Jan Lubinski, Katarzyna Jaworska, Katarzyna Durda, Elżbieta Złowocka, Jacek Gronwald, Tomasz Huzarski, Tomasz Byrski, Cezary Cybulski, Aleksandra Toloczko-Grabarek, Ana Osorio, Javier Benitez, Mercedes Duran, Maria-Isabel Tejada, Ute Hamann, Matti Rookus, Flora E van Leeuwen, Cora M Aalfs, Hanne E J Meijers-Heijboer, Christi J van Asperen, K E P van Roozendaal, Nicoline Hoogerbrugge, J Margriet Collée, Oskar Th Johannsson & SWE-BRCA SWE-BRCA, 2012 apr, I : Human Mutation. 33, 4, s. 690-702 13 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  8. Additional aberrations of the ETV6 and RUNX1 genes have no prognostic impact in 229 t(12;21)(p13;q22)-positive B-cell precursor acute lymphoblastic leukaemias treated according to the NOPHO-ALL-2000 protocol

    Gisela Barbany, Mette K. Andersen, Kirsti Autio, Georg Borgstrom, Lucia Cavalier Franco, Irina Golovleva, Sverre Heim, Kristina Heinonen, Randi Hovland, Bertil Johansson, Johann H. Johannsson, Eigil Kjeldsen, Ann Nordgren, Lars Palmqvist & Erik Forestier, 2012, I : Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis. 36, 7, s. 936-938

    Forskningsoutput: TidskriftsbidragLetter

  9. Analysis of giant cell tumour of bone cells for Noonan syndrome/Cherubism-related mutations.

    Linda Moskovszky, Bernadine Idowu, Richard Taylor, Fredrik Mertens, Nicholas Athanasou & Adrienne Flanagan, 2012, I : Journal of Oral Pathology & Medicine.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Yuan C. Ding, Lesley McGuffog, Sue Healey, Eitan Friedman, Yael Laitman, Shani Paluch-Shimon, Bella Kaufman, Annelie Liljegren, Annika Lindblom, Håkan Olsson, Ulf Kristoffersson, Marie Stenmark-Askmalm, Beatrice Melin, Susan M. Domchek, Katherine L. Nathanson, Timothy R. Rebbeck, Anna Jakubowska, Jan Lubinski, Katarzyna Jaworska, Katarzyna Durda & 141 andra, Jacek Gronwald, Tomasz Huzarski, Cezary Cybulski, Tomasz Byrski, Ana Osorio, Teresa Ramony Cajal, Alexandra V. Stavropoulou, Javier Benitez, Ute Hamann, Matti Rookus, Cora M. Aalfs, Judith L. de Lange, Hanne E. J. Meijers-Heijboer, Jan C. Oosterwijk, Christi J. van Asperen, Encarna B. Gomez Garcia, Nicoline Hoogerbrugge, Agnes Jager, Rob B. van der Luijt, Douglas F. Easton, Susan Peock, Debra Frost, Steve D. Ellis, Radka Platte, Elena Fineberg, D. Gareth Evans, Fiona Lalloo, Louise Izatt, Ros Eeles, Julian Adlard, Rosemarie Davidson, Diana Eccles, Trevor Cole, Jackie Cook, Carole Brewer, Marc Tischkowitz, Andrew K. Godwin, Harsh Pathak, Dominique Stoppa-Lyonnet, Olga M. Sinilnikova, Sylvie Mazoyer, Laure Barjhoux, Melanie Leone, Marion Gauthier-Villars, Virginie Caux-Moncoutier, Antoine de Pauw, Agnes Hardouin, Pascaline Berthet, Helene Dreyfus, Sandra Fert Ferrer, Marie-Agnes Collonge-Rame, Johanna Sokolowska, Saundra Buys, Mary Daly, Alex Miron, Mary Beth Terry, Wendy Chung, Esther M. John, Melissa Southey, David Goldgar, Christian F. Singer, Muy-Kheng Maria Tea, Daphne Gschwantler-Kaulich, Anneliese Fink-Retter, Thomas V. O. Hansen, Bent Ejlertsen, Oskar T. Johannsson, Kenneth Offit, Kara Sarrel, Mia M. Gaudet, Joseph Vijai, Mark Robson, Marion R. Piedmonte, Lesley Andrews, David Cohn, Leslie R. DeMars, Paul DiSilvestro, Gustavo Rodriguez, Amanda Ewart Toland, Marco Montagna, Simona Agata, Evgeny Imyanitov, Claudine Isaacs, Ramunas Janavicius, Conxi Lazaro, Ignacio Blanco, Susan J. Ramus, Lara Sucheston, Beth Y. Karlan, Jenny Gross, Patricia A. Ganz, Mary S. Beattie, Rita K. Schmutzler, Barbara Wappenschmidt, Alfons Meindl, Norbert Arnold, Dieter Niederacher, Sabine Preisler-Adams, Dorotehea Gadzicki, Raymonda Varon-Mateeva, Helmut Deissler, Andrea Gehrig, Christian Sutter, Karin Kast, Heli Nevanlinna, Kristiina Aittomaki, Jacques Simard, Amanda B. Spurdle, Jonathan Beesley, Xiaoqing Chen, Gail E. Tomlinson, Jeffrey Weitzel, Judy E. Garber, Olufunmilayo I. Olopade, Wendy S. Rubinstein, Nadine Tung, Joanne L. Blum, Steven A. Narod, Sean Brummel, Daniel L. Gillen, Noralane Lindor, Zachary Fredericksen, Vernon S. Pankratz, Fergus J. Couch, Paolo Radice, Paolo Peterlongo, Mark H. Greene, Jennifer T. Loud, Phuong L. Mai, Irene L. Andrulis, Gord Glendon, Hilmi Ozcelik, Anne-Marie Gerdes, Mads Thomassen, Uffe Birk Jensen, Anne-Bine Skytte, Maria A. Caligo, Andrew Lee, Georgia Chenevix-Trench, Antonis C. Antoniou & Susan L. Neuhausen, 2012, I : Cancer Epidemiology Biomarkers & Prevention. 21, 8, s. 1362-1370

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Kelly L. Bolton, Georgia Chenevix-Trench, Cindy Goh, Siegal Sadetzki, Susan J. Ramus, Beth Y. Karlan, Diether Lambrechts, Evelyn Despierre, Daniel Barrowdale, Lesley McGuffog, Sue Healey, Douglas F. Easton, Olga Sinilnikova, Javier Benitez, Maria J. Garcia, Susan Neuhausen, Mitchell H. Gail, Patricia Hartge, Susan Peock, Debra Frost & 55 andra, Gareth Evans, Rosalind Eeles, Andrew K. Godwin, Mary B. Daly, Ava Kwong, Edmond S. K. Ma, Conxi Lazaro, Ignacio Blanco, Marco Montagna, Emma D'Andrea, Maria Ornella Nicoletto, Sharon E. Johnatty, Susanne Krueger, Allan Jensen, Estrid Hogdall, Ellen L. Goode, Brooke L. Fridley, Jennifer T. Loud, Mark H. Greene, Phuong L. Mai, Angela Chetrit, Flora Lubin, Galit Hirsh-Yechezkel, Gord Glendon, Irene L. Andrulis, Amanda E. Toland, Leigha Senter, Martin E. Gore, Charlie Gourley, Caroline O. Michie, Honglin Song, Jonathan Tyrer, Alice S. Whittemore, Valerie McGuire, Weiva Sieh, Ulf Kristoffersson, Håkan Olsson, Åke Borg, Douglas A. Levine, Linda Steele, Mary S. Beattie, Salina Chan, Robert L. Nussbaum, Kirsten B. Moysich, Jenny Gross, Ilana Cass, Christine Walsh, Andrew J. Li, Ronald Leuchter, Ora Gordon, Montserrat Garcia-Closas, Simon A. Gayther, Stephen J. Chanock, Antonis C. Antoniou & Paul D. P. Pharoah, 2012, I : JAMA: The Journal of the American Medical Association. 307, 4, s. 382-390

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Charles Walther, David Gisselsson Nord, Linda Magnusson, Jenny Nilsson, Dorthe Grabau, Carl-Magnus Kullendorff, Karolin Hansén Nord & Fredrik Mertens, 2012, I : Journal of Pediatric Hematology/Oncology.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  13. Characterisation of amplification patterns and target genes at chromosome 11q13 in CCND1-amplified sporadic and familial breast tumours.

    Karolina Holm, Johan Staaf, Göran B Jönsson, Johan Vallon-Christersson, Haukur Gunnarsson, Adalgeir Arason, Linda Magnusson, Rosa B Barkardottir, Cecilia Hegardt, Markus Ringnér & Åke Borg, 2012, I : Breast Cancer Research and Treatment. 133, 2, s. 583-594

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Elaine O'Meara, Deirdre Stack, Cheng-Han Lee, A. Julian Garvin, Thomas Morris, Pedram Argani, Jeong S. Han, Jenny Karlsson, David Gisselsson Nord, Ivo Leuschner, Manfred Gessler, Norbert Graf, Jonathan A. Fletcher & Maureen J. O'Sullivan, 2012, I : Journal of Pathology. 227, 1, s. 72-80

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  16. 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.

    Fergus J Couch, Mia M Gaudet, Antonis C Antoniou, Susan J Ramus, Karoline B Kuchenbaecker, Penny Soucy, Jonathan Beesley, Xiaoqing Chen, Xianshu Wang, Tomas Kirchhoff, Lesley McGuffog, Daniel Barrowdale, Andrew Lee, Sue Healey, Olga M Sinilnikova, Irene L Andrulis, Hilmi Ozcelik, Anna Marie Mulligan, Mads Thomassen, Anne-Marie Gerdes & 170 andra, Uffe Birk Jensen, Anne-Bine Skytte, Torben A Kruse, Maria A Caligo, Anna von Wachenfeldt, Gisela Barbany-Bustinza, Niklas Loman, Maria Soller, Hans Ehrencrona, Per Karlsson, Katherine L Nathanson, Timothy R Rebbeck, Susan M Domchek, Ania Jakubowska, Jan Lubinski, Katarzyna Jaworska, Katarzyna Durda, Elzbieta Zlowocka, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Cezary Cybulski, Bohdan Górski, Ana Osorio, Mercedes Durán, María Isabel Tejada, Javier Benitez, Ute Hamann, Frans B L Hogervorst, Theo A van Os, Flora E van Leeuwen, Hanne E J Meijers-Heijboer, Juul Wijnen, Marinus J Blok, Marleen Kets, Maartje J Hooning, Rogier A Oldenburg, Margreet G E M Ausems, Susan Peock, Debra Frost, Steve D Ellis, Radka Platte, Elena Fineberg, D Gareth Evans, Chris Jacobs, Rosalind A Eeles, Julian Adlard, Rosemarie Davidson, Diana M Eccles, Trevor Cole, Jackie Cook, Joan Paterson, Carole Brewer, Fiona Douglas, Shirley V Hodgson, Patrick J Morrison, Lisa Walker, Mary E Porteous, M John Kennedy, Lucy E Side, Betsy Bove, Andrew K Godwin, Dominique Stoppa-Lyonnet, Marion Fassy-Colcombet, Laurent Castera, François Cornelis, Sylvie Mazoyer, Mélanie Léoné, Nadia Boutry-Kryza, Brigitte Bressac-de Paillerets, Olivier Caron, Pascal Pujol, Isabelle Coupier, Capucine Delnatte, Linda Akloul, Henry T Lynch, Carrie L Snyder, Saundra S Buys, Mary B Daly, Marybeth Terry, Wendy K Chung, Esther M John, Alexander Miron, Melissa C Southey, John L Hopper, David E Goldgar, Christian F Singer, Christine Rappaport, Muy-Kheng M Tea, Anneliese Fink-Retter, Thomas V O Hansen, Finn C Nielsen, Aðalgeir Arason, Joseph Vijai, Sohela Shah, Kara Sarrel, Mark E Robson, Marion Piedmonte, Kelly Phillips, Jack Basil, Wendy S Rubinstein, John Boggess, Katie Wakeley, Amanda Ewart-Toland, Marco Montagna, Simona Agata, Evgeny N Imyanitov, Claudine Isaacs, Ramunas Janavicius, Conxi Lazaro, Ignacio Blanco, Lidia Feliubadalo, Joan Brunet, Simon A Gayther, Paul P D Pharoah, Kunle O Odunsi, Beth Y Karlan, Christine S Walsh, Edith Olah, Soo Hwang Teo, Patricia A Ganz, Mary S Beattie, Elizabeth J van Rensburg, Cecelia M Dorfling, Orland Diez, Ava Kwong, Rita K Schmutzler, Barbara Wappenschmidt, Christoph Engel, Alfons Meindl, Nina Ditsch, Norbert Arnold, Simone Heidemann, Dieter Niederacher, Sabine Preisler-Adams, Dorothea Gadzicki, Raymonda Varon-Mateeva, Helmut Deissler, Andrea Gehrig, Christian Sutter, Karin Kast, Britta Fiebig, Wolfram Heinritz, Trinidad Caldes, Miguel de la Hoya, Taru A Muranen, Heli Nevanlinna, Marc D Tischkowitz, Amanda B Spurdle, Susan L Neuhausen, Yuan Chun Ding, Noralane M Lindor, Zachary Fredericksen, V Shane Pankratz, Paolo Peterlongo, Siranoush Manoukian, Bernard Peissel, Daniela Zaffaroni, Monica Barile, Loris Bernard, Alessandra Viel, Giuseppe Giannini, Liliana Varesco, Paolo Radice, Mark H Greene, Phuong L Mai, Douglas F Easton, Georgia Chenevix-Trench, Kenneth Offit & Jacques Simard, 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

  17. 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

    Jan J. Molenaar, Jan Koster, Marli E. Ebus, Peter van Sluis, Ellen M. Westerhout, Katleen de Preter, David Gisselsson Nord, Ingrid Øra, Frank Speleman, Huib N. Caron & Rogier Versteeg, 2012, I : Genes, Chromosomes and Cancer. 51, 1, s. 10-19

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Meena Kanduri, Millaray Marincevic, Anna M. Halldorsdottir, Larry Mansouri, Katarina Junevik, Stavroula Ntoufa, Hanna Goransson Kultima, Anders Isaksson, Gunnar Juliusson, Per-Ola Andersson, Hans Ehrencrona, Kostas Stamatopoulos & Richard Rosenquist, 2012, I : Epigenetics. 7, 12, s. 1435-1442

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  19. Editorial: Genetics and Democracy

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

    Forskningsoutput: TidskriftsbidragLetter

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

    Madelene Olsson, Margery K. Herrington, Roger D. Reidelberger, Johan Permert, Samuel Gebre-Medhin & Urban Arnelo, 2012, I : Scandinavian Journal of Gastroenterology. 47, 2, s. 191-196

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Gemma Macchia, Domenico Trombetta, Emely Möller, Fredrik Mertens, Clelia T Storlazzi, Maria Debiec-Rychter, Raf Sciot & Karolin Hansén Nord, 2012, I : Laboratory Investigation. 92, 5, s. 735-743

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Emil Ygland, Franco Taroni, Cinzia Gellera, Morten Dunø, Petra Johnels, Maria Soller & Andreas Puschmann, 2012, I : European Journal of Neurology. 19, suppl1, s. 727-727

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  23. 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.

    Yuesheng Jin, Emely Möller, Karolin Hansén Nord, Nils Mandahl, Fredrik Vult von Steyern, Henryk Domanski, Adrian Mariño-Enríquez, Linda Magnusson, Jenny Nilsson, Raf Sciot, Christopher D M Fletcher, Maria Debiec-Rychter & Fredrik Mertens, 2012, I : Genes, Chromosomes and Cancer. 51, 5, s. 510-520

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  24. Genetics and democracy-what is the issue?

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Anna Staffas, Meena Kanduri, Randi Hovland, Richard Rosenquist, Hans Beier Ommen, Jonas Abrahamsson, Erik Forestier, Kirsi Jahnukainen, Olafur G. Jonsson, Bernward Zeller, Josefine Palle, Gudmar Lonnerholm, Henrik Hasle, Hans Ehrencrona & Lars Palmqvist, 2012, I : Blood. 119, 4, s. 1087-1088

    Forskningsoutput: TidskriftsbidragLetter

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

    Catarina Lundin, Lars Hjorth, Mikael Behrendtz, Ann Nordgren, Lars Palmqvist, Mette Klarskov Andersen, Andrea Biloglav, Erik Forestier, Kajsa Paulsson & Bertil Johansson, 2012, I : Genes, Chromosomes and Cancer. 51, s. 196-206

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Tarja Niini, Ilari Scheinin, Leo Lahti, Suvi Savola, Fredrik Mertens, Jaakko Hollmen, Tom Bohling, Aarne Kivioja, Karolin Hansén Nord & Sakari Knuutila, 2012, I : Cancer Genetics. 205, 11, s. 588-593

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  28. 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

    Vasilios Zachariadis, Jacqueline Schoumans, Gisela Barbany, Mats Heyman, Erik Forestier, Bertil Johansson, Magnus Nordenskjold & Ann Nordgren, 2012, I : British Journal of Haematology. 159, 4, s. 488-491

    Forskningsoutput: TidskriftsbidragLetter

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

    Lu Wang, Toru Motoi, Raya Khanin, Adam Olshen, Fredrik Mertens, Julia Bridge, Paola Dal Cin, Cristina R. Antonescu, Samuel Singer, Meera Hameed, Judith V. M. G. Bovee, Pancras C. W. Hogendoorn, Nicholas Socci & Marc Ladanyi, 2012, I : Genes, Chromosomes and Cancer. 51, 2, s. 127-139

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Salvatore Romeo, Judith V. M. G. Bovee, Herman M. Kroon, Roberto Tirabosco, Cristina Natali, Lucia Zanatta, Raf Sciot, Fredrik Mertens, Nick Athanasou, Marco Alberghini, Karoly Szuhai, Pancras C. W. Hogendoorn & Angelo Paolo Dei Tos, 2012, I : Virchows Archiv: an international journal of pathology. 461, 5, s. 561-570

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Anna Margret Halldorsdottir, Meena Kanduri, Millaray Marincevic, Larry Mansouri, Anders Isaksson, Hanna Goransson, Tomas Axelsson, Prasoon Agarwal, Helena Jernberg-Wiklund, Kostas Stamatopoulos, Birgitta Sander, Hans Ehrencrona & Richard Rosenquist, 2012, I : American Journal of Hematology. 87, 4, s. 361-367

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Domenico Trombetta, Gemma Macchia, Nils Mandahl, Karolin Hansén Nord & Fredrik Mertens, 2012, I : Cancer Genetics. 205, 7-8, s. 410-413

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Leona A Doyle, Wei-Lien Wang, Paola Dal Cin, Dolores Lopez-Terrada, Fredrik Mertens, Alexander J F Lazar, Christopher D M Fletcher & Jason L Hornick, 2012, I : American Journal of Surgical Pathology. 36, 10, s. 1444-1451

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Hao Zhang, Xuehua Chen, Yuesheng Jin, Bingya Liu & Liang Zhou, 2012, I : European Archives of Oto-Rhino-Laryngology. 269, 2, s. 607-614

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Samuel Gebre-Medhin, Karolin Hansén Nord, Emely Möller, Nils Mandahl, Linda Magnusson, Jenny Nilsson, Vickie Y Jo, Fredrik Vult von Steyern, Otte Brosjö, Olle Larsson, Henryk Domanski, Raf Sciot, Maria Debiec-Rychter, Christopher D M Fletcher & Fredrik Mertens, 2012, I : American Journal of Pathology. 181, 3, s. 1069-1077

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Johan Staaf, Göran B Jönsson, Mats Jönsson, Anna Karlsson, Sofi Isaksson, Annette Salomonsson, Helen Pettersson, Maria Soller, Sven-Börje Ewers, Leif Johansson, Per Jönsson & Maria Planck, 2012, I : BMC Medical Genomics. 5

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Fiona M. Ross, Herve Avet-Loiseau, Genevieve Ameye, Norma C. Gutierrez, Peter Liebisch, Sheila O'Connor, Klara Dalva, Sonia Fabris, Adele M. Testi, Marie Jarosova, Clare Hodkinson, Anna Collin, Gitte Kerndrup, Petr Kuglik, Dariusz Ladon, Paolo Bernasconi, Brigitte Maes, Zuzana Zemanova, Kyra Michalova, Lucienne Michau & 10 andra, Kai Neben, N. Emil U. Hermansen, Katrina Rack, Alberto Rocci, Rebecca Protheroe, Laura Chiecchio, Helene A. Poirel, Pieter Sonneveld, Mette Nyegaard & Hans E. Johnsen, 2012, I : Haematologica. 97, 8, s. 1272-1277

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Karina Meden Sorensen, Milad El-Segaier, Eva Fernlund, Ab Errami, Patrice Bouvagnet, Nancy Nehme, Jesper Steensberg, Vibeke Hjortdal, Maria Soller, Mohaddeseh Behjati, Thomas Werge, Maria Kirchoff, Jan Schouten, Niels Tommerup, Paal Skytt Andersen & Lars Allan Larsen, 2012, I : American Journal of Medical Genetics. Part A. 158A, 4, s. 720-725

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  43. Smooth muscle actin expression in primary bone tumours

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Arezoo Mohajeri, Lars-Gunnar Kindblom, Vaiyapuri P Sumathi, Otte Brosjö, Linda Magnusson, Jenny Nilsson, Karolin Hansén Nord & Fredrik Mertens, 2012, I : Cancer Genetics. 205, 12, s. 673-6

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

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

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

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

    Göran B Jönsson, Johan Staaf, Johan Vallon-Christersson, Markus Ringnér, Sofia Gruvberger, Lao Saal, Karolina Holm, Cecilia Hegardt, Adalgeir Arason, Rainer Fagerholm, Camilla Olsson, Dorthe Grabau, Ellinor Johnsson, Kristina Lövgren, Linda Magnusson, Paivi Heikkilä, Bjarni A Agnarsson, Oskar Th Johannsson, Per Malmström, Mårten Fernö & 5 andra, Håkan Olsson, Niklas Loman, Heli Nevanlinna, Rosa Bjork Barkardottir & Åke Borg, 2012, I : Cancer Research. 72, 16, s. 4028-4036

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  47. Tumor-initiating cells in childhood neuroblastoma: Letter

    Sofie Mohlin, Alexander Pietras, Caroline Wigerup, Ingrid Øra, Michael Andäng, Kenneth Nilsson, Tor Olofsson, David Gisselsson Nord & Sven Påhlman, 2012, I : Cancer Research. 72, 3, s. 821-822

    Forskningsoutput: TidskriftsbidragLetter