Avdelningen för klinisk genetik

Organisation: avdelning

Fler filtreringsmöjligheter
  1. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

    Couch, F. J., Kuchenbaecker, K. B., Michailidou, K., Mendoza-Fandino, G. A., Nord, S., Lilyquist, J., Olswold, C., Hallberg, E., Agata, S., Ahsan, H., Aittomäki, K., Ambrosone, C., Andrulis, I. L., Anton-Culver, H., Arndt, V., Arun, B. K., Arver, B., Barile, M., Barkardottir, R. B., Barrowdale, D. & 229 andraBeckmann, L., Beckmann, M. W., Benitez, J., Blank, S. V., Blomqvist, C., Bogdanova, N. V., Bojesen, S. E., Bolla, M. K., Bonanni, B., Brauch, H., Brenner, H., Burwinkel, B., Buys, S., Caldes, T., Caligo, M. A., Canzian, F., Carpenter, J., Chang-Claude, J., Chanock, S. J., Chung, W. K., Claes, K. B. M., Cox, A., Cross, S. S., Cunningham, J. M., Czene, K., Daly, M. B., Damiola, F., Darabi, H., de la Hoya, M., Devilee, P., Diez, O., Ding, Y. C., Dolcetti, R., Domchek, S. M., Dorfling, C. M., Dos Santos Silva, I., Dumont, M., Dunning, A. M., Eccles, D. M., Hans Ehrencrona, Ekici, A. B., Eliassen, A. H., Ellis, S., Fasching, P. A., Figueroa, J., Flesch-Janys, D., Asta Försti, Fostira, F., Foulkes, W. D., Friebel, T., Friedman, E., Frost, D., Gabrielson, M., Gammon, M. D., Ganz, P. A., Gapstur, S. M., Garber, J., Gaudet, M., Gayther, S. A., Gerdes, A-M., Ghoussaini, M., Giles, G. G., Glendon, G., Godwin, A. K., Goldberg, M. S., Goldgar, D. E., González-Neira, A., Greene, M. H., Gronwald, J., Guénel, P., Gunter, M., Haeberle, L., Haiman, C. A., Hamann, U., Hansen, T. V. O., Hart, S., Healey, S., Heikkinen, T., Henderson, B. E., Herzog, J., Hogervorst, F. B. L., Hollestelle, A., Hooning, M. J., Hoover, R. N., Hopper, J. L., Humphreys, K., Hunter, D. J., Huzarski, T., Imyanitov, E. N., Isaacs, C., Jakubowska, A., James, P., Janavicius, R., Jensen, U. B., John, E. M., Jones, M., Kabisch, M., Kar, S., Karlan, B. Y., Khan, S., Khaw, K. T., Kibriya, M. G., Knight, J. A., Ko, Y-D., Konstantopoulou, I., Kosma, V-M., Kristensen, V., Kwong, A., Laitman, Y., Lambrechts, D., Lazaro, C., Lee, E., Le Marchand, L., Lester, J., Lindblom, A., Lindor, N., Lindstrom, S., Liu, J., Long, J., Lubinski, J., Mai, P. L., Makalic, E., Malone, K. E., Mannermaa, A., Manoukian, S., Margolin, S., Marme, F., Martens, J. W. M., McGuffog, L., Meindl, A., Miller, A., Milne, R. L., Miron, P., Montagna, M., Mazoyer, S., Mulligan, A. M., Muranen, T. A., Nathanson, K. L., Neuhausen, S. L., Nevanlinna, H., Nordestgaard, B. G., Nussbaum, R. L., Offit, K., Olah, E., Olopade, O. I., Olson, J. E., Osorio, A., Park, S. K., Peeters, P. H., Peissel, B., Peterlongo, P., Peto, J., Phelan, C. M., Pilarski, R., Poppe, B., Pylkäs, K., Radice, P., Rahman, N., Rantala, J., Rappaport, C., Rennert, G., Richardson, A. L., Robson, M., Romieu, I., Rudolph, A., Rutgers, E. J., Sanchez, M-J., Santella, R. M., Sawyer, E. J., Schmidt, D. F., Schmidt, M. K., Schmutzler, R. K., Schumacher, F., Scott, R., Senter, L., Sharma, P., Simard, J., Singer, C. F., Sinilnikova, O. M., Soucy, P., Southey, M., Steinemann, D., Stenmark-Askmalm, M., Stoppa-Lyonnet, D., Swerdlow, A., Szabo, C. I., Tamimi, R., Tapper, W., Teixeira, M. R., Teo, S-H., Terry, M. B., Thomassen, M., Thompson, D., Tihomirova, L., Toland, A. E., Tollenaar, R. A. E. M., Tomlinson, I., Truong, T., Tsimiklis, H., Teulé, A., Tumino, R., Tung, N., Turnbull, C., Ursin, G., van Deurzen, C. H. M., van Rensburg, E. J., Varon-Mateeva, R., Wang, Z., Wang-Gohrke, S., Weiderpass, E., Weitzel, J. N., Whittemore, A. S., Wildiers, H., Winqvist, R., Yang, X. R., Yannoukakos, D., Yao, S., Zamora, M. P., Zheng, W., Hall, P., Kraft, P., Vachon, C., Slager, S., Chenevix-Trench, G., Pharoah, P. P. D., Monteiro, A. N., García-Closas, M., Easton, D. F. & Antoniou, A. C., 2016 apr 27, I : Nature Communications. 7, 11375.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  2. Establishment and characterisation of a human clear cell sarcoma model in nude mice

    Crnalic, S., Panagopoulos, I., Boquist, L., Nils Mandahl, Stenling, R. & Lofvenberg, R., 2002, I : International Journal of Cancer. 101, 6, s. 505-511

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. Laboratory recommendations for scoring deep molecular responses following treatment for chronic myeloid leukemia.

    Cross, N. C. P., White, H. E., Colomer, D., Ehrencrona, H., Foroni, L., Gottardi, E., Lange, T., Lion, T., Machova Polakova, K., Dulucq, S., Martinelli, G., Oppliger Leibundgut, E., Pallisgaard, N., Barbany, G., Sacha, T., Talmaci, R., Izzo, B., Saglio, G., Pane, F., Müller, M. C. & 1 andraHochhaus, A., 2015, I : Leukemia. 29, 5, s. 999-1003

    Forskningsoutput: TidskriftsbidragÖversiktsartikel

  4. No Genomic Aberrations in Langerhans Cell Histiocytosis as Assessed by Diverse Molecular Technologies

    da Costa, C. E. T., Szuhai, K., van Eijk, R., Hoogeboom, M., Sciot, R., Fredrik Mertens, Bjorgvinsdottir, H., Debiec-Rychter, M., de Krijger, R. R., Hogendoorn, P. C. W., Egeler, R. M. & Annels, N. E., 2009, I : Genes, Chromosomes and Cancer. 48, 3, s. 239-249

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. Amylin inhibits bone resorption while the calcitonin receptor controls bone formation in vivo

    Dacquin, R., Davey, RA., Laplace, C., Levasseur, G., Morris, HA., Goldring, SR., Samuel Gebre-Medhin, Galson, DL., Zajac, JD. & Karsenty, G., 2004, I : Journal of Cell Biology. 164, 4, s. 509-514

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  6. Genetic Characterization of Bone and Soft Tissue Tumors

    Dahlen, A., 2005, Department of Clinical Genetics, Lund University. 117 s.

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  7. Clustering of deletions on chromosome 13 in benign and low-malignant lipomatous tumors

    Dahlén, A., Debiec-Rychter, M., Pedeutour, F., Domanski, H. A., Mattias Höglund, Bauer, H. C. F., Anders Rydholm, Sciot, R., Nils Mandahl & Fredrik Mertens, 2003 feb 20, I : International Journal of Cancer. 103, 5, s. 616-623 8 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  8. Activation of the GLI Oncogene through Fusion with the beta-Actin Gene (ACTB) in a Group of Distinctive Pericytic Neoplasms: Pericytoma with t(7;12).

    Dahlén, A., Fletcher, C. D. M., Fredrik Mertens, Fletcher, J. A., Perez-Atayde, A. R., Hicks, M. J., Debiec-Rychter, M., Sciot, R., Wejde, J., Wedin, R., Nils Mandahl & Panagopoulos, I., 2004, I : American Journal of Pathology. 164, 5, s. 1645-1653

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  9. Analysis of the distribution and frequency of trisomy 7 in vivo in synovia from patients with osteoarthritis and pigmented villonodular synovitis

    Dahlén, A., Broberg, K., Domanski, H. A., S Toksvig-Larsen, Lindstrand, A., N Mandahl & F Mertens, 2001 nov, I : Cancer Genetics and Cytogenetics. 131, 1, s. 19-24 6 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  10. Fusion, disruption, and expression of HMGA2 in bone and soft tissue chondromas

    Dahlén, A., Fredrik Mertens, Anders Rydholm, Brosjö, O., Wejde, J., Nils Mandahl & Panagopoulos, I., 2003 nov, I : Modern Pathology. 16, 11, s. 1132-1140 9 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  11. Molecular genetic characterization of the genomic ACTB-GLI fusion in pericytoma with t(7;12).

    Dahlén, A., Fredrik Mertens, Nils Mandahl & Panagopoulos, I., 2004, I : Biochemical and Biophysical Research Communications. 325, 4, s. 1318-1323

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  12. Methylated RASSF1A in malignant peripheral nerve sheath tumors identifies neurofibromatosis type 1 patients with inferior prognosis.

    Danielsen, S. A., Lind, G. E., Kolberg, M., Høland, M., Bjerkehagen, B., Sundby Hall, K., van den Berg, E., Fredrik Mertens, Smeland, S., Picci, P. & Lothe, R. A., 2015, I : Neuro-Oncology. 17, 1, s. 63-69

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  13. Epigenetic target genes in malignant peripheral nerve sheath tumours identified as surrogate prognostic biomarkers

    Danielsen, S. A., Lind, G. E., Hall, K. S., Smeland, S., van den Berg, E., Fredrik Mertens, Kolberg, M. & Lothe, R. A., 2010, I : EJC Supplements. 8, 5, s. 163

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  14. Trisomy 19 as the sole chromosomal abnormality in proliferative chronic myelomonocytic leukemia

    Daskalakis, M., Mauritzson, N., Bertil Johansson, Bouabdallah, K., Onida, F., Kunzmann, R., Mueller-Berndorff, H., Schmitt-Graeff, A. & Luebbert, M., 2006, I : Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis. 30, 8, s. 1043-1047

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  15. Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12

    Josef Davidsson, Collin, A., Oereberg, M. & David Gisselsson Nord, 2008, I : Clinical Genetics. 73, 1, s. 44-49

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  16. The hypermethylome of pediatric acute lymphoblastic leukemia

    Josef Davidsson, Henrik Lilljebjörn, Anna Andersson, Srinivas Veerla, Heldrup, J., Behrendtz, M., Thoas Fioretos & Bertil Johansson, 2008, I : Cellular Oncology. 30, 3, s. 252-252

    Forskningsoutput: TidskriftsbidragPublicerat konferensabstract

  17. Genetic and epigenetic characterization of pediatric high hyperdiploid acute lymphoblastic leukemia

    Josef Davidsson, 2009, Lund University, Faculty of Medicine. 193 s.

    Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

  18. Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: An array-based genotype-phenotype correlation and a comprehensive review of previously published cases.

    Josef Davidsson, Collin, A., Olsson, M. E., Lundgren, J. & Soller, M., 2008, I : Epilepsy Research. Jun 6, s. 69-79

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  19. dup(19)(q12q13.2): Array-based Genotype-Phenotype Correlation of a New Possibly Obesity-related Syndrome.

    Josef Davidsson, Jahnke, K., Forsgren, M., Collin, A. & Soller, M., 2010, I : Obesity. 18, s. 580-587

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  20. The DNA methylome of pediatric acute lymphoblastic leukemia.

    Josef Davidsson, Henrik Lilljebjörn, Anna Andersson, Srinivas Veerla, Heldrup, J., Behrendtz, M., Thoas Fioretos & Bertil Johansson, 2009, I : Human Molecular Genetics. Aug 13, s. 4054-4065

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  21. Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations.

    Josef Davidsson, Kajsa Paulsson, David Lindgren, Henrik Lilljebjörn, Chaplin, T., Forestier, E., Andersen, M. K., Nordgren, A., Rosenquist, R., Thoas Fioretos, Young, B. D. & Bertil Johansson, 2010, I : Leukemia. 24, s. 924-931

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  22. Delection of the SCN gene cluster on 2q24.4 is associated with severe epilepsy an array-based genotype-phenotype correlation and a comprehensive review of previously published area

    Josef Davidsson, Collin, A., Engman Olsson, M., Lundgren, J. & Soller, M., 2008, I : Epilepsy Res. 81, 1, s. 69-79

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  23. Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU

    Depienne, C., Nava, C., Keren, B., Heide, S., Rastetter, A., Passemard, S., Chantot-Bastaraud, S., Moutard, M. L., Agrawal, P. B., VanNoy, G., Stoler, J. M., Amor, D. J., Billette de Villemeur, T., Doummar, D., Alby, C., Cormier-Daire, V., Garel, C., Marzin, P., Scheidecker, S., de Saint-Martin, A. & 31 andraHirsch, E., Korff, C., Bottani, A., Faivre, L., Verloes, A., Orzechowski, C., Burglen, L., Leheup, B., Roume, J., Andrieux, J., Sheth, F., Datar, C., Parker, M. J., Pasquier, L., Odent, S., Naudion, S., Delrue, M. A., Le Caignec, C., Vincent, M., Isidor, B., Renaldo, F., Stewart, F., Toutain, A., Koehler, U., Häckl, B., von Stülpnagel, C., Kluger, G., Møller, R. S., Tord Jonson, Soller, M. & DDD Study, 2017, I : Human Genetics. 136, 4, s. 463-479 17 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  24. Genetic profiling of colorectal cancer liver metastases by combined comparative genomic hybridization and G-banding analysis

    Diep, CB., Parada, LA., Teixeira, MR., Eknaes, M., Nesland, JM., Bertil Johansson & Lothe, RA., 2003, I : Genes, Chromosomes and Cancer. 36, 2, s. 189-197

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  25. Genome characteristics of primary carcinomas, local recurrences, carcinomatoses, and liver metastases from colorectal cancer patients

    Diep, C. B., Teixeira, M. R., Thorstensen, L., Wiig, J. N., Eknaes, M., Nesland, J. M., Giercksky, K-E., Bertil Johansson & Lothe, R. A., 2004, I : Molecular Cancer. 3, 6.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  26. 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

  27. A Population-Based Single Nucleotide Polymorphism Array Analysis of Genomic Aberrations in Younger Adult Acute Lymphoblastic Leukemia Patients

    Dirse, V., Bertasiute, A., Gineikiene, E., Zvirblis, T., Dambrauskiene, R., Gerbutavicius, R., Juozaityte, E., Malciute, L., Kajsa Paulsson & Griskevicius, L., 2015, I : Genes, Chromosomes and Cancer. 54, 5, s. 326-333

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  28. Single nucleotide polymorphism array analysis of clonal evolution in younger adult acute lymphoblastic leukemia

    Dirse, V., Gineikiene, E., Zvirblis, T., Bertasiute, R., Kajsa Paulsson & Griskevicius, L., 2016, I : Leukemia & Lymphoma. 57, 11, s. 2716-2719 4 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  29. Fine-needle aspiration of neurilemoma (schwannoma). A clinicocytopathologic study of 116 patients

    Domanski, H. A., Åkerman, M., Jacob Engellau, Pelle Gustafson, Fredrik Mertens & Anders Rydholm, 2006 jun, I : Diagnostic Cytopathology. 34, 6, s. 403-412 10 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  30. Core-needle biopsy performed by the cytopathologist: a technique to complement fine-needle aspiration of soft tissue and bone lesions

    Domanski, H. A., Åkerman, M., Carlén, B., Jacob Engellau, Pelle Gustafson, Jonsson, K., Fredrik Mertens & Anders Rydholm, 2005 aug 25, I : Cancer. 105, 4, s. 229-239 11 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  31. Distinct cytologic features of spindle cell lipoma - A cytologic-histologic study with clinical, radiologic, electron microscopic, and cytogenetic correlations

    Domanski, H., Carlén, B., Jonsson, K., Fredrik Mertens & Åkerman, M., 2001, I : Cancer. 93, 6, s. 381-389

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  32. Low-grade fibromyxoid sarcoma is difficult to diagnose by fine needle aspiration cytology: a cytomorphological study of eight cases.

    Domanski, H., Fredrik Mertens, Panagopoulos, I. & Åkerman, M., 2009, I : Cytopathology. 20, s. 304-314

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  33. FNA Cytology of Soft Tissue and Bone Tumors

    Domanski, H. A. & Charles S. Walther, 2017, Karger. (Monographs in Clinical Cytology; vol. 22)

    Forskningsoutput: Bok/rapportBok

  34. Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein.

    Dominguez, M., Drost, M., Therkildsen, C., Rambech, E., Hans Ehrencrona, Angleys, M., Lau Hansen, T., de Wind, N., Mef Nilbert & Juel Rasmussen, L., 2014, I : Molecular Genetics & Genomic Medicine. 2, 4, s. 352-355

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  35. Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.

    Dondorp, W., de Wert, G., Bombard, Y., Bianchi, D. W., Bergmann, C., Borry, P., Chitty, L. S., Fellmann, F., Forzano, F., Hall, A., Henneman, L., Howard, H. C., Lucassen, A., Ormond, K., Peterlin, B., Radojkovic, D., Rogowski, W., Soller, M., Tibben, A., Tranebjærg, L. & 2 andravan El, C. G. & Cornel, M. C., 2015, I : European Journal of Human Genetics. 23, 11, s. 1438-1450

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  36. Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations.

    Dondorp, W., de Wert, G., Bombard, Y., Bianchi, D. W., Bergmann, C., Borry, P., Chitty, L. S., Fellmann, F., Forzano, F., Hall, A., Henneman, L., Howard, H. C., Lucassen, A., Ormond, K., Peterlin, B., Radojkovic, D., Rogowski, W., Soller, M., Tibben, A., Tranebjærg, L. & 2 andravan El, C. G. & Cornel, M. C., 2015, I : European Journal of Human Genetics.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  37. The utility of fluorescence in situ hybridization (FISH) in the diagnosis of myxoid soft tissue neoplasms

    Downs-Kelly, E., Goldblum, J. R., Patel, R. M., Weiss, S. W., Folpe, A. L., Fredrik Mertens, Hartke, M., Tubbs, R. R. & Skacel, M., 2008, I : American Journal of Surgical Pathology. 32, 1, s. 8-13

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  38. 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

  39. 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

  40. Nuclear expression of STAT6 distinguishes solitary fibrous tumor from histologic mimics

    Doyle, L. A., Vivero, M., Fletcher, C. D. M., Fredrik Mertens & Hornick, J. L., 2014, I : Modern Pathology. 27, 3, s. 390-395

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift