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Ausgewählte Publikationen

Figlioli G, Köhler A, Chen B, Elisei R, Romei C, Cipollini M, Cristaudo A, Bambi F, Paolicchi E, Hoffmann P, Herms S, Kalemba M, Kula D, Pastor S, Marcos R, Velázquez A, Jarzab B, Landi S, Hemminki K, Försti A, Gemignani F. Novel genome-wide association study-based candidate Loci for differentiated thyroid cancer risk. J Clin Endocrinol Metab. 2014 Oct;99(10):E2084-92.

Woltmann A, Chen B, Lascorz J, Johansson R, Eyfjörd JE, Hamann U, Manjer J, Enquist-Olsson K, Henriksson R, Herms S, Hoffmann P, Hemminki K, Lenner P, Försti A. Systematic pathway enrichment analysis of a genome-wide association study on breast cancer survival reveals an influence of genes involved in cell adhesion and calcium signaling on the patients' clinical outcome. PLoS One. 2014 Jun 2;9(6):e98229.

Hemminki K, Musak L, Vymetalkova V, Smerhovsky Z, Halasova E, Osina O, Letkova L, Försti A, Vodickova L, Buchancova J, Vodicka P. Cyclin D1 splice site variant triggers chromosomal aberrations in healthy humans. Leukemia. 2014;28:721-2.

Weinhold N, Johnson DC, Rawstron AC, Försti A, Doughty C, Vijayakrishnan J, Broderick P, Dahir NB, Begum DB, Hosking FJ, Yong K, Walker BA, Hoffmann P, Mühleisen TW, Langer C, Dörner E, Jöckel KH, Eisele L, Nöthen MM, Hose D, Davies FE, Goldschmidt H, Morgan GJ, Hemminki K, Houlston RS. Inherited genetic susceptibility to monoclonal gammopathy of unknown significance. Blood 2014;123:2513-17.

Weinhold N, Försti A, da Silva Filho MI, Nickel J, Campo C, Hoffmann P, Nöthen MM, Hose D, Goldschmidt H, Jauch A, Langer C, Hegenbart U, Schönland SO, Hemminki K. Immunoglobulin light chain amyloidosis shares genetic susceptibility with multiple myeloma. Leukemia 2014 Nov;28(11):2254-6.

Hemminki K, Fallah M, Hemminki A. Collection and Use of Family History in Oncology Clinics.J Clin Oncol 2014; 32(29):3344-5.

Letzte Aktualisierung: 16.06.2015 Seitenanfang