Benutzerspezifische Werkzeuge

Publikationen - 2011

Carrai,M., Steinke,V., Vodicka,P., Pardini,B., Rahner,N., Holinski-Feder,E., Morak,M., Schackert,H.K., Gorgens,H., Stemmler,S., Betz,B., Kloor,M., Engel,C., Buttner,R., Naccarati,A., Vodickova,L., Novotny,J., Stein,A., Hemminki,K., Propping,P., Forsti,A., Canzian,F., Barale,R., and Campa,D. (2011). Association between TAS2R38 gene polymorphisms and colorectal cancer risk: a case-control study in two independent populations of Caucasian origin. PLoS. One. 6, e20464.
Serra,A., Schuchardt,K., Genuneit,J., Leriche,C., Gorgens,H.S., Schackert,H.K., and Fitze,G. (2011). The role of RET genomic variants in infantile hypertrophic pyloric stenosis. Eur. J. Pediatr. Surg. 21, 389-394.
Venkatachalam,R., Verwiel,E.T., Kamping,E.J., Hoenselaar,E., Gorgens,H., Schackert,H.K., van Krieken,J.H., Ligtenberg,M.J., Hoogerbrugge,N., van Kessel,A.G., and Kuiper,R.P. (2011). Identification of candidate predisposing copy number variants in familial and early-onset colorectal cancer patients. Int. J. Cancer 129, 1635-1642.
Morak,M., Koehler,U., Schackert,H.K., Steinke,V., Royer-Pokora,B., Schulmann,K., Kloor,M., Hochter,W., Weingart,J., Keiling,C., Massdorf,T., and Holinski-Feder,E. (2011). Biallelic MLH1 SNP cDNA expression or constitutional promoter methylation can hide genomic rearrangements causing Lynch syndrome. J. Med. Genet. 48, 513-519.
Ruckert,F., Gorgens,H., Richter,I., Krex,D., Schackert,G., Kuhlisch,E., Fitze,G., Saeger,H.D., Pilarsky,C., Grutzmann,R., and Schackert,H.K. (2011). RET-protooncogene variants in patients with sporadic neoplasms of the digestive tract and the central nervous system. Int. J. Colorectal Dis. 26, 835-840.
Kern,A., Gorgens,H., Dittert,D.D., Kruger,S., Richter,K.K., Schackert,H.K., Saeger,H.D., Baretton,G., and Pistorius,S. (2011). Mutational status of KIT and PDGFRA and expression of PDGFRA are not associated with prognosis after curative resection of primary gastrointestinal stromal tumors (GISTs). J. Surg. Oncol. 104, 59-65.
Hardt,K., Heick,S.B., Betz,B., Goecke,T., Yazdanparast,H., Kuppers,R., Servan,K., Steinke,V., Rahner,N., Morak,M., Holinski-Feder,E., Engel,C., Moslein,G., Schackert,H.K., von Knebel,D.M., Pox,C., Hegemann,J.H., and Royer-Pokora,B. (2011). Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies. Fam. Cancer 10, 273-284.
Kuiper,R.P., Vissers,L.E., Venkatachalam,R., Bodmer,D., Hoenselaar,E., Goossens,M., Haufe,A., Kamping,E., Niessen,R.C., Hogervorst,F.B., Gille,J.J., Redeker,B., Tops,C.M., van Gijn,M.E., van den Ouweland,A.M., Rahner,N., Steinke,V., Kahl,P., Holinski-Feder,E., Morak,M., Kloor,M., Stemmler,S., Betz,B., Hutter,P., Bunyan,D.J., Syngal,S., Culver,J.O., Graham,T., Chan,T.L., Nagtegaal,I.D., van Krieken,J.H., Schackert,H.K., Hoogerbrugge,N., van Kessel,A.G., and Ligtenberg,M.J. (2011). Recurrence and variability of germline EPCAM deletions in Lynch syndrome. Hum. Mutat. 32, 407-414.
Kempers,M.J., Kuiper,R.P., Ockeloen,C.W., Chappuis,P.O., Hutter,P., Rahner,N., Schackert,H.K., Steinke,V., Holinski-Feder,E., Morak,M., Kloor,M., Buttner,R., Verwiel,E.T., van Krieken,J.H., Nagtegaal,I.D., Goossens,M., van der Post,R.S., Niessen,R.C., Sijmons,R.H., Kluijt,I., Hogervorst,F.B., Leter,E.M., Gille,J.J., Aalfs,C.M., Redeker,E.J., Hes,F.J., Tops,C.M., van Nesselrooij,B.P., van Gijn,M.E., Gomez Garcia,E.B., Eccles,D.M., Bunyan,D.J., Syngal,S., Stoffel,E.M., Culver,J.O., Palomares,M.R., Graham,T., Velsher,L., Papp,J., Olah,E., Chan,T.L., Leung,S.Y., van Kessel,A.G., Kiemeney,L.A., Hoogerbrugge,N., and Ligtenberg,M.J. (2011). Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study. Lancet Oncol. 12, 49-55.
Kloor,M., Voigt,A.Y., Schackert,H.K., Schirmacher,P., von Knebel,D.M., and Blaker,H. (2011). Analysis of EPCAM protein expression in diagnostics of Lynch syndrome. J. Clin. Oncol. 29, 223-227.
Huhn,S., Ingelfinger,D., Bermejo,J.L., Bevier,M., Pardini,B., Naccarati,A., Steinke,V., Rahner,N., Holinski-Feder,E., Morak,M., Schackert,H.K., Gorgens,H., Pox,C.P., Goecke,T., Kloor,M., Loeffler,M., Buttner,R., Vodickova,L., Novotny,J., Demir,K., Cruciat,C.M., Renneberg,R., Huber,W., Niehrs,C., Boutros,M., Propping,P., Vodieka,P., Hemminki,K., and Forsti,A. (2011). Polymorphisms in CTNNBL1 in relation to colorectal cancer with evolutionary implications. Int. J. Mol. Epidemiol. Genet. 2, 36-50.