Uni Basel Research Database

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Publications

Showing records 1 - 20 (of 28)

Publication: JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)

ID	Author	Year	Title	Publisher
1193604	von Kanel, Thomas; Gerber, Dominik; Schaller, André; Baumer, Alessandra; Wey, Eva; Jackson, Christopher B; Gisler, Franziska M; Heinimann, Karl; Gallati, Sabina	2010	Quantitative 1-step DNA methylation analysis with native genomic DNA as template	Clinical chemistry
1197045	Zlobec, Inti; Kovac, Michal; Erzberger, Priska; Molinari, Francesca; Bihl, Michel P; Rufle, Alexander; Foerster, Anja; Frattini, Milo; Terracciano, Luigi; Heinimann, Karl; Lugli, Alessandro	2010	Combined analysis of specific KRAS mutation, BRAF and microsatellite instability identifies prognostic subgroups of sporadic and hereditary colorectal cancer	International journal of cancer
1193370	Zlobec, I; Molinari, F; Kovac, M; Bihl, M P; Altermatt, H J; Diebold, J; Frick, H; Germer, M; Horcic, M; Montani, M; Singer, G; Yurtsever, H; Zettl, A; Terracciano, L; Mazzucchelli, L; Saletti, P; Frattini, M; Heinimann, K; Lugli, A	2010	Prognostic and predictive value of TOPK stratified by KRAS and BRAF gene alterations in sporadic, hereditary and metastatic colorectal cancer patients	British journal of cancer
4596629	Zimmermann, Bettina M.; Shaw, David; Heinimann, Karl; Knabben, Laura; Elger, Bernice; Koné, Insa	2020	How the "control-fate continuum" helps explain the genetic testing decision-making process: a grounded theory study	European journal of human genetics : EJHG : the official journal of the European Society of Human Genetics
1197046	Vasen, H F A; Möslein, G; Alonso, A; Aretz, S; Bernstein, I; Bertario, L; Blanco, I; Bulow, S; Burn, J; Capella, G; Colas, C; Engel, C; Frayling, I; Rahner, N; Hes, F J; Hodgson, S; Mecklin, J-P; Møller, P; Myrhøj, T; Nagengast, F M; Parc, Y; Ponz de Leon, M; Renkonen-Sinisalo, L; Sampson, J R; Stormorken, A; Tejpar, S; Thomas, H J W; Wijnen, J; Lubinski, J; Järvinen, H; Claes, E; Heinimann, K; Karagiannis, J A; Lindblom, A; Dove-Edwin, I; Müller, H	2010	Recommendations to improve identification of hereditary and familial colorectal cancer in Europe	Familial cancer
1196145	Templeton, Arnoud; Marra, Giancarlo; Valtorta, Emanuele; Heinimann, Karl; Müller, Hansjakob; Köberle, Dieter; Gillessen, Silke	2009	Concordant colon tumors in monozygotic twins previously treated for prostate cancer	Familial cancer
1194306	Out, Astrid A; Tops, Carli M J; Nielsen, Maartje; Weiss, Marjan M; van Minderhout, Ivonne J H M; Fokkema, Ivo F A C; Buisine, Marie-Pierre; Claes, Kathleen; Colas, Chrystelle; Fodde, Riccardo; Fostira, Florentia; Franken, Patrick F; Gaustadnes, Mette; Heinimann, Karl; Hodgson, Shirley V; Hogervorst, Frans B L; Holinski-Feder, Elke; Lagerstedt-Robinson, Kristina; Olschwang, Sylviane; van den Ouweland, Ans M W; Redeker, Egbert J W; Scott, Rodney J; Vankeirsbilck, Bruno; Grønlund, Rikke Veggerby; Wijnen, Juul T; Wikman, Friedrik P; Aretz, Stefan; Sampson, Julian R; Devilee, Peter; den Dunnen, Johan T; Hes, Frederik J	2010	Leiden Open Variation Database of the MUTYH gene	Human mutation
1195332	Oliveira, J; Santos, R; Soares-Silva, I; Jorge, P; Vieira, E; Oliveira, M E; Moreira, A; Coelho, T; Ferreira, J C; Fonseca, M J; Barbosa, C; Prats, J; Aríztegui, M L; Martins, M L; Moreno, T; Heinimann, K; Barbot, C; Pascual-Pascual, S I; Cabral, A; Fineza, I; Santos, M; Bronze-da-Rocha, E	2008	LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients	Clinical genetics
1194552	Necker, Judith; Kovac, Michal; Attenhofer, Michèle; Reichlin, Bruno; Heinimann, Karl	2011	Detection of APC germ line mosaicism in patients with de novo familial adenomatous polyposis : a plea for the protein truncation test	Journal of medical genetics
1193587	Montani, Matteo; Heinimann, Karl; von Teichman, Adriana; Rudolph, Thomas; Perren, Aurel; Moch, Holger	2010	VHL-gene deletion in single renal tubular epithelial cells and renal tubular cysts : further evidence for a cyst-dependent progression pathway of clear cell renal carcinoma in von Hippel-Lindau disease	American journal of surgical pathology
1193845	Kovac, Michal; Laczko, Endre; Haider, Ritva; Jiricny, Josef; Mueller, Hansjakob; Heinimann, Karl; Marra, Giancarlo	2011	Familial colorectal cancer: eleven years of data from a registry program in Switzerland	Familial cancer
1194068	Kantelinen, J; Kansikas, M; Korhonen, M K; Ollila, S; Heinimann, K; Kariola, R; Nyström, M	2010	MutSbeta exceeds MutSalpha in dinucleotide loop repair	British journal of cancer
1195322	Jaeger,E; Webb,E; Howarth,K; Carvajal-Carmona,L; Rowan,A; Broderick,P; Walther,A; Spain,S; Pittman,A; Kemp,Z; Sullivan,K; Heinimann,K; Lubbe,S; Domingo,E; Barclay,E; Martin,L; Gorman,M; Chandler,I; Vijayakrishnan,J; Wood,W; Papaemmanuil,E; Penegar,S; Qureshi,M; CORGI,Consortium; Farrington,S; Tenesa,A; Cazier,JB; Kerr,D; Gray,R; Peto,J; Dunlop,M; Campbell,H; Thomas,H; Houlston,R; Tomlinson,I	2008	Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk	Nature genetics
4374174	Itin, Peter H.; Heinimann, Karl; Attenhofer, Michèle; Boesch, Nemya; De Lorenzo, Rosaria; Trüb, Swantje; Burger, Bettina	2010	Precalcaneal congenital fibrolipomatous hamartomas: is there a pathogenetic relationship with Gardner Syndrome?	European journal of dermatology : EJD
1192681	Gloor, Monika; Fasler, Susanne; Fischmann, Arne; Haas, Tanja; Bieri, Oliver; Heinimann, Karl; Wetzel, Stephan G; Scheffler, Klaus; Fischer, Dirk	2011	Quantification of fat infiltration in oculopharyngeal muscular dystrophy : comparison of three MR imaging methods	Journal of magnetic resonance imaging
1197044	Ganster, Christina; Wernstedt, Annekatrin; Kehrer-Sawatzki, Hildegard; Messiaen, Ludwine; Schmidt, Konrad; Rahner, Nils; Heinimann, Karl; Fonatsch, Christa; Zschocke, Johannes; Wimmer, Katharina	2010	Functional PMS2 hybrid alleles containing a pseudogene-specific missense variant trace back to a single ancient intrachromosomal recombination event	Human mutation
1195683	Fischmann, Arne; Gloor, Monika; Fasler, Susanne; Haas, Tanja; Rodoni Wetzel, Rachele; Bieri, Oliver; Wetzel, Stephan; Heinimann, Karl; Scheffler, Klaus; Fischer, Dirk	2011	Muscular involvement assessed by MRI correlates to motor function measurement values in oculopharyngeal muscular dystrophy	Journal of neurology
1193020	Filges,Isabel; Röthlisberger,Benno; Noppen,Christoph; Boesch,Nemya; Wenzel,Friedel; Necker,Judith; Binkert,Franz; Huber,Andreas R; Heinimann,Karl; Miny,Peter	2009	Familial 14.5 Mb interstitial deletion 13q21.1-13q21.33 : clinical and array-CGH study of a benign phenotype in a three-generation family	American journal of medical genetics
1194674	Filges, Isabel; Röthlisberger, Benno; Wenzel, Friedel; Heinimann, Karl; Huber, Andreas R; Miny, Peter	2008	Mosaic ring chromosome 8 : clinical and array-CGH findings in partial trisomy 8	American journal of medical genetics. Part A
1192680	Filges, Isabel; Röthlisberger, Benno; Boesch, Nemya; Weber, Peter; Wenzel, Friedel; Huber, Andreas R; Heinimann, Karl; Miny, Peter	2010	Interstitial deletion 1q42 in a patient with agenesis of corpus callosum : Phenotype-genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndrome	American journal of medical genetics. Part A

Showing records 1 - 20 (of 28)

11/05/2024

Research Database / FORSCHUNGSDATENBANK