Items where Author is "Heinimann, K."

2022

Sarki, M. and Ming, C. and Aissaoui, S. and Bürki, N. and Caiata-Zufferey, M. and Erlanger, T. E. and Graffeo-Galbiati, R. and Heinimann, K. and Heinzelmann-Schwarz, V. and Monnerat, C. and Probst-Hensch, N. and Rabaglio, M. and Zurrer-Härdi, U. and Chappuis, P. O. and Katapodi, M. C. and Cascade Consortium, . (2022) Intention to inform relatives, rates of cascade testing, and preference for patient-mediated communication in families concerned with hereditary breast and ovarian cancer and lynch syndrome: the Swiss CASCADE Cohort. Cancers (Basel), 14 (7). p. 1636.

Sarki, M. and Ming, C. and Aceti, M. and Fink, G. and Aissaoui, S. and Bürki, N. and Graffeo, R. and Heinimann, K. and Caiata Zufferey, M. and Monnerat, C. and Rabaglio, M. and Zürrer-Härdi, U. and Chappuis, P. O. and Katapodi, M. C. and The Cascade Consortium, . (2022) Relatives from hereditary breast and ovarian cancer and lynch syndrome families forgoing genetic testing: findings from the Swiss CASCADE cohort. J Pers Med, 12 (10). p. 1740.

2016

De Geyter, C. and M'Rabet, N. and De Geyter, J. and Zhang, H. and Heinimann, K.. (2016) Response to Sierra-Delgado et al. Genetics in Medicine, 18 (8). pp. 857-858.

2014

De Geyter, C. and M'Rabet, N. and De Geyter, J. and Zurcher, S. and Moffat, R. and Bosch, N. and Zhang, H. and Heinimann, K.. (2014) Similar prevalence of expanded CGG repeat lengths in the fragile X mental retardation I gene among infertile women and among women with proven fertility : a prospective study. Genetics in medicine, Vol. 16, H. 5. pp. 374-378.

2013

Peyer, A. K. and Abicht, A. and Heinimann, K. and Sinnreich, M. and Fischer, D.. (2013) Quinine sulfate as a therapeutic option in a patient with slow channel congenital myasthenic syndrome. Neuromuscular disorders, Vol. 23, H. 7. pp. 571-574.

Heng, B. C. and Heinimann, K. and Miny, P. and Iezzi, G. and Glatz, K. and Scherberich, A. and Zulewski, H. and Fussenegger, M.. (2013) mRNA transfection-based, feeder-free, induced pluripotent stem cells derived from adipose tissue of a 50-year-old patient. Metabolic Engineering, 18. pp. 9-24.

2011

Filges, I. and Röthlisberger, B. and Blattner, A. and Boesch, N. and Demougin, P. and Wenzel, F. and Huber, A. R. and Heinimann, K. and Weber, P. and Miny, P.. (2011) Deletion in Xp22.11 : PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism. Clinical genetics, Vol. 79, H. 1. pp. 79-85.

Burger, B. and Cattani, N. and Trueb, S. and de Lorenzo, R. and Albertini, M. and Bontognali, E. and Itin, C. and Schaub, N. and Itin, P. H. and Heinimann, K.. (2011) Prevalence of skin lesions in familial adenomatous polyposis : a marker for presymptomatic diagnosis? The Oncologist, 16 (12). pp. 1698-1705.

2010

Kantelinen, J. and Kansikas, M. and Korhonen, M. K. and Ollila, S. and Heinimann, K. and Kariola, R. and Nyström, M.. (2010) MutSbeta exceeds MutSalpha in dinucleotide loop repair. British journal of cancer, Vol. 102, no. 6. pp. 1068-1073.

Zlobec, I. and Molinari, F. and Kovac, M. and Bihl, M. P. and Altermatt, H. J. and Diebold, J. and Frick, H. and Germer, M. and Horcic, M. and Montani, M. and Singer, G. and Yurtsever, H. and Zettl, A. and Terracciano, L. and Mazzucchelli, L. and Saletti, P. and Frattini, M. and Heinimann, K. and 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, Vol. 102, no. 1. pp. 151-161.

Vasen, H. F. A. and Möslein, G. and Alonso, A. and Aretz, S. and Bernstein, I. and Bertario, L. and Blanco, I. and Bulow, S. and Burn, J. and Capella, G. and Colas, C. and Engel, C. and Frayling, I. and Rahner, N. and Hes, F. J. and Hodgson, S. and Mecklin, J.-P. and Møller, P. and Myrhøj, T. and Nagengast, F. M. and Parc, Y. and Ponz de Leon, M. and Renkonen-Sinisalo, L. and Sampson, J. R. and Stormorken, A. and Tejpar, S. and Thomas, H. J. W. and Wijnen, J. and Lubinski, J. and Järvinen, H. and Claes, E. and Heinimann, K. and Karagiannis, J. A. and Lindblom, A. and Dove-Edwin, I. and Müller, H.. (2010) Recommendations to improve identification of hereditary and familial colorectal cancer in Europe. Familial cancer, Vol. 9, H. 2. pp. 109-115.

2008

Jaeger, E. and Webb, E. and Howarth, K. and Carvajal-Carmona, L. and Rowan, A. and Broderick, P. and Walther, A. and Spain, S. and Pittman, A. and Kemp, Z. and Sullivan, K. and Heinimann, K. and Lubbe, S. and Domingo, E. and Barclay, E. and Martin, L. and Gorman, M. and Chandler, I. and Vijayakrishnan, J. and Wood, W. and Papaemmanuil, E. and Penegar, S. and Qureshi, M. and Corgi, Consortium and Farrington, S. and Tenesa, A. and Cazier, J. B. and Kerr, D. and Gray, R. and Peto, J. and Dunlop, M. and Campbell, H. and Thomas, H. and Houlston, R. and Tomlinson, I.. (2008) Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk. Nature genetics, Vol. 40, H. 1. pp. 26-28.

Oliveira, J. and Santos, R. and Soares-Silva, I. and Jorge, P. and Vieira, E. and Oliveira, M. E. and Moreira, A. and Coelho, T. and Ferreira, J. C. and Fonseca, M. J. and Barbosa, C. and Prats, J. and Aríztegui, M. L. and Martins, M. L. and Moreno, T. and Heinimann, K. and Barbot, C. and Pascual-Pascual, S. I. and Cabral, A. and Fineza, I. and Santos, M. and Bronze-da-Rocha, E.. (2008) LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients. Clinical genetics, Vol. 74, H. 6. pp. 502-512.

Filges, I. and Röthlisberger, B. and Wenzel, F. and Heinimann, K. and Huber, A. R. and Miny, P.. (2008) Mosaic ring chromosome 8 : clinical and array-CGH findings in partial trisomy 8. American journal of medical genetics. Part A, Vol. 146, H. 21. pp. 2837-2841.