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Oncology Reports|October 19, 1999
Hypothesis: more mutations to cure cancer?F Eisinger, H Sobol, D BirnbaumCommunity Genetics|February 13, 2004
French physicians' knowledge about hereditary breast/ovarian cancer: the need for continuing vocational training in geneticsC Julian-Reynier, F Eisinger, J P Moatti, et al.European Journal of Human Genetics : EJHG|April 26, 2000
Physicians' attitudes towards mammography and prophylactic surgery for hereditary breast/ovarian cancer risk and subsequently published guidelinesC Julian-Reynier, F Eisinger, J P Moatti, et al.Annales De Chirurgie|January 1, 1994
[Genetics and cancer of the breast]H Sobol, Y J Bignon, F Eisinger, et al.Annales D'Endocrinologie|April 6, 1999
[Impact of recent oncogenetic progress on the management of high risk breast cancer patients: the example of BRCA1 and BRCA2 genes]H Sobol, F Eisinger, R Sauvan, et al.International Journal of Cancer|February 14, 1998
Loss of heterozygosity at loci from chromosome arm 22Q in human sporadic breast carcinomasF Allione, F Eisinger, P Parc, et al.Anticancer Research|November 20, 2001
PS2 expression in BRCA1-associated breast cancersE Charafe-Jauffre, F Eisinger, M P Mathoulin-Portier, et al.Psycho-Oncology|December 9, 2008
Subjective interpretation of inconclusive BRCA1/2 cancer genetic test results and transmission of information to the relativesC Cypowyj, F Eisinger, L Huiart, et al.Community Genetics|August 28, 2004
Information-seeking behaviour and psycho-social interactions during the genetic testing processC Cypowyj, F Eisinger, M Morin, et al.International Journal of Oncology|December 15, 2000
Tamoxifen and breast cancer risk in women harboring a BRCA1 germline mutation: computed efficacy, effectiveness and impactF Eisinger, E Charafe-Jauffret, J Jacquemier, et al.Pageof 16