Author

Cécile Boisson

Observed names: C Boisson, C. Boisson, Cecile Boisson

Observed institutions: Inserm, École Pratique des Hautes Études, Fondation Jean Dausset-CEPH, Hôpital Saint-Antoine, Centre Hospitalier Sainte-Anne, Institut Curie

OpenAlex ID: A5007871237

Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan

1996 · Berton Zbar, Takeshi Kishida, et al. · Human Mutation · 503

Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444

1995 · Reiner Caspari, Sylciane Olschwang, et al. · Human Molecular Genetics · 369

MSH2 in contrast to MLH1 and MSH6 is frequently inactivated by exonic and promoter rearrangements in hereditary nonpolyposis colorectal cancer.

2002 · Françoise Charbonnier, Sylviane Olschwang, et al. · PubMed · 125

Germline mutation profile of the VHL gene in von Hippel‐Lindau disease and in sporadic hemangioblastoma

1998 · Sylviane Olschwang, Stéphane Richard, et al. · Human Mutation · 105

Peutz-Jeghers families unlinked toSTK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma

2001 · Sylviane Olschwang, Cécile Boisson, et al. · Journal of Medical Genetics · 91

Heterogeneity of mesothelioma cell lines as defined by altered genomic structure and expression of theNF2 gene

1998 · Brigitte Deguen, Laurence Goutebroze, et al. · International Journal of Cancer · 60

DNA-Based Presymptomatic Diagnosis for the von Hippel-Lindau Disease by Linkage Analysis

1995 · S. Olschwang, C. Boisson, et al. · European Journal of Human Genetics · 6

[Familial adenomatous polyposis coli in the Czech population. I. Detection of an additional 3 mutations out of a total of 7 in exon 15 of the APC gene].

1997 · V Jirásek, S Olschwang, et al. · PubMed

Works count: 8

Citation count: 1,259

H-index: 6

I10-index: 6