Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1974 3
1975 3
1976 2
1979 1
1980 3
1981 2
1984 3
1986 5
1987 2
1988 2
1989 1
1990 6
1991 1
1992 9
1993 9
1994 6
1995 10
1996 5
1997 2
1998 3
1999 1
2000 5
2001 5
2002 3
2003 2
2004 6
2005 4
2006 6
2007 5
2008 6
2009 11
2010 4
2011 3
2012 1
2013 3
2014 1
2015 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

140 results

Results by year

Filters applied: . Clear all
Page 1
Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers.
Bougeard G, Renaux-Petel M, Flaman JM, Charbonnier C, Fermey P, Belotti M, Gauthier-Villars M, Stoppa-Lyonnet D, Consolino E, Brugières L, Caron O, Benusiglio PR, Bressac-de Paillerets B, Bonadona V, Bonaïti-Pellié C, Tinat J, Baert-Desurmont S, Frebourg T. Bougeard G, et al. Among authors: bonaiti pellie c. J Clin Oncol. 2015 Jul 20;33(21):2345-52. doi: 10.1200/JCO.2014.59.5728. Epub 2015 May 26. J Clin Oncol. 2015. PMID: 26014290
Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.
Bonadona V, Bonaïti B, Olschwang S, Grandjouan S, Huiart L, Longy M, Guimbaud R, Buecher B, Bignon YJ, Caron O, Colas C, Noguès C, Lejeune-Dumoulin S, Olivier-Faivre L, Polycarpe-Osaer F, Nguyen TD, Desseigne F, Saurin JC, Berthet P, Leroux D, Duffour J, Manouvrier S, Frébourg T, Sobol H, Lasset C, Bonaïti-Pellié C; French Cancer Genetics Network. Bonadona V, et al. Among authors: bonaiti pellie c. JAMA. 2011 Jun 8;305(22):2304-10. doi: 10.1001/jama.2011.743. JAMA. 2011. PMID: 21642682
Genetic study of scaphocephaly.
Lajeunie E, Le Merrer M, Bonaïti-Pellie C, Marchac D, Renier D. Lajeunie E, et al. Among authors: bonaiti pellie c. Am J Med Genet. 1996 Mar 29;62(3):282-5. doi: 10.1002/(SICI)1096-8628(19960329)62:3<282::AID-AJMG15>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8882788
Segregation analysis in nonsyndromic holoprosencephaly.
Odent S, Le Marec B, Munnich A, Le Merrer M, Bonaïti-Pellié C. Odent S, et al. Among authors: bonaiti pellie c. Am J Med Genet. 1998 May 1;77(2):139-43. Am J Med Genet. 1998. PMID: 9605287
Genetic study of nonsyndromic coronal craniosynostosis.
Lajeunie E, Le Merrer M, Bonaïti-Pellie C, Marchac D, Renier D. Lajeunie E, et al. Among authors: bonaiti pellie c. Am J Med Genet. 1995 Feb 13;55(4):500-4. doi: 10.1002/ajmg.1320550422. Am J Med Genet. 1995. PMID: 7762595
[Li-Fraumeni syndrome: update, new data and guidelines for clinical management].
Frebourg T, Abel A, Bonaiti-Pellie C, Brugières L, Berthet P, Bressac-de Paillerets B, Chevrier A, Chompret A, Cohen-Haguenauer O, Delattre O, Feingold J, Feunteun J, Frappaz D, Fricker JP, Gesta P, Jonveaux P, Kalifa C, Lasset C, Leheup B, Limacher JM, Longy M, Nogues C, Oppenheim D, Sommelet D, Soubrier F, Stoll C, Stoppa-Lyonnet D, Tristant H. Frebourg T, et al. Among authors: bonaiti pellie c. Bull Cancer. 2001 Jun;88(6):581-7. Bull Cancer. 2001. PMID: 11459705 Free article. Review. French.
[Cancer genetics: estimation of the needs of the population in France for the next ten years].
Bonaïti-Pellié C, Andrieu N, Arveux P, Bonadona V, Buecher B, Delpech M, Jolly D, Julian-Reynier C, Luporsi E, Noguès C, Nowak F, Olschwang S, Orsi F, Pujol P, Saurin JC, Sinilnikova O, Stoppa-Lyonnet D, Thépot F. Bonaïti-Pellié C, et al. Bull Cancer. 2009 Sep;96(9):875-900. doi: 10.1684/bdc.2009.0943. Bull Cancer. 2009. PMID: 19751997 Free article. Review. French.
[Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas].
Olschwang S, Bonaïti-Pellié C, Feingold J, Frébourg T, Grandjouan S, Lasset C, Laurent-Puig P, Lecuru F, Millat B, Sobol H, Thomas G, Eisinger F. Olschwang S, et al. Among authors: bonaiti pellie c. Pathol Biol (Paris). 2006 May;54(4):215-29. doi: 10.1016/j.patbio.2006.02.008. Epub 2006 May 4. Pathol Biol (Paris). 2006. PMID: 16677780 Review. French.
Segregation analysis of Alagille syndrome.
Dhorne-Pollet S, Deleuze JF, Hadchouel M, Bonaïti-Pellié C. Dhorne-Pollet S, et al. Among authors: bonaiti pellie c. J Med Genet. 1994 Jun;31(6):453-7. doi: 10.1136/jmg.31.6.453. J Med Genet. 1994. PMID: 8071971 Free PMC article.
Fragile site (16) (q22). III. Segregation analysis.
Müller B, Feichtinger W, Bonaïti-Pellié C, Schmid M. Müller B, et al. Among authors: bonaiti pellie c. Hum Genet. 1992 Aug;89(6):612-4. doi: 10.1007/BF00221948. Hum Genet. 1992. PMID: 1511978
140 results