-
1
-
-
34248170114
-
Meta-analysis of BRCA1 and BRCA2 penetrance
-
Chen S, Parmigiani G. Meta-analysis of BRCA1 and BRCA2 penetrance. J Clin Oncol 2007;25:1329-33.
-
(2007)
J Clin Oncol
, vol.25
, pp. 1329-1333
-
-
Chen, S.1
Parmigiani, G.2
-
2
-
-
79958071334
-
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 Y-J, Caron O, Colas C, Noguès C, Lejeune-Dumoulin S, Olivier-Faivre L. Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome. JAMA 2011;305:2304-10.
-
(2011)
JAMA
, vol.305
, pp. 2304-2310
-
-
Bonadona, V.1
Bonaïti, B.2
Olschwang, S.3
Grandjouan, S.4
Huiart, L.5
Longy, M.6
Guimbaud, R.7
Buecher, B.8
Bignon, Y.-J.9
Caron, O.10
Colas, C.11
Noguès, C.12
Lejeune-Dumoulin, S.13
Olivier-Faivre, L.14
-
3
-
-
11144356022
-
Identification et prise en charge des prédispositions héréditaires aux cancers du sein et de l'ovaire (mise à jour 2004)
-
Eisinger F, Bressac B, Castaigne D, Cottu PH, Lansac J, Lefranc JP, Lesur A, Nogues C, Pierret J, Puy-Pernias S, Sobol H, Tardivon A, Tristant H, Villet R. Identification et prise en charge des prédispositions héréditaires aux cancers du sein et de l'ovaire (mise à jour 2004). Bull Cancer 2004;91:219-37.
-
(2004)
Bull Cancer
, vol.91
, pp. 219-237
-
-
Eisinger, F.1
Bressac, B.2
Castaigne, D.3
Cottu, P.H.4
Lansac, J.5
Lefranc, J.P.6
Lesur, A.7
Nogues, C.8
Pierret, J.9
Puy-Pernias, S.10
Sobol, H.11
Tardivon, A.12
Tristant, H.13
Villet, R.14
-
4
-
-
34447340945
-
Management of an inherited predisposition to breast cancer
-
Robson M, Offit K. Management of an inherited predisposition to breast cancer. N Engl J Med 2007;357:154-62.
-
(2007)
N Engl J Med
, vol.357
, pp. 154-162
-
-
Robson, M.1
Offit, K.2
-
5
-
-
2442678871
-
Identification et prise en charge du syndrome HNPCC (Hereditary NonPolyposis Colon Cancer), prédisposition héréditaire aux cancers du côlon, du rectum et de l'utérus
-
Olschwang S, Bonaiti C, Feingold J, Frebourg T, Grandjouan S, Lasset C, Laurent-Puig P, Lecuru F, Millat B, Sobol H, Thomas G, Eisinger F. Identification et prise en charge du syndrome HNPCC (Hereditary NonPolyposis Colon Cancer), prédisposition héréditaire aux cancers du côlon, du rectum et de l'utérus. Bull Cancer 2004;91:303-15.
-
(2004)
Bull Cancer
, vol.91
, pp. 303-315
-
-
Olschwang, S.1
Bonaiti, C.2
Feingold, J.3
Frebourg, T.4
Grandjouan, S.5
Lasset, C.6
Laurent-Puig, P.7
Lecuru, F.8
Millat, B.9
Sobol, H.10
Thomas, G.11
Eisinger, F.12
-
6
-
-
33749067855
-
Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review
-
Lindor NM, Petersen GM, Hadley DW, Kinney AY, Miesfeldt S, Lu KH, Lynch P, Burke W, Press N. Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review. JAMA 2006;296:1507-17.
-
(2006)
JAMA
, vol.296
, pp. 1507-1517
-
-
Lindor, N.M.1
Petersen, G.M.2
Hadley, D.W.3
Kinney, A.Y.4
Miesfeldt, S.5
Lu, K.H.6
Lynch, P.7
Burke, W.8
Press, N.9
-
7
-
-
33646446067
-
Risk prediction models for familial breast cancer
-
Antoniou AC, Easton DF. Risk prediction models for familial breast cancer. Future Oncol 2006;2:257-74.
-
(2006)
Future Oncol
, vol.2
, pp. 257-274
-
-
Antoniou, A.C.1
Easton, D.F.2
-
8
-
-
0031917403
-
Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2
-
Parmigiani G, Berry D, Aguilar O. Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2. Am J Hum Genet 1998;62:145-58.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 145-158
-
-
Parmigiani, G.1
Berry, D.2
Aguilar, O.3
-
9
-
-
7944237307
-
The BOADICEA model of genetic susceptibility to breast and ovarian cancer
-
Antoniou AC, Pharoah PP, Smith P, Easton DF. The BOADICEA model of genetic susceptibility to breast and ovarian cancer. Br J Cancer 2004;91:1580-90.
-
(2004)
Br J Cancer
, vol.91
, pp. 1580-1590
-
-
Antoniou, A.C.1
Pharoah, P.P.2
Smith, P.3
Easton, D.F.4
-
10
-
-
1842680082
-
A breast cancer prediction model incorporating familial and personal risk factors
-
Tyrer J, Duffy SW, Cuzick J. A breast cancer prediction model incorporating familial and personal risk factors. Stat Med 2004;23:111-1130.
-
(2004)
Stat Med
, vol.23
, pp. 111-1130
-
-
Tyrer, J.1
Duffy, S.W.2
Cuzick, J.3
-
11
-
-
2942726188
-
A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO
-
Evans DG, Eccles DM, Rahman N, Young K, Bulman M, Amir E, Shenton A, Howell A, Lalloo F. A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO. J Med Genet 2004;41:474-80.
-
(2004)
J Med Genet
, vol.41
, pp. 474-480
-
-
Evans, D.G.1
Eccles, D.M.2
Rahman, N.3
Young, K.4
Bulman, M.5
Amir, E.6
Shenton, A.7
Howell, A.8
Lalloo, F.9
-
12
-
-
33644872552
-
Update on the Manchester Scoring System for BRCA1 and BRCA2 testing
-
Evans DG, Lalloo F, Wallace A, Rahman N. Update on the Manchester Scoring System for BRCA1 and BRCA2 testing. J Med Genet 2005;42:e39.
-
(2005)
J Med Genet
, vol.42
-
-
Evans, D.G.1
Lalloo, F.2
Wallace, A.3
Rahman, N.4
-
14
-
-
79960502227
-
Nouveau système de score pour le diagnostic des prédispositions aux cancers du sein et de l'ovaire associées à BRCA1/2
-
Bonaïti B, Alarcon F, Bonadona V, et al. Nouveau système de score pour le diagnostic des prédispositions aux cancers du sein et de l'ovaire associées à BRCA1/2. Bull Cancer 2011;98:779-95.
-
(2011)
Bull Cancer
, vol.98
, pp. 779-795
-
-
Bonaïti, B.1
Alarcon, F.2
Bonadona, V.3
-
15
-
-
72749102465
-
Addition of pathology and biomarker information significantly improves the performance of the Manchester scoring system for BRCA1 and BRCA2 testing
-
Evans DG, Lalloo F, Cramer A, Jones EA, Knox F, Amir E, Howell A. Addition of pathology and biomarker information significantly improves the performance of the Manchester scoring system for BRCA1 and BRCA2 testing. J Med Genet 2009;46:811-17.
-
(2009)
J Med Genet
, vol.46
, pp. 811-817
-
-
Evans, D.G.1
Lalloo, F.2
Cramer, A.3
Jones, E.A.4
Knox, F.5
Amir, E.6
Howell, A.7
-
16
-
-
0036569877
-
The pathology of familial breast cancer: predictive value of immunohistochemical markers estrogen receptor, progesterone receptor, HER-2, and p53 in patients with mutations in BRCA1 and BRCA2
-
Lakhani SR, Van de Vijver MJ, Jacquemier J, Anderson TJ, Osin PP, McGuffog L, Easton DF. The pathology of familial breast cancer: predictive value of immunohistochemical markers estrogen receptor, progesterone receptor, HER-2, and p53 in patients with mutations in BRCA1 and BRCA2. J Clin Oncol 2002;20:2310-18.
-
(2002)
J Clin Oncol
, vol.20
, pp. 2310-2318
-
-
Lakhani, S.R.1
Van de Vijver, M.J.2
Jacquemier, J.3
Anderson, T.J.4
Osin, P.P.5
McGuffog, L.6
Easton, D.F.7
-
17
-
-
0033498602
-
Germline mutation and genome instability
-
Olschwang S. Germline mutation and genome instability. Eur J Cancer Prev 1999;8 (Suppl 1):S33-7.
-
(1999)
Eur J Cancer Prev
, vol.8
, Issue.1
-
-
Olschwang, S.1
-
18
-
-
33845654907
-
Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: a kin-cohort study in Ontario Canada
-
Risch HA, McLaughlin JR, Cole DE, Rosen B, Bradley L, Fan I, Tang J, Li S, Zhang S, Shaw PA, Narod SA. Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: a kin-cohort study in Ontario, Canada. J Natl Cancer Inst 2006;98:1694-706.
-
(2006)
J Natl Cancer Inst
, vol.98
, pp. 1694-1706
-
-
Risch, H.A.1
McLaughlin, J.R.2
Cole, D.E.3
Rosen, B.4
Bradley, L.5
Fan, I.6
Tang, J.7
Li, S.8
Zhang, S.9
Shaw, P.A.10
Narod, S.A.11
-
19
-
-
24944434401
-
Cancer risks in BRCA2 families: estimates for sites other than breast and ovary
-
van Asperen CJ, Brohet RM, Meijers-Heijboer EJ, Hoogerbrugge N, Verhoef S, Vasen HF, Ausems MG, Menko FH, Gomez Garcia EB, Klijn JG, Hogervorst FB, van Houwelingen JC, van't Veer LJ, Rookus MA, van Leeuwen FE. Cancer risks in BRCA2 families: estimates for sites other than breast and ovary. J Med Genet 2005;42:711-19.
-
(2005)
J Med Genet
, vol.42
, pp. 711-719
-
-
van Asperen, C.J.1
Brohet, R.M.2
Meijers-Heijboer, E.J.3
Hoogerbrugge, N.4
Verhoef, S.5
Vasen, H.F.6
Ausems, M.G.7
Menko, F.H.8
Gomez Garcia, E.B.9
Klijn, J.G.10
Hogervorst, F.B.11
van Houwelingen, J.C.12
van't Veer, L.J.13
Rookus, M.A.14
van Leeuwen, F.E.15
-
21
-
-
0033611747
-
Mixture models for cancer survival analysis: application to population-based data with covariates
-
De Angelis R, Capocaccia R, Hakulinen T, Soderman B, Verdecchia A. Mixture models for cancer survival analysis: application to population-based data with covariates. Stat Med 1999;18:441-54.
-
(1999)
Stat Med
, vol.18
, pp. 441-454
-
-
De Angelis, R.1
Capocaccia, R.2
Hakulinen, T.3
Soderman, B.4
Verdecchia, A.5
-
22
-
-
78651393080
-
Estimating penetrance from multiple case families with predisposing mutations: extension of the 'genotype-restricted likelihood' (GRL) method
-
Bonaiti B, Bonadona V, Perdry H, Andrieu N, Bonaiti-Pellie C. Estimating penetrance from multiple case families with predisposing mutations: extension of the 'genotype-restricted likelihood' (GRL) method. Eur J Hum Genet 2011;19:173-9.
-
(2011)
Eur J Hum Genet
, vol.19
, pp. 173-179
-
-
Bonaiti, B.1
Bonadona, V.2
Perdry, H.3
Andrieu, N.4
Bonaiti-Pellie, C.5
-
23
-
-
46949090897
-
Cancer incidence and mortality in France over the period 1980-2005
-
Belot A, Grosclaude P, Bossard N, Jougla E, Benhamou E, Delafosse P, Guizard AV, Molinie F, Danzon A, Bara S, Bouvier AM, Tretarre B, Binder-Foucard F, Colonna M, Daubisse L, Hedelin G, Launoy G, Le Stang N, Maynadie M, Monnereau A, Troussard X, Faivre J, Collignon A, Janoray I, Arveux P, Buemi A, Raverdy N, Schvartz C, Bovet M, Cherie-Challine L, Esteve J, Remontet L, Velten M. Cancer incidence and mortality in France over the period 1980-2005. Rev Epidemiol Sante Publique 2008;56:159-75.
-
(2008)
Rev Epidemiol Sante Publique
, vol.56
, pp. 159-175
-
-
Belot, A.1
Grosclaude, P.2
Bossard, N.3
Jougla, E.4
Benhamou, E.5
Delafosse, P.6
Guizard, A.V.7
Molinie, F.8
Danzon, A.9
Bara, S.10
Bouvier, A.M.11
Tretarre, B.12
Binder-Foucard, F.13
Colonna, M.14
Daubisse, L.15
Hedelin, G.16
Launoy, G.17
Le Stang, N.18
Maynadie, M.19
Monnereau, A.20
Troussard, X.21
Faivre, J.22
Collignon, A.23
Janoray, I.24
Arveux, P.25
Buemi, A.26
Raverdy, N.27
Schvartz, C.28
Bovet, M.29
Cherie-Challine, L.30
Esteve, J.31
Remontet, L.32
Velten, M.33
more..
-
24
-
-
52049086689
-
Clinical and pathologic characteristics of patients with BRCA-positive and BRCA-negative breast cancer
-
Atchley DP, Albarracin CT, Lopez A, Valero V, Amos CI, Gonzalez-Angulo AM, Hortobagyi GN, Arun BK. Clinical and pathologic characteristics of patients with BRCA-positive and BRCA-negative breast cancer. J Clin Oncol 2008;26:4282-8.
-
(2008)
J Clin Oncol
, vol.26
, pp. 4282-4288
-
-
Atchley, D.P.1
Albarracin, C.T.2
Lopez, A.3
Valero, V.4
Amos, C.I.5
Gonzalez-Angulo, A.M.6
Hortobagyi, G.N.7
Arun, B.K.8
-
25
-
-
34247381115
-
Locoregional relapse and distant metastasis in conservatively managed triple negative early-stage breast cancer
-
Haffty BG, Yang Q, Reiss M, Kearney T, Higgins SA, Weidhaas J, Harris L, Hait W, Toppmeyer D. Locoregional relapse and distant metastasis in conservatively managed triple negative early-stage breast cancer. J Clin Oncol 2006;24:5652-7.
-
(2006)
J Clin Oncol
, vol.24
, pp. 5652-5657
-
-
Haffty, B.G.1
Yang, Q.2
Reiss, M.3
Kearney, T.4
Higgins, S.A.5
Weidhaas, J.6
Harris, L.7
Hait, W.8
Toppmeyer, D.9
-
26
-
-
0037033733
-
A comprehensive model for familial breast cancer incorporating BRCA1 BRCA2 and other genes
-
Antoniou AC, Pharoah PD, McMullan G, Day NE, Stratton MR, Peto J, Ponder BJ, Easton DF. A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes. Br J Cancer 2002;86:76-83.
-
(2002)
Br J Cancer
, vol.86
, pp. 76-83
-
-
Antoniou, A.C.1
Pharoah, P.D.2
McMullan, G.3
Day, N.E.4
Stratton, M.R.5
Peto, J.6
Ponder, B.J.7
Easton, D.F.8
-
27
-
-
38649137993
-
High frequency of BRCA1/2 germline mutations in consecutive ovarian cancer patients in Poland
-
Brozek I, Ochman K, Debniak J, Morzuch L, Ratajska M, Stepnowska M, Stukan M, Emerich J, Limon J. High frequency of BRCA1/2 germline mutations in consecutive ovarian cancer patients in Poland. Gynecol Oncol 2008;108:433-7.
-
(2008)
Gynecol Oncol
, vol.108
, pp. 433-437
-
-
Brozek, I.1
Ochman, K.2
Debniak, J.3
Morzuch, L.4
Ratajska, M.5
Stepnowska, M.6
Stukan, M.7
Emerich, J.8
Limon, J.9
-
28
-
-
34247138331
-
Prediction of BRCA1/2 mutation status in patients with ovarian cancer from a hospital-based cohort
-
Jacobi CE, van Ierland Y, van Asperen CJ, Hallensleben E, Devilee P, Jan Fleuren G, Kenter GG. Prediction of BRCA1/2 mutation status in patients with ovarian cancer from a hospital-based cohort. Genet Med 2007;9:173-9.
-
(2007)
Genet Med
, vol.9
, pp. 173-179
-
-
Jacobi, C.E.1
van Ierland, Y.2
van Asperen, C.J.3
Hallensleben, E.4
Devilee, P.5
Jan Fleuren, G.6
Kenter, G.G.7
-
29
-
-
0033927850
-
BRCA1 and BRCA2 mutation analysis of 208 Ashkenazi Jewish women with ovarian cancer
-
Moslehi R, Chu W, Karlan B, Fishman D, Risch H, Fields A, Smotkin D, Ben-David Y, Rosenblatt J, Russo D, Schwartz P, Tung N, Warner E, Rosen B, Friedman J, Brunet JS, Narod SA. BRCA1 and BRCA2 mutation analysis of 208 Ashkenazi Jewish women with ovarian cancer. Am J Hum Genet 2000;66:1259-72.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1259-1272
-
-
Moslehi, R.1
Chu, W.2
Karlan, B.3
Fishman, D.4
Risch, H.5
Fields, A.6
Smotkin, D.7
Ben-David, Y.8
Rosenblatt, J.9
Russo, D.10
Schwartz, P.11
Tung, N.12
Warner, E.13
Rosen, B.14
Friedman, J.15
Brunet, J.S.16
Narod, S.A.17
-
30
-
-
0035098503
-
Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer
-
Risch HA, McLaughlin JR, Cole DE, Rosen B, Bradley L, Kwan E, Jack E, Vesprini DJ, Kuperstein G, Abrahamson JL, Fan I, Wong B, Narod SA. Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer. Am J Hum Genet 2001;68:700-10.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 700-710
-
-
Risch, H.A.1
McLaughlin, J.R.2
Cole, D.E.3
Rosen, B.4
Bradley, L.5
Kwan, E.6
Jack, E.7
Vesprini, D.J.8
Kuperstein, G.9
Abrahamson, J.L.10
Fan, I.11
Wong, B.12
Narod, S.A.13
-
31
-
-
70149091959
-
PEL: an unbiased method for estimating age-dependent genetic disease risk from pedigree data unselected for family history
-
Alarcon F, Bourgain C, Gauthier-Villars M, Plante-Bordeneuve V, Stoppa-Lyonnet D, Bonaiti-Pellie C. PEL: an unbiased method for estimating age-dependent genetic disease risk from pedigree data unselected for family history. Genet Epidemiol 2009;33:379-85.
-
(2009)
Genet Epidemiol
, vol.33
, pp. 379-385
-
-
Alarcon, F.1
Bourgain, C.2
Gauthier-Villars, M.3
Plante-Bordeneuve, V.4
Stoppa-Lyonnet, D.5
Bonaiti-Pellie, C.6
-
32
-
-
84933476595
-
Four-Generation families in France
-
Pennec S. Four-Generation families in France. Popul Eng Sel 1997;9:75-101.
-
(1997)
Popul Eng Sel
, vol.9
, pp. 75-101
-
-
Pennec, S.1
-
33
-
-
33847780446
-
How many children and how many siblings in France in the last century?
-
Toulemon L. How many children and how many siblings in France in the last century? Popul Societies 2001;373:1-4.
-
(2001)
Popul Societies
, vol.373
, pp. 1-4
-
-
Toulemon, L.1
-
34
-
-
0015183542
-
A general model for the genetic analysis of pedigree data
-
Elston RC, Stewart J. A general model for the genetic analysis of pedigree data. Hum Hered 1971;21:523-42.
-
(1971)
Hum Hered
, vol.21
, pp. 523-542
-
-
Elston, R.C.1
Stewart, J.2
-
35
-
-
70350072363
-
Oncogénétique: estimation des besoins de la populations en France pour les 10 ans à venir
-
Bonaiti-Pellie C, Andrieu N, Arveux P, Bonadona V, Buecher B, Delpech M, Jolly D, Julian-Reynier C, Luporsi E, Nogues C, Nowak F, Olschwang S, Orsi F, Pujol P, Saurin JC, Sinilnikova O, Stoppa-Lyonnet D, Thepot F. Oncogénétique: estimation des besoins de la populations en France pour les 10 ans à venir. Bull Cancer 2009;96:875-900.
-
(2009)
Bull Cancer
, vol.96
, pp. 875-900
-
-
Bonaiti-Pellie, C.1
Andrieu, N.2
Arveux, P.3
Bonadona, V.4
Buecher, B.5
Delpech, M.6
Jolly, D.7
Julian-Reynier, C.8
Luporsi, E.9
Nogues, C.10
Nowak, F.11
Olschwang, S.12
Orsi, F.13
Pujol, P.14
Saurin, J.C.15
Sinilnikova, O.16
Stoppa-Lyonnet, D.17
Thepot, F.18
-
36
-
-
47149086213
-
Predicting the likelihood of carrying a BRCA1 or BRCA2 mutation: validation of BOADICEA, BRCAPRO, IBIS, Myriad and the Manchester scoring system using data from UK genetics clinics
-
Antoniou AC, Hardy R, Walker L, Evans DG, Shenton A, Eeles R, Shanley S, Pichert G, Izatt L, Rose S, Douglas F, Eccles D, Morrison PJ, Scott J, Zimmern RL, Easton DF, Pharoah PD. Predicting the likelihood of carrying a BRCA1 or BRCA2 mutation: validation of BOADICEA, BRCAPRO, IBIS, Myriad and the Manchester scoring system using data from UK genetics clinics. J Med Genet 2008;45:425-31.
-
(2008)
J Med Genet
, vol.45
, pp. 425-431
-
-
Antoniou, A.C.1
Hardy, R.2
Walker, L.3
Evans, D.G.4
Shenton, A.5
Eeles, R.6
Shanley, S.7
Pichert, G.8
Izatt, L.9
Rose, S.10
Douglas, F.11
Eccles, D.12
Morrison, P.J.13
Scott, J.14
Zimmern, R.L.15
Easton, D.F.16
Pharoah, P.D.17
-
37
-
-
0033843018
-
Why are the majority of hereditary cases of early-onset breast cancer sporadic? A simulation study
-
Cui J, Hopper JL. Why are the majority of hereditary cases of early-onset breast cancer sporadic? A simulation study. Cancer Epidemiol Biomarkers Prev 2000;9:805-12.
-
(2000)
Cancer Epidemiol Biomarkers Prev
, vol.9
, pp. 805-812
-
-
Cui, J.1
Hopper, J.L.2
|