-
1
-
-
2942532130
-
Prevalence of familial pancreatic cancer in Germany
-
Bartsch DK, Kress R, Sina-Frey M, Grutzmann R, Gerdes B, Pilarsky C et al.(2004) Prevalence of familial pancreatic cancer in Germany. Int J Cancer110: 902-906
-
(2004)
Int J Cancer
, vol.110
, pp. 902-906
-
-
Bartsch, D.K.1
Kress, R.2
Sina-Frey, M.3
Grutzmann, R.4
Gerdes, B.5
Pilarsky, C.6
-
2
-
-
0028059330
-
Frequent somaticmutations and homozygous deletions of the p16 (MTS1) gene inpancreatic adenocarcinoma
-
Caldas C, Hahn SA, da Costa LT, Redston MS, Schutte M, Seymour AB,Weinstein CL, Hruban RH, Yeo CJ, Kern SE (1994) Frequent somaticmutations and homozygous deletions of the p16 (MTS1) gene inpancreatic adenocarcinoma. Nat Genet 8: 27-32
-
(1994)
Nat Genet
, vol.8
, pp. 27-32
-
-
Caldas, C.1
Hahn, S.A.2
Da Costa, L.T.3
Redston, M.S.4
Schutte, M.5
Seymour, A.B.6
Weinstein, C.L.7
Hruban, R.H.8
Yeo, C.J.9
Kern, S.E.10
-
3
-
-
84858795627
-
-
Canadian Cancer Society CanadianCancer Society
-
Canadian Cancer Society (2010) Canadian Cancer Statistics. CanadianCancer Society.
-
(2010)
Canadian Cancer Statistics
-
-
-
4
-
-
84860282103
-
CDKN2A is the main susceptibility gene in Italianpancreatic cancer families
-
Genoa Pancreatic CancerStudy Group
-
TorontoGhiorzo P, Fornarini G, Sciallero S, Battistuzzi L, Belli F, Bernard L,Bonelli L, Borgonovo G, Bruno W, De Cian F, Decensi A, Filauro M,Faravelli F, Gozza A, Gargiulo S, Mariette F, Nasti S, Pastorino L,Queirolo P, Savarino V, Varesco L, Scarrà GB. Genoa Pancreatic CancerStudy Group (2012) CDKN2A is the main susceptibility gene in Italianpancreatic cancer families. J Med Genet 49: 164-170
-
(2012)
J Med Genet
, vol.49
, pp. 164-170
-
-
Torontoghiorzo, P.1
Fornarini, G.2
Sciallero, S.3
Battistuzzi, L.4
Belli, F.5
Bernard, L.6
Bonelli, L.7
Borgonovo, G.8
Bruno, W.9
De Cian, F.10
Decensi, A.11
Filauro, M.12
Faravelli, F.13
Gozza, A.14
Gargiulo, S.15
Mariette, F.16
Nasti, S.17
Pastorino, L.18
Queirolo, P.19
Savarino, V.20
Varesco, L.21
Scarrà, G.B.22
more..
-
5
-
-
77955273537
-
-
Lyon France International Agency forResearch on Cancer
-
Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM (2010)GLOBOCAN 2008 v1.2 cancer incidence and mortality worldwide: IARCCancerBase No. 10 (Internet). Lyon, France: International Agency forResearch on Cancer; available from http://globocan.iarc.fr
-
(2010)
GLOBOCAN 2008 v1.2 Cancer Incidence and Mortality Worldwide: IARCCancerBase No 10 (Internet)
-
-
Ferlay, J.1
Shin, H.R.2
Bray, F.3
Forman, D.4
Mathers, C.5
Parkin, D.M.6
-
6
-
-
0028199186
-
Family history and the risk of liver, gallbladder, and pancreatic cancer
-
Fernandez E, La Vecchia C, D'Avanzo B, Negri E, Franceschi S (1994)Family history and the risk of liver, gallbladder, and pancreatic cancer.Cancer Epidemiol Biomarkers Prev 3: 209-212
-
(1994)
Cancer Epidemiol Biomarkers Prev
, vol.3
, pp. 209-212
-
-
Fernandez, E.1
La Vecchia, C.2
D'Avanzo, B.3
Negri, E.4
Franceschi, S.5
-
7
-
-
0030593038
-
DPC4, acandidate tumor suppressor gene at human chromosome 18q21.1
-
Hahn SA, Schutte M, Hoque AT, Moskaluk CA, da Costa LT, Rozenblum E,Weinstein CL, Fischer A, Yeo CJ, Hruban RH, Kern SE (1996) DPC4, acandidate tumor suppressor gene at human chromosome 18q21.1.Science 271: 350-353
-
(1996)
Science
, vol.271
, pp. 350-353
-
-
Hahn, S.A.1
Schutte, M.2
Hoque, A.T.3
Moskaluk, C.A.4
Da Costa, L.T.5
Rozenblum, E.6
Weinstein, C.L.7
Fischer, A.8
Yeo, C.J.9
Hruban, R.H.10
Kern, S.E.11
-
8
-
-
64849092309
-
Exomic sequencing identifiesPALB2 as a pancreatic cancer susceptibility gene
-
Jones S, Hruban RH, Kamiyama M, Borges M, Zhang X, Parsons DW,Lin JC, Palmisano E, Brune K, Jaffee EM, Iacobuzio-Donahue CA, MaitraA, Parmigiani G, Kern SE, Velculescu VE, Kinzler KW, Vogelstein B,Eshleman JR, Goggins M, Klein AP (2009) Exomic sequencing identifiesPALB2 as a pancreatic cancer susceptibility gene. Science 324: 217
-
(2009)
Science
, vol.324
, pp. 217
-
-
Jones, S.1
Hruban, R.H.2
Kamiyama, M.3
Borges, M.4
Zhang, X.5
Parsons, D.W.6
Lin, J.C.7
Palmisano, E.8
Brune, K.9
Jaffee, E.M.10
Iacobuzio-Donahue, C.A.11
Maitra, A.12
Parmigiani, G.13
Kern, S.E.14
Velculescu, V.E.15
Kinzler, K.W.16
Vogelstein, B.17
Eshleman, J.R.18
Goggins, M.19
Klein, A.P.20
more..
-
9
-
-
0035409832
-
Familialpancreatic cancer
-
Klein AP, Hruban RH, Brune KA, Petersen GM, Goggins M (2001) Familialpancreatic cancer. Cancer J 7: 266-273
-
(2001)
Cancer J
, vol.7
, pp. 266-273
-
-
Klein, A.P.1
Hruban, R.H.2
Brune, K.A.3
Petersen, G.M.4
Goggins, M.5
-
10
-
-
0034650411
-
Inherited predisposition to pancreatic adenocarcinoma:role of family history and germ-line p16, BRCA1,and BRCA2 mutations
-
Lal G, Liu G, Schmocker B, Kaurah P, Ozcelik H, Narod SA, Redston M,Gallinger S (2000) Inherited predisposition to pancreatic adenocarcinoma:role of family history and germ-line p16, BRCA1,and BRCA2 mutations. Cancer Res 60: 409-416
-
(2000)
Cancer Res
, vol.60
, pp. 409-416
-
-
Lal, G.1
Liu, G.2
Schmocker, B.3
Kaurah, P.4
Ozcelik, H.5
Narod, S.A.6
Redston, M.7
Gallinger, S.8
-
11
-
-
80054820265
-
An emerging entity: Pancreatic adenocarcinomaassociated with a known BRCA mutation: Clinical descriptors, treatmentimplications, and future directions
-
Lowery MA, Kelsen DP, Stadler ZK, Yu KH, Janjigian YY, Ludwig E,D'Adamo DR, Salo-Mullen E, Robson ME, Allen PJ, Kurtz RC, O'ReillyEM (2011) An emerging entity: pancreatic adenocarcinomaassociated with a known BRCA mutation: clinical descriptors, treatmentimplications, and future directions. Oncologist 16: 1397-1402
-
(2011)
Oncologist
, vol.16
, pp. 1397-1402
-
-
Lowery, M.A.1
Kelsen, D.P.2
Stadler, Z.K.3
Yu, K.H.4
Janjigian, Y.Y.5
Ludwig, E.6
D'Adamo, D.R.7
Salo-Mullen, E.8
Robson, M.E.9
Allen, P.J.10
Kurtz, R.C.11
O'Reilly, E.M.12
-
12
-
-
0030137718
-
Mutation analysis of theBRCA2 gene in 49 site-specific breast cancer families
-
Phelan CM, Lancaster JM, Tonin P, Gumbs C, Cochran C,Carter R, Ghadirian P, Perret C, Moslehi R, Dion F, Faucher MC,Dole K, Karimi S, Foulkes W, Lounis H, Warner E, Goss P, Anderson D,Larsson C, Narod SA, Futreal PA (1996) Mutation analysis of theBRCA2 gene in 49 site-specific breast cancer families. Nat Genet 13:120-122
-
(1996)
Nat Genet
, vol.13
, pp. 120-122
-
-
Phelan, C.M.1
Lancaster, J.M.2
Tonin, P.3
Gumbs, C.4
Cochran, C.5
Carter, R.6
Ghadirian, P.7
Perret, C.8
Moslehi, R.9
Dion, F.10
Faucher, M.C.11
Dole, K.12
Karimi, S.13
Foulkes, W.14
Lounis, H.15
Warner, E.16
Goss, P.17
Anderson, D.18
Larsson, C.19
Narod, S.A.20
Futreal, P.A.21
more..
-
13
-
-
0028308492
-
P53 mutations in pancreatic carcinoma and evidence ofcommon involvement of homocopolymer tracts in DNA microdeletions
-
Redston MS, Caldas C, Seymour AB, Hruban RH, da Costa L, Yeo CJ,Kern SE (1994) p53 mutations in pancreatic carcinoma and evidence ofcommon involvement of homocopolymer tracts in DNA microdeletions.Cancer Res 54: 3025-3033
-
(1994)
Cancer Res
, vol.54
, pp. 3025-3033
-
-
Redston, M.S.1
Caldas, C.2
Seymour, A.B.3
Hruban, R.H.4
Da Costa, L.5
Yeo, C.J.6
Kern, S.E.7
-
14
-
-
33845654907
-
Population BRCA1 and BRCA2mutation frequencies and cancer penetrances: A kin-cohort study inOntario, Canada
-
Risch HA, McLaughlin JR, Cole DEC, Rosen B, Bradley L, Fan I, Ang J,Li S, Zhang S, Shaw PA, Narod SA (2006) Population BRCA1 and BRCA2mutation frequencies and cancer penetrances: a kin-cohort study inOntario, Canada. J Natl Cancer Inst 98: 1694-1706
-
(2006)
J Natl Cancer Inst
, vol.98
, pp. 1694-1706
-
-
Risch, H.A.1
McLaughlin, J.R.2
Cole, D.E.C.3
Rosen, B.4
Bradley, L.5
Fan, I.6
Ang, J.7
Li, S.8
Zhang, S.9
Shaw, P.A.10
Narod, S.A.11
-
15
-
-
84863830403
-
ATM mutations inpatients with hereditary pancreatic cancer
-
Roberts NJ, Jiao Y, Yu J, Kopelovich L, Petersen GM, Bondy ML,Gallinger S, Schwartz AG, Syngal S, Cote ML, Axilbund J, Schulick R,Ali SZ, Eshleman JR, Velculescu VE, Goggins M, Vogelstein B, PapadopoulosN, Hruban RH, Kinzler KW, Klein AP (2011) ATM mutations inpatients with hereditary pancreatic cancer. Cancer Discov 2: 41-46
-
(2011)
Cancer Discov
, vol.2
, pp. 41-46
-
-
Roberts, N.J.1
Jiao, Y.2
Yu, J.3
Kopelovich, L.4
Petersen, G.M.5
Bondy, M.L.6
Gallinger, S.7
Schwartz, A.G.8
Syngal, S.9
Cote, M.L.10
Axilbund, J.11
Schulick, R.12
Ali, S.Z.13
Eshleman, J.R.14
Velculescu, V.E.15
Goggins, M.16
Vogelstein, B.17
Papadopoulos, N.18
Hruban, R.H.19
Kinzler, K.W.20
Klein, A.P.21
more..
-
16
-
-
0035184065
-
STK11/LKB1Peutz-Jeghers gene inactivation in intraductal papillary-mucinousneoplasms of the pancreas
-
Sato N, Rosty C, Jansen M, Fukushima N, Ueki T, Yeo CJ, Cameron JL,Iacobuzio-Donahue CA, Hruban RH, Goggins M (2001) STK11/LKB1Peutz-Jeghers gene inactivation in intraductal papillary-mucinousneoplasms of the pancreas. Am J Pathol 159: 2017-2022
-
(2001)
Am J Pathol
, vol.159
, pp. 2017-2022
-
-
Sato, N.1
Rosty, C.2
Jansen, M.3
Fukushima, N.4
Ueki, T.5
Yeo, C.J.6
Cameron, J.L.7
Iacobuzio-Donahue, C.A.8
Hruban, R.H.9
Goggins, M.10
-
17
-
-
0033523268
-
Cancer risks in BRCA2mutation carriers
-
The Breast Cancer Linkage Consortium
-
The Breast Cancer Linkage Consortium (1999) Cancer risks in BRCA2mutation carriers. J Natl Cancer Inst 91: 1310-1316
-
(1999)
J Natl Cancer Inst
, vol.91
, pp. 1310-1316
-
-
-
18
-
-
0037130887
-
Cancer Incidence in BRCA1 mutation carriers
-
Breast Cancer Linkage Consortium
-
Thompson D, Easton DF, Breast Cancer Linkage Consortium (2002)Cancer Incidence in BRCA1 mutation carriers. J Natl Cancer Inst 94:1358-1365
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 1358-1365
-
-
Thompson, D.1
Easton, D.F.2
-
19
-
-
27144532118
-
In vivo therapeutic responses contingent on Fanconianemia/BRCA2 status of the tumor
-
van der Heijden MS, Brody JR, Dezentje DA, Gallmeier E, Cunningham SC,Swartz MJ, DeMarzo AM, Offerhaus GJ, Isacoff WH, Hruban RH,Kern SE (2005) In vivo therapeutic responses contingent on Fanconianemia/BRCA2 status of the tumor. Clin Cancer Res 11: 7508-7515
-
(2005)
Clin Cancer Res
, vol.11
, pp. 7508-7515
-
-
Van Der Heijden, M.S.1
Brody, J.R.2
Dezentje, D.A.3
Gallmeier, E.4
Cunningham, S.C.5
Swartz, M.J.6
Demarzo, A.M.7
Offerhaus, G.J.8
Isacoff, W.H.9
Hruban, R.H.10
Kern, S.E.11
-
20
-
-
84860605783
-
Colorectal and other cancerrisks for carriers and noncarriers from families with a DNA mismatchrepair gene mutation: A prospective cohort study
-
Win AK, Young JP, Lindor NM, Tucker KM, Ahnen DJ, Young GP,Buchanan DD, Clendenning M, Giles GG, Winship I, Macrae FA,Goldblatt J, Southey MC, Arnold J, Thibodeau SN, Gunawardena SR,Bapat B, Baron JA, Casey G, Gallinger S, Le Marchand L, Newcomb PA,Haile RW, Hopper JL, Jenkins MA (2012) Colorectal and other cancerrisks for carriers and noncarriers from families with a DNA mismatchrepair gene mutation: a prospective cohort study. J Clin Oncol 30:958-964
-
(2012)
J Clin Oncol
, vol.30
, pp. 958-964
-
-
Win, A.K.1
Young, J.P.2
Lindor, N.M.3
Tucker, K.M.4
Ahnen, D.J.5
Young, G.P.6
Buchanan, D.D.7
Clendenning, M.8
Giles, G.G.9
Winship, I.10
MacRae, F.A.11
Goldblatt, J.12
Southey, M.C.13
Arnold, J.14
Thibodeau, S.N.15
Gunawardena, S.R.16
Bapat, B.17
Baron, J.A.18
Casey, G.19
Gallinger, S.20
Le Marchand, L.21
Newcomb, P.A.22
Haile, R.W.23
Hopper, J.L.24
Jenkins, M.A.25
more..
|