-
2
-
-
0035088092
-
The role of genetic factors in the etiology of pancreatic adenocarcinoma: An update
-
Chappuis PO, Ghadirian P, Foulkes WD: The role of genetic factors in the etiology of pancreatic adenocarcinoma: an update. Cancer Invest 2001; 191: 65-75.
-
(2001)
Cancer Invest
, vol.191
, pp. 65-75
-
-
Chappuis, P.O.1
Ghadirian, P.2
Foulkes, W.D.3
-
3
-
-
84865543465
-
Interplay between smoking-induced genotoxicity and altered signaling in pancreatic carcinogenesis
-
Momi N, Kaur S, Ponnusamy MP, Kumar S, Wittel UA, Batra SK: Interplay between smoking-induced genotoxicity and altered signaling in pancreatic carcinogenesis. Carcinogenesis 2012; 33: 1617-1628.
-
(2012)
Carcinogenesis
, vol.33
, pp. 1617-1628
-
-
Momi, N.1
Kaur, S.2
Ponnusamy, M.P.3
Kumar, S.4
Wittel, U.A.5
Batra, S.K.6
-
4
-
-
37349014799
-
Pancreatic cancer-associated diabetes mellitus: Prevalence and temporal association with diagnosis of cancer
-
Chari ST, Leibson CL, Rabe KG, Timmons LJ, Ransom J, de Andrade M, Petersen GM: Pancreatic cancer-associated diabetes mellitus: prevalence and temporal association with diagnosis of cancer. Gastroenterology 2008; 134: 95-101.
-
(2008)
Gastroenterology
, vol.134
, pp. 95-101
-
-
Chari, S.T.1
Leibson, C.L.2
Rabe, K.G.3
Timmons, L.J.4
Ransom, J.5
De Andrade, M.6
Petersen, G.M.7
-
5
-
-
33947191596
-
Body mass index and pancreatic cancer risk: A meta-analysis of prospective studies
-
Larsson SC, Orsini N, Wolk A: Body mass index and pancreatic cancer risk: a meta-analysis of prospective studies. Int J Cancer 2007; 120: 1993-1998.
-
(2007)
Int J Cancer
, vol.120
, pp. 1993-1998
-
-
Larsson, S.C.1
Orsini, N.2
Wolk, A.3
-
6
-
-
0036893825
-
Risk of pancreatic adenocarcinoma in chronic pancreatitis
-
Malka D, Hammel P, Maire F, Rufat P, Madeira I, Pessione F, Levy P, Ruszniewski P: Risk of pancreatic adenocarcinoma in chronic pancreatitis. Gut 2002; 51: 849-852.
-
(2002)
Gut
, vol.51
, pp. 849-852
-
-
Malka, D.1
Hammel, P.2
Maire, F.3
Rufat, P.4
Madeira, I.5
Pessione, F.6
Levy, P.7
Ruszniewski, P.8
-
7
-
-
80051700067
-
Pancreatic cancer
-
Vincent A, Herman J, Schulick R, Hruban RH, Goggins M: Pancreatic cancer. Lancet 2011; 378: 607-620.
-
(2011)
Lancet
, vol.378
, pp. 607-620
-
-
Vincent, A.1
Herman, J.2
Schulick, R.3
Hruban, R.H.4
Goggins, M.5
-
8
-
-
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: Inherited predisposition to pancreatic adenocarcinoma: role of family history and germ-line p16, BRCA1, and BRCA2 mutations. Cancer Res 2000; 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
-
9
-
-
0034464147
-
Very high risk of cancer in familial Peutz-Jeghers syndrome
-
Giardiello FM, Brensinger JD, Tersmette AC, Goodman SN, Petersen GM, Booker SV, Cruz-Correa M, Offerhaus JA: Very high risk of cancer in familial Peutz-Jeghers syndrome. Gastroenterology 2000; 119: 1447-1453.
-
(2000)
Gastroenterology
, vol.119
, pp. 1447-1453
-
-
Giardiello, F.M.1
Brensinger, J.D.2
Tersmette, A.C.3
Goodman, S.N.4
Petersen, G.M.5
Booker, S.V.6
Cruz-Correa, M.7
Offerhaus, J.A.8
-
10
-
-
0029129816
-
Increased risk of pancreatic cancer in melanoma-prone kindreds with p16INK4 mutations
-
Goldstein AM, Fraser MC, Struewing JP, Hussussian CJ, Ranade K, Zametkin DP, Fontaine LS, Organic SM, Dracopoli NC, Clark WH Jr, et al: Increased risk of pancreatic cancer in melanoma-prone kindreds with p16INK4 mutations. N Engl J Med 1995; 333: 970-974.
-
(1995)
N Engl J Med
, vol.333
, pp. 970-974
-
-
Goldstein, A.M.1
Fraser, M.C.2
Struewing, J.P.3
Hussussian, C.J.4
Ranade, K.5
Zametkin, D.P.6
Fontaine, L.S.7
Organic, S.M.8
Dracopoli, N.C.9
Clark Jr., W.H.10
-
11
-
-
33646577163
-
Genetics and biology of pancreatic ductal adenocarcinoma
-
Hezel AF, Kimmelman AC, Stanger BZ, Bardeesy N, Depinho RA: Genetics and biology of pancreatic ductal adenocarcinoma. Genes Dev 2006; 20: 1218-1249.
-
(2006)
Genes Dev
, vol.20
, pp. 1218-1249
-
-
Hezel, A.F.1
Kimmelman, A.C.2
Stanger, B.Z.3
Bardeesy, N.4
Depinho, R.A.5
-
12
-
-
77950461601
-
Origins and functional impact of copy number variation in the human genome
-
Conrad DF, Pinto D, Redon R, Feuk L, Gokcumen O, Zhang Y, Aerts J, Andrews TD, Barnes C, Campbell P, Fitzgerald T, Hu M, Ihm CH, Kristiansson K, Macarthur DG, Macdonald JR, Onyiah I, Pang AW, Robson S, Stirrups K, Valsesia A, Walter K, Wei J, Tyler-Smith C, Carter NP, Lee C, Scherer SW, Hurles ME: Origins and functional impact of copy number variation in the human genome. Nature 2010; 464: 704-712.
-
(2010)
Nature
, vol.464
, pp. 704-712
-
-
Conrad, D.F.1
Pinto, D.2
Redon, R.3
Feuk, L.4
Gokcumen, O.5
Zhang, Y.6
Aerts, J.7
Andrews, T.D.8
Barnes, C.9
Campbell, P.10
Fitzgerald, T.11
Hu, M.12
Ihm, C.H.13
Kristiansson, K.14
MacArthur, D.G.15
MacDonald, J.R.16
Onyiah, I.17
Pang, A.W.18
Robson, S.19
Stirrups, K.20
Valsesia, A.21
Walter, K.22
Wei, J.23
Tyler-Smith, C.24
Carter, N.P.25
Lee, C.26
Scherer, S.W.27
Hurles, M.E.28
more..
-
13
-
-
40849109768
-
Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles
-
Bruder CE, Piotrowski A, Gijsbers AA, Andersson R, Erickson S, Diaz de Stahl T, Menzel U, Sandgren J, von Tell D, Poplawski A, Crowley M, Crasto C, Partridge EC, Tiwari H, Allison DB, Komorowski J, van Ommen GJ, Boomsma DI, Pedersen NL, den Dunnen JT, Wirdefeldt K, Dumanski JP: Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles. Am J Hum Genet 2008; 82: 763-771.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 763-771
-
-
Bruder, C.E.1
Piotrowski, A.2
Gijsbers, A.A.3
Andersson, R.4
Erickson, S.5
Diaz De-Stahl, T.6
Menzel, U.7
Sandgren, J.8
Von Tell, D.9
Poplawski, A.10
Crowley, M.11
Crasto, C.12
Partridge, E.C.13
Tiwari, H.14
Allison, D.B.15
Komorowski, J.16
Van Ommen, G.J.17
Boomsma, D.I.18
Pedersen, N.L.19
Den Dunnen, J.T.20
Wirdefeldt, K.21
Dumanski, J.P.22
more..
-
15
-
-
58049209786
-
Population-specific GSTM1 copy number variation
-
Huang RS, Chen P, Wisel S, Duan S, Zhang W, Cook EH, Das S, Cox NJ, Dolan ME: Population-specific GSTM1 copy number variation. Hum Mol Genet 2009; 18: 366-372.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 366-372
-
-
Huang, R.S.1
Chen, P.2
Wisel, S.3
Duan, S.4
Zhang, W.5
Cook, E.H.6
Das, S.7
Cox, N.J.8
Dolan, M.E.9
-
16
-
-
79961144450
-
Copy number variation across European populations
-
Chen W, Hayward C, Wright AF, Hicks AA, Vitart V, Knott S, Wild SH, Pramstaller PP, Wilson JF, Rudan I, Porteous DJ: Copy number variation across European populations. PLoS One 2011; 6:e23087.
-
(2011)
PLoS One
, vol.6
-
-
Chen, W.1
Hayward, C.2
Wright, A.F.3
Hicks, A.A.4
Vitart, V.5
Knott, S.6
Wild, S.H.7
Pramstaller, P.P.8
Wilson, J.F.9
Rudan, I.10
Porteous, D.J.11
-
17
-
-
84855379048
-
Copy number variation at 6q13 functions as a long-range regulator and is associated with pancreatic cancer risk
-
Huang L, Yu D, Wu C, Zhai K, Jiang G, Cao G, Wang C, Liu Y, Sun M, Li Z, Tan W, Lin D: Copy number variation at 6q13 functions as a long-range regulator and is associated with pancreatic cancer risk. Carcinogenesis 2012; 33: 94-100.
-
(2012)
Carcinogenesis
, vol.33
, pp. 94-100
-
-
Huang, L.1
Yu, D.2
Wu, C.3
Zhai, K.4
Jiang, G.5
Cao, G.6
Wang, C.7
Liu, Y.8
Sun, M.9
Li, Z.10
Tan, W.11
Lin, D.12
-
18
-
-
69349097813
-
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
-
Amundadottir L, Kraft P, Stolzenberg-Solomon RZ, Fuchs CS, Petersen GM, Arslan AA, Bueno-de-Mesquita HB, et al: Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer. Nat Genet 2009; 41: 986-990.
-
(2009)
Nat Genet
, vol.41
, pp. 986-990
-
-
Amundadottir, L.1
Kraft, P.2
Stolzenberg-Solomon, R.Z.3
Fuchs, C.S.4
Petersen, G.M.5
Arslan, A.A.6
Bueno-De-Mesquita, H.B.7
-
19
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
Iafrate AJ, Feuk L, Rivera MN, Listewnik ML, Donahoe PK, Qi Y, Scherer SW, Lee C: Detection of large-scale variation in the human genome. Nat Genet 2004; 36: 949-951.
-
(2004)
Nat Genet
, vol.36
, pp. 949-951
-
-
Iafrate, A.J.1
Feuk, L.2
Rivera, M.N.3
Listewnik, M.L.4
Donahoe, P.K.5
Qi, Y.6
Scherer, S.W.7
Lee, C.8
-
20
-
-
33748323156
-
A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism
-
Koolen DA, Vissers LE, Pfundt R, de Leeuw N, Knight SJ, Regan R, Kooy RF, Reyniers E, Romano C, Fichera M, Schinzel A, Baumer A, Anderlid BM, Schoumans J, Knoers NV, van Kessel AG, Sistermans EA, Veltman JA, Brunner HG, de Vries BB: A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism. Nat Genet 2006; 38: 999-1001.
-
(2006)
Nat Genet
, vol.38
, pp. 999-1001
-
-
Koolen, D.A.1
Vissers, L.E.2
Pfundt, R.3
De Leeuw, N.4
Knight, S.J.5
Regan, R.6
Kooy, R.F.7
Reyniers, E.8
Romano, C.9
Fichera, M.10
Schinzel, A.11
Baumer, A.12
Anderlid, B.M.13
Schoumans, J.14
Knoers, N.V.15
Van Kessel, A.G.16
Sistermans, E.A.17
Veltman, J.A.18
Brunner, H.G.19
De Vries, B.B.20
more..
-
21
-
-
33748300645
-
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability
-
Shaw-Smith C, Pittman AM, Willatt L, Martin H, Rickman L, Gribble S, Curley R, Cumming S, Dunn C, Kalaitzopoulos D, Porter K, Prigmore E, Krepischi-Santos AC, Varela MC, Koiffmann CP, Lees AJ, Rosenberg C, Firth HV, de Silva R, Carter NP: Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability. Nat Genet 2006; 38: 1032-1037.
-
(2006)
Nat Genet
, vol.38
, pp. 1032-1037
-
-
Shaw-Smith, C.1
Pittman, A.M.2
Willatt, L.3
Martin, H.4
Rickman, L.5
Gribble, S.6
Curley, R.7
Cumming, S.8
Dunn, C.9
Kalaitzopoulos, D.10
Porter, K.11
Prigmore, E.12
Krepischi-Santos, A.C.13
Varela, M.C.14
Koiffmann, C.P.15
Lees, A.J.16
Rosenberg, C.17
Firth, H.V.18
De Silva, R.19
Carter, N.P.20
more..
-
22
-
-
33751257500
-
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders
-
Jacquemont ML, Sanlaville D, Redon R, Raoul O, Cormier-Daire V, Lyonnet S, Amiel J, Le Merrer M, Heron D, de Blois MC, Prieur M, Vekemans M, Carter NP, Munnich A, Colleaux L, Philippe A: Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders. J Med Genet 2006; 43: 843-849.
-
(2006)
J Med Genet
, vol.43
, pp. 843-849
-
-
Jacquemont, M.L.1
Sanlaville, D.2
Redon, R.3
Raoul, O.4
Cormier-Daire, V.5
Lyonnet, S.6
Amiel, J.7
Le Merrer, M.8
Heron, D.9
De Blois, M.C.10
Prieur, M.11
Vekemans, M.12
Carter, N.P.13
Munnich, A.14
Colleaux, L.15
Philippe, A.16
-
23
-
-
33751329250
-
Global variation in copy number in the human genome
-
Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD, Fiegler H, Shapero MH, Carson AR, Chen W, Cho EK, Dallaire S, Freeman JL, Gonzalez JR, Gratacos M, Huang J, Kalaitzopoulos D, Komura D, MacDonald JR, Marshall CR, Mei R, Montgomery L, Nishimura K, Okamura K, Shen F, Somerville MJ, Tchinda J, Valsesia A, Woodwark C, Yang F, Zhang J, Zerjal T, Armengol L, Conrad DF, Estivill X, Tyler-Smith C, Carter NP, Aburatani H, Lee C, Jones KW, Scherer SW, Hurles ME: Global variation in copy number in the human genome. Nature 2006; 444: 444-454.
-
(2006)
Nature
, vol.444
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.R.3
Feuk, L.4
Perry, G.H.5
Andrews, T.D.6
Fiegler, H.7
Shapero, M.H.8
Carson, A.R.9
Chen, W.10
Cho, E.K.11
Dallaire, S.12
Freeman, J.L.13
Gonzalez, J.R.14
Gratacos, M.15
Huang, J.16
Kalaitzopoulos, D.17
Komura, D.18
MacDonald, J.R.19
Marshall, C.R.20
Mei, R.21
Montgomery, L.22
Nishimura, K.23
Okamura, K.24
Shen, F.25
Somerville, M.J.26
Tchinda, J.27
Valsesia, A.28
Woodwark, C.29
Yang, F.30
Zhang, J.31
Zerjal, T.32
Armengol, L.33
Conrad, D.F.34
Estivill, X.35
Tyler-Smith, C.36
Carter, N.P.37
Aburatani, H.38
Lee, C.39
Jones, K.W.40
Scherer, S.W.41
Hurles, M.E.42
more..
-
24
-
-
48349105094
-
Impact of whole genome amplification on analysis of copy number variants
-
Pugh TJ, Delaney AD, Farnoud N, Flibotte S, Griffith M, Li HI, Qian H, Farinha P, Gascoyne RD, Marra MA: Impact of whole genome amplification on analysis of copy number variants. Nucleic Acids Res 2008; 36:e80.
-
(2008)
Nucleic Acids Res
, vol.36
-
-
Pugh, T.J.1
Delaney, A.D.2
Farnoud, N.3
Flibotte, S.4
Griffith, M.5
Li, H.I.6
Qian, H.7
Farinha, P.8
Gascoyne, R.D.9
Marra, M.A.10
-
25
-
-
84864204856
-
Are risk factors associated with outcomes in pancreatic cancer?
-
Wang DS, Wang ZQ, Zhang L, Qiu MZ, Luo HY, Ren C, Zhang DS, Wang FH, Li YH, Xu RH: Are risk factors associated with outcomes in pancreatic cancer? PLoS One 2012; 7: e41984.
-
(2012)
PLoS One
, vol.7
-
-
Wang, D.S.1
Wang, Z.Q.2
Zhang, L.3
Qiu, M.Z.4
Luo, H.Y.5
Ren, C.6
Zhang, D.S.7
Wang, F.H.8
Li, Y.H.9
Xu, R.H.10
-
26
-
-
41649088291
-
Copy-number variants in patients with a strong family history of pancreatic cancer
-
Lucito R, Suresh S, Walter K, Pandey A, Lakshmi B, Krasnitz A, Sebat J, Wigler M, Klein AP, Brune K, Palmisano E, Maitra A, Goggins M, Hruban RH: Copy-number variants in patients with a strong family history of pancreatic cancer. Cancer Biol Ther 2007; 6: 1592-1599.
-
(2007)
Cancer Biol Ther
, vol.6
, pp. 1592-1599
-
-
Lucito, R.1
Suresh, S.2
Walter, K.3
Pandey, A.4
Lakshmi, B.5
Krasnitz, A.6
Sebat, J.7
Wigler, M.8
Klein, A.P.9
Brune, K.10
Palmisano, E.11
Maitra, A.12
Goggins, M.13
Hruban, R.H.14
-
27
-
-
33746741125
-
Copy number variation: New insights in genome diversity
-
Freeman JL, Perry GH, Feuk L, Redon R, Mc-Carroll SA, Altshuler DM, Aburatani H, Jones KW, Tyler-Smith C, Hurles ME, Carter NP, Scherer SW, Lee C: Copy number variation: new insights in genome diversity. Genome Res 2006; 16: 949-961.
-
(2006)
Genome Res
, vol.16
, pp. 949-961
-
-
Freeman, J.L.1
Perry, G.H.2
Feuk, L.3
Redon, R.4
Mc-Carroll, S.A.5
Altshuler, D.M.6
Aburatani, H.7
Jones, K.W.8
Tyler-Smith, C.9
Hurles, M.E.10
Carter, N.P.11
Scherer, S.W.12
Lee, C.13
|