-
1
-
-
79958043675
-
-
National Cancer Institute, Bethesda, MD, USA
-
Howlader NNA, Krapcho M, Neyman N, Aminou R, Waldron W, Altekruse SF, Kosary CL, Ruhl J, Tatalovich Z, Cho H, Mariotto A, Eisner MP, Lewis DR, Chen HS, Feuer EJ, Cronin KA, Edwards BK. SEER Cancer Statistics Review 1975-2008 2011, National Cancer Institute, Bethesda, MD, USA.
-
(2011)
SEER Cancer Statistics Review 1975-2008
-
-
Howlader, N.N.A.1
Krapcho, M.2
Neyman, N.3
Aminou, R.4
Waldron, W.5
Altekruse, S.F.6
Kosary, C.L.7
Ruhl, J.8
Tatalovich, Z.9
Cho, H.10
Mariotto, A.11
Eisner, M.P.12
Lewis, D.R.13
Chen, H.S.14
Feuer, E.J.15
Cronin, K.A.16
Edwards, B.K.17
-
2
-
-
84855792427
-
Cancer statistics, 2012
-
10.3322/caac.20138, 22237781
-
Siegel R, Naishadham D, Jemal A. Cancer statistics, 2012. CA Cancer J Clin 2012, 62(1):10-29. 10.3322/caac.20138, 22237781.
-
(2012)
CA Cancer J Clin
, vol.62
, Issue.1
, pp. 10-29
-
-
Siegel, R.1
Naishadham, D.2
Jemal, A.3
-
3
-
-
2542431689
-
BRCA1, BRCA2, and Hereditary Breast Cancer
-
Marcel Dekker Inc, New York, NY, USA, Pasqualini JR
-
Bove B, Dunbrack RL, Godwin AK. BRCA1, BRCA2, and Hereditary Breast Cancer. Breast Cancer: Prognosis, Treatment and Prevention 2002, 555-624. Marcel Dekker Inc, New York, NY, USA, Pasqualini JR.
-
(2002)
Breast Cancer: Prognosis, Treatment and Prevention
, pp. 555-624
-
-
Bove, B.1
Dunbrack, R.L.2
Godwin, A.K.3
-
4
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
10.1126/science.7545954, 7545954
-
Miki Y, Swensen J, Shattuck-Eidens D, Futreal PA, Harshman K, Tavtigian S, Liu Q, Cochran C, Bennett LM, Ding W, et al. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 1994, 266(5182):66-71. 10.1126/science.7545954, 7545954.
-
(1994)
Science
, vol.266
, Issue.5182
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Eidens, D.3
Futreal, P.A.4
Harshman, K.5
Tavtigian, S.6
Liu, Q.7
Cochran, C.8
Bennett, L.M.9
Ding, W.10
-
5
-
-
0028006563
-
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
-
10.1126/science.8091231, 8091231
-
Wooster R, Neuhausen SL, Mangion J, Quirk Y, Ford D, Collins N, Nguyen K, Seal S, Tran T, Averill D, et al. Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13. Science 1994, 265(5181):2088-2090. 10.1126/science.8091231, 8091231.
-
(1994)
Science
, vol.265
, Issue.5181
, pp. 2088-2090
-
-
Wooster, R.1
Neuhausen, S.L.2
Mangion, J.3
Quirk, Y.4
Ford, D.5
Collins, N.6
Nguyen, K.7
Seal, S.8
Tran, T.9
Averill, D.10
-
6
-
-
0142178215
-
Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2
-
10.1126/science.1088759, 14576434
-
King MC, Marks JH, Mandell JB. Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2. Science 2003, 302(5645):643-646. 10.1126/science.1088759, 14576434.
-
(2003)
Science
, vol.302
, Issue.5645
, pp. 643-646
-
-
King, M.C.1
Marks, J.H.2
Mandell, J.B.3
-
7
-
-
33645084562
-
Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer
-
10.1001/jama.295.12.1379, 16551709
-
Walsh T, Casadei S, Coats KH, Swisher E, Stray SM, Higgins J, Roach KC, Mandell J, Lee MK, Ciernikova S, et al. Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer. Jama 2006, 295(12):1379-1388. 10.1001/jama.295.12.1379, 16551709.
-
(2006)
Jama
, vol.295
, Issue.12
, pp. 1379-1388
-
-
Walsh, T.1
Casadei, S.2
Coats, K.H.3
Swisher, E.4
Stray, S.M.5
Higgins, J.6
Roach, K.C.7
Mandell, J.8
Lee, M.K.9
Ciernikova, S.10
-
8
-
-
0030936323
-
PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer
-
10.1126/science.275.5308.1943, 9072974
-
Li J, Yen C, Liaw D, Podsypanina K, Bose S, Wang SI, Puc J, Miliaresis C, Rodgers L, McCombie R, et al. PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer. Science 1997, 275(5308):1943-1947. 10.1126/science.275.5308.1943, 9072974.
-
(1997)
Science
, vol.275
, Issue.5308
, pp. 1943-1947
-
-
Li, J.1
Yen, C.2
Liaw, D.3
Podsypanina, K.4
Bose, S.5
Wang, S.I.6
Puc, J.7
Miliaresis, C.8
Rodgers, L.9
McCombie, R.10
-
9
-
-
20544474516
-
Cancer risks and mortality in heterozygous ATM mutation carriers
-
10.1093/jnci/dji141, 15928302
-
Thompson D, Duedal S, Kirner J, McGuffog L, Last J, Reiman A, Byrd P, Taylor M, Easton DF. Cancer risks and mortality in heterozygous ATM mutation carriers. J Natl Cancer Inst 2005, 97(11):813-822. 10.1093/jnci/dji141, 15928302.
-
(2005)
J Natl Cancer Inst
, vol.97
, Issue.11
, pp. 813-822
-
-
Thompson, D.1
Duedal, S.2
Kirner, J.3
McGuffog, L.4
Last, J.5
Reiman, A.6
Byrd, P.7
Taylor, M.8
Easton, D.F.9
-
10
-
-
18544389716
-
Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations
-
10.1038/ng879, 11967536
-
Meijers-Heijboer H, van den Ouweland A, Klijn J, Wasielewski M, de Snoo A, Oldenburg R, Hollestelle A, Houben M, Crepin E, van Veghel-Plandsoen M, et al. Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat Genet 2002, 31(1):55-59. 10.1038/ng879, 11967536.
-
(2002)
Nat Genet
, vol.31
, Issue.1
, pp. 55-59
-
-
Meijers-Heijboer, H.1
van den Ouweland, A.2
Klijn, J.3
Wasielewski, M.4
de Snoo, A.5
Oldenburg, R.6
Hollestelle, A.7
Houben, M.8
Crepin, E.9
van Veghel-Plandsoen, M.10
-
11
-
-
33750465216
-
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles
-
10.1038/ng1902, 17033622
-
Seal S, Thompson D, Renwick A, Elliott A, Kelly P, Barfoot R, Chagtai T, Jayatilake H, Ahmed M, Spanova K, et al. Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Nat Genet 2006, 38(11):1239-1241. 10.1038/ng1902, 17033622.
-
(2006)
Nat Genet
, vol.38
, Issue.11
, pp. 1239-1241
-
-
Seal, S.1
Thompson, D.2
Renwick, A.3
Elliott, A.4
Kelly, P.5
Barfoot, R.6
Chagtai, T.7
Jayatilake, H.8
Ahmed, M.9
Spanova, K.10
-
12
-
-
33745200945
-
Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2
-
10.1016/j.molcel.2006.05.022, 16793542
-
Xia B, Sheng Q, Nakanishi K, Ohashi A, Wu J, Christ N, Liu X, Jasin M, Couch FJ, Livingston DM. Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2. Mol Cell 2006, 22(6):719-729. 10.1016/j.molcel.2006.05.022, 16793542.
-
(2006)
Mol Cell
, vol.22
, Issue.6
, pp. 719-729
-
-
Xia, B.1
Sheng, Q.2
Nakanishi, K.3
Ohashi, A.4
Wu, J.5
Christ, N.6
Liu, X.7
Jasin, M.8
Couch, F.J.9
Livingston, D.M.10
-
13
-
-
33745225487
-
Germline mutations 657del5 of the NBS1 gene contribute significantly to the incidence of breast cancer in Central Poland
-
10.1002/ijc.21853, 16770759
-
Steffen J, Nowakowska D, Niwinska A, Czapczak D, Kluska A, Piatkowska M, Wisniewska A, Paszko Z. Germline mutations 657del5 of the NBS1 gene contribute significantly to the incidence of breast cancer in Central Poland. Int J Cancer 2006, 119(2):472-475. 10.1002/ijc.21853, 16770759.
-
(2006)
Int J Cancer
, vol.119
, Issue.2
, pp. 472-475
-
-
Steffen, J.1
Nowakowska, D.2
Niwinska, A.3
Czapczak, D.4
Kluska, A.5
Piatkowska, M.6
Wisniewska, A.7
Paszko, Z.8
-
14
-
-
33747884830
-
RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability
-
3006189, 16474176
-
Heikkinen K, Rapakko K, Karppinen SM, Erkko H, Knuutila S, Lundan T, Mannermaa A, Borresen-Dale AL, Borg A, Barkardottir RB, et al. RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability. Carcinogenesis 2006, 27(8):1593-1599. 3006189, 16474176.
-
(2006)
Carcinogenesis
, vol.27
, Issue.8
, pp. 1593-1599
-
-
Heikkinen, K.1
Rapakko, K.2
Karppinen, S.M.3
Erkko, H.4
Knuutila, S.5
Lundan, T.6
Mannermaa, A.7
Borresen-Dale, A.L.8
Borg, A.9
Barkardottir, R.B.10
-
15
-
-
15544384884
-
Gene expression profiling of breast cancer: a new tumor marker
-
10.1200/JCO.2005.12.005, 15755970
-
Van't Veer LJ, Paik S, Hayes DF, Van't Veer LJ, Paik S, Hayes DF. Gene expression profiling of breast cancer: a new tumor marker. J Clin Oncol 2005, 23(8):1631-1635. 10.1200/JCO.2005.12.005, 15755970.
-
(2005)
J Clin Oncol
, vol.23
, Issue.8
, pp. 1631-1635
-
-
Van't Veer, L.J.1
Paik, S.2
Hayes, D.F.3
Van't Veer, L.J.4
Paik, S.5
Hayes, D.F.6
-
16
-
-
33646365369
-
Intronic alterations in BRCA1 and BRCA2: effect on mRNA splicing fidelity and expression
-
10.1002/humu.20319, 16619214
-
Chen X, Truong TT, Weaver J, Bove BA, Cattie K, Armstrong BA, Daly MB, Godwin AK. Intronic alterations in BRCA1 and BRCA2: effect on mRNA splicing fidelity and expression. Hum Mutat 2006, 27(5):427-435. 10.1002/humu.20319, 16619214.
-
(2006)
Hum Mutat
, vol.27
, Issue.5
, pp. 427-435
-
-
Chen, X.1
Truong, T.T.2
Weaver, J.3
Bove, B.A.4
Cattie, K.5
Armstrong, B.A.6
Daly, M.B.7
Godwin, A.K.8
-
17
-
-
42449136232
-
Allelic imbalance in BRCA1 and BRCA2 gene expression is associated with an increased breast cancer risk
-
10.1093/hmg/ddn022, 18204050
-
Chen X, Weaver J, Bove BA, Vanderveer LA, Weil SC, Miron A, Daly MB, Godwin AK. Allelic imbalance in BRCA1 and BRCA2 gene expression is associated with an increased breast cancer risk. Hum Mol Genet 2008, 17(9):1336-1348. 10.1093/hmg/ddn022, 18204050.
-
(2008)
Hum Mol Genet
, vol.17
, Issue.9
, pp. 1336-1348
-
-
Chen, X.1
Weaver, J.2
Bove, B.A.3
Vanderveer, L.A.4
Weil, S.C.5
Miron, A.6
Daly, M.B.7
Godwin, A.K.8
-
18
-
-
5444256188
-
Allele-specific gene expression differences in humans
-
13 Spec No 2
-
Buckland PR. Allele-specific gene expression differences in humans. Hum Mol Genet 2004, 13 Spec No 2:R255-R260.
-
(2004)
Hum Mol Genet
-
-
Buckland, P.R.1
-
19
-
-
84855847820
-
SNP-based large-scale identification of allele-specific gene expression in human B cells
-
10.1016/j.gene.2011.11.058, 22178530
-
Song MY, Kim HE, Kim S, Choi IH, Lee JK. SNP-based large-scale identification of allele-specific gene expression in human B cells. Gene 2012, 493(2):211-218. 10.1016/j.gene.2011.11.058, 22178530.
-
(2012)
Gene
, vol.493
, Issue.2
, pp. 211-218
-
-
Song, M.Y.1
Kim, H.E.2
Kim, S.3
Choi, I.H.4
Lee, J.K.5
-
20
-
-
70350651269
-
Global patterns of cis variation in human cells revealed by high-density allelic expression analysis
-
10.1038/ng.473, 19838192
-
Ge B, Pokholok DK, Kwan T, Grundberg E, Morcos L, Verlaan DJ, Le J, Koka V, Lam KC, Gagne V, et al. Global patterns of cis variation in human cells revealed by high-density allelic expression analysis. Nat Genet 2009, 41(11):1216-1222. 10.1038/ng.473, 19838192.
-
(2009)
Nat Genet
, vol.41
, Issue.11
, pp. 1216-1222
-
-
Ge, B.1
Pokholok, D.K.2
Kwan, T.3
Grundberg, E.4
Morcos, L.5
Verlaan, D.J.6
Le, J.7
Koka, V.8
Lam, K.C.9
Gagne, V.10
-
21
-
-
70449101927
-
Whole-genome genotyping on bead arrays
-
10.1007/978-1-59745-538-1_13, 19381978
-
Gunderson KL. Whole-genome genotyping on bead arrays. Methods Mol Biol 2009, 529:197-213. 10.1007/978-1-59745-538-1_13, 19381978.
-
(2009)
Methods Mol Biol
, vol.529
, pp. 197-213
-
-
Gunderson, K.L.1
-
22
-
-
43149120213
-
SNP-specific array-based allele-specific expression analysis
-
10.1101/gr.073254.107, 2336807, 18369178
-
Bjornsson HT, Albert TJ, Ladd-Acosta CM, Green RD, Rongione MA, Middle CM, Irizarry RA, Broman KW, Feinberg AP. SNP-specific array-based allele-specific expression analysis. Genome Res 2008, 18(5):771-779. 10.1101/gr.073254.107, 2336807, 18369178.
-
(2008)
Genome Res
, vol.18
, Issue.5
, pp. 771-779
-
-
Bjornsson, H.T.1
Albert, T.J.2
Ladd-Acosta, C.M.3
Green, R.D.4
Rongione, M.A.5
Middle, C.M.6
Irizarry, R.A.7
Broman, K.W.8
Feinberg, A.P.9
-
23
-
-
40149090710
-
Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression
-
10.1371/journal.pgen.1000006, 2265535, 18454203
-
Serre D, Gurd S, Ge B, Sladek R, Sinnett D, Harmsen E, Bibikova M, Chudin E, Barker DL, Dickinson T, et al. Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression. PLoS Genet 2008, 4(2):e1000006. 10.1371/journal.pgen.1000006, 2265535, 18454203.
-
(2008)
PLoS Genet
, vol.4
, Issue.2
-
-
Serre, D.1
Gurd, S.2
Ge, B.3
Sladek, R.4
Sinnett, D.5
Harmsen, E.6
Bibikova, M.7
Chudin, E.8
Barker, D.L.9
Dickinson, T.10
-
24
-
-
74049142035
-
Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity
-
10.1002/humu.21134, 19830809
-
Tchatchou S, Riedel A, Lyer S, Schmutzhard J, Strobel-Freidekind O, Gronert-Sum S, Mietag C, D'Amato M, Schlehe B, Hemminki K, et al. Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity. Hum Mutat 2010, 31(1):60-66. 10.1002/humu.21134, 19830809.
-
(2010)
Hum Mutat
, vol.31
, Issue.1
, pp. 60-66
-
-
Tchatchou, S.1
Riedel, A.2
Lyer, S.3
Schmutzhard, J.4
Strobel-Freidekind, O.5
Gronert-Sum, S.6
Mietag, C.7
D'Amato, M.8
Schlehe, B.9
Hemminki, K.10
-
25
-
-
34748821761
-
The role of site accessibility in microRNA target recognition
-
10.1038/ng2135, 17893677
-
Kertesz M, Iovino N, Unnerstall U, Gaul U, Segal E. The role of site accessibility in microRNA target recognition. Nat Genet 2007, 39(10):1278-1284. 10.1038/ng2135, 17893677.
-
(2007)
Nat Genet
, vol.39
, Issue.10
, pp. 1278-1284
-
-
Kertesz, M.1
Iovino, N.2
Unnerstall, U.3
Gaul, U.4
Segal, E.5
-
26
-
-
77950930978
-
High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta
-
2871261, 20403199
-
Daelemans C, Ritchie ME, Smits G, Abu-Amero S, Sudbery IM, Forrest MS, Campino S, Clark TG, Stanier P, Kwiatkowski D, et al. High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta. BMC Genet 2010, 11:25. 2871261, 20403199.
-
(2010)
BMC Genet
, vol.11
, pp. 25
-
-
Daelemans, C.1
Ritchie, M.E.2
Smits, G.3
Abu-Amero, S.4
Sudbery, I.M.5
Forrest, M.S.6
Campino, S.7
Clark, T.G.8
Stanier, P.9
Kwiatkowski, D.10
-
27
-
-
84864927713
-
-
Emerging functional and mechanistic paradigms of mammalian long non-coding RNAs. Nucleic Acids Res, Khalil AM
-
Moran VA. Perera RJ 2012, Emerging functional and mechanistic paradigms of mammalian long non-coding RNAs. Nucleic Acids Res, Khalil AM.
-
(2012)
Perera RJ
-
-
Moran, V.A.1
-
28
-
-
79957840356
-
Long noncoding RNAs and human disease
-
10.1016/j.tcb.2011.04.001, 21550244
-
Wapinski O, Chang HY. Long noncoding RNAs and human disease. Trends Cell Biol 2011, 21(6):354-361. 10.1016/j.tcb.2011.04.001, 21550244.
-
(2011)
Trends Cell Biol
, vol.21
, Issue.6
, pp. 354-361
-
-
Wapinski, O.1
Chang, H.Y.2
-
29
-
-
33747829927
-
Whole-genome genotyping
-
Gunderson KL, Steemers FJ, Ren H, Ng P, Zhou L, Tsan C, Chang W, Bullis D, Musmacker J, King C, et al. Whole-genome genotyping. Methods Enzymol 2006, 410:359-376.
-
(2006)
Methods Enzymol
, vol.410
, pp. 359-376
-
-
Gunderson, K.L.1
Steemers, F.J.2
Ren, H.3
Ng, P.4
Zhou, L.5
Tsan, C.6
Chang, W.7
Bullis, D.8
Musmacker, J.9
King, C.10
-
30
-
-
77953872952
-
Genetic susceptibility to breast cancer
-
10.1016/j.molonc.2010.04.011, 20542480
-
Mavaddat N, Antoniou AC, Easton DF, Garcia-Closas M. Genetic susceptibility to breast cancer. Mol Oncol 2010, 4(3):174-191. 10.1016/j.molonc.2010.04.011, 20542480.
-
(2010)
Mol Oncol
, vol.4
, Issue.3
, pp. 174-191
-
-
Mavaddat, N.1
Antoniou, A.C.2
Easton, D.F.3
Garcia-Closas, M.4
-
31
-
-
34250006413
-
Genome-wide association study identifies novel breast cancer susceptibility loci
-
10.1038/nature05887, 2714974, 17529967
-
Easton DF, Pooley KA, Dunning AM, Pharoah PD, Thompson D, Ballinger DG, Struewing JP, Morrison J, Field H, Luben R, et al. Genome-wide association study identifies novel breast cancer susceptibility loci. Nature 2007, 447(7148):1087-1093. 10.1038/nature05887, 2714974, 17529967.
-
(2007)
Nature
, vol.447
, Issue.7148
, pp. 1087-1093
-
-
Easton, D.F.1
Pooley, K.A.2
Dunning, A.M.3
Pharoah, P.D.4
Thompson, D.5
Ballinger, D.G.6
Struewing, J.P.7
Morrison, J.8
Field, H.9
Luben, R.10
-
32
-
-
34250001297
-
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
-
10.1038/ng2075, 3493132, 17529973
-
Hunter DJ, Kraft P, Jacobs KB, Cox DG, Yeager M, Hankinson SE, Wacholder S, Wang Z, Welch R, Hutchinson A, et al. A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat Genet 2007, 39(7):870-874. 10.1038/ng2075, 3493132, 17529973.
-
(2007)
Nat Genet
, vol.39
, Issue.7
, pp. 870-874
-
-
Hunter, D.J.1
Kraft, P.2
Jacobs, K.B.3
Cox, D.G.4
Yeager, M.5
Hankinson, S.E.6
Wacholder, S.7
Wang, Z.8
Welch, R.9
Hutchinson, A.10
-
33
-
-
34250002140
-
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer
-
10.1038/ng2064, 17529974
-
Stacey SN, Manolescu A, Sulem P, Rafnar T, Gudmundsson J, Gudjonsson SA, Masson G, Jakobsdottir M, Thorlacius S, Helgason A, et al. Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer. Nat Genet 2007, 39(7):865-869. 10.1038/ng2064, 17529974.
-
(2007)
Nat Genet
, vol.39
, Issue.7
, pp. 865-869
-
-
Stacey, S.N.1
Manolescu, A.2
Sulem, P.3
Rafnar, T.4
Gudmundsson, J.5
Gudjonsson, S.A.6
Masson, G.7
Jakobsdottir, M.8
Thorlacius, S.9
Helgason, A.10
-
34
-
-
84862776961
-
Genome-wide association analysis identifies three new breast cancer susceptibility loci
-
10.1038/ng.1049, 22267197
-
Ghoussaini M, Fletcher O, Michailidou K, Turnbull C, Schmidt MK, Dicks E, Dennis J, Wang Q, Humphreys MK, Luccarini C, et al. Genome-wide association analysis identifies three new breast cancer susceptibility loci. Nat Genet 2012, 44(3):312-318. 10.1038/ng.1049, 22267197.
-
(2012)
Nat Genet
, vol.44
, Issue.3
, pp. 312-318
-
-
Ghoussaini, M.1
Fletcher, O.2
Michailidou, K.3
Turnbull, C.4
Schmidt, M.K.5
Dicks, E.6
Dennis, J.7
Wang, Q.8
Humphreys, M.K.9
Luccarini, C.10
-
35
-
-
58149347486
-
Genome-wide association studies: potential next steps on a genetic journey
-
10.1093/hmg/ddn289, 2782356, 18852205
-
McCarthy MI, Hirschhorn JN. Genome-wide association studies: potential next steps on a genetic journey. Hum Mol Genet 2008, 17(R2):R156-R165. 10.1093/hmg/ddn289, 2782356, 18852205.
-
(2008)
Hum Mol Genet
, vol.17
, Issue.R2
-
-
McCarthy, M.I.1
Hirschhorn, J.N.2
-
36
-
-
58149357365
-
Genome-wide association studies in cancer
-
10.1093/hmg/ddn287, 18852198
-
Easton DF, Eeles RA. Genome-wide association studies in cancer. Hum Mol Genet 2008, 17(R2):R109-R115. 10.1093/hmg/ddn287, 18852198.
-
(2008)
Hum Mol Genet
, vol.17
, Issue.R2
-
-
Easton, D.F.1
Eeles, R.A.2
-
37
-
-
79953738130
-
Quantifying the underestimation of relative risks from genome-wide association studies
-
10.1371/journal.pgen.1001337, 3060077, 21437273
-
Spencer C, Hechter E, Vukcevic D, Donnelly P. Quantifying the underestimation of relative risks from genome-wide association studies. PLoS Genet 2011, 7(3):e1001337. 10.1371/journal.pgen.1001337, 3060077, 21437273.
-
(2011)
PLoS Genet
, vol.7
, Issue.3
-
-
Spencer, C.1
Hechter, E.2
Vukcevic, D.3
Donnelly, P.4
-
38
-
-
45149099137
-
Allele-specific up-regulation of FGFR2 increases susceptibility to breast cancer
-
10.1371/journal.pbio.0060108, 2365982, 18462018
-
Meyer KB, Maia AT, O'Reilly M, Teschendorff AE, Chin SF, Caldas C, Ponder BA. Allele-specific up-regulation of FGFR2 increases susceptibility to breast cancer. PLoS Biol 2008, 6(5):e108. 10.1371/journal.pbio.0060108, 2365982, 18462018.
-
(2008)
PLoS Biol
, vol.6
, Issue.5
-
-
Meyer, K.B.1
Maia, A.T.2
O'Reilly, M.3
Teschendorff, A.E.4
Chin, S.F.5
Caldas, C.6
Ponder, B.A.7
-
39
-
-
68149180901
-
The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer
-
10.1038/ng.403, 2763485, 19561607
-
Pomerantz MM, Ahmadiyeh N, Jia L, Herman P, Verzi MP, Doddapaneni H, Beckwith CA, Chan JA, Hills A, Davis M, et al. The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer. Nat Genet 2009, 41(8):882-884. 10.1038/ng.403, 2763485, 19561607.
-
(2009)
Nat Genet
, vol.41
, Issue.8
, pp. 882-884
-
-
Pomerantz, M.M.1
Ahmadiyeh, N.2
Jia, L.3
Herman, P.4
Verzi, M.P.5
Doddapaneni, H.6
Beckwith, C.A.7
Chan, J.A.8
Hills, A.9
Davis, M.10
-
40
-
-
33845622039
-
Single nucleotide polymorphisms in the DMBT1 promoter and the progression of breast cancer
-
10.1002/ijc.22182, 17066405
-
Lei H, Hemminki K, Johansson R, Altieri A, Enquist K, Henriksson R, Lenner P, Forsti A. Single nucleotide polymorphisms in the DMBT1 promoter and the progression of breast cancer. Int J Cancer 2007, 120(2):447-449. 10.1002/ijc.22182, 17066405.
-
(2007)
Int J Cancer
, vol.120
, Issue.2
, pp. 447-449
-
-
Lei, H.1
Hemminki, K.2
Johansson, R.3
Altieri, A.4
Enquist, K.5
Henriksson, R.6
Lenner, P.7
Forsti, A.8
-
41
-
-
34447295401
-
Genetic mapping in mice identifies DMBT1 as a candidate modifier of mammary tumors and breast cancer risk
-
10.2353/ajpath.2007.060512, 1899446, 17525270
-
Blackburn AC, Hill LZ, Roberts AL, Wang J, Aud D, Jung J, Nikolcheva T, Allard J, Peltz G, Otis CN, et al. Genetic mapping in mice identifies DMBT1 as a candidate modifier of mammary tumors and breast cancer risk. Am J Pathol 2007, 170(6):2030-2041. 10.2353/ajpath.2007.060512, 1899446, 17525270.
-
(2007)
Am J Pathol
, vol.170
, Issue.6
, pp. 2030-2041
-
-
Blackburn, A.C.1
Hill, L.Z.2
Roberts, A.L.3
Wang, J.4
Aud, D.5
Jung, J.6
Nikolcheva, T.7
Allard, J.8
Peltz, G.9
Otis, C.N.10
-
42
-
-
13144297794
-
DMBT1 expression is down-regulated in breast cancer
-
10.1186/1471-2407-4-46, 514551, 15301691
-
Braidotti P, Nuciforo PG, Mollenhauer J, Poustka A, Pellegrini C, Moro A, Bulfamante G, Coggi G, Bosari S, Pietra GG. DMBT1 expression is down-regulated in breast cancer. BMC cancer 2004, 4:46. 10.1186/1471-2407-4-46, 514551, 15301691.
-
(2004)
BMC cancer
, vol.4
, pp. 46
-
-
Braidotti, P.1
Nuciforo, P.G.2
Mollenhauer, J.3
Poustka, A.4
Pellegrini, C.5
Moro, A.6
Bulfamante, G.7
Coggi, G.8
Bosari, S.9
Pietra, G.G.10
-
43
-
-
10744220690
-
Carcinogen inducibility in vivo and down-regulation of DMBT1 during breast carcinogenesis
-
10.1002/gcc.10309, 23229310
-
Mollenhauer J, Helmke B, Medina D, Bergmann G, Gassler N, Muller H, Lyer S, Diedrichs L, Renner M, Wittig R, et al. Carcinogen inducibility in vivo and down-regulation of DMBT1 during breast carcinogenesis. Genes, Chromosomes & Cancer 2004, 39(3):185-194. 10.1002/gcc.10309, 23229310.
-
(2004)
Genes, Chromosomes & Cancer
, vol.39
, Issue.3
, pp. 185-194
-
-
Mollenhauer, J.1
Helmke, B.2
Medina, D.3
Bergmann, G.4
Gassler, N.5
Muller, H.6
Lyer, S.7
Diedrichs, L.8
Renner, M.9
Wittig, R.10
-
44
-
-
76049095642
-
Mapping allele-specific DNA methylation: a new tool for maximizing information from GWAS
-
10.1016/j.ajhg.2010.01.021, 2820186, 20159108
-
Tycko B. Mapping allele-specific DNA methylation: a new tool for maximizing information from GWAS. Am J Hum Genet 2010, 86(2):109-112. 10.1016/j.ajhg.2010.01.021, 2820186, 20159108.
-
(2010)
Am J Hum Genet
, vol.86
, Issue.2
, pp. 109-112
-
-
Tycko, B.1
-
45
-
-
1542515338
-
A census of human cancer genes
-
10.1038/nrc1299, 2665285, 14993899
-
Futreal PA, Coin L, Marshall M, Down T, Hubbard T, Wooster R, Rahman N, Stratton MR. A census of human cancer genes. Nat Rev Cancer 2004, 4(3):177-183. 10.1038/nrc1299, 2665285, 14993899.
-
(2004)
Nat Rev Cancer
, vol.4
, Issue.3
, pp. 177-183
-
-
Futreal, P.A.1
Coin, L.2
Marshall, M.3
Down, T.4
Hubbard, T.5
Wooster, R.6
Rahman, N.7
Stratton, M.R.8
-
46
-
-
80052719960
-
Expanding DNA diagnostic panel testing: is more better?
-
10.1586/erm.11.58, 21902532
-
Klee EW, Hoppman-Chaney NL, Ferber MJ. Expanding DNA diagnostic panel testing: is more better?. Expert Rev Mol Diagn 2011, 11(7):703-709. 10.1586/erm.11.58, 21902532.
-
(2011)
Expert Rev Mol Diagn
, vol.11
, Issue.7
, pp. 703-709
-
-
Klee, E.W.1
Hoppman-Chaney, N.L.2
Ferber, M.J.3
-
47
-
-
0028050103
-
A common region of deletion on chromosome 17q in both sporadic and familial epithelial ovarian tumors distal to BRCA1
-
1918278, 7942844
-
Godwin AK, Vanderveer L, Schultz DC, Lynch HT, Altomare DA, Buetow KH, Daly M, Getts LA, Masny A, Rosenblum N, et al. A common region of deletion on chromosome 17q in both sporadic and familial epithelial ovarian tumors distal to BRCA1. Am J Hum Genet 1994, 55(4):666-677. 1918278, 7942844.
-
(1994)
Am J Hum Genet
, vol.55
, Issue.4
, pp. 666-677
-
-
Godwin, A.K.1
Vanderveer, L.2
Schultz, D.C.3
Lynch, H.T.4
Altomare, D.A.5
Buetow, K.H.6
Daly, M.7
Getts, L.A.8
Masny, A.9
Rosenblum, N.10
-
48
-
-
0023277545
-
Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
-
Chomczynski P, Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem 1987, 162(1):156-159.
-
(1987)
Anal Biochem
, vol.162
, Issue.1
, pp. 156-159
-
-
Chomczynski, P.1
Sacchi, N.2
-
49
-
-
69649109364
-
Circos: an information aesthetic for comparative genomics
-
10.1101/gr.092759.109, 2752132, 19541911
-
Krzywinski M, Schein J, Birol I, Connors J, Gascoyne R, Horsman D, Jones SJ, Marra MA. Circos: an information aesthetic for comparative genomics. Genome Res 2009, 19(9):1639-1645. 10.1101/gr.092759.109, 2752132, 19541911.
-
(2009)
Genome Res
, vol.19
, Issue.9
, pp. 1639-1645
-
-
Krzywinski, M.1
Schein, J.2
Birol, I.3
Connors, J.4
Gascoyne, R.5
Horsman, D.6
Jones, S.J.7
Marra, M.A.8
-
50
-
-
78049259700
-
Computational analysis of whole-genome differential allelic expression data in human
-
10.1371/journal.pcbi.1000849, 2900287, 20628616
-
Wagner JR, Ge B, Pokholok D, Gunderson KL, Pastinen T, Blanchette M. Computational analysis of whole-genome differential allelic expression data in human. PLoS Comput Biol 2010, 6(7):e1000849. 10.1371/journal.pcbi.1000849, 2900287, 20628616.
-
(2010)
PLoS Comput Biol
, vol.6
, Issue.7
-
-
Wagner, J.R.1
Ge, B.2
Pokholok, D.3
Gunderson, K.L.4
Pastinen, T.5
Blanchette, M.6
-
51
-
-
0001677717
-
Controlling the False Discovery Rate: A practical and powerful approach to multiple testing
-
Benjamini Y, Hochberg Y. Controlling the False Discovery Rate: A practical and powerful approach to multiple testing. J R Stat Soc 1995, 57:289-300.
-
(1995)
J R Stat Soc
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
|