-
1
-
-
0037370476
-
The genetics and genomics of cancer
-
Balmain A, Gray J, Ponder BA: The genetics and genomics of cancer. Nat Genet 33:238-244 (2003).
-
(2003)
Nat Genet
, vol.33
, pp. 238-244
-
-
Balmain, A.1
Gray, J.2
Ponder, B.A.3
-
2
-
-
16244403039
-
Cancer incidence and mortality in Europe. 2004
-
Boyle P, Ferlay J: Cancer incidence and mortality in Europe. 2004. Ann Oncol 16:481-488 (2005).
-
(2005)
Ann Oncol
, vol.16
, pp. 481-488
-
-
Boyle, P.1
Ferlay, J.2
-
3
-
-
34447264706
-
Prevalence of BRCA1 and BRCA2 genomic rearrangements in a cohort of consecutive Italian breast and/or ovarian cancer families
-
Buffone A, Capalbo C, Ricevuto E, Sidoni T, Ottini L, et al: Prevalence of BRCA1 and BRCA2 genomic rearrangements in a cohort of consecutive Italian breast and/or ovarian cancer families. Breast Cancer Res Treat 106:289-296 (2007).
-
(2007)
Breast Cancer Res Treat
, vol.106
, pp. 289-296
-
-
Buffone, A.1
Capalbo, C.2
Ricevuto, E.3
Sidoni, T.4
Ottini, L.5
-
4
-
-
0036218046
-
Genome-wide detection of chromosomal imbalances in tumors using BAC microarrays
-
Cai WW, Mao JH, Chow CW, Damani S, Balmain A, Bradley A: Genome-wide detection of chromosomal imbalances in tumors using BAC microarrays. Nat Biotechnol 20:393-396 (2002).
-
(2002)
Nat Biotechnol
, vol.20
, pp. 393-396
-
-
Cai, W.W.1
Mao, J.H.2
Chow, C.W.3
Damani, S.4
Balmain, A.5
Bradley, A.6
-
5
-
-
34548107829
-
The contribution of germline rearrangements to the spectrum of BRCA2 mutations
-
Casilli F, Tournier I, Sinilnikova OM, Coulet F, Soubrier F, et al: The contribution of germline rearrangements to the spectrum of BRCA2 mutations. J Med Genet 43:e49 (2006).
-
(2006)
J Med Genet
, vol.43
-
-
Casilli, F.1
Tournier, I.2
Sinilnikova, O.M.3
Coulet, F.4
Soubrier, F.5
-
6
-
-
0038207967
-
Haploinsufficiency and reduced expression of genes localized to the 8p chromosomal region in human prostate tumors
-
Chaib H, MacDonald JW, Vessella RL, Washburn JG, Quinn JE, et al: Haploinsufficiency and reduced expression of genes localized to the 8p chromosomal region in human prostate tumors. Genes Chromosomes Cancer 37:306-313 (2003).
-
(2003)
Genes Chromosomes Cancer
, vol.37
, pp. 306-313
-
-
Chaib, H.1
MacDonald, J.W.2
Vessella, R.L.3
Washburn, J.G.4
Quinn, J.E.5
-
7
-
-
0036835501
-
Loss of heterozygosity at microsatellite markers from region p11-21 of chromosome 8 in microdissected breast tumor but not in peritumoral cells
-
Charafe-Jauffret E, Moulin JF, Ginestier C, Bechlian D, Conte N, et al: Loss of heterozygosity at microsatellite markers from region p11-21 of chromosome 8 in microdissected breast tumor but not in peritumoral cells. Int J Oncol 21:989-996 (2002).
-
(2002)
Int J Oncol
, vol.21
, pp. 989-996
-
-
Charafe-Jauffret, E.1
Moulin, J.F.2
Ginestier, C.3
Bechlian, D.4
Conte, N.5
-
8
-
-
43149125640
-
Scanning the human genome at kilobase resolution
-
Chen J, Kim YC, Jung YC, Xuan Z, Dworkin G, et al: Scanning the human genome at kilobase resolution. Genome Res 18:751-762 (2008).
-
(2008)
Genome Res
, vol.18
, pp. 751-762
-
-
Chen, J.1
Kim, Y.C.2
Jung, Y.C.3
Xuan, Z.4
Dworkin, G.5
-
9
-
-
34250006413
-
Genome-wide association study identifies novel breast cancer susceptibility loci
-
Easton DF, Pooley KA, Dunning AM, Pharoah PD, Thompson D, et al: Genome-wide association study identifies novel breast cancer susceptibility loci. Nature 447:1087-1093 (2007).
-
(2007)
Nature
, vol.447
, pp. 1087-1093
-
-
Easton, D.F.1
Pooley, K.A.2
Dunning, A.M.3
Pharoah, P.D.4
Thompson, D.5
-
10
-
-
46749157576
-
MLPA screening in the BRCA1 gene from 1,506 German hereditary breast cancer cases: Novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases
-
Engert S, Wappenschmidt B, Betz B, Kast K, Kutsche M, et al: MLPA screening in the BRCA1 gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases. Hum Mutat 29:948-958 (2008).
-
(2008)
Hum Mutat
, vol.29
, pp. 948-958
-
-
Engert, S.1
Wappenschmidt, B.2
Betz, B.3
Kast, K.4
Kutsche, M.5
-
12
-
-
34547730931
-
Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk
-
Frank B, Bermejo JL, Hemminki K, Sutter C, Wappenschmidt B, et al: Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk. Carcinogenesis 28:1442-1445 (2007).
-
(2007)
Carcinogenesis
, vol.28
, pp. 1442-1445
-
-
Frank, B.1
Bermejo, J.L.2
Hemminki, K.3
Sutter, C.4
Wappenschmidt, B.5
-
13
-
-
18644382608
-
Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families
-
Gad S, Caux-Moncoutier V, Pages-Berhouet S, Gauthier-Villars M, Coupier I, et al: Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families. Oncogene 21:6841-6847 (2002a).
-
(2002)
Oncogene
, vol.21
, pp. 6841-6847
-
-
Gad, S.1
Caux-Moncoutier, V.2
Pages-Berhouet, S.3
Gauthier-Villars, M.4
Coupier, I.5
-
14
-
-
0036850003
-
Bar code screening on combed DNA for large rearrangements of the BRCA1 and BRCA2 genes in French breast cancer families
-
Gad S, Klinger M, Caux-Moncoutier V, Pages-Berhouet S, Gauthier-Villars M, et al: Bar code screening on combed DNA for large rearrangements of the BRCA1 and BRCA2 genes in French breast cancer families. J Med Genet 39:817-821 (2002b).
-
(2002)
J Med Genet
, vol.39
, pp. 817-821
-
-
Gad, S.1
Klinger, M.2
Caux-Moncoutier, V.3
Pages-Berhouet, S.4
Gauthier-Villars, M.5
-
15
-
-
34247490187
-
-
Gutierrez-Enriquez S, de la Hoya M, Martinez-Bouzas C, Sanchez de Abajo A, Ramon y Cajal T, et al: Screening for large rearrangements of the BRCA2 gene in Spanish families with breast/ovarian cancer. Breast Cancer Res Treat 103:103-107 (2007).
-
Gutierrez-Enriquez S, de la Hoya M, Martinez-Bouzas C, Sanchez de Abajo A, Ramon y Cajal T, et al: Screening for large rearrangements of the BRCA2 gene in Spanish families with breast/ovarian cancer. Breast Cancer Res Treat 103:103-107 (2007).
-
-
-
-
16
-
-
28744446802
-
Large BRCA1 gene deletions are found in 3% of German high-risk breast cancer families
-
Hartmann C, John AL, Klaes R, Hofmann W, Bielen R, et al: Large BRCA1 gene deletions are found in 3% of German high-risk breast cancer families. Hum Mutat 24:534 (2004).
-
(2004)
Hum Mutat
, vol.24
, pp. 534
-
-
Hartmann, C.1
John, A.L.2
Klaes, R.3
Hofmann, W.4
Bielen, R.5
-
17
-
-
0029561598
-
The glutathione S-transferase supergene family: Regulation of GST and the contribution of the isoenzymes to cancer chemoprotection and drug resistance
-
Hayes JD, Pulford DJ: The glutathione S-transferase supergene family: regulation of GST and the contribution of the isoenzymes to cancer chemoprotection and drug resistance. Crit Rev Biochem Mol Biol 30:445-600 (1995).
-
(1995)
Crit Rev Biochem Mol Biol
, vol.30
, pp. 445-600
-
-
Hayes, J.D.1
Pulford, D.J.2
-
18
-
-
0344394343
-
Familial breast cancer: Scope for more susceptibility genes?
-
Hemminki K, Granstrom C: Familial breast cancer: scope for more susceptibility genes? Breast Cancer Res Treat 82:17-22 (2003).
-
(2003)
Breast Cancer Res Treat
, vol.82
, pp. 17-22
-
-
Hemminki, K.1
Granstrom, C.2
-
19
-
-
0037054932
-
Attributable risks for familial breast cancer by proband status and morphology: A nationwide epidemiologic study from Sweden
-
Hemminki K, Granstrom C, Czene K: Attributable risks for familial breast cancer by proband status and morphology: a nationwide epidemiologic study from Sweden. Int J Cancer 100:214-219 (2002).
-
(2002)
Int J Cancer
, vol.100
, pp. 214-219
-
-
Hemminki, K.1
Granstrom, C.2
Czene, K.3
-
20
-
-
29444450702
-
Common deletions and SNPs are in linkage disequilibrium in the human genome
-
Hinds DA, Kloek AP, Jen M, Chen X, Frazer KA: Common deletions and SNPs are in linkage disequilibrium in the human genome. Nat Genet 38:82-85 (2006).
-
(2006)
Nat Genet
, vol.38
, pp. 82-85
-
-
Hinds, D.A.1
Kloek, A.P.2
Jen, M.3
Chen, X.4
Frazer, K.A.5
-
21
-
-
0037380994
-
Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method
-
Hogervorst FB, Nederlof PM, Gille JJ, McElgunn CJ, Grippeling M, et al: Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method. Cancer Res 63:1449-1453 (2003).
-
(2003)
Cancer Res
, vol.63
, pp. 1449-1453
-
-
Hogervorst, F.B.1
Nederlof, P.M.2
Gille, J.J.3
McElgunn, C.J.4
Grippeling, M.5
-
22
-
-
34248525150
-
Completing the map of human genetic variation
-
Human Genome Structural Variation Working Group
-
Human Genome Structural Variation Working Group, Eichler EE, Nickerson DA, Altshuler D, Bowcock AM, et al: Completing the map of human genetic variation. Nature 447:161-165 (2007).
-
(2007)
Nature
, vol.447
, pp. 161-165
-
-
Eichler, E.E.1
Nickerson, D.A.2
Altshuler, D.3
Bowcock, A.M.4
-
23
-
-
34250001297
-
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
-
Hunter DJ, Kraft P, Jacobs KB, Cox DG, Yeager M, et al: A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat Genet 39:870-874 (2007).
-
(2007)
Nat Genet
, vol.39
, pp. 870-874
-
-
Hunter, D.J.1
Kraft, P.2
Jacobs, K.B.3
Cox, D.G.4
Yeager, M.5
-
24
-
-
36148976077
-
Influence of cytochrome P450 polymorphisms on drug therapies: Pharmacogenetic, pharmacoepigenetic, and clinical aspects
-
Ingelman-Sundberg M, Sim SC, Gomez A, Rodriguez-Antona C: Influence of cytochrome P450 polymorphisms on drug therapies: Pharmacogenetic, pharmacoepigenetic, and clinical aspects. Pharmacol Therap 116:496-526 (2007).
-
(2007)
Pharmacol Therap
, vol.116
, pp. 496-526
-
-
Ingelman-Sundberg, M.1
Sim, S.C.2
Gomez, A.3
Rodriguez-Antona, C.4
-
25
-
-
0027136288
-
Inherited amplification of an active gene in cytochrome P450 CYP2D locus as a cause of ultrarapid metabolism of debrisoquine
-
Johansson L, Lundquist E, Bertilsson L, Dahl ML, Sjoqvist F, Ingelmann-Sundberg M: Inherited amplification of an active gene in cytochrome P450 CYP2D locus as a cause of ultrarapid metabolism of debrisoquine. Proc Natl Acad Sci USA 90:11825-11829 (1993).
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 11825-11829
-
-
Johansson, L.1
Lundquist, E.2
Bertilsson, L.3
Dahl, M.L.4
Sjoqvist, F.5
Ingelmann-Sundberg, M.6
-
26
-
-
0026495364
-
Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
-
Kallioniemi A, Kallioniemi OP, Sudar D, Rutovitz D, Gray JW, et al: Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 258:818-821 (1992).
-
(1992)
Science
, vol.258
, pp. 818-821
-
-
Kallioniemi, A.1
Kallioniemi, O.P.2
Sudar, D.3
Rutovitz, D.4
Gray, J.W.5
-
27
-
-
15144340686
-
Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomas
-
Kerangueven F, Noguchi T, Coulier F, Allione F, Wargniez V, et al: Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomas. Cancer Res 57:5469-5474 (1997).
-
(1997)
Cancer Res
, vol.57
, pp. 5469-5474
-
-
Kerangueven, F.1
Noguchi, T.2
Coulier, F.3
Allione, F.4
Wargniez, V.5
-
29
-
-
0034644185
-
Environmental and heritable factors in the causation of cancer - analyses of cohorts of twins from Sweden, Denmark, and Finland
-
Lichtenstein P, Holm NV, Verkasalo PK, Iliadou A, Kaprio J, et al: Environmental and heritable factors in the causation of cancer - analyses of cohorts of twins from Sweden, Denmark, and Finland. N Engl J Med 343:78-85 (2000).
-
(2000)
N Engl J Med
, vol.343
, pp. 78-85
-
-
Lichtenstein, P.1
Holm, N.V.2
Verkasalo, P.K.3
Iliadou, A.4
Kaprio, J.5
-
30
-
-
0036466858
-
Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population
-
Meindl A: Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population. Int J Cancer 97:472-480 (2002).
-
(2002)
Int J Cancer
, vol.97
, pp. 472-480
-
-
Meindl, A.1
-
31
-
-
0032878514
-
Single amino acids determine specificity of binding of protein kinase A regulatory subunits by protein kinase A anchoring proteins
-
Miki K, Eddy EM: Single amino acids determine specificity of binding of protein kinase A regulatory subunits by protein kinase A anchoring proteins. J Biol Chem 274:29057-29062 (1999).
-
(1999)
J Biol Chem
, vol.274
, pp. 29057-29062
-
-
Miki, K.1
Eddy, E.M.2
-
32
-
-
0038364017
-
Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families
-
Montagna M, Dalla Palma M, Menin C, Agata S, De Nicolo A, et al: Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families. Hum Mol Genet 12:1055-1061 (2003).
-
(2003)
Hum Mol Genet
, vol.12
, pp. 1055-1061
-
-
Montagna, M.1
Dalla Palma, M.2
Menin, C.3
Agata, S.4
De Nicolo, A.5
-
33
-
-
22244453416
-
A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays
-
Nannya Y, Sanada M, Nakazaki K, Hosoya N, Wang L, et al: A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays. Cancer Res 65:6071-6079 (2005).
-
(2005)
Cancer Res
, vol.65
, pp. 6071-6079
-
-
Nannya, Y.1
Sanada, M.2
Nakazaki, K.3
Hosoya, N.4
Wang, L.5
-
34
-
-
0037181715
-
What options for treatment of hereditary breast cancer?
-
Narod S: What options for treatment of hereditary breast cancer? Lancet 359:1451-1452 (2002).
-
(2002)
Lancet
, vol.359
, pp. 1451-1452
-
-
Narod, S.1
-
35
-
-
0036178190
-
Current understanding of the epidemiology and clinical implications of BRCA1 and BRCA2 mutations for ovarian cancer
-
Narod SA, Boyd J: Current understanding of the epidemiology and clinical implications of BRCA1 and BRCA2 mutations for ovarian cancer. Curr Opin Obstet Gynecol 14:19-26 (2002).
-
(2002)
Curr Opin Obstet Gynecol
, vol.14
, pp. 19-26
-
-
Narod, S.A.1
Boyd, J.2
-
36
-
-
0035030368
-
Breast cancer genetics: What we know and what we need
-
Nathanson KL, Wooster R, Weber BL: Breast cancer genetics: what we know and what we need. Nat Med 7:552-556 (2001).
-
(2001)
Nat Med
, vol.7
, pp. 552-556
-
-
Nathanson, K.L.1
Wooster, R.2
Weber, B.L.3
-
37
-
-
14944385553
-
Global cancer statistics, 2002
-
Parkin DM, Bray F, Ferlay J, Pisani P: Global cancer statistics, 2002. CA Cancer J Clin 55:74-108 (2005).
-
(2005)
CA Cancer J Clin
, vol.55
, pp. 74-108
-
-
Parkin, D.M.1
Bray, F.2
Ferlay, J.3
Pisani, P.4
-
38
-
-
41149140876
-
The fine-scale and complex architecture of human copy number variation
-
Perry GH, Ben-Dor A, Tsalenko A, Sampas N, Rodriguez-Revenga L, et al: The fine-scale and complex architecture of human copy number variation. Am J Hum Genet 82:685-695 (2008).
-
(2008)
Am J Hum Genet
, vol.82
, pp. 685-695
-
-
Perry, G.H.1
Ben-Dor, A.2
Tsalenko, A.3
Sampas, N.4
Rodriguez-Revenga, L.5
-
39
-
-
0033516265
-
Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer
-
Peto J, Collins N, Barfoot R, Seal S, Warren W, et al: Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer. J Natl Cancer Inst 91:943-949 (1999).
-
(1999)
J Natl Cancer Inst
, vol.91
, pp. 943-949
-
-
Peto, J.1
Collins, N.2
Barfoot, R.3
Seal, S.4
Warren, W.5
-
40
-
-
28044442055
-
Five genes from chromosomal band 8p22 are significantly down-regulated in ovarian carcinoma: N33 and EFA6R have a potential impact on overall survival
-
Pils D, Horak P, Gleiss A, Sax C, Fabjani G, et al: Five genes from chromosomal band 8p22 are significantly down-regulated in ovarian carcinoma: N33 and EFA6R have a potential impact on overall survival. Cancer 104:2417-2429 (2005).
-
(2005)
Cancer
, vol.104
, pp. 2417-2429
-
-
Pils, D.1
Horak, P.2
Gleiss, A.3
Sax, C.4
Fabjani, G.5
-
41
-
-
0033587111
-
Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinoma
-
Pineau P, Nagai H, Prigent S, Wei Y, Gyapay G, et al: Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinoma. Oncogene 18:3127-3134 (1999).
-
(1999)
Oncogene
, vol.18
, pp. 3127-3134
-
-
Pineau, P.1
Nagai, H.2
Prigent, S.3
Wei, Y.4
Gyapay, G.5
-
42
-
-
17344371740
-
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
-
Pinkel D, Segraves R, Sudar D, Clark S, Poole I, et al: High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat Genet 20:207-211 (1998).
-
(1998)
Nat Genet
, vol.20
, pp. 207-211
-
-
Pinkel, D.1
Segraves, R.2
Sudar, D.3
Clark, S.4
Poole, I.5
-
43
-
-
33751329250
-
Global variation in copy number in the human genome
-
Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, et al: Global variation in copy number in the human genome. Nature 444:444-454 (2006).
-
(2006)
Nature
, vol.444
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.R.3
Feuk, L.4
Perry, G.H.5
-
44
-
-
0035955718
-
An isoform of the coactivator AIB1 that increases hormone and growth factor sensitivity is overexpressed in breast cancer
-
Reiter R, Wellstein A, Riegel AT: An isoform of the coactivator AIB1 that increases hormone and growth factor sensitivity is overexpressed in breast cancer. J Biol Chem 276:39736-39741 (2001).
-
(2001)
J Biol Chem
, vol.276
, pp. 39736-39741
-
-
Reiter, R.1
Wellstein, A.2
Riegel, A.T.3
-
45
-
-
1242338795
-
Association of homozygous wild-type glutathione S-transferase M1 genotype with increased breast cancer risk
-
Roodi N, Dupont WD, Moore JH, Parl FF: Association of homozygous wild-type glutathione S-transferase M1 genotype with increased breast cancer risk. Cancer Res 64:1233-1236 (2004).
-
(2004)
Cancer Res
, vol.64
, pp. 1233-1236
-
-
Roodi, N.1
Dupont, W.D.2
Moore, J.H.3
Parl, F.F.4
-
46
-
-
3543023204
-
Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification
-
Schouten JP, McElgunn CJ, Waaijer R, Zwijnenburg D, Diepvens F, Pals G: Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification. Nucleic Acids Res 30:e57 (2002).
-
(2002)
Nucleic Acids Res
, vol.30
-
-
Schouten, J.P.1
McElgunn, C.J.2
Waaijer, R.3
Zwijnenburg, D.4
Diepvens, F.5
Pals, G.6
-
47
-
-
3242808027
-
Large-scale copy number polymorphism in the human genome
-
Sebat J, Lakshmi B, Troge J, Alexander J, Young J, et al: Large-scale copy number polymorphism in the human genome. Science 305:525-528 (2004).
-
(2004)
Science
, vol.305
, pp. 525-528
-
-
Sebat, J.1
Lakshmi, B.2
Troge, J.3
Alexander, J.4
Young, J.5
-
48
-
-
0037704396
-
Identification of a new tumor suppressor gene located at chromosome 8p21.3-22
-
Seibold S, Rudroff C, Weber M, Galle J, Wanner C, Marx M: Identification of a new tumor suppressor gene located at chromosome 8p21.3-22. FASEB J 17:1180-1182 (2003).
-
(2003)
FASEB J
, vol.17
, pp. 1180-1182
-
-
Seibold, S.1
Rudroff, C.2
Weber, M.3
Galle, J.4
Wanner, C.5
Marx, M.6
-
49
-
-
20544462642
-
Segmental duplications and copy number variation in the human genome
-
Sharp AJ, Locke DP, McGrath SD, Cheng Z, Bailey JA, et al: Segmental duplications and copy number variation in the human genome. Am J Hum Genet 77:78-88 (2005).
-
(2005)
Am J Hum Genet
, vol.77
, pp. 78-88
-
-
Sharp, A.J.1
Locke, D.P.2
McGrath, S.D.3
Cheng, Z.4
Bailey, J.A.5
-
50
-
-
0033816360
-
Characterization of the glutathione S-transferase GSTT1 deletion: Discrimination of all genotypes by polymerase chain reaction indicates a trimodular genotype-phenotype correlation
-
Sprenger R, Schlagenhaufer R, Kerb R, Bruhn C, Brockmöller J, et al: Characterization of the glutathione S-transferase GSTT1 deletion: discrimination of all genotypes by polymerase chain reaction indicates a trimodular genotype-phenotype correlation. Pharmacogenetics 10:557-565 (2000).
-
(2000)
Pharmacogenetics
, vol.10
, pp. 557-565
-
-
Sprenger, R.1
Schlagenhaufer, R.2
Kerb, R.3
Bruhn, C.4
Brockmöller, J.5
-
51
-
-
0037169354
-
Cancer susceptibility and the functions of BRCA1 and BRCA2
-
Venkitaraman AR: Cancer susceptibility and the functions of BRCA1 and BRCA2 . Cell 108:171-182 (2002).
-
(2002)
Cell
, vol.108
, pp. 171-182
-
-
Venkitaraman, A.R.1
-
52
-
-
4444353421
-
Glutathione S-transferases M1, T1, and P1 and breast cancer: A pooled analysis
-
Vogl FD, Taioli E, Maugard C, Zheng W, Pinto LF, et al: Glutathione S-transferases M1, T1, and P1 and breast cancer: a pooled analysis. Cancer Epidemiol Biomarkers Prev 13:1473-1479 (2004).
-
(2004)
Cancer Epidemiol Biomarkers Prev
, vol.13
, pp. 1473-1479
-
-
Vogl, F.D.1
Taioli, E.2
Maugard, C.3
Zheng, W.4
Pinto, L.F.5
-
53
-
-
33645084562
-
Spectrum of mutations in BRCA1 , BRCA2, CHEK2 and TP53 in families at high risk of breast cancer
-
Walsh T, Casadei S, Coats KH, Swisher E, Stray SM, et al: Spectrum of mutations in BRCA1 , BRCA2, CHEK2 and TP53 in families at high risk of breast cancer. JAMA 295:1379-1388 (2006).
-
(2006)
JAMA
, vol.295
, pp. 1379-1388
-
-
Walsh, T.1
Casadei, S.2
Coats, K.H.3
Swisher, E.4
Stray, S.M.5
-
54
-
-
34548076029
-
Evidence for common ancestral origin of a recurring BRCA1 genomic rearrangement identified in high-risk Hispanic families
-
Weitzel JN, Lagos VI, Herzog JS, Judkins T, Hendrickson B, et al: Evidence for common ancestral origin of a recurring BRCA1 genomic rearrangement identified in high-risk Hispanic families. Cancer Epidemiol Biomarkers Prev 16:1615-1620 (2007).
-
(2007)
Cancer Epidemiol Biomarkers Prev
, vol.16
, pp. 1615-1620
-
-
Weitzel, J.N.1
Lagos, V.I.2
Herzog, J.S.3
Judkins, T.4
Hendrickson, B.5
-
55
-
-
0038054378
-
Transfer of chromosome 8 into two breast cancer cell lines: Total exclusion of three regions indicates location of putative in vitro growth suppressor genes
-
Wilson P, Cuthbert A, Marsh A, Arnold J, Flanagan J, et al: Transfer of chromosome 8 into two breast cancer cell lines: total exclusion of three regions indicates location of putative in vitro growth suppressor genes. Cancer Genet Cytogenet 143:100-112 (2003).
-
(2003)
Cancer Genet Cytogenet
, vol.143
, pp. 100-112
-
-
Wilson, P.1
Cuthbert, A.2
Marsh, A.3
Arnold, J.4
Flanagan, J.5
-
56
-
-
33344469939
-
Identification of frequent chromosome copy number polymorphisms by use of high-resolution single-nucleotide-polymorphism arrays
-
Wirtenberger M, Hemminki K, Burwinkel B: Identification of frequent chromosome copy number polymorphisms by use of high-resolution single-nucleotide-polymorphism arrays. Am J Hum Genet 78:520-522 (2006).
-
(2006)
Am J Hum Genet
, vol.78
, pp. 520-522
-
-
Wirtenberger, M.1
Hemminki, K.2
Burwinkel, B.3
-
57
-
-
0037685164
-
Breast and ovarian cancer
-
Wooster R, Weber BL: Breast and ovarian cancer. N Engl J Med 348:2339-2347 (2003).
-
(2003)
N Engl J Med
, vol.348
, pp. 2339-2347
-
-
Wooster, R.1
Weber, B.L.2
-
58
-
-
0032917458
-
Localization of a tumor suppressor gene associated with the progression of human breast carcinoma within a 1-cM interval of 8p22-p23.1
-
Yokota T, Yoshimoto M, Akiyama F, Sakamoto G, Kasumi F, et al: Localization of a tumor suppressor gene associated with the progression of human breast carcinoma within a 1-cM interval of 8p22-p23.1. Cancer 85:447-452 (1999).
-
(1999)
Cancer
, vol.85
, pp. 447-452
-
-
Yokota, T.1
Yoshimoto, M.2
Akiyama, F.3
Sakamoto, G.4
Kasumi, F.5
|