-
2
-
-
84877028141
-
Comprehensive molecular portraits of human breast tumours
-
Cancer Genome Atlas Network. Comprehensive molecular portraits of human breast tumours. Nature. 2012;490:61-70.
-
(2012)
Nature.
, vol.490
, pp. 61-70
-
-
-
3
-
-
84856210264
-
Cancer predisposing BARD1 mutations in breast-ovarian cancer families
-
Ratajska M, Antoszewska E, Piskorz A, et al. Cancer predisposing BARD1 mutations in breast-ovarian cancer families. Breast Cancer Res Treat. 2012;131:89-97.
-
(2012)
Breast Cancer Res Treat.
, vol.131
, pp. 89-97
-
-
Ratajska, M.1
Antoszewska, E.2
Piskorz, A.3
-
4
-
-
79952741549
-
Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer
-
Casadei S, Norquist BM, Walsh T, et al. Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer. Cancer Res. 2011;71:2222-2229.
-
(2011)
Cancer Res.
, vol.71
, pp. 2222-2229
-
-
Casadei, S.1
Norquist, B.M.2
Walsh, T.3
-
5
-
-
33846625493
-
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
-
Rahman N, Seal S, Thompson D, et al. PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. Nat Genet. 2007;39:165-167.
-
(2007)
Nat Genet.
, vol.39
, pp. 165-167
-
-
Rahman, N.1
Seal, S.2
Thompson, D.3
-
6
-
-
33750465216
-
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles
-
Seal S, Thompson D, Renwick A, et al. Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Nat Genet. 2006;38:1239-1241.
-
(2006)
Nat Genet.
, vol.38
, pp. 1239-1241
-
-
Seal, S.1
Thompson, D.2
Renwick, A.3
-
7
-
-
67650090387
-
Variations in the NBN/NBS1 gene and the risk of breast cancer in non-BRCA1/2 French Canadian families with high risk of breast cancer [serial online]
-
Desjardins S, Beauparlant JC, Labrie Y, Ouellette G, Durocher F. Variations in the NBN/NBS1 gene and the risk of breast cancer in non-BRCA1/2 French Canadian families with high risk of breast cancer [serial online]. BMC Cancer. 2009;9:181.
-
(2009)
BMC Cancer.
, vol.9
, pp. 181
-
-
Desjardins, S.1
Beauparlant, J.C.2
Labrie, Y.3
Ouellette, G.4
Durocher, F.5
-
8
-
-
38349052915
-
Nijmegen breakage syndrome mutations and risk of breast cancer
-
Bogdanova N, Feshchenko S, Schurmann P, et al. Nijmegen breakage syndrome mutations and risk of breast cancer. Int J Cancer. 2008;122:802-806.
-
(2008)
Int J Cancer.
, vol.122
, pp. 802-806
-
-
Bogdanova, N.1
Feshchenko, S.2
Schurmann, P.3
-
9
-
-
84863532805
-
Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families
-
Osorio A, Endt D, Fernandez F, et al. Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families. Hum Mol Genet. 2012;21:2889-2898.
-
(2012)
Hum Mol Genet.
, vol.21
, pp. 2889-2898
-
-
Osorio, A.1
Endt, D.2
Fernandez, F.3
-
10
-
-
80054973810
-
Mutations in BRIP1 confer high risk of ovarian cancer
-
Rafnar T, Gudbjartsson DF, Sulem P, et al. Mutations in BRIP1 confer high risk of ovarian cancer. Nat Genet. 2011;43:1104-1107.
-
(2011)
Nat Genet.
, vol.43
, pp. 1104-1107
-
-
Rafnar, T.1
Gudbjartsson, D.F.2
Sulem, P.3
-
11
-
-
77951720395
-
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene
-
Meindl A, Hellebrand H, Wiek C, et al. Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. Nat Genet. 2010;42:410-414.
-
(2010)
Nat Genet.
, vol.42
, pp. 410-414
-
-
Meindl, A.1
Hellebrand, H.2
Wiek, C.3
-
12
-
-
84860320440
-
Germline RAD51C mutations confer susceptibility to ovarian cancer
-
author reply 476
-
Loveday C, Turnbull C, Ruark E, et al. Germline RAD51C mutations confer susceptibility to ovarian cancer. Nat Genet. 2012;44: 475-476; author reply 476.
-
(2012)
Nat Genet.
, vol.44
, pp. 475-476
-
-
Loveday, C.1
Turnbull, C.2
Ruark, E.3
-
13
-
-
84863944009
-
Genetic/Familial High-Risk Assessment: Breast and Ovarian
-
Fort Washington, PA: NCCN; Accessed April 1, 2014
-
National Comprehensive Cancer Network (NCCN). Genetic/Familial High-Risk Assessment: Breast and Ovarian. NCCN Clinical Practice Guidelines in Oncology. Fort Washington, PA: NCCN; 2014. Available at: http://www.nccn.org/professionals/physician-gls/pdf/genetics-screening.pdf. Accessed April 1, 2014.
-
(2014)
NCCN Clinical Practice Guidelines in Oncology
-
-
-
14
-
-
77955439715
-
Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing
-
Walsh T, Lee MK, Casadei S, et al. Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing. Proc Natl Acad Sci U S A. 2010;107: 12629-12633.
-
(2010)
Proc Natl Acad Sci U S A.
, vol.107
, pp. 12629-12633
-
-
Walsh, T.1
Lee, M.K.2
Casadei, S.3
-
15
-
-
81055126264
-
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing
-
Walsh T, Casadei S, Lee MK, et al. Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. Proc Natl Acad Sci U S A. 2011; 108:18032-18037.
-
(2011)
Proc Natl Acad Sci U S A.
, vol.108
, pp. 18032-18037
-
-
Walsh, T.1
Casadei, S.2
Lee, M.K.3
-
16
-
-
62449249871
-
Beyond Li Fraumeni syndrome: Clinical characteristics of families with p53 germline mutations
-
Gonzalez KD, Noltner KA, Buzin CH, et al. Beyond Li Fraumeni syndrome: clinical characteristics of families with p53 germline mutations. J Clin Oncol. 2009;27:1250-1256.
-
(2009)
J Clin Oncol.
, vol.27
, pp. 1250-1256
-
-
Gonzalez, K.D.1
Noltner, K.A.2
Buzin, C.H.3
-
17
-
-
34249989159
-
Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer
-
Kaurah P, MacMillan A, Boyd N, et al. Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer. JAMA. 2007;297:2360-2372.
-
(2007)
JAMA
, vol.297
, pp. 2360-2372
-
-
Kaurah, P.1
MacMillan, A.2
Boyd, N.3
-
18
-
-
0035211026
-
Incidence of gastric cancer and breast cancer in CDH1 (E-cadherin) mutation carriers from hereditary diffuse gastric cancer families
-
Pharoah PD, Guilford P, Caldas C. Incidence of gastric cancer and breast cancer in CDH1 (E-cadherin) mutation carriers from hereditary diffuse gastric cancer families. Gastroenterology. 2001;121:1348-1353.
-
(2001)
Gastroenterology.
, vol.121
, pp. 1348-1353
-
-
Pharoah, P.D.1
Guilford, P.2
Caldas, C.3
-
19
-
-
2342458960
-
Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome
-
Pilarski R, Eng C. Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome. J Med Genet. 2004;41:323-326.
-
(2004)
J Med Genet.
, vol.41
, pp. 323-326
-
-
Pilarski, R.1
Eng, C.2
-
20
-
-
84855985283
-
Lifetime cancer risks in individuals with germline PTEN mutations
-
Tan MH, Mester JL, Ngeow J, Rybicki LA, Orloff MS, Eng C. Lifetime cancer risks in individuals with germline PTEN mutations. Clin Cancer Res. 2012;18:400-407.
-
(2012)
Clin Cancer Res.
, vol.18
, pp. 400-407
-
-
Tan, M.H.1
Mester, J.L.2
Ngeow, J.3
Rybicki, L.A.4
Orloff, M.S.5
Eng, C.6
-
21
-
-
33746491583
-
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles
-
Renwick A, Thompson D, Seal S, et al. ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles. Nat Genet. 2006;38:873-875.
-
(2006)
Nat Genet.
, vol.38
, pp. 873-875
-
-
Renwick, A.1
Thompson, D.2
Seal, S.3
-
22
-
-
39149141409
-
CHEK2∗1100delC genotyping for clinical assessment of breast cancer risk: Meta-analyses of 26, 000 patient cases and 27, 000 controls
-
Weischer M, Bojesen SE, Ellervik C, Tybjaerg-Hansen A, Nordestgaard BG. CHEK2∗1100delC genotyping for clinical assessment of breast cancer risk: meta-analyses of 26, 000 patient cases and 27, 000 controls. J Clin Oncol. 2008;26:542-548.
-
(2008)
J Clin Oncol.
, vol.26
, pp. 542-548
-
-
Weischer, M.1
Bojesen, S.E.2
Ellervik, C.3
Tybjaerg-Hansen, A.4
Nordestgaard, B.G.5
-
23
-
-
33744782567
-
Frequency and spectrum of cancers in the Peutz-Jeghers syndrome
-
Hearle N, Schumacher V, Menko FH, et al. Frequency and spectrum of cancers in the Peutz-Jeghers syndrome. Clin Cancer Res. 2006;12:3209-3215.
-
(2006)
Clin Cancer Res.
, vol.12
, pp. 3209-3215
-
-
Hearle, N.1
Schumacher, V.2
Menko, F.H.3
-
24
-
-
2942527434
-
Relative frequency and morphology of cancers in STK11 mutation carriers
-
Lim W, Olschwang S, Keller JJ, et al. Relative frequency and morphology of cancers in STK11 mutation carriers. Gastroenterology. 2004;126:1788-1794.
-
(2004)
Gastroenterology.
, vol.126
, pp. 1788-1794
-
-
Lim, W.1
Olschwang, S.2
Keller, J.J.3
-
25
-
-
77149149958
-
Cancer predisposing mis-sense and protein truncating BARD1 mutations in non-BRCA1 or BRCA2 breast cancer families
-
De Brakeleer S, De Greve J, Loris R, et al. Cancer predisposing mis-sense and protein truncating BARD1 mutations in non-BRCA1 or BRCA2 breast cancer families. Hum Mutat. 2010;31:E1175-E1185.
-
(2010)
Hum Mutat.
, vol.31
, pp. E1175-E1185
-
-
De Brakeleer, S.1
De Greve, J.2
Loris, R.3
-
26
-
-
38449120192
-
Cancer risk of heterozygotes with the NBN founder mutation
-
Seemanova E, Jarolim P, Seeman P, et al. Cancer risk of heterozygotes with the NBN founder mutation. J Natl Cancer Inst. 2007;99: 1875-1880.
-
(2007)
J Natl Cancer Inst.
, vol.99
, pp. 1875-1880
-
-
Seemanova, E.1
Jarolim, P.2
Seeman, P.3
-
27
-
-
84874083026
-
Current evidence on the relationship between 2 polymorphisms in the NBS1 gene and breast cancer risk: A meta-analysis
-
Zhang ZH, Yang LS, Huang F, Hao JH, Su PY, Sun YH. Current evidence on the relationship between 2 polymorphisms in the NBS1 gene and breast cancer risk: a meta-analysis. Asian Pac J Cancer Prev. 2012;13:5375-5379.
-
(2012)
Asian Pac J Cancer Prev.
, vol.13
, pp. 5375-5379
-
-
Zhang, Z.H.1
Yang, L.S.2
Huang, F.3
Hao, J.H.4
Su, P.Y.5
Sun, Y.H.6
-
28
-
-
80052264429
-
Germline mutations in RAD51D confer susceptibility to ovarian cancer
-
Loveday C, Turnbull C, Ramsay E, et al. Germline mutations in RAD51D confer susceptibility to ovarian cancer. Nat Genet. 2011; 43:879-882.
-
(2011)
Nat Genet.
, vol.43
, pp. 879-882
-
-
Loveday, C.1
Turnbull, C.2
Ramsay, E.3
-
29
-
-
85028163189
-
Development of a next generation sequencing panel to assess hereditary cancer risk that includes clinical diagnostic analysis of the BRCA1 and BRCA2 genes
-
October 22-26, 2013; Boston, Massachusetts
-
Roa BB, Bowles K, Bhatnagar S, et al. Development of a next generation sequencing panel to assess hereditary cancer risk that includes clinical diagnostic analysis of the BRCA1 and BRCA2 genes. Paper presented at: 2013 American Society of Human Genetics (ASHG) Annual Meeting; October 22-26, 2013; Boston, Massachusetts.
-
Paper Presented At: 2013 American Society of Human Genetics (ASHG) Annual Meeting
-
-
Roa, B.B.1
Bowles, K.2
Bhatnagar, S.3
-
30
-
-
42149139456
-
ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007
-
Richards CS, Bale S, Bellissimo DB, et al. ACMG recommendations for standards for interpretation and reporting of sequence variations: revisions 2007. Genet Med. 2008;10:294-300.
-
(2008)
Genet Med.
, vol.10
, pp. 294-300
-
-
Richards, C.S.1
Bale, S.2
Bellissimo, D.B.3
-
31
-
-
0037087536
-
Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: Analysis of 10, 000 individuals
-
Frank TS, Deffenbaugh AM, Reid JE, et al. Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10, 000 individuals. J Clin Oncol. 2002;20:1480-1490.
-
(2002)
J Clin Oncol.
, vol.20
, pp. 1480-1490
-
-
Frank, T.S.1
Deffenbaugh, A.M.2
Reid, J.E.3
-
32
-
-
84907597238
-
A comprehensive laboratory-based program for classification of variants of uncertain significance in hereditary cancer genes
-
Eggington JM, Bowles KR, Moyes K, et al. A comprehensive laboratory-based program for classification of variants of uncertain significance in hereditary cancer genes. Clin Genet. 2014;86:229-237.
-
(2014)
Clin Genet.
, vol.86
, pp. 229-237
-
-
Eggington, J.M.1
Bowles, K.R.2
Moyes, K.3
-
33
-
-
78650389153
-
A PALB2 mutation associated with high risk of breast cancer [serial online]
-
Southey MC, Teo ZL, Dowty JG, et al. A PALB2 mutation associated with high risk of breast cancer [serial online]. Breast Cancer Res. 2010;12:R109.
-
(2010)
Breast Cancer Res.
, vol.12
, pp. R109
-
-
Southey, M.C.1
Teo, Z.L.2
Dowty, J.G.3
-
34
-
-
84862776557
-
Rare germline mutations in PALB2 and breast cancer risk: A population-based study
-
Tischkowitz M, Capanu M, Sabbaghian N, et al. Rare germline mutations in PALB2 and breast cancer risk: a population-based study. Hum Mutat. 2012;33:674-680.
-
(2012)
Hum Mutat.
, vol.33
, pp. 674-680
-
-
Tischkowitz, M.1
Capanu, M.2
Sabbaghian, N.3
-
35
-
-
65649112112
-
The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype
-
Heikkinen T, Karkkainen H, Aaltonen K, et al. The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype. Clin Cancer Res. 2009;15:3214-3222.
-
(2009)
Clin Cancer Res.
, vol.15
, pp. 3214-3222
-
-
Heikkinen, T.1
Karkkainen, H.2
Aaltonen, K.3
-
36
-
-
0035921190
-
Two metachronous tumors in the radiotherapy fields of a patient with Li-Fraumeni syndrome
-
Limacher JM, Frebourg T, Natarajan-Ame S, Bergerat JP. Two metachronous tumors in the radiotherapy fields of a patient with Li-Fraumeni syndrome. Int J Cancer. 2001;96:238-242.
-
(2001)
Int J Cancer.
, vol.96
, pp. 238-242
-
-
Limacher, J.M.1
Frebourg, T.2
Natarajan-Ame, S.3
Bergerat, J.P.4
-
37
-
-
0032522623
-
Multiple primary cancers in families with Li-Fraumeni syndrome
-
Hisada M, Garber JE, Fung CY, Fraumeni JF Jr, Li FP. Multiple primary cancers in families with Li-Fraumeni syndrome. J Natl Cancer Inst. 1998;90:606-611.
-
(1998)
J Natl Cancer Inst.
, vol.90
, pp. 606-611
-
-
Hisada, M.1
Garber, J.E.2
Fung, C.Y.3
Fraumeni, J.F.4
Li, F.P.5
-
38
-
-
0028168643
-
P53-deficient mice are extremely susceptible to radiation-induced tumorigenesis
-
Kemp CJ, Wheldon T, Balmain A. p53-deficient mice are extremely susceptible to radiation-induced tumorigenesis. Nat Genet. 1994;8: 66-69.
-
(1994)
Nat Genet.
, vol.8
, pp. 66-69
-
-
Kemp, C.J.1
Wheldon, T.2
Balmain, A.3
-
39
-
-
80053594059
-
Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer
-
Cybulski C, Wokolorczyk D, Jakubowska A, et al. Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer. J Clin Oncol. 2011;29:3747-3752.
-
(2011)
J Clin Oncol.
, vol.29
, pp. 3747-3752
-
-
Cybulski, C.1
Wokolorczyk, D.2
Jakubowska, A.3
-
40
-
-
20544474516
-
Cancer risks and mortalityin heterozygous ATM mutation carriers
-
Thompson D, Duedal S, Kirner J, et al. Cancer risks and mortalityin heterozygous ATM mutation carriers. J Natl Cancer Inst. 2005;97:813-822.
-
(2005)
J Natl Cancer Inst.
, vol.97
, pp. 813-822
-
-
Thompson, D.1
Duedal, S.2
Kirner, J.3
-
41
-
-
18544389716
-
Low-penetrance susceptibility to breast cancer due to CHEK2(∗)1100delC in noncarriers of BRCA1 or BRCA2 mutations
-
Meijers-Heijboer H, van den Ouweland A, Klijn J, et al. Low-penetrance susceptibility to breast cancer due to CHEK2(∗)1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat Genet. 2002;31:55-59.
-
(2002)
Nat Genet.
, vol.31
, pp. 55-59
-
-
Meijers-Heijboer, H.1
Van Den Ouweland, A.2
Klijn, J.3
-
42
-
-
3042582651
-
CHEK2∗1100-delC and susceptibility to breast cancer: A collaborative analysis involving 10, 860 breast cancer cases and 9, 065 controls from 10 studies
-
CHEK2 Breast Cancer Case-Control Consortium. CHEK2∗1100-delC and susceptibility to breast cancer: a collaborative analysis involving 10, 860 breast cancer cases and 9, 065 controls from 10 studies. Am J Hum Genet. 2004;74:1175-1182.
-
(2004)
Am J Hum Genet.
, vol.74
, pp. 1175-1182
-
-
-
43
-
-
79954560252
-
Synthetic lethality of PARP inhibition in cancers lacking BRCA1 and BRCA2 mutations
-
Dedes KJ, Wilkerson PM, Wetterskog D, Weigelt B, Ashworth A, Reis-Filho JS. Synthetic lethality of PARP inhibition in cancers lacking BRCA1 and BRCA2 mutations. Cell Cycle. 2011;10:1192-1199.
-
(2011)
Cell Cycle.
, vol.10
, pp. 1192-1199
-
-
Dedes, K.J.1
Wilkerson, P.M.2
Wetterskog, D.3
Weigelt, B.4
Ashworth, A.5
Reis-Filho, J.S.6
-
44
-
-
78649321855
-
The PARP inhibitor olaparib induces significant killing of ATM-deficient lymphoid tumor cells in vitro and in vivo
-
Weston VJ, Oldreive CE, Skowronska A, et al. The PARP inhibitor olaparib induces significant killing of ATM-deficient lymphoid tumor cells in vitro and in vivo. Blood. 2010;116:4578-4587.
-
(2010)
Blood.
, vol.116
, pp. 4578-4587
-
-
Weston, V.J.1
Oldreive, C.E.2
Skowronska, A.3
-
45
-
-
64849092309
-
Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene [serial online]
-
Jones S, Hruban RH, Kamiyama M, et al. Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene [serial online]. Science. 2009;324:217.
-
(2009)
Science.
, vol.324
, pp. 217
-
-
Jones, S.1
Hruban, R.H.2
Kamiyama, M.3
-
46
-
-
79961127649
-
Germline PALB2 mutation analysis in breast-pancreas cancer families
-
Stadler ZK, Salo-Mullen E, Sabbaghian N, et al. Germline PALB2 mutation analysis in breast-pancreas cancer families. J Med Genet. 2011;48:523-525.
-
(2011)
J Med Genet.
, vol.48
, pp. 523-525
-
-
Stadler, Z.K.1
Salo-Mullen, E.2
Sabbaghian, N.3
-
47
-
-
67650979375
-
Increased colorectal cancer incidence in obligate carriers of heterozygous mutations in MUTYH
-
494, e481; quiz 725-486
-
Jones N, Vogt S, Nielsen M, et al. Increased colorectal cancer incidence in obligate carriers of heterozygous mutations in MUTYH. Gastroenterology. 2009;137:489-494, 494, e481; quiz 725-486.
-
(2009)
Gastroenterology.
, vol.137
, pp. 489-494
-
-
Jones, N.1
Vogt, S.2
Nielsen, M.3
-
48
-
-
33644747476
-
Risk of colorectal cancer in monoallelic and biallelic carriers of MYH mutations: A population-based case-family study
-
Jenkins MA, Croitoru ME, Monga N, et al. Risk of colorectal cancer in monoallelic and biallelic carriers of MYH mutations: a population-based case-family study. Cancer Epidemiol Biomarkers Prev. 2006;15:312-314.
-
(2006)
Cancer Epidemiol Biomarkers Prev.
, vol.15
, pp. 312-314
-
-
Jenkins, M.A.1
Croitoru, M.E.2
Monga, N.3
-
49
-
-
85028140681
-
Genetic/Familial High-Risk Assessment: Colorectal
-
Fort Washington, PA: NCCN; Accessed April 1, 2014
-
National Comprehensive Cancer Network (NCCN). Genetic/Familial High-Risk Assessment: Colorectal. NCCN Clinical Practice Guidelines in Oncology. Fort Washington, PA: NCCN; 2014. Available at: http://www.nccn.org/professionals/physician-gls/pdf/genetics-colon.pdf. Accessed April 1, 2014.
-
(2014)
NCCN Clinical Practice Guidelines in Oncology
-
-
-
50
-
-
84873412474
-
International Cancer of the Pancreas Screening (CAPS) Consortium summit on the management of patients with increased risk for familial pancreatic cancer
-
Canto MI, Harinck F, Hruban RH, et al. International Cancer of the Pancreas Screening (CAPS) Consortium summit on the management of patients with increased risk for familial pancreatic cancer. Gut. 2013;62:339-347.
-
(2013)
Gut.
, vol.62
, pp. 339-347
-
-
Canto, M.I.1
Harinck, F.2
Hruban, R.H.3
-
51
-
-
0031029633
-
Probability of carrying a mutation of breast-ovarian cancer gene BRCA1 based on family history
-
Berry DA, Parmigiani G, Sanchez J, Schildkraut J, Winer E. Probability of carrying a mutation of breast-ovarian cancer gene BRCA1 based on family history. J Natl Cancer Inst. 1997;89:227-238.
-
(1997)
J Natl Cancer Inst.
, vol.89
, pp. 227-238
-
-
Berry, D.A.1
Parmigiani, G.2
Sanchez, J.3
Schildkraut, J.4
Winer, E.5
-
52
-
-
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;62:145-158.
-
(1998)
Am J Hum Genet.
, vol.62
, pp. 145-158
-
-
Parmigiani, G.1
Berry, D.2
Aguilar, O.3
|