Related Content
Search Google Scholar for:
|
|
Science 21 December 1990: Vol. 250. no. 4988, pp. 1684 - 1689 DOI: 10.1126/science.2270482
|
|
Articles
Science, Vol 250, Issue 4988, 1684-1689
Copyright © 1990 by American Association for the Advancement of Science
Linkage of early-onset familial breast cancer to chromosome 17q21
JM Hall,
MK Lee,
B Newman,
JE Morrow,
LA Anderson,
B Huey,
and
MC King
School of Public Health, University of California, Berkeley 94720.
Human breast cancer is usually caused by genetic alterations of somatic cells of the breast, but occasionally, susceptibility to the disease is inherited. Mapping the genes responsible for inherited breast cancer may also allow the identification of early lesions that are critical for the development of breast cancer in the general population. Chromosome 17q21 appears to be the locale of a gene for inherited susceptibility to breast cancer in families with early-onset disease. Genetic analysis yields a lod score (logarithm of the likelihood ratio for linkage) of 5.98 for linkage of breast cancer susceptibility to D17S74 in early-onset families and negative lod scores in families with late-onset disease. Likelihood ratios in favor of linkage heterogeneity among families ranged between 2000:1 and greater than 10(6):1 on the basis of multipoint analysis of four loci in the region.
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
- Polymorphic Variants in Hereditary Pancreatic Cancer Genes Are Not Associated with Pancreatic Cancer Risk.
- R. R. McWilliams, W. R. Bamlet, M. de Andrade, D. N. Rider, F. J. Couch, J. M. Cunningham, M. E. Matsumoto, K. G. Rabe, T. J. Hammer, and G. M. Petersen (2009)
Cancer Epidemiol. Biomarkers Prev.
18, 2549-2552
| Abstract »
| Full Text »
| PDF »
- Cancer Prevention: From 1727 to Milestones of the Past 100 Years.
- S. M. Lippman and E. T. Hawk (2009)
Cancer Res.
69, 5269-5284
| Abstract »
| Full Text »
| PDF »
- Cancer Prevention Research: Back to the Future.
- S. M. Lippman (2009)
Cancer Prevention Research
2, 503-513
| Full Text »
| PDF »
- Evidence for an Inherited Predisposition Contributing to the Risk for Rotator Cuff Disease.
- R. Z. Tashjian, J. M. Farnham, F. S. Albright, C. C. Teerlink, and L. A. Cannon-Albright (2009)
J. Bone Joint Surg. Am.
91, 1136-1142
| Abstract »
| Full Text »
| PDF »
- Two mutations of BRCA2 gene at exon and splicing site in a woman who underwent oncogenetic counseling.
- M. Pensabene, I. Spagnoletti, I. Capuano, C. Condello, S. Pepe, A. Contegiacomo, G. Lombardi, G. Bevilacqua, and M. A. Caligo (2009)
Ann. Onc.
20, 874-878
| Abstract »
| Full Text »
| PDF »
- Age-dependent penetrance of different germline mutations in the BRCA1 gene.
- F Al-Mulla, J M Bland, D Serratt, J Miller, C Chu, and G T Taylor (2009)
J. Clin. Pathol.
62, 350-356
| Abstract »
| Full Text »
| PDF »
- How Is a Statistical Link Established Between a Human Outcome and a Genetic Variant?.
- Guang Guo and D. E. Adkins (2008)
Sociological Methods Research
37, 201-226
| Abstract »
| PDF »
- BRCA1 Is Required for Meiotic Spindle Assembly and Spindle Assembly Checkpoint Activation in Mouse Oocytes.
- B. Xiong, S. Li, J.-S. Ai, S. Yin, Y.-C. OuYang, S.-C. Sun, D.-Y. Chen, and Q.-Y. Sun (2008)
Biol Reprod
79, 718-726
| Abstract »
| Full Text »
| PDF »
- Hereditary breast cancer: from molecular pathology to tailored therapies.
- D S P Tan, C Marchio, and J S Reis-Filho (2008)
J. Clin. Pathol.
61, 1073-1082
| Abstract »
| Full Text »
| PDF »
- Genetic and Genomic Discovery Using Family Studies.
- I. B. Borecki and M. A. Province (2008)
Circulation
118, 1057-1063
| Full Text »
| PDF »
- Tilting at Quixotic Trait Loci (QTL): An Evolutionary Perspective on Genetic Causation.
- K. M. Weiss (2008)
Genetics
179, 1741-1756
| Abstract »
| Full Text »
| PDF »
- LOT: a tool for linkage analysis of ordinal traits for pedigree data.
- M. Zhang, R. Feng, X. Chen, B. Hu, and H. Zhang (2008)
Bioinformatics
24, 1737-1739
| Abstract »
| Full Text »
| PDF »
- Functional Analysis of the Transcription Repressor PLU-1/JARID1B.
- A. G. Scibetta, S. Santangelo, J. Coleman, D. Hall, T. Chaplin, J. Copier, S. Catchpole, J. Burchell, and J. Taylor-Papadimitriou (2007)
Mol. Cell. Biol.
27, 7220-7235
| Abstract »
| Full Text »
| PDF »
- Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screening.
- A Smith, A Moran, M C Boyd, M Bulman, A Shenton, L Smith, R Iddenden, E R Woodward, F Lalloo, E R Maher, et al. (2007)
J. Med. Genet.
44, 10-15
| Abstract »
| Full Text »
| PDF »
- Ashkenazi Jews and Breast Cancer: The Consequences of Linking Ethnic Identity to Genetic Disease.
- S. I. Brandt-Rauf, V. H. Raveis, N. F. Drummond, J. A. Conte, and S. M. Rothman (2006)
Am J Public Health
96, 1979-1988
| Abstract »
| Full Text »
| PDF »
- ASCO/SSO Review of Current Role of Risk-Reducing Surgery in Common Hereditary Cancer Syndromes.
- J. G. Guillem, W. C. Wood, J. F. Moley, A. Berchuck, B. Y. Karlan, D. G. Mutch, R. F. Gagel, J. Weitzel, M. Morrow, B. L. Weber, et al. (2006)
J. Clin. Oncol.
24, 4642-4660
| Abstract »
| Full Text »
| PDF »
- Familial Aggregation of Illness Chronicity in Recurrent, Early-Onset Major Depression Pedigrees.
- F. M. Mondimore, P. P. Zandi, D. F. MacKinnon, M. G. McInnis, E. B. Miller, R. P. Crowe, W. A. Scheftner, D. H. Marta, M. M. Weissman, D. F. Levinson, et al. (2006)
Am J Psychiatry
163, 1554-1560
| Abstract »
| Full Text »
| PDF »
- Genetic Dissection of Complex Traits.
- E. S. Lander and N. J. Schork (2006)
Focus
4, 442
| Abstract »
| Full Text »
| PDF »
- Genetic Analysis of Chromosome Pairing, Recombination, and Cell Cycle Control during First Meiotic Prophase in Mammals.
- P. E. Cohen, S. E. Pollack, and J. W. Pollard (2006)
Endocr. Rev.
27, 398-426
| Abstract »
| Full Text »
| PDF »
- Deliberate Deceit of Family Members: A Challenge to Providers of Clinical Genetics Services.
- J. T. Loud, N. E. Weissman, J. A. Peters, R. M. Giusti, B. S. Wilfond, W. Burke, and M. H. Greene (2006)
J. Clin. Oncol.
24, 1643-1646
| Full Text »
| PDF »
- BRCA1: cell cycle checkpoint, genetic instability, DNA damage response and cancer evolution.
- C.-X. Deng (2006)
Nucleic Acids Res.
34, 1416-1426
| Abstract »
| Full Text »
| PDF »
- Lymphocytes of BRCA1 and BRCA2 germ-line mutation carriers, with or without breast cancer, are not abnormally sensitive to the chromosome damaging effect of moderate folate deficiency.
- S. Beetstra, C. Salisbury, J. Turner, M. Altree, R. McKinnon, G. Suthers, and M. Fenech (2006)
Carcinogenesis
27, 517-524
| Abstract »
| Full Text »
| PDF »
- Clinical Correlates and Familial Aggregation of Age at Onset in Bipolar Disorder.
- P.-I Lin, M. G. McInnis, J. B. Potash, V. Willour, D. F. MacKinnon, J. R. DePaulo, and P. P. Zandi (2006)
Am J Psychiatry
163, 240-246
| Abstract »
| Full Text »
| PDF »
- Detection of Genes for Ordinal Traits in Nuclear Families and a Unified Approach for Association Studies.
- H. Zhang, X. Wang, and Y. Ye (2006)
Genetics
172, 693-699
| Abstract »
| Full Text »
| PDF »
- Tumor suppressor genetics.
- S. R. Payne and C. J. Kemp (2005)
Carcinogenesis
26, 2031-2045
| Abstract »
| Full Text »
| PDF »
- Relationship Between a High-Risk Haplotype in the DTNBP1 (Dysbindin) Gene and Clinical Features of Schizophrenia.
- A. H. Fanous, E. J. van den Oord, B. P. Riley, S. H. Aggen, M. C. Neale, F. A. O'Neill, D. Walsh, and K. S. Kendler (2005)
Am J Psychiatry
162, 1824-1832
| Abstract »
| Full Text »
| PDF »
- The Role of the BRCA1 Tumor Suppressor in DNA Double-Strand Break Repair.
- J. Zhang and S. N. Powell (2005)
Mol. Cancer Res.
3, 531-539
| Abstract »
| Full Text »
| PDF »
- A Haplotype-Based Case-Control Study of BRCA1 and Sporadic Breast Cancer Risk.
- M. L. Freedman, K. L. Penney, D. O. Stram, S. Riley, R. McKean-Cowdin, L. Le Marchand, D. Altshuler, and C. A. Haiman (2005)
Cancer Res.
65, 7516-7522
| Abstract »
| Full Text »
| PDF »
- Critical Junctures in Genetic Medicine: The Transformation of DNA Lab Science to Commercial Pharmacogenomics.
- S. S. Turner (2005)
Journal of Business and Technical Communication
19, 328-352
| Abstract »
| PDF »
- Early Adult-Onset POAG Linked to 15q11-13 Using Ordered Subset Analysis.
- R. R. Allingham, J. L. Wiggs, E. R. Hauser, K. R. Larocque-Abramson, C. Santiago-Turla, B. Broomer, E. A. Del Bono, F. L. Graham, J. L. Haines, M. A. Pericak-Vance, et al. (2005)
Invest. Ophthalmol. Vis. Sci.
46, 2002-2005
| Abstract »
| Full Text »
| PDF »
- Neurogenetics II: complex disorders.
- A F Wright (2005)
J. Neurol. Neurosurg. Psychiatry
76, 623-631
| Abstract »
| Full Text »
| PDF »
- A novel BRCA2 mutation in an Indonesian family found with a new, rapid, and sensitive mutation detection method based on pooled denaturing gradient gel electrophoresis and targeted sequencing.
- D Purnomosari, D K Paramita, T Aryandono, G Pals, and P J van Diest (2005)
J. Clin. Pathol.
58, 493-499
| Abstract »
| Full Text »
| PDF »
- N-(4-Hydroxyphenyl)retinamide is more potent than other phenylretinamides in inhibiting the growth of BRCA1-mutated breast cancer cells.
- A.-M. Simeone, C.-X. Deng, G. J. Kelloff, V. E. Steele, M. M. Johnson, and A. M. Tari (2005)
Carcinogenesis
26, 1000-1007
| Abstract »
| Full Text »
| PDF »
- An Autosome-Wide Scan for Linkage Disequilibrium-Based Association in Sporadic Breast Cancer Cases in Eastern Finland: Three Candidate Regions Found.
- J. M. Hartikainen, H. Tuhkanen, V. Kataja, A. M. Dunning, A. Antoniou, P. Smith, A. Arffman, M. Pirskanen, D. F. Easton, M. Eskelinen, et al. (2005)
Cancer Epidemiol. Biomarkers Prev.
14, 75-80
| Abstract »
| Full Text »
| PDF »
- Haplotype-Based Localization of an Alcohol Dependence Gene to the 5q34 {gamma}-Aminobutyric Acid Type A Gene Cluster.
- M. Radel, R. L. Vallejo, N. Iwata, R. Aragon, J. C. Long, M. Virkkunen, and D. Goldman (2005)
Arch Gen Psychiatry
62, 47-55
| Abstract »
| Full Text »
| PDF »
- Linkage analysis of ordinal traits for pedigree data.
- R. Feng, J. F. Leckman, and H. Zhang (2004)
PNAS
101, 16739-16744
| Abstract »
| Full Text »
| PDF »
- Functional Phe31Ile polymorphism in Aurora A and risk of breast carcinoma.
- T. Sun, X. Miao, J. Wang, W. Tan, Y. Zhou, C. Yu, and D. Lin (2004)
Carcinogenesis
25, 2225-2230
| Abstract »
| Full Text »
| PDF »
- Age at onset in mesial temporal lobe epilepsy with a history of febrile seizures.
- J. Janszky, I. Janszky, and A. Ebner (2004)
Neurology
63, 1296-1298
| Abstract »
| Full Text »
| PDF »
- Low-Density Lipoprotein Particle Size Loci in Familial Combined Hyperlipidemia: Evidence for Multiple Loci From a Genome Scan.
- M. D. Badzioch, R. P. Igo Jr, F. Gagnon, J. D. Brunzell, R. M. Krauss, A. G. Motulsky, E. M. Wijsman, and G. P. Jarvik (2004)
Arterioscler Thromb Vasc Biol
24, 1942-1950
| Abstract »
| Full Text »
| PDF »
- Truncating BRCA1 Mutations Are Uncommon in a Cohort of Hereditary Prostate Cancer Families with Evidence of Linkage to 17q Markers.
- K. A. Zuhlke, J. J. Madeoy, J. Beebe-Dimmer, K. A. White, A. Griffin, E. M. Lange, S. B. Gruber, E. A. Ostrander, and K. A. Cooney (2004)
Clin. Cancer Res.
10, 5975-5980
| Abstract »
| Full Text »
| PDF »
- Oncogenes and Tumor Suppressor Genes in Breast Cancer: Potential Diagnostic and Therapeutic Applications.
- C. Osborne, P. Wilson, and D. Tripathy (2004)
Oncologist
9, 361-377
| Abstract »
| Full Text »
| PDF »
- Substantial reduction in risk of breast cancer associated with genetic polymorphisms in the promoters of the matrix metalloproteinase-2 and tissue inhibitor of metalloproteinase-2 genes.
- Y. Zhou, C. Yu, X. Miao, W. Tan, G. Liang, P. Xiong, T. Sun, and D. Lin (2004)
Carcinogenesis
25, 399-404
| Abstract »
| Full Text »
| PDF »
- Functional Dissection of Transcription Factor ZBRK1 Reveals Zinc Fingers with Dual Roles in DNA-binding and BRCA1-dependent Transcriptional Repression.
- W. Tan, L. Zheng, W.-H. Lee, and T. G. Boyer (2004)
J. Biol. Chem.
279, 6576-6587
| Abstract »
| Full Text »
| PDF »
- BRCA1 c.2845insA is a recurring mutation with a founder effect in Singapore Malay women with early onset breast/ovarian cancer.
- J-H Sng, A B Ali, S C Lee, D Zahar, J E L Wong, V Blake, A Sharif, G Cross, and P T C Iau (2003)
J. Med. Genet.
40, e117-117
| Full Text »
| PDF »
- Stroma Adjacent to Metastatic Mature Teratoma after Chemotherapy for Testicular Germ Cell Tumors Is Derived from the Same Progenitor Cells as the Teratoma.
- D. W. Brandli, T. M. Ulbright, R. S. Foster, O. W. Cummings, S. Zhang, C. J. Sweeney, J. N. Eble, and L. Cheng (2003)
Cancer Res.
63, 6063-6068
| Abstract »
| Full Text »
| PDF »
- Genetic loading in familial migraine with aura.
- S E Noble-Topham, M Z Cader, D A Dyment, G P A Rice, J D Brown, and G C Ebers (2003)
J. Neurol. Neurosurg. Psychiatry
74, 1128-1130
| Abstract »
| Full Text »
| PDF »
- Breast and Ovarian Cancer.
- R. Wooster and B. L. Weber (2003)
N. Engl. J. Med.
348, 2339-2347
| Full Text »
| PDF »
- Roles of BRCA1 in DNA damage repair: a link between development and cancer.
- C.-X. Deng and R.-H. Wang (2003)
Hum. Mol. Genet.
12, R113-123
| Abstract »
| Full Text »
| PDF »
- Clinical challenges posed by new biotechnology.
- D Castle (2003)
Postgrad. Med. J.
79, 65-66
| Full Text »
| PDF »
- Finding genetic contributions to sporadic disease: A recessive locus at 12q24 commonly contributes to patent ductus arteriosus.
- A. Mani, S.-M. Meraji, R. Houshyar, J. Radhakrishnan, A. Mani, M. Ahangar, T. M. Rezaie, M.-A. Taghavinejad, B. Broumand, H. Zhao, et al. (2002)
PNAS
99, 15054-15059
| Abstract »
| Full Text »
| PDF »
- Cancer Incidence in BRCA1 Mutation Carriers.
- D. Thompson, D. F. Easton, and the Breast Cancer Linkage Consortium (2002)
J Natl Cancer Inst
94, 1358-1365
| Abstract »
| Full Text »
| PDF »
- Cancer Risk Estimates for BRCA1 Mutation Carriers Identified in a Risk Evaluation Program.
- M. S. Brose, T. R. Rebbeck, K. A. Calzone, J. E. Stopfer, K. L. Nathanson, and B. L. Weber (2002)
J Natl Cancer Inst
94, 1365-1372
| Abstract »
| Full Text »
| PDF »
- Sex hormone-binding globulin polymorphisms in familial and sporadic breast cancer.
- A. Forsti, Q. Jin, E. Grzybowska, M. Soderberg, H. Zientek, M. Sieminska, J. Rogozinska-Szczepka, E. Chmielik, B. Utracka-Hutka, and K. Hemminki (2002)
Carcinogenesis
23, 1315-1320
| Abstract »
| Full Text »
| PDF »
- A multigenerational family with multiple sclerosis.
- D. A. Dyment, M. Z. Cader, C. J. Willer, N. Risch, A. D. Sadovnick, and G. C. Ebers (2002)
Brain
125, 1474-1482
| Abstract »
| Full Text »
| PDF »
- BRCA1 transcriptionally regulates genes involved in breast tumorigenesis.
- P. L. Welcsh, M. K. Lee, R. M. Gonzalez-Hernandez, D. J. Black, M. Mahadevappa, E. M. Swisher, J. A. Warrington, and M.-C. King (2002)
PNAS
99, 7560-7565
| Abstract »
| Full Text »
| PDF »
- Variation in BRCA1 Cancer Risks by Mutation Position.
- D. Thompson and D. Easton (2002)
Cancer Epidemiol. Biomarkers Prev.
11, 329-336
| Abstract »
| Full Text »
| PDF »
- Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility.
- M M de Jong, I M Nolte, G J te Meerman, W T A van der Graaf, J C Oosterwijk, J H Kleibeuker, M Schaapveld, and E G E de Vries (2002)
J. Med. Genet.
39, 225-242
| Abstract »
| Full Text »
| PDF »
- Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes.
- E. K. Silverman, J. D. Mosley, L. J. Palmer, M. Barth, J. M. Senter, A. Brown, J. M. Drazen, D. J. Kwiatkowski, H. A. Chapman, E. J. Campbell, et al. (2002)
Hum. Mol. Genet.
11, 623-632
| Abstract »
| Full Text »
| PDF »
- BRCA1 and BRCA2 Mutation Frequency in Women Evaluated in a Breast Cancer Risk Evaluation Clinic.
- H. A. Shih, F. J. Couch, K. L. Nathanson, M. A. Blackwood, T. R. Rebbeck, K. A. Armstrong, K. Calzone, J. Stopfer, S. Seal, M. R. Stratton, et al. (2002)
J. Clin. Oncol.
20, 994-999
| Abstract »
| Full Text »
| PDF »
- Comorbid Bipolar Disorder and Panic Disorder in Families With a High Prevalence of Bipolar Disorder.
- D. F. MacKinnon, P. P. Zandi, J. Cooper, J. B. Potash, S. G. Simpson, E. Gershon, J. Nurnberger, T. Reich, and J. R. DePaulo (2002)
Am J Psychiatry
159, 30-35
| Abstract »
| Full Text »
| PDF »
- Tamoxifen and Breast Cancer Incidence Among Women With Inherited Mutations in BRCA1 and BRCA2: National Surgical Adjuvant Breast and Bowel Project (NSABP-P1) Breast Cancer Prevention Trial.
- M.-C. King, S. Wieand, K. Hale, M. Lee, T. Walsh, K. Owens, J. Tait, L. Ford, B. K. Dunn, J. Costantino, et al. (2001)
JAMA
286, 2251-2256
| Abstract »
| Full Text »
| PDF »
- Clinical Characteristics of Prostate Cancer in an Analysis of Linkage to Four Putative Susceptibility Loci.
- E. L. Goode, J. L. Stanford, M. A. Peters, M. Janer, M. Gibbs, S. Kolb, M. D. Badzioch, L. Hood, E. A. Ostrander, and G. P. Jarvik (2001)
Clin. Cancer Res.
7, 2739-2749
| Abstract »
| Full Text »
| PDF »
- The Genetic Epidemiology of Cancer: Interpreting Family and Twin Studies and Their Implications for Molecular Genetic Approaches.
- N. Risch (2001)
Cancer Epidemiol. Biomarkers Prev.
10, 733-741
| Abstract »
| Full Text »
| PDF »
- Pathological Features and BRCA1 Mutation Screening in Premenopausal Breast Cancer Patients.
- J. Chang, S. G. Hilsenbeck, J. H. Sng, J. Wong, and G. C. Ragu (2001)
Clin. Cancer Res.
7, 1739-1742
| Abstract »
| Full Text »
| PDF »
- Admixture Analysis of Age at Onset in Bipolar I Affective Disorder.
- F. Bellivier, J.-L. Golmard, C. Henry, M. Leboyer, and F. Schurhoff (2001)
Arch Gen Psychiatry
58, 510-512
| Full Text »
| PDF »
- BRCA1 and BRCA2 and the genetics of breast and ovarian cancer.
- P. L. Welcsh and M.-C. King (2001)
Hum. Mol. Genet.
10, 705-713
| Abstract »
| Full Text »
| PDF »
- Allele-sharing among affected relatives: non-parametric methods for identifying genes.
- M.-C. Shih and A. S Whittemore (2001)
Statistical Methods in Medical Research
10, 27-55
| Abstract »
| PDF »
- Genetic Disease, Genetic Testing, and the Clinician.
- K. C. Smith (2001)
JAMA
285, 91
| Full Text »
| PDF »
- Allelic imbalance on chromosomes 13 and 17 and mutation analysis of BRCA1 and BRCA2 genes in monozygotic twins concordant for breast cancer.
- A. Forsti, L. Luo, I. Vorechovsky, M. Soderberg, P. Lichtenstein, and K. Hemminki (2001)
Carcinogenesis
22, 27-33
| Abstract »
| Full Text »
| PDF »
- Familial Breast and Ovarian Cancer: A Swedish Population-based Register Study.
- H. Anderson, A. Bladstrom, H. Olsson, and T. R. Moller (2000)
Am. J. Epidemiol.
152, 1154-1163
| Abstract »
| Full Text »
| PDF »
- Statistical designs for familial aggregation.
- K.-Y. Liang and T. H Beaty (2000)
Statistical Methods in Medical Research
9, 543-562
| Abstract »
| PDF »
- Effect of Radiotherapy After Breast-Conserving Treatment in Women With Breast Cancer and Germline BRCA1/2 Mutations.
- L. J. Pierce, M. Strawderman, S. A. Narod, I. Oliviotto, A. Eisen, L. Dawson, D. Gaffney, L. J. Solin, A. Nixon, J. Garber, et al. (2000)
J. Clin. Oncol.
18, 3360-3369
| Abstract »
| Full Text »
| PDF »
- Randomized Trial of a Specialist Genetic Assessment Service for Familial Breast Cancer.
- K. Brain, J. Gray, P. Norman, E. France, C. Anglim, G. Barton, E. Parsons, A. Clarke, H. Sweetland, M. Tischkowitz, et al. (2000)
J Natl Cancer Inst
92, 1345-1351
| Abstract »
| Full Text »
| PDF »
- Why Are the Majority of Hereditary Cases of Early-Onset Breast Cancer Sporadic? A Simulation Study.
- J. Cui and J. L. Hopper (2000)
Cancer Epidemiol. Biomarkers Prev.
9, 805-812
| Abstract »
| Full Text »
- Familial Aggregation: Sorting Susceptibility From Shared Environment.
- G. M. Petersen (2000)
J Natl Cancer Inst
92, 1114-1115
| Full Text »
| PDF »
- Genetic and Hormonal Risk Factors in Breast Cancer.
- A.-M. Martin and B. L. Weber (2000)
J Natl Cancer Inst
92, 1126-1135
| Abstract »
| Full Text »
| PDF »
- Intention to Undergo Prophylactic Bilateral Mastectomy in Women at Increased Risk of Developing Hereditary Breast Cancer.
- B. Meiser, P. Butow, M. Friedlander, V. Schnieden, M. Gattas, J. Kirk, G. Suthers, E. Haan, and K. Tucker (2000)
J. Clin. Oncol.
18, 2250-2257
| Abstract »
| Full Text »
| PDF »
- Attitudes to genetic testing for breast cancer susceptibility in women at increased risk of developing hereditary breast cancer.
- B. MEISER, P. BUTOW, A. BARRATT, G. SUTHERS, M. SMITH, A. COLLEY, E. THOMPSON, and K. TUCKER (2000)
J. Med. Genet.
37, 472-476
| Full Text »
- Functional Assay for BRCA1: Mutagenesis of the COOH-Terminal Region Reveals Critical Residues for Transcription Activation.
- F. Hayes, C. Cayanan, D. Barillà, and A. N. A. Monteiro (2000)
Cancer Res.
60, 2411-2418
| Abstract »
| Full Text »
- BRCA1 and E-Cadherin Promoter Hypermethylation and Gene Inactivation in Cancer--Association or Mechanism?.
- E. R. Fearon (2000)
J Natl Cancer Inst
92, 515-517
| Full Text »
| PDF »
- Promoter Hypermethylation and BRCA1 Inactivation in Sporadic Breast and Ovarian Tumors.
- M. Esteller, J. M. Silva, G. Dominguez, F. Bonilla, X. Matias-Guiu, E. Lerma, E. Bussaglia, J. Prat, I. C. Harkes, E. A. Repasky, et al. (2000)
J Natl Cancer Inst
92, 564-569
| Abstract »
| Full Text »
| PDF »
- Risk assessment in first degree female relatives of breast cancer patients using the alkaline Comet assay.
- N. Rajeswari, Y.R. Ahuja, U. Malini, S. Chandrashekar, N. Balakrishna, K.V. Rao, and A. Khar (2000)
Carcinogenesis
21, 557-561
| Abstract »
| Full Text »
| PDF »
- Establishment of a radiation- and estrogen-induced breast cancer model.
- G. M. Calaf and T. K. Hei (2000)
Carcinogenesis
21, 769-776
| Abstract »
| Full Text »
| PDF »
- Communicating Genetic Risk: Pros, Cons, and Counsel.
- R. T. Penson, M. V. Seiden, K. M. Shannon, M. L. Lubratovich, M. Roche, B. A. Chabner, and T. J. Lynch Jr. (2000)
Oncologist
5, 152-161
| Abstract »
| Full Text »
- Age and sex based genetic locus heterogeneity in type 1 diabetes.
- A. D Paterson and A. Petronis (2000)
J. Med. Genet.
37, 186-191
| Abstract »
| Full Text »
- A model protocol evaluating the introduction of genetic assessment for women with a family history of breast cancer.
- J. Gray, K. Brain, P. Norman, C. Anglim, L. France, G. Barton, L. Branston, E. Parsons, A. Clarke, J. Sampson, et al. (2000)
J. Med. Genet.
37, 192-196
| Abstract »
| Full Text »
- Why do women attend familial breast cancer clinics?.
- K. Brain, J. Gray, P. Norman, E. Parsons, A. Clarke, C. Rogers, R. Mansel, and P. Harper (2000)
J. Med. Genet.
37, 197-202
| Abstract »
| Full Text »
- Cancer Risk Estimates for Family Members of a Population-based Family Registry for Breast and Ovarian Cancer.
- A. Ziogas, M. Gildea, P. Cohen, D. Bringman, T. H. Taylor, D. Seminara, D. Barker, G. Casey, R. Haile, S.-Y. Liao, et al. (2000)
Cancer Epidemiol. Biomarkers Prev.
9, 103-111
| Abstract »
| Full Text »
- Interactions of the Nijmegen Breakage Syndrome Protein with ATM and BRCA1.
- X. WU, G. RATHBUN, W.S. LANE, D.T. WEAVER, and D.M. LIVINGSTON (2000)
Cold Spring Harb Symp Quant Biol
65, 535-546
| Abstract »
| PDF »
- Chromosomal Instability and Cancer Predisposition: Insights from Studies on the Breast Cancer Susceptibility Gene, BRCA2.
- A.R. VENKITARAMAN (2000)
Cold Spring Harb Symp Quant Biol
65, 567-572
| Abstract »
| PDF »
- Genetic Polymorphisms and Risk of Breast Cancer.
- S. S. Coughlin and M. Piper (1999)
Cancer Epidemiol. Biomarkers Prev.
8, 1023-1032
| Full Text »
- Survival in Hereditary Breast Cancer Associated With Germline Mutations of BRCA2.
- L. C. Verhoog, C.T.M. Brekelmans, C. Seynaeve, G. Dahmen, A. N. van Geel, C.C.M. Bartels, M.M.A. Tilanus-Linthorst, A. Wagner, P. Devilee, D.J.J. Halley, et al. (1999)
J. Clin. Oncol.
17, 3396-3402
| Abstract »
| Full Text »
| PDF »
- BRCA1/BRCA2 Germline Mutations in Locally Recurrent Breast Cancer Patients After Lumpectomy and Radiation Therapy: Implications for Breast-Conserving Management in Patients With BRCA1/BRCA2 Mutations.
- B. C. Turner, E. Harrold, E. Matloff, T. Smith, A. A. Gumbs, M. Beinfield, B. Ward, M. Skolnick, P. M. Glazer, A. Thomas, et al. (1999)
J. Clin. Oncol.
17, 3017-3024
| Abstract »
| Full Text »
| PDF »
- Linkage analysis of 56 multiplex families excludes the Cowden disease gene PTEN as a major contributor to familial breast cancer.
- Y. Y. SHUGART, C. COUR, H. RENARD, G. LENOIR, D. GOLDGAR, D. TEARE, D. EASTON, N. RAHMAN, R. GUSTERTON, S. SEAL, et al. (1999)
J. Med. Genet.
36, 720-721
| Full Text »
- Association of BRCA1 with the hRad50-hMre11-p95 Complex and the DNA Damage Response.
- Q. Zhong, C. Chen, S. Li, Y. Chen, C. Wang, J. Xiao, P. Chen, Z. D. Sharp, and W. Lee (1999)
Science
285, 747-750
| Abstract »
| Full Text »
- Prevalence of BRCA1 and BRCA2 Gene Mutations in Patients With Early-Onset Breast Cancer.
- J. Peto, N. Collins, R. Barfoot, S. Seal, W. Warren, N. Rahman, D. F. Easton, C. Evans, J. Deacon, and M. R. Stratton (1999)
J Natl Cancer Inst
91, 943-949
| Abstract »
| Full Text »
| PDF »
- Positive Regulation of the BRCA1 Promoter.
- S. Thakur and C. M. Croce (1999)
J. Biol. Chem.
274, 8837-8843
| Abstract »
| Full Text »
| PDF »
- Hereditary Factors in Gynecologic Cancer.
- H. T. Lynch, M. J. Casey, T. G. Shaw, and J. F. Lynch (1998)
Oncologist
3, 319-338
| Abstract »
| Full Text »
|
|