Breast cancer genetics in African Americans
暂无分享,去创建一个
O. Olopade | M. Tainsky | J. Fackenthal | G. Dunston | F. Collins | C. Whitfield-Broome | Carolyn Whitfield-Broome
[1] O. Olopade,et al. Male breast cancer in Cowden syndrome patients with germlinePTEN mutations , 2001, Journal of medical genetics.
[2] J. Carpten,et al. Recruitment experience in the first phase of the African American Hereditary Prostate Cancer (AAHPC) study. , 2000, Annals of epidemiology.
[3] C. Adebamowo,et al. Protein truncating BRCA1 and BRCA2 mutations in African women with pre-menopausal breast cancer , 2000, Human Genetics.
[4] E. Gillanders,et al. Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[5] Olufunmilayo I. Olopade,et al. Prevalence of BRCA1 and BRCA2 mutations among clinic-based African American families with breast cancer , 2000, Human Genetics.
[6] C. Isaacs,et al. Spiritual faith and genetic testing decisions among high-risk breast cancer probands. , 2000, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[7] M. King,et al. Insights into the functions of BRCA1 and BRCA2. , 2000, Trends in genetics : TIG.
[8] A. Godwin,et al. Novel germline BRCA1 mutation (155del4) in an African American with early‐onset breast cancer , 1999, Human mutation.
[9] H. Mefford,et al. Evidence for a BRCA1 founder mutation in families of West African ancestry. , 1999, American journal of human genetics.
[10] R. Modali,et al. BRCA1 mutations in African Americans , 1999, Human Genetics.
[11] C. Adebamowo,et al. Case‐controlled study of the epidemiological risk factors for breast cancer in Nigeria , 1999, The British journal of surgery.
[12] I. Andrulis,et al. Frequency of p53 mutations in breast carcinomas from Ashkenazi Jewish carriers of BRCA1 mutations. , 1999, Journal of the National Cancer Institute.
[13] P. Underhill,et al. Global sequence diversity of BRCA2: analysis of 71 breast cancer families and 95 control individuals of worldwide populations. , 1999, Human molecular genetics.
[14] E. Smith,et al. Pattern of breast cancer among white-American, African-American, and nonimmigrant west-African women. , 1998, Journal of the National Medical Association.
[15] S. Cummings,et al. Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[16] M. King,et al. Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study. , 1998, American journal of human genetics.
[17] M. King,et al. Frequency of breast cancer attributable to BRCA1 in a population-based series of American women. , 1998, JAMA.
[18] J Chang-Claude,et al. Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium. , 1998, American journal of human genetics.
[19] J. Klijn,et al. Survival and tumour characteristics of breast-cancer patients with germline mutations of BRCA1 , 1998, The Lancet.
[20] W. Neufeld-Kaiser,et al. Predisposition genetic testing for late-onset disorders in adults. A position paper of the National Society of Genetic Counselors. , 1997, JAMA.
[21] C. Isaacs,et al. Ethnic differences in knowledge and attitudes about BRCA1 testing in women at increased risk. , 1997, Patient education and counseling.
[22] D. Page,et al. BRCA1 and BRCA2 hereditary breast carcinoma phenotypes , 1997 .
[23] P. Tonin,et al. Brca2 hereditary breast cancer pathophenotype , 1997, Breast Cancer Research and Treatment.
[24] M. Stratton. Pathology of familial breast cancer: differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases , 1997, The Lancet.
[25] F. Couch,et al. BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer. , 1997, The New England journal of medicine.
[26] H. Mefford,et al. BRCA2 in American families with four or more cases of breast or ovarian cancer: recurrent and novel mutations, variable expression, penetrance, and the possibility of families whose cancer is not attributable to BRCA1 or BRCA2. , 1997, American journal of human genetics.
[27] P. Laurent-Puig,et al. BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic. Institut Curie Breast Cancer Group. , 1997, American journal of human genetics.
[28] S. Cummings,et al. Recurrent germ-line BRCA1 mutations in extended African American families with early-onset breast cancer. , 1997, American journal of human genetics.
[29] H. Hanafusa,et al. Evidence for a transcriptional activation function of BRCA1 C-terminal region. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[30] M. Fiddler,et al. Practice-based competencies for accreditation of and training in graduate programs in genetic counseling , 1996, Journal of Genetic Counseling.
[31] J. Rommens,et al. The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds , 1996, Nature Genetics.
[32] G M Lenoir,et al. Hereditary breast cancer: Pathobiology, prognosis, and BRCA1 and BRCA2 gene linkage , 1996, Cancer.
[33] Robin L. Bennett,et al. Recommendations for standardized human pedigree nomenclature , 1995, Journal of Genetic Counseling.
[34] Francis S. Collins,et al. Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer , 1994, Nature Genetics.
[35] Steven E. Bayer,et al. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. , 1994, Science.
[36] M. Skolnick,et al. BRCA1 mutations in primary breast and ovarian carcinomas. , 1994, Science.
[37] G. Palos. Cultural heritage: cancer screening and early detection. , 1994, Seminars in oncology nursing.
[38] C. Varricchio,et al. Efforts to recruit the economically disadvantaged to national clinical trials. , 1994, Seminars in oncology nursing.
[39] T. Ades,et al. American Cancer Society urban demonstration projects: models for successful intervention. , 1994, Seminars in oncology nursing.
[40] C. Redmond,et al. Histological characteristics of breast carcinoma in blacks and whites. , 1994, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[41] J. Vadgama,et al. Mutation analysis of BRCA1 gene in African-American patients with breast cancer. , 2000, Journal of the National Medical Association.
[42] M. West,et al. Racial differences in breast carcinoma survival , 2000, Cancer.
[43] L. Strong,et al. TP53 mutation and haplotype analysis of two large African American families , 1999, Human mutation.
[44] M. Stratton,et al. The genetics of familial breast cancer and their practical implications. , 1994, European journal of cancer.
[45] D. Easton. The inherited component of cancer. , 1994, British medical bulletin.
[46] A. Lippman,et al. Prenatal Genetic Testing and Screening: Constructing Needs and Reinforcing Inequities , 2020, American Journal of Law & Medicine.
[47] S. Kessler. 2 – The Psychological Foundations of Genetic Counseling , 1979 .