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1. Full Text Familial Breast Cancer
by Lalloo, F and Evans, D G
Clinical Genetics, ISSN 0009-9163, 08/2012, Volume 82, Issue 2, pp. 105 - 114
Since the localization and discovery of the first high‐risk breast cancer (BC) genes in 1990, there has been a substantial progress in unravelling its familial... 
familial | breast cancer | BRCA1 | BRCA2 | TP53 | Breast cancer | Familial | BRCA2 MUTATION CARRIERS | SURGICAL ADJUVANT BREAST | OVARIAN-CANCER | ESTROGEN-RECEPTOR | GENETICS & HEREDITY | GERMLINE MUTATIONS | RISK-REDUCING SURGERY | SUSCEPTIBILITY GENE | CONFER SUSCEPTIBILITY | STAR P-2 TRIAL | GENOME-WIDE ASSOCIATION | Breast Neoplasms - therapy | Genes, p53 | Genetic Predisposition to Disease | Breast Neoplasms - genetics | Humans | Genes, BRCA2 | Family | Female | Penetrance | Breast Neoplasms - diagnosis | Genes, BRCA1 | Genetic aspects | Tumor proteins | Genes | Genomics | Risk factors | BRCA2 protein | BRCA1 protein | Risk groups | p53 protein
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2. Genetics and breast cancer
by Lynch, Henry T
ISBN 0442249195, xii, 253
Genetic counseling | Breast | Familial and genetic | Breast neoplasms | Genetic aspects | Cancer
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3. Full Text Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers
by Kuchenbaecker, Karoline B and Hopper, John L and Barnes, Daniel R and Phillips, Kelly-Anne and Mooij, Thea M and Roos-Blom, Marie-José and Jervis, Sarah and van Leeuwen, Flora E and Milne, Roger L and Andrieu, Nadine and Goldgar, David E and Terry, Mary Beth and Rookus, Matti A and Easton, Douglas F and Antoniou, Antonis C and McGuffog, Lesley and Evans, D. Gareth and Barrowdale, Daniel and Frost, Debra and Adlard, Julian and Ong, Kai-ren and Izatt, Louise and Tischkowitz, Marc and Eeles, Ros and Davidson, Rosemarie and Hodgson, Shirley and Ellis, Steve and Nogues, Catherine and Lasset, Christine and Stoppa-Lyonnet, Dominique and Fricker, Jean-Pierre and Faivre, Laurence and Berthet, Pascaline and Hooning, Maartje J and van der Kolk, Lizet E and Kets, Carolien M and Adank, Muriel A and John, Esther M and Chung, Wendy K and Andrulis, Irene L and Southey, Melissa and Daly, Mary B and Buys, Saundra S and Osorio, Ana and Engel, Christoph and Kast, Karin and Schmutzler, Rita K and Caldes, Trinidad and Jakubowska, Anna and Simard, Jacques and Friedlander, Michael L and McLachlan, Sue-Anne and Machackova, Eva and Foretova, Lenka and Tan, Yen Y and Singer, Christian F and Olah, Edith and Gerdes, Anne-Marie and Arver, Brita and Olsson, Håkan and BRCA1 BRCA2 Cohort Consortium and BRCA1 and BRCA2 Cohort Consortium and and the BRCA1 and BRCA2 Cohort Consortium and Lund University and Lunds Melanomstudiegrupp and EpiHealth: Epidemiology for Health and Lund Melanoma Study Group and BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation and Lunds universitet
JAMA, ISSN 0098-7484, 06/2017, Volume 317, Issue 23, pp. 2402 - 2416
IMPORTANCE: The clinical management of BRCA1 and BRCA2 mutation carriers requires accurate, prospective cancer risk estimates. OBJECTIVES: To estimate... 
PENETRANCE | POSITION | WOMEN | MEDICINE, GENERAL & INTERNAL | SERIES | FAMILIES | SUSCEPTIBILITY | MODEL | Age Distribution | Prospective Studies | Age Factors | Risk Assessment | Humans | Middle Aged | Incidence | Neoplasms, Second Primary - epidemiology | Ovarian Neoplasms - epidemiology | Ovarian Neoplasms - genetics | Breast Neoplasms - genetics | Time Factors | Aged, 80 and over | Genes, BRCA2 | Adult | Family | Female | Aged | Genes, BRCA1 | Mutation | Neoplasms, Second Primary - genetics | Breast Neoplasms - epidemiology | BRCA2 protein | Ovarian carcinoma | BRCA1 protein | Health risks | Oncology | Population studies | Breast cancer | Estimates | Ovarian cancer | Carriers | Consortia | Design modifications | Risk assessment | Data collection | Breast | Genetics | Diagnosis | Genetic testing | Position (location) | Age | Cancer | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Cancer and Oncology | Medicin och hälsovetenskap | Cancer och onkologi
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4. Full Text Genetic susceptibility to breast cancer
by Mavaddat, Nasim and Antoniou, Antonis C and Easton, Douglas F and Garcia-Closas, Montserrat
Molecular Oncology, ISSN 1574-7891, 2010, Volume 4, Issue 3, pp. 174 - 191
Genetic and lifestyle/environmental factors are implicated in the aetiology of breast cancer. This review summarizes the current state of knowledge on rare... 
Pathology | BRCA1/2 mutation carriers | Breast cancer | Aetiology of breast cancer | Genetic susceptibility | BRCA2 MUTATION CARRIERS | REDUCING SALPINGO-OOPHORECTOMY | DEL PROMOTER POLYMORPHISM | AFRICAN-AMERICAN WOMEN | ESTROGEN-RECEPTOR | PROGESTERONE-RECEPTOR STATUS | BILATERAL PROPHYLACTIC MASTECTOMY | KERATINOCYTE GROWTH-FACTOR | ONCOLOGY | FAMILIAL BREAST | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Genome-Wide Association Study | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Humans | Genes, BRCA2 | Female | Heterozygote | Penetrance | Genes, BRCA1 | Mutation | Polymorphism, Genetic | BRCA2 protein | Genetic variance | BRCA1 protein | Hormone replacement therapy | Genomes | Environmental factors | Health risk assessment | Ovarian cancer | Tumors | Reviews | Review | BRCA1 | 2 mutation carriers
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5. Familial breast cancer: Genetics and counseling
by Thakur, S and Phadke, S.R
Familial breast cancer: Genetics and counseling, 12/2005
Hereditary breast cancer (HBC) accounts for 5-10% of all breast cancer cases. A family history of breast cancer has long been ecognized as a significant risk... 
Familial breast cancer, BRCA1, BRCA2, genetic counseling
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6. Breast Cancer Screening and Diagnosis
by Bevers, TB and Anderson, BO and Bonaccio, E and Buys, S and Daly, MB and Dempsey, PJ and Farrar, WB and Fleming, I and Garber, JE and Harris, RE and Heerdt, AS and Helvie, M and Huff, JG and Khakpour, N and Khan, SA and Krontiras, H and Lyman, G and Rafferty, E and Shaw, S and Smith, ML and Tsangaris, TN and Williams, C and Yaneeklov, T
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, ISSN 1540-1405, 11/2009, Volume 7, Issue 10, pp. 1060 - 1096
carcinoma in situ | risk assessment | screening | ATYPICAL LOBULAR HYPERPLASIA | mammography | HIGH FAMILIAL RISK | diagnosis | FOLLOW-UP | RANDOMIZED-TRIAL | NCCN Clinical Practice Guidelines | CARCINOMA IN-SITU | HODGKINS-DISEASE | CORE-NEEDLE-BIOPSY | ONCOLOGY | breast carcinoma | FILM MAMMOGRAPHY | biopsy | SURGICAL EXCISION | hyperplasia | FIELD DIGITAL MAMMOGRAPHY
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7. Breast Cancer Screening
by Euhus, David and Di Carlo, Philip A and Khouri, Nagi F
Surgical Clinics of North America, ISSN 0039-6109, 10/2015, Volume 95, Issue 5, pp. 991 - 1011
Breast cancer screening has become a controversial topic. Understanding the points of contention requires an appreciation of the conceptual framework... 
Screening | Mammographic density | Breast cancer | Breast MRI | Mammography | SURGERY | COST-EFFECTIVENESS | SOCIETY GUIDELINES | HIGH FAMILIAL RISK | DIGITAL MAMMOGRAPHY | BACKGROUND PARENCHYMAL ENHANCEMENT | POSITRON EMISSION MAMMOGRAPHY | REPLACEMENT THERAPY | DENSE BREASTS | SELF-EXAMINATION | COMPUTER-AIDED DETECTION | Gynecological Examination | Magnetic Resonance Imaging | Early Detection of Cancer - methods | Humans | Sensitivity and Specificity | Female | Breast Neoplasms - diagnosis
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8. Full Text Breast Cancer 1 MRI for breast cancer screening, diagnosis, and treatment
by Morrow, M and Waters, J and Morris, E
LANCET, ISSN 0140-6736, 11/2011, Volume 378, Issue 9805, pp. 1804 - 1811
MRI is used widely both for screening women who are at increased risk of breast cancer and for treatment selection. Prospective studies confirm that MRI... 
PREOPERATIVE MRI | WOMEN | MEDICINE, GENERAL & INTERNAL | SURGICAL ADJUVANT BREAST | CONTRALATERAL BREAST | NEOADJUVANT CHEMOTHERAPY | CONSERVING SURGERY | MUTATION CARRIERS | HIGH FAMILIAL RISK | TUMOR RESPONSE | ESTROGEN-RECEPTOR | Breast cancer | Mammography | Family medical history | Mutation | Womens health
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9. Full Text ATM and breast cancer susceptibility
by Ahmed, M and Rahman, N
Oncogene, ISSN 0950-9232, 09/2006, Volume 25, Issue 43, pp. 5906 - 5911
ATM was originally identified by positional cloning as the gene that underlies the autosomal recessive condition ataxia-telangiectasia. The encoded protein... 
Breast cancer genes | ATM | Ataxiatelangiectasia | Breast cancer susceptibility | VARIANTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | DNA-DAMAGE | HETEROZYGOTES | ATAXIA-TELANGIECTASIA GENE | RISK | breast cancer susceptibility | MISSENSE MUTATIONS | breast cancer genes | FUNCTIONAL CONSEQUENCES | CELL BIOLOGY | ataxia-telangiectasia | ONCOLOGY | FAMILIAL BREAST | FREQUENCY | GENETICS & HEREDITY | EARLY-ONSET | Genetic Predisposition to Disease | Humans | Protein-Serine-Threonine Kinases - genetics | Ataxia Telangiectasia Mutated Proteins | DNA-Binding Proteins - genetics | Breast Neoplasms - genetics | DNA Repair | Tumor Suppressor Proteins - genetics | Cell Cycle Proteins - genetics | Female | DNA Damage | Mutation | Genetic Carrier Screening | Breast Neoplasms - epidemiology | Proteins | Breast cancer | Epidemiology | Genes | DNA damage
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10. Full Text Detection of Breast Cancer With Addition of Annual Screening Ultrasound or a Single Screening MRI to Mammography in Women With Elevated Breast Cancer Risk
by Berg, Wendie A and Zhang, Zheng and Lehrer, Daniel and Jong, Roberta A and Pisano, Etta D and Barr, Richard G and Böhm-Vélez, Marcela and Mahoney, Mary C and Evans, W. Phil and Larsen, Linda H and Morton, Marilyn J and Mendelson, Ellen B and Farria, Dione M and Cormack, Jean B and Marques, Helga S and Adams, Amanda and Yeh, Nolin M and Gabrielli, Glenna and ACRIN 6666 Investigators, for the and ACRIN 6666 Investigators
JAMA, ISSN 0098-7484, 04/2012, Volume 307, Issue 13, pp. 1394 - 1404
CONTEXT Annual ultrasound screening may detect small, node-negative breast cancers that are not seen on mammography. Magnetic resonance imaging (MRI) may... 
TRIAL | MEDICINE, GENERAL & INTERNAL | HIGH FAMILIAL RISK | SURVEILLANCE | SONOGRAPHY | ULTRASONOGRAPHY | DENSE BREASTS | PROSPECTIVE MULTICENTER COHORT | Predictive Value of Tests | Humans | Middle Aged | Risk Factors | Mammography | False Positive Reactions | Young Adult | Magnetic Resonance Imaging | Biopsy | Breast Neoplasms - pathology | Sensitivity and Specificity | Ultrasonography | Aged, 80 and over | Adult | Female | Aged | Breast Neoplasms - diagnostic imaging | Cancer patients | Usage | Medical examination | Magnetic resonance imaging | Breast cancer | Diagnosis | Methods | Cancer | Ultrasonic imaging | Nuclear magnetic resonance--NMR | Medical diagnosis | Womens health
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