X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (399) 399
female (351) 351
breast neoplasms - genetics (244) 244
oncology (233) 233
adult (224) 224
index medicus (222) 222
middle aged (213) 213
breast cancer (199) 199
brca1 (192) 192
ovarian neoplasms - genetics (182) 182
breast/ovarian cancer (177) 177
mutation (169) 169
ovarian cancer (159) 159
genetics & heredity (149) 149
genetic testing (146) 146
cancer (135) 135
genetic predisposition to disease (134) 134
genes, brca1 (132) 132
male (129) 129
genetic aspects (128) 128
women (127) 127
aged (125) 125
ovarian-cancer (125) 125
risk (123) 123
brca2 (114) 114
genes, brca2 (107) 107
risk factors (107) 107
genetic counseling (105) 105
breast-cancer (96) 96
hereditary breast (94) 94
susceptibility (88) 88
brca1 protein - genetics (82) 82
breast-ovarian cancer (78) 78
research (78) 78
families (76) 76
genetic screening (73) 73
genetics (73) 73
brca2 protein - genetics (70) 70
human genetics (62) 62
genes (61) 61
gene mutations (59) 59
pedigree (59) 59
surveys and questionnaires (58) 58
health aspects (56) 56
hereditary breast/ovarian cancer (54) 54
prevalence (54) 54
epidemiology (52) 52
genetic testing - psychology (52) 52
medicine & public health (52) 52
mutations (52) 52
risk assessment (50) 50
breast (49) 49
breast neoplasms - epidemiology (49) 49
population (49) 49
biomedicine (48) 48
aged, 80 and over (47) 47
breast neoplasms - psychology (47) 47
family (47) 47
decision-making (46) 46
diagnosis (46) 46
family-history (46) 46
germline mutations (46) 46
public, environmental & occupational health (46) 46
genetic research (43) 43
health knowledge, attitudes, practice (43) 43
article (41) 41
dna mutational analysis (41) 41
impact (41) 41
gene (39) 39
skin and connective tissue diseases (39) 39
oncology, experimental (38) 38
analysis (36) 36
ovarian neoplasms - psychology (36) 36
adolescent (35) 35
endocrine system diseases (35) 35
identification (35) 35
ovarian neoplasms - epidemiology (35) 35
attitudes (34) 34
carriers (34) 34
ethics (34) 34
breast neoplasms - diagnosis (33) 33
heterozygote (33) 33
neoplasms - genetics (33) 33
young adult (33) 33
breast-ovarian-cancer (31) 31
decision making (31) 31
germ-line mutation (31) 31
high-risk (31) 31
brca1 protein (30) 30
psychology (30) 30
cancer research (29) 29
founder effect (29) 29
nonpolyposis colorectal-cancer (29) 29
communication (28) 28
founder mutations (28) 28
genetic predisposition to disease - psychology (28) 28
medical genetics (28) 28
mutation - genetics (28) 28
psychological distress (28) 28
brca2 protein (27) 27
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (497) 497
Japanese (17) 17
Chinese (6) 6
German (4) 4
French (2) 2
Dutch (1) 1
Korean (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Current Breast Cancer Reports, ISSN 1943-4588, 9/2013, Volume 5, Issue 3, pp. 170 - 182
Journal Article
WESTERN JOURNAL OF NURSING RESEARCH, ISSN 0193-9459, 01/2015, Volume 37, Issue 1, pp. 66 - 84
Women with pathogenic BRCA genetic mutations face high risks for cancer development. Estimates vary among mutation carriers, with lifetime risks ranging from... 
MUTATION CARRIERS | NURSING | HEREDITARY BREAST | PREVENTION | ORAL-CONTRACEPTIVE USE | FAMILY-HISTORY | oncology | phenomenology | BRCA | SUPPORT | genetics | BREAST-OVARIAN CANCER | qualitative | genomics | PROPHYLACTIC OOPHORECTOMY | YOUNG-WOMEN
Journal Article
Journal Article
Qualitative Health Research, ISSN 1049-7323, 4/2011, Volume 21, Issue 4, pp. 502 - 519
Journal Article
Familial Cancer, ISSN 1389-9600, 7/2016, Volume 15, Issue 3, pp. 493 - 496
Cancer risk assessment, genetic counseling and genetic testing have experienced advances and changes over the past two decades due to improved technology,... 
Human Genetics | Cancer genetics | Biomedicine | Genetic counseling | Hereditary cancer | Cancer Research | Hereditary breast–ovarian cancer | Genetic testing | Epidemiology | Biomedicine general | Lynch syndrome | SURGERY | Hereditary breast-ovarian cancer | ONCOLOGY | COLORECTAL-CANCER | FAMILIES | GENETICS & HEREDITY | BLOCKADE | Risk Assessment - methods | Genetic Counseling - psychology | Genetic Counseling - legislation & jurisprudence | Hereditary Breast and Ovarian Cancer Syndrome - diagnosis | Insurance Coverage - trends | United States | Humans | Colorectal Neoplasms, Hereditary Nonpolyposis - psychology | DNA Repair Enzymes - genetics | DNA Mismatch Repair - genetics | Molecular Targeted Therapy | Risk Assessment - legislation & jurisprudence | Insurance Coverage - legislation & jurisprudence | Colorectal Neoplasms, Hereditary Nonpolyposis - diagnosis | Hereditary Breast and Ovarian Cancer Syndrome - psychology | Genetic Counseling - economics | Genetic Testing - trends | Insurance Coverage - economics | Hereditary Breast and Ovarian Cancer Syndrome - genetics | Genetic Predisposition to Disease | Colorectal Neoplasms, Hereditary Nonpolyposis - drug therapy | Insurance, Health - trends | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Genetic Testing - legislation & jurisprudence | Hereditary Breast and Ovarian Cancer Syndrome - drug therapy | Insurance, Health - legislation & jurisprudence | BRCA1 Protein - genetics | Genetic Counseling - trends | Genetic Testing - economics | Risk Assessment - trends | BRCA2 Protein - genetics | Insurance, Health - economics | Risk assessment | Medical genetics | Genetic research | Health aspects | Cancer | Ovarian cancer
Journal Article
HEALTH PSYCHOLOGY, ISSN 0278-6133, 11/2002, Volume 21, Issue 6, pp. 564 - 572
The Multidimensional Impact of Cancer Risk Assessment (MICRA) is a new tool to measure the specific impact of result disclosure after genetic testing. The... 
FAMILY HISTORY | DISTRESS | SUSCEPTIBILITY | cancer risk assessment | BRCA1 | PSYCHOLOGY, CLINICAL | BREAST-OVARIAN-CANCER | WOMEN | cancer genetics | FOLLOW-UP CARE | RECOMMENDATIONS | genetic testing | MUTATIONS | INHERITED PREDISPOSITION
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 05/2011, Volume 19, Issue 5, pp. 500 - 506
Journal Article