scholarly article | Q13442814 |
P50 | author | Jeannette M Beasley | Q56948903 |
Polly A Newcomb | Q89454622 | ||
P2093 | author name string | Julie R Hunt | |
Rachel M Ceballos | |||
Allyson Templeton | |||
Scot Peterson | |||
P2860 | cites work | Hereditary nonpolyposis colorectal cancer family members' perceptions about the duty to inform and health professionals' role in disseminating genetic information | Q33555443 |
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Who should be sent for genetic testing in hereditary colorectal cancer syndromes? | Q36905417 | ||
Anticipating dissemination of cancer genomics in public health: a theoretical approach to psychosocial and behavioral challenges | Q37004702 | ||
Psychological opportunities and hazards in predictive genetic testing for cancer risk | Q38558424 | ||
Colorectal cancer survivors undergoing genetic testing for hereditary non-polyposis colorectal cancer: motivational factors and psychosocial functioning | Q40170903 | ||
Genetic testing for colon cancer among African-Americans in North Carolina | Q40371466 | ||
Should healthcare providers have a duty to warn family members of individuals with an HNPCC-causing mutation? A survey of patients from the Ontario Familial Colon Cancer Registry | Q42550928 | ||
Correlates of intentions to obtain genetic counseling and colorectal cancer gene testing among at-risk relatives from three ethnic groups. | Q45249001 | ||
Motivations and psychosocial impact of genetic testing for HNPCC. | Q48664154 | ||
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A social network analysis of communication about hereditary nonpolyposis colorectal cancer genetic testing and family functioning | Q52018395 | ||
Intention to learn results of genetic testing for hereditary colon cancer. | Q52177858 | ||
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Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer. | Q53226230 | ||
Medical privacy and the disclosure of personal medical information: the beliefs and experiences of those with genetic and other clinical conditions. | Q54856182 | ||
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Genetics as a tool to improve cancer outcomes: ethics and policy | Q57577428 | ||
Attitudes toward genetic testing for colon cancer risk | Q71776540 | ||
How families communicate about HNPCC genetic testing: Findings from a qualitative study | Q73293994 | ||
Knowledge, attitudes, and interest in breast-ovarian cancer gene testing: a survey of a large African-American kindred with a BRCA1 mutation | Q77208085 | ||
Colon cancer screening practices following genetic testing for hereditary nonpolyposis colon cancer (HNPCC) mutations | Q80794920 | ||
P433 | issue | 3 | |
P921 | main subject | colorectal cancer | Q188874 |
colorectal carcinoma | Q25493920 | ||
P304 | page(s) | 415-420 | |
P577 | publication date | 2008-09-01 | |
P1433 | published in | Genetic Testing and Molecular Biomarkers | Q15753742 |
P1476 | title | Colorectal cancer cases and relatives of cases indicate similar willingness to receive and disclose genetic information | |
P478 | volume | 12 |
Q30513982 | Genetics, genomics, and cancer risk assessment: State of the Art and Future Directions in the Era of Personalized Medicine |
Q37639436 | How do researchers manage genetic results in practice? The experience of the multinational Colon Cancer Family Registry |
Q37130341 | Impact of genetic risk assessment on nutrition-related lifestyle behaviours |
Q34515650 | Preferences regarding genetic research results: comparing veterans and nonveterans responses |
Q43406156 | Survey report of gamete donors' and recipients' preferences regarding disclosure of third party reproduction outcomes and genetic risk information |
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