The Prospect of Genome-guided Preventive Medicine: A Need and Opportunity for Genetic Counselors
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[1] D. Lobach,et al. Factors Influencing Uptake of Pharmacogenetic Testing in a Diverse Patient Population , 2009, Public Health Genomics.
[2] Muin J Khoury,et al. Health care provider and consumer awareness, perceptions, and use of direct-to-consumer personal genomic tests, United States, 2008 , 2009, Genetics in Medicine.
[3] L. Acheson,et al. Reconsidering the family history in primary care , 2004, Journal of General Internal Medicine.
[4] Chris M. R. Smerecnik,et al. Educating the general public about multifactorial genetic disease: applying a theory-based framework to understand current public knowledge , 2008, Genetics in Medicine.
[5] Lawrence H. Kushi,et al. Erratum: American Cancer Society guidelines on nutrition and physical activity for cancer prevention: Reducing the risk of cancer with healthy food choices and physical activity (CA - A Cancer Journal for Clinicians (2006) 56, (254-281)) , 2007 .
[6] J. Kai,et al. Informing patients of familial diabetes mellitus risk: How do they respond? A cross-sectional survey , 2008, BMC health services research.
[7] Dianne Davis,et al. Association of Numeracy and Diabetes Control , 2008, Annals of Internal Medicine.
[8] Judy H. Cho,et al. Finding the missing heritability of complex diseases , 2009, Nature.
[9] L. Adès,et al. Guidelines for the diagnosis and management of Marfan syndrome. , 2007, Heart, lung & circulation.
[10] W. Burke,et al. Pharmacogenetic testing: not as simple as it seems , 2008, Genetics in Medicine.
[11] T. Marteau,et al. Genetic risk and behavioural change , 2001, BMJ : British Medical Journal.
[12] L. Wilkins-Haug,et al. Gynecologists' Training, Knowledge, and Experiences in Genetics: A Survey , 2000, Obstetrics and gynecology.
[13] Sue-Jane Wang,et al. Family history: a comprehensive genetic risk assessment method for the chronic conditions of adulthood. , 1997, American journal of medical genetics.
[14] Kurt C Stange,et al. A sense of priorities for the healthcare commons. , 2006, American journal of preventive medicine.
[15] S. Michie,et al. Psychological and Behavioral Responses to Genetic Test Results Indicating Increased Risk of Obesity: Does the Causal Pathway from Gene to Obesity Matter? , 2009, Public Health Genomics.
[16] S. Ellard,et al. Patients' understanding of genetic susceptibility testing in mainstream medicine: qualitative study on thrombophilia , 2007, BMC Health Services Research.
[17] Identifying future models for delivering genetic services: a nominal group study in primary care , 2005, BMC family practice.
[18] M. Zwahlen,et al. Swiss primary care physicians' knowledge, attitudes and perception towards genetic testing for hereditary breast cancer , 2004, Familial Cancer.
[19] G. Petersen,et al. The use and interpretation of commercial APC gene testing for familial adenomatous polyposis. , 1997, The New England journal of medicine.
[20] M. Scheuner. Genetic evaluation for coronary artery disease , 2003, Genetics in Medicine.
[21] P. Goodson,et al. Texas physicians' perceptions of genomic medicine as an innovation , 2004, Clinical genetics.
[22] R. Pagon. Genetic testing for disease susceptibilities: consequences for genetic counseling. , 2002, Trends in molecular medicine.
[23] M. Khoury,et al. Public awareness and use of direct-to-consumer genetic tests: results from 3 state population-based surveys, 2006. , 2009, American journal of public health.
[24] Brenda Wilson,et al. A systematic review of perceived risks, psychological and behavioral impacts of genetic testing , 2008, Genetics in Medicine.
[25] Rowena J Dolor,et al. Evidence-based guidelines for cardiovascular disease prevention in women: 2007 update. , 2007, Journal of the American College of Cardiology.
[26] M. Davidson. Primary care for children and adolescents with Down syndrome. , 2008, Pediatric clinics of North America.
[27] M. Khoury,et al. Personal utility and genomic information: Look before you leap , 2009, Genetics in Medicine.
[28] Paul G Shekelle,et al. Delivery of genomic medicine for common chronic adult diseases: a systematic review. , 2008, JAMA.
[29] L. Acheson. Fostering applications of genetics in primary care: what will it take? , 2003 .
[30] M. Young,et al. A Qualitative Study of Health Professionals' Views Regarding Provision of Information About Health-Protective Behaviors During Genetic Consultation for Breast Cancer , 2006, Journal of Genetic Counseling.
[31] Raluca Mihaescu,et al. Evaluation of risk prediction updates from commercial genome-wide scans , 2009, Genetics in Medicine.
[32] Muin J. Khoury,et al. Letting the genome out of the bottle--will we get our wish? , 2008, The New England journal of medicine.
[33] M. Aitken,et al. A model for the development of genetics education programs for health professionals , 2007, Genetics in Medicine.
[34] C. Isaacs,et al. Utilization of breast cancer screening in a clinically based sample of women after BRCA1/2 testing. , 2002, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[35] E. Hoffman,et al. Nondisease genetic testing: reporting of muscle SNPs shows effects on self-concept and health orientation scales , 2005, European Journal of Human Genetics.
[36] C. Apovian,et al. Nutrition Recommendations and Interventions for Diabetes–2006 , 2006, Diabetes Care.
[37] A. Stockdale,et al. Interviews with primary care physicians regarding taking and interpreting the cancer family history. , 2008, Family practice.
[38] Peter Kraft,et al. Beyond odds ratios — communicating disease risk based on genetic profiles , 2009, Nature Reviews Genetics.
[39] G. Bonsel,et al. Genetic knowledge and counselling skills of Dutch cardiologists: sufficient for the genomics era? , 2003, European heart journal.
[40] Jon Emery,et al. Guidelines for preventive activities in general practice. , 2001, Australian family physician.
[41] Bruce S. Ling,et al. Family history and colorectal cancer screening: a survey of physician knowledge and practice patterns , 2002, American Journal of Gastroenterology.
[42] M. Hopkins,et al. The current clinical practice of pharmacogenetic testing in Europe: TPMT and HER2 as case studies , 2006, The Pharmacogenomics Journal.
[43] N. Qureshi,et al. Genetics Support to Primary Care Practitioners—A Demonstration Project , 2007, Journal of Genetic Counseling.
[44] K. Frazer,et al. Human genetic variation and its contribution to complex traits , 2009, Nature Reviews Genetics.
[45] M. Gantley,et al. Tensions between policy makers and general practitioners in implementing new genetics: grounded theory interview study , 1999, BMJ.
[46] A. Folsom,et al. Accuracy of proband reported family history: The NHLBI Family Heart Study (FHS) , 1999, Genetic epidemiology.
[47] Christine L. Moskalik,et al. Development and Evaluation of a Genetics Literacy Assessment Instrument for Undergraduates , 2008, Genetics.
[48] D. Goldstein. Common genetic variation and human traits. , 2009, The New England journal of medicine.
[49] Julie O. Culver,et al. Genetic Cancer Risk Assessment and Counseling: Recommendations of the National Society of Genetic Counselors , 2004, Journal of Genetic Counseling.
[50] K. Silvey,et al. Outcomes of genetics services: Creating an inclusive definition and outcomes menu for public health and clinical genetics services , 2009, American journal of medical genetics. Part C, Seminars in medical genetics.
[51] L. Leviton,et al. Knowledge, Attitudes, and Behaviors of Alabama's Primary Care Physicians Regarding Cancer Genetics , 2000, Academic medicine : journal of the Association of American Medical Colleges.
[52] N. Qureshi,et al. The Impact of Genetic Outreach Education and Support to Primary Care on Practitioner’s Confidence and Competence in Dealing with Familial Cancers , 2008, Public Health Genomics.
[53] Penny Kyler,et al. Educational Needs in Genetic Medicine: Primary Care Perspectives , 2008, Public Health Genomics.
[54] R. Wootton,et al. Telemedicine and clinical genetics: Establishing a successful service , 2001, Journal of telemedicine and telecare.
[55] Robert Cook-Deegan,et al. Disclosure of APOE genotype for risk of Alzheimer's disease. , 2009, The New England journal of medicine.
[56] Nina Ditsch,et al. Hereditary breast and ovarian cancer: new genes, new treatments, new concepts. , 2011, Deutsches Arzteblatt international.
[57] D. Seibert,et al. Twenty questions in genetic medicine—an assessment of World Wide Web databases for genetics information at the point of care , 2008, Genetics in Medicine.
[58] Argyrios Ziogas,et al. Validation of family history data in cancer family registries. , 2003, American journal of preventive medicine.
[59] Pamela W Duncan,et al. Sex Differences in Stroke Recovery , 2005, Preventing chronic disease.
[60] S. Metcalfe,et al. Needs assessment study of genetics education for general practitioners in Australia , 2002, Genetics in Medicine.
[61] J. Beaumont,et al. Familial risk for common diseases in primary care: the Family Healthware Impact Trial. , 2009, American journal of preventive medicine.
[62] L. Acheson. Fostering applications of genetics in primary care: What will it take? , 2003, Genetics in Medicine.
[63] Muin J. Khoury,et al. Developing Family Healthware, a Family History Screening Tool to Prevent Common Chronic Diseases , 2008, Preventing chronic disease.
[64] HER2 status in breast cancer--an example of pharmacogenetic testing. , 2007, Journal of the Royal Society of Medicine.
[65] S. Teutsch,et al. Recommendations from the EGAPP Working Group: can tumor gene expression profiling improve outcomes in patients with breast cancer? , 2009, Genetics in Medicine.
[66] S. Nanri,et al. Reliability of family history of lifestyle‐related diseases on questionnaire , 2009, Pediatrics international : official journal of the Japan Pediatric Society.
[67] R. Zori,et al. Telegenetic medicine: improved access to services in an underserved area , 2006, Journal of telemedicine and telecare.
[68] M. Greene,et al. Hereditary breast/ovarian and colorectal cancer genetics knowledge in a national sample of US physicians , 2005, Journal of Medical Genetics.
[69] J. Mackay,et al. An assessment of the efficacy of cancer genetic counselling using real-time videoconferencing technology (telemedicine) compared to face-to-face consultations. , 2005, European journal of cancer.
[70] R. Bennett,et al. A New Definition of Genetic Counseling: National Society of Genetic Counselors’ Task Force Report , 2006, Journal of Genetic Counseling.
[71] Brian H Shirts,et al. Changing interpretations, stable genes: responsibilities of patients, professionals, and policy makers in the clinical interpretation of complex genetic information , 2008, Genetics in Medicine.
[72] Patricia Goodson,et al. Barriers to the provision of genetic services by primary care physicians: A systematic review of the literature , 2003, Genetics in Medicine.
[73] Constance K Haan,et al. Evidence-Based Guidelines for Cardiovascular Disease Prevention in Women , 2004, Arteriosclerosis, thrombosis, and vascular biology.
[74] M. McCarthy,et al. Genome-wide association studies for complex traits: consensus, uncertainty and challenges , 2008, Nature Reviews Genetics.
[75] M. P. Eiff,et al. Will the learners be learned? , 2002, Genetics in Medicine.
[76] W. GREGORY FEERO,et al. Position Paper: New Standards and Enhanced Utility for Family Health History Information in the Electronic Health Record: An Update from the American Health Information Community's Family Health History Multi-Stakeholder Workgroup , 2008, J. Am. Medical Informatics Assoc..
[77] J. Tobin,et al. Attitudes about Genetics in Underserved, Culturally Diverse Populations , 2005, Public Health Genomics.
[78] S. Paik,et al. Prediction of adjuvant chemotherapy benefit in endocrine responsive, early breast cancer using multigene assays. , 2009, Breast.
[79] B. Psaty,et al. Personalized medicine in the era of genomics. , 2007, JAMA.
[80] S. Kardia,et al. Exploring the Public Understanding of Basic Genetic Concepts , 2004, Journal of Genetic Counseling.
[81] S. Kalishman,et al. Revitalizing problem based learning: student and tutor attitudes towards a structured tutorial , 2007, Medical teacher.
[82] B. Biesecker,et al. Process studies in genetic counseling: peering into the black box. , 2001, American journal of medical genetics.
[83] W. Meschino,et al. Interactive Genetic Counseling Role-Play: A Novel Educational Strategy for Family Physicians , 2008, Journal of Genetic Counseling.
[84] B. Maher. Personal genomes: The case of the missing heritability , 2008, Nature.
[85] Farzad Mostashari,et al. Health care as if health mattered. , 2008, JAMA.
[86] Awareness of family health history as a risk factor for disease--United States, 2004. , 2004, MMWR. Morbidity and mortality weekly report.
[87] A. Guttmacher,et al. Science & society: Educating health-care professionals about genetics and genomics , 2007, Nature Reviews Genetics.
[88] R. Pickering,et al. Feasibility and acceptability of providing nurse counsellor genetics clinics in primary care. , 2006, Journal of advanced nursing.
[89] D. L. Doyle,et al. Billing for Medical Genetics and Genetic Counseling Services: A National Survey , 2010, Journal of Genetic Counseling.
[90] Stephen B. Thomas,et al. The Use of Family Health Histories to Address Health Disparities in an African American Community , 2007, Health promotion practice.
[91] S. Hodgson,et al. Nurse-led cancer genetics clinics in primary and secondary care in varied ethnic population areas: interaction with primary care to improve ascertainment of individuals from ethnic minorities , 2007, Familial Cancer.
[92] M. Thun,et al. American Cancer Society Guidelines on Nutrition and Physical Activity for Cancer Prevention: Reducing the Risk of Cancer With Healthy Food Choices and Physical Activity , 2002, CA: a cancer journal for clinicians.
[93] T. Trotter,et al. Family History in Pediatric Primary Care , 2007, Pediatrics.
[94] Julie O. Culver,et al. Results of a randomized study of telephone versus in-person breast cancer risk counseling. , 2006, Patient education and counseling.
[95] K. Hemminki,et al. Familial risks for cancer as the basis for evidence-based clinical referral and counseling. , 2008, The oncologist.
[96] J. Kai,et al. Genomic medicine for underserved minority populations in family medicine. , 2005, American family physician.
[97] M. McCarthy,et al. Variation in TCF7L2 Influences Therapeutic Response to Sulfonylureas , 2007, Diabetes.
[98] R. Green,et al. A New Scale Measuring Psychologic Impact of Genetic Susceptibility Testing for Alzheimer Disease , 2009, Alzheimer disease and associated disorders.
[99] Judith Wylie-Rosett,et al. Nutrition Recommendations and Interventions for Diabetes , 2008, Diabetes Care.
[100] B. Husaini,et al. HEDIS Prevention Performance Indicators, Prevention Quality Assessment and Healthy People 2010 , 2005, Journal of health care for the poor and underserved.
[101] M. Khoury,et al. Expanding the definition of a positive family history for early-onset coronary heart disease , 2006, Genetics in Medicine.
[102] J. Florez,et al. The clinical application of genetic testing in type 2 diabetes: a patient and physician survey , 2009, Diabetologia.
[103] J. Mouchawar,et al. Colorado family physicians' knowledge of hereditary breast cancer and related practice. , 2009, Journal of cancer education : the official journal of the American Association for Cancer Education.
[104] R. Hinton,et al. The family history: reemergence of an established tool. , 2008, Critical care nursing clinics of North America.
[105] J. Higgins,et al. The impact of a genetics education program on physicians’ knowledge and genetic counseling referral patterns , 2007, Medical teacher.
[106] 'Over-the-counter' genetic testing: what does it really mean for primary care? , 2009, The British journal of general practice : the journal of the Royal College of General Practitioners.
[107] A. Caspi,et al. Predictive value of family history on severity of illness: the case for depression, anxiety, alcohol dependence, and drug dependence. , 2009, Archives of general psychiatry.
[108] D. Wattendorf,et al. Family history: the three-generation pedigree. , 2005, American family physician.
[109] N. Dawson,et al. Reporting BRCA test results to primary care physicians , 2001, Genetics in Medicine.
[110] A. Guttmacher,et al. Genomic medicine: who will practice it? A call to open arms. , 2001, American journal of medical genetics.
[111] J. Austoker,et al. Education improves general practitioner (GP) management of familial breast/ovarian cancer: findings from a cluster randomised controlled trial , 2002, Journal of medical genetics.
[112] P. Kaplan,et al. Gaucher disease type 1: revised recommendations on evaluations and monitoring for adult patients. , 2004, Seminars in hematology.
[113] J. Witte,et al. The Scientific Foundation for Personal Genomics: Recommendations from a National Institutes of Health–Centers for Disease Control and Prevention Multidisciplinary Workshop , 2009, Genetics in Medicine.
[114] G. Guyatt,et al. How to use an article about genetic association: C: What are the results and will they help me in caring for my patients? , 2009, JAMA.
[115] J. Ioannidis. Personalized Genetic Prediction: Too Limited, Too Expensive, or Too Soon? , 2009, Annals of Internal Medicine.
[116] Joseph Biederman,et al. Attention-Deficit/Hyperactivity Disorder: A Selective Overview , 2005, Biological Psychiatry.
[117] M. Khoury,et al. Family history of type 2 diabetes: A population-based screening tool for prevention? , 2006, Genetics in Medicine.
[118] R. Green,et al. Health Behavior Changes After Genetic Risk Assessment for Alzheimer Disease: The REVEAL Study , 2008, Alzheimer disease and associated disorders.
[119] Judith Wylie-Rosett,et al. Diet and Lifestyle Recommendations Revision 2006: A Scientific Statement From the American Heart Association Nutrition Committee , 2006, Circulation.
[120] T. Manolio,et al. How to Interpret a Genome-wide Association Study Topic Collections , 2022 .
[121] P. Basch. Quality of health care delivered to adults in the United States. , 2003, New England Journal of Medicine.
[122] Kurt C Stange,et al. Family history-taking in community family practice: Implications for genetic screening , 2000, Genetics in Medicine.
[123] Gynecologists. ACOG Practice Bulletin No. 103: Hereditary breast and ovarian cancer syndrome. , 2009, Obstetrics and gynecology.
[124] M. Khoury,et al. Family history and prevalence of diabetes in the US population: 6-year results from the National Health and Nutrition Examination Survey (NHANES, 1999 2004). , 2007, Diabetes.
[125] S. Langlois,et al. Assessment of the Effectiveness of Genetic Counseling by Telephone Compared to a Clinic Visit , 2003, Journal of Genetic Counseling.
[126] F. Hu,et al. TCF7L2, dietary carbohydrate, and risk of type 2 diabetes in US women. , 2009, The American journal of clinical nutrition.
[127] G. Bepler,et al. Responses to Online GSTM1 Genetic Test Results among Smokers Related to Patients with Lung Cancer: A Pilot Study , 2009, Cancer Epidemiology Biomarkers & Prevention.
[128] G. Montgomery,et al. A Model of Disease-Specific Worry in Heritable Disease: The Influence of Family History, Perceived Risk and Worry About Other Illnesses , 2006, Journal of Behavioral Medicine.