A blueprint for maternal and child health primary care physician education in medical genetics and genomic medicine: Recommendations of the united states secretary for health and human services advisory committee on heritable disorders in newborns and children

Genetics in Medicine

Volumn 12, Issue 2, 2010, Pages 77-80

  Kemper, Alex R ^a   Trotter, Tracy L ^b   Lloyd Puryear, Michele A ^c   Kyler, Penny ^c   Feero, W Gregory ^d   Howell, R Rodney ^e  

^a DUKE CLINICAL RESEARCH INSTITUTE   (United States)

^b San Ramon Valley Primary Care   (United States)

^c U S DEPARTMENT OF HEALTH AND HUMAN SERVICES   (United States)

^d NATIONAL INSTITUTES OF HEALTH   (United States)

^e UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

Author keywords

Child health services; Education; Genetics; Maternal health services; Medical; Primary health care

Indexed keywords

CHILD HEALTH; CHILD HEALTH CARE; CONTINUING EDUCATION; CONTINUING EDUCATION PROVIDER; DISEASE CONTROL; GENETIC DISORDER; GENETIC SERVICE; HEALTH CARE DELIVERY; HEALTH CARE PERSONNEL; HEALTH CARE PLANNING; HEALTH SERVICE; HUMAN; INTERNET; MATERNAL WELFARE; MEDICAL EDUCATION; MEDICAL GENETICS; NOTE; PRIMARY HEALTH CARE; RESIDENCY EDUCATION;

ADVISORY COMMITTEES; CENTERS FOR DISEASE CONTROL AND PREVENTION (U.S.); CHILD WELFARE; CHILD, PRESCHOOL; EDUCATION, MEDICAL, CONTINUING; FEMALE; GENETIC DISEASES, INBORN; GENETICS, MEDICAL; GENOMICS; GUIDELINES AS TOPIC; HUMANS; INFANT, NEWBORN; MATERNAL WELFARE; NATIONAL INSTITUTES OF HEALTH (U.S.); PHYSICIANS, FAMILY; UNITED STATES;

EID: 77149154993     PISSN: 10983600     EISSN: None     Source Type: Journal    
DOI: 10.1097/GIM.0b013e3181cb78fa     Document Type: Note

References (17)

1. Dolan SM, Moore C. Linking family history in obstetric and pediatric care: assessing risk for genetic disease and birth defects. Pediatrics 2007;120: S66-S70.
2. Guttmacher AE, Collins FS, Carmona RH. The family history-more important than ever. N Engl J Med 2004;351:2333-2336.
3. Committee on Genetics, American College of Obstetricians and Gynecologists. ACOG Committee Opinion. Number 325, December 2005. Update on carrier screening for cystic fibrosis. Obstet Gynecol 2005, 106. 1465-1468.
4. ACOG Committee on Practice Bulletins. ACOG Practice Bulletin No. 77: screening for fetal chromosomal abnormalities. Obstet Gynecol 2007;77: 217-228.
5. Watson MS, Mann MY, Lloyd-Puryear MA, Rinaldo P, Howell RR. Newborn screening: toward a uniform screening panel and system-executive summary. Genet Med 2006;8:1S-11S.
6. Morgan MA, Driscoll DA, Mennuti MT, Schulkin J. Practice patterns of obstetrician-gynecologists regarding preconception and prenatal screening for cystic fibrosis. Genet Med 2004;6:450-455.
7. Ginsburg GS, McCarthy JJ. Personalized medicine: revolutionizing drug discovery and patient care. Trends Biotechnol 2001;19:491-496.
8. Bailey DB, Armstrong D, Kemper AR, Skinner D, Warren SF. Supporting family adaption to presymptomatic and "untreatable" conditions in an era of expanded newborn screening. J Pediatr Psychol 2009;34:648-661.
9. Kupila A, Keskinen P, Simell T, et al. Genetic risk determines the emergence of diabetes-associated autoantibodies in young children. Diabetes 2002;51:646-651. (Pubitemid 34760171)
10. Koster ES, Raaijmakers JA, Koppelman GH, et al. Pharmacogenetics of anti-inflammatory treatment in children with asthma: rationale and design of the PACMAN cohort. Pharmacogenomics 2009;10:1351-1361.
11. Cooksey JA, Forte G, Flanagan PA, Benkendorf J, Blitzer MG. The medical genetics workforce: an analysis of clinical geneticist subgroups. Genet Med 2006;8:603-614.
12. Khoury MJ, Gwinn M, Yoon PW, Dowling N, Moore CA, Bradley L. The continuum of translation research in genomic medicine: how can we accelerate the appropriate integration of human genome discoveries into health care and disease prevention? Genet Med 2007;9:655-674.
13. Zerhouni EA. Translational research: moving discovery to practice. Clin Pharmacol Ther 2007;81:126-128.
14. Yarnall KSH, Pollak KI, Ostbye T, Krause KM, Michener JL. Primary care: is there enough time for prevention? Am J Public Health 2003;93:635-641.
15. Suther S, Goodson P. Barriers to the provision of genetic services by primary care physicians: a systematic review of the literature. Genet Med 2003;5: 70-76.
16. National Coalition for Health Professional Education in Genetics. Core Competencies in genetics for health professionals. Available at: http:// www.nchpeg.org/core/Core-Comps-English-2007.pdf. Accessed October 14, 2009.
17. Young PC, Glade GB, Stoddard GJ, Norlin C. Evaluation of a learning collaborative to improve the delivery of preventive services by pediatric practices. Pediatrics 2006;117:1469-1476.