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Publications

Recent Publications

  1. Offit K, Kohut K, Clagett B, Wadsworth EA, Lafaro KJ, Cummings S, White M, Sagi M, Bernstein D, Davis JG.: Cancer genetic testing and assisted reproduction. Oct 10; 24(29): 4775-82. 2007.
  2. Carter EM, Davis JG, Raggio CL.: Advances in understanding etiology of achondroplasia and review of management. Current Opinion in Pediatrics. Feb; 19(1): 32-7. 2007.
  3. Sills ES, Burns MJ, Parker LD, Carroll LP, Kephart LL, Dyer CS, Papenhausen PR, Davis JG. Further phenotypic delineation of subtelomeric (terminal) 4q deletion with emphasis on intracranial and reproductive anatomy. Feb 12;2:9. 2007.
  4. Giampietro, P.F., Raggio, C., Davis, J.G.: Marfan Syndrome: orthopedic and genetic review. Current Opinion in Pediatrics 14(1): 35-41, 2002.
  5. Kauff, N.D., Scheuer, L., Robson, M.E., Glogowski, E., Kelly, B., Barakat, R., Heerdt, A., Borgen, P.I., Davis, J.G., Offit, K.: Insurance reimbursement for risk-reducing mastectomy and oophorectomy in women with BRCA1 or BRCA 2 mutations. Genetics in Medicine, 3(6):442-5, 2001.
  6. Wajnrajch, M.P., Gertner, J.M., Huma, Z., Popovic, J., Lin, K., Verlander, P.C., Batish, S.D., Giampietro, P.F., Davis, J.G., New, M.I., Auerbach, A.D.: Evaluation of growth and hormonal status in patients referred to the International Fanconi Anemia Registry. Pediatrics, 107(4): 744-54, 2001.
  7. Davis, J.G., Berkwitz, R., Stern, K.: Genetics for Primary Health Care Professionals. Text and Disc., Weill-Cornell Publication, 2000.
  8. Do, T., Giampietro, P.F., Burke, S.W., Davis, J.G., Raggio, C., Schneider, R., Boachie-Adjei, O., Brill, P.: The incidence of protrusio acetabuli in Marfan syndrome and its relationship to bone density. Journal of Pediatric Orthopedic, 20(6): 718-21, 2000.
  9. Davis, J.G.: ACMG's continuing medical education program: a new initiative. Genetics in Medicine, 1(4)127-9, 1999.
  10. Giampietro, P.F., Auerbach, A.D., Elias, E.R., Gutman, A., Zellers, N.F., and Davis, J.G.: A new recessive syndrome characterized by increased levels of chromosome breakage and several features which overlap with Fanconi Anemia. American Journal of Medical Genetics, 70: 70-75, 1998.
  11. Davis, J.G.: Population screening for hemochromatosis: The evolving role of genetic analysis. Annals of InternalMedicine, 129: 905, 1998.
  12. Davis, J.G.: Cancer and the Environment. Predictive Genetic Tests: Problems and Pitfalls. Ann. NY Acad. of Sciences,, 883: 42-46, 1997.
  13. Touchette, N., Holtzman, N.A., Davis, J.G., Feetharn, S.: Toward the 21st Century Incorporating Genetics in to Primary Health Care. Cold Spring Harbor Laboratory Press, 1997.
  14. Giampietro, P.F., Verlander, P.C., Davis, J.G., and Auerbach, A.D.: Diagnosis of Fanconi Anemia in patients without congenital malformations: an International Fanconi anemia registry study. Am. J. Med. Genet., 68:58-61, 1997.

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