Jessica G. Davis, M.D.

Medical Genetics


Recent Publications

  1. Minkis K, Aksentijevich I, Goldbach-Mansky R, Magro C, Scott R, Davis JG, Sardana N, Herzog R. Interleukin 1 Receptor Antagonist Deficiency Presenting as Infantile Pustulosis Mimicking Infantile Pustular Psoriasis. Arch Dermatol. 2012
    Mar 19. [Epub ahead of print] PubMed PMID: 22431714.
  2. Carter EM, Montuori L, Davis JG, Raggio CL. The Kathryn O. and Alan C. Greenberg Center for Skeletal Dysplasias: an interdisciplinary approach. HSS J. 2008 Sep;4(2):112-6. Epub 2008 May 28. PubMed PMID: 18815853; PubMed Central PMCID: PMC2553170.
  3. Chervenak FA, McCullough LB, Sharma G, Davis J, Gross S. Enhancing patient autonomy with risk assessment and invasive diagnosis: an ethical solution to a clinical challenge. Am J Obstet Gynecol. 2008 Jul;199(1):19.e1-4. Epub 2008 Mar 20. Review. PubMed PMID: 18355783.
  4. Manzini MC, Gleason D, Chang BS, Hill RS, Barry BJ, Partlow JN, Poduri A, Currier S, Galvin-Parton P, Shapiro LR, Schmidt K, Davis JG, Basel-Vanagaite L Seidahmed MZ, Salih MA, Dobyns WB, Walsh CA. Ethnically diverse causes of Walker-Warburg syndrome (WWS): FCMD mutations are a more commn cause of WWS outside of the Middle East. Hum Mutat. 2008 Nov;29(11):E231-41. PubMed PMID: 18752264; PubMed Central PMCID: PMC2577713.
  5. 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.
  6. 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.
  7. 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.
  8. Giampietro, P.F., Raggio, C., Davis, J.G.: Marfan Syndrome: orthopedic and genetic review. Current Opinion in Pediatrics 14(1): 35-41, 2002.
  9. 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.
  10. 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.
  11. Davis, J.G., Berkwitz, R., Stern, K.: Genetics for Primary Health Care Professionals. Text and Disc., Weill-Cornell Publication, 2000.
  12. 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.
  13. Davis, J.G.: ACMG's continuing medical education program: a new initiative. Genetics in Medicine, 1(4)127-9, 1999.
  14. 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.
  15. Davis, J.G.: Population screening for hemochromatosis: The evolving role of genetic analysis. Annals of InternalMedicine, 129: 905, 1998.
  16. Davis, J.G.: Cancer and the Environment. Predictive Genetic Tests: Problems and Pitfalls. Ann. NY Acad. of Sciences,, 883: 42-46, 1997.
  17. 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.
  18. 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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