|
Kelly
Jackson
Certified Genetic Counselor
Instructor, Pediatrics/Medicine
|
| August
1992-May 1994 |
Master
of Science in Genetic Counseling, University of Pittsburgh,
Graduate School of Public Health, Department of Human
Genetics, Pittsburgh, PA; Thesis title"An Exon-2 Peripherin/RDS
Mutation Causes Macular and Peripheral Retinal Degeneration |
| August
1986-May 1990 |
Bachelor
of Arts in Biology and Psychology Washington University
in St. Louis, Missouri |
|
| January
1995 - present |
Genetic
Counselor, Tulane University Medical School Human Genetics
Program, Hayward Genetics Center. Responsibilities include
clinic coordination for weekly clinic at Tulane and
three satellite clinics; cancer genetic counseling for
Tulane community; staff, community and allied health
care provider education on cancer genetics and human
genetics; clinical research; lysosomal storage disease
registry local coordinator; lectures to medical students
about genetic counseling and cancer genetics Instructor
of Pediatrics and Clinical Medicine in Hematology/Oncology,
November 1, 1996. |
| |
American
Society of Human Genetics, National Society of Genetic
Counselors, current state representative for region
III of NSGC; member, metabolic / lysosomal disease special
interest group, member, cancer special interest group,
Psi Chi, National Psychology Honor Society Alpha Phi
Omega, National Co-ed Service Fraternity, Louisiana
Breast Cancer Task Force. |
|
|
American
Board of Genetic Counseling, 1996 |
| |
Selected
as a member of the New Orleans City Business Power Generation
for 2003. |
| SELECTED
PUBLICATIONS / ABSTRACTS: |
| |
Andersson
HC, Krousel-Wood MA, Jackson KE, Rice J, Lubin IM. Medical
genetic test reporting in molecular cystic fibrosis
and factor V Leiden tests based on reports solicited
from North American laboratories. Genetics in Medicine
4 (5): 324-327, 2002. |
| |
Krousel-Wood
MA, Andersson HA, Rice J, Jackson KE, Rosner ER, Lubin
IM. Physicians' perceived usefulness of and satisfaction
with test reports for cystic fibrosis (delta F 508)
and factor V Leiden. Genetics in Medicine 5 (3): 2002. |
| |
Jackson
KE, Krousel-Wood MA, Lubin IM, Andersson HC (2001).
Medical Genetic Test Report . Platform presentation
at the American College of Medical Genetics meeting,
Miami, March, 2001. |
| |
Jackson
KE, Tsien F, Marble M (2000). Brief Clinical Report:
Phenotypic Features in a Boy with Monosomy 18 Mosaicism.
Am J Med Genet 95:229-232. |
| |
Jackson
KE, Prieto-Carrasquero M, Li S, Marble M (1999). Phenotypic
features of a patient with mosaic trisomy 18 and 45,X;
comparison with three previous cases. Poster presentation
at the 1999 American Society of Human Genetics meeting
and Platform presentation at the 1999 Southern Genetics
Group meeting. |
| |
Morava,
E., Jackson KE, Marble, M., Andersson, HC, Shapira,
E. (1997). Congenital Anophthalmia, an Overview of Eleven
Patients. Poster presentation at the American Society
of Human Genetics meeting, October, 1997. |
| |
Jackson,
KE, Tsien, F., Marble M. (1996). Near Normal Cognitive
Development in a Patient with Non-Mosaic Robertsonian
Trisomy 13 in Blood, Found to have Mosaicism for the
Balanced/ Unbalanced Translocation in Skin Fibroblasts.
Poster presentation at the American Society of Human
Genetics meeting, October, 1996. |
| |
Gorin
MB, Jackson KE, Ferrell RE, Sheffield VC, Jacobson SG,
Gass JDM, Mitchell EB, Stone EM (1995). A Peripherin/Retinal
Degeneration Slow Mutation (Pro-210-Arg) Associated
with Macular and Peripheral Retinal Degeneration. Ophthalmology,
102:246-255. |
| |
Green
RP, Cohn SM, Sacchettini JC, Jackson KE, Gordon JI (1992).
The Mouse Intestinal Fatty Acid Binding Protein Gene:
Nucleotide Sequence, Pattern of Developmental and Regional
Expression, and Proposed Structure of Its Protein Product.
DNA and Cell Biology 11(1): 31-41. |
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