Jamie Caroline Fong, MS, CGC
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Jamie Caroline Fong, MS, CGC
Assistant Professor
Positions
- Assistant Professor
-
Molecular & Human Genetics - Clinic Program
Baylor College of Medicine
Houston
Education
- BA from University of California - Berkeley
- 12/2000 - Berkeley, California United States
- Molecular and Cell Biology
- MS from Sarah Lawrence College
- 05/2008 - Bronxville, New York United States
- Genetic Counseling
Certifications
- Certified Genetic Counselor
- American Board of Genetic Counseling
- Licensed Genetic Counselor
- State of California Dept of Public Health
Professional Interests
- Adult Neurodegenerative Disease
- Predictive Genetic Testing/Counseling
- Clinical Research
Selected Publications
- Minikel EV, Vallabh SM, Orseth MC, Brandel JP, Haik S, Laplanche JL, Zerr I, Parchi P, Capellari S, Safar J, Kenny J, Fong JC, et al "Age of onset in genetic prion disease and the design of preventative clinical trials." Neurology. 2019 Jul;93(2):e125-34. Pubmed PMID: 31171647
- Olney NT, Alquezar C, Ramos EM, Nana AL, Fong JC, Karydas AM, Taylor JB, Stephens ML, Argouarch AR, Van Berlo VA, Dokuru DR, Scherr EH, Jicha GA, Dillon WP, Desikan RS, DeMay M, Seeley WW, Coppola G, Miller BL, Kao AW "Linking tuberous sclerosis complex, excessive mTOR signaling, and age-related neurodegeneration: a new association between TSC1 mutation and frontotemporal dementia." Acta Neuropath. 2017 Nov;134(5):813-6. Pubmed PMID: 28828560
- Takada LT, Kim MO, Cleveland RW, Wong K, Forner SA, Gala II, Fong JC, Geschwind MD "Genetic prion disease: experience of a rapidly progressive dementia center in the United States and a review of the literature." Am J Med Genet B Neuropsychiatr Genet. 2017 Jan;174(1):36-69. Pubmed PMID: 27943639
- Fong JC, Rojas JC, Bang J, Legati A, Rankin KP, Forner S, Miller ZA, Karydas AM, Coppola G, Grouse CK, Ralph J, Miller BL, Geschwind MD "Genetic prion disease caused by PRNP Q160X mutation presenting with an orbitofrontal syndrome, cyclic diarrhea, and peripheral neuropathy." J Alzheimers Dis. 2017 Nov;55(1):249-58. Pubmed PMID: 27716661
- Lee SE, Khazenzon AM, Trujillo AJ, Guo CC, Yokoyama JS, Sha SJ, Takada LT, Karydas AM, Block NR, Coppola G, Pribadi M, Geschwind DH, Rademakers R, Fong JC, Weiner MW, Boxer AL, Kramer JH, Rosen HJ, Miller BL, Seeley WW "Altered network connectivity in frontotemporal dementia with C9orf72 hexanucleotide repeat expansion." Brain. 2014 Nov;137(11):3047-60. Pubmed PMID: 25273996
- Sha SJ, Takada LT, Rankin KP, Yokoyama JS, Rutherford NJ, Fong JC, Khan B, Karydas A, Baker MC, DeJesus-Hernandez M, Pribadi M, Coppola G, Geschwind DH, Rademakers R, Lee SE, Seeley W, Miller BL, Boxer AL "Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features." Neurology. 2012 Sep;79(10):1002-11. Pubmed PMID: 22875087
- Fong JC, Karydas AM, Goldman JS "Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion." Alzheimers Res Ther. 2012 Sep;4(4) Pubmed PMID: 22808918
- Steele NZ, Bright AR, Lee SE, Fong JC, Bonham LW, Karydas A, Karbassi ID, Pribadi M, Meservey MA, Gallen MC, Ramos EM, Liaquat K, Hoffman CC, Krasner MR, Dodge W, L Miller B, Coppola G, Rankin KP, Yokoyama JS, Higgins JJ "Frequency of frontotemporal dementia gene variants in C9ORF72, MAPT, and GRN in academic versus commercial laboratory cohorts." Adv Genomics Genet. 2018;8:23-33. Pubmed PMID: 31031559
Memberships
- National Society of Genetic Counselors
- Member
- Alzheimer’s Association International Society to Advance Alzheimer’s Research and Treatment (ISTAART)
- Member
- International Society for Frontotemporal Dementias (ISFTD)
- Member
- ClinGen Parkinson's Disease Gene Curation Expert Panel
- Member
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