Dr. Sue Ann Wee is a board certified and fellowship-trained laser, cosmetic and general dermatologist who received her doctorate of medicine from Stanford Medical School. She completed dermatology residency at New York University’s Ronald O. Perelman Department of Dermatology, followed by a fellowship in laser and cosmetic dermatology at SkinCare Physicians in Massachusetts. Dr. Wee has published in numerous academic journals and is a leading expert in treating aesthetic skin concerns in individuals of all skin tones, blending artistry with innovative, precise and scientifically validated techniques. She believes in a compassionate partnership with her patients.
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New York Rising Stars 2014
New York Rising Stars 2013
Medical School: Stanford University School of Medicine
Graduation Year: 2002
Professional Webpage: https://www.drsueannwee.com/
Howard Hughes Medical Institute Research Training Fellowship for Medical Students
First prize, 16th Annual Conrad Stritzler Memorial Resident Competition for best oral presentation
National Alopecia Areata Foundation Research Grant Award
Stanford Medical Scholars Grant Award
Winner, 3rd Annual New Physician Creative Arts Contest
Dr. Wee is a member of the American Academy of Dermatology and the American Society for Dermatologic Surgery.
The Art & Science Of Facial Proportions in Dermatology ,
Photodynamic Therapy for Actinic Keratoses and Cutaneous Oncology ,
Profiling genomic expression in disorders of epidermal proliferation identifies Egr-1 as a potent regulator of epidermal growth.,
Gene expression profiling in human squamous cell carcinoma, basal cell carcinoma, and psoriasis identifies distinct patterns of gene expression.,
Gene expression profiling reveals distinct patterns of gene expression in normal, senescent, terminally differentiated, and immortalized keratinocytes.
Clinical and pathological features of posttransplantation lymphoproliferative disorders presenting with skin involvement in 4 patients. ,
Choi CM, Bogart M, Wee SA, Burstein R, Arndt K, Dover J. Predicting migraine responsiveness to botulinum toxin type A injections. Arch Dermatol. 2010;146(2): 159-163.
Wee SA, Dover JS. Effective treatment of psychotropic drug-induced facial hyperpigmentation with a 755-nm Q-switched Alexandrite laser . Dermatol Surg. 2008;34(11):1609-12.
Kaminer MS, Bogart M, Choi C, Wee SA. Long-term efficacy of anchored barbed sutures in the face and neck. Dermatol Surg. 2008; 34(8):1041-7.
Fang M, Wee SA, Ronski K, Fan H, Tao S, Lin Q. Evidence of EGR1 as a differentially expressed gene among proliferative skin diseases. Genomic Med. 2007; 1(1-2):–85.
Wee SA. Multiple eruptive keratoacanthomas, de novo. Dermatol Online J. 2004 Nov 30;10(3):19.
Wee SA, Possick P. Necrobiosis lipoidica. Dermatol Online J. 2004 Nov 30;10(3):18.
Beynet DP, Wee SA, Horwitz SS, Kohler S, Horning S, Hoppe R, Kim YH. Clinical and pathological features of posttransplantation lymphoproliferative disorders presenting with skin involvement in 4 patients. Arch Dermatol. 2004 Sep; 140(9):1140-6 (also oral presentation at The Dermatologic Society of Greater New York 2005).
Wee SA, Lin Q, Tao S, Fan H, Khavari PA. Profiling genomic expression in disorders of epidermal proliferation identifies Egr-1 as a potent regulator of epidermal growth. J Invest Dermatol. 2001;117(2):477.
Dajee M, Wee SA, Tao S, Khavari PA. Non-invasive topical immunization by a peptide vaccine against hepatitis B and rubella virus. J Invest Dermatol 2001; 117(2): 435.
Fan H, Wee SA, Khavari PA (abstract and poster). Sonic hedgehog opposes epithelial cell cycle arrest. J Invest Dermatol 1999; 112(4):525.
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