Patient Offices
- Address
-
1184 Fifth Avenue, 2nd Floor
Gaucher and Porphyria Disease patients only
New York , NY 10029
- Tel
- 212-241-0915
- Office Hours
- Tuesday 9:00 AM - 4:00 PM
- Wednesday 9:00 AM - 4:00 PM
- Thursday 9:00 AM - 4:00 PM
- Friday 9:00 AM - 12:00 PM
- Disabled Access
- Yes
Business Offices
- Address
-
Atran Berg Laboratory Building Floor 1st Floor, Room AB1-50
1428 Madison Avenue
New York, NY 10029
- Tel
- 212-241-8384
Manisha Balwani
ASSISTANT PROFESSOR Genetics and Genomic Sciences
ASSISTANT PROFESSOR Medicine
Overview
| Specialty |
Clinical Genetics - MD
, Internal Medicine
|
| Clinical Interests |
Cancer Genetics |
| |
Gaucher’s Disease |
| |
Porphyrias |
| Gender |
Female |
| E-mail |
manisha.balwani@mssm.edu |
| Education and Training |
MBBS, Topiwala National Medical College |
| |
M.S., University of Pittsburgh |
| |
Fellowship, Mount Sinai School of Medicine |
| |
Fellowship, Mount Sinai School of Medicine |
| |
Residency, North Shore University Hospital at Forest Hills |
| |
Residency, Internal Medicine, North Shore Univ. Hosp. at Forest Hills |
| |
Fellowship, Biochemical Genetics, Mount Sinai Hospital |
| |
Fellowship, Medical Genetics, Mount Sinai Hospital |
Board Certification: Internal Medicine, Clinical Genetics
Training
| Education and Training |
MBBS, Topiwala National Medical College |
| |
M.S., University of Pittsburgh |
| |
Fellowship, Mount Sinai School of Medicine |
| |
Fellowship, Mount Sinai School of Medicine |
| |
Residency, North Shore University Hospital at Forest Hills |
| |
Residency, Internal Medicine, North Shore Univ. Hosp. at Forest Hills |
| |
Fellowship, Biochemical Genetics, Mount Sinai Hospital |
| |
Fellowship, Medical Genetics, Mount Sinai Hospital |
| Board Certification |
Clinical Genetics - MD |
| |
Internal Medicine |
Clinical Practice
| Specialty |
Clinical Genetics - MD
, Internal Medicine
|
| Clinical Interests |
Cancer Genetics |
| |
Gaucher’s Disease |
| |
Porphyrias |
| Board Certification |
Clinical Genetics - MD |
| |
Internal Medicine |
Research
Current Research: Modifier Genes in Type I Gaucher disease
Publications
Sansaricq C, Pardo S, Balwani M, Raymond K, Grace M. Biochemical and molecular diagnosis of lipoamide dehydrogenase deficiency in a North American Ashkenazi Jewish family. J Inherit Metab Dis 2006 February; 29(1): 203-204.
Grace ME, Balwani M, Nazarenko I, Prakash-Cheng A, Desnick RJ. Type I Gaucher Disease: Null and Hypomorphic Novel Chitotriosidase Gene Mutations-Implications for Diagnosis and Therapeutic Monitoring. Hum Mutat 2006;.
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