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Patient Offices

Address
5 East 98th Street
11th Floor
New York, NY 10029
Tel
212-241-0034
Fax
212-289-7738
Office Hours
Monday 8:00 AM - 5:00 PM
Tuesday 8:00 AM - 5:00 PM
Wednesday 8:00 AM - 5:00 PM
Thursday 8:00 AM - 5:00 PM
Friday 8:00 AM - 5:00 PM
Disabled Access
Yes

Insurance Plans Accepted

  • Aetna U.S. Healthcare
  • Aetna U.S. Healthcare - HMO
  • Best Doctor
  • Devon Health Services
  • Fidelis Care NY - HMO
  • First Health
  • Group Health Insurance, Inc.
  • Healthnet-Empire BCBS
  • Island Group
  • Medicaid
  • Medicare
  • Neighborhood Health Providers, LLC
  • Oxford Health Plans
  • Railroad Medicare
  • United Healthcare

Disclaimer - Please note that the insurance accepted list may not be complete. Prior to scheduling an appointment, please contact the doctors' office to verify their participation in your plan.

Business Offices

Address
19 East 98th Street Floor 8th Floor
New York, NY 10029
Tel
212-241-8035
Fax
212-996-9688

Joseph A. Odin

ASSOCIATE PROFESSOR  Medicine, Liver Diseases

Overview

Subspecialty Gastroenterology
Clinical Interests Liver Disease
Languages English
  Spanish
Gender Male
E-mail joseph.odin@mountsinai.org
Education and Training MD, Mount Sinai Sch. of Medicine CUNY
  M.D., Mount Sinai School of Medicine
  Ph.D., C.U.N.Y.
  Cum Laude, Cornell University
  Residency, Internal Medicine, Mount Sinai Hospital
  Fellowship, Gastroenterology, Johns Hopkins Hospital
Awards 2006
Liver Scholar Award
American Liver Foundation
  2003
Research Excellence in GI and Liver Disease Award

Dr. Odin is an assistant professor in the Division of Liver Diseases with an interest in patients with autoimmune liver diseases, including primary biliary cirrhosis, primary sclerosing cholangitis, and autoimmune hepatitis, and those with hepatitis C infection (HCV). This interest is both clinical and translational research oriented.
His research program focuses on the importance of clearance of apoptotic or dying cells from the liver in the regulation of chronic inflammatory responses in each of the above diseases. The roles of bile duct epithelial cells, macrophages, and dendritic cells in this process are of particular interest. Systems have been developed to analyze these cell types in vitro and in vivo.  The overall research aim is to identify environmental, including toxins and vitamin D, and genetic factors, that influence this process in order to identify novel means of decreasing chronic liver inflammation. This research program is a continuation of studies regarding the pathogenesis of Primary Biliary Cirrhosis (PBC) that he began as a postdoctoral fellow at Johns Hopkins School of Medicine. Much of this work is part of the PBC Research Center at Mount Sinai and has been funded at various times by a K08 award from the NIH /NIDDK, the Artzt Family Foundation Trust, the New York City Speaker's Fund, The American Liver Foundation and the Hirschl/Weill-Caulier Trust. Dr. Odin was also the recipient of a Research Excellence in GI and Liver Disease (REGAL) Award presented by the American Gastroenterologic Association. The studies of autoimmune liver disease are performed in collaboration with Nancy Bach, M.D.  and the studies of HCV infection are partly in collaboration with Andrea Branch, Ph.D. Current members of the laboratory include Jorge Allina, M.D., Carmen Stanca, M.D., and John Garber, M.D.
In his clinical practice, Dr. Odin accepts patients with all types of liver disease. Those with HCV infection are treated with pegylated-interferon/ ribavirin combination therapy under the watchful eye of myself and a physician assistant. Patient support groups are available for those with HCV infection and PBC. Those with end-stage liver disease are referred to RMTI physicians at Mount Sinai for evaluation for liver transplantation. Eligible patients are referred to a number of available clinical trials if interested. Dr. Odin is the principal investigator or co-investigator for several of these clinical trials. Currently, enrollment is available in clinical trials for those with primary biliary cirrhosis, chronic hepatitis C infection, and chronic hepatitis B infection.
Dr. Odin completed his postdoctoral fellowship in the Division of Gastroenterology and Hepatology at the Johns Hopkins School of Medicine in 2000. Prior to this, he was an Internal Medicine resident at Mount Sinai. Following acceptance into the Medical Scientist Training Program at the Mount Sinai School of Medicine in 1986, he was awarded his Ph.D. degree in 1991 upon completion of his doctoral dissertation under the supervision of Dr. Jay Unkeless. He received his M.D. degree in 1993, at which time he was selected for an NIDDK Medical Student of the Year Award and an American Federation for Clinical Research Student Award. Currently, he is a member of the American Association for the Study of Liver Diseases and the American Gastroenterology Association.

Training

Education and Training MD, Mount Sinai Sch. of Medicine CUNY
  M.D., Mount Sinai School of Medicine
  Ph.D., C.U.N.Y.
  Cum Laude, Cornell University
  Residency, Internal Medicine, Mount Sinai Hospital
  Fellowship, Gastroenterology, Johns Hopkins Hospital
Board Certification Gastroenterology

Clinical Practice

Subspecialty Gastroenterology
Clinical Interests Liver Disease
Languages English
  Spanish
Board Certification Gastroenterology

Research

Research

  •  PBC
  • PSC
  • Autoimmune Liver Disease
  • Hepatic Immunology

Dr. Odin's research program focuses on the importance of clearance of apoptic or dying cells from the liver in the regulation of chronic inflammatory responses in each of the above diseases. The roles of bile duct epithelial cells, macrophages, and dendritic cells in this process are of particular interest. Systems have been developed to analyze these cell types in vitro and in vivo. The overall research aim is to identify environmental, including toxins and vitamin D, and genetic factors, that influence this process in order to identify novel means of decreasing chronic liver inflammation. The research program is a continuation of studies regarding the pathogenesis of Primary Biliary Chirrhosis (PBC) that he began as a postdoctoral fellow at Johns Hopkins School of Medicine. Much of this work is part of the PBC Research Center at Mount Sinai and has been funded at various times by a K08 Award from the NIH/NIDDK, the Artzt Family Foundation and the Hirschl/Weill-Caulier Trust. Dr. Odin was also the recipient of a Research Excellence in GI and Liver Disease (REGAL) Award presented by the American Gastroenterological Association. The studies of autoimmune liver disease are performed in collaboration with Nancy Bach, M.D., and the studies of HCV infection are partly in collaboration with Andrea Branch, Ph.D. Current members of the laboratory include Jorge Allina, M.D., Carmen Stanca, M.D., and John Garber, M.D.

  • Macrophage Function in HCV infection
  • Safety and efficacy of viramidine in HCV treatment
  • Autoimmune Liver Disease Pathogenesis
  • Apoptotic Cells as Sources of Immunogen in Primary Biliary Cirrhosis
  • Apoptosis Signaling Mechanisms in the Mitochondria
  • The Role of Environmental Toxins in PBC
Bile Duct Cells, HeLa Cells

Publications

Allina J, Hu B, Fiel MI, Sullivan DM, Thung SN, Bronk SF, Huebert RC, van de Water J, LaRusso NF, Gershwin ME, Gores GJ, Odin JA. Biliary epithelial cell phagocytosis of apoptotic cells and T cell targeting in primary biliary cirrhosis. J Autoimmunty;.


Ala A, Stanca CM, Bu-Ghanim M, Ahmado I, Branch AD, Schiano TD, Odin JA, Bach N. Increased prevalence of primary biliary cirrhosis near superfund toxic waste sites. Hepatology 2006; 43: 525-531.


Stanca CM, Bach N, Krause C, Tandon N, Freni MA, Gutierrez JA, Bodian C, Schiano TD, Branch AD, Odin JA. Evaluation of fatigue in U.S. patients with primary biliary cirrhosis. Am J Gastroenterol 2005; 100: 1104-1109.


Benzeno S, Narla G, Allina J, Cheng GZ, Reeves HL, Banck MS, Odin JA, Diehl JA, Germain D, Friedman SL. Cyclin-dependent kinase inhibition by the KLF6 tumor suppressor protein through interaction with cyclin D1. Cancer Res 2004 Jun 1; 64(11): 3885-3891.


Matsumura S, Van De Water J, Leung P, Odin JA, Yamamoto K, Gores GJ, Mostov K, Ansari AA, Coppel RL, Shiratori Y, Gershwin ME. Caspase induction by IgA antimitochondrial antibody: IgA-mediated biliary injury in primary biliary cirrhosis. Hepatology 2004; 39(5): 1415-1422.


Sasaki M, Allina J, Odin JA, Thung SN, Coppel R, Nakanuma Y, Gershwin ME. Autoimmune Cholangitis in the SJL/J mouse is antigen non-specific. Develop Immunol 2003; 9(2): 103-111.


Bach N, Odin JA. Primary biliary cirrhosis: the Mount Sinai perspective. Mt Sinai J Med 2003 Sep; 70(4): 242-250.


Bai J, Odin JA. Apoptosis and the liver: in relation to autoimmune disease. Autoimmunity Reviews 2003; 2: 36-42.


Odin JA, Huebert RC, Casciola-Rosen L , LaRusso NF, Rosen A . Bcl-2-dependent oxidation of pyruvate dehydrogenase-E2, a primary biliary cirrhosis autoantigen, during apoptosis. J Clin Invest 2001; 108(2): 223-232.


Zhang F, Odin JA, Shen Z, Lin CT, Unkeless JC, Jacobson K. Lateral mobility of Fc gamma RIIa is reduced by protein kinase C activation. FEBS Lett 1995; 376(1-2): 77-80.


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