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Nancy Bach

Researcher at Icahn School of Medicine at Mount Sinai

Publications -  31
Citations -  2699

Nancy Bach is an academic researcher from Icahn School of Medicine at Mount Sinai. The author has contributed to research in topics: Liver transplantation & Primary biliary cirrhosis. The author has an hindex of 19, co-authored 31 publications receiving 2473 citations. Previous affiliations of Nancy Bach include City University of New York & Mount Sinai Hospital.

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Features and outcomes of 899 patients with drug-induced liver injury: The DILIN prospective study

Naga Chalasani, +77 more
- 01 Jun 2015 - 
TL;DR: In this article, the authors present characteristics and subgroup analyses from the first 1257 patients enrolled in the study, and conclude that there are no differences in outcomes of patients with short vs long latency of DILI.
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The histological features of chronic hepatitis C and autoimmune chronic hepatitis: a comparative analysis.

TL;DR: For example, the authors examined biopsy specimens from 50 patients with chronic hepatitis C and 21 patients with autoimmune chronic hepatitis and found that bile duct damage was more common in chronic hepatitis than in hepatitis C.
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Primary biliary cirrhosis in monozygotic and dizygotic twins: Genetics, epigenetics, and environment ☆

TL;DR: The concordance rate of PBC in identical twins is among the highest reported in autoimmunity, and discordant pairs were identified, indicating that either epigenetic factors and/or environment play a critical role.
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Increased prevalence of primary biliary cirrhosis near superfund toxic waste sites

TL;DR: Toxin exposure may be a risk factor influencing the clustering of PBC cases and significant clusters of both PBC‐OLT and PSC‐MSSM were identified surrounding SFS.
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Assessment of hepatitis C virus RNA and genotype from 6807 patients with chronic hepatitis C in the United States

TL;DR: Hepatitis C virus (HCV) RNA status and HCV genotype have become important tools in the diagnosis and monitoring of therapy in chronic HCV infection and African–American patients were more likely to be infected with genotype 1 when compared with Caucasian, Hispanic or Asian Pacific Islanders.