Genomic analysis of lean individuals with NAFLD identifies monogenic disorders in a prospective cohort study-Reference-Cited by-同舟云学术

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Genomic analysis of lean individuals with NAFLD identifies monogenic disorders in a prospective cohort study

Published:2023-04 Issue:4 Volume:5 Page:100692
ISSN:2589-5559
Container-title:JHEP Reports
language:en
Short-container-title:JHEP Reports

Author:

Zheng Melanie,Huang Daniel Q.,Konkwo Chigoziri,Agrawal Saaket,Khera Amit V.^ORCID,Loomba Rohit,Vilarinho Sílvia,Ajmera Veeral^ORCID

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

National Institute of Environmental Health Sciences

Doris Duke Charitable Foundation

U.S. Department of Defense

National Center for Advancing Translational Sciences

National Institute on Alcohol Abuse and Alcoholism

National Heart, Lung, and Blood Institute

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology,Immunology and Allergy,Internal Medicine

Reference23 articles.

1. Mechanisms and disease consequences of nonalcoholic fatty liver disease;Loomba;Cell,2021

2. Risk for development of severe liver disease in lean patients with nonalcoholic fatty liver disease: a long-term follow-up study;Hagström;Hepatol Commun,2018

3. Histological severity and clinical outcomes of nonalcoholic fatty liver disease in nonobese patients;Leung;Hepatology,2017

4. Clinical utility of genomic analysis in adults with idiopathic liver disease;Hakim;J Hepatol,2019

5. Emerging role of genomic analysis in clinical evaluation of lean individuals with NAFLD;Vilarinho;Hepatology,2021

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1. Prevalence of Liver Steatosis and Fibrosis in Adults With Primary Hypobetaliproteinemia: Results From the HYPOCHOL Study;Clinical Gastroenterology and Hepatology;2024-07

2. Rare monogenic causes of steatotic liver disease masquerading as MASLD;Journal of Hepatology;2024-06

3. Genetics of liver disease in adults;Hepatology Communications;2024-03-29

4. Associations of PNPLA3 and LEP genetic polymorphisms with metabolic-associated fatty liver disease in Thai people living with human immunodeficiency virus;World Journal of Hepatology;2024-03-27

5. Combination of heterozygous APOB gene mutation with PNPLA3 and TM6SF2 variants promotes steatotic liver disease, cirrhosis and HCC development;Liver International;2024-02-29

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