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388 results for “alcoholic fatty liver disease”

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zenodo40/100

Figure S1. Mediation analysis on the effect of insulin resistance on intraocular pressure. Figure S2. Forest plot showing the OR (95% CI) for EIOP of ALD versus NAFLD and the OR (95% CI) for EIOP of drinkers versus non-drinkers. Abbreviations: OR, odds ratio; CI, confidence interval; ALD, alcoholic liver disease; NAFLD, non-alcoholic fatty liver disease.

<p>Figure S1. Mediation analysis on the effect of insulin resistance on intraocular pressure.</p> <p>Figure S2. Forest plot showing the OR (95% CI) for EIOP of ALD versus NAFLD and the OR (95% CI) for EIOP of drinkers versus non-drinkers. Abbreviations: OR, odds ratio; CI, confidence interval; ALD, alcoholic liver disease; NAFLD, non-alcoholic fatty liver disease.</p>

opencc-by-4.0Oct 2022View details →
zenodo40/100

VISION Invited lecture - Bariatric surgery and non-alcoholic fatty liver disease

<p>Recording and presentation&nbsp;of the invited lecture that took place online on 16&nbsp;June 2021&nbsp;- <strong>Pantelis Antonakis, MD, PhD -&nbsp;Bariatric surgery and non-alcoholic fatty liver disease.</strong></p> <p>Bariatric surgery is a documented solution for morbid obesity. Additionally to excess weight loss, significant improvement in comorbidities is an established benefit after bariatric operations. In recent years, non-alcoholic fatty liver disease (NAFLD) has emerged as one of these comorbidities. Herein we will review the data supporting the positive effect of bariatric surgery in patients with NAFLD.</p>

opencc-by-4.0Jul 2021View details →
zenodo40/100

Dihydrosphingolipids are associated with steatosis and increased fibrosis damage in human and animal models of non-alcoholic fatty liver disease

<p>Data sets used for the&nbsp;article entitled:&nbsp;&quot;Accumulation of dihydrosphingolipids and neutral lipids is related to steatosis and fibrosis damage in human and animal models of non-alcoholic fatty liver disease&quot;</p> <p>- Patient data: DATA Patients JLR.xlsx</p> <p>- Mouse&nbsp;data:&nbsp;DATA Mice.xlsx</p>

opencc-by-4.0Feb 2022View details →
ClinicalTrials.gov40/100

Study of Semaglutide for Non-Alcoholic Fatty Liver Disease (NAFLD), a Metabolic Syndrome With Insulin Resistance, Increased Hepatic Lipids, and Increased Cardiovascular Disease Risk (The SLIM LIVER St

ClinicalTrials.gov study NCT04216589. IPD Sharing: YES. Countries: 2. Publications: 2.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov40/100

Study of Various Treatments in Non-alcoholic Fatty Liver Disease (NAFLD) Patients Who Have Aspects of Non-alcoholic Steatohepatitis (NASH)

ClinicalTrials.gov study NCT04147195. IPD Sharing: YES. Countries: 3. Publications: 1.

controlledIPD-YESFeb 2026View details →
zenodo36/100

Raw data related to: Randomised Clinical Trial: Calorie Restriction Regimen with Tomato Juice Supplementation Ameliorates Oxidative Stress and Preserves a Proper Immune Surveillance Modulating Mitochondrial Bioenergetics of T-Lymphocytes in Obese Children Affected by Non-Alcoholic Fatty Liver Disease (NAFLD)

<p><strong>Abstract</strong></p> <p>Fatty liver disease is a serious complication of childhood obesity. Calorie-restricted regimen&nbsp;(RCR) is one of the e ective therapy for this condition. Aim of the study was to evaluate the effect&nbsp;of lycopene-rich tomato sauce with oregano and basil extracts in obese children with fatty liver on&nbsp;RCR. 61 obese children with fatty liver were enrolled, 52 completed the study. A randomized cross&nbsp;over clinical trial was performed. Participants were assigned to RCR alone or with a supplement of&nbsp;lycopene-rich tomato juice for 60 days; subsequently, the groups were switched to the alternative&nbsp;regimen for the next 60 days. Reduction in BMI, HOMA-IR, cholesterol, triglycerides, liver size,&nbsp;and steatosis was more profound in tomato-supplemented group. Leptin decreased in both groups&nbsp;whereas adiponectin raised only after tomato supplementation. RCR is associated with the impaired&nbsp;engagement of T-cells glycolysis and proliferation, tomato-supplementation resulted in glycolytic&nbsp;metabolic activation of T-cells. Tomato juice ameliorates glucose and lipid metabolism in obese&nbsp;children, improve oxidative and inflammatory state and modulates the mitochondrial metabolism&nbsp;of T-cells contributing to a maintenance of a proper immune surveillance in children, impaired by&nbsp;RCR. The addition of tomato to RCR could be considered a protective and preventive support to&nbsp;obese child.</p> <p><strong>Progetto giovani ricercatori&nbsp;</strong>[GR-2016-02363725] dal titolo: &quot;Immune Tolerance, Metabolism and Multiple Sclerosis: Novel Molecular Tools to Monitor Disease Pathogenesis and Progression&quot;</p>

opencc-by-4.0Mar 2020View details →
dryad36/100

Association of fat-to-muscle ratio with non-alcoholic fatty liver disease: a single-centre retrospective study

<p><strong>Objectives</strong>: Sarcopenia is a known risk factor for non-alcoholic fatty liver disease (NAFLD). Studies evaluating the association between the fat-to-muscle ratio (FMR) and NAFLD are limited. Therefore, the aim of our study was to investigate the association between FMR and NAFLD.</p> <p><strong>Design:</strong> A retrospective study was conducted on the individuals who underwent health examination in Wuhan Union Hospital between January 2020 and November 2021. Clinical data were collected from electronic medical records.</p> <p><strong>Setting:</strong> Our study was conducted in a hospital in China.</p> <p><strong>Participants:</strong> A total of 1,592 participants aged ≥40 years who underwent body composition analysis and liver ultrasonography were retrospectively reviewed.</p> <p><strong>Primary outcome measures:</strong> Liver ultrasonography was used to assess liver steatosis, and the Fibrosis-4 Index (FIB-4) was used to calculate the risk scores for liver fibrosis. The 10-year atherosclerotic cardiovascular disease (ASCVD) risk prediction model was used to calculate ASCVD risk scores.</p> <p><strong>Results:</strong> The FMR was significantly higher in individuals with NAFLD than in those without NAFLD (P&lt;0.001). The prevalence of NAFLD gradually increased from FMR tertile 1 (reference) to tertile 2 (OR=1.49, 95% CI: 1.13–1.97) and tertile 3 (OR=2.85, 95% CI: 2.08–3.90). In addition, patients with NAFLD in FMR tertile 3 had a significantly higher risk of liver fibrosis (OR=4.48, 95% CI: 2.12–9.50) and ASCVD (OR=4.63, 95% CI: 2.62–8.19) than those in FMR tertile 1 after adjustment for multiple confounders.</p> <p><strong>Conclusion:</strong> In this study, we found a significant association between FMR and NAFLD. A higher FMR indicates a higher risk of NAFLD in the study population and a higher risk of liver fibrosis and ASCVD in NAFLD patients.</p>

opencc-zeroSep 2023View details →
ClinicalTrials.gov36/100

Prevalence of Non-alcoholic Fatty Liver Disease (NAFLD) in Hispanics With Diabetes Mellitus Type 2 (T2DM) and Role of Treatment

ClinicalTrials.gov study NCT01002547. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov36/100

Insulin Resistance in Non-alcoholic Fatty Liver Disease

ClinicalTrials.gov study NCT00252499. IPD Sharing: Not stated. Countries: 1. Publications: 2.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov36/100

Non-Alcoholic Fatty Liver Disease in a Saudi Cohort With Type 2 Diabetes Mellitus

ClinicalTrials.gov study NCT05697991. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov36/100

The Impact of Different Exercise Modes on Bile Acid Levels and Liver Function in Patients With Non-alcoholic Fatty Liver Disease

ClinicalTrials.gov study NCT06338449. IPD Sharing: UNDECIDED. Countries: 1. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov36/100

Impact of Lifestyle Interventions on Cognitive Decline in Non-alcoholic Fatty Liver Disease

ClinicalTrials.gov study NCT07294963. IPD Sharing: YES. Countries: 1. Publications: 4.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov36/100

Insulin Resistance in Non-alcoholic Fatty Liver Disease

ClinicalTrials.gov study NCT01289639. IPD Sharing: Not stated. Countries: 1. Publications: 2.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov36/100

Fetuin-A, a Promising Serum Biomarker for Diagnosis of Non-Alcoholic Fatty Liver Disease

ClinicalTrials.gov study NCT06097039. IPD Sharing: NO. Countries: 1. Publications: 6.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov36/100

The Effect Of NS-0200 Versus Placebo On Hepatic Fat Content In Patients With Non Alcoholic Fatty Liver Disease

ClinicalTrials.gov study NCT02546609. IPD Sharing: NO. Countries: 1. Publications: 2.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov36/100

A Study To Assess Pharmacodynamics, Safety And Tolerability Of PF-05221304 And PF-06865571 Co-Administered For 6 Weeks In Adults With Non-Alcoholic Fatty Liver Disease.

ClinicalTrials.gov study NCT03776175. IPD Sharing: YES. Countries: 1. Publications: 1.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov36/100

Study of the Safety and Tolerability of AXA1125 and AXA1957 in Subjects With Non-Alcoholic Fatty Liver Disease (NAFLD)

ClinicalTrials.gov study NCT04073368. IPD Sharing: Not stated. Countries: 1. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov36/100

Sitagliptin Versus Placebo in the Treatment of Non-alcoholic Fatty Liver Disease

ClinicalTrials.gov study NCT01963845. IPD Sharing: Not stated. Countries: 1. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov36/100

Fucoidan Improves the Metabolic Profiles of Patients With Non-alcoholic Fatty Liver Disease (NAFLD)

ClinicalTrials.gov study NCT02875392. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov36/100

Efficacy of a Natural Components Mixture in the Treatment of Non Alcoholic Fatty Liver Disease (NAFLD)

ClinicalTrials.gov study NCT02369536. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →

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International Brain Laboratory public data

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