Area of research
Epidemiology · Pathology and Forensic Medicine
Research interest
Research interests include Liver Disease Diagnosis and Treatment, Alcohol Consumption and Health Effects, Genetic factors in colorectal cancer, and Genetic Associations and Epidemiology.
Meta‐Analysis: Effects of Steatotic Liver Disease‐Associated Genetic Risk Alleles on Longitudinal Outcomes
Meta-Analysis: Effects of Steatotic Liver Disease-Associated Genetic Risk Alleles on Longitudinal Outcomes.
PNPLA3 in Alcohol-Related Liver Disease.
Interpreting elevated liver blood test results through a genetic lens: A genome-wide association study.
Genetic variation in <i>TERT</i> modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis: results from a genome-wide case-control study.
The rs72613567:TA polymorphism in HSD17B13 is associated with survival benefit after development of hepatocellular carcinoma.
High producer variant of lipoprotein lipase may protect from hepatocellular carcinoma in alcohol-associated cirrhosis
Performance of routine risk scores for predicting cirrhosis-related morbidity in the community.
PSD3 downregulation confers protection against fatty liver disease.
The rs429358 Locus in Apolipoprotein E Is Associated With Hepatocellular Carcinoma in Patients With Cirrhosis.
Genetic Variation of <i>SAMM50</i> Is Not an Independent Risk Factor for Alcoholic Hepatocellular Carcinoma in Caucasian Patients.
rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysis.
Loss of hepatic Mboat7 leads to liver fibrosis.
Nonalcoholic fatty liver disease stratification by liver lipidomics
Genetic architectures of proximal and distal colorectal cancer are partly distinct
Genetic architectures of proximal and distal colorectal cancer are partly distinct
Nonalcoholic fatty liver disease stratification by liver lipidomics.
Identifying Novel Susceptibility Genes for Colorectal Cancer Risk From a Transcriptome-Wide Association Study of 125,478 Subjects
Combined effects of PNPLA3, TM6SF2 and HSD17B13 variants on severity of biopsy-proven non-alcoholic fatty liver disease.
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease.
The rs738409 G Allele in PNPLA3 Is Associated With a Reduced Risk of COVID-19 Mortality and Hospitalization.
Variants in PCSK7, PNPLA3 and TM6SF2 are risk factors for the development of cirrhosis in hereditary haemochromatosis.
Cumulative Burden of Colorectal Cancer–Associated Genetic Variants Is More Strongly Associated With Early-Onset vs Late-Onset Cancer
Loss of hepatic Mboat7 leads to liver fibrosis
Genetic Variation in HSD17B13 Reduces the Risk of Developing Cirrhosis and Hepatocellular Carcinoma in Alcohol Misusers.
Genome-Wide Association Study for Alcohol-Related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1.
Genetic architectures of proximal and distal colorectal cancer are partly distinct
Copy number variants in lipid metabolism genes are associated with gallstones disease in men.
Genome-wide analysis of 944,133 individuals provides insights into the etiology of hemorrhoidal disease
Genetic architectures of proximal and distal colorectal cancer are partly distinct