Associated Papers
Integrated Cross-Platform Analysis Reveals Candidate Variants and Linkage Disequilibrium-Defined Loci Associated with Osteoporosis in Korean Postmenopausal Women.
Kim SK et al.
Diagnostics (basel, Switzerland), 2026
Whole exome sequencing and machine learning germline analysis of individuals presenting with extreme phenotypes of high and low risk of developing tobacco-associated lung adenocarcinoma.
Patiño-García A et al.
Ebiomedicine, 2024
38484556 (PubMed )
Supplement: mmc1.xlsx › Supp_Table_2
A case of NASH with genetic predisposition successfully treated with an SGLT2 inhibitor: a possible involvement of mitochondrial dysfunction.
Nakajima R et al.
Endocrinology, Diabetes & Metabolism Case Reports, 2022
Screening for rare variants in the PNPLA3 gene in obese liver biopsy patients.
Zegers D et al.
Clinics and Research in Hepatology and Gastroenterology, 2016
The rs2294918 E434K variant modulates patatin-like phospholipase domain-containing 3 expression and liver damage.
Donati B et al.
Hepatology (baltimore, Md.), 2016
Hepatic patatin-like phospholipase domain-containing protein 3 sequence, single nucleotide polymorphism presence, protein confirmation, and responsiveness to energy balance in dairy cows.
McCann CC et al.
Journal of Dairy Science, 2014
Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease.
Romeo S et al.
Nature Genetics, 2008
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