| Year |
Citation |
Score |
| 2020 |
Teo K, Abeysekera KWM, Adams L, Aigner E, Anstee QM, Banales JM, Banerjee R, Basu P, Berg T, Bhatnagar P, Buch S, Canbay A, Caprio S, Chatterjee A, Ida Chen YD, ... ... Kozlitina J, et al. rs641738C>T near MBOAT7 is associated with liver fat, ALT, and fibrosis in NAFLD: a meta-analysis. Journal of Hepatology. PMID 32882372 DOI: 10.1016/J.Jhep.2020.08.027 |
0.343 |
|
| 2020 |
Kozlitina J. Genetic Risk Factors and Disease Modifiers of Nonalcoholic Steatohepatitis. Gastroenterology Clinics of North America. 49: 25-44. PMID 32033763 DOI: 10.1016/J.Gtc.2019.09.001 |
0.349 |
|
| 2019 |
Dongiovanni P, Meroni M, Baselli GA, Mancina RM, Ruscica M, Longo M, Rametta R, Cespiati A, Pelusi S, Ferri N, Ranzani V, Nobili V, Pihlajamaki J, Fracanzani AL, Badiali S, ... ... Kozlitina J, et al. PCSK7 gene variation bridges atherogenic dyslipidemia with hepatic inflammation in NAFLD patients. Journal of Lipid Research. PMID 30918065 DOI: 10.1194/Jlr.P090449 |
0.362 |
|
| 2019 |
Newton CA, Oldham JM, Ley B, Anand V, Adegunsoye A, Liu G, Batra K, Torrealba J, Kozlitina J, Glazer C, Strek ME, Wolters PJ, Noth I, Garcia CK. Telomere Length and Genetic Variant Associations with Interstitial Lung Disease Progression and Survival. The European Respiratory Journal. PMID 30635297 DOI: 10.1183/13993003.01641-2018 |
0.314 |
|
| 2018 |
Abul-Husn NS, Cheng X, Li AH, Xin Y, Schurmann C, Stevis P, Liu Y, Kozlitina J, Stender S, Wood GC, Stepanchick AN, Still MD, McCarthy S, O'Dushlaine C, Packer JS, et al. A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease. The New England Journal of Medicine. 378: 1096-1106. PMID 29562163 DOI: 10.1056/Nejmoa1712191 |
0.362 |
|
| 2017 |
Stender S, Kozlitina J, Nordestgaard BG, Tybjærg-Hansen A, Hobbs HH, Cohen JC. Adiposity amplifies the genetic risk of fatty liver disease conferred by multiple loci. Nature Genetics. PMID 28436986 DOI: 10.1038/Ng.3855 |
0.379 |
|
| 2016 |
Kozlitina J, Zhou H, Brown PN, Rohm RJ, Pan Y, Ayanoglu G, Du X, Rimmer E, Reilly DF, Roddy TP, Cully DF, Vogt TF, Blom D, Hoek M. Plasma Levels of Risk-Variant APOL1 Do Not Associate with Renal Disease in a Population-Based Cohort. Journal of the American Society of Nephrology : Jasn. PMID 27005919 DOI: 10.1681/Asn.2015101121 |
0.326 |
|
| 2016 |
Mancina RM, Dongiovanni P, Petta S, Pingitore P, Meroni M, Rametta R, Borén J, Montalcini T, Pujia A, Wiklund O, Hindy G, Spagnuolo R, Motta BM, Pipitone RM, Craxì A, ... ... Kozlitina J, et al. The MBOAT7-TMC4 Variant rs641738 Increases Risk of Nonalcoholic Fatty Liver Disease in Individuals of European Descent. Gastroenterology. PMID 26850495 DOI: 10.1053/J.Gastro.2016.01.032 |
0.348 |
|
| 2015 |
Kozlitina J, Schucany WR. A robust distribution-free test for genetic association studies of quantitative traits. Statistical Applications in Genetics and Molecular Biology. 14: 443-64. PMID 26426896 DOI: 10.1515/Sagmb-2014-0050 |
0.556 |
|
| 2014 |
Kozlitina J, Smagris E, Stender S, Nordestgaard BG, Zhou HH, Tybjærg-Hansen A, Vogt TF, Hobbs HH, Cohen JC. Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease. Nature Genetics. 46: 352-6. PMID 24531328 DOI: 10.1038/Ng.2901 |
0.357 |
|
| 2011 |
Friedman DJ, Kozlitina J, Genovese G, Jog P, Pollak MR. Population-based risk assessment of APOL1 on renal disease. Journal of the American Society of Nephrology : Jasn. 22: 2098-105. PMID 21997396 DOI: 10.1681/Asn.2011050519 |
0.301 |
|
| 2011 |
Kozlitina J, Boerwinkle E, Cohen JC, Hobbs HH. Dissociation between APOC3 variants, hepatic triglyceride content and insulin resistance. Hepatology (Baltimore, Md.). 53: 467-74. PMID 21274868 DOI: 10.1002/Hep.24072 |
0.333 |
|
| 2010 |
Kozlitina J, Xing C, Pertsemlidis A, Schucany WR. Power of genetic association studies with fixed and random genotype frequencies. Annals of Human Genetics. 74: 429-38. PMID 20645958 DOI: 10.1111/J.1469-1809.2010.00598.X |
0.555 |
|
| 2009 |
Romeo S, Yin W, Kozlitina J, Pennacchio LA, Boerwinkle E, Hobbs HH, Cohen JC. Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans. The Journal of Clinical Investigation. 119: 70-9. PMID 19075393 DOI: 10.1172/Jci37118 |
0.318 |
|
| 2008 |
Romeo S, Kozlitina J, Xing C, Pertsemlidis A, Cox D, Pennacchio LA, Boerwinkle E, Cohen JC, Hobbs HH. Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease. Nature Genetics. 40: 1461-5. PMID 18820647 DOI: 10.1038/Ng.257 |
0.371 |
|
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