Publications:

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Genetic variants in HFE are associated with non-alcoholic fatty liver disease in lean individuals.

Jhep Reports : Innovation In Hepatology

Sun, Zewen Z; Pan, Xingchen X; Tian, Aowen A; Surakka, Ida I; Wang, Tao T; Jiao, Xu X; He, Shanshan S; Song, Jinfang J; Tian, Xin X; Tong, Dan D; Wen, Jianping J; Zhang, Yonggang Y; Liu, Wanqing W; Chen, Peng P

Publication Date: 2023-07

Variant appearance in text: rs9992651

PubMed Link: 37235137

Variant Present in the following documents:

• mmc1.pdf
• mmc4.pdf

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Assessing causal relationships between sarcopenia and nonalcoholic fatty liver disease: A bidirectional Mendelian randomization study.

Frontiers In Nutrition

Zhao, Ze-Hua ZH; Zou, Juanjuan J; Huang, Xin X; Fan, Yu-Chen YC; Wang, Kai K

Publication Date: 2022

Variant appearance in text: rs9992651

PubMed Link: 36438727

Variant Present in the following documents:

• Main text
• fnut-09-971913.pdf

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Metabolic subtypes of patients with NAFLD exhibit distinctive cardiovascular risk profiles.

Hepatology (Baltimore, Md.)

Martínez-Arranz, Ibon I; Bruzzone, Chiara C; Noureddin, Mazen M; Gil-Redondo, Ruben R; Mincholé, Itziar I; Bizkarguenaga, Maider M; Arretxe, Enara E; Iruarrizaga-Lejarreta, Marta M; Fernández-Ramos, David D; Lopitz-Otsoa, Fernando F; Mayo, Rebeca R; Embade, Nieves N; Newberry, Elizabeth E; Mittendorf, Bettina B; Izquierdo-Sánchez, Laura L; Smid, Vaclav V; Arnold, Jorge J; Iruzubieta, Paula P; Pérez Castaño, Ylenia Y; Krawczyk, Marcin M; Marigorta, Urko M UM; Morrison, Martine C MC; Kleemann, Robert R; Martín-Duce, Antonio A; Hayardeny, Liat L; Vitek, Libor L; Bruha, Radan R; Aller de la Fuente, Rocío R; Crespo, Javier J; Romero-Gomez, Manuel M; Banales, Jesus M JM; Arrese, Marco M; Cusi, Kenneth K; Bugianesi, Elisabetta E; Klein, Samuel S; Lu, Shelly C SC; Anstee, Quentin M QM; Millet, Oscar O; Davidson, Nicholas O NO; Alonso, Cristina C; Mato, José M JM

Publication Date: 2022-10

Variant appearance in text: rs9992651

PubMed Link: 35220605

Variant Present in the following documents:

• Main text
• HEP-76-1121.pdf

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HSD17B13: A Potential Therapeutic Target for NAFLD.

Frontiers In Molecular Biosciences

Zhang, Hai-Bo HB; Su, Wen W; Xu, Hu H; Zhang, Xiao-Yan XY; Guan, You-Fei YF

Publication Date: 2021

Variant appearance in text: rs9992651

PubMed Link: 35071330

Variant Present in the following documents:

• Main text

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Identification of 90 NAFLD GWAS loci and establishment of NAFLD PRS and causal role of NAFLD in coronary artery disease.

Hgg Advances

Miao, Zong Z; Garske, Kristina M KM; Pan, David Z DZ; Koka, Amogha A; Kaminska, Dorota D; Männistö, Ville V; Sinsheimer, Janet S JS; Pihlajamäki, Jussi J; Pajukanta, Päivi P

Publication Date: 2022-01-13

Variant appearance in text: rs9992651

PubMed Link: 35047847

Variant Present in the following documents:

• Main text
• main.pdf
• mmc3.pdf

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Association of Genetic Risk Score With NAFLD in An Ethnically Diverse Cohort.

Hepatology Communications

Wang, Jun J; Conti, David V DV; Bogumil, David D; Sheng, Xin X; Noureddin, Mazen M; Wilkens, Lynne R LR; Le Marchand, Loic L; Rosen, Hugo R HR; Haiman, Christopher A CA; Setiawan, Veronica Wendy VW

Publication Date: 2021-10

Variant appearance in text: rs9992651

PubMed Link: 34558842

Variant Present in the following documents:

• Main text
• HEP4-5-1689.pdf

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Is HSD17B13 Genetic Variant a Protector for Liver Dysfunction? Future Perspective as a Potential Therapeutic Target.

Journal Of Personalized Medicine

Motomura, Takashi T; Amirneni, Sriram S; Diaz-Aragon, Ricardo R; Faccioli, Lanuza A P LAP; Malizio, Michelle R MR; Coard, Michael C MC; Kocas-Kilicarslan, Zehra N ZN; Frau, Carla C; Haep, Nils N; Ostrowska, Alina A; Florentino, Rodrigo M RM; Soto-Gutierrez, Alejandro A

Publication Date: 2021-06-30

Variant appearance in text: rs9992651

PubMed Link: 34208839

Variant Present in the following documents:

• Main text
• jpm-11-00619.pdf

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A closer look at the mysterious HSD17B13.

Journal Of Lipid Research

Dong, X Charlie XC

Publication Date: 2020-11

Variant appearance in text: rs9992651

PubMed Link: 33008926

Variant Present in the following documents:

• Main text

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An exploratory phenome wide association study linking asthma and liver disease genetic variants to electronic health records from the Estonian Biobank.

Plos One

James, Glen G; Reisberg, Sulev S; Lepik, Kaido K; Galwey, Nicholas N; Avillach, Paul P; Kolberg, Liis L; Mägi, Reedik R; Esko, Tõnu T; Alexander, Myriam M; Waterworth, Dawn D; Loomis, A Katrina AK; Vilo, Jaak J

Publication Date: 2019

Variant appearance in text: rs9992651

PubMed Link: 30978214

Variant Present in the following documents:

• Main text
• pone.0215026.pdf

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