Publications:

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Genetic Polymorphisms and Diversity in Nonalcoholic Fatty Liver Disease (NAFLD): A Mini Review.

Biomedicines

Sulaiman, Siti Aishah SA; Dorairaj, Vicneswarry V; Adrus, Muhammad Nafiz Haidi MNH

Publication Date: 2022-12-30

Variant appearance in text: rs2070666

PubMed Link: 36672614

Variant Present in the following documents:

• Main text
• biomedicines-11-00106.pdf

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Unique genetic variants of lean nonalcoholic fatty liver disease: a retrospective cohort study.

Bmc Endocrine Disorders

Li, Jie J; Wu, Na N; Yang, Yukun Y; Zhai, Xiangyu X; Yuan, Fan F; Zhang, Fengwei F; Yu, Ning N; Li, Dong D; Wang, Ruirui R; Wang, Jianying J; Zhang, Lei L; Shi, Yi Y; He, Guang G; Liu, Baocheng B

Publication Date: 2023-01-10

Variant appearance in text: rs2070666

PubMed Link: 36627697

Variant Present in the following documents:

• Main text
• 12902_2022_Article_1234.pdf

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Update on genetics and epigenetics in metabolic associated fatty liver disease.

Therapeutic Advances In Endocrinology And Metabolism

Zhu, Xiaopeng X; Xia, Mingfeng M; Gao, Xin X

Publication Date: 2022

Variant appearance in text: rs2070666

PubMed Link: 36325500

Variant Present in the following documents:

• Main text
• 10.1177_20420188221132138.pdf

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Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports

Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-10-14

Variant appearance in text: rs2070666

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2

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Expanding the phenotypic spectrum of non-alcoholic fatty liver disease and hypertriglyceridemia.

Frontiers In Nutrition

Meroni, Marica M; Longo, Miriam M; Paolini, Erika E; Tria, Giada G; Ripolone, Michela M; Napoli, Laura L; Moggio, Maurizio M; Fracanzani, Anna Ludovica AL; Dongiovanni, Paola P

Publication Date: 2022

Variant appearance in text: rs2070666

PubMed Link: 36185699

Variant Present in the following documents:

• Main text
• fnut-09-967899.pdf

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A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation

Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-09-08

Variant appearance in text: rs2070666

PubMed Link: 36075891

Variant Present in the following documents:

• 41439_2022_208_MOESM3_ESM.xlsx, sheet 2

View BVdb publication page

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Association between APOC3 polymorphisms and non-alcoholic fatty liver disease risk: a meta-analysis.

African Health Sciences

Wang, Jun J; Ye, Chuncui C; Fei, Sujuan S

Publication Date: 2020-12

Variant appearance in text: rs2070666

PubMed Link: 34394242

Variant Present in the following documents:

• AFHS2004-1800.pdf

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Association between PNPLA3 rs738409 polymorphism and nonalcoholic fatty liver disease: a systematic review and meta-analysis.

Bmc Endocrine Disorders

Salari, Nader N; Darvishi, Niloufar N; Mansouri, Kamran K; Ghasemi, Hooman H; Hosseinian-Far, Melika M; Darvishi, Fateme F; Mohammadi, Masoud M

Publication Date: 2021-06-19

Variant appearance in text: rs2070666

PubMed Link: 34147109

Variant Present in the following documents:

• 12902_2021_Article_789.pdf

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APOC3 rs2070667 Associates with Serum Triglyceride Profile and Hepatic Inflammation in Nonalcoholic Fatty Liver Disease.

Biomed Research International

Xu, Qing-Yang QY; Li, Han H; Cao, Hai-Xia HX; Pan, Qin Q; Fan, Jian-Gao JG

Publication Date: 2020

Variant appearance in text: rs2070666

PubMed Link: 33294458

Variant Present in the following documents:

• Main text
• BMRI2020-8869674.pdf

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Prevalence, clinical characteristics, risk factors, and indicators for lean Chinese adults with nonalcoholic fatty liver disease.

World Journal Of Gastroenterology

Zeng, Jing J; Yang, Rui-Xu RX; Sun, Chao C; Pan, Qin Q; Zhang, Rui-Nan RN; Chen, Guang-Yu GY; Hu, Ying Y; Fan, Jian-Gao JG

Publication Date: 2020-04-21

Variant appearance in text: rs2070666

PubMed Link: 32351294

Variant Present in the following documents:

• Main text
• WJG-26-1792.pdf

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Association between Genetic Variant of Apolipoprotein C3 and Incident Hypertension Stratified by Obesity and Physical Activity in Korea.

Nutrients

Jo, Garam G; Kwak, So-Young SY; Kim, Ji Young JY; Lim, Hyunjung H; Shin, Min-Jeong MJ

Publication Date: 2018-10-30

Variant appearance in text: rs2070666

PubMed Link: 30380775

Variant Present in the following documents:

• nutrients-10-01595.pdf

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Disturbed Vitamin A Metabolism in Non-Alcoholic Fatty Liver Disease (NAFLD).

Nutrients

Saeed, Ali A; Dullaart, Robin P F RPF; Schreuder, Tim C M A TCMA; Blokzijl, Hans H; Faber, Klaas Nico KN

Publication Date: 2017-12-29

Variant appearance in text: rs2070666

PubMed Link: 29286303

Variant Present in the following documents:

• nutrients-10-00029.pdf

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Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation

Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H

Publication Date: 2017

Variant appearance in text: rs2070666

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

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Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports

Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC

Publication Date: 2015-12-08

Variant appearance in text: rs2070666

PubMed Link: 26549847

Variant Present in the following documents:

• mmc3.xlsx, sheet 1

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