Publications:

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G Allele of the rs1801282 Polymorphism in PPARγ Gene Confers an Increased Risk of Obesity and Hypercholesterolemia, While T Allele of the rs3856806 Polymorphism Displays a Protective Role Against Dyslipidemia: A Systematic Review and Meta-Analysis.

Frontiers In Endocrinology

Li, Shujin S; He, Chuan C; Nie, Haiyan H; Pang, Qianyin Q; Wang, Ruixia R; Zeng, Zhifu Z; Song, Yongyan Y

Publication Date: 2022

Variant appearance in text: PPARG: 1431C>T

PubMed Link: 35846293

Variant Present in the following documents:

• Main text
• fendo-13-919087.pdf

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PPARγ Gene Polymorphisms, Metabolic Disorders, and Coronary Artery Disease.

Frontiers In Cardiovascular Medicine

Song, Yongyan Y; Li, Shujin S; He, Chuan C

Publication Date: 2022

Variant appearance in text: PPARG: 1431C>T

PubMed Link: 35402540

Variant Present in the following documents:

• Main text
• fcvm-09-808929.pdf

View BVdb publication page

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Comprehensive analysis of important pharmacogenes in Koreans using the DMET™ platform.

Translational And Clinical Pharmacology

Kim, Byungwook B; Yoon, Deok Yong DY; Lee, SeungHwan S; Jang, In-Jin IJ; Yu, Kyung-Sang KS; Cho, Joo-Youn JY; Oh, Jaeseong J

Publication Date: 2021-09

Variant appearance in text: PPARG: 1431C>T

PubMed Link: 34621706

Variant Present in the following documents:

• tcp-29-135-s001.xls, sheet 1

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Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes.

Frontiers In Genetics

Feng, Wei-Xing WX; Zhuo, Xiu-Wei XW; Liu, Zhi-Mei ZM; Li, Jiu-Wei JW; Zhang, Wei-Hua WH; Wu, Yun Y; Han, Tong-Li TL; Fang, Fang F

Publication Date: 2021

Variant appearance in text: PPARG: 1431C>T

PubMed Link: 34054912

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

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Six years' experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemias.

Bmc Medical Genomics

Dron, Jacqueline S JS; Wang, Jian J; McIntyre, Adam D AD; Iacocca, Michael A MA; Robinson, John F JF; Ban, Matthew R MR; Cao, Henian H; Hegele, Robert A RA

Publication Date: 2020-02-10

Variant appearance in text: PPARG: 1431C>T

PubMed Link: 32041611

Variant Present in the following documents:

• 12920_2020_669_MOESM1_ESM.xlsx, sheet 3

View BVdb publication page

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PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology

Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S

Publication Date: 2019-10-22

Variant appearance in text: PPARG: 1431C>T

PubMed Link: 31640808

Variant Present in the following documents:

• 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1

View BVdb publication page

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A pan-cancer analysis of synonymous mutations.

Nature Communications

Sharma, Yogita Y; Miladi, Milad M; Dukare, Sandeep S; Boulay, Karine K; Caudron-Herger, Maiwen M; Groß, Matthias M; Backofen, Rolf R; Diederichs, Sven S

Publication Date: 2019-06-12

Variant appearance in text: PPARG: 1431C>T

PubMed Link: 31189880

Variant Present in the following documents:

• 41467_2019_10489_MOESM7_ESM.xlsx, sheet 1

View BVdb publication page

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Association of MTTP gene variants with pediatric NAFLD: A candidate-gene-based analysis of single nucleotide variations in obese children.

Plos One

Dai, Dongling D; Wen, Feiqiu F; Zhou, Shaoming S; Su, Zhe Z; Liu, Guosheng G; Wang, Mingbang M; Zhou, Jianli J; He, Fusheng F

Publication Date: 2017

Variant appearance in text: PPARG: 1431C>T

PubMed Link: 28953935

Variant Present in the following documents:

• pone.0185396.s001.xls, sheet 3
• pone.0185396.s001.xls, sheet 1
• pone.0185396.s001.xls, sheet 2

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Sporadic hemangioblastomas are characterized by cryptic VHL inactivation.

Acta Neuropathologica Communications

Shankar, Ganesh M GM; Taylor-Weiner, Amaro A; Lelic, Nina N; Jones, Robert T RT; Kim, James C JC; Francis, Joshua M JM; Abedalthagafi, Malak M; Borges, Lawrence F LF; Coumans, Jean-Valery JV; Curry, William T WT; Nahed, Brian V BV; Shin, John H JH; Paek, Sun Ha SH; Park, Sung-Hye SH; Stewart, Chip C; Lawrence, Michael S MS; Cibulskis, Kristian K; Thorner, Aaron R AR; Van Hummelen, Paul P; Stemmer-Rachamimov, Anat O AO; Batchelor, Tracy T TT; Carter, Scott L SL; Hoang, Mai P MP; Santagata, Sandro S; Louis, David N DN; Barker, Fred G FG; Meyerson, Matthew M; Getz, Gad G; Brastianos, Priscilla K PK; Cahill, Daniel P DP

Publication Date: 2014-12-24

Variant appearance in text: PPARG: 1431C>T

PubMed Link: 25589003

Variant Present in the following documents:

• 40478_2014_167_MOESM1_ESM.xlsx, sheet 6

View BVdb publication page

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Low-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study.

Bmc Cancer

Küry, Sébastien S; Buecher, Bruno B; Robiou-du-Pont, Sébastien S; Scoul, Catherine C; Colman, Hélène H; Le Neel, Tanguy T; Le Houérou, Claire C; Faroux, Roger R; Ollivry, Jean J; Lafraise, Bernard B; Chupin, Louis-Dominique LD; Sébille, Véronique V; Bézieau, Stéphane S

Publication Date: 2008-11-07

Variant appearance in text: PPARG: 1431C>T

PubMed Link: 18992148

Variant Present in the following documents:

• Main text
• 1471-2407-8-326-S4.xls, sheet 1
• 1471-2407-8-326-S3.xls, sheet 1
• 1471-2407-8-326.pdf
• 1471-2407-8-326-S2.xls, sheet 1

View BVdb publication page

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