Publications:

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Comprehensive proteogenomic characterization of early duodenal cancer reveals the carcinogenesis tracks of different subtypes.

Nature Communications

Li, Lingling L; Jiang, Dongxian D; Liu, Hui H; Guo, Chunmei C; Zhao, Rui R; Zhang, Qiao Q; Xu, Chen C; Qin, Zhaoyu Z; Feng, Jinwen J; Liu, Yang Y; Wang, Haixing H; Chen, Weijie W; Zhang, Xue X; Li, Bin B; Bai, Lin L; Tian, Sha S; Tan, Subei S; Yu, Zixiang Z; Chen, Lingli L; Huang, Jie J; Zhao, Jian-Yuan JY; Hou, Yingyong Y; Ding, Chen C

Publication Date: 2023-03-29

Variant appearance in text: rs2076167

PubMed Link: 36991000

Variant Present in the following documents:

• 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3

View BVdb publication page

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The Influence of the Differentiation of Genes Encoding Peroxisome Proliferator-Activated Receptors and Their Coactivators on Nutrient and Energy Metabolism.

Nutrients

Maciejewska-Skrendo, Agnieszka A; Massidda, Myosotis M; Tocco, Filippo F; Leźnicka, Katarzyna K

Publication Date: 2022-12-18

Variant appearance in text: rs2076167

PubMed Link: 36558537

Variant Present in the following documents:

• Main text
• nutrients-14-05378.pdf

View BVdb publication page

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Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem

Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS

Publication Date: 2022-11

Variant appearance in text: PPARD: N163N; rs2076167

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

View BVdb publication page

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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: PPARD: N163N

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM13_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM10_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM6_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM11_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM4_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM2_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM5_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM12_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM9_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM3_ESM.xlsx, sheet 2

View BVdb publication page

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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: PPARD: N163N

PubMed Link: 36075891

Variant Present in the following documents:

• 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
• 41439_2022_208_MOESM3_ESM.xlsx, sheet 2

View BVdb publication page

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Genomic, transcriptomic, and metabolomic profiles of hiPSC-derived dopamine neurons from clinically discordant brothers with identical PRKN deletions.

Npj Parkinson'S Disease

Cukier, Holly N HN; Kim, Hyunjin H; Griswold, Anthony J AJ; Codreanu, Simona G SG; Prince, Lisa M LM; Sherrod, Stacy D SD; McLean, John A JA; Dykxhoorn, Derek M DM; Ess, Kevin C KC; Hedera, Peter P; Bowman, Aaron B AB; Neely, M Diana MD

Publication Date: 2022-06-29

Variant appearance in text: rs2076167

PubMed Link: 35768426

Variant Present in the following documents:

• 41531_2022_346_MOESM2_ESM.xlsx, sheet 1

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: PPARD: N163N; rs2076167

PubMed Link: 34621706

Variant Present in the following documents:

• tcp-29-135-s001.xls, sheet 1

View BVdb publication page

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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: PPARD: 489C>T; rs2076167

PubMed Link: 34054912

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology

Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA

Publication Date: 2021

Variant appearance in text: PPARD: N163N; rs2076167

PubMed Link: 33791233

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Identification of a nonsense mutation in TNNI3K associated with cardiac conduction disease.

Journal Of Clinical Laboratory Analysis

Liu, Jiang J; Liu, Da D; Li, Muzheng M; Wu, Keke K; Liu, Na N; Zhao, Chenyu C; Shi, Xiaoliu X; Liu, Qiming Q

Publication Date: 2020-09

Variant appearance in text: PPARD: N163N; rs2076167

PubMed Link: 32529721

Variant Present in the following documents:

• JCLA-34-e23418-s003.xls, sheet 1

View BVdb publication page

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Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.

Bmc Cardiovascular Disorders

Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M

Publication Date: 2020-02-11

Variant appearance in text: PPARD: 489C>T; rs2076167

PubMed Link: 32046637

Variant Present in the following documents:

• 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1

View BVdb publication page

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Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports

Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA

Publication Date: 2019-10-09

Variant appearance in text: PPARD: N163N; rs2076167

PubMed Link: 31597922

Variant Present in the following documents:

• 41598_2019_50891_MOESM5_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM9_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM7_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM6_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM4_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM8_ESM.xlsx, sheet 1

View BVdb publication page

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Multiple genetic mutations caused by NKX6.3 depletion contribute to gastric tumorigenesis.

Scientific Reports

Yoon, Jung Hwan JH; Kim, Olga O; Eun, Jung Woo JW; Choi, Sung Sook SS; Ashktorab, Hassan H; Smoot, Duane T DT; Nam, Suk Woo SW; Park, Won Sang WS

Publication Date: 2018-12-04

Variant appearance in text: rs2076167

PubMed Link: 30514953

Variant Present in the following documents:

• 41598_2018_35733_MOESM2_ESM.xlsx, sheet 1

View BVdb publication page

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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology

Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P

Publication Date: 2018

Variant appearance in text: PPARD: 489C>T; rs2076167

PubMed Link: 30319441

Variant Present in the following documents:

• Table_7.xlsx, sheet 1
• Table_6.xlsx, sheet 1

View BVdb publication page

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The Role of Peroxisome Proliferator-Activated Receptors and Their Transcriptional Coactivators Gene Variations in Human Trainability: A Systematic Review.

International Journal Of Molecular Sciences

Petr, Miroslav M; Stastny, Petr P; Zajac, Adam A; Tufano, James J JJ; Maciejewska-Skrendo, Agnieszka A

Publication Date: 2018-05-15

Variant appearance in text: rs2076167

PubMed Link: 29762540

Variant Present in the following documents:

• Main text
• ijms-19-01472.pdf

View BVdb publication page

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Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget

Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH

Publication Date: 2017-11-10

Variant appearance in text: PPARD: N163N; rs2076167

PubMed Link: 29221171

Variant Present in the following documents:

• oncotarget-08-95841-s002.xlsx, sheet 1
• oncotarget-08-95841-s002.xlsx, sheet 4

View BVdb publication page

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Genes to predict VO2max trainability: a systematic review.

Bmc Genomics

Williams, Camilla J CJ; Williams, Mark G MG; Eynon, Nir N; Ashton, Kevin J KJ; Little, Jonathan P JP; Wisloff, Ulrik U; Coombes, Jeff S JS

Publication Date: 2017-11-14

Variant appearance in text: rs2076167

PubMed Link: 29143670

Variant Present in the following documents:

• Main text
• 12864_2017_Article_4192.pdf

View BVdb publication page

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Genetic variants of increased waist circumference in psychosis.

Psychiatric Genetics

Hukic, Dzana S DS; Ösby, Urban U; Olsson, Eric E; Hilding, Agneta A; Östenson, Claes-Göran CG; Gu, Harvest F HF; Ehrenborg, Ewa E; Edman, Gunnar G; Schalling, Martin M; Lavebratt, Catharina C; Frisén, Louise L

Publication Date: 2017-12

Variant appearance in text: rs2076167

PubMed Link: 28737528

Variant Present in the following documents:

• ypg-27-210.pdf

View BVdb publication page

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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: rs2076167

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

View BVdb publication page

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Role of Helicobacter pylori infection in pathogenesis of gastric carcinoma.

World Journal Of Gastrointestinal Pathophysiology

Zhang, Rong-Guang RG; Duan, Guang-Cai GC; Fan, Qing-Tang QT; Chen, Shuai-Yin SY

Publication Date: 2016-02-15

Variant appearance in text: rs2076167

PubMed Link: 26909232

Variant Present in the following documents:

• Main text

View BVdb publication page

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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: PPARD: N163N; rs2076167

PubMed Link: 26549847

Variant Present in the following documents:

• mmc3.xlsx, sheet 3
• mmc3.xlsx, sheet 1
• mmc3.xlsx, sheet 2

View BVdb publication page

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Susceptible gene of stasis-stagnation constitution from genome-wide association study related to cardiovascular disturbance and possible regulated traditional Chinese medicine.

Bmc Complementary And Alternative Medicine

Huang, Kuo-Chin KC; Huang, Hung-Jin HJ; Chen, Ching-Chu CC; Chang, Chwen-Tzuei CT; Wang, Tzu-Yuan TY; Chen, Rong-Hsing RH; Chen, Yu-Chian YC; Tsai, Fuu-Jen FJ

Publication Date: 2015-07-14

Variant appearance in text: rs2076167

PubMed Link: 26169365

Variant Present in the following documents:

• Main text

View BVdb publication page

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Role of peroxisome proliferator-activated receptors gene polymorphisms in type 2 diabetes and metabolic syndrome.

World Journal Of Diabetes

Dong, Chen C; Zhou, Hui H; Shen, Chong C; Yu, Lu-Gang LG; Ding, Yi Y; Zhang, Yong-Hong YH; Guo, Zhi-Rong ZR

Publication Date: 2015-05-15

Variant appearance in text: rs2076167

PubMed Link: 25987964

Variant Present in the following documents:

• Main text

View BVdb publication page

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Integrative and systemic approaches for evaluating PPARβ/δ (PPARD) function.

Nuclear Receptor Signaling

Giordano Attianese, Greta M P GM; Desvergne, Béatrice B

Publication Date: 2015

Variant appearance in text: PPARD: 489C>T; rs2076167

PubMed Link: 25945080

Variant Present in the following documents:

• Main text
• nrs-13-001.pdf

View BVdb publication page

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Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget

Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S

Publication Date: 2015-06-20

Variant appearance in text: PPARD: N163N; rs2076167

PubMed Link: 25944692

Variant Present in the following documents:

• oncotarget-06-15375-s005.xlsx, sheet 2

View BVdb publication page

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The Affymetrix DMET Plus platform reveals unique distribution of ADME-related variants in ethnic Arabs.

Disease Markers

Wakil, Salma M SM; Nguyen, Cao C; Muiya, Nzioka P NP; Andres, Editha E; Lykowska-Tarnowska, Agnieszka A; Baz, Batoul B; Tahir, Asma I AI; Meyer, Brian F BF; Morahan, Grant G; Dzimiri, Nduna N

Publication Date: 2015

Variant appearance in text: rs2076167

PubMed Link: 25802476

Variant Present in the following documents:

• 542543.f1.xlsx, sheet 1

View BVdb publication page

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Whole-genome sequencing of the world's oldest people.

Plos One

Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK

Publication Date: 2014

Variant appearance in text: PPARD: N163N; rs2076167

PubMed Link: 25390934

Variant Present in the following documents:

• pone.0112430.s004.xlsx, sheet 1

View BVdb publication page

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CardioGxE, a catalog of gene-environment interactions for cardiometabolic traits.

Biodata Mining

Parnell, Laurence D LD; Blokker, Britt A BA; Dashti, Hassan S HS; Nesbeth, Paula-Dene PD; Cooper, Brittany Elle BE; Ma, Yiyi Y; Lee, Yu-Chi YC; Hou, Ruixue R; Lai, Chao-Qiang CQ; Richardson, Kris K; Ordovás, José M JM

Publication Date: 2014

Variant appearance in text: rs2076167

PubMed Link: 25368670

Variant Present in the following documents:

• Main text
• 1756-0381-7-21.pdf

View BVdb publication page

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The RPTEC/TERT1 cell line models key renal cell responses to the environmental toxicants, benzo[a]pyrene and cadmium.

Toxicology Reports

Simon, B R BR; Wilson, M J MJ; Wickliffe, J K JK

Publication Date: 2014

Variant appearance in text: rs2076167

PubMed Link: 25126521

Variant Present in the following documents:

• mmc1.xls, sheet 1

View BVdb publication page

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Polymorphisms of peroxisome proliferator-activated receptors and survival of lung cancer and upper aero-digestive tract cancers.

Lung Cancer (Amsterdam, Netherlands)

Yang, Ying Y; Burke, Rita V RV; Jeon, Christie Y CY; Chang, Shen-Chih SC; Chang, Po-Yin PY; Morgenstern, Hal H; Tashkin, Donald P DP; Mao, Jenny J; Cozen, Wendy W; Mack, Thomas M TM; Rao, Jianyu J; Zhang, Zuo-Feng ZF

Publication Date: 2014-09

Variant appearance in text: rs2076167

PubMed Link: 25043640

Variant Present in the following documents:

• Main text

View BVdb publication page

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Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.

Febs Open Bio

Szeto, Carol Ying-Ying CY; Lin, Chi Ho CH; Choi, Siu Chung SC; Yip, Timothy T C TT; Ngan, Roger Kai-Cheong RK; Tsao, George Sai-Wah GS; Li Lung, Maria M

Publication Date: 2014

Variant appearance in text: rs2076167

PubMed Link: 24490137

Variant Present in the following documents:

• mmc5.xlsx, sheet 2

View BVdb publication page

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Variants of the PPARD gene and their clinicopathological significance in colorectal cancer.

Plos One

Ticha, Ivana I; Gnosa, Sebastian S; Lindblom, Annika A; Liu, Tao T; Sun, Xiao-Feng XF

Publication Date: 2013

Variant appearance in text: PPARD: 489C>T; rs2076167

PubMed Link: 24391853

Variant Present in the following documents:

• Main text

View BVdb publication page

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Polymorphisms in PPAR Genes (PPARD, PPARG, and PPARGC1A) and the Risk of Chronic Kidney Disease in Japanese: Cross-Sectional Data from the J-MICC Study.

Ppar Research

Hishida, Asahi A; Wakai, Kenji K; Naito, Mariko M; Tamura, Takashi T; Kawai, Sayo S; Hamajima, Nobuyuki N; Oze, Isao I; Imaizumi, Takeshi T; Turin, Tanvir Chowdhury TC; Suzuki, Sadao S; Kheradmand, Motahare M; Mikami, Haruo H; Ohnaka, Keizo K; Watanabe, Yoshiyuki Y; Arisawa, Kokichi K; Kubo, Michiaki M; Tanaka, Hideo H

Publication Date: 2013

Variant appearance in text: PPARD: Asn163Asn; rs2076167

PubMed Link: 24288525

Variant Present in the following documents:

• Main text
• PPAR2013-980471.pdf

View BVdb publication page

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Effect of a poly(ADP-ribose) polymerase-1 inhibitor against esophageal squamous cell carcinoma cell lines.

Cancer Science

Nasuno, Tomomitsu T; Mimaki, Sachiyo S; Okamoto, Makito M; Esumi, Hiroyasu H; Tsuchihara, Katsuya K

Publication Date: 2014-02

Variant appearance in text: PPARD: N163N; rs2076167

PubMed Link: 24219164

Variant Present in the following documents:

• cas0105-0202-SD2.xlsx, sheet 1
• cas0105-0202-SD3.xlsx, sheet 1

View BVdb publication page

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Genetic variants of peroxisome proliferator-activated receptor δ are associated with gastric cancer.

Digestive Diseases And Sciences

Jeon, Christie C; Chang, Shen-Chih SC; Mu, Lina L; Zhao, Jinkou J; Rao, Jian-Yu JY; Lu, Qing-Yi QY; Zhang, Zuo-Feng ZF

Publication Date: 2013-10

Variant appearance in text: rs2076167

PubMed Link: 23907334

Variant Present in the following documents:

• Main text

View BVdb publication page

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Profile of participants and genotype distributions of 108 polymorphisms in a cross-sectional study of associations of genotypes with lifestyle and clinical factors: a project in the Japan Multi-Institutional Collaborative Cohort (J-MICC) Study.

Journal Of Epidemiology

Wakai, Kenji K; Hamajima, Nobuyuki N; Okada, Rieko R; Naito, Mariko M; Morita, Emi E; Hishida, Asahi A; Kawai, Sayo S; Nishio, Kazuko K; Yin, Guang G; Asai, Yatami Y; Matsuo, Keitaro K; Hosono, Satoyo S; Ito, Hidemi H; Watanabe, Miki M; Kawase, Takakazu T; Suzuki, Takeshi T; Tajima, Kazuo K; Tanaka, Keitaro K; Higaki, Yasuki Y; Hara, Megumi M; Imaizumi, Takeshi T; Taguchi, Naoto N; Nakamura, Kazuyo K; Nanri, Hinako H; Sakamoto, Tatsuhiko T; Horita, Mikako M; Shinchi, Koichi K; Kita, Yoshikuni Y; Turin, Tanvir Chowdhury TC; Rumana, Nahid N; Matsui, Kenji K; Miura, Katsuyuki K; Ueshima, Hirotsugu H; Takashima, Naoyuki N; Nakamura, Yasuyuki Y; Suzuki, Sadao S; Ando, Ryosuke R; Hosono, Akihiro A; Imaeda, Nahomi N; Shibata, Kiyoshi K; Goto, Chiho C; Hattori, Nami N; Fukatsu, Mitsuru M; Yamada, Tamaki T; Tokudome, Shinkan S; Takezaki, Toshiro T; Niimura, Hideshi H; Hirasada, Kazuyo K; Nakamura, Akihiko A; Tatebo, Masaya M; Ogawa, Shin S; Tsunematsu, Noriko N; Chiba, Shirabe S; Mikami, Haruo H; Kono, Suminori S; Ohnaka, Keizo K; Takayanagi, Ryoichi R; Watanabe, Yoshiyuki Y; Ozaki, Etsuko E; Shigeta, Masako M; Kuriyama, Nagato N; Yoshikawa, Aya A; Matsui, Daisuke D; Watanabe, Isao I; Inoue, Kaoru K; Ozasa, Kotaro K; Mitani, Satoko S; Arisawa, Kokichi K; Uemura, Hirokazu H; Hiyoshi, Mineyoshi M; Takami, Hidenobu H; Yamaguchi, Miwa M; Nakamoto, Mariko M; Takeda, Hideo H; Kubo, Michiaki M; Tanaka, Hideo H; ,

Publication Date: 2011

Variant appearance in text: PPARD: Asn163Asn; rs2076167

PubMed Link: 21467728

Variant Present in the following documents:

• Main text

View BVdb publication page

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Single nucleotide polymorphisms in the Wnt and BMP pathways and colorectal cancer risk in a Spanish cohort.

Plos One

Fernández-Rozadilla, Ceres C; de Castro, Luisa L; Clofent, Juan J; Brea-Fernández, Alejandro A; Bessa, Xavier X; Abulí, Anna A; Andreu, Montserrat M; Jover, Rodrigo R; Xicola, Rosa R; Llor, Xavier X; Castells, Antoni A; Castellví-Bel, Sergi S; Carracedo, Angel A; Ruiz-Ponte, Clara C; ,

Publication Date: 2010-09-09

Variant appearance in text: PPARD: N163N; rs2076167

PubMed Link: 20844743

Variant Present in the following documents:

• Main text
• pone.0012673.pdf

View BVdb publication page

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Interaction between Calpain 5, Peroxisome proliferator-activated receptor-gamma and Peroxisome proliferator-activated receptor-delta genes: a polygenic approach to obesity.

Cardiovascular Diabetology

Sáez, María E ME; Grilo, Antonio A; Morón, Francisco J FJ; Manzano, Luis L; Martínez-Larrad, María T MT; González-Pérez, Antonio A; Serrano-Hernando, Javier J; Ruiz, Agustín A; Ramírez-Lorca, Reposo R; Serrano-Ríos, Manuel M

Publication Date: 2008-07-25

Variant appearance in text: rs2076167

PubMed Link: 18657264

Variant Present in the following documents:

• Main text
• 1475-2840-7-23.pdf

View BVdb publication page

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Association study of Wnt signaling pathway genes in bipolar disorder.

Archives Of General Psychiatry

Zandi, Peter P PP; Belmonte, Pamela L PL; Willour, Virginia L VL; Goes, Fernando S FS; Badner, Judith A JA; Simpson, Sylvia G SG; Gershon, Elliot S ES; McMahon, Francis J FJ; DePaulo, J Raymond JR; Potash, James B JB; , ; ,

Publication Date: 2008-07

Variant appearance in text: rs2076167

PubMed Link: 18606951

Variant Present in the following documents:

• Main text

View BVdb publication page

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SNP genotyping on a genome-wide amplified DOP-PCR template.

Nucleic Acids Research

Grant, Struan F A SF; Steinlicht, Simone S; Nentwich, Ulrike U; Kern, Rainer R; Burwinkel, Barbara B; Tolle, Ralf R

Publication Date: 2002-11-15

Variant appearance in text: rs2076167

PubMed Link: 12434007

Variant Present in the following documents:

• Main text

View BVdb publication page

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