PLPP3 c.811-3316G>A

Variant ID: 1-56965664-C-T

NM_003713.4(PLPP3):c.811-3316G>A

This variant was identified in 14 publications

View GRCh38 version.




Publications:


Etiologic Puzzle of Coronary Artery Disease: How Important Is Genetic Component?

Life (Basel, Switzerland)
Butnariu, Lăcrămioara Ionela LI; Florea, Laura L; Badescu, Minerva Codruta MC; Țarcă, Elena E; Costache, Irina-Iuliana II; Gorduza, Eusebiu Vlad EV
Publication Date: 2022-06-09

Variant appearance in text: rs9970807
PubMed Link: 35743896
Variant Present in the following documents:
  • life-12-00865.pdf
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Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control.

Diabetologia
Tremblay, Johanne J; Haloui, Mounsif M; Attaoua, Redha R; Tahir, Ramzan R; Hishmih, Camil C; Harvey, François F; Marois-Blanchet, François-Christophe FC; Long, Carole C; Simon, Paul P; Santucci, Lara L; Hizel, Candan C; Chalmers, John J; Marre, Michel M; Harrap, Stephen S; Cífková, Renata R; Krajčoviechová, Alena A; Matthews, David R DR; Williams, Bryan B; Poulter, Neil N; Zoungas, Sophia S; Colagiuri, Stephen S; Mancia, Giuseppe G; Grobbee, Diederick E DE; Rodgers, Anthony A; Liu, Liusheng L; Agbessi, Mawussé M; Bruat, Vanessa V; Favé, Marie-Julie MJ; Harwood, Michelle P MP; Awadalla, Philip P; Woodward, Mark M; Hussin, Julie G JG; Hamet, Pavel P
Publication Date: 2021-09

Variant appearance in text: rs9970807
PubMed Link: 34226943
Variant Present in the following documents:
  • 125_2021_5491_MOESM1_ESM.pdf
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Genetic variant at coronary artery disease and ischemic stroke locus 1p32.2 regulates endothelial responses to hemodynamics.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Krause, Matthew D MD; Huang, Ru-Ting RT; Wu, David D; Shentu, Tzu-Pin TP; Harrison, Devin L DL; Whalen, Michael B MB; Stolze, Lindsey K LK; Di Rienzo, Anna A; Moskowitz, Ivan P IP; Civelek, Mete M; Romanoski, Casey E CE; Fang, Yun Y
Publication Date: 2018-11-27

Variant appearance in text: rs9970807
PubMed Link: 30429326
Variant Present in the following documents:
  • pnas.1810568115.sapp.pdf
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Tissue-specific Network Analysis of Genetic Variants Associated with Coronary Artery Disease.

Scientific Reports
Miao, Xiao X; Chen, Xinlin X; Xie, Zhijun Z; Lin, Honghuang H
Publication Date: 2018-07-31

Variant appearance in text: rs9970807
PubMed Link: 30065343
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_29904.pdf
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Integrated Human Evaluation of the Lysophosphatidic Acid Pathway as a Novel Therapeutic Target in Atherosclerosis.

Molecular Therapy. Methods & Clinical Development
Aldi, Silvia S; Matic, Ljubica Perisic LP; Hamm, Gregory G; van Keulen, Daniëlle D; Tempel, Dennie D; Holmstrøm, Kim K; Szwajda, Agnieszka A; Nielsen, Boye Schnack BS; Emilsson, Valur V; Ait-Belkacem, Rima R; Lengquist, Mariette M; Paulsson-Berne, Gabrielle G; Eriksson, Per P; Lindeman, Jan H N JHN; Gool, Alain J AJ; Stauber, Jonathan J; Hedin, Ulf U; Hurt-Camejo, Eva E
Publication Date: 2018-09-21

Variant appearance in text: rs9970807
PubMed Link: 30003117
Variant Present in the following documents:
  • Main text
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Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes.

Cardiovascular Diabetology
Charmet, Romain R; Duffy, Seamus S; Keshavarzi, Sareh S; Gyorgy, Beata B; Marre, Michel M; Rossing, Peter P; McKnight, Amy Jayne AJ; Maxwell, Alexander P AP; Ahluwalia, Tarun Veer Singh TVS; Paterson, Andrew D AD; Trégouët, David-Alexandre DA; Hadjadj, Samy S
Publication Date: 2018-04-25

Variant appearance in text: rs9970807
PubMed Link: 29695241
Variant Present in the following documents:
  • Main text
  • 12933_2018_Article_705.pdf
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Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia.

Scientific Reports
Han, Yi Y; Dorajoo, Rajkumar R; Chang, Xuling X; Wang, Ling L; Khor, Chiea-Chuen CC; Sim, Xueling X; Cheng, Ching-Yu CY; Shi, Yuan Y; Tham, Yih Chung YC; Zhao, Wanting W; Chee, Miao Ling ML; Sabanayagam, Charumathi C; Chee, Miao Li ML; Tan, Nicholas N; Wong, Tien Yin TY; Tai, E-Shyong ES; Liu, Jianjun J; Goh, Daniel Y T DYT; Yuan, Jian-Min JM; Koh, Woon-Puay WP; van Dam, Rob M RM; Low, Adrian F AF; Chan, Mark Yan-Yee MY; Friedlander, Yechiel Y; Heng, Chew-Kiat CK
Publication Date: 2017-12-20

Variant appearance in text: rs9970807
PubMed Link: 29263402
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_18214.pdf
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Impact of a Genetic Risk Score for Coronary Artery Disease on Reducing Cardiovascular Risk: A Pilot Randomized Controlled Study.

Frontiers In Cardiovascular Medicine
Knowles, Joshua W JW; Zarafshar, Shirin S; Pavlovic, Aleksandra A; Goldstein, Benjamin A BA; Tsai, Sandra S; Li, Jin J; McConnell, Michael V MV; Absher, Devin D; Ashley, Euan A EA; Kiernan, Michaela M; Ioannidis, John P A JPA; Assimes, Themistocles L TL
Publication Date: 2017

Variant appearance in text: rs9970807
PubMed Link: 28856136
Variant Present in the following documents:
  • Main text
View BVdb publication page



Transcriptional networks specifying homeostatic and inflammatory programs of gene expression in human aortic endothelial cells.

Elife
Hogan, Nicholas T NT; Whalen, Michael B MB; Stolze, Lindsey K LK; Hadeli, Nizar K NK; Lam, Michael T MT; Springstead, James R JR; Glass, Christopher K CK; Romanoski, Casey E CE
Publication Date: 2017-06-06

Variant appearance in text: rs9970807
PubMed Link: 28585919
Variant Present in the following documents:
  • Main text
  • elife-22536.pdf
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The Genetic Architecture of Coronary Artery Disease: Current Knowledge and Future Opportunities.

Current Atherosclerosis Reports
Hartiala, Jaana J; Schwartzman, William S WS; Gabbay, Julian J; Ghazalpour, Anatole A; Bennett, Brian J BJ; Allayee, Hooman H
Publication Date: 2017-02

Variant appearance in text: rs9970807
PubMed Link: 28130654
Variant Present in the following documents:
  • Main text
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Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies.

Genome Biology
Joehanes, Roby R; Zhang, Xiaoling X; Huan, Tianxiao T; Yao, Chen C; Ying, Sai-Xia SX; Nguyen, Quang Tri QT; Demirkale, Cumhur Yusuf CY; Feolo, Michael L ML; Sharopova, Nataliya R NR; Sturcke, Anne A; Schäffer, Alejandro A AA; Heard-Costa, Nancy N; Chen, Han H; Liu, Po-Ching PC; Wang, Richard R; Woodhouse, Kimberly A KA; Tanriverdi, Kahraman K; Freedman, Jane E JE; Raghavachari, Nalini N; Dupuis, Josée J; Johnson, Andrew D AD; O'Donnell, Christopher J CJ; Levy, Daniel D; Munson, Peter J PJ
Publication Date: 2017-01-25

Variant appearance in text: rs9970807
PubMed Link: 28122634
Variant Present in the following documents:
  • 13059_2016_1142_MOESM1_ESM.pdf
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From Loci to Biology: Functional Genomics of Genome-Wide Association for Coronary Disease.

Circulation Research
Nurnberg, Sylvia T ST; Zhang, Hanrui H; Hand, Nicholas J NJ; Bauer, Robert C RC; Saleheen, Danish D; Reilly, Muredach P MP; Rader, Daniel J DJ
Publication Date: 2016-02-19

Variant appearance in text: rs9970807
PubMed Link: 26892960
Variant Present in the following documents:
  • Main text
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Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach.

European Journal Of Human Genetics : Ejhg
Versmissen, Jorie J; Oosterveer, Daniëlla M DM; Yazdanpanah, Mojgan M; Dehghan, Abbas A; Hólm, Hilma H; Erdman, Jeanette J; Aulchenko, Yurii S YS; Thorleifsson, Gudmar G; Schunkert, Heribert H; Huijgen, Roeland R; Vongpromek, Ranitha R; Uitterlinden, André G AG; Defesche, Joep C JC; van Duijn, Cornelia M CM; Mulder, Monique M; Dadd, Tony T; Karlsson, Hróbjartur D HD; Ordovas, Jose J; Kindt, Iris I; Jarman, Amelia A; Hofman, Albert A; van Vark-van der Zee, Leonie L; Blommesteijn-Touw, Adriana C AC; Kwekkeboom, Jaap J; Liem, Anho H AH; van der Ouderaa, Frans J FJ; Calandra, Sebastiano S; Bertolini, Stefano S; Averna, Maurizio M; Langslet, Gisle G; Ose, Leiv L; Ros, Emilio E; Almagro, Fátima F; de Leeuw, Peter W PW; Civeira, Fernando F; Masana, Luis L; Pintó, Xavier X; Simoons, Maarten L ML; Schinkel, Arend F L AF; Green, Martin R MR; Zwinderman, Aeilko H AH; Johnson, Keith J KJ; Schaefer, Arne A; Neil, Andrew A; Witteman, Jacqueline C M JC; Humphries, Steve E SE; Kastelein, John J P JJ; Sijbrands, Eric J G EJ
Publication Date: 2015-03

Variant appearance in text: rs9970807
PubMed Link: 24916650
Variant Present in the following documents:
  • Main text
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Randomized trial of personal genomics for preventive cardiology: design and challenges.

Circulation. Cardiovascular Genetics
Knowles, Joshua W JW; Assimes, Themistocles L TL; Kiernan, Michaela M; Pavlovic, Aleksandra A; Goldstein, Benjamin A BA; Yank, Veronica V; McConnell, Michael V MV; Absher, Devin D; Bustamante, Carlos C; Ashley, Euan A EA; Ioannidis, John P A JP
Publication Date: 2012-06

Variant appearance in text: rs9970807
PubMed Link: 22715281
Variant Present in the following documents:
  • Main text
View BVdb publication page