SMAD3 c.207-1603C>T

Variant ID: 15-67455630-C-T

NM_005902.3(SMAD3):c.207-1603C>T

This variant was identified in 34 publications

View GRCh38 version.




Publications:


Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation.

Nature Communications
Saarentaus, Elmo C EC; Karjalainen, Juha J; Rämö, Joel T JT; Kiiskinen, Tuomo T; Havulinna, Aki S AS; Mehtonen, Juha J; Hautakangas, Heidi H; Ruotsalainen, Sanni S; Tamlander, Max M; Mars, Nina N; , ; Toppila-Salmi, Sanna S; Pirinen, Matti M; Kurki, Mitja M; Ripatti, Samuli S; Daly, Mark M; Palotie, Tuula T; Mäkitie, Antti A; Palotie, Aarno A
Publication Date: 2023-01-18

Variant appearance in text: rs56062135
PubMed Link: 36653354
Variant Present in the following documents:
  • 41467_2022_Article_33626.pdf
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Association Between Genetic Risk, Adherence to Healthy Lifestyle Behavior, and Thyroid Cancer Risk.

Jama Network Open
Feng, Xiuming X; Wang, Fei F; Yang, Wenjun W; Zheng, Yuan Y; Liu, Chaoqun C; Huang, Lulu L; Li, Longman L; Cheng, Hong H; Cai, Haiqing H; Li, Xiangzhi X; Chen, Xing X; Yang, Xiaobo X
Publication Date: 2022-12-01

Variant appearance in text: rs56062135
PubMed Link: 36508215
Variant Present in the following documents:
  • jamanetwopen-e2246311-s001.pdf
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Genetic Factors for Coronary Heart Disease and Their Mechanisms: A Meta-Analysis and Comprehensive Review of Common Variants from Genome-Wide Association Studies.

Diagnostics (Basel, Switzerland)
Zarkasi, Khairul Anwar KA; Abdullah, Noraidatulakma N; Abdul Murad, Nor Azian NA; Ahmad, Norfazilah N; Jamal, Rahman R
Publication Date: 2022-10-21

Variant appearance in text: rs56062135
PubMed Link: 36292250
Variant Present in the following documents:
  • diagnostics-12-02561.pdf
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Smad3 regulates smooth muscle cell fate and mediates adverse remodeling and calcification of the atherosclerotic plaque.

Nature Cardiovascular Research
Cheng, Paul P; Wirka, Robert C RC; Kim, Juyong Brian JB; Kim, Hyun-Jung HJ; Nguyen, Trieu T; Kundu, Ramendra R; Zhao, Quanyi Q; Sharma, Disha D; Pedroza, Albert A; Nagao, Manabu M; Iyer, Dharini D; Fischbein, Michael P MP; Quertermous, Thomas T
Publication Date: 2022-04

Variant appearance in text: rs56062135
PubMed Link: 36246779
Variant Present in the following documents:
  • Main text
  • nihms-1785285.pdf
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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: rs56062135
PubMed Link: 35743896
Variant Present in the following documents:
  • life-12-00865.pdf
View BVdb publication page



Genetic susceptibility to hereditary non-medullary thyroid cancer.

Hereditary Cancer In Clinical Practice
Kamani, Tina T; Charkhchi, Parsa P; Zahedi, Afshan A; Akbari, Mohammad R MR
Publication Date: 2022-03-07

Variant appearance in text: rs56062135
PubMed Link: 35255942
Variant Present in the following documents:
  • Main text
  • 13053_2022_Article_215.pdf
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Molecular Mechanisms of Eosinophilic Esophagitis.

International Journal Of Molecular Sciences
Zhernov, Yury V YV; Vysochanskaya, Sonya O SO; Sukhov, Vitaly A VA; Zaostrovtseva, Olga K OK; Gorshenin, Denis S DS; Sidorova, Ekaterina A EA; Mitrokhin, Oleg V OV
Publication Date: 2021-12-07

Variant appearance in text: rs56062135
PubMed Link: 34947981
Variant Present in the following documents:
  • Main text
  • ijms-22-13183.pdf
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Molecular Mechanisms of Eosinophilic Esophagitis.

International Journal Of Molecular Sciences
Zhernov, Yury V YV; Vysochanskaya, Sonya O SO; Sukhov, Vitaly A VA; Zaostrovtseva, Olga K OK; Gorshenin, Denis S DS; Sidorova, Ekaterina A EA; Mitrokhin, Oleg V OV
Publication Date: 2021-12-07

Variant appearance in text: rs56062135
PubMed Link: 34947981
Variant Present in the following documents:
  • Main text
  • ijms-22-13183.pdf
View BVdb publication page



Polygenic risk for coronary artery disease in the Scottish and English population.

Bmc Cardiovascular Disorders
Yang, Chuhua C; Starnecker, Fabian F; Pang, Shichao S; Chen, Zhifen Z; Güldener, Ulrich U; Li, Ling L; Heinig, Matthias M; Schunkert, Heribert H
Publication Date: 2021-12-07

Variant appearance in text: rs56062135
PubMed Link: 34876023
Variant Present in the following documents:
  • 12872_2021_2398_MOESM1_ESM.pdf
View BVdb publication page



Cardiovascular risk factor mediation of the effects of education and Genetic Risk Score on cardiovascular disease: a prospective observational cohort study of the Framingham Heart Study.

Bmj Open
Powell, Katie L KL; Stephens, Sebastien R SR; Stephens, Alexandre S AS
Publication Date: 2021-01-12

Variant appearance in text: rs56062135
PubMed Link: 33436477
Variant Present in the following documents:
  • bmjopen-2020-045210.draft_revisions.pdf
View BVdb publication page



Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight
Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL
Publication Date: 2020-09-03

Variant appearance in text: rs56062135
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



Age-of-onset information helps identify 76 genetic variants associated with allergic disease.

Plos Genetics
Ferreira, Manuel A R MAR; Vonk, Judith M JM; Baurecht, Hansjörg H; Marenholz, Ingo I; Tian, Chao C; Hoffman, Joshua D JD; Helmer, Quinta Q; Tillander, Annika A; Ullemar, Vilhelmina V; Lu, Yi Y; Grosche, Sarah S; Rüschendorf, Franz F; Granell, Raquel R; Brumpton, Ben M BM; Fritsche, Lars G LG; Bhatta, Laxmi L; Gabrielsen, Maiken E ME; Nielsen, Jonas B JB; Zhou, Wei W; Hveem, Kristian K; Langhammer, Arnulf A; Holmen, Oddgeir L OL; Løset, Mari M; Abecasis, Gonçalo R GR; Willer, Cristen J CJ; Emami, Nima C NC; Cavazos, Taylor B TB; Witte, John S JS; Szwajda, Agnieszka A; , ; , ; Hinds, David A DA; Hübner, Norbert N; Weidinger, Stephan S; Magnusson, Patrik Ke PK; Jorgenson, Eric E; Karlsson, Robert R; Paternoster, Lavinia L; Boomsma, Dorret I DI; Almqvist, Catarina C; Lee, Young-Ae YA; Koppelman, Gerard H GH
Publication Date: 2020-06

Variant appearance in text: rs56062135
PubMed Link: 32603359
Variant Present in the following documents:
  • Main text
  • pgen.1008725.pdf
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Precision Medicine and Cardiovascular Health: Insights from Mendelian Randomization Analyses.

Korean Circulation Journal
Spiller, Wes W; Jung, Keum Ji KJ; Lee, Ji Young JY; Jee, Sun Ha SH
Publication Date: 2020-02

Variant appearance in text: rs56062135
PubMed Link: 31845553
Variant Present in the following documents:
  • Main text
  • kcj-50-91.pdf
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2018 George Lyman Duff Memorial Lecture: Genetics and Genomics of Coronary Artery Disease: A Decade of Progress.

Arteriosclerosis, Thrombosis, And Vascular Biology
McPherson, Ruth R
Publication Date: 2019-10

Variant appearance in text: rs56062135
PubMed Link: 31462092
Variant Present in the following documents:
  • Main text
  • atv-39-1925.pdf
View BVdb publication page



Genome-Wide Association Studies of Hypertension and Several Other Cardiovascular Diseases.

Pulse (Basel, Switzerland)
Wang, Yan Y; Wang, Ji-Guang JG
Publication Date: 2019-04

Variant appearance in text: rs56062135
PubMed Link: 31049317
Variant Present in the following documents:
  • Main text
View BVdb publication page



Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies.

The Lancet. Respiratory Medicine
Pividori, Milton M; Schoettler, Nathan N; Nicolae, Dan L DL; Ober, Carole C; Im, Hae Kyung HK
Publication Date: 2019-06

Variant appearance in text: rs56062135
PubMed Link: 31036433
Variant Present in the following documents:
  • Main text
View BVdb publication page



Bayesian multiple logistic regression for case-control GWAS.

Plos Genetics
Banerjee, Saikat S; Zeng, Lingyao L; Schunkert, Heribert H; Söding, Johannes J
Publication Date: 2018-12

Variant appearance in text: rs56062135
PubMed Link: 30596640
Variant Present in the following documents:
  • Main text
View BVdb publication page



The Role of the NIS (SLC5A5) Gene in Papillary Thyroid Cancer: A Systematic Review.

International Journal Of Endocrinology
de Morais, Rafael Martins RM; Sobrinho, Alaor Barra AB; de Souza Silva, Calliandra Maria CM; de Oliveira, Jamila Reis JR; da Silva, Izabel Cristina Rodrigues ICR; de Toledo Nóbrega, Otávio O
Publication Date: 2018

Variant appearance in text: rs56062135
PubMed Link: 30595693
Variant Present in the following documents:
  • Main text
  • IJE2018-9128754.pdf
View BVdb publication page



Thyroid cancers of follicular origin in a genomic light: in-depth overview of common and unique molecular marker candidates.

Molecular Cancer
Pstrąg, Natalia N; Ziemnicka, Katarzyna K; Bluyssen, Hans H; Wesoły, Joanna J
Publication Date: 2018-08-08

Variant appearance in text: rs56062135
PubMed Link: 30089490
Variant Present in the following documents:
  • Main text
  • 12943_2018_Article_866.pdf
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A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases.

Nature Genetics
Zhu, Zhaozhong Z; Lee, Phil H PH; Chaffin, Mark D MD; Chung, Wonil W; Loh, Po-Ru PR; Lu, Quan Q; Christiani, David C DC; Liang, Liming L
Publication Date: 2018-06

Variant appearance in text: rs56062135
PubMed Link: 29785011
Variant Present in the following documents:
  • Main text
  • nihms955373.pdf
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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: rs56062135
PubMed Link: 29695241
Variant Present in the following documents:
  • Main text
  • 12933_2018_Article_705.pdf
View BVdb publication page



The role of SMAD3 in the genetic predisposition to papillary thyroid carcinoma.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Wang, Yanqiang Y; He, Huiling H; Liyanarachchi, Sandya S; Genutis, Luke K LK; Li, Wei W; Yu, Lianbo L; Phay, John E JE; Shen, Rulong R; Brock, Pamela P; de la Chapelle, Albert A
Publication Date: 2018-09

Variant appearance in text: rs56062135
PubMed Link: 29300379
Variant Present in the following documents:
  • Main text
View BVdb publication page



Proficiency of data interpretation: identification of signaling SNPs/specific loci for coronary artery disease.

Database : The Journal Of Biological Databases And Curation
Cheema, Asma N AN; Rosenthal, Samantha L SL; Ilyas Kamboh, M M
Publication Date: 2017-01-01

Variant appearance in text: rs56062135
PubMed Link: 29220472
Variant Present in the following documents:
  • Main text
  • bax078.pdf
View BVdb publication page



Transforming growth factor-β signaling pathway-associated genes SMAD2 and TGFBR2 are implicated in metabolic syndrome in a Taiwanese population.

Scientific Reports
Lin, Eugene E; Kuo, Po-Hsiu PH; Liu, Yu-Li YL; Yang, Albert C AC; Tsai, Shih-Jen SJ
Publication Date: 2017-10-19

Variant appearance in text: rs56062135
PubMed Link: 29051557
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_14025.pdf
View BVdb publication page



Fine-mapping inflammatory bowel disease loci to single-variant resolution.

Nature
Huang, Hailiang H; Fang, Ming M; Jostins, Luke L; Umićević Mirkov, Maša M; Boucher, Gabrielle G; Anderson, Carl A CA; Andersen, Vibeke V; Cleynen, Isabelle I; Cortes, Adrian A; Crins, François F; D'Amato, Mauro M; Deffontaine, Valérie V; Dmitrieva, Julia J; Docampo, Elisa E; Elansary, Mahmoud M; Farh, Kyle Kai-How KK; Franke, Andre A; Gori, Ann-Stephan AS; Goyette, Philippe P; Halfvarson, Jonas J; Haritunians, Talin T; Knight, Jo J; Lawrance, Ian C IC; Lees, Charlie W CW; Louis, Edouard E; Mariman, Rob R; Meuwissen, Theo T; Mni, Myriam M; Momozawa, Yukihide Y; Parkes, Miles M; Spain, Sarah L SL; Théâtre, Emilie E; Trynka, Gosia G; Satsangi, Jack J; van Sommeren, Suzanne S; Vermeire, Severine S; Xavier, Ramnik J RJ; , ; Weersma, Rinse K RK; Duerr, Richard H RH; Mathew, Christopher G CG; Rioux, John D JD; McGovern, Dermot P B DPB; Cho, Judy H JH; Georges, Michel M; Daly, Mark J MJ; Barrett, Jeffrey C JC
Publication Date: 2017-07-13

Variant appearance in text: rs56062135
PubMed Link: 28658209
Variant Present in the following documents:
  • NIHMS72714-supplement-Supplementary_Table_1.xlsx, sheet 2
View BVdb publication page



Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy.

Plos Genetics
Byars, Sean G SG; Huang, Qin Qin QQ; Gray, Lesley-Ann LA; Bakshi, Andrew A; Ripatti, Samuli S; Abraham, Gad G; Stearns, Stephen C SC; Inouye, Michael M
Publication Date: 2017-06

Variant appearance in text: rs56062135
PubMed Link: 28640878
Variant Present in the following documents:
  • pgen.1006328.s006.pdf
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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: rs56062135
PubMed Link: 28585919
Variant Present in the following documents:
  • Main text
View BVdb publication page



Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.

Journal Of The American College Of Cardiology
Webb, Thomas R TR; Erdmann, Jeanette J; Stirrups, Kathleen E KE; Stitziel, Nathan O NO; Masca, Nicholas G D NG; Jansen, Henning H; Kanoni, Stavroula S; Nelson, Christopher P CP; Ferrario, Paola G PG; König, Inke R IR; Eicher, John D JD; Johnson, Andrew D AD; Hamby, Stephen E SE; Betsholtz, Christer C; Ruusalepp, Arno A; Franzén, Oscar O; Schadt, Eric E EE; Björkegren, Johan L M JL; Weeke, Peter E PE; Auer, Paul L PL; Schick, Ursula M UM; Lu, Yingchang Y; Zhang, He H; Dube, Marie-Pierre MP; Goel, Anuj A; Farrall, Martin M; Peloso, Gina M GM; Won, Hong-Hee HH; Do, Ron R; van Iperen, Erik E; Kruppa, Jochen J; Mahajan, Anubha A; Scott, Robert A RA; Willenborg, Christina C; Braund, Peter S PS; van Capelleveen, Julian C JC; Doney, Alex S F AS; Donnelly, Louise A LA; Asselta, Rosanna R; Merlini, Pier A PA; Duga, Stefano S; Marziliano, Nicola N; Denny, Josh C JC; Shaffer, Christian C; El-Mokhtari, Nour Eddine NE; Franke, Andre A; Heilmann, Stefanie S; Hengstenberg, Christian C; Hoffmann, Per P; Holmen, Oddgeir L OL; Hveem, Kristian K; Jansson, Jan-Håkan JH; Jöckel, Karl-Heinz KH; Kessler, Thorsten T; Kriebel, Jennifer J; Laugwitz, Karl L KL; Marouli, Eirini E; Martinelli, Nicola N; McCarthy, Mark I MI; Van Zuydam, Natalie R NR; Meisinger, Christa C; Esko, Tõnu T; Mihailov, Evelin E; Escher, Stefan A SA; Alver, Maris M; Moebus, Susanne S; Morris, Andrew D AD; Virtamo, Jarma J; Nikpay, Majid M; Olivieri, Oliviero O; Provost, Sylvie S; AlQarawi, Alaa A; Robertson, Neil R NR; Akinsansya, Karen O KO; Reilly, Dermot F DF; Vogt, Thomas F TF; Yin, Wu W; Asselbergs, Folkert W FW; Kooperberg, Charles C; Jackson, Rebecca D RD; Stahl, Eli E; Müller-Nurasyid, Martina M; Strauch, Konstantin K; Varga, Tibor V TV; Waldenberger, Melanie M; , ; Zeng, Lingyao L; Chowdhury, Rajiv R; Salomaa, Veikko V; Ford, Ian I; Jukema, J Wouter JW; Amouyel, Philippe P; Kontto, Jukka J; , ; Nordestgaard, Børge G BG; Ferrières, Jean J; Saleheen, Danish D; Sattar, Naveed N; Surendran, Praveen P; Wagner, Aline A; Young, Robin R; Howson, Joanna M M JM; Butterworth, Adam S AS; Danesh, John J; Ardissino, Diego D; Bottinger, Erwin P EP; Erbel, Raimund R; Franks, Paul W PW; Girelli, Domenico D; Hall, Alistair S AS; Hovingh, G Kees GK; Kastrati, Adnan A; Lieb, Wolfgang W; Meitinger, Thomas T; Kraus, William E WE; Shah, Svati H SH; McPherson, Ruth R; Orho-Melander, Marju M; Melander, Olle O; Metspalu, Andres A; Palmer, Colin N A CN; Peters, Annette A; Rader, Daniel J DJ; Reilly, Muredach P MP; Loos, Ruth J F RJ; Reiner, Alex P AP; Roden, Dan M DM; Tardif, Jean-Claude JC; Thompson, John R JR; Wareham, Nicholas J NJ; Watkins, Hugh H; Willer, Cristen J CJ; Samani, Nilesh J NJ; Schunkert, Heribert H; Deloukas, Panos P; Kathiresan, Sekar S; ,
Publication Date: 2017-02-21

Variant appearance in text: rs56062135
PubMed Link: 28209224
Variant Present in the following documents:
  • Main text
View BVdb publication page



A genome-wide association study yields five novel thyroid cancer risk loci.

Nature Communications
Gudmundsson, Julius J; Thorleifsson, Gudmar G; Sigurdsson, Jon K JK; Stefansdottir, Lilja L; Jonasson, Jon G JG; Gudjonsson, Sigurjon A SA; Gudbjartsson, Daniel F DF; Masson, Gisli G; Johannsdottir, Hrefna H; Halldorsson, Gisli H GH; Stacey, Simon N SN; Helgason, Hannes H; Sulem, Patrick P; Senter, Leigha L; He, Huiling H; Liyanarachchi, Sandya S; Ringel, Matthew D MD; Aguillo, Esperanza E; Panadero, Angeles A; Prats, Enrique E; Garcia-Castaño, Almudena A; De Juan, Ana A; Rivera, Fernando F; Xu, Li L; Kiemeney, Lambertus A LA; Eyjolfsson, Gudmundur I GI; Sigurdardottir, Olof O; Olafsson, Isleifur I; Kristvinsson, Hoskuldur H; Netea-Maier, Romana T RT; Jonsson, Thorvaldur T; Mayordomo, Jose I JI; Plantinga, Theo S TS; Hjartarson, Hannes H; Hrafnkelsson, Jon J; Sturgis, Erich M EM; Thorsteinsdottir, Unnur U; Rafnar, Thorunn T; de la Chapelle, Albert A; Stefansson, Kari K
Publication Date: 2017-02-14

Variant appearance in text: rs56062135
PubMed Link: 28195142
Variant Present in the following documents:
  • Main text
  • ncomms14517-s1.pdf
  • ncomms14517.pdf
View BVdb publication page



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: rs56062135
PubMed Link: 28130654
Variant Present in the following documents:
  • Main text
View BVdb publication page



Integrative functional genomics identifies regulatory mechanisms at coronary artery disease loci.

Nature Communications
Miller, Clint L CL; Pjanic, Milos M; Wang, Ting T; Nguyen, Trieu T; Cohain, Ariella A; Lee, Jonathan D JD; Perisic, Ljubica L; Hedin, Ulf U; Kundu, Ramendra K RK; Majmudar, Deshna D; Kim, Juyong B JB; Wang, Oliver O; Betsholtz, Christer C; Ruusalepp, Arno A; Franzén, Oscar O; Assimes, Themistocles L TL; Montgomery, Stephen B SB; Schadt, Eric E EE; Björkegren, Johan L M JLM; Quertermous, Thomas T
Publication Date: 2016-07-08

Variant appearance in text: rs56062135
PubMed Link: 27386823
Variant Present in the following documents:
  • Main text
View BVdb publication page



The impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular disease.

Embo Molecular Medicine
Kessler, Thorsten T; Vilne, Baiba B; Schunkert, Heribert H
Publication Date: 2016-07

Variant appearance in text: rs56062135
PubMed Link: 27189168
Variant Present in the following documents:
  • Main text
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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: rs56062135
PubMed Link: 26892960
Variant Present in the following documents:
  • Main text
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Experimental Biology for the Identification of Causal Pathways in Atherosclerosis.

Cardiovascular Drugs And Therapy
Guo, Yanhong Y; Garcia-Barrio, Minerva T MT; Wang, Laiyuan L; Chen, Y Eugene YE
Publication Date: 2016-02

Variant appearance in text: rs56062135
PubMed Link: 26847647
Variant Present in the following documents:
  • Main text
  • 10557_2016_Article_6644.pdf
View BVdb publication page



A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.

Nature Genetics
Nikpay, Majid M; Goel, Anuj A; Won, Hong-Hee HH; Hall, Leanne M LM; Willenborg, Christina C; Kanoni, Stavroula S; Saleheen, Danish D; Kyriakou, Theodosios T; Nelson, Christopher P CP; Hopewell, Jemma C JC; Webb, Thomas R TR; Zeng, Lingyao L; Dehghan, Abbas A; Alver, Maris M; Armasu, Sebastian M SM; Auro, Kirsi K; Bjonnes, Andrew A; Chasman, Daniel I DI; Chen, Shufeng S; Ford, Ian I; Franceschini, Nora N; Gieger, Christian C; Grace, Christopher C; Gustafsson, Stefan S; Huang, Jie J; Hwang, Shih-Jen SJ; Kim, Yun Kyoung YK; Kleber, Marcus E ME; Lau, King Wai KW; Lu, Xiangfeng X; Lu, Yingchang Y; Lyytikäinen, Leo-Pekka LP; Mihailov, Evelin E; Morrison, Alanna C AC; Pervjakova, Natalia N; Qu, Liming L; Rose, Lynda M LM; Salfati, Elias E; Saxena, Richa R; Scholz, Markus M; Smith, Albert V AV; Tikkanen, Emmi E; Uitterlinden, Andre A; Yang, Xueli X; Zhang, Weihua W; Zhao, Wei W; de Andrade, Mariza M; de Vries, Paul S PS; van Zuydam, Natalie R NR; Anand, Sonia S SS; Bertram, Lars L; Beutner, Frank F; Dedoussis, George G; Frossard, Philippe P; Gauguier, Dominique D; Goodall, Alison H AH; Gottesman, Omri O; Haber, Marc M; Han, Bok-Ghee BG; Huang, Jianfeng J; Jalilzadeh, Shapour S; Kessler, Thorsten T; König, Inke R IR; Lannfelt, Lars L; Lieb, Wolfgang W; Lind, Lars L; Lindgren, Cecilia M CM; Lokki, Marja-Liisa ML; Magnusson, Patrik K PK; Mallick, Nadeem H NH; Mehra, Narinder N; Meitinger, Thomas T; Memon, Fazal-Ur-Rehman FU; Morris, Andrew P AP; Nieminen, Markku S MS; Pedersen, Nancy L NL; Peters, Annette A; Rallidis, Loukianos S LS; Rasheed, Asif A; Samuel, Maria M; Shah, Svati H SH; Sinisalo, Juha J; Stirrups, Kathleen E KE; Trompet, Stella S; Wang, Laiyuan L; Zaman, Khan S KS; Ardissino, Diego D; Boerwinkle, Eric E; Borecki, Ingrid B IB; Bottinger, Erwin P EP; Buring, Julie E JE; Chambers, John C JC; Collins, Rory R; Cupples, L Adrienne LA; Danesh, John J; Demuth, Ilja I; Elosua, Roberto R; Epstein, Stephen E SE; Esko, Tõnu T; Feitosa, Mary F MF; Franco, Oscar H OH; Franzosi, Maria Grazia MG; Granger, Christopher B CB; Gu, Dongfeng D; Gudnason, Vilmundur V; Hall, Alistair S AS; Hamsten, Anders A; Harris, Tamara B TB; Hazen, Stanley L SL; Hengstenberg, Christian C; Hofman, Albert A; Ingelsson, Erik E; Iribarren, Carlos C; Jukema, J Wouter JW; Karhunen, Pekka J PJ; Kim, Bong-Jo BJ; Kooner, Jaspal S JS; Kullo, Iftikhar J IJ; Lehtimäki, Terho T; Loos, Ruth J F RJF; Melander, Olle O; Metspalu, Andres A; März, Winfried W; Palmer, Colin N CN; Perola, Markus M; Quertermous, Thomas T; Rader, Daniel J DJ; Ridker, Paul M PM; Ripatti, Samuli S; Roberts, Robert R; Salomaa, Veikko V; Sanghera, Dharambir K DK; Schwartz, Stephen M SM; Seedorf, Udo U; Stewart, Alexandre F AF; Stott, David J DJ; Thiery, Joachim J; Zalloua, Pierre A PA; O'Donnell, Christopher J CJ; Reilly, Muredach P MP; Assimes, Themistocles L TL; Thompson, John R JR; Erdmann, Jeanette J; Clarke, Robert R; Watkins, Hugh H; Kathiresan, Sekar S; McPherson, Ruth R; Deloukas, Panos P; Schunkert, Heribert H; Samani, Nilesh J NJ; Farrall, Martin M
Publication Date: 2015-10

Variant appearance in text: rs56062135
PubMed Link: 26343387
Variant Present in the following documents:
  • Main text
  • emss-64693.pdf
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