NOA1 c.1515+731C>A

Variant ID: 4-57838583-G-T

NM_032313.2(NOA1):c.1515+731C>A

This variant was identified in 23 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: rs17087335
PubMed Link: 35743896
Variant Present in the following documents:
  • life-12-00865.pdf
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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: rs17087335
PubMed Link: 34876023
Variant Present in the following documents:
  • 12872_2021_2398_MOESM1_ESM.pdf
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Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression.

Nature Genetics
Võsa, Urmo U; Claringbould, Annique A; Westra, Harm-Jan HJ; Bonder, Marc Jan MJ; Deelen, Patrick P; Zeng, Biao B; Kirsten, Holger H; Saha, Ashis A; Kreuzhuber, Roman R; Yazar, Seyhan S; Brugge, Harm H; Oelen, Roy R; de Vries, Dylan H DH; van der Wijst, Monique G P MGP; Kasela, Silva S; Pervjakova, Natalia N; Alves, Isabel I; Favé, Marie-Julie MJ; Agbessi, Mawussé M; Christiansen, Mark W MW; Jansen, Rick R; Seppälä, Ilkka I; Tong, Lin L; Teumer, Alexander A; Schramm, Katharina K; Hemani, Gibran G; Verlouw, Joost J; Yaghootkar, Hanieh H; Sönmez Flitman, Reyhan R; Brown, Andrew A; Kukushkina, Viktorija V; Kalnapenkis, Anette A; Rüeger, Sina S; Porcu, Eleonora E; Kronberg, Jaanika J; Kettunen, Johannes J; Lee, Bernett B; Zhang, Futao F; Qi, Ting T; Hernandez, Jose Alquicira JA; Arindrarto, Wibowo W; Beutner, Frank F; , ; , ; Dmitrieva, Julia J; Elansary, Mahmoud M; Fairfax, Benjamin P BP; Georges, Michel M; Heijmans, Bastiaan T BT; Hewitt, Alex W AW; Kähönen, Mika M; Kim, Yungil Y; Knight, Julian C JC; Kovacs, Peter P; Krohn, Knut K; Li, Shuang S; Loeffler, Markus M; Marigorta, Urko M UM; Mei, Hailang H; Momozawa, Yukihide Y; Müller-Nurasyid, Martina M; Nauck, Matthias M; Nivard, Michel G MG; Penninx, Brenda W J H BWJH; Pritchard, Jonathan K JK; Raitakari, Olli T OT; Rotzschke, Olaf O; Slagboom, Eline P EP; Stehouwer, Coen D A CDA; Stumvoll, Michael M; Sullivan, Patrick P; 't Hoen, Peter A C PAC; Thiery, Joachim J; Tönjes, Anke A; van Dongen, Jenny J; van Iterson, Maarten M; Veldink, Jan H JH; Völker, Uwe U; Warmerdam, Robert R; Wijmenga, Cisca C; Swertz, Morris M; Andiappan, Anand A; Montgomery, Grant W GW; Ripatti, Samuli S; Perola, Markus M; Kutalik, Zoltan Z; Dermitzakis, Emmanouil E; Bergmann, Sven S; Frayling, Timothy T; van Meurs, Joyce J; Prokisch, Holger H; Ahsan, Habibul H; Pierce, Brandon L BL; Lehtimäki, Terho T; Boomsma, Dorret I DI; Psaty, Bruce M BM; Gharib, Sina A SA; Awadalla, Philip P; Milani, Lili L; Ouwehand, Willem H WH; Downes, Kate K; Stegle, Oliver O; Battle, Alexis A; Visscher, Peter M PM; Yang, Jian J; Scholz, Markus M; Powell, Joseph J; Gibson, Greg G; Esko, Tõnu T; Franke, Lude L
Publication Date: 2021-09

Variant appearance in text: rs17087335
PubMed Link: 34475573
Variant Present in the following documents:
  • Main text
  • NIHMS1723987-supplement-Supplementary_Note.pdf
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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: rs17087335
PubMed Link: 33436477
Variant Present in the following documents:
  • bmjopen-2020-045210.draft_revisions.pdf
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Sarcopenia-related traits and coronary artery disease: a bi-directional Mendelian randomization study.

Aging
Liu, Hui-Min HM; Zhang, Qiang Q; Shen, Wen-Di WD; Li, Bo-Yang BY; Lv, Wan-Qiang WQ; Xiao, Hong-Mei HM; Deng, Hong-Wen HW
Publication Date: 2020-02-16

Variant appearance in text: rs17087335
PubMed Link: 32062614
Variant Present in the following documents:
  • Main text
  • aging-12-102815.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: rs17087335
PubMed Link: 31845553
Variant Present in the following documents:
  • Main text
  • kcj-50-91.pdf
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Evaluation of the role of STAP1 in Familial Hypercholesterolemia.

Scientific Reports
Danyel, Magdalena M; Ott, Claus-Eric CE; Grenkowitz, Thomas T; Salewsky, Bastian B; Hicks, Andrew A AA; Fuchsberger, Christian C; Steinhagen-Thiessen, Elisabeth E; Bobbert, Thomas T; Kassner, Ursula U; Demuth, Ilja I
Publication Date: 2019-08-19

Variant appearance in text: rs17087335
PubMed Link: 31427613
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_48402.pdf
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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: rs17087335
PubMed Link: 31049317
Variant Present in the following documents:
  • Main text
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Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank.

Diabetologia
Fall, Tove T; Gustafsson, Stefan S; Orho-Melander, Marju M; Ingelsson, Erik E
Publication Date: 2018-10

Variant appearance in text: rs17087335
PubMed Link: 30003307
Variant Present in the following documents:
  • 125_2018_4686_MOESM1_ESM.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: rs17087335
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: rs17087335
PubMed Link: 29263402
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_18214.pdf
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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: rs17087335
PubMed Link: 29220472
Variant Present in the following documents:
  • Main text
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: rs17087335
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: rs17087335
PubMed Link: 28585919
Variant Present in the following documents:
  • Main text
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: rs17087335
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: rs17087335
PubMed Link: 28122634
Variant Present in the following documents:
  • Main text
  • 13059_2016_1142_MOESM1_ESM.pdf
  • 13059_2016_Article_1142.pdf
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The genetic overlap between mood disorders and cardiometabolic diseases: a systematic review of genome wide and candidate gene studies.

Translational Psychiatry
Amare, A T AT; Schubert, K O KO; Klingler-Hoffmann, M M; Cohen-Woods, S S; Baune, B T BT
Publication Date: 2017-01-24

Variant appearance in text: rs17087335
PubMed Link: 28117839
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: rs17087335
PubMed Link: 27189168
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs17087335
PubMed Link: 26892960
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs17087335
PubMed Link: 26847647
Variant Present in the following documents:
  • Main text
  • 10557_2016_Article_6644.pdf
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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: rs17087335
PubMed Link: 26343387
Variant Present in the following documents:
  • Main text
  • emss-64693.pdf
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Prediction of Causal Candidate Genes in Coronary Artery Disease Loci.

Arteriosclerosis, Thrombosis, And Vascular Biology
Brænne, Ingrid I; Civelek, Mete M; Vilne, Baiba B; Di Narzo, Antonio A; Johnson, Andrew D AD; Zhao, Yuqi Y; Reiz, Benedikt B; Codoni, Veronica V; Webb, Thomas R TR; Foroughi Asl, Hassan H; Hamby, Stephen E SE; Zeng, Lingyao L; Trégouët, David-Alexandre DA; Hao, Ke K; Topol, Eric J EJ; Schadt, Eric E EE; Yang, Xia X; Samani, Nilesh J NJ; Björkegren, Johan L M JL; Erdmann, Jeanette J; Schunkert, Heribert H; Lusis, Aldons J AJ; ,
Publication Date: 2015-10

Variant appearance in text: rs17087335
PubMed Link: 26293461
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry.

Plos Genetics
N'Diaye, Amidou A; Chen, Gary K GK; Palmer, Cameron D CD; Ge, Bing B; Tayo, Bamidele B; Mathias, Rasika A RA; Ding, Jingzhong J; Nalls, Michael A MA; Adeyemo, Adebowale A; Adoue, Véronique V; Ambrosone, Christine B CB; Atwood, Larry L; Bandera, Elisa V EV; Becker, Lewis C LC; Berndt, Sonja I SI; Bernstein, Leslie L; Blot, William J WJ; Boerwinkle, Eric E; Britton, Angela A; Casey, Graham G; Chanock, Stephen J SJ; Demerath, Ellen E; Deming, Sandra L SL; Diver, W Ryan WR; Fox, Caroline C; Harris, Tamara B TB; Hernandez, Dena G DG; Hu, Jennifer J JJ; Ingles, Sue A SA; John, Esther M EM; Johnson, Craig C; Keating, Brendan B; Kittles, Rick A RA; Kolonel, Laurence N LN; Kritchevsky, Stephen B SB; Le Marchand, Loic L; Lohman, Kurt K; Liu, Jiankang J; Millikan, Robert C RC; Murphy, Adam A; Musani, Solomon S; Neslund-Dudas, Christine C; North, Kari E KE; Nyante, Sarah S; Ogunniyi, Adesola A; Ostrander, Elaine A EA; Papanicolaou, George G; Patel, Sanjay S; Pettaway, Curtis A CA; Press, Michael F MF; Redline, Susan S; Rodriguez-Gil, Jorge L JL; Rotimi, Charles C; Rybicki, Benjamin A BA; Salako, Babatunde B; Schreiner, Pamela J PJ; Signorello, Lisa B LB; Singleton, Andrew B AB; Stanford, Janet L JL; Stram, Alex H AH; Stram, Daniel O DO; Strom, Sara S SS; Suktitipat, Bhoom B; Thun, Michael J MJ; Witte, John S JS; Yanek, Lisa R LR; Ziegler, Regina G RG; Zheng, Wei W; Zhu, Xiaofeng X; Zmuda, Joseph M JM; Zonderman, Alan B AB; Evans, Michele K MK; Liu, Yongmei Y; Becker, Diane M DM; Cooper, Richard S RS; Pastinen, Tomi T; Henderson, Brian E BE; Hirschhorn, Joel N JN; Lettre, Guillaume G; Haiman, Christopher A CA
Publication Date: 2011-10

Variant appearance in text: rs17087335
PubMed Link: 21998595
Variant Present in the following documents:
  • Main text
  • pgen.1002298.pdf
View BVdb publication page