FURIN c.-159-2262C>G

Variant ID: 15-91416550-C-G

NM_002569.2(FURIN):c.-159-2262C>G

This variant was identified in 67 publications

View GRCh38 version.




Publications:


Establishing the role of the FES tyrosine kinase in the pathogenesis, pathophysiology, and severity of sepsis and its outcomes.

Frontiers In Immunology
Laight, Brian J BJ; Jawa, Natasha A NA; Tyryshkin, Kathrin K; Maslove, David M DM; Boyd, J Gordon JG; Greer, Peter A PA
Publication Date: 2023

Variant appearance in text: rs17514846
PubMed Link: 37122758
Variant Present in the following documents:
  • Main text
  • fimmu-14-1145826.pdf
View BVdb publication page



The FES Gene at the 15q26 Coronary-Artery-Disease Locus Inhibits Atherosclerosis.

Circulation Research
Karamanavi, Elisavet E; McVey, David G DG; van der Laan, Sander W SW; Stanczyk, Paulina J PJ; Morris, Gavin E GE; Wang, Yifan Y; Yang, Wei W; Chan, Kenneth K; Poston, Robin N RN; Luo, Jun J; Zhou, Xinmiao X; Gong, Peng P; Jones, Peter D PD; Cao, Junjun J; Kostogrys, Renata B RB; Webb, Tom R TR; Pasterkamp, Gerard G; Yu, Haojie H; Xiao, Qingzhong Q; Greer, Peter A PA; Stringer, Emma J EJ; Samani, Nilesh J NJ; Ye, Shu S
Publication Date: 2022-12-02

Variant appearance in text: rs17514846
PubMed Link: 36321446
Variant Present in the following documents:
  • Main text
  • res-131-1004.pdf
  • res-131-1004-s007.pdf
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Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond.

Scientific Reports
Gaddis, Nathan N; Mathur, Ravi R; Marks, Jesse J; Zhou, Linran L; Quach, Bryan B; Waldrop, Alex A; Levran, Orna O; Agrawal, Arpana A; Randesi, Matthew M; Adelson, Miriam M; Jeffries, Paul W PW; Martin, Nicholas G NG; Degenhardt, Louisa L; Montgomery, Grant W GW; Wetherill, Leah L; Lai, Dongbing D; Bucholz, Kathleen K; Foroud, Tatiana T; Porjesz, Bernice B; Runarsdottir, Valgerdur V; Tyrfingsson, Thorarinn T; Einarsson, Gudmundur G; Gudbjartsson, Daniel F DF; Webb, Bradley Todd BT; Crist, Richard C RC; Kranzler, Henry R HR; Sherva, Richard R; Zhou, Hang H; Hulse, Gary G; Wildenauer, Dieter D; Kelty, Erin E; Attia, John J; Holliday, Elizabeth G EG; McEvoy, Mark M; Scott, Rodney J RJ; Schwab, Sibylle G SG; Maher, Brion S BS; Gruza, Richard R; Kreek, Mary Jeanne MJ; Nelson, Elliot C EC; Thorgeirsson, Thorgeir T; Stefansson, Kari K; Berrettini, Wade H WH; Gelernter, Joel J; Edenberg, Howard J HJ; Bierut, Laura L; Hancock, Dana B DB; Johnson, Eric Otto EO
Publication Date: 2022-10-07

Variant appearance in text: rs17514846
PubMed Link: 36207451
Variant Present in the following documents:
  • Main text
  • 41598_2022_Article_21003.pdf
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The emerging role of furin in neurodegenerative and neuropsychiatric diseases.

Translational Neurodegeneration
Zhang, Yi Y; Gao, Xiaoqin X; Bai, Xue X; Yao, Shanshan S; Chang, Yan-Zhong YZ; Gao, Guofen G
Publication Date: 2022-08-23

Variant appearance in text: rs17514846
PubMed Link: 35996194
Variant Present in the following documents:
  • Main text
  • 40035_2022_Article_313.pdf
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Genome-wide variance quantitative trait locus analysis suggests small interaction effects in blood pressure traits.

Scientific Reports
Shi, Gang G
Publication Date: 2022-07-25

Variant appearance in text: rs17514846
PubMed Link: 35879408
Variant Present in the following documents:
  • Main text
  • 41598_2022_Article_16908.pdf
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Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci.

Molecular Psychiatry
Deak, Joseph D JD; Zhou, Hang H; Galimberti, Marco M; Levey, Daniel F DF; Wendt, Frank R FR; Sanchez-Roige, Sandra S; Hatoum, Alexander S AS; Johnson, Emma C EC; Nunez, Yaira Z YZ; Demontis, Ditte D; Børglum, Anders D AD; Rajagopal, Veera M VM; Jennings, Mariela V MV; Kember, Rachel L RL; Justice, Amy C AC; Edenberg, Howard J HJ; Agrawal, Arpana A; Polimanti, Renato R; Kranzler, Henry R HR; Gelernter, Joel J
Publication Date: 2022-10

Variant appearance in text: rs17514846
PubMed Link: 35879402
Variant Present in the following documents:
  • Main text
  • 41380_2022_Article_1709.pdf
View BVdb publication page



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: rs17514846
PubMed Link: 35743896
Variant Present in the following documents:
  • life-12-00865.pdf
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FURIN Promoter Methylation Predicts the Risk of Incident Diabetes: A Prospective Analysis in the Gusu Cohort.

Frontiers In Endocrinology
He, Yan Y; Li, Yinan Y; Zhang, Jianan J; Chen, Linan L; Li, Jing J; Zhang, Min M; Zhang, Qiu Q; Lu, Ying Y; Jiang, Jun J; Zhang, Xiaolong X; Hu, Jianwei J; Ding, Yi Y; Zhang, Mingzhi M; Peng, Hao H
Publication Date: 2022

Variant appearance in text: rs17514846
PubMed Link: 35399937
Variant Present in the following documents:
  • Main text
  • fendo-13-873012.pdf
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Pathogenesis of premature coronary artery disease: Focus on risk factors and genetic variants.

Genes & Diseases
Wang, Haiming H; Liu, Zifan Z; Shao, Junjie J; Jiang, Min M; Lu, Xuechun X; Lin, Lejian L; Wang, Lin L; Xu, Qiang Q; Zhang, Haomin H; Li, Xin X; Zhou, Jingjing J; Chen, Yundai Y; Zhang, Ran R
Publication Date: 2022-03

Variant appearance in text: rs17514846
PubMed Link: 35224153
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Evidence for Shared Genetic Aetiology Between Schizophrenia, Cardiometabolic, and Inflammation-Related Traits: Genetic Correlation and Colocalization Analyses.

Schizophrenia Bulletin Open
Perry, Benjamin I BI; Bowker, Nicholas N; Burgess, Stephen S; Wareham, Nicholas J NJ; Upthegrove, Rachel R; Jones, Peter B PB; Langenberg, Claudia C; Khandaker, Golam M GM
Publication Date: 2022-01

Variant appearance in text: rs17514846
PubMed Link: 35156041
Variant Present in the following documents:
  • Main text
  • sgac001.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: rs17514846
PubMed Link: 34876023
Variant Present in the following documents:
  • 12872_2021_2398_MOESM1_ESM.pdf
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Genetic Control of Human Infection with SARS-CoV-2.

Russian Journal Of Genetics
Kucher, A N AN; Babushkina, N P NP; Sleptcov, A A AA; Nazarenko, M S MS
Publication Date: 2021

Variant appearance in text: rs17514846
PubMed Link: 34248311
Variant Present in the following documents:
  • Main text
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Shared genetic architecture between neuroticism, coronary artery disease and cardiovascular risk factors.

Translational Psychiatry
Torgersen, Kristin K; Bahrami, Shahram S; Frei, Oleksandr O; Shadrin, Alexey A; Connell, Kevin S O' KSO; Smeland, Olav B OB; Munkhaugen, John J; Djurovic, Srdjan S; Dammen, Toril T; Andreassen, Ole A OA
Publication Date: 2021-06-17

Variant appearance in text: rs17514846
PubMed Link: 34226488
Variant Present in the following documents:
  • Main text
View BVdb publication page



Germline Genetic Variants of Viral Entry and Innate Immunity May Influence Susceptibility to SARS-CoV-2 Infection: Toward a Polygenic Risk Score for Risk Stratification.

Frontiers In Immunology
Grolmusz, Vince Kornél VK; Bozsik, Anikó A; Papp, János J; Patócs, Attila A
Publication Date: 2021

Variant appearance in text: rs17514846
PubMed Link: 33763088
Variant Present in the following documents:
  • Main text
  • fimmu-12-653489.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: rs17514846
PubMed Link: 33436477
Variant Present in the following documents:
  • bmjopen-2020-045210.draft_revisions.pdf
View BVdb publication page



Mouse Models of Human Proprotein Convertase Insufficiency.

Endocrine Reviews
Shakya, Manita M; Lindberg, Iris I
Publication Date: 2021-05-25

Variant appearance in text: rs17514846
PubMed Link: 33382413
Variant Present in the following documents:
  • Main text
View BVdb publication page



Assessing COVID-19 susceptibility through analysis of the genetic and epigenetic diversity of ACE2-mediated SARS-CoV-2 entry.

Pharmacogenomics
Ragia, Georgia G; Manolopoulos, Vangelis G VG
Publication Date: 2020-12

Variant appearance in text: rs17514846
PubMed Link: 33243086
Variant Present in the following documents:
  • Main text
  • pgs-2020-0092.pdf
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Tissue Proteases and Immune Responses: Influencing Factors of COVID-19 Severity and Mortality.

Pathogens (Basel, Switzerland)
Mulinari Turin de Oliveira, Natália N; Fernandes da Silva Figueiredo, Isabella I; Cristine Malaquias da Silva, Liziane L; Sauruk da Silva, Karien K; Regis Bueno, Laryssa L; Barbosa da Luz, Bruna B; Rita Corso, Cláudia C; de Paula Werner, Maria Fernanda MF; Soares Fernandes, Elizabeth E; Maria-Ferreira, Daniele D
Publication Date: 2020-10-06

Variant appearance in text: rs17514846
PubMed Link: 33036180
Variant Present in the following documents:
  • Main text
  • pathogens-09-00817.pdf
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Association between HindIII (rs320) variant in the lipoprotein lipase gene and the presence of coronary artery disease and stroke among the Saudi population.

Saudi Journal Of Biological Sciences
Bogari, Neda M NM; Aljohani, Ashwag A; Dannoun, Anas A; Elkhateeb, Osama O; Porqueddu, Masimo M; Amin, Amr A AA; Bogari, Dema N DN; Taher, Mohiuddin M MM; Buba, Faruk F; Allam, Reem M RM; Bogari, Mustafa N MN; Alamanni, Francesco F
Publication Date: 2020-08

Variant appearance in text: rs17514846
PubMed Link: 32714026
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Prioritization of causal genes for coronary artery disease based on cumulative evidence from experimental and in silico studies.

Scientific Reports
Shadrina, Alexandra S AS; Shashkova, Tatiana I TI; Torgasheva, Anna A AA; Sharapov, Sodbo Z SZ; Klarić, Lucija L; Pakhomov, Eugene D ED; Alexeev, Dmitry G DG; Wilson, James F JF; Tsepilov, Yakov A YA; Joshi, Peter K PK; Aulchenko, Yurii S YS
Publication Date: 2020-06-26

Variant appearance in text: rs17514846
PubMed Link: 32591598
Variant Present in the following documents:
  • Main text
  • 41598_2020_67001_MOESM6_ESM.pdf
View BVdb publication page



Single-cell expression and Mendelian randomization analyses identify blood genes associated with lifespan and chronic diseases.

Communications Biology
Chignon, Arnaud A; Bon-Baret, Valentin V; Boulanger, Marie-Chloé MC; Li, Zhonglin Z; Argaud, Deborah D; Bossé, Yohan Y; Thériault, Sébastien S; Arsenault, Benoit J BJ; Mathieu, Patrick P
Publication Date: 2020-05-01

Variant appearance in text: rs17514846
PubMed Link: 32358504
Variant Present in the following documents:
  • Main text
View BVdb publication page



Exome-Wide Association Study Reveals Several Susceptibility Genes and Pathways Associated With Acute Coronary Syndromes in Han Chinese.

Frontiers In Genetics
Zheng, Qiwen Q; Zhang, Yan Y; Jiang, Jie J; Jia, Jia J; Fan, Fangfang F; Gong, Yanjun Y; Wang, Zhi Z; Shi, Qiuping Q; Chen, Dafang D; Huo, Yong Y
Publication Date: 2020

Variant appearance in text: rs17514846
PubMed Link: 32328087
Variant Present in the following documents:
  • Main text
  • fgene-11-00336.pdf
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FURIN Expression in Vascular Endothelial Cells Is Modulated by a Coronary Artery Disease-Associated Genetic Variant and Influences Monocyte Transendothelial Migration.

Journal Of The American Heart Association
Yang, Xu X; Yang, Wei W; McVey, David G DG; Zhao, Guojun G; Hu, Jinfu J; Poston, Robin N RN; Ren, Meixia M; Willeit, Karin K; Coassin, Stefan S; Willeit, Johann J; Webb, Thomas R TR; Samani, Nilesh J NJ; Mayr, Manuel M; Kiechl, Stefan S; Ye, Shu S
Publication Date: 2020-02-18

Variant appearance in text: rs17514846
PubMed Link: 32067586
Variant Present in the following documents:
  • Main text
  • JAH3-9-e014333.pdf
View BVdb publication page



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: rs17514846
PubMed Link: 31845553
Variant Present in the following documents:
  • Main text
  • kcj-50-91.pdf
View BVdb publication page



Functional Genomics and CRISPR Applied to Cardiovascular Research and Medicine.

Arteriosclerosis, Thrombosis, And Vascular Biology
Li, Fang F; Shi, Jianting J; Lu, Hong S HS; Zhang, Hanrui H
Publication Date: 2019-09

Variant appearance in text: rs17514846
PubMed Link: 31433696
Variant Present in the following documents:
  • Main text
View BVdb publication page



Improved detection of common variants in coronary artery disease and blood pressure using a pleiotropy cFDR method.

Scientific Reports
Mao, Xiang-Jie XJ; Zhang, Qiang Q; Xu, Fei F; Gao, Pan P; Sun, Nan N; Wang, Bo B; Tang, Qi-Xin QX; Hao, Yi-Bin YB; Sun, Chang-Qing CQ
Publication Date: 2019-07-17

Variant appearance in text: rs17514846
PubMed Link: 31316127
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic and epigenetic regulation of human aging and longevity.

Biochimica Et Biophysica Acta. Molecular Basis Of Disease
Morris, Brian J BJ; Willcox, Bradley J BJ; Donlon, Timothy A TA
Publication Date: 2019-07-01

Variant appearance in text: rs17514846
PubMed Link: 31109447
Variant Present in the following documents:
  • Main text
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: rs17514846
PubMed Link: 31049317
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study of medication-use and associated disease in the UK Biobank.

Nature Communications
Wu, Yeda Y; Byrne, Enda M EM; Zheng, Zhili Z; Kemper, Kathryn E KE; Yengo, Loic L; Mallett, Andrew J AJ; Yang, Jian J; Visscher, Peter M PM; Wray, Naomi R NR
Publication Date: 2019-04-23

Variant appearance in text: rs17514846
PubMed Link: 31015401
Variant Present in the following documents:
  • 41467_2019_9572_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page



The Genetics of Aging: A Vertebrate Perspective.

Cell
Singh, Param Priya PP; Demmitt, Brittany A BA; Nath, Ravi D RD; Brunet, Anne A
Publication Date: 2019-03-21

Variant appearance in text: rs17514846
PubMed Link: 30901541
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic Evidence for the Association between Schizophrenia and Breast Cancer.

Journal Of Psychiatry And Brain Science
Shi, Jiajun J; Wu, Lang L; Zheng, Wei W; Wen, Wanqing W; Wang, Shuyang S; Shu, Xiang X; Long, Jirong J; Shen, Chen-Yang CY; Wu, Pei-Ei PE; Saloustros, Emmanouil E; Chang-Claude, Jenny J; Brenner, Hermann H; Shu, Xiao-Ou XO; Cai, Qiuyin Q
Publication Date: 2018

Variant appearance in text: rs17514846
PubMed Link: 30854469
Variant Present in the following documents:
  • Main text
  • nihms-1001247.pdf
View BVdb publication page



FURIN Inhibition Reduces Vascular Remodeling and Atherosclerotic Lesion Progression in Mice.

Arteriosclerosis, Thrombosis, And Vascular Biology
Yakala, Gopala K GK; Cabrera-Fuentes, Hector A HA; Crespo-Avilan, Gustavo E GE; Rattanasopa, Chutima C; Burlacu, Alexandrina A; George, Benjamin L BL; Anand, Kaviya K; Mayan, David Castaño DC; Corlianò, Maria M; Hernández-Reséndiz, Sauri S; Wu, Zihao Z; Schwerk, Anne M K AMK; Tan, Amberlyn L J ALJ; Trigueros-Motos, Laia L; Chèvre, Raphael R; Chua, Tricia T; Kleemann, Robert R; Liehn, Elisa A EA; Hausenloy, Derek J DJ; Ghosh, Sujoy S; Singaraja, Roshni R RR
Publication Date: 2019-03

Variant appearance in text: rs17514846
PubMed Link: 30651003
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances.

Elife
Timmers, Paul Rhj PR; Mounier, Ninon N; Lall, Kristi K; Fischer, Krista K; Ning, Zheng Z; Feng, Xiao X; Bretherick, Andrew D AD; Clark, David W DW; , ; Shen, Xia X; Esko, Tõnu T; Kutalik, Zoltán Z; Wilson, James F JF; Joshi, Peter K PK
Publication Date: 2019-01-15

Variant appearance in text: rs17514846
PubMed Link: 30642433
Variant Present in the following documents:
  • elife-39856.pdf
View BVdb publication page



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: rs17514846
PubMed Link: 30003307
Variant Present in the following documents:
  • 125_2018_4686_MOESM1_ESM.pdf
View BVdb publication page



Influence of a Coronary Artery Disease-Associated Genetic Variant on FURIN Expression and Effect of Furin on Macrophage Behavior.

Arteriosclerosis, Thrombosis, And Vascular Biology
Zhao, Guojun G; Yang, Wei W; Wu, Jingchun J; Chen, Bairu B; Yang, Xu X; Chen, Junhui J; McVey, David G DG; Andreadi, Catherine C; Gong, Peng P; Webb, Tom R TR; Samani, Nilesh J NJ; Ye, Shu S
Publication Date: 2018-08

Variant appearance in text: rs17514846
PubMed Link: 29976768
Variant Present in the following documents:
  • Main text
  • atv-38-1837.pdf
View BVdb publication page



Weighted Multi-marker Genetic Risk Scores for Incident Coronary Heart Disease among Individuals of African, Latino and East-Asian Ancestry.

Scientific Reports
Iribarren, Carlos C; Lu, Meng M; Jorgenson, Eric E; Martínez, Manuel M; Lluis-Ganella, Carla C; Subirana, Isaac I; Salas, Eduardo E; Elosua, Roberto R
Publication Date: 2018-05-01

Variant appearance in text: rs17514846
PubMed Link: 29717161
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_25128.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: rs17514846
PubMed Link: 29695241
Variant Present in the following documents:
  • Main text
  • 12933_2018_Article_705.pdf
View BVdb publication page



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: rs17514846
PubMed Link: 29263402
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_18214.pdf
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Human longevity: 25 genetic loci associated in 389,166 UK biobank participants.

Aging
Pilling, Luke C LC; Kuo, Chia-Ling CL; Sicinski, Kamil K; Tamosauskaite, Jone J; Kuchel, George A GA; Harries, Lorna W LW; Herd, Pamela P; Wallace, Robert R; Ferrucci, Luigi L; Melzer, David D
Publication Date: 2017-12-06

Variant appearance in text: rs17514846
PubMed Link: 29227965
Variant Present in the following documents:
  • Main text
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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: rs17514846
PubMed Link: 29220472
Variant Present in the following documents:
  • Main text
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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: rs17514846
PubMed Link: 28640878
Variant Present in the following documents:
  • pgen.1006328.s006.pdf
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A comparison of Cox and logistic regression for use in genome-wide association studies of cohort and case-cohort design.

European Journal Of Human Genetics : Ejhg
Staley, James R JR; Jones, Edmund E; Kaptoge, Stephen S; Butterworth, Adam S AS; Sweeting, Michael J MJ; Wood, Angela M AM; Howson, Joanna M M JMM
Publication Date: 2017-06

Variant appearance in text: rs17514846
PubMed Link: 28594416
Variant Present in the following documents:
  • Main text
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ADAM19: A Novel Target for Metabolic Syndrome in Humans and Mice.

Mediators Of Inflammation
Weerasekera, Lakshini L; Rudnicka, Caroline C; Sang, Qing-Xiang QX; Curran, Joanne E JE; Johnson, Matthew P MP; Moses, Eric K EK; Göring, Harald H H HH; Blangero, John J; Hricova, Jana J; Schlaich, Markus M; Matthews, Vance B VB
Publication Date: 2017

Variant appearance in text: rs17514846
PubMed Link: 28265178
Variant Present in the following documents:
  • Main text
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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: rs17514846
PubMed Link: 28209224
Variant Present in the following documents:
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Heart Disease and Stroke Statistics-2017 Update: A Report From the American Heart Association.

Circulation
Benjamin, Emelia J EJ; Blaha, Michael J MJ; Chiuve, Stephanie E SE; Cushman, Mary M; Das, Sandeep R SR; Deo, Rajat R; de Ferranti, Sarah D SD; Floyd, James J; Fornage, Myriam M; Gillespie, Cathleen C; Isasi, Carmen R CR; Jiménez, Monik C MC; Jordan, Lori Chaffin LC; Judd, Suzanne E SE; Lackland, Daniel D; Lichtman, Judith H JH; Lisabeth, Lynda L; Liu, Simin S; Longenecker, Chris T CT; Mackey, Rachel H RH; Matsushita, Kunihiro K; Mozaffarian, Dariush D; Mussolino, Michael E ME; Nasir, Khurram K; Neumar, Robert W RW; Palaniappan, Latha L; Pandey, Dilip K DK; Thiagarajan, Ravi R RR; Reeves, Mathew J MJ; Ritchey, Matthew M; Rodriguez, Carlos J CJ; Roth, Gregory A GA; Rosamond, Wayne D WD; Sasson, Comilla C; Towfighi, Amytis A; Tsao, Connie W CW; Turner, Melanie B MB; Virani, Salim S SS; Voeks, Jenifer H JH; Willey, Joshua Z JZ; Wilkins, John T JT; Wu, Jason Hy JH; Alger, Heather M HM; Wong, Sally S SS; Muntner, Paul P; ,
Publication Date: 2017-03-07

Variant appearance in text: rs17514846
PubMed Link: 28122885
Variant Present in the following documents:
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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: rs17514846
PubMed Link: 28122634
Variant Present in the following documents:
  • 13059_2016_1142_MOESM1_ESM.pdf
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Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans.

Plos One
Franceschini, Nora N; Carty, Cara L CL; Lu, Yingchang Y; Tao, Ran R; Sung, Yun Ju YJ; Manichaikul, Ani A; Haessler, Jeff J; Fornage, Myriam M; Schwander, Karen K; Zubair, Niha N; Bien, Stephanie S; Hindorff, Lucia A LA; Guo, Xiuqing X; Bielinski, Suzette J SJ; Ehret, Georg G; Kaufman, Joel D JD; Rich, Stephen S SS; Carlson, Christopher S CS; Bottinger, Erwin P EP; North, Kari E KE; Rao, D C DC; Chakravarti, Aravinda A; Barrett, Paula Q PQ; Loos, Ruth J F RJ; Buyske, Steven S; Kooperberg, Charles C
Publication Date: 2016

Variant appearance in text: rs17514846
PubMed Link: 27736895
Variant Present in the following documents:
  • pone.0164132.s001.pdf
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Coronary Artery Calcification and Rheumatoid Arthritis: Lack of Relationship to Risk Alleles for Coronary Artery Disease in the General Population.

Arthritis & Rheumatology (Hoboken, N.J.)
Ferraz-Amaro, Iván I; Winchester, Robert R; Gregersen, Peter K PK; Reynolds, Richard J RJ; Wasko, Mary Chester MC; Oeser, Anette A; Chung, Cecilia P CP; Stein, C Michael CM; Giles, Jon T JT; Bathon, Joan M JM
Publication Date: 2017-03

Variant appearance in text: rs17514846
PubMed Link: 27696788
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Variants in human papillomavirus receptor and associated genes are associated with type-specific HPV infection and lesion progression of the cervix.

Oncotarget
Zou, Jian J; Cao, Zhu Z; Zhang, Jianyang J; Chen, Tingting T; Yang, Shizhou S; Huang, Yongjie Y; Hong, Die D; Li, Yang Y; Chen, Xiaojing X; Wang, Xinyu X; Cheng, Xiaodong X; Lu, Weiguo W; Xie, Xing X
Publication Date: 2016-06-28

Variant appearance in text: rs17514846
PubMed Link: 27223085
Variant Present in the following documents:
  • Main text
  • oncotarget-07-40135.pdf
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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: rs17514846
PubMed Link: 27189168
Variant Present in the following documents:
  • Main text
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