GOSR2 c.477+736T>C

Variant ID: 17-45013271-T-C

NM_004287.3(GOSR2):c.477+736T>C

This variant was identified in 51 publications

View GRCh38 version.




Publications:


Multivariate Genome-wide Association Analysis by Iterative Hard Thresholding.

Bioinformatics (Oxford, England)
Chu, Benjamin B BB; Ko, Seyoon S; Zhou, Jin J JJ; Jensen, Aubrey A; Zhou, Hua H; Sinsheimer, Janet S JS; Lange, Kenneth K
Publication Date: 2023-04-17

Variant appearance in text: rs17608766
PubMed Link: 37067496
Variant Present in the following documents:
  • btad193_supplementary_data.pdf
View BVdb publication page



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: rs17608766
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Common genetic variation associated with Mendelian disease severity revealed through cryptic phenotype analysis.

Nature Communications
Blair, David R DR; Hoffmann, Thomas J TJ; Shieh, Joseph T JT
Publication Date: 2022-06-27

Variant appearance in text: rs17608766
PubMed Link: 35760791
Variant Present in the following documents:
  • 41467_2022_31030_MOESM1_ESM.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: rs17608766
PubMed Link: 34876023
Variant Present in the following documents:
  • 12872_2021_2398_MOESM1_ESM.pdf
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Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.

Nature Communications
Georges, Adrien A; Yang, Min-Lee ML; Berrandou, Takiy-Eddine TE; Bakker, Mark K MK; Dikilitas, Ozan O; Kiando, Soto Romuald SR; Ma, Lijiang L; Satterfield, Benjamin A BA; Sengupta, Sebanti S; Yu, Mengyao M; Deleuze, Jean-François JF; Dupré, Delia D; Hunker, Kristina L KL; Kyryachenko, Sergiy S; Liu, Lu L; Sayoud-Sadeg, Ines I; Amar, Laurence L; Brummett, Chad M CM; Coleman, Dawn M DM; d'Escamard, Valentina V; de Leeuw, Peter P; Fendrikova-Mahlay, Natalia N; Kadian-Dodov, Daniella D; Li, Jun Z JZ; Lorthioir, Aurélien A; Pappaccogli, Marco M; Prejbisz, Aleksander A; Smigielski, Witold W; Stanley, James C JC; Zawistowski, Matthew M; Zhou, Xiang X; Zöllner, Sebastian S; , ; , ; , ; Amouyel, Philippe P; De Buyzere, Marc L ML; Debette, Stéphanie S; Dobrowolski, Piotr P; Drygas, Wojciech W; Gornik, Heather L HL; Olin, Jeffrey W JW; Piwonski, Jerzy J; Rietzschel, Ernst R ER; Ruigrok, Ynte M YM; Vikkula, Miikka M; Warchol Celinska, Ewa E; Januszewicz, Andrzej A; Kullo, Iftikhar J IJ; Azizi, Michel M; , ; Jeunemaitre, Xavier X; Persu, Alexandre A; Kovacic, Jason C JC; Ganesh, Santhi K SK; Bouatia-Naji, Nabila N
Publication Date: 2021-10-15

Variant appearance in text: rs17608766
PubMed Link: 34654805
Variant Present in the following documents:
  • 41467_2021_26174_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.

Nature Communications
Georges, Adrien A; Yang, Min-Lee ML; Berrandou, Takiy-Eddine TE; Bakker, Mark K MK; Dikilitas, Ozan O; Kiando, Soto Romuald SR; Ma, Lijiang L; Satterfield, Benjamin A BA; Sengupta, Sebanti S; Yu, Mengyao M; Deleuze, Jean-François JF; Dupré, Delia D; Hunker, Kristina L KL; Kyryachenko, Sergiy S; Liu, Lu L; Sayoud-Sadeg, Ines I; Amar, Laurence L; Brummett, Chad M CM; Coleman, Dawn M DM; d'Escamard, Valentina V; de Leeuw, Peter P; Fendrikova-Mahlay, Natalia N; Kadian-Dodov, Daniella D; Li, Jun Z JZ; Lorthioir, Aurélien A; Pappaccogli, Marco M; Prejbisz, Aleksander A; Smigielski, Witold W; Stanley, James C JC; Zawistowski, Matthew M; Zhou, Xiang X; Zöllner, Sebastian S; , ; , ; , ; Amouyel, Philippe P; De Buyzere, Marc L ML; Debette, Stéphanie S; Dobrowolski, Piotr P; Drygas, Wojciech W; Gornik, Heather L HL; Olin, Jeffrey W JW; Piwonski, Jerzy J; Rietzschel, Ernst R ER; Ruigrok, Ynte M YM; Vikkula, Miikka M; Warchol Celinska, Ewa E; Januszewicz, Andrzej A; Kullo, Iftikhar J IJ; Azizi, Michel M; Jeunemaitre, Xavier X; Persu, Alexandre A; Kovacic, Jason C JC; Ganesh, Santhi K SK; Bouatia-Naji, Nabila N
Publication Date: 2021-10-15

Variant appearance in text: rs17608766
PubMed Link: 34654805
Variant Present in the following documents:
  • 41467_2021_26174_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



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: rs17608766
PubMed Link: 34226943
Variant Present in the following documents:
  • 125_2021_5491_MOESM1_ESM.pdf
View BVdb publication page



Hypertension in African Populations: Review and Computational Insights.

Genes
Mabhida, Sihle E SE; Mashatola, Lebohang L; Kaur, Mandeep M; Sharma, Jyoti R JR; Apalata, Teke T; Muhamed, Babu B; Benjeddou, Mongi M; Johnson, Rabia R
Publication Date: 2021-04-06

Variant appearance in text: rs17608766
PubMed Link: 33917487
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation.

Circulation. Genomic And Precision Medicine
Weng, Lu-Chen LC; Hall, Amelia Weber AW; Choi, Seung Hoan SH; Jurgens, Sean J SJ; Haessler, Jeffrey J; Bihlmeyer, Nathan A NA; Grarup, Niels N; Lin, Honghuang H; Teumer, Alexander A; Li-Gao, Ruifang R; Yao, Jie J; Guo, Xiuqing X; Brody, Jennifer A JA; Müller-Nurasyid, Martina M; Schramm, Katharina K; Verweij, Niek N; van den Berg, Marten E ME; van Setten, Jessica J; Isaacs, Aaron A; Ramírez, Julia J; Warren, Helen R HR; Padmanabhan, Sandosh S; Kors, Jan A JA; de Boer, Rudolf A RA; van der Meer, Peter P; Sinner, Moritz F MF; Waldenberger, Melanie M; Psaty, Bruce M BM; Taylor, Kent D KD; Völker, Uwe U; Kanters, Jørgen K JK; Li, Man M; Alonso, Alvaro A; Perez, Marco V MV; Vaartjes, Ilonca I; Bots, Michiel L ML; Huang, Paul L PL; Heckbert, Susan R SR; Lin, Henry J HJ; Kornej, Jelena J; Munroe, Patricia B PB; van Duijn, Cornelia M CM; Asselbergs, Folkert W FW; Stricker, Bruno H BH; van der Harst, Pim P; Kääb, Stefan S; Peters, Annette A; Sotoodehnia, Nona N; Rotter, Jerome I JI; Mook-Kanamori, Dennis O DO; Dörr, Marcus M; Felix, Stephan B SB; Linneberg, Allan A; Hansen, Torben T; Arking, Dan E DE; Kooperberg, Charles C; Benjamin, Emelia J EJ; Lunetta, Kathryn L KL; Ellinor, Patrick T PT; Lubitz, Steven A SA
Publication Date: 2020-10

Variant appearance in text: rs17608766
PubMed Link: 32822252
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic and functional insights into the fractal structure of the heart.

Nature
Meyer, Hannah V HV; Dawes, Timothy J W TJW; Serrani, Marta M; Bai, Wenjia W; Tokarczuk, Paweł P; Cai, Jiashen J; de Marvao, Antonio A; Henry, Albert A; Lumbers, R Thomas RT; Gierten, Jakob J; Thumberger, Thomas T; Wittbrodt, Joachim J; Ware, James S JS; Rueckert, Daniel D; Matthews, Paul M PM; Prasad, Sanjay K SK; Costantino, Maria L ML; Cook, Stuart A SA; Birney, Ewan E; O'Regan, Declan P DP
Publication Date: 2020-08

Variant appearance in text: rs17608766
PubMed Link: 32814899
Variant Present in the following documents:
  • Main text
View BVdb publication page



Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated With Brugada Syndrome: SADS-TW BrS Registry.

Circulation. Genomic And Precision Medicine
Jimmy Juang, Jyh-Ming JM; Liu, Yen-Bin YB; Julius Chen, Ching-Yu CY; Yu, Qi-You QY; Chattopadhyay, Amrita A; Lin, Lian-Yu LY; Chen, Wen-Jone WJ; Yu, Chih-Chien CC; Huang, Hui-Chun HC; Ho, Li-Ting LT; Lai, Ling-Ping LP; Hwang, Juey-Jen JJ; Lin, Ting-Tse TT; Liao, Min-Tsun MT; Chen, Jien-Jiun JJ; Sherri Yeh, Shih-Fan SF; Chuang, Jing-Yuan JY; Yang, Dun-Hui DH; Lin, Jiunn-Lee JL; Lu, Tzu-Pin TP; Chuang, Eric Y EY; Ackerman, Michael J MJ
Publication Date: 2020-08

Variant appearance in text: rs17608766
PubMed Link: 32490690
Variant Present in the following documents:
  • hcg-13-e002797-s001.pdf
View BVdb publication page



Causal Factors for Knee, Hip, and Hand Osteoarthritis: A Mendelian Randomization Study in the UK Biobank.

Arthritis & Rheumatology (Hoboken, N.J.)
Funck-Brentano, Thomas T; Nethander, Maria M; Movérare-Skrtic, Sofia S; Richette, Pascal P; Ohlsson, Claes C
Publication Date: 2019-10

Variant appearance in text: rs17608766
PubMed Link: 31099188
Variant Present in the following documents:
  • ART-71-1634-s001.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: rs17608766
PubMed Link: 31049317
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetics of Hypertension in African Americans and Others of African Descent.

International Journal Of Molecular Sciences
Zilbermint, Mihail M; Hannah-Shmouni, Fady F; Stratakis, Constantine A CA
Publication Date: 2019-03-02

Variant appearance in text: rs17608766
PubMed Link: 30832344
Variant Present in the following documents:
  • Main text
  • ijms-20-01081.pdf
View BVdb publication page



Hypertension and Cerebral Microangiopathy (Cerebral Small Vessel Disease): Genetic and Epigenetic Aspects of Their Relationship.

Acta Naturae
Dobrynina, L A LA; Zabitova, M R MR; Kalashnikova, L A LA; Gnedovskaya, E V EV; Piradov, M A MA
Publication Date: 2018

Variant appearance in text: rs17608766
PubMed Link: 30116610
Variant Present in the following documents:
  • Main text
  • AN20758251-10-02-004.pdf
View BVdb publication page



Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.

Genome Biology
Prins, Bram P BP; Mead, Timothy J TJ; Brody, Jennifer A JA; Sveinbjornsson, Gardar G; Ntalla, Ioanna I; Bihlmeyer, Nathan A NA; van den Berg, Marten M; Bork-Jensen, Jette J; Cappellani, Stefania S; Van Duijvenboden, Stefan S; Klena, Nikolai T NT; Gabriel, George C GC; Liu, Xiaoqin X; Gulec, Cagri C; Grarup, Niels N; Haessler, Jeffrey J; Hall, Leanne M LM; Iorio, Annamaria A; Isaacs, Aaron A; Li-Gao, Ruifang R; Lin, Honghuang H; Liu, Ching-Ti CT; Lyytikäinen, Leo-Pekka LP; Marten, Jonathan J; Mei, Hao H; Müller-Nurasyid, Martina M; Orini, Michele M; Padmanabhan, Sandosh S; Radmanesh, Farid F; Ramirez, Julia J; Robino, Antonietta A; Schwartz, Molly M; van Setten, Jessica J; Smith, Albert V AV; Verweij, Niek N; Warren, Helen R HR; Weiss, Stefan S; Alonso, Alvaro A; Arnar, David O DO; Bots, Michiel L ML; de Boer, Rudolf A RA; Dominiczak, Anna F AF; Eijgelsheim, Mark M; Ellinor, Patrick T PT; Guo, Xiuqing X; Felix, Stephan B SB; Harris, Tamara B TB; Hayward, Caroline C; Heckbert, Susan R SR; Huang, Paul L PL; Jukema, J W JW; Kähönen, Mika M; Kors, Jan A JA; Lambiase, Pier D PD; Launer, Lenore J LJ; Li, Man M; Linneberg, Allan A; Nelson, Christopher P CP; Pedersen, Oluf O; Perez, Marco M; Peters, Annette A; Polasek, Ozren O; Psaty, Bruce M BM; Raitakari, Olli T OT; Rice, Kenneth M KM; Rotter, Jerome I JI; Sinner, Moritz F MF; Soliman, Elsayed Z EZ; Spector, Tim D TD; Strauch, Konstantin K; Thorsteinsdottir, Unnur U; Tinker, Andrew A; Trompet, Stella S; Uitterlinden, André A; Vaartjes, Ilonca I; van der Meer, Peter P; Völker, Uwe U; Völzke, Henry H; Waldenberger, Melanie M; Wilson, James G JG; Xie, Zhijun Z; Asselbergs, Folkert W FW; Dörr, Marcus M; van Duijn, Cornelia M CM; Gasparini, Paolo P; Gudbjartsson, Daniel F DF; Gudnason, Vilmundur V; Hansen, Torben T; Kääb, Stefan S; Kanters, Jørgen K JK; Kooperberg, Charles C; Lehtimäki, Terho T; Lin, Henry J HJ; Lubitz, Steven A SA; Mook-Kanamori, Dennis O DO; Conti, Francesco J FJ; Newton-Cheh, Christopher H CH; Rosand, Jonathan J; Rudan, Igor I; Samani, Nilesh J NJ; Sinagra, Gianfranco G; Smith, Blair H BH; Holm, Hilma H; Stricker, Bruno H BH; Ulivi, Sheila S; Sotoodehnia, Nona N; Apte, Suneel S SS; van der Harst, Pim P; Stefansson, Kari K; Munroe, Patricia B PB; Arking, Dan E DE; Lo, Cecilia W CW; Jamshidi, Yalda Y
Publication Date: 2018-07-17

Variant appearance in text: rs17608766
PubMed Link: 30012220
Variant Present in the following documents:
  • Main text
View BVdb publication page



ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals.

Circulation. Genomic And Precision Medicine
Bihlmeyer, Nathan A NA; Brody, Jennifer A JA; Smith, Albert Vernon AV; Warren, Helen R HR; Lin, Honghuang H; Isaacs, Aaron A; Liu, Ching-Ti CT; Marten, Jonathan J; Radmanesh, Farid F; Hall, Leanne M LM; Grarup, Niels N; Mei, Hao H; Müller-Nurasyid, Martina M; Huffman, Jennifer E JE; Verweij, Niek N; Guo, Xiuqing X; Yao, Jie J; Li-Gao, Ruifang R; van den Berg, Marten M; Weiss, Stefan S; Prins, Bram P BP; van Setten, Jessica J; Haessler, Jeffrey J; Lyytikäinen, Leo-Pekka LP; Li, Man M; Alonso, Alvaro A; Soliman, Elsayed Z EZ; Bis, Joshua C JC; Austin, Tom T; Chen, Yii-Der Ida YI; Psaty, Bruce M BM; Harrris, Tamara B TB; Launer, Lenore J LJ; Padmanabhan, Sandosh S; Dominiczak, Anna A; Huang, Paul L PL; Xie, Zhijun Z; Ellinor, Patrick T PT; Kors, Jan A JA; Campbell, Archie A; Murray, Alison D AD; Nelson, Christopher P CP; Tobin, Martin D MD; Bork-Jensen, Jette J; Hansen, Torben T; Pedersen, Oluf O; Linneberg, Allan A; Sinner, Moritz F MF; Peters, Annette A; Waldenberger, Melanie M; Meitinger, Thomas T; Perz, Siegfried S; Kolcic, Ivana I; Rudan, Igor I; de Boer, Rudolf A RA; van der Meer, Peter P; Lin, Henry J HJ; Taylor, Kent D KD; de Mutsert, Renée R; Trompet, Stella S; Jukema, J Wouter JW; Maan, Arie C AC; Stricker, Bruno H C BHC; Rivadeneira, Fernando F; Uitterlinden, André A; Völker, Uwe U; Homuth, Georg G; Völzke, Henry H; Felix, Stephan B SB; Mangino, Massimo M; Spector, Timothy D TD; Bots, Michiel L ML; Perez, Marco M; Raitakari, Olli T OT; Kähönen, Mika M; Mononen, Nina N; Gudnason, Vilmundur V; Munroe, Patricia B PB; Lubitz, Steven A SA; van Duijn, Cornelia M CM; Newton-Cheh, Christopher H CH; Hayward, Caroline C; Rosand, Jonathan J; Samani, Nilesh J NJ; Kanters, Jørgen K JK; Wilson, James G JG; Kääb, Stefan S; Polasek, Ozren O; van der Harst, Pim P; Heckbert, Susan R SR; Rotter, Jerome I JI; Mook-Kanamori, Dennis O DO; Eijgelsheim, Mark M; Dörr, Marcus M; Jamshidi, Yalda Y; Asselbergs, Folkert W FW; Kooperberg, Charles C; Lehtimäki, Terho T; Arking, Dan E DE; Sotoodehnia, Nona N
Publication Date: 2018-01

Variant appearance in text: rs17608766
PubMed Link: 29874175
Variant Present in the following documents:
  • Main text
  • hcg-11-e001758.pdf
  • hcg-11-e001758-s001.pdf
View BVdb publication page



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: rs17608766
PubMed Link: 29695241
Variant Present in the following documents:
  • Main text
View BVdb publication page



Brief Overview of a Decade of Genome-Wide Association Studies on Primary Hypertension.

International Journal Of Endocrinology
Azam, Afifah Binti AB; Azizan, Elena Aisha Binti EAB
Publication Date: 2018

Variant appearance in text: rs17608766
PubMed Link: 29666641
Variant Present in the following documents:
  • Main text
  • IJE2018-7259704.pdf
View BVdb publication page



Genomics of Cardiovascular Measures of Autonomic Tone.

Journal Of Cardiovascular Pharmacology
Sigurdsson, Martin I MI; Waldron, Nathan H NH; Bortsov, Andrey V AV; Smith, Shad B SB; Maixner, William W
Publication Date: 2018-03

Variant appearance in text: rs17608766
PubMed Link: 29300220
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs17608766
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



G-T haplotype established by rs3785889-rs16941382 in GOSR2 gene is associated with coronary artery disease in Chinese Han population.

Oncotarget
Pan, Shuo S; Guan, Gong-Chang GC; Lv, Ying Y; Liu, Zhong-Wei ZW; Liu, Fu-Qiang FQ; Zhang, Yong Y; Zhu, Shun-Ming SM; Zhang, Rong-Huai RH; Zhao, Na N; Shi, Shuang S; Nakayama, Tomohiro T; Wang, Jun-Kui JK
Publication Date: 2017-10-10

Variant appearance in text: rs17608766
PubMed Link: 29137253
Variant Present in the following documents:
  • Main text
  • oncotarget-08-82165.pdf
View BVdb publication page



Towards Precision Medicine for Hypertension: A Review of Genomic, Epigenomic, and Microbiomic Effects on Blood Pressure in Experimental Rat Models and Humans.

Physiological Reviews
Padmanabhan, Sandosh S; Joe, Bina B
Publication Date: 2017-10-01

Variant appearance in text: rs17608766
PubMed Link: 28931564
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos.

Scientific Reports
Sofer, Tamar T; Wong, Quenna Q; Hartwig, Fernando P FP; Taylor, Kent K; Warren, Helen R HR; Evangelou, Evangelos E; Cabrera, Claudia P CP; Levy, Daniel D; Kramer, Holly H; Lange, Leslie A LA; Horta, Bernardo L BL; , ; Kerr, Kathleen F KF; Reiner, Alex P AP; Franceschini, Nora N
Publication Date: 2017-09-04

Variant appearance in text: rs17608766
PubMed Link: 28871152
Variant Present in the following documents:
  • 41598_2017_9019_MOESM1_ESM.pdf
View BVdb publication page



Is There a Role for Genomics in the Management of Hypertension?

International Journal Of Molecular Sciences
Burrello, Jacopo J; Monticone, Silvia S; Buffolo, Fabrizio F; Tetti, Martina M; Veglio, Franco F; Williams, Tracy A TA; Mulatero, Paolo P
Publication Date: 2017-05-26

Variant appearance in text: rs17608766
PubMed Link: 28587112
Variant Present in the following documents:
  • Main text
  • ijms-18-01131.pdf
View BVdb publication page



Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms.

Nature Genetics
Howson, Joanna M M JMM; Zhao, Wei W; Barnes, Daniel R DR; Ho, Weang-Kee WK; Young, Robin R; Paul, Dirk S DS; Waite, Lindsay L LL; Freitag, Daniel F DF; Fauman, Eric B EB; Salfati, Elias L EL; Sun, Benjamin B BB; Eicher, John D JD; Johnson, Andrew D AD; Sheu, Wayne H H WHH; Nielsen, Sune F SF; Lin, Wei-Yu WY; Surendran, Praveen P; Malarstig, Anders A; Wilk, Jemma B JB; Tybjærg-Hansen, Anne A; Rasmussen, Katrine L KL; Kamstrup, Pia R PR; Deloukas, Panos P; Erdmann, Jeanette J; Kathiresan, Sekar S; Samani, Nilesh J NJ; Schunkert, Heribert H; Watkins, Hugh H; , ; Do, Ron R; Rader, Daniel J DJ; Johnson, Julie A JA; Hazen, Stanley L SL; Quyyumi, Arshed A AA; Spertus, John A JA; Pepine, Carl J CJ; Franceschini, Nora N; Justice, Anne A; Reiner, Alex P AP; Buyske, Steven S; Hindorff, Lucia A LA; Carty, Cara L CL; North, Kari E KE; Kooperberg, Charles C; Boerwinkle, Eric E; Young, Kristin K; Graff, Mariaelisa M; Peters, Ulrike U; Absher, Devin D; Hsiung, Chao A CA; Lee, Wen-Jane WJ; Taylor, Kent D KD; Chen, Ying-Hsiang YH; Lee, I-Te IT; Guo, Xiuqing X; Chung, Ren-Hua RH; Hung, Yi-Jen YJ; Rotter, Jerome I JI; Juang, Jyh-Ming J JJ; Quertermous, Thomas T; Wang, Tzung-Dau TD; Rasheed, Asif A; Frossard, Philippe P; Alam, Dewan S DS; Majumder, Abdulla Al Shafi AAS; Di Angelantonio, Emanuele E; Chowdhury, Rajiv R; , ; Chen, Yii-Der Ida YI; Nordestgaard, Børge G BG; Assimes, Themistocles L TL; Danesh, John J; Butterworth, Adam S AS; Saleheen, Danish D
Publication Date: 2017-07

Variant appearance in text: rs17608766
PubMed Link: 28530674
Variant Present in the following documents:
  • Main text
View BVdb publication page



Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.

The Journal Of Clinical Investigation
Wild, Philipp S PS; Felix, Janine F JF; Schillert, Arne A; Teumer, Alexander A; Chen, Ming-Huei MH; Leening, Maarten J G MJG; Völker, Uwe U; Großmann, Vera V; Brody, Jennifer A JA; Irvin, Marguerite R MR; Shah, Sanjiv J SJ; Pramana, Setia S; Lieb, Wolfgang W; Schmidt, Reinhold R; Stanton, Alice V AV; Malzahn, Dörthe D; Smith, Albert Vernon AV; Sundström, Johan J; Minelli, Cosetta C; Ruggiero, Daniela D; Lyytikäinen, Leo-Pekka LP; Tiller, Daniel D; Smith, J Gustav JG; Monnereau, Claire C; Di Tullio, Marco R MR; Musani, Solomon K SK; Morrison, Alanna C AC; Pers, Tune H TH; Morley, Michael M; Kleber, Marcus E ME; Aragam, Jayashri J; Benjamin, Emelia J EJ; Bis, Joshua C JC; Bisping, Egbert E; Broeckel, Ulrich U; Cheng, Susan S; Deckers, Jaap W JW; Del Greco M, Fabiola F; Edelmann, Frank F; Fornage, Myriam M; Franke, Lude L; Friedrich, Nele N; Harris, Tamara B TB; Hofer, Edith E; Hofman, Albert A; Huang, Jie J; Hughes, Alun D AD; Kähönen, Mika M; Investigators, Knhi K; Kruppa, Jochen J; Lackner, Karl J KJ; Lannfelt, Lars L; Laskowski, Rafael R; Launer, Lenore J LJ; Leosdottir, Margrét M; Lin, Honghuang H; Lindgren, Cecilia M CM; Loley, Christina C; MacRae, Calum A CA; Mascalzoni, Deborah D; Mayet, Jamil J; Medenwald, Daniel D; Morris, Andrew P AP; Müller, Christian C; Müller-Nurasyid, Martina M; Nappo, Stefania S; Nilsson, Peter M PM; Nuding, Sebastian S; Nutile, Teresa T; Peters, Annette A; Pfeufer, Arne A; Pietzner, Diana D; Pramstaller, Peter P PP; Raitakari, Olli T OT; Rice, Kenneth M KM; Rivadeneira, Fernando F; Rotter, Jerome I JI; Ruohonen, Saku T ST; Sacco, Ralph L RL; Samdarshi, Tandaw E TE; Schmidt, Helena H; Sharp, Andrew S P ASP; Shields, Denis C DC; Sorice, Rossella R; Sotoodehnia, Nona N; Stricker, Bruno H BH; Surendran, Praveen P; Thom, Simon S; Töglhofer, Anna M AM; Uitterlinden, André G AG; Wachter, Rolf R; Völzke, Henry H; Ziegler, Andreas A; Münzel, Thomas T; März, Winfried W; Cappola, Thomas P TP; Hirschhorn, Joel N JN; Mitchell, Gary F GF; Smith, Nicholas L NL; Fox, Ervin R ER; Dueker, Nicole D ND; Jaddoe, Vincent W V VWV; Melander, Olle O; Russ, Martin M; Lehtimäki, Terho T; Ciullo, Marina M; Hicks, Andrew A AA; Lind, Lars L; Gudnason, Vilmundur V; Pieske, Burkert B; Barron, Anthony J AJ; Zweiker, Robert R; Schunkert, Heribert H; Ingelsson, Erik E; Liu, Kiang K; Arnett, Donna K DK; Psaty, Bruce M BM; Blankenberg, Stefan S; Larson, Martin G MG; Felix, Stephan B SB; Franco, Oscar H OH; Zeller, Tanja T; Vasan, Ramachandran S RS; Dörr, Marcus M
Publication Date: 2017-05-01

Variant appearance in text: rs17608766
PubMed Link: 28394258
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Examination of previously identified associations within the Genetic Analysis Workshop 19 data.

Bmc Proceedings
Howey, Richard A J RA; Eu-Ahsunthornwattana, Jakris J; Darlay, Rebecca R; Cordell, Heather J HJ
Publication Date: 2016

Variant appearance in text: rs17608766
PubMed Link: 27980618
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  • Main text
  • 12919_2016_Article_12.pdf
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The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.

Nature Genetics
Ehret, Georg B GB; Ferreira, Teresa T; Chasman, Daniel I DI; Jackson, Anne U AU; Schmidt, Ellen M EM; Johnson, Toby T; Thorleifsson, Gudmar G; Luan, Jian'an J; Donnelly, Lousie A LA; Kanoni, Stavroula S; Petersen, Ann-Kristin AK; Pihur, Vasyl V; Strawbridge, Rona J RJ; Shungin, Dmitry D; Hughes, Maria F MF; Meirelles, Osorio O; Kaakinen, Marika M; Bouatia-Naji, Nabila N; Kristiansson, Kati K; Shah, Sonia S; Kleber, Marcus E ME; Guo, Xiuqing X; Lyytikäinen, Leo-Pekka LP; Fava, Cristiano C; Eriksson, Niclas N; Nolte, Ilja M IM; Magnusson, Patrik K PK; Salfati, Elias L EL; Rallidis, Loukianos S LS; Theusch, Elizabeth E; Smith, Andrew J P AJP; Folkersen, Lasse L; Witkowska, Kate K; Pers, Tune H TH; Joehanes, Roby R; Kim, Stuart K SK; Lataniotis, Lazaros L; Jansen, Rick R; Johnson, Andrew D AD; Warren, Helen H; Kim, Young Jin YJ; Zhao, Wei W; Wu, Ying Y; Tayo, Bamidele O BO; Bochud, Murielle M; , ; , ; , ; Absher, Devin D; Adair, Linda S LS; Amin, Najaf N; Arking, Dan E DE; Axelsson, Tomas T; Baldassarre, Damiano D; Balkau, Beverley B; Bandinelli, Stefania S; Barnes, Michael R MR; Barroso, Inês I; Bevan, Stephen S; Bis, Joshua C JC; Bjornsdottir, Gyda G; Boehnke, Michael M; Boerwinkle, Eric E; Bonnycastle, Lori L LL; Boomsma, Dorret I DI; Bornstein, Stefan R SR; Brown, Morris J MJ; Burnier, Michel M; Cabrera, Claudia P CP; Chambers, John C JC; Chang, I-Shou IS; Cheng, Ching-Yu CY; Chines, Peter S PS; Chung, Ren-Hua RH; Collins, Francis S FS; Connell, John M JM; Döring, Angela A; Dallongeville, Jean J; Danesh, John J; de Faire, Ulf U; Delgado, Graciela G; Dominiczak, Anna F AF; Doney, Alex S F ASF; Drenos, Fotios F; Edkins, Sarah S; Eicher, John D JD; Elosua, Roberto R; Enroth, Stefan S; Erdmann, Jeanette J; Eriksson, Per P; Esko, Tonu T; Evangelou, Evangelos E; Evans, Alun A; Fall, Tove T; Farrall, Martin M; Felix, Janine F JF; Ferrières, Jean J; Ferrucci, Luigi L; Fornage, Myriam M; Forrester, Terrence T; Franceschini, Nora N; Duran, Oscar H Franco OHF; Franco-Cereceda, Anders A; Fraser, Ross M RM; Ganesh, Santhi K SK; Gao, He H; Gertow, Karl K; Gianfagna, Francesco F; Gigante, Bruna B; Giulianini, Franco F; Goel, Anuj A; Goodall, Alison H AH; Goodarzi, Mark O MO; Gorski, Mathias M; Gräßler, Jürgen J; Groves, Christopher C; Gudnason, Vilmundur V; Gyllensten, Ulf U; Hallmans, Göran G; Hartikainen, Anna-Liisa AL; Hassinen, Maija M; Havulinna, Aki S AS; Hayward, Caroline C; Hercberg, Serge S; Herzig, Karl-Heinz KH; Hicks, Andrew A AA; Hingorani, Aroon D AD; Hirschhorn, Joel N JN; Hofman, Albert A; Holmen, Jostein J; Holmen, Oddgeir Lingaas OL; Hottenga, Jouke-Jan JJ; Howard, Phil P; Hsiung, Chao A CA; Hunt, Steven C SC; Ikram, M Arfan MA; Illig, Thomas T; Iribarren, Carlos C; Jensen, Richard A RA; Kähönen, Mika M; Kang, Hyun H; Kathiresan, Sekar S; Keating, Brendan J BJ; Khaw, Kay-Tee KT; Kim, Yun Kyoung YK; Kim, Eric E; Kivimaki, Mika M; Klopp, Norman N; Kolovou, Genovefa G; Komulainen, Pirjo P; Kooner, Jaspal S JS; Kosova, Gulum G; Krauss, Ronald M RM; Kuh, Diana D; Kutalik, Zoltan Z; Kuusisto, Johanna J; Kvaløy, Kirsti K; Lakka, Timo A TA; Lee, Nanette R NR; Lee, I-Te IT; Lee, Wen-Jane WJ; Levy, Daniel D; Li, Xiaohui X; Liang, Kae-Woei KW; Lin, Honghuang H; Lin, Li L; Lindström, Jaana J; Lobbens, Stéphane S; Männistö, Satu S; Müller, Gabriele G; Müller-Nurasyid, Martina M; Mach, François F; Markus, Hugh S HS; Marouli, Eirini E; McCarthy, Mark I MI; McKenzie, Colin A CA; Meneton, Pierre P; Menni, Cristina C; Metspalu, Andres A; Mijatovic, Vladan V; Moilanen, Leena L; Montasser, May E ME; Morris, Andrew D AD; Morrison, Alanna C AC; Mulas, Antonella A; Nagaraja, Ramaiah R; Narisu, Narisu N; Nikus, Kjell K; O'Donnell, Christopher J CJ; O'Reilly, Paul F PF; Ong, Ken K KK; Paccaud, Fred F; Palmer, Cameron D CD; Parsa, Afshin A; Pedersen, Nancy L NL; Penninx, Brenda W BW; Perola, Markus M; Peters, Annette A; Poulter, Neil N; Pramstaller, Peter P PP; Psaty, Bruce M BM; Quertermous, Thomas T; Rao, Dabeeru C DC; Rasheed, Asif A; Rayner, N William N W R NWNWR; Renström, Frida F; Rettig, Rainer R; Rice, Kenneth M KM; Roberts, Robert R; Rose, Lynda M LM; Rossouw, Jacques J; Samani, Nilesh J NJ; Sanna, Serena S; Saramies, Jouko J; Schunkert, Heribert H; Sebert, Sylvain S; Sheu, Wayne H-H WH; Shin, Young-Ah YA; Sim, Xueling X; Smit, Johannes H JH; Smith, Albert V AV; Sosa, Maria X MX; Spector, Tim D TD; Stančáková, Alena A; Stanton, Alice A; Stirrups, Kathleen E KE; Stringham, Heather M HM; Sundstrom, Johan J; Swift, Amy J AJ; Syvänen, Ann-Christine AC; Tai, E-Shyong ES; Tanaka, Toshiko T; Tarasov, Kirill V KV; Teumer, Alexander A; Thorsteinsdottir, Unnur U; Tobin, Martin D MD; Tremoli, Elena E; Uitterlinden, Andre G AG; Uusitupa, Matti M; Vaez, Ahmad A; Vaidya, Dhananjay D; van Duijn, Cornelia M CM; van Iperen, Erik P A EPA; Vasan, Ramachandran S RS; Verwoert, Germaine C GC; Virtamo, Jarmo J; Vitart, Veronique V; Voight, Benjamin F BF; Vollenweider, Peter P; Wagner, Aline A; Wain, Louise V LV; Wareham, Nicholas J NJ; Watkins, Hugh H; Weder, Alan B AB; Westra, Harm-Jan HJ; Wilks, Rainford R; Wilsgaard, Tom T; Wilson, James F JF; Wong, Tien Y TY; Yang, Tsun-Po TP; Yao, Jie J; Yengo, Loic L; Zhang, Weihua W; Zhao, Jing Hua JH; Zhu, Xiaofeng X; Bovet, Pascal P; Cooper, Richard S RS; Mohlke, Karen L KL; Saleheen, Danish D; Lee, Jong-Young JY; Elliott, Paul P; Gierman, Hinco J HJ; Willer, Cristen J CJ; Franke, Lude L; Hovingh, G Kees GK; Taylor, Kent D KD; Dedoussis, George G; Sever, Peter P; Wong, Andrew A; Lind, Lars L; Assimes, Themistocles L TL; Njølstad, Inger I; Schwarz, Peter Eh PE; Langenberg, Claudia C; Snieder, Harold H; Caulfield, Mark J MJ; Melander, Olle O; Laakso, Markku M; Saltevo, Juha J; Rauramaa, Rainer R; Tuomilehto, Jaakko J; Ingelsson, Erik E; Lehtimäki, Terho T; Hveem, Kristian K; Palmas, Walter W; März, Winfried W; Kumari, Meena M; Salomaa, Veikko V; Chen, Yii-Der I YI; Rotter, Jerome I JI; Froguel, Philippe P; Jarvelin, Marjo-Riitta MR; Lakatta, Edward G EG; Kuulasmaa, Kari K; Franks, Paul W PW; Hamsten, Anders A; Wichmann, H-Erich HE; Palmer, Colin N A CNA; Stefansson, Kari K; Ridker, Paul M PM; Loos, Ruth J F RJF; Chakravarti, Aravinda A; Deloukas, Panos P; Morris, Andrew P AP; Newton-Cheh, Christopher C; Munroe, Patricia B PB
Publication Date: 2016-10

Variant appearance in text: rs17608766
PubMed Link: 27618452
Variant Present in the following documents:
  • Main text
  • NIHMS810971-supplement-1.pdf
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Utility of blood pressure genetic risk score in admixed Hispanic samples.

Journal Of Human Hypertension
Beecham, A H AH; Wang, L L; Vasudeva, N N; Liu, Z Z; Dong, C C; Goldschmidt-Clermont, P J PJ; Pericak-Vance, M A MA; Rundek, T T; Seo, D D; Blanton, S H SH; Sacco, R L RL; Beecham, G W GW
Publication Date: 2016-12

Variant appearance in text: rs17608766
PubMed Link: 27251080
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Identifying Novel Gene Variants in Coronary Artery Disease and Shared Genes With Several Cardiovascular Risk Factors.

Circulation Research
LeBlanc, Marissa M; Zuber, Verena V; Andreassen, Bettina Kulle BK; Witoelar, Aree A; Zeng, Lingyao L; Bettella, Francesco F; Wang, Yunpeng Y; McEvoy, Linda K LK; Thompson, Wesley K WK; Schork, Andrew J AJ; Reppe, Sjur S; Barrett-Connor, Elizabeth E; Ligthart, Symen S; Dehghan, Abbas A; Gautvik, Kaare M KM; Nelson, Christopher P CP; Schunkert, Heribert H; Samani, Nilesh J NJ; , ; Ridker, Paul M PM; Chasman, Daniel I DI; Aukrust, Pål P; Djurovic, Srdjan S; Frigessi, Arnoldo A; Desikan, Rahul S RS; Dale, Anders M AM; Andreassen, Ole A OA
Publication Date: 2016-01-08

Variant appearance in text: rs17608766
PubMed Link: 26487741
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Integrative network analysis reveals molecular mechanisms of blood pressure regulation.

Molecular Systems Biology
Huan, Tianxiao T; Meng, Qingying Q; Saleh, Mohamed A MA; Norlander, Allison E AE; Joehanes, Roby R; Zhu, Jun J; Chen, Brian H BH; Zhang, Bin B; Johnson, Andrew D AD; Ying, Saixia S; Courchesne, Paul P; Raghavachari, Nalini N; Wang, Richard R; Liu, Poching P; , ; O'Donnell, Christopher J CJ; Vasan, Ramachandran R; Munson, Peter J PJ; Madhur, Meena S MS; Harrison, David G DG; Yang, Xia X; Levy, Daniel D
Publication Date: 2015-04-16

Variant appearance in text: rs17608766
PubMed Link: 25882670
Variant Present in the following documents:
  • Main text
  • MSB-11-799.pdf
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Meta-analysis of correlated traits via summary statistics from GWASs with an application in hypertension.

American Journal Of Human Genetics
Zhu, Xiaofeng X; Feng, Tao T; Tayo, Bamidele O BO; Liang, Jingjing J; Young, J Hunter JH; Franceschini, Nora N; Smith, Jennifer A JA; Yanek, Lisa R LR; Sun, Yan V YV; Edwards, Todd L TL; Chen, Wei W; Nalls, Mike M; Fox, Ervin E; Sale, Michele M; Bottinger, Erwin E; Rotimi, Charles C; , ; Liu, Yongmei Y; McKnight, Barbara B; Liu, Kiang K; Arnett, Donna K DK; Chakravati, Aravinda A; Cooper, Richard S RS; Redline, Susan S
Publication Date: 2015-01-08

Variant appearance in text: rs17608766
PubMed Link: 25500260
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Measurement of absolute copy number variation reveals association with essential hypertension.

Bmc Medical Genomics
Marques, Francine Z FZ; Prestes, Priscilla R PR; Pinheiro, Leonardo B LB; Scurrah, Katrina K; Emslie, Kerry R KR; Tomaszewski, Maciej M; Harrap, Stephen B SB; Charchar, Fadi J FJ
Publication Date: 2014-07-15

Variant appearance in text: rs17608766
PubMed Link: 25027169
Variant Present in the following documents:
  • Main text
  • 1755-8794-7-44.pdf
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Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.

American Journal Of Human Genetics
Simino, Jeannette J; Shi, Gang G; Bis, Joshua C JC; Chasman, Daniel I DI; Ehret, Georg B GB; Gu, Xiangjun X; Guo, Xiuqing X; Hwang, Shih-Jen SJ; Sijbrands, Eric E; Smith, Albert V AV; Verwoert, Germaine C GC; Bragg-Gresham, Jennifer L JL; Cadby, Gemma G; Chen, Peng P; Cheng, Ching-Yu CY; Corre, Tanguy T; de Boer, Rudolf A RA; Goel, Anuj A; Johnson, Toby T; Khor, Chiea-Chuen CC; , ; Lluís-Ganella, Carla C; Luan, Jian'an J; Lyytikäinen, Leo-Pekka LP; Nolte, Ilja M IM; Sim, Xueling X; Sõber, Siim S; van der Most, Peter J PJ; Verweij, Niek N; Zhao, Jing Hua JH; Amin, Najaf N; Boerwinkle, Eric E; Bouchard, Claude C; Dehghan, Abbas A; Eiriksdottir, Gudny G; Elosua, Roberto R; Franco, Oscar H OH; Gieger, Christian C; Harris, Tamara B TB; Hercberg, Serge S; Hofman, Albert A; James, Alan L AL; Johnson, Andrew D AD; Kähönen, Mika M; Khaw, Kay-Tee KT; Kutalik, Zoltan Z; Larson, Martin G MG; Launer, Lenore J LJ; Li, Guo G; Liu, Jianjun J; Liu, Kiang K; Morrison, Alanna C AC; Navis, Gerjan G; Ong, Rick Twee-Hee RT; Papanicolau, George J GJ; Penninx, Brenda W BW; Psaty, Bruce M BM; Raffel, Leslie J LJ; Raitakari, Olli T OT; Rice, Kenneth K; Rivadeneira, Fernando F; Rose, Lynda M LM; Sanna, Serena S; Scott, Robert A RA; Siscovick, David S DS; Stolk, Ronald P RP; Uitterlinden, Andre G AG; Vaidya, Dhananjay D; van der Klauw, Melanie M MM; Vasan, Ramachandran S RS; Vithana, Eranga Nishanthie EN; Völker, Uwe U; Völzke, Henry H; Watkins, Hugh H; Young, Terri L TL; Aung, Tin T; Bochud, Murielle M; Farrall, Martin M; Hartman, Catharina A CA; Laan, Maris M; Lakatta, Edward G EG; Lehtimäki, Terho T; Loos, Ruth J F RJ; Lucas, Gavin G; Meneton, Pierre P; Palmer, Lyle J LJ; Rettig, Rainer R; Snieder, Harold H; Tai, E Shyong ES; Teo, Yik-Ying YY; van der Harst, Pim P; Wareham, Nicholas J NJ; Wijmenga, Cisca C; Wong, Tien Yin TY; Fornage, Myriam M; Gudnason, Vilmundur V; Levy, Daniel D; Palmas, Walter W; Ridker, Paul M PM; Rotter, Jerome I JI; van Duijn, Cornelia M CM; Witteman, Jacqueline C M JC; Chakravarti, Aravinda A; Rao, Dabeeru C DC
Publication Date: 2014-07-03

Variant appearance in text: rs17608766
PubMed Link: 24954895
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Pathogenesis of coronary artery disease: focus on genetic risk factors and identification of genetic variants.

The Application Of Clinical Genetics
Sayols-Baixeras, Sergi S; Lluís-Ganella, Carla C; Lucas, Gavin G; Elosua, Roberto R
Publication Date: 2014

Variant appearance in text: rs17608766
PubMed Link: 24520200
Variant Present in the following documents:
  • Main text
  • tacg-7-015.pdf
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Identifying common genetic variants in blood pressure due to polygenic pleiotropy with associated phenotypes.

Hypertension (Dallas, Tex. : 1979)
Andreassen, Ole A OA; McEvoy, Linda K LK; Thompson, Wesley K WK; Wang, Yunpeng Y; Reppe, Sjur S; Schork, Andrew J AJ; Zuber, Verena V; Barrett-Connor, Elizabeth E; Gautvik, Kaare K; Aukrust, Pål P; Karlsen, Tom H TH; Djurovic, Srdjan S; Desikan, Rahul S RS; Dale, Anders M AM; ,
Publication Date: 2014-04

Variant appearance in text: rs17608766
PubMed Link: 24396023
Variant Present in the following documents:
  • Main text
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Genetic influences on trajectories of systolic blood pressure across childhood and adolescence.

Circulation. Cardiovascular Genetics
Howe, Laura D LD; Parmar, Priyakumari G PG; Paternoster, Lavinia L; Warrington, Nicole M NM; Kemp, John P JP; Briollais, Laurent L; Newnham, John P JP; Timpson, Nicholas J NJ; Smith, George Davey GD; Ring, Susan M SM; Evans, David M DM; Tilling, Kate K; Pennell, Craig E CE; Beilin, Lawrie J LJ; Palmer, Lyle J LJ; Lawlor, Debbie A DA
Publication Date: 2013-12

Variant appearance in text: rs17608766
PubMed Link: 24200906
Variant Present in the following documents:
  • Main text
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Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease.

Plos One
Bhatnagar, Pallav P; Barron-Casella, Emily E; Bean, Christopher J CJ; Milton, Jacqueline N JN; Baldwin, Clinton T CT; Steinberg, Martin H MH; Debaun, Michael M; Casella, James F JF; Arking, Dan E DE
Publication Date: 2013

Variant appearance in text: rs17608766
PubMed Link: 24058526
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  • Main text
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Gentrepid V2.0: a web server for candidate disease gene prediction.

Bmc Bioinformatics
Ballouz, Sara S; Liu, Jason Y JY; George, Richard A RA; Bains, Naresh N; Liu, Arthur A; Oti, Martin M; Gaeta, Bruno B; Fatkin, Diane D; Wouters, Merridee A MA
Publication Date: 2013-08-16

Variant appearance in text: rs17608766
PubMed Link: 23947436
Variant Present in the following documents:
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A haplotype of the GOSR2 gene is associated with myocardial infarction in Japanese men.

Genetic Testing And Molecular Biomarkers
Pan, Shuo S; Nakayama, Tomohiro T; Sato, Naoyuki N; Izumi, Yoichi Y; Soma, Masayoshi M; Aoi, Noriko N; Ma, Yitong Y; Hinohara, Shigeaki S; Doba, Nobutaka N
Publication Date: 2013-06

Variant appearance in text: rs17608766
PubMed Link: 23675987
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Overlap between common genetic polymorphisms underpinning kidney traits and cardiovascular disease phenotypes: the CKDGen consortium.

American Journal Of Kidney Diseases : The Official Journal Of The National Kidney Foundation
Olden, Matthias M; Teumer, Alexander A; Bochud, Murielle M; Pattaro, Cristian C; Köttgen, Anna A; Turner, Stephen T ST; Rettig, Rainer R; Chen, Ming-Huei MH; Dehghan, Abbas A; Bastardot, Francois F; Schmidt, Reinhold R; Vollenweider, Peter P; Schunkert, Heribert H; Reilly, Muredach P MP; Fornage, Myriam M; Launer, Lenore J LJ; Verwoert, Germaine C GC; Mitchell, Gary F GF; Bis, Joshua C JC; O'Donnell, Christopher J CJ; Cheng, Ching-Yu CY; Sim, Xueling X; Siscovick, David S DS; Coresh, Josef J; Kao, W H Linda WH; Fox, Caroline S CS; O'Seaghdha, Conall M CM; ,
Publication Date: 2013-06

Variant appearance in text: rs17608766
PubMed Link: 23474010
Variant Present in the following documents:
  • Main text
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Current genomics in cardiovascular medicine.

Current Genomics
Sawhney, Vinit V; Brouilette, Scott S; Abrams, Dominic D; Schilling, Richard R; O'Brien, Benjamin B
Publication Date: 2012-09

Variant appearance in text: rs17608766
PubMed Link: 23450299
Variant Present in the following documents:
  • Main text
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SNPs identified as modulators of ECG traits in the general population do not markedly affect ECG traits during acute myocardial infarction nor ventricular fibrillation risk in this condition.

Plos One
Pazoki, Raha R; de Jong, Jonas S S G JS; Marsman, Roos F RF; Bruinsma, Nienke N; Dekker, Lukas R C LR; Wilde, Arthur A M AA; Bezzina, Connie R CR; Tanck, Michael W T MW
Publication Date: 2013

Variant appearance in text: rs17608766
PubMed Link: 23437344
Variant Present in the following documents:
  • Main text
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Genes for blood pressure: an opportunity to understand hypertension.

European Heart Journal
Ehret, Georg B GB; Caulfield, Mark J MJ
Publication Date: 2013-04

Variant appearance in text: rs17608766
PubMed Link: 23303660
Variant Present in the following documents:
  • Main text
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Hypothesis-based analysis of gene-gene interactions and risk of myocardial infarction.

Plos One
Lucas, Gavin G; Lluís-Ganella, Carla C; Subirana, Isaac I; Musameh, Muntaser D MD; Gonzalez, Juan Ramon JR; Nelson, Christopher P CP; Sentí, Mariano M; , ; , ; Schwartz, Stephen M SM; Siscovick, David D; O'Donnell, Christopher J CJ; Melander, Olle O; Salomaa, Veikko V; Purcell, Shaun S; Altshuler, David D; Samani, Nilesh J NJ; Kathiresan, Sekar S; Elosua, Roberto R
Publication Date: 2012

Variant appearance in text: rs17608766
PubMed Link: 22876292
Variant Present in the following documents:
  • pone.0041730.s001.pdf
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Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.

European Heart Journal
Fedorowski, Artur A; Franceschini, Nora N; Brody, Jennifer J; Liu, Chunyu C; Verwoert, Germaine C GC; Boerwinkle, Eric E; Couper, David D; Rice, Kenneth M KM; Rotter, Jerome I JI; Mattace-Raso, Francesco F; Uitterlinden, Andre A; Hofman, Albert A; Almgren, Peter P; Sjögren, Marketa M; Hedblad, Bo B; Larson, Martin G MG; Newton-Cheh, Christopher C; Wang, Thomas J TJ; Rose, Kathryn M KM; Psaty, Bruce M BM; Levy, Daniel D; Witteman, Jacqueline J; Melander, Olle O
Publication Date: 2012-09

Variant appearance in text: rs17608766
PubMed Link: 22504314
Variant Present in the following documents:
  • Main text
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A review of genetics, arterial stiffness, and blood pressure in African Americans.

Journal Of Cardiovascular Translational Research
Hall, Jennifer L JL; Duprez, Daniel A DA; Barac, Ana A; Rich, Stephen S SS
Publication Date: 2012-06

Variant appearance in text: rs17608766
PubMed Link: 22492025
Variant Present in the following documents:
  • Main text
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Epidemiology and genetics of sudden cardiac death.

Circulation
Deo, Rajat R; Albert, Christine M CM
Publication Date: 2012-01-31

Variant appearance in text: rs17608766
PubMed Link: 22294707
Variant Present in the following documents:
  • Main text
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Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.

Nature
, ; Ehret, Georg B GB; Munroe, Patricia B PB; Rice, Kenneth M KM; Bochud, Murielle M; Johnson, Andrew D AD; Chasman, Daniel I DI; Smith, Albert V AV; Tobin, Martin D MD; Verwoert, Germaine C GC; Hwang, Shih-Jen SJ; Pihur, Vasyl V; Vollenweider, Peter P; O'Reilly, Paul F PF; Amin, Najaf N; Bragg-Gresham, Jennifer L JL; Teumer, Alexander A; Glazer, Nicole L NL; Launer, Lenore L; Zhao, Jing Hua JH; Aulchenko, Yurii Y; Heath, Simon S; Sõber, Siim S; Parsa, Afshin A; Luan, Jian'an J; Arora, Pankaj P; Dehghan, Abbas A; Zhang, Feng F; Lucas, Gavin G; Hicks, Andrew A AA; Jackson, Anne U AU; Peden, John F JF; Tanaka, Toshiko T; Wild, Sarah H SH; Rudan, Igor I; Igl, Wilmar W; Milaneschi, Yuri Y; Parker, Alex N AN; Fava, Cristiano C; Chambers, John C JC; Fox, Ervin R ER; Kumari, Meena M; Go, Min Jin MJ; van der Harst, Pim P; Kao, Wen Hong Linda WH; Sjögren, Marketa M; Vinay, D G DG; Alexander, Myriam M; Tabara, Yasuharu Y; Shaw-Hawkins, Sue S; Whincup, Peter H PH; Liu, Yongmei Y; Shi, Gang G; Kuusisto, Johanna J; Tayo, Bamidele B; Seielstad, Mark M; Sim, Xueling X; Nguyen, Khanh-Dung Hoang KD; Lehtimäki, Terho T; Matullo, Giuseppe G; Wu, Ying Y; Gaunt, Tom R TR; Onland-Moret, N Charlotte NC; Cooper, Matthew N MN; Platou, Carl G P CG; Org, Elin E; Hardy, Rebecca R; Dahgam, Santosh S; Palmen, Jutta J; Vitart, Veronique V; Braund, Peter S PS; Kuznetsova, Tatiana T; Uiterwaal, Cuno S P M CS; Adeyemo, Adebowale A; Palmas, Walter W; Campbell, Harry H; Ludwig, Barbara B; Tomaszewski, Maciej M; Tzoulaki, Ioanna I; Palmer, Nicholette D ND; , ; , ; , ; , ; , ; Aspelund, Thor T; Garcia, Melissa M; Chang, Yen-Pei C YP; O'Connell, Jeffrey R JR; Steinle, Nanette I NI; Grobbee, Diederick E DE; Arking, Dan E DE; Kardia, Sharon L SL; Morrison, Alanna C AC; Hernandez, Dena D; Najjar, Samer S; McArdle, Wendy L WL; Hadley, David D; Brown, Morris J MJ; Connell, John M JM; Hingorani, Aroon D AD; Day, Ian N M IN; Lawlor, Debbie A DA; Beilby, John P JP; Lawrence, Robert W RW; Clarke, Robert R; Hopewell, Jemma C JC; Ongen, Halit H; Dreisbach, Albert W AW; Li, Yali Y; Young, J Hunter JH; Bis, Joshua C JC; Kähönen, Mika M; Viikari, Jorma J; Adair, Linda S LS; Lee, Nanette R NR; Chen, Ming-Huei MH; Olden, Matthias M; Pattaro, Cristian C; Bolton, Judith A Hoffman JA; Köttgen, Anna A; Bergmann, Sven S; Mooser, Vincent V; Chaturvedi, Nish N; Frayling, Timothy M TM; Islam, Muhammad M; Jafar, Tazeen H TH; Erdmann, Jeanette J; Kulkarni, Smita R SR; Bornstein, Stefan R SR; Grässler, Jürgen J; Groop, Leif L; Voight, Benjamin F BF; Kettunen, Johannes J; Howard, Philip P; Taylor, Andrew A; Guarrera, Simonetta S; Ricceri, Fulvio F; Emilsson, Valur V; Plump, Andrew A; Barroso, Inês I; Khaw, Kay-Tee KT; Weder, Alan B AB; Hunt, Steven C SC; Sun, Yan V YV; Bergman, Richard N RN; Collins, Francis S FS; Bonnycastle, Lori L LL; Scott, Laura J LJ; Stringham, Heather M HM; Peltonen, Leena L; Perola, Markus M; Vartiainen, Erkki E; Brand, Stefan-Martin SM; Staessen, Jan A JA; Wang, Thomas J TJ; Burton, Paul R PR; Soler Artigas, Maria M; Dong, Yanbin Y; Snieder, Harold H; Wang, Xiaoling X; Zhu, Haidong H; Lohman, Kurt K KK; Rudock, Megan E ME; Heckbert, Susan R SR; Smith, Nicholas L NL; Wiggins, Kerri L KL; Doumatey, Ayo A; Shriner, Daniel D; Veldre, Gudrun G; Viigimaa, Margus M; Kinra, Sanjay S; Prabhakaran, Dorairaj D; Tripathy, Vikal V; Langefeld, Carl D CD; Rosengren, Annika A; Thelle, Dag S DS; Corsi, Anna Maria AM; Singleton, Andrew A; Forrester, Terrence T; Hilton, Gina G; McKenzie, Colin A CA; Salako, Tunde T; Iwai, Naoharu N; Kita, Yoshikuni Y; Ogihara, Toshio T; Ohkubo, Takayoshi T; Okamura, Tomonori T; Ueshima, Hirotsugu H; Umemura, Satoshi S; Eyheramendy, Susana S; Meitinger, Thomas T; Wichmann, H-Erich HE; Cho, Yoon Shin YS; Kim, Hyung-Lae HL; Lee, Jong-Young JY; Scott, James J; Sehmi, Joban S JS; Zhang, Weihua W; Hedblad, Bo B; Nilsson, Peter P; Smith, George Davey GD; Wong, Andrew A; Narisu, Narisu N; Stančáková, Alena A; Raffel, Leslie J LJ; Yao, Jie J; Kathiresan, Sekar S; O'Donnell, Christopher J CJ; Schwartz, Stephen M SM; Ikram, M Arfan MA; Longstreth, W T WT; Mosley, Thomas H TH; Seshadri, Sudha S; Shrine, Nick R G NR; Wain, Louise V LV; Morken, Mario A MA; Swift, Amy J AJ; Laitinen, Jaana J; Prokopenko, Inga I; Zitting, Paavo P; Cooper, Jackie A JA; Humphries, Steve E SE; Danesh, John J; Rasheed, Asif A; Goel, Anuj A; Hamsten, Anders A; Watkins, Hugh H; Bakker, Stephan J L SJ; van Gilst, Wiek H WH; Janipalli, Charles S CS; Mani, K Radha KR; Yajnik, Chittaranjan S CS; Hofman, Albert A; Mattace-Raso, Francesco U S FU; Oostra, Ben A BA; Demirkan, Ayse A; Isaacs, Aaron A; Rivadeneira, Fernando F; Lakatta, Edward G EG; Orru, Marco M; Scuteri, Angelo A; Ala-Korpela, Mika M; Kangas, Antti J AJ; Lyytikäinen, Leo-Pekka LP; Soininen, Pasi P; Tukiainen, Taru T; Würtz, Peter P; Ong, Rick Twee-Hee RT; Dörr, Marcus M; Kroemer, Heyo K HK; Völker, Uwe U; Völzke, Henry H; Galan, Pilar P; Hercberg, Serge S; Lathrop, Mark M; Zelenika, Diana D; Deloukas, Panos P; Mangino, Massimo M; Spector, Tim D TD; Zhai, Guangju G; Meschia, James F JF; Nalls, Michael A MA; Sharma, Pankaj P; Terzic, Janos J; Kumar, M V Kranthi MV; Denniff, Matthew M; Zukowska-Szczechowska, Ewa E; Wagenknecht, Lynne E LE; Fowkes, F Gerald R FG; Charchar, Fadi J FJ; Schwarz, Peter E H PE; Hayward, Caroline C; Guo, Xiuqing X; Rotimi, Charles C; Bots, Michiel L ML; Brand, Eva E; Samani, Nilesh J NJ; Polasek, Ozren O; Talmud, Philippa J PJ; Nyberg, Fredrik F; Kuh, Diana D; Laan, Maris M; Hveem, Kristian K; Palmer, Lyle J LJ; van der Schouw, Yvonne T YT; Casas, Juan P JP; Mohlke, Karen L KL; Vineis, Paolo P; Raitakari, Olli O; Ganesh, Santhi K SK; Wong, Tien Y TY; Tai, E Shyong ES; Cooper, Richard S RS; Laakso, Markku M; Rao, Dabeeru C DC; Harris, Tamara B TB; Morris, Richard W RW; Dominiczak, Anna F AF; Kivimaki, Mika M; Marmot, Michael G MG; Miki, Tetsuro T; Saleheen, Danish D; Chandak, Giriraj R GR; Coresh, Josef J; Navis, Gerjan G; Salomaa, Veikko V; Han, Bok-Ghee BG; Zhu, Xiaofeng X; Kooner, Jaspal S JS; Melander, Olle O; Ridker, Paul M PM; Bandinelli, Stefania S; Gyllensten, Ulf B UB; Wright, Alan F AF; Wilson, James F JF; Ferrucci, Luigi L; Farrall, Martin M; Tuomilehto, Jaakko J; Pramstaller, Peter P PP; Elosua, Roberto R; Soranzo, Nicole N; Sijbrands, Eric J G EJ; Altshuler, David D; Loos, Ruth J F RJ; Shuldiner, Alan R AR; Gieger, Christian C; Meneton, Pierre P; Uitterlinden, Andre G AG; Wareham, Nicholas J NJ; Gudnason, Vilmundur V; Rotter, Jerome I JI; Rettig, Rainer R; Uda, Manuela M; Strachan, David P DP; Witteman, Jacqueline C M JC; Hartikainen, Anna-Liisa AL; Beckmann, Jacques S JS; Boerwinkle, Eric E; Vasan, Ramachandran S RS; Boehnke, Michael M; Larson, Martin G MG; Järvelin, Marjo-Riitta MR; Psaty, Bruce M BM; Abecasis, Gonçalo R GR; Chakravarti, Aravinda A; Elliott, Paul P; van Duijn, Cornelia M CM; Newton-Cheh, Christopher C; Levy, Daniel D; Caulfield, Mark J MJ; Johnson, Toby T
Publication Date: 2011-09-11

Variant appearance in text: rs17608766
PubMed Link: 21909115
Variant Present in the following documents:
  • Main text
  • NIHMS314865-supplement-3.pdf
  • nihms314865.pdf
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Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.

Nature Genetics
Sotoodehnia, Nona N; Isaacs, Aaron A; de Bakker, Paul I W PI; Dörr, Marcus M; Newton-Cheh, Christopher C; Nolte, Ilja M IM; van der Harst, Pim P; Müller, Martina M; Eijgelsheim, Mark M; Alonso, Alvaro A; Hicks, Andrew A AA; Padmanabhan, Sandosh S; Hayward, Caroline C; Smith, Albert Vernon AV; Polasek, Ozren O; Giovannone, Steven S; Fu, Jingyuan J; Magnani, Jared W JW; Marciante, Kristin D KD; Pfeufer, Arne A; Gharib, Sina A SA; Teumer, Alexander A; Li, Man M; Bis, Joshua C JC; Rivadeneira, Fernando F; Aspelund, Thor T; Köttgen, Anna A; Johnson, Toby T; Rice, Kenneth K; Sie, Mark P S MP; Wang, Ying A YA; Klopp, Norman N; Fuchsberger, Christian C; Wild, Sarah H SH; Mateo Leach, Irene I; Estrada, Karol K; Völker, Uwe U; Wright, Alan F AF; Asselbergs, Folkert W FW; Qu, Jiaxiang J; Chakravarti, Aravinda A; Sinner, Moritz F MF; Kors, Jan A JA; Petersmann, Astrid A; Harris, Tamara B TB; Soliman, Elsayed Z EZ; Munroe, Patricia B PB; Psaty, Bruce M BM; Oostra, Ben A BA; Cupples, L Adrienne LA; Perz, Siegfried S; de Boer, Rudolf A RA; Uitterlinden, André G AG; Völzke, Henry H; Spector, Timothy D TD; Liu, Fang-Yu FY; Boerwinkle, Eric E; Dominiczak, Anna F AF; Rotter, Jerome I JI; van Herpen, Gé G; Levy, Daniel D; Wichmann, H-Erich HE; van Gilst, Wiek H WH; Witteman, Jacqueline C M JC; Kroemer, Heyo K HK; Kao, W H Linda WH; Heckbert, Susan R SR; Meitinger, Thomas T; Hofman, Albert A; Campbell, Harry H; Folsom, Aaron R AR; van Veldhuisen, Dirk J DJ; Schwienbacher, Christine C; O'Donnell, Christopher J CJ; Volpato, Claudia Beu CB; Caulfield, Mark J MJ; Connell, John M JM; Launer, Lenore L; Lu, Xiaowen X; Franke, Lude L; Fehrmann, Rudolf S N RS; te Meerman, Gerard G; Groen, Harry J M HJ; Weersma, Rinse K RK; van den Berg, Leonard H LH; Wijmenga, Cisca C; Ophoff, Roel A RA; Navis, Gerjan G; Rudan, Igor I; Snieder, Harold H; Wilson, James F JF; Pramstaller, Peter P PP; Siscovick, David S DS; Wang, Thomas J TJ; Gudnason, Vilmundur V; van Duijn, Cornelia M CM; Felix, Stephan B SB; Fishman, Glenn I GI; Jamshidi, Yalda Y; Stricker, Bruno H Ch BH; Samani, Nilesh J NJ; Kääb, Stefan S; Arking, Dan E DE
Publication Date: 2010-12

Variant appearance in text: rs17608766
PubMed Link: 21076409
Variant Present in the following documents:
  • Main text
  • NIHMS247823-supplement-1.pdf
  • nihms247823.pdf
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Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.

Jama
Vasan, Ramachandran S RS; Glazer, Nicole L NL; Felix, Janine F JF; Lieb, Wolfgang W; Wild, Philipp S PS; Felix, Stephan B SB; Watzinger, Norbert N; Larson, Martin G MG; Smith, Nicholas L NL; Dehghan, Abbas A; Grosshennig, Anika A; Schillert, Arne A; Teumer, Alexander A; Schmidt, Reinhold R; Kathiresan, Sekar S; Lumley, Thomas T; Aulchenko, Yurii S YS; König, Inke R IR; Zeller, Tanja T; Homuth, Georg G; Struchalin, Maksim M; Aragam, Jayashri J; Bis, Joshua C JC; Rivadeneira, Fernando F; Erdmann, Jeanette J; Schnabel, Renate B RB; Dörr, Marcus M; Zweiker, Robert R; Lind, Lars L; Rodeheffer, Richard J RJ; Greiser, Karin Halina KH; Levy, Daniel D; Haritunians, Talin T; Deckers, Jaap W JW; Stritzke, Jan J; Lackner, Karl J KJ; Völker, Uwe U; Ingelsson, Erik E; Kullo, Iftikhar I; Haerting, Johannes J; O'Donnell, Christopher J CJ; Heckbert, Susan R SR; Stricker, Bruno H BH; Ziegler, Andreas A; Reffelmann, Thorsten T; Redfield, Margaret M MM; Werdan, Karl K; Mitchell, Gary F GF; Rice, Kenneth K; Arnett, Donna K DK; Hofman, Albert A; Gottdiener, John S JS; Uitterlinden, Andre G AG; Meitinger, Thomas T; Blettner, Maria M; Friedrich, Nele N; Wang, Thomas J TJ; Psaty, Bruce M BM; van Duijn, Cornelia M CM; Wichmann, H-Erich HE; Munzel, Thomas F TF; Kroemer, Heyo K HK; Benjamin, Emelia J EJ; Rotter, Jerome I JI; Witteman, Jacqueline C JC; Schunkert, Heribert H; Schmidt, Helena H; Völzke, Henry H; Blankenberg, Stefan S
Publication Date: 2009-07-08

Variant appearance in text: rs17608766
PubMed Link: 19584346
Variant Present in the following documents:
  • Main text
View BVdb publication page