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
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
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
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
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
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
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
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
Towards Precision Medicine for Hypertension: A Review of Genomic, Epigenomic, and Microbiomic Effects on Blood Pressure in Experimental Rat Models and Humans.
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
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
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.
The Journal Of Clinical Investigation
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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; 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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
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
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
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
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
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
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; ,
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
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
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
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; ,
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
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
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
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Nature
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Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.
Nature Genetics
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Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.
Jama
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