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25 matches for
Soliman EZ,
showing the first 20.
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
Christophersen IE,
Rienstra M,
Roselli C,
Yin X,
Geelhoed B,
Barnard J,
Lin H,
Arking DE,
Smith AV,
Albert CM,
Chaffin M,
Tucker NR
and 150 more — show all
Li M,
Klarin D,
Bihlmeyer NA,
Low SK,
Weeke PE,
Müller-Nurasyid M,
Smith JG,
Brody JA,
Niemeijer MN,
Dörr M,
Trompet S,
Huffman J,
Gustafsson S,
Schurmann C,
Kleber ME,
Lyytikäinen LP,
Seppälä I,
Malik R,
Horimoto ARVR,
Perez M,
Sinisalo J,
Aeschbacher S,
Thériault S,
Yao J,
Radmanesh F,
Weiss S,
Teumer A,
Choi SH,
Weng LC,
Clauss S,
Deo R,
Rader DJ,
Shah SH,
Sun A,
Hopewell JC,
Debette S,
Chauhan G,
Yang Q,
Worrall BB,
Paré G,
Kamatani Y,
Hagemeijer YP,
Verweij N,
Siland JE,
Kubo M,
Smith JD,
Van Wagoner DR,
Bis JC,
Perz S,
Psaty BM,
Ridker PM,
Magnani JW,
Harris TB,
Launer LJ,
Shoemaker MB,
Padmanabhan S,
Haessler J,
Bartz TM,
Waldenberger M,
Lichtner P,
Arendt M,
Krieger JE,
Kähönen M,
Risch L,
Mansur AJ,
Peters A,
Smith BH,
Lind L,
Scott SA,
Lu Y,
Bottinger EB,
Hernesniemi J,
Lindgren CM,
Wong JA,
Huang J,
Eskola M,
Morris AP,
Ford I,
Reiner AP,
Delgado G,
Chen LY,
Chen YI,
Sandhu RK,
Li M,
Boerwinkle E,
Eisele L,
Lannfelt L,
Rost N,
Anderson CD,
Taylor KD,
Campbell A,
Magnusson PK,
Porteous D,
Hocking LJ,
Vlachopoulou E,
Pedersen NL,
Nikus K,
Orho-Melander M,
Hamsten A,
Heeringa J,
Denny JC,
Kriebel J,
Darbar D,
Newton-Cheh C,
Shaffer C,
Macfarlane PW,
Heilmann-Heimbach S,
Almgren P,
Huang PL,
Sotoodehnia N,
Soliman EZ,
Uitterlinden AG,
Hofman A,
Franco OH,
Völker U,
Jöckel KH,
Sinner MF,
Lin HJ,
Guo X,
Dichgans M,
Ingelsson E,
Kooperberg C,
Melander O,
Loos RJF,
Laurikka J,
Conen D,
Rosand J,
van der Harst P,
Lokki ML,
Kathiresan S,
Pereira A,
Jukema JW,
Hayward C,
Rotter JI,
März W,
Lehtimäki T,
Stricker BH,
Chung MK,
Felix SB,
Gudnason V,
Alonso A,
Roden DM,
Kääb S,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Tanaka T,
Lunetta KL,
Lubitz SA,
Ellinor PT
METASTROKE Consortium of the ISGC · Neurology Working Group of the CHARGE Consortium and 1 more consortia
Nature genetics · 2017 · PMID 28416818
12 pages+
Multi-ethnic genome-wide association study for atrial fibrillation
Roselli C,
Chaffin MD,
Weng LC,
Aeschbacher S,
Ahlberg G,
Albert CM,
Almgren P,
Alonso A,
Anderson CD,
Aragam KG,
Arking DE,
Barnard J
and 206 more — show all
Bartz TM,
Benjamin EJ,
Bihlmeyer NA,
Bis JC,
Bloom HL,
Boerwinkle E,
Bottinger EB,
Brody JA,
Calkins H,
Campbell A,
Cappola TP,
Carlquist J,
Chasman DI,
Chen LY,
Chen YI,
Choi EK,
Choi SH,
Christophersen IE,
Chung MK,
Cole JW,
Conen D,
Cook J,
Crijns HJ,
Cutler MJ,
Damrauer SM,
Daniels BR,
Darbar D,
Delgado G,
Denny JC,
Dichgans M,
Dörr M,
Dudink EA,
Dudley SC,
Esa N,
Esko T,
Eskola M,
Fatkin D,
Felix SB,
Ford I,
Franco OH,
Geelhoed B,
Grewal RP,
Gudnason V,
Guo X,
Gupta N,
Gustafsson S,
Gutmann R,
Hamsten A,
Harris TB,
Hayward C,
Heckbert SR,
Hernesniemi J,
Hocking LJ,
Hofman A,
Horimoto ARVR,
Huang J,
Huang PL,
Huffman J,
Ingelsson E,
Ipek EG,
Ito K,
Jimenez-Conde J,
Johnson R,
Jukema JW,
Kääb S,
Kähönen M,
Kamatani Y,
Kane JP,
Kastrati A,
Kathiresan S,
Katschnig-Winter P,
Kavousi M,
Kessler T,
Kietselaer BL,
Kirchhof P,
Kleber ME,
Knight S,
Krieger JE,
Kubo M,
Launer LJ,
Laurikka J,
Lehtimäki T,
Leineweber K,
Lemaitre RN,
Li M,
Lim HE,
Lin HJ,
Lin H,
Lind L,
Lindgren CM,
Lokki ML,
London B,
Loos RJF,
Low SK,
Lu Y,
Lyytikäinen LP,
Macfarlane PW,
Magnusson PK,
Mahajan A,
Malik R,
Mansur AJ,
Marcus GM,
Margolin L,
Margulies KB,
März W,
McManus DD,
Melander O,
Mohanty S,
Montgomery JA,
Morley MP,
Morris AP,
Müller-Nurasyid M,
Natale A,
Nazarian S,
Neumann B,
Newton-Cheh C,
Niemeijer MN,
Nikus K,
Nilsson P,
Noordam R,
Oellers H,
Olesen MS,
Orho-Melander M,
Padmanabhan S,
Pak HN,
Paré G,
Pedersen NL,
Pera J,
Pereira A,
Porteous D,
Psaty BM,
Pulit SL,
Pullinger CR,
Rader DJ,
Refsgaard L,
Ribasés M,
Ridker PM,
Rienstra M,
Risch L,
Roden DM,
Rosand J,
Rosenberg MA,
Rost N,
Rotter JI,
Saba S,
Sandhu RK,
Schnabel RB,
Schramm K,
Schunkert H,
Schurman C,
Scott SA,
Seppälä I,
Shaffer C,
Shah S,
Shalaby AA,
Shim J,
Shoemaker MB,
Siland JE,
Sinisalo J,
Sinner MF,
Slowik A,
Smith AV,
Smith BH,
Smith JG,
Smith JD,
Smith NL,
Soliman EZ,
Sotoodehnia N,
Stricker BH,
Sun A,
Sun H,
Svendsen JH,
Tanaka T,
Tanriverdi K,
Taylor KD,
Teder-Laving M,
Teumer A,
Thériault S,
Trompet S,
Tucker NR,
Tveit A,
Uitterlinden AG,
Van Der Harst P,
Van Gelder IC,
Van Wagoner DR,
Verweij N,
Vlachopoulou E,
Völker U,
Wang B,
Weeke PE,
Weijs B,
Weiss R,
Weiss S,
Wells QS,
Wiggins KL,
Wong JA,
Woo D,
Worrall BB,
Yang PS,
Yao J,
Yoneda ZT,
Zeller T,
Zeng L,
Lubitz SA,
Lunetta KL,
Ellinor PT
Nature genetics · 2018 · PMID 29892015
12 pages+
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity
van Setten J,
Brody JA,
Jamshidi Y,
Swenson BR,
Butler AM,
Campbell H,
Del Greco FM,
Evans DS,
Gibson Q,
Gudbjartsson DF,
Kerr KF,
Krijthe BP
and 114 more — show all
Lyytikäinen LP,
Müller C,
Müller-Nurasyid M,
Nolte IM,
Padmanabhan S,
Ritchie MD,
Robino A,
Smith AV,
Steri M,
Tanaka T,
Teumer A,
Trompet S,
Ulivi S,
Verweij N,
Yin X,
Arnar DO,
Asselbergs FW,
Bader JS,
Barnard J,
Bis J,
Blankenberg S,
Boerwinkle E,
Bradford Y,
Buckley BM,
Chung MK,
Crawford D,
den Hoed M,
Denny JC,
Dominiczak AF,
Ehret GB,
Eijgelsheim M,
Ellinor PT,
Felix SB,
Franco OH,
Franke L,
Harris TB,
Holm H,
Ilaria G,
Iorio A,
Kähönen M,
Kolcic I,
Kors JA,
Lakatta EG,
Launer LJ,
Lin H,
Lin HJ,
Loos RJF,
Lubitz SA,
Macfarlane PW,
Magnani JW,
Leach IM,
Meitinger T,
Mitchell BD,
Munzel T,
Papanicolaou GJ,
Peters A,
Pfeufer A,
Pramstaller PP,
Raitakari OT,
Rotter JI,
Rudan I,
Samani NJ,
Schlessinger D,
Silva Aldana CT,
Sinner MF,
Smith JD,
Snieder H,
Soliman EZ,
Spector TD,
Stott DJ,
Strauch K,
Tarasov KV,
Thorsteinsdottir U,
Uitterlinden AG,
Van Wagoner DR,
Völker U,
Völzke H,
Waldenberger M,
Jan Westra H,
Wild PS,
Zeller T,
Alonso A,
Avery CL,
Bandinelli S,
Benjamin EJ,
Cucca F,
Dörr M,
Ferrucci L,
Gasparini P,
Gudnason V,
Hayward C,
Heckbert SR,
Hicks AA,
Jukema JW,
Kääb S,
Lehtimäki T,
Liu Y,
Munroe PB,
Parsa A,
Polasek O,
Psaty BM,
Roden DM,
Schnabel RB,
Sinagra G,
Stefansson K,
Stricker BH,
van der Harst P,
van Duijn CM,
Wilson JF,
Gharib SA,
de Bakker PIW,
Isaacs A,
Arking DE,
Sotoodehnia N
Nature communications · 2018 · PMID 30046033 · open access
12 pages+
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Ntalla I,
Weng LC,
Cartwright JH,
Hall AW,
Sveinbjornsson G,
Tucker NR,
Choi SH,
Chaffin MD,
Roselli C,
Barnes MR,
Mifsud B,
Warren HR
and 175 more — show all
Hayward C,
Marten J,
Cranley JJ,
Concas MP,
Gasparini P,
Boutin T,
Kolcic I,
Polasek O,
Rudan I,
Araujo NM,
Lima-Costa MF,
Ribeiro ALP,
Souza RP,
Tarazona-Santos E,
Giedraitis V,
Ingelsson E,
Mahajan A,
Morris AP,
Del Greco M F,
Foco L,
Gögele M,
Hicks AA,
Cook JP,
Lind L,
Lindgren CM,
Sundström J,
Nelson CP,
Riaz MB,
Samani NJ,
Sinagra G,
Ulivi S,
Kähönen M,
Mishra PP,
Mononen N,
Nikus K,
Caulfield MJ,
Dominiczak A,
Padmanabhan S,
Montasser ME,
O'Connell JR,
Ryan K,
Shuldiner AR,
Aeschbacher S,
Conen D,
Risch L,
Thériault S,
Hutri-Kähönen N,
Lehtimäki T,
Lyytikäinen LP,
Raitakari OT,
Barnes CLK,
Campbell H,
Joshi PK,
Wilson JF,
Isaacs A,
Kors JA,
van Duijn CM,
Huang PL,
Gudnason V,
Harris TB,
Launer LJ,
Smith AV,
Bottinger EP,
Loos RJF,
Nadkarni GN,
Preuss MH,
Correa A,
Mei H,
Wilson J,
Meitinger T,
Müller-Nurasyid M,
Peters A,
Waldenberger M,
Mangino M,
Spector TD,
Rienstra M,
van de Vegte YJ,
van der Harst P,
Verweij N,
Kääb S,
Schramm K,
Sinner MF,
Strauch K,
Cutler MJ,
Fatkin D,
London B,
Olesen M,
Roden DM,
Benjamin Shoemaker M,
Gustav Smith J,
Biggs ML,
Bis JC,
Brody JA,
Psaty BM,
Rice K,
Sotoodehnia N,
De Grandi A,
Fuchsberger C,
Pattaro C,
Pramstaller PP,
Ford I,
Wouter Jukema J,
Macfarlane PW,
Trompet S,
Dörr M,
Felix SB,
Völker U,
Weiss S,
Havulinna AS,
Jula A,
Sääksjärvi K,
Salomaa V,
Guo X,
Heckbert SR,
Lin HJ,
Rotter JI,
Taylor KD,
Yao J,
de Mutsert R,
Maan AC,
Mook-Kanamori DO,
Noordam R,
Cucca F,
Ding J,
Lakatta EG,
Qian Y,
Tarasov KV,
Levy D,
Lin H,
Newton-Cheh CH,
Lunetta KL,
Murray AD,
Porteous DJ,
Smith BH,
Stricker BH,
Uitterlinden A,
van den Berg ME,
Haessler J,
Jackson RD,
Kooperberg C,
Peters U,
Reiner AP,
Whitsel EA,
Alonso A,
Arking DE,
Boerwinkle E,
Ehret GB,
Soliman EZ,
Avery CL,
Gogarten SM,
Kerr KF,
Laurie CC,
Seyerle AA,
Stilp A,
Assa S,
Abdullah Said M,
Yldau van der Ende M,
Lambiase PD,
Orini M,
Ramirez J,
Van Duijvenboden S,
Arnar DO,
Gudbjartsson DF,
Holm H,
Sulem P,
Thorleifsson G,
Thorolfsdottir RB,
Thorsteinsdottir U,
Benjamin EJ,
Tinker A,
Stefansson K,
Ellinor PT,
Jamshidi Y,
Lubitz SA,
Munroe PB
Nature communications · 2020 · PMID 32439900 · open access
12 pages+
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Young WJ,
Lahrouchi N,
Isaacs A,
Duong T,
Foco L,
Ahmed F,
Brody JA,
Salman R,
Noordam R,
Benjamins JW,
Haessler J,
Lyytikäinen LP
and 154 more — show all
Repetto L,
Concas MP,
van den Berg ME,
Weiss S,
Baldassari AR,
Bartz TM,
Cook JP,
Evans DS,
Freudling R,
Hines O,
Isaksen JL,
Lin H,
Mei H,
Moscati A,
Müller-Nurasyid M,
Nursyifa C,
Qian Y,
Richmond A,
Roselli C,
Ryan KA,
Tarazona-Santos E,
Thériault S,
van Duijvenboden S,
Warren HR,
Yao J,
Raza D,
Aeschbacher S,
Ahlberg G,
Alonso A,
Andreasen L,
Bis JC,
Boerwinkle E,
Campbell A,
Catamo E,
Cocca M,
Cutler MJ,
Darbar D,
De Grandi A,
De Luca A,
Ding J,
Ellervik C,
Ellinor PT,
Felix SB,
Froguel P,
Fuchsberger C,
Gögele M,
Graff C,
Graff M,
Guo X,
Hansen T,
Heckbert SR,
Huang PL,
Huikuri HV,
Hutri-Kähönen N,
Ikram MA,
Jackson RD,
Junttila J,
Kavousi M,
Kors JA,
Leal TP,
Lemaitre RN,
Lin HJ,
Lind L,
Linneberg A,
Liu S,
MacFarlane PW,
Mangino M,
Meitinger T,
Mezzavilla M,
Mishra PP,
Mitchell RN,
Mononen N,
Montasser ME,
Morrison AC,
Nauck M,
Nauffal V,
Navarro P,
Nikus K,
Pare G,
Patton KK,
Pelliccione G,
Pittman A,
Porteous DJ,
Pramstaller PP,
Preuss MH,
Raitakari OT,
Reiner AP,
Ribeiro ALP,
Rice KM,
Risch L,
Schlessinger D,
Schotten U,
Schurmann C,
Shen X,
Shoemaker MB,
Sinagra G,
Sinner MF,
Soliman EZ,
Stoll M,
Strauch K,
Tarasov K,
Taylor KD,
Tinker A,
Trompet S,
Uitterlinden A,
Völker U,
Völzke H,
Waldenberger M,
Weng LC,
Whitsel EA,
Wilson JG,
Avery CL,
Conen D,
Correa A,
Cucca F,
Dörr M,
Gharib SA,
Girotto G,
Grarup N,
Hayward C,
Jamshidi Y,
Järvelin MR,
Jukema JW,
Kääb S,
Kähönen M,
Kanters JK,
Kooperberg C,
Lehtimäki T,
Lima-Costa MF,
Liu Y,
Loos RJF,
Lubitz SA,
Mook-Kanamori DO,
Morris AP,
O'Connell JR,
Olesen MS,
Orini M,
Padmanabhan S,
Pattaro C,
Peters A,
Psaty BM,
Rotter JI,
Stricker B,
van der Harst P,
van Duijn CM,
Verweij N,
Wilson JF,
Arking DE,
Ramirez J,
Lambiase PD,
Sotoodehnia N,
Mifsud B,
Newton-Cheh C,
Munroe PB
Nature communications · 2022 · PMID 36050321 · open access
12 pages+
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease
Young WJ,
Haessler J,
Benjamins JW,
Repetto L,
Yao J,
Isaacs A,
Harper AR,
Ramirez J,
Garnier S,
van Duijvenboden S,
Baldassari AR,
Concas MP
and 82 more — show all
Duong T,
Foco L,
Isaksen JL,
Mei H,
Noordam R,
Nursyifa C,
Richmond A,
Santolalla ML,
Sitlani CM,
Soroush N,
Thériault S,
Trompet S,
Aeschbacher S,
Ahmadizar F,
Alonso A,
Brody JA,
Campbell A,
Correa A,
Darbar D,
De Luca A,
Deleuze JF,
Ellervik C,
Fuchsberger C,
Goel A,
Grace C,
Guo X,
Hansen T,
Heckbert SR,
Jackson RD,
Kors JA,
Lima-Costa MF,
Linneberg A,
Macfarlane PW,
Morrison AC,
Navarro P,
Porteous DJ,
Pramstaller PP,
Reiner AP,
Risch L,
Schotten U,
Shen X,
Sinagra G,
Soliman EZ,
Stoll M,
Tarazona-Santos E,
Tinker A,
Trajanoska K,
Villard E,
Warren HR,
Whitsel EA,
Wiggins KL,
Arking DE,
Avery CL,
Conen D,
Girotto G,
Grarup N,
Hayward C,
Jukema JW,
Mook-Kanamori DO,
Olesen MS,
Padmanabhan S,
Psaty BM,
Pattaro C,
Ribeiro ALP,
Rotter JI,
Stricker BH,
van der Harst P,
van Duijn CM,
Verweij N,
Wilson JG,
Orini M,
Charron P,
Watkins H,
Kooperberg C,
Lin HJ,
Wilson JF,
Kanters JK,
Sotoodehnia N,
Mifsud B,
Lambiase PD,
Tereshchenko LG,
Munroe PB
Nature communications · 2023 · PMID 36918541 · open access
12 pages+
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
Roselli C,
Surakka I,
Olesen MS,
Sveinbjornsson G,
Marston NA,
Choi SH,
Holm H,
Chaffin M,
Gudbjartsson D,
Hill MC,
Aegisdottir H,
Albert CM
and 145 more — show all
Alonso A,
Anderson CD,
Arking DE,
Arnar DO,
Barnard J,
Benjamin EJ,
Braunwald E,
Brumpton B,
Campbell A,
Chami N,
Chasman DI,
Cho K,
Choi EK,
Christophersen IE,
Chung MK,
Conen D,
Crijns HJ,
Cutler MJ,
Czuba T,
Damrauer SM,
Dichgans M,
Dörr M,
Dudink E,
Duong T,
Erikstrup C,
Esko T,
Fatkin D,
Faul JD,
Ferreira M,
Freitag DF,
Ganesh SK,
Gaziano JM,
Geelhoed B,
Ghouse J,
Gieger C,
Giulianini F,
Graham SE,
Gudnason V,
Guo X,
Haggerty C,
Hayward C,
Heckbert SR,
Hveem K,
Ito K,
Johnson R,
Jukema JW,
Jurgens SJ,
Kääb S,
Kane JP,
Kany S,
Kardia SLR,
Kavousi M,
Khurshid S,
Kamanu FK,
Kirchhof P,
Kleber ME,
Knight S,
Komuro I,
Krieger JE,
Launer LJ,
Li D,
Lin H,
Lin HJ,
Loos RJF,
Lotta L,
Lubitz SA,
Lunetta KL,
Macfarlane PW,
Magnusson PKE,
Malik R,
Mantineo H,
Marcus GM,
März W,
McManus DD,
Melander O,
Melloni GEM,
Meyre PB,
Miyazawa K,
Mohanty S,
Monfort LM,
Müller-Nurasyid M,
Nafissi NA,
Natale A,
Nazarian S,
Ostrowski SR,
Pak HN,
Pang S,
Pedersen OB,
Pedersen NL,
Pereira AC,
Pirruccello JP,
Preuss M,
Psaty BM,
Pullinger CR,
Rader DJ,
Rämö JT,
Ridker PM,
Rienstra M,
Risch L,
Roden DM,
Rotter JI,
Sabatine MS,
Schunkert H,
Shah SH,
Shim J,
Shoemaker MB,
Simonson B,
Sinner MF,
Smit RAJ,
Smith JA,
Smith NL,
Smith JG,
Soliman EZ,
Sørensen E,
Sotoodehnia N,
Strbian D,
Stricker BH,
Teder-Laving M,
Sun YV,
Thériault S,
Thorolfsdottir RB,
Thorsteinsdottir U,
Tveit A,
van der Harst P,
van Meurs J,
Wang B,
Weiss S,
Wells QS,
Weng LC,
Wilson PW,
Xiao L,
Yang PS,
Yao J,
Yoneda ZT,
Zeller T,
Zeng L,
Zhao W,
Zhao W,
Zhou X,
Zöllner S,
Ruff CT,
Bundgaard H,
Willer C,
Stefansson K,
Ellinor PT
BioBank Japan Project · Regeneron Genetics Center and 1 more consortia
Nature genetics · 2025 · PMID 40050429
12 pages+
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits
van Setten J,
Verweij N,
Mbarek H,
Niemeijer MN,
Trompet S,
Arking DE,
Brody JA,
Gandin I,
Grarup N,
Hall LM,
Hemerich D,
Lyytikäinen LP
and 49 more — show all
Mei H,
Müller-Nurasyid M,
Prins BP,
Robino A,
Smith AV,
Warren HR,
Asselbergs FW,
Boomsma DI,
Caulfield MJ,
Eijgelsheim M,
Ford I,
Hansen T,
Harris TB,
Heckbert SR,
Hottenga JJ,
Iorio A,
Kors JA,
Linneberg A,
MacFarlane PW,
Meitinger T,
Nelson CP,
Raitakari OT,
Silva Aldana CT,
Sinagra G,
Sinner M,
Soliman EZ,
Stoll M,
Uitterlinden A,
van Duijn CM,
Waldenberger M,
Alonso A,
Gasparini P,
Gudnason V,
Jamshidi Y,
Kääb S,
Kanters JK,
Lehtimäki T,
Munroe PB,
Peters A,
Samani NJ,
Sotoodehnia N,
Ulivi S,
Wilson JG,
de Geus EJC,
Jukema JW,
Stricker B,
van der Harst P,
de Bakker PIW,
Isaacs A
European journal of human genetics : EJHG · 2019 · PMID 30679814 · open access
11 pages
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans
Evans DS,
Avery CL,
Nalls MA,
Li G,
Barnard J,
Smith EN,
Tanaka T,
Butler AM,
Buxbaum SG,
Alonso A,
Arking DE,
Berenson GS
and 49 more — show all
Bis JC,
Buyske S,
Carty CL,
Chen W,
Chung MK,
Cummings SR,
Deo R,
Eaton CB,
Fox ER,
Heckbert SR,
Heiss G,
Hindorff LA,
Hsueh WC,
Isaacs A,
Jamshidi Y,
Kerr KF,
Liu F,
Liu Y,
Lohman KK,
Magnani JW,
Maher JF,
Mehra R,
Meng YA,
Musani SK,
Newton-Cheh C,
North KE,
Psaty BM,
Redline S,
Rotter JI,
Schnabel RB,
Schork NJ,
Shohet RV,
Singleton AB,
Smith JD,
Soliman EZ,
Srinivasan SR,
Taylor HA Jr,
Van Wagoner DR,
Wilson JG,
Young T,
Zhang ZM,
Zonderman AB,
Evans MK,
Ferrucci L,
Murray SS,
Tranah GJ,
Whitsel EA,
Reiner AP,
Sotoodehnia N
CHARGE QRS Consortium
Human molecular genetics · 2016 · PMID 27577874
9 pages
Fifteen Genetic Loci Associated With the Electrocardiographic P Wave
Christophersen IE,
Magnani JW,
Yin X,
Barnard J,
Weng LC,
Arking DE,
Niemeijer MN,
Lubitz SA,
Avery CL,
Duan Q,
Felix SB,
Bis JC
and 40 more — show all
Kerr KF,
Isaacs A,
Müller-Nurasyid M,
Müller C,
North KE,
Reiner AP,
Tinker LF,
Kors JA,
Teumer A,
Petersmann A,
Sinner MF,
Buzkova P,
Smith JD,
Van Wagoner DR,
Völker U,
Waldenberger M,
Peters A,
Meitinger T,
Limacher MC,
Wilhelmsen KC,
Psaty BM,
Hofman A,
Uitterlinden A,
Krijthe BP,
Zhang ZM,
Schnabel RB,
Kääb S,
van Duijn C,
Rotter JI,
Sotoodehnia N,
Dörr M,
Li Y,
Chung MK,
Soliman EZ,
Alonso A,
Whitsel EA,
Stricker BH,
Benjamin EJ,
Heckbert SR,
Ellinor PT
Circulation. Cardiovascular genetics · 2017 · PMID 28794112
7 pages
GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals
Méndez-Giráldez R,
Gogarten SM,
Below JE,
Yao J,
Seyerle AA,
Highland HM,
Kooperberg C,
Soliman EZ,
Rotter JI,
Kerr KF,
Ryckman KK,
Taylor KD
and 13 more — show all
Petty LE,
Shah SJ,
Conomos MP,
Sotoodehnia N,
Cheng S,
Heckbert SR,
Sofer T,
Guo X,
Whitsel EA,
Lin HJ,
Hanis CL,
Laurie CC,
Avery CL
Scientific reports · 2017 · PMID 29213071 · open access
7 pages
Genome-wide association study of PR interval
Pfeufer A,
van Noord C,
Marciante KD,
Arking DE,
Larson MG,
Smith AV,
Tarasov KV,
Müller M,
Sotoodehnia N,
Sinner MF,
Verwoert GC,
Li M
and 53 more — show all
Kao WH,
Köttgen A,
Coresh J,
Bis JC,
Psaty BM,
Rice K,
Rotter JI,
Rivadeneira F,
Hofman A,
Kors JA,
Stricker BH,
Uitterlinden AG,
van Duijn CM,
Beckmann BM,
Sauter W,
Gieger C,
Lubitz SA,
Newton-Cheh C,
Wang TJ,
Magnani JW,
Schnabel RB,
Chung MK,
Barnard J,
Smith JD,
Van Wagoner DR,
Vasan RS,
Aspelund T,
Eiriksdottir G,
Harris TB,
Launer LJ,
Najjar SS,
Lakatta E,
Schlessinger D,
Uda M,
Abecasis GR,
Müller-Myhsok B,
Ehret GB,
Boerwinkle E,
Chakravarti A,
Soliman EZ,
Lunetta KL,
Perz S,
Wichmann HE,
Meitinger T,
Levy D,
Gudnason V,
Ellinor PT,
Sanna S,
Kääb S,
Witteman JC,
Alonso A,
Benjamin EJ,
Heckbert SR
Nature genetics · 2010 · PMID 20062060 · open access
6 pages
Genetic loci associated with heart rate variability and their effects on cardiac disease risk
Nolte IM,
Munoz ML,
Tragante V,
Amare AT,
Jansen R,
Vaez A,
von der Heyde B,
Avery CL,
Bis JC,
Dierckx B,
van Dongen J,
Gogarten SM
and 153 more — show all
Goyette P,
Hernesniemi J,
Huikari V,
Hwang SJ,
Jaju D,
Kerr KF,
Kluttig A,
Krijthe BP,
Kumar J,
van der Laan SW,
Lyytikäinen LP,
Maihofer AX,
Minassian A,
van der Most PJ,
Müller-Nurasyid M,
Nivard M,
Salvi E,
Stewart JD,
Thayer JF,
Verweij N,
Wong A,
Zabaneh D,
Zafarmand MH,
Abdellaoui A,
Albarwani S,
Albert C,
Alonso A,
Ashar F,
Auvinen J,
Axelsson T,
Baker DG,
de Bakker PIW,
Barcella M,
Bayoumi R,
Bieringa RJ,
Boomsma D,
Boucher G,
Britton AR,
Christophersen I,
Dietrich A,
Ehret GB,
Ellinor PT,
Eskola M,
Felix JF,
Floras JS,
Franco OH,
Friberg P,
Gademan MGJ,
Geyer MA,
Giedraitis V,
Hartman CA,
Hemerich D,
Hofman A,
Hottenga JJ,
Huikuri H,
Hutri-Kähönen N,
Jouven X,
Junttila J,
Juonala M,
Kiviniemi AM,
Kors JA,
Kumari M,
Kuznetsova T,
Kuznetsova T,
Laurie CC,
Lefrandt JD,
Li Y,
Li Y,
Liao D,
Limacher MC,
Lin HJ,
Lindgren CM,
Lubitz SA,
Mahajan A,
McKnight B,
Zu Schwabedissen HM,
Milaneschi Y,
Mononen N,
Morris AP,
Nalls MA,
Navis G,
Neijts M,
Nikus K,
North KE,
O'Connor DT,
Ormel J,
Perz S,
Peters A,
Psaty BM,
Raitakari OT,
Risbrough VB,
Sinner MF,
Siscovick D,
Smit JH,
Smith NL,
Soliman EZ,
Sotoodehnia N,
Staessen JA,
Stein PK,
Stilp AM,
Stolarz-Skrzypek K,
Strauch K,
Sundström J,
Swenne CA,
Syvänen AC,
Tardif JC,
Taylor KD,
Teumer A,
Thornton TA,
Tinker LE,
Uitterlinden AG,
van Setten J,
Voss A,
Waldenberger M,
Wilhelmsen KC,
Willemsen G,
Wong Q,
Zhang ZM,
Zonderman AB,
Cusi D,
Evans MK,
Greiser HK,
van der Harst P,
Hassan M,
Ingelsson E,
Järvelin MR,
Kääb S,
Kähönen M,
Kivimaki M,
Kooperberg C,
Kuh D,
Lehtimäki T,
Lind L,
Nievergelt CM,
O'Donnell CJ,
Oldehinkel AJ,
Penninx B,
Reiner AP,
Riese H,
van Roon AM,
Rioux JD,
Rotter JI,
Sofer T,
Stricker BH,
Tiemeier H,
Vrijkotte TGM,
Asselbergs FW,
Brundel BJJM,
Heckbert SR,
Whitsel EA,
den Hoed M,
Snieder H,
de Geus EJC
Nature communications · 2017 · PMID 28613276 · open access
6 pages
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Sotoodehnia N,
Isaacs A,
de Bakker PI,
Dörr M,
Newton-Cheh C,
Nolte IM,
van der Harst P,
Müller M,
Eijgelsheim M,
Alonso A,
Hicks AA,
Padmanabhan S
and 91 more — show all
Hayward C,
Smith AV,
Polasek O,
Giovannone S,
Fu J,
Magnani JW,
Marciante KD,
Pfeufer A,
Gharib SA,
Teumer A,
Li M,
Bis JC,
Rivadeneira F,
Aspelund T,
Köttgen A,
Johnson T,
Rice K,
Sie MP,
Wang YA,
Klopp N,
Fuchsberger C,
Wild SH,
Mateo Leach I,
Estrada K,
Völker U,
Wright AF,
Asselbergs FW,
Qu J,
Chakravarti A,
Sinner MF,
Kors JA,
Petersmann A,
Harris TB,
Soliman EZ,
Munroe PB,
Psaty BM,
Oostra BA,
Cupples LA,
Perz S,
de Boer RA,
Uitterlinden AG,
Völzke H,
Spector TD,
Liu FY,
Boerwinkle E,
Dominiczak AF,
Rotter JI,
van Herpen G,
Levy D,
Wichmann HE,
van Gilst WH,
Witteman JC,
Kroemer HK,
Kao WH,
Heckbert SR,
Meitinger T,
Hofman A,
Campbell H,
Folsom AR,
van Veldhuisen DJ,
Schwienbacher C,
O'Donnell CJ,
Volpato CB,
Caulfield MJ,
Connell JM,
Launer L,
Lu X,
Franke L,
Fehrmann RS,
te Meerman G,
Groen HJ,
Weersma RK,
van den Berg LH,
Wijmenga C,
Ophoff RA,
Navis G,
Rudan I,
Snieder H,
Wilson JF,
Pramstaller PP,
Siscovick DS,
Wang TJ,
Gudnason V,
van Duijn CM,
Felix SB,
Fishman GI,
Jamshidi Y,
Stricker BH,
Samani NJ,
Kääb S,
Arking DE
Nature genetics · 2010 · PMID 21076409 · open access
5 pages
Genome-Wide Associations of Global Electrical Heterogeneity ECG Phenotype: The ARIC (Atherosclerosis Risk in Communities) Study and CHS (Cardiovascular Health Study)
Tereshchenko LG,
Sotoodehnia N,
Sitlani CM,
Ashar FN,
Kabir M,
Biggs ML,
Morley MP,
Waks JW,
Soliman EZ,
Buxton AE,
Biering-Sørensen T,
Solomon SD
and 4 more — show all
Journal of the American Heart Association · 2018 · PMID 29622589 · open access
5 pages
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
Prins BP,
Mead TJ,
Brody JA,
Sveinbjornsson G,
Ntalla I,
Bihlmeyer NA,
van den Berg M,
Bork-Jensen J,
Cappellani S,
Van Duijvenboden S,
Klena NT,
Gabriel GC
and 101 more — show all
Liu X,
Gulec C,
Grarup N,
Haessler J,
Hall LM,
Iorio A,
Isaacs A,
Li-Gao R,
Lin H,
Liu CT,
Lyytikäinen LP,
Marten J,
Mei H,
Müller-Nurasyid M,
Orini M,
Padmanabhan S,
Radmanesh F,
Ramirez J,
Robino A,
Schwartz M,
van Setten J,
Smith AV,
Verweij N,
Warren HR,
Weiss S,
Alonso A,
Arnar DO,
Bots ML,
de Boer RA,
Dominiczak AF,
Eijgelsheim M,
Ellinor PT,
Guo X,
Felix SB,
Harris TB,
Hayward C,
Heckbert SR,
Huang PL,
Jukema JW,
Kähönen M,
Kors JA,
Lambiase PD,
Launer LJ,
Li M,
Linneberg A,
Nelson CP,
Pedersen O,
Perez M,
Peters A,
Polasek O,
Psaty BM,
Raitakari OT,
Rice KM,
Rotter JI,
Sinner MF,
Soliman EZ,
Spector TD,
Strauch K,
Thorsteinsdottir U,
Tinker A,
Trompet S,
Uitterlinden A,
Vaartjes I,
van der Meer P,
Völker U,
Völzke H,
Waldenberger M,
Wilson JG,
Xie Z,
Asselbergs FW,
Dörr M,
van Duijn CM,
Gasparini P,
Gudbjartsson DF,
Gudnason V,
Hansen T,
Kääb S,
Kanters JK,
Kooperberg C,
Lehtimäki T,
Lin HJ,
Lubitz SA,
Mook-Kanamori DO,
Conti FJ,
Newton-Cheh CH,
Rosand J,
Rudan I,
Samani NJ,
Sinagra G,
Smith BH,
Holm H,
Stricker BH,
Ulivi S,
Sotoodehnia N,
Apte SS,
van der Harst P,
Stefansson K,
Munroe PB,
Arking DE,
Lo CW,
Jamshidi Y
Genome biology · 2018 · PMID 30012220 · open access
4 pages
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
Ellinor PT,
Lunetta KL,
Albert CM,
Glazer NL,
Ritchie MD,
Smith AV,
Arking DE,
Müller-Nurasyid M,
Krijthe BP,
Lubitz SA,
Bis JC,
Chung MK
and 77 more — show all
Dörr M,
Ozaki K,
Roberts JD,
Smith JG,
Pfeufer A,
Sinner MF,
Lohman K,
Ding J,
Smith NL,
Smith JD,
Rienstra M,
Rice KM,
Van Wagoner DR,
Magnani JW,
Wakili R,
Clauss S,
Rotter JI,
Steinbeck G,
Launer LJ,
Davies RW,
Borkovich M,
Harris TB,
Lin H,
Völker U,
Völzke H,
Milan DJ,
Hofman A,
Boerwinkle E,
Chen LY,
Soliman EZ,
Voight BF,
Li G,
Chakravarti A,
Kubo M,
Tedrow UB,
Rose LM,
Ridker PM,
Conen D,
Tsunoda T,
Furukawa T,
Sotoodehnia N,
Xu S,
Kamatani N,
Levy D,
Nakamura Y,
Parvez B,
Mahida S,
Furie KL,
Rosand J,
Muhammad R,
Psaty BM,
Meitinger T,
Perz S,
Wichmann HE,
Witteman JC,
Kao WH,
Kathiresan S,
Roden DM,
Uitterlinden AG,
Rivadeneira F,
McKnight B,
Sjögren M,
Newman AB,
Liu Y,
Gollob MH,
Melander O,
Tanaka T,
Stricker BH,
Felix SB,
Alonso A,
Darbar D,
Barnard J,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Gudnason V,
Kääb S
Nature genetics · 2012 · PMID 22544366
3 pages
Genome-wide association studies of the PR interval in African Americans
Smith JG,
Magnani JW,
Palmer C,
Meng YA,
Soliman EZ,
Musani SK,
Kerr KF,
Schnabel RB,
Lubitz SA,
Sotoodehnia N,
Redline S,
Pfeufer A
and 16 more — show all
Müller M,
Evans DS,
Nalls MA,
Liu Y,
Newman AB,
Zonderman AB,
Evans MK,
Deo R,
Ellinor PT,
Paltoo DN,
Newton-Cheh C,
Benjamin EJ,
Mehra R,
Alonso A,
Heckbert SR,
Fox ER
Candidate-gene Association Resource (CARe) Consortium
PLoS genetics · 2011 · PMID 21347284 · open access
2 pages
GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations
Swenson BR,
Louie T,
Lin HJ,
Méndez-Giráldez R,
Below JE,
Laurie CC,
Kerr KF,
Highland H,
Thornton TA,
Ryckman KK,
Kooperberg C,
Soliman EZ
and 18 more — show all
Seyerle AA,
Guo X,
Taylor KD,
Yao J,
Heckbert SR,
Darbar D,
Petty LE,
McKnight B,
Cheng S,
Bello NA,
Whitsel EA,
Hanis CL,
Nalls MA,
Evans DS,
Rotter JI,
Sofer T,
Avery CL,
Sotoodehnia N
PloS one · 2019 · PMID 31251759 · open access
2 pages
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
Benjamin EJ,
Rice KM,
Arking DE,
Pfeufer A,
van Noord C,
Smith AV,
Schnabel RB,
Bis JC,
Boerwinkle E,
Sinner MF,
Dehghan A,
Lubitz SA
and 44 more — show all
D'Agostino RB Sr,
Lumley T,
Ehret GB,
Heeringa J,
Aspelund T,
Newton-Cheh C,
Larson MG,
Marciante KD,
Soliman EZ,
Rivadeneira F,
Wang TJ,
Eiríksdottir G,
Levy D,
Psaty BM,
Li M,
Chamberlain AM,
Hofman A,
Vasan RS,
Harris TB,
Rotter JI,
Kao WH,
Agarwal SK,
Stricker BH,
Wang K,
Launer LJ,
Smith NL,
Chakravarti A,
Uitterlinden AG,
Wolf PA,
Sotoodehnia N,
Köttgen A,
van Duijn CM,
Meitinger T,
Mueller M,
Perz S,
Steinbeck G,
Wichmann HE,
Lunetta KL,
Heckbert SR,
Gudnason V,
Alonso A,
Kääb S,
Ellinor PT,
Witteman JC
Nature genetics · 2009 · PMID 19597492 · open access
1 page
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