| Year |
Citation |
Score |
| 2024 |
Lin AE, Bapat AC, Xiao L, Niroula A, Ye J, Wong WJ, Agrawal M, Farady CJ, Boettcher A, Hergott CB, McConkey M, Flores-Bringas P, Shkolnik V, Bick AG, Milan D, ... ... Ellinor PT, et al. Clonal Hematopoiesis of Indeterminate Potential With Loss of Enhances Risk for Atrial Fibrillation Through Inflammasome Activation. Circulation. PMID 38357791 DOI: 10.1161/CIRCULATIONAHA.123.065597 |
0.378 |
|
| 2023 |
Raghavan A, Pirruccello JP, Ellinor PT, Lindsay ME. Using Genomics to Identify Novel Therapeutic Targets for Aortic Disease. Arteriosclerosis, Thrombosis, and Vascular Biology. PMID 38095107 DOI: 10.1161/ATVBAHA.123.318771 |
0.315 |
|
| 2023 |
Arduini A, Fleming SJ, Xiao L, Hall AW, Akkad AD, Chaffin M, Bendinelli KJ, Tucker NR, Papangeli I, Mantineo H, Babadi M, Stegmann CM, García-Cardeña G, Lindsay ME, Klattenhoff C, ... Ellinor PT, et al. Transcriptional profile of the rat cardiovascular system at single cell resolution. Biorxiv : the Preprint Server For Biology. PMID 38014050 DOI: 10.1101/2023.11.14.567085 |
0.67 |
|
| 2023 |
Schuermans A, Vlasschaert C, Nauffal V, Cho SMJ, Uddin MM, Nakao T, Niroula A, Klarqvist MDR, Weeks LD, Lin AE, Saadatagah S, Lannery K, Wong M, Hornsby W, Lubitz SA, ... ... Ellinor PT, et al. Clonal haematopoiesis of indeterminate potential predicts incident cardiac arrhythmias. European Heart Journal. PMID 37952204 DOI: 10.1093/eurheartj/ehad670 |
0.308 |
|
| 2023 |
Wang Y, Selvaraj MS, Li X, Li Z, Holdcraft JA, Arnett DK, Bis JC, Blangero J, Boerwinkle E, Bowden DW, Cade BE, Carlson JC, Carson AP, Chen YI, Curran JE, ... ... Ellinor PT, et al. Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study. American Journal of Human Genetics. 110: 1704-1717. PMID 37802043 DOI: 10.1016/j.ajhg.2023.09.003 |
0.314 |
|
| 2023 |
Rämö JT, Kany S, Hou CR, Friedman SF, Roselli C, Nauffal V, Koyama S, Karjalainen J, Maddah M, Palotie A, Ellinor PT, Pirruccello JP. The Cardiovascular Impact and Genetics of Pericardial Adiposity. Medrxiv : the Preprint Server For Health Sciences. PMID 37502935 DOI: 10.1101/2023.07.16.23292729 |
0.322 |
|
| 2023 |
Jameson HS, Hanley A, Hill MC, Xiao L, Ye J, Bapat A, Ronzier E, Hall AW, Hucker WJ, Clauss S, Barazza M, Silber E, Mina J, Tucker NR, Mills RW, ... ... Ellinor PT, et al. Loss of the Atrial Fibrillation-Related Gene, , Results in Atrial Dilation and Arrhythmias. Circulation Research. PMID 37449401 DOI: 10.1161/CIRCRESAHA.123.323029 |
0.765 |
|
| 2023 |
Wang Y, Selvaraj MS, Li X, Li Z, Holdcraft JA, Arnett DK, Bis JC, Blangero J, Boerwinkle E, Bowden DW, Cade BE, Carlson JC, Carson AP, Chen YI, Curran JE, ... ... Ellinor PT, et al. Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study. Medrxiv : the Preprint Server For Health Sciences. PMID 37425772 DOI: 10.1101/2023.06.28.23291966 |
0.324 |
|
| 2023 |
Einson J, Glinos D, Boerwinkle E, Castaldi P, Darbar D, de Andrade M, Ellinor P, Fornage M, Gabriel S, Germer S, Gibbs R, Hersh CP, Johnsen J, Kaplan R, Konkle BA, et al. Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants. Genetics. PMID 37348055 DOI: 10.1093/genetics/iyad115 |
0.323 |
|
| 2023 |
Klarin D, Devineni P, Sendamarai AK, Angueira AR, Graham SE, Shen YH, Levin MG, Pirruccello JP, Surakka I, Karnam PR, Roychowdhury T, Li Y, Wang M, Aragam KG, Paruchuri K, ... ... Ellinor PT, et al. Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program. Nature Genetics. PMID 37308786 DOI: 10.1038/s41588-023-01420-z |
0.35 |
|
| 2023 |
Wang X, Khurshid S, Choi SH, Friedman S, Weng LC, Reeder C, Pirruccello JP, Singh P, Lau ES, Venn R, Diamant N, Di Achille P, Philippakis A, Anderson CD, Ho JE, ... Ellinor PT, et al. Genetic Susceptibility to Atrial Fibrillation Identified via Deep Learning of 12-Lead Electrocardiograms. Circulation. Genomic and Precision Medicine. e003808. PMID 37278238 DOI: 10.1161/CIRCGEN.122.003808 |
0.314 |
|
| 2023 |
Pham C, Andrzejczyk K, Jurgens SJ, Deprez RL, Palm KCA, Vermeer AMC, Nijman J, Christiaans I, van Dessel PFHM, Beekman L, Choi SH, Lubitz SA, Skoric-Milosavljevic D, van den Bersselaar L, Jansen PR, ... ... Ellinor PT, et al. Genetic Burden of in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias. Circulation. Genomic and Precision Medicine. e003975. PMID 37199186 DOI: 10.1161/CIRCGEN.122.003975 |
0.381 |
|
| 2023 |
Nauffal V, Di Achille P, Klarqvist MDR, Cunningham JW, Hill MC, Pirruccello JP, Weng LC, Morrill VN, Choi SH, Khurshid S, Friedman SF, Nekoui M, Roselli C, Ng K, Philippakis AA, ... ... Ellinor PT, et al. Genetics of myocardial interstitial fibrosis in the human heart and association with disease. Nature Genetics. PMID 37081215 DOI: 10.1038/s41588-023-01371-5 |
0.391 |
|
| 2023 |
Wang X, Ryu J, Kim J, Ramirez A, Mayo KR, Condon H, Vaitinadin NS, Ohno-Machado L, Talavera GA, Ellinor PT, Lubitz SA, Choi SH. Common and rare variants associated with cardiometabolic traits across 98,622 whole-genome sequences in the All of Us research program. Journal of Human Genetics. PMID 37072623 DOI: 10.1038/s10038-023-01147-z |
0.399 |
|
| 2023 |
Khurshid S, Lazarte J, Pirruccello JP, Weng LC, Choi SH, Hall AW, Wang X, Friedman SF, Nauffal V, Biddinger KJ, Aragam KG, Batra P, Ho JE, Philippakis AA, Ellinor PT, et al. Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass. Nature Communications. 14: 1558. PMID 36944631 DOI: 10.1038/s41467-023-37173-w |
0.725 |
|
| 2023 |
Simonson B, Chaffin M, Hill MC, Atwa O, Guedira Y, Bhasin H, Hall AW, Hayat S, Baumgart S, Bedi KC, Margulies KB, Klattenhoff CA, Ellinor PT. Single-nucleus RNA sequencing in ischemic cardiomyopathy reveals common transcriptional profile underlying end-stage heart failure. Cell Reports. 42: 112086. PMID 36790929 DOI: 10.1016/j.celrep.2023.112086 |
0.709 |
|
| 2023 |
Einson J, Glinos D, Boerwinkle E, Castaldi P, Darbar D, de Andrade M, Ellinor P, Fornage M, Gabriel S, Germer S, Gibbs R, Hersh CP, Johnsen J, Kaplan R, Konkle BA, et al. Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants. Biorxiv : the Preprint Server For Biology. PMID 36778406 DOI: 10.1101/2023.01.31.526505 |
0.323 |
|
| 2022 |
Aragam KG, Jiang T, Goel A, Kanoni S, Wolford BN, Atri DS, Weeks EM, Wang M, Hindy G, Zhou W, Grace C, Roselli C, Marston NA, Kamanu FK, Surakka I, ... ... Ellinor PT, et al. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants. Nature Genetics. 54: 1803-1815. PMID 36474045 DOI: 10.1038/s41588-022-01233-6 |
0.33 |
|
| 2022 |
Levin MG, Tsao NL, Singhal P, Liu C, Vy HMT, Paranjpe I, Backman JD, Bellomo TR, Bone WP, Biddinger KJ, Hui Q, Dikilitas O, Satterfield BA, Yang Y, Morley MP, ... ... Ellinor PT, et al. Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure. Nature Communications. 13: 6914. PMID 36376295 DOI: 10.1038/s41467-022-34216-6 |
0.365 |
|
| 2022 |
Yengo L, Vedantam S, Marouli E, Sidorenko J, Bartell E, Sakaue S, Graff M, Eliasen AU, Jiang Y, Raghavan S, Miao J, Arias JD, Graham SE, Mukamel RE, Spracklen CN, ... ... Ellinor PT, et al. A saturated map of common genetic variants associated with human height. Nature. PMID 36224396 DOI: 10.1038/s41586-022-05275-y |
0.407 |
|
| 2022 |
Halford JL, Morrill VN, Choi SH, Jurgens SJ, Melloni G, Marston NA, Weng LC, Nauffal V, Hall AW, Gunn S, Austin-Tse CA, Pirruccello JP, Khurshid S, Rehm HL, Benjamin EJ, ... ... Ellinor PT, et al. Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes. Nature Communications. 13: 5767. PMID 36180445 DOI: 10.1038/s41467-022-33534-z |
0.709 |
|
| 2022 |
Young WJ, Lahrouchi N, Isaacs A, Duong T, Foco L, Ahmed F, Brody JA, Salman R, Noordam R, Benjamins JW, Haessler J, Lyytikäinen LP, Repetto L, Concas MP, van den Berg ME, ... ... Ellinor PT, et al. Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. Nature Communications. 13: 5144. PMID 36050321 DOI: 10.1038/s41467-022-32821-z |
0.472 |
|
| 2022 |
Halford JL, Morrill VN, Choi SH, Jurgens SJ, Melloni G, Marston NA, Weng LC, Nauffal V, Hall AW, Gunn S, Austin-Tse CA, Pirruccello JP, Khurshid S, Rehm HL, Benjamin EJ, ... ... Ellinor PT, et al. Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes. Nature Communications. 13: 5106. PMID 36042188 DOI: 10.1038/s41467-022-32009-5 |
0.726 |
|
| 2022 |
Marston NA, Garfinkel AC, Kamanu FK, Melloni GM, Roselli C, Jarolim P, Berg DD, Bhatt DL, Bonaca MP, Cannon CP, Giugliano RP, O'Donoghue ML, Raz I, Scirica BM, Braunwald E, ... ... Ellinor PT, et al. A polygenic risk score predicts atrial fibrillation in cardiovascular disease. European Heart Journal. PMID 35980763 DOI: 10.1093/eurheartj/ehac460 |
0.337 |
|
| 2022 |
Glinos DA, Garborcauskas G, Hoffman P, Ehsan N, Jiang L, Gokden A, Dai X, Aguet F, Brown KL, Garimella K, Bowers T, Costello M, Ardlie K, Jian R, Tucker NR, ... Ellinor PT, et al. Transcriptome variation in human tissues revealed by long-read sequencing. Nature. PMID 35922509 DOI: 10.1038/s41586-022-05035-y |
0.315 |
|
| 2022 |
Lazarte J, Jurgens SJ, Choi SH, Khurshid S, Morrill VN, Weng LC, Nauffal V, Pirruccello JP, Halford JL, Hegele RA, Ellinor PT, Lunetta KL, Lubitz SA. LMNA Variants and Risk of Adult-Onset Cardiac Disease. Journal of the American College of Cardiology. 80: 50-59. PMID 35772917 DOI: 10.1016/j.jacc.2022.04.035 |
0.374 |
|
| 2022 |
Chaffin M, Papangeli I, Simonson B, Akkad AD, Hill MC, Arduini A, Fleming SJ, Melanson M, Hayat S, Kost-Alimova M, Atwa O, Ye J, Bedi KC, Nahrendorf M, Kaushik VK, ... ... Ellinor PT, et al. Single-nucleus profiling of human dilated and hypertrophic cardiomyopathy. Nature. PMID 35732739 DOI: 10.1038/s41586-022-04817-8 |
0.313 |
|
| 2022 |
Pirruccello JP, Di Achille P, Nauffal V, Nekoui M, Friedman SF, Klarqvist MDR, Chaffin MD, Weng LC, Cunningham JW, Khurshid S, Roselli C, Lin H, Koyama S, Ito K, Kamatani Y, ... ... Ellinor PT, et al. Genetic analysis of right heart structure and function in 40,000 people. Nature Genetics. 54: 792-803. PMID 35697867 DOI: 10.1038/s41588-022-01090-3 |
0.352 |
|
| 2022 |
Biddinger KJ, Jurgens SJ, Maamari D, Gaziano L, Choi SH, Morrill VN, Halford JL, Khera AV, Lubitz SA, Ellinor PT, Aragam KG. Rare and Common Genetic Variation Underlying the Risk of Hypertrophic Cardiomyopathy in a National Biobank. Jama Cardiology. PMID 35583889 DOI: 10.1001/jamacardio.2022.1061 |
0.343 |
|
| 2022 |
Yoneda ZT, Anderson KC, Ye F, Quintana JA, O'Neill MJ, Sims RA, Sun L, Glazer AM, Davogustto G, El-Harasis M, Laws JL, Saldivar BN, Crawford DM, Stricker T, Wells Q, ... ... Ellinor PT, et al. Mortality Among Patients With Early-Onset Atrial Fibrillation and Rare Variants in Cardiomyopathy and Arrhythmia Genes. Jama Cardiology. PMID 35544069 DOI: 10.1001/jamacardio.2022.0810 |
0.375 |
|
| 2022 |
Patel AP, Dron JS, Wang M, Pirruccello JP, Ng K, Natarajan P, Lebo M, Ellinor PT, Aragam KG, Khera AV. Association of Pathogenic DNA Variants Predisposing to Cardiomyopathy With Cardiovascular Disease Outcomes and All-Cause Mortality. Jama Cardiology. PMID 35544052 DOI: 10.1001/jamacardio.2022.0901 |
0.301 |
|
| 2022 |
Taub MA, Conomos MP, Keener R, Iyer KR, Weinstock JS, Yanek LR, Lane J, Miller-Fleming TW, Brody JA, Raffield LM, McHugh CP, Jain D, Gogarten SM, Laurie CA, Keramati A, ... ... Ellinor PT, et al. Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed. Cell Genomics. 2. PMID 35530816 DOI: 10.1016/j.xgen.2021.100084 |
0.372 |
|
| 2022 |
Nauffal V, Morrill VN, Jurgens SJ, Choi SH, Hall AW, Weng LC, Halford JL, Austin-Tse C, Haggerty CM, Harris SL, Wong EK, Alonso A, Arking DE, Benjamin EJ, Boerwinkle E, ... ... Ellinor PT, et al. Monogenic and Polygenic Contributions to QTc Prolongation in the Population. Circulation. PMID 35389749 DOI: 10.1161/CIRCULATIONAHA.121.057261 |
0.761 |
|
| 2022 |
Wainschtein P, Jain D, Zheng Z, Cupples LA, Shadyab AH, McKnight B, Shoemaker BM, Mitchell BD, Psaty BM, Kooperberg C, Liu CT, Albert CM, Roden D, Chasman DI, Darbar D, ... ... Ellinor PT, et al. Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data. Nature Genetics. PMID 35256806 DOI: 10.1038/s41588-021-00997-7 |
0.394 |
|
| 2022 |
Roselli C, Yu M, Nauffal V, Georges A, Yang Q, Love K, Weng LC, Delling FN, Maurya SR, Schrölkamp M, Tfelt-Hansen J, Hagège A, Jeunemaitre X, Debette S, Amouyel P, ... ... Ellinor PT, et al. Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse. European Heart Journal. PMID 35245370 DOI: 10.1093/eurheartj/ehac049 |
0.34 |
|
| 2022 |
Barc J, Tadros R, Glinge C, Chiang DY, Jouni M, Simonet F, Jurgens SJ, Baudic M, Nicastro M, Potet F, Offerhaus JA, Walsh R, Choi SH, Verkerk AO, Mizusawa Y, ... ... Ellinor PT, et al. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nature Genetics. PMID 35210625 DOI: 10.1038/s41588-021-01007-6 |
0.442 |
|
| 2022 |
Jurgens SJ, Choi SH, Morrill VN, Chaffin M, Pirruccello JP, Halford JL, Weng LC, Nauffal V, Roselli C, Hall AW, Oetjens MT, Lagerman B, vanMaanen DP, Aragam KG, Lunetta KL, ... ... Ellinor PT, et al. Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank. Nature Genetics. PMID 35177841 DOI: 10.1038/s41588-021-01011-w |
0.747 |
|
| 2022 |
O' Brien S, Holmes AP, Johnson DM, Kabir SN, O' Shea C, O' Reilly M, Avezzu A, Reyat JS, Hall AW, Apicella C, Ellinor PT, Niederer S, Tucker NR, Fabritz L, Kirchhof P, et al. Increased atrial effectiveness of flecainide conferred by altered biophysical properties of sodium channels. Journal of Molecular and Cellular Cardiology. 166: 23-35. PMID 35114252 DOI: 10.1016/j.yjmcc.2022.01.009 |
0.71 |
|
| 2021 |
Hindy G, Dornbos P, Chaffin MD, Liu DJ, Wang M, Selvaraj MS, Zhang D, Park J, Aguilar-Salinas CA, Antonacci-Fulton L, Ardissino D, Arnett DK, Aslibekyan S, Atzmon G, Ballantyne CM, ... ... Ellinor PT, et al. Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes. American Journal of Human Genetics. PMID 34932938 DOI: 10.1016/j.ajhg.2021.11.021 |
0.322 |
|
| 2021 |
Pirruccello JP, Chaffin MD, Chou EL, Fleming SJ, Lin H, Nekoui M, Khurshid S, Friedman SF, Bick AG, Arduini A, Weng LC, Choi SH, Akkad AD, Batra P, Tucker NR, ... ... Ellinor PT, et al. Deep learning enables genetic analysis of the human thoracic aorta. Nature Genetics. PMID 34837083 DOI: 10.1038/s41588-021-00962-4 |
0.708 |
|
| 2021 |
Yoneda ZT, Anderson KC, Quintana JA, O'Neill MJ, Sims RA, Glazer AM, Shaffer CM, Crawford DM, Stricker T, Ye F, Wells Q, Stevenson LW, Michaud GF, Darbar D, Lubitz SA, ... Ellinor PT, et al. Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes. Jama Cardiology. PMID 34495297 DOI: 10.1001/jamacardio.2021.3370 |
0.378 |
|
| 2021 |
Lumbers RT, Shah S, Lin H, Czuba T, Henry A, Swerdlow DI, Mälarstig A, Andersson C, Verweij N, Holmes MV, Ärnlöv J, Svensson P, Hemingway H, Sallah N, Almgren P, ... ... Ellinor PT, et al. The genomics of heart failure: design and rationale of the HERMES consortium. Esc Heart Failure. PMID 34480422 DOI: 10.1002/ehf2.13517 |
0.307 |
|
| 2021 |
Khurshid S, Mars N, Haggerty CM, Huang Q, Weng LC, Hartzel DN, Lunetta KL, Ashburner JM, Anderson CD, Benjamin EJ, Salomaa V, Ellinor PT, Fornwalt BK, Ripatti S, Trinquart L, et al. Predictive Accuracy of a Clinical and Genetic Risk Model for Atrial Fibrillation. Circulation. Genomic and Precision Medicine. CIRCGEN121003355. PMID 34463125 DOI: 10.1161/CIRCGEN.121.003355 |
0.301 |
|
| 2021 |
Choi SH, Jurgens SJ, Haggerty CM, Hall AW, Halford JL, Morrill VN, Weng LC, Lagerman B, Mirshahi T, Pettinger M, Guo X, Lin HJ, Alonso A, Soliman EZ, Kornej J, ... ... Ellinor PT, et al. Rare Coding Variants Associated with Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-ancestry Analysis. Circulation. Genomic and Precision Medicine. PMID 34319147 DOI: 10.1161/CIRCGEN.120.003300 |
0.779 |
|
| 2021 |
Chalazan B, Mol D, Darbar FA, Ornelas-Loredo A, Al-Azzam B, Chen Y, Tofovic D, Sridhar A, Alzahrani Z, Ellinor P, Darbar D. Association of Rare Genetic Variants and Early-Onset Atrial Fibrillation in Ethnic Minority Individuals. Jama Cardiology. PMID 33950154 DOI: 10.1001/jamacardio.2021.0994 |
0.419 |
|
| 2021 |
Taliun D, Harris DN, Kessler MD, Carlson J, Szpiech ZA, Torres R, Taliun SAG, Corvelo A, Gogarten SM, Kang HM, Pitsillides AN, LeFaive J, Lee SB, Tian X, Browning BL, ... ... Ellinor PT, et al. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program. Nature. 590: 290-299. PMID 33568819 DOI: 10.1038/s41586-021-03205-y |
0.32 |
|
| 2020 |
Khurshid S, Kartoun U, Ashburner JM, Trinquart L, Philippakis A, Khera AV, Ellinor PT, Ng K, Lubitz SA. Performance of Atrial Fibrillation Risk Prediction Models in Over Four Million Individuals. Circulation. Arrhythmia and Electrophysiology. PMID 33295794 DOI: 10.1161/CIRCEP.120.008997 |
0.301 |
|
| 2020 |
Hall AW, Chaffin M, Roselli C, Lin H, Lubitz SA, Bianchi V, Geeven G, Bedi K, Margulies KB, de Laat W, Tucker NR, Ellinor PT. Epigenetic Analyses of Human Left Atrial Tissue Identifies Gene Networks Underlying Atrial Fibrillation. Circulation. Genomic and Precision Medicine. PMID 33155827 DOI: 10.1161/CIRCGEN.120.003085 |
0.763 |
|
| 2020 |
Xiao L, Salem JE, Clauss S, Hanley A, Bapat A, Hulsmans M, Iwamoto Y, Wojtkiewicz G, Cetinbas M, Schloss MJ, Tedeschi J, Lebrun-Vignes B, Lundby A, Sadreyev RI, Moslehi JJ, ... ... Ellinor PT, et al. Ibrutinib-Mediated Atrial Fibrillation Due to Inhibition of CSK. Circulation. PMID 33092403 DOI: 10.1161/CIRCULATIONAHA.120.049210 |
0.304 |
|
| 2020 |
Bick AG, Weinstock JS, Nandakumar SK, Fulco CP, Bao EL, Zekavat SM, Szeto MD, Liao X, Leventhal MJ, Nasser J, Chang K, Laurie C, Burugula BB, Gibson CJ, Lin AE, ... ... Ellinor PT, et al. Inherited causes of clonal haematopoiesis in 97,691 whole genomes. Nature. PMID 33057201 DOI: 10.1038/s41586-020-2819-2 |
0.364 |
|
| 2020 |
Walsh R, Lahrouchi N, Tadros R, Kyndt F, Glinge C, Postema PG, Amin AS, Nannenberg EA, Ware JS, Whiffin N, Mazzarotto F, Škorić-Milosavljević D, Krijger C, Arbelo E, Babuty D, ... ... Ellinor PT, et al. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 32893267 DOI: 10.1038/S41436-020-00946-5 |
0.321 |
|
| 2020 |
Weng LC, Hall AW, Choi SH, Jurgens SJ, Haessler J, Bihlmeyer NA, Grarup N, Lin H, Teumer A, Li-Gao R, Yao J, Guo X, Brody JA, Müller-Nurasyid M, Schramm K, ... ... Ellinor PT, et al. Genetic Determinants of Electrocardiographic P-wave Duration and Relation to Atrial Fibrillation. Circulation. Genomic and Precision Medicine. PMID 32822252 DOI: 10.1161/CIRCGEN.119.002874 |
0.773 |
|
| 2020 |
van Ouwerkerk AF, Hall AW, Kadow ZA, Lazarevic S, Reyat JS, Tucker NR, Nadadur RD, Bosada FM, Bianchi V, Ellinor PT, Fabritz L, Martin JF, de Laat W, Kirchhof P, Moskowitz IP, et al. Epigenetic and Transcriptional Networks Underlying Atrial Fibrillation. Circulation Research. 127: 34-50. PMID 32717170 DOI: 10.1161/CIRCRESAHA.120.316574 |
0.763 |
|
| 2020 |
Roselli C, Rienstra M, Ellinor PT. Genetics of Atrial Fibrillation in 2020: GWAS, Genome Sequencing, Polygenic Risk, and Beyond. Circulation Research. 127: 21-33. PMID 32716721 DOI: 10.1161/CIRCRESAHA.120.316575 |
0.436 |
|
| 2020 |
Ntalla I, Weng LC, Cartwright JH, Hall AW, Sveinbjornsson G, Tucker NR, Choi SH, Chaffin MD, Roselli C, Barnes MR, Mifsud B, Warren HR, Hayward C, Marten J, Cranley JJ, ... ... Ellinor PT, et al. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. Nature Communications. 11: 2542. PMID 32439900 DOI: 10.1038/S41467-020-15706-X |
0.777 |
|
| 2020 |
Lahrouchi N, Tadros R, Crotti L, Mizusawa Y, Postema PG, Beekman L, Walsh R, Hasegawa K, Barc J, Ernsting M, Turkowski KL, Mazzanti A, Beckmann BM, Shimamoto K, Diamant UB, ... ... Ellinor PT, et al. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. Circulation. PMID 32429735 DOI: 10.1161/Circulationaha.120.045956 |
0.363 |
|
| 2020 |
Tucker NR, Chaffin M, Fleming SJ, Hall AW, Parsons VA, Bedi KC, Akkad AD, Herndon CN, Arduini A, Papangeli I, Roselli C, Aguet F, Choi SH, Ardlie KG, Babadi M, ... ... Ellinor PT, et al. Transcriptional and Cellular Diversity of the Human Heart. Circulation. PMID 32403949 DOI: 10.1161/Circulationaha.119.045401 |
0.749 |
|
| 2020 |
Pirruccello JP, Bick A, Wang M, Chaffin M, Friedman S, Yao J, Guo X, Venkatesh BA, Taylor KD, Post WS, Rich S, Lima JAC, Rotter JI, Philippakis A, Lubitz SA, ... Ellinor PT, et al. Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy. Nature Communications. 11: 2254. PMID 32382064 DOI: 10.1038/s41467-020-15823-7 |
0.425 |
|
| 2020 |
Kember RL, Levin MG, Cousminer DL, Tsao N, Judy R, Schur GM, Lubitz SA, Ellinor PT, McCormack SE, Grant SFA, Rader DJ, Voight BF, Damrauer SM. Genetically Determined Birthweight Associates with Atrial Fibrillation: A Mendelian Randomization Study. Circulation. Genomic and Precision Medicine. PMID 32340472 DOI: 10.1161/CIRCGEN.119.002553 |
0.414 |
|
| 2020 |
van Ouwerkerk AF, Bosada F, Liu J, Zhang J, van Duijvenboden K, Chaffin M, Tucker N, Pijnappels DA, Ellinor PT, Barnett P, de Vries AA, Christoffels VM. Identification of Functional Variant Enhancers Associated with Atrial Fibrillation. Circulation Research. PMID 32248749 DOI: 10.1161/CIRCRESAHA.119.316006 |
0.477 |
|
| 2020 |
Yamak A, Hu D, Mittal N, Buikema JW, Ditta S, Lutz PG, Moog-Lutz C, Ellinor PT, Domian IJ. Loss of Asb2 Impairs Cardiomyocyte Differentiation and Leads to Congenital Double Outlet Right Ventricle. Iscience. 23: 100959. PMID 32179481 DOI: 10.1016/j.isci.2020.100959 |
0.312 |
|
| 2020 |
Shoemaker MB, Husser D, Roselli C, Al Jazairi M, Chrispin J, Kühne M, Neumann B, Knight S, Sun H, Mohanty S, Shaffer C, Thériault S, Rinke LL, Siland JE, Crawford DM, ... ... Ellinor P, et al. Genetic Susceptibility for Atrial Fibrillation in Patients Undergoing Atrial Fibrillation Ablation. Circulation. Arrhythmia and Electrophysiology. PMID 32078373 DOI: 10.1161/Circep.119.007676 |
0.377 |
|
| 2020 |
Shah S, Henry A, Roselli C, Lin H, Sveinbjörnsson G, Fatemifar G, Hedman ÅK, Wilk JB, Morley MP, Chaffin MD, Helgadottir A, Verweij N, Dehghan A, Almgren P, Andersson C, ... ... Ellinor PT, et al. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure. Nature Communications. 11: 163. PMID 31919418 DOI: 10.1038/S41467-019-13690-5 |
0.502 |
|
| 2019 |
Kowalski MH, Qian H, Hou Z, Rosen JD, Tapia AL, Shan Y, Jain D, Argos M, Arnett DK, Avery C, Barnes KC, Becker LC, Bien SA, Bis JC, Blangero J, ... ... Ellinor PT, et al. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. Plos Genetics. 15: e1008500. PMID 31869403 DOI: 10.1371/Journal.Pgen.1008500 |
0.308 |
|
| 2019 |
Wang B, Lunetta K, Dupuis J, Lubitz SA, Trinquart L, Yao L, Ellinor PT, Benjamin EJ, Lin H. Integrative Omics Approach to Identifying Genes Associated with Atrial Fibrillation. Circulation Research. PMID 31801406 DOI: 10.1161/Circresaha.119.315179 |
0.442 |
|
| 2019 |
Choi SH, Jurgens SJ, Weng LC, Pirruccello JP, Roselli C, Chaffin M, Lee C, Hall AW, Khera AV, Lunetta K, Lubitz SA, Ellinor PT. Monogenic and Polygenic Contributions to Atrial Fibrillation Risk: Results from a National Biobank. Circulation Research. PMID 31691645 DOI: 10.1161/CIRCRESAHA.119.315686 |
0.774 |
|
| 2019 |
Zhang M, Hill MC, Kadow ZA, Suh JH, Tucker NR, Hall AW, Tran TT, Swinton PS, Leach JP, Margulies KB, Ellinor PT, Li N, Martin JF. Long-range enhancer-promoter interactions prevent predisposition to atrial fibrillation. Proceedings of the National Academy of Sciences of the United States of America. PMID 31636200 DOI: 10.1073/Pnas.1907418116 |
0.747 |
|
| 2019 |
van Ouwerkerk AF, Bosada FM, van Duijvenboden K, Hill MC, Montefiori LE, Scholman KT, Liu J, de Vries AAF, Boukens BJ, Ellinor PT, Goumans MJTH, Efimov IR, Nobrega MA, Barnett P, Martin JF, et al. Identification of atrial fibrillation associated genes and functional non-coding variants. Nature Communications. 10: 4755. PMID 31628324 DOI: 10.1038/S41467-019-12721-5 |
0.449 |
|
| 2019 |
Toomer KA, Yu M, Fulmer D, Guo L, Moore KS, Moore R, Drayton KD, Glover J, Peterson N, Ramos-Ortiz S, Drohan A, Catching BJ, Stairley R, Wessels A, Lipschutz JH, ... ... Ellinor PT, et al. Primary cilia defects causing mitral valve prolapse. Science Translational Medicine. 11. PMID 31118289 DOI: 10.1126/Scitranslmed.Aax0290 |
0.376 |
|
| 2019 |
Yu M, Georges A, Tucker NR, Kyryachenko S, Toomer K, Schott JJ, Delling FN, Fernandez-Friera L, Solis J, Ellinor PT, Levine RA, Slaugenhaupt SA, Hagège AA, Dina C, Jeunemaitre X, et al. Genome-Wide Association Study-Driven Gene-Set Analyses, Genetic, and Functional Follow-Up Suggest GLIS1 as a Susceptibility Gene for Mitral Valve Prolapse. Circulation. Genomic and Precision Medicine. 12: e002497. PMID 31112420 DOI: 10.1161/CIRCGEN.119.002497 |
0.44 |
|
| 2019 |
Ko D, Benson MD, Ngo D, Yang Q, Larson MG, Wang TJ, Trinquart L, McManus DD, Lubitz SA, Ellinor PT, Vasan RS, Gerszten RE, Benjamin EJ, Lin H. Proteomics Profiling and Risk of New-Onset Atrial Fibrillation: Framingham Heart Study. Journal of the American Heart Association. 8: e010976. PMID 30841775 DOI: 10.1161/Jaha.118.010976 |
0.376 |
|
| 2019 |
Ellervik C, Roselli C, Christophersen IE, Alonso A, Pietzner M, Sitlani CM, Trompet S, Arking DE, Geelhoed B, Guo X, Kleber ME, Lin HJ, Lin H, MacFarlane P, Selvin E, ... ... Ellinor P, et al. Assessment of the Relationship Between Genetic Determinants of Thyroid Function and Atrial Fibrillation: A Mendelian Randomization Study. Jama Cardiology. PMID 30673084 DOI: 10.1001/Jamacardio.2018.4635 |
0.352 |
|
| 2019 |
Salem JE, Shoemaker MB, Bastarache L, Shaffer CM, Glazer AM, Kroncke B, Wells QS, Shi M, Straub P, Jarvik GP, Larson EB, Velez Edwards DR, Edwards TL, Davis LK, Hakonarson H, ... ... Ellinor PT, et al. Association of Thyroid Function Genetic Predictors With Atrial Fibrillation: A Phenome-Wide Association Study and Inverse-Variance Weighted Average Meta-analysis. Jama Cardiology. PMID 30673079 DOI: 10.1001/Jamacardio.2018.4615 |
0.307 |
|
| 2018 |
Choe WS, Kang JH, Choi EK, Shin SY, Lubitz SA, Ellinor PT, Oh S, Lim HE. A Genetic Risk Score for Atrial Fibrillation Predicts the Response to Catheter Ablation. Korean Circulation Journal. PMID 30808078 DOI: 10.4070/kcj.2018.0161 |
0.346 |
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| 2018 |
Choi SH, Weng LC, Roselli C, Lin H, Haggerty CM, Shoemaker MB, Barnard J, Arking DE, Chasman DI, Albert CM, Chaffin M, Tucker NR, Smith JD, Gupta N, Gabriel S, ... ... Ellinor PT, et al. Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation. Jama. 320: 2354-2364. PMID 30535219 DOI: 10.1001/Jama.2018.18179 |
0.423 |
|
| 2018 |
Ahlberg G, Refsgaard L, Lundegaard PR, Andreasen L, Ranthe MF, Linscheid N, Nielsen JB, Melbye M, Haunsø S, Sajadieh A, Camp L, Olesen SP, Rasmussen S, Lundby A, Ellinor PT, et al. Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation. Nature Communications. 9: 4316. PMID 30333491 DOI: 10.1038/S41467-018-06618-Y |
0.355 |
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| 2018 |
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, Lyytikäinen LP, Müller C, Müller-Nurasyid M, ... ... Ellinor PT, et al. PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity. Nature Communications. 9: 2904. PMID 30046033 DOI: 10.1038/S41467-018-04766-9 |
0.494 |
|
| 2018 |
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, Liu X, Gulec C, Grarup N, ... ... Ellinor PT, et al. Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6. Genome Biology. 19: 87. PMID 30012220 DOI: 10.1186/S13059-018-1457-6 |
0.409 |
|
| 2018 |
Roselli C, Chaffin MD, Weng LC, Aeschbacher S, Ahlberg G, Albert CM, Almgren P, Alonso A, Anderson CD, Aragam KG, Arking DE, Barnard J, Bartz TM, Benjamin EJ, Bihlmeyer NA, ... ... Ellinor PT, et al. Multi-ethnic genome-wide association study for atrial fibrillation. Nature Genetics. PMID 29892015 DOI: 10.1038/S41588-018-0133-9 |
0.481 |
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| 2018 |
Bihlmeyer NA, Brody JA, Smith AV, Warren HR, Lin H, Isaacs A, Liu CT, Marten J, Radmanesh F, Hall LM, Grarup N, Mei H, Müller-Nurasyid M, Huffman JE, Verweij N, ... ... Ellinor PT, et al. ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals. Circulation. Genomic and Precision Medicine. 11: e001758. PMID 29874175 DOI: 10.1161/Circgen.117.001758 |
0.337 |
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| 2018 |
Macri V, Brody JA, Arking DE, Hucker WJ, Yin X, Lin H, Mills RW, Sinner MF, Lubitz SA, Liu CT, Morrison AC, Alonso A, Li N, Fedorov VV, Janssen PM, ... ... Ellinor PT, et al. Common Coding Variants in Are Associated With the Nav1.8 Late Current and Cardiac Conduction. Circulation. Genomic and Precision Medicine. 11: e001663. PMID 29752399 DOI: 10.1161/CIRCGEN.116.001663 |
0.403 |
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| 2018 |
Lin H, van Setten J, Smith AV, Bihlmeyer NA, Warren HR, Brody JA, Radmanesh F, Hall L, Grarup N, Müller-Nurasyid M, Boutin T, Verweij N, Lin HJ, Li-Gao R, van den Berg ME, ... ... Ellinor PT, et al. Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval. Circulation. Genomic and Precision Medicine. 11: e002037. PMID 29748316 DOI: 10.1161/CIRCGEN.117.002037 |
0.393 |
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| 2017 |
Weng LC, Choi SH, Klarin D, Smith JG, Loh PR, Chaffin M, Roselli C, Hulme OL, Lunetta KL, Dupuis J, Benjamin EJ, Newton-Cheh C, Kathiresan S, Ellinor PT, Lubitz SA. Heritability of Atrial Fibrillation. Circulation. Cardiovascular Genetics. 10. PMID 29237688 DOI: 10.1161/Circgenetics.117.001838 |
0.424 |
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| 2017 |
Staerk L, Wang B, Lunetta KL, Helm RH, Ko D, Sherer JA, Ellinor PT, Lubitz SA, McManus DD, Vasan RS, Benjamin EJ, Trinquart L. Association Between Leukocyte Telomere Length and the Risk of Incident Atrial Fibrillation: The Framingham Heart Study. Journal of the American Heart Association. 6. PMID 29138179 DOI: 10.1161/Jaha.117.006541 |
0.305 |
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| 2017 |
Tucker NR, Dolmatova EV, Lin H, Cooper RR, Ye J, Hucker WJ, Jameson HS, Parsons VA, Weng LC, Mills RW, Sinner MF, Imakaev M, Leyton-Mange J, Vlahakes G, Benjamin EJ, ... ... Ellinor PT, et al. Diminished PRRX1 Expression Is Associated With Increased Risk of Atrial Fibrillation and Shortening of the Cardiac Action Potential. Circulation. Cardiovascular Genetics. 10. PMID 28974514 DOI: 10.1161/Circgenetics.117.001902 |
0.45 |
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| 2017 |
Weng LC, Lunetta KL, Müller-Nurasyid M, Smith AV, Thériault S, Weeke PE, Barnard J, Bis JC, Lyytikäinen LP, Kleber ME, Martinsson A, Lin HJ, Rienstra M, Trompet S, Krijthe BP, ... ... Ellinor PT, et al. Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium. Scientific Reports. 7: 11303. PMID 28900195 DOI: 10.1038/S41598-017-09396-7 |
0.321 |
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| 2017 |
Bapat A, Anderson CD, Ellinor PT, Lubitz SA. Genomic basis of atrial fibrillation. Heart (British Cardiac Society). PMID 28893835 DOI: 10.1136/Heartjnl-2016-311027 |
0.393 |
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| 2017 |
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, Goyette P, Hernesniemi J, Huikari V, ... ... Ellinor PT, et al. Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk. Nature Communications. 8: 16140. PMID 28767105 DOI: 10.1038/Ncomms16140 |
0.35 |
|
| 2017 |
Christophersen IE, Rienstra M, Roselli C, Yin X, Geelhoed B, Barnard J, Lin H, Arking DE, Smith AV, Albert CM, Chaffin M, Tucker NR, Li M, Klarin D, Bihlmeyer NA, ... ... Ellinor PT, et al. Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nature Genetics. 49: 1286. PMID 28747752 DOI: 10.1038/ng0817-1286c |
0.364 |
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| 2017 |
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, Goyette P, Hernesniemi J, Huikari V, ... ... Ellinor PT, et al. Genetic loci associated with heart rate variability and their effects on cardiac disease risk. Nature Communications. 8: 15805. PMID 28613276 DOI: 10.1038/Ncomms15805 |
0.414 |
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| 2017 |
Fatkin D, Santiago CF, Huttner IG, Lubitz SA, Ellinor PT. Genetics of Atrial Fibrillation: State of the Art in 2017. Heart, Lung & Circulation. PMID 28601532 DOI: 10.1016/j.hlc.2017.04.008 |
0.517 |
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| 2017 |
Low SK, Takahashi A, Ebana Y, Ozaki K, Christophersen IE, Ellinor PT, Ogishima S, Yamamoto M, Satoh M, Sasaki M, Yamaji T, Iwasaki M, Tsugane S, Tanaka K, et al. Identification of six new genetic loci associated with atrial fibrillation in the Japanese population. Nature Genetics. PMID 28416822 DOI: 10.1038/Ng.3842 |
0.462 |
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| 2017 |
Christophersen IE, Rienstra M, Roselli C, Yin X, Geelhoed B, Barnard J, Lin H, Arking DE, Smith AV, Albert CM, Chaffin M, Tucker NR, Li M, Klarin D, Bihlmeyer NA, ... ... Ellinor PT, et al. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nature Genetics. PMID 28416818 DOI: 10.1038/Ng.3843 |
0.489 |
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| 2017 |
van den Berg ME, Warren HR, Cabrera CP, Verweij N, Mifsud B, Haessler J, Bihlmeyer NA, Fu YP, Weiss S, Lin HJ, Grarup N, Li-Gao R, Pistis G, Shah N, Brody JA, ... ... Ellinor PT, et al. Discovery of novel heart rate-associated loci using the Exome Chip. Human Molecular Genetics. PMID 28379579 DOI: 10.1093/Hmg/Ddx113 |
0.362 |
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| 2017 |
Marouli E, Graff M, Medina-Gomez C, Lo KS, Wood AR, Kjaer TR, Fine RS, Lu Y, Schurmann C, Highland HM, Rüeger S, Thorleifsson G, Justice AE, Lamparter D, Stirrups KE, ... ... Ellinor PT, et al. Rare and low-frequency coding variants alter human adult height. Nature. PMID 28146470 DOI: 10.1038/Nature21039 |
0.312 |
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| 2017 |
Lin H, Yin X, Xie Z, Lunetta KL, Lubitz SA, Larson MG, Ko D, Magnani JW, Mendelson MM, Liu C, McManus DD, Levy D, Ellinor PT, Benjamin EJ. Methylome-wide Association Study of Atrial Fibrillation in Framingham Heart Study. Scientific Reports. 7: 40377. PMID 28067321 DOI: 10.1038/Srep40377 |
0.382 |
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| 2016 |
Chatterjee NA, Giulianini F, Geelhoed B, Lunetta KL, Misialek JR, Niemeijer MN, Rienstra M, Rose LM, Smith AV, Arking DE, Ellinor PT, Heeringa J, Lin H, Lubitz SA, Soliman EZ, et al. Genetic Obesity and the Risk of Atrial Fibrillation- Causal Estimates from Mendelian Randomization. Circulation. PMID 27974350 DOI: 10.1161/Circulationaha.116.024921 |
0.306 |
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| 2016 |
Ye J, Tucker NR, Weng LC, Clauss S, Lubitz SA, Ellinor PT. A Functional Variant Associated with Atrial Fibrillation Regulates PITX2c Expression through TFAP2a. American Journal of Human Genetics. PMID 27866707 DOI: 10.1016/j.ajhg.2016.10.001 |
0.361 |
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| 2016 |
Lin H, Mueller-Nurasyid M, Smith AV, Arking DE, Barnard J, Bartz TM, Lunetta KL, Lohman K, Kleber ME, Lubitz SA, Geelhoed B, Trompet S, Niemeijer MN, Kacprowski T, Chasman DI, ... ... Ellinor PT, et al. Gene-gene Interaction Analyses for Atrial Fibrillation. Scientific Reports. 6: 35371. PMID 27824142 DOI: 10.1038/Srep35371 |
0.392 |
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| 2016 |
Lubitz SA, Yin X, Lin H, Kolek M, Smith JG, Trompet S, Rienstra M, Rost NS, Teixeira P, Almgren P, Anderson CD, Chen LY, Engström G, Ford I, Furie KL, ... ... Ellinor PT, et al. Genetic Risk Prediction of Atrial Fibrillation. Circulation. PMID 27793994 DOI: 10.1161/Circulationaha.116.024143 |
0.332 |
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| 2016 |
Tucker NR, Mahida S, Ye J, Abraham EJ, Mina JA, Parsons VA, McLellan MA, Shea MA, Hanley A, Benjamin EJ, Milan DJ, Lin H, Ellinor PT. Gain of function mutations in GATA6 lead to atrial fibrillation. Heart Rhythm : the Official Journal of the Heart Rhythm Society. PMID 27756709 DOI: 10.1016/j.hrthm.2016.10.014 |
0.383 |
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| 2016 |
Lubitz SA, Brody JA, Bihlmeyer NA, Roselli C, Weng LC, Christophersen IE, Alonso A, Boerwinkle E, Gibbs RA, Bis JC, Cupples LA, Mohler PJ, Nickerson DA, Muzny D, ... ... Ellinor PT, et al. Whole Exome Sequencing in Atrial Fibrillation. Plos Genetics. 12: e1006284. PMID 27589061 DOI: 10.1371/Journal.Pgen.1006284 |
0.468 |
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| 2016 |
Kim EJ, Yin X, Fontes JD, Magnani JW, Lubitz SA, McManus DD, Seshadri S, Vasan RS, Ellinor PT, Larson MG, Benjamin EJ, Rienstra M. Atrial fibrillation without comorbidities: Prevalence, incidence and prognosis (from the Framingham Heart Study). American Heart Journal. 177: 138-44. PMID 27297859 DOI: 10.1016/J.Ahj.2016.03.023 |
0.321 |
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| 2016 |
Wang X, Tucker NR, Rizki G, Mills R, Krijger PH, de Wit E, Subramanian V, Bartell E, Nguyen XX, Ye J, Leyton-Mange J, Dolmatova EV, van der Harst P, de Laat W, Ellinor PT, et al. Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures. Elife. 5. PMID 27162171 DOI: 10.7554/Elife.10557 |
0.392 |
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| 2016 |
Hucker WJ, Saini H, Lubitz SA, Ellinor PT. Atrial Fibrillation Genetics: Is There a Practical Clinical Value Now or in the Future? The Canadian Journal of Cardiology. PMID 27094126 DOI: 10.1016/J.Cjca.2016.02.032 |
0.366 |
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| 2016 |
Ma JF, Yang F, Mahida SN, Zhao L, Chen X, Zhang ML, Sun Z, Yao Y, Zhang YX, Zheng GY, Dong J, Feng MJ, Zhang R, Sun J, Li S, ... ... Ellinor PT, et al. TBX5 mutations contribute to early-onset atrial fibrillation in Chinese and Caucasians. Cardiovascular Research. PMID 26762269 DOI: 10.1093/cvr/cvw003 |
0.35 |
|
| 2016 |
Santhanakrishnan R, Wang N, Larson MG, Magnani JW, McManus DD, Lubitz SA, Ellinor PT, Cheng S, Vasan RS, Lee DS, Wang TJ, Levy D, Benjamin EJ, Ho JE. Atrial Fibrillation Begets Heart Failure and Vice Versa: Temporal Associations and Differences in Preserved vs. Reduced Ejection Fraction. Circulation. PMID 26746177 DOI: 10.1161/CIRCULATIONAHA.115.018614 |
0.32 |
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| 2016 |
Tucker NR, Clauss S, Ellinor PT. Common variation in atrial fibrillation: navigating the path from genetic association to mechanism. Cardiovascular Research. 109: 493-501. PMID 26733238 DOI: 10.1093/cvr/cvv283 |
0.424 |
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| 2015 |
Kirchhof P, Breithardt G, Bax J, Benninger G, Blomstrom-Lundqvist C, Boriani G, Brandes A, Brown H, Brueckmann M, Calkins H, Calvert M, Christoffels V, Crijns H, Dobrev D, Ellinor P, et al. A roadmap to improve the quality of atrial fibrillation management: proceedings from the fifth Atrial Fibrillation Network/European Heart Rhythm Association consensus conference. Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. PMID 26481149 DOI: 10.1093/Europace/Euv304 |
0.316 |
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| 2015 |
Dina C, Bouatia-Naji N, Tucker N, Delling FN, Toomer K, Durst R, Perrocheau M, Fernandez-Friera L, Solis J, Le Tourneau T, Chen MH, Probst V, Bosse Y, Pibarot P, ... ... Ellinor PT, et al. Genetic association analyses highlight biological pathways underlying mitral valve prolapse. Nature Genetics. PMID 26301497 DOI: 10.1038/Ng.3383 |
0.345 |
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| 2015 |
Choi EK, Park JH, Lee JY, Nam CM, Hwang MK, Uhm JS, Joung B, Ko YG, Lee MH, Lubitz SA, Ellinor PT, Pak HN. Korean Atrial Fibrillation (AF) Network: Genetic Variants for AF Do Not Predict Ablation Success. Journal of the American Heart Association. 4. PMID 26272656 DOI: 10.1161/JAHA.115.002046 |
0.319 |
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| 2015 |
Shim J, Park JH, Lee JY, Uhm JS, Joung B, Lee MH, Ellinor PT, Pak HN. eNOS3 Genetic Polymorphism Is Related to Post-Ablation Early Recurrence of Atrial Fibrillation. Yonsei Medical Journal. 56: 1244-50. PMID 26256966 DOI: 10.3349/ymj.2015.56.5.1244 |
0.342 |
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| 2015 |
Rahman F, Wang N, Yin X, Ellinor PT, Lubitz SA, LeLorier PA, McManus DD, Sullivan LM, Seshadri S, Vasan RS, Benjamin EJ, Magnani JW. Atrial flutter: Clinical risk factors and adverse outcomes in the Framingham Heart Study. Heart Rhythm : the Official Journal of the Heart Rhythm Society. PMID 26226213 DOI: 10.1016/J.Hrthm.2015.07.031 |
0.329 |
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| 2015 |
Christophersen IE, Ellinor PT. Genetics of atrial fibrillation: from families to genomes. Journal of Human Genetics. 61: 61-70. PMID 25994868 DOI: 10.1038/jhg.2015.44 |
0.461 |
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| 2015 |
Jabbari J, Olesen MS, Yuan L, Nielsen JB, Liang B, Macri V, Christophersen IE, Nielsen N, Sajadieh A, Ellinor PT, Grunnet M, Haunsø S, Holst AG, Svendsen JH, Jespersen T. Common and rare variants in SCN10A modulate the risk of atrial fibrillation. Circulation. Cardiovascular Genetics. 8: 64-73. PMID 25691686 DOI: 10.1161/Circgenetics.113.000442 |
0.335 |
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| 2014 |
Sinner MF, Tucker NR, Lunetta KL, Ozaki K, Smith JG, Trompet S, Bis JC, Lin H, Chung MK, Nielsen JB, Lubitz SA, Krijthe BP, Magnani JW, Ye J, Gollob MH, ... ... Ellinor PT, et al. Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation. Circulation. 130: 1225-35. PMID 25124494 DOI: 10.1161/Circulationaha.114.009892 |
0.441 |
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| 2014 |
Tada H, Shiffman D, Smith JG, Sjögren M, Lubitz SA, Ellinor PT, Louie JZ, Catanese JJ, Engström G, Devlin JJ, Kathiresan S, Melander O. Twelve-single nucleotide polymorphism genetic risk score identifies individuals at increased risk for future atrial fibrillation and stroke. Stroke; a Journal of Cerebral Circulation. 45: 2856-62. PMID 25123217 DOI: 10.1161/STROKEAHA.114.006072 |
0.327 |
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| 2014 |
Lundby A, Rossin EJ, Steffensen AB, Acha MR, Newton-Cheh C, Pfeufer A, Lynch SN, Olesen SP, Brunak S, Ellinor PT, Jukema JW, Trompet S, Ford I, Macfarlane PW, et al. Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics. Nature Methods. 11: 868-74. PMID 24952909 DOI: 10.1038/Nmeth.2997 |
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| 2014 |
Magnani JW, Brody JA, Prins BP, Arking DE, Lin H, Yin X, Liu CT, Morrison AC, Zhang F, Spector TD, Alonso A, Bis JC, Heckbert SR, Lumley T, Sitlani CM, ... ... Ellinor PT, et al. Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. Circulation. Cardiovascular Genetics. 7: 365-73. PMID 24951663 DOI: 10.1161/Circgenetics.113.000098 |
0.443 |
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| 2014 |
Lin H, Yin X, Lunetta KL, Dupuis J, McManus DD, Lubitz SA, Magnani JW, Joehanes R, Munson PJ, Larson MG, Levy D, Ellinor PT, Benjamin EJ. Whole blood gene expression and atrial fibrillation: the Framingham Heart Study. Plos One. 9: e96794. PMID 24805109 DOI: 10.1371/Journal.Pone.0096794 |
0.378 |
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| 2014 |
Ho JE, Yin X, Levy D, Vasan RS, Magnani JW, Ellinor PT, McManus DD, Lubitz SA, Larson MG, Benjamin EJ. Galectin 3 and incident atrial fibrillation in the community. American Heart Journal. 167: 729-34.e1. PMID 24766984 DOI: 10.1016/j.ahj.2014.02.009 |
0.338 |
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| 2014 |
Tucker NR, Ellinor PT. Emerging directions in the genetics of atrial fibrillation. Circulation Research. 114: 1469-82. PMID 24763465 DOI: 10.1161/CIRCRESAHA.114.302225 |
0.447 |
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| 2014 |
Magnani JW, Yin X, McManus DD, Chuang ML, Cheng S, Lubitz SA, Arora G, Manning WJ, Ellinor PT, Benjamin EJ. Genetic loci associated with atrial fibrillation: relation to left atrial structure in the Framingham Heart Study. Journal of the American Heart Association. 3: e000616. PMID 24695651 DOI: 10.1161/JAHA.113.000616 |
0.452 |
|
| 2014 |
Macri V, Mahida SN, Zhang ML, Sinner MF, Dolmatova EV, Tucker NR, McLellan M, Shea MA, Milan DJ, Lunetta KL, Benjamin EJ, Ellinor PT. A novel trafficking-defective HCN4 mutation is associated with early-onset atrial fibrillation. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 1055-62. PMID 24607718 DOI: 10.1016/j.hrthm.2014.03.002 |
0.372 |
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| 2014 |
Wyse DG, Van Gelder IC, Ellinor PT, Go AS, Kalman JM, Narayan SM, Nattel S, Schotten U, Rienstra M. Lone atrial fibrillation: does it exist? Journal of the American College of Cardiology. 63: 1715-23. PMID 24530673 DOI: 10.1016/J.Jacc.2014.01.023 |
0.34 |
|
| 2014 |
Lubitz SA, Lunetta KL, Lin H, Arking DE, Trompet S, Li G, Krijthe BP, Chasman DI, Barnard J, Kleber ME, Dörr M, Ozaki K, Smith AV, Müller-Nurasyid M, Walter S, ... ... Ellinor PT, et al. Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese. Journal of the American College of Cardiology. 63: 1200-10. PMID 24486271 DOI: 10.1016/J.Jacc.2013.12.015 |
0.392 |
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| 2014 |
Mahida S, Mills RW, Tucker NR, Simonson B, Macri V, Lemoine MD, Das S, Milan DJ, Ellinor PT. Overexpression of KCNN3 results in sudden cardiac death. Cardiovascular Research. 101: 326-34. PMID 24296650 DOI: 10.1093/cvr/cvt269 |
0.388 |
|
| 2014 |
Lin H, Sinner MF, Brody JA, Arking DE, Lunetta KL, Rienstra M, Lubitz SA, Magnani JW, Sotoodehnia N, McKnight B, McManus DD, Boerwinkle E, Psaty BM, Rotter JI, Bis JC, ... ... Ellinor PT, et al. Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 452-7. PMID 24239840 DOI: 10.1016/J.Hrthm.2013.11.012 |
0.479 |
|
| 2014 |
Lin H, Dolmatova EV, Morley MP, Lunetta KL, McManus DD, Magnani JW, Margulies KB, Hakonarson H, del Monte F, Benjamin EJ, Cappola TP, Ellinor PT. Gene expression and genetic variation in human atria. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 266-71. PMID 24177373 DOI: 10.1016/J.Hrthm.2013.10.051 |
0.369 |
|
| 2013 |
Ganesh SK, Arnett DK, Assimes TL, Assimes TL, Basson CT, Chakravarti A, Ellinor PT, Engler MB, Goldmuntz E, Herrington DM, Hershberger RE, Hong Y, Johnson JA, Kittner SJ, McDermott DA, et al. Genetics and genomics for the prevention and treatment of cardiovascular disease: update: a scientific statement from the American Heart Association. Circulation. 128: 2813-51. PMID 24297835 DOI: 10.1161/01.Cir.0000437913.98912.1D |
0.363 |
|
| 2013 |
Mandyam MC, Soliman EZ, Alonso A, Dewland TA, Heckbert SR, Vittinghoff E, Cummings SR, Ellinor PT, Chaitman BR, Stocke K, Applegate WB, Arking DE, Butler J, Loehr LR, Magnani JW, et al. The QT interval and risk of incident atrial fibrillation. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 10: 1562-8. PMID 23872693 DOI: 10.1016/J.Hrthm.2013.07.023 |
0.31 |
|
| 2013 |
Nielsen JB, Pietersen A, Graff C, Lind B, Struijk JJ, Olesen MS, Haunsø S, Gerds TA, Ellinor PT, Køber L, Svendsen JH, Holst AG. Risk of atrial fibrillation as a function of the electrocardiographic PR interval: results from the Copenhagen ECG Study. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 10: 1249-56. PMID 23608590 DOI: 10.1016/j.hrthm.2013.04.012 |
0.327 |
|
| 2013 |
den Hoed M, Eijgelsheim M, Esko T, Brundel BJ, Peal DS, Evans DM, Nolte IM, Segrè AV, Holm H, Handsaker RE, Westra HJ, Johnson T, Isaacs A, Yang J, Lundby A, ... ... Ellinor PT, et al. Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nature Genetics. 45: 621-31. PMID 23583979 DOI: 10.1038/Ng.2610 |
0.478 |
|
| 2013 |
Khan AM, Lubitz SA, Sullivan LM, Sun JX, Levy D, Vasan RS, Magnani JW, Ellinor PT, Benjamin EJ, Wang TJ. Low serum magnesium and the development of atrial fibrillation in the community: the Framingham Heart Study. Circulation. 127: 33-8. PMID 23172839 DOI: 10.1161/CIRCULATIONAHA.111.082511 |
0.305 |
|
| 2013 |
Sinner MF, Wang N, Fox CS, Fontes JD, Rienstra M, Magnani JW, Vasan RS, Calderwood AH, Pencina M, Sullivan LM, Ellinor PT, Benjamin EJ. Relation of circulating liver transaminase concentrations to risk of new-onset atrial fibrillation. The American Journal of Cardiology. 111: 219-24. PMID 23127690 DOI: 10.1016/J.Amjcard.2012.09.021 |
0.336 |
|
| 2012 |
Rosenberg MA, Das S, Quintero Pinzon P, Knight AC, Sosnovik DE, Ellinor PT, Rosenzweig A. A Novel Transgenic Mouse Model of Cardiac Hypertrophy and Atrial Fibrillation. Journal of Atrial Fibrillation. 4: 415. PMID 28496713 DOI: 10.4022/jafib.415 |
0.328 |
|
| 2012 |
Lubitz SA, Ellinor PT. Personalized medicine and atrial fibrillation: will it ever happen? Bmc Medicine. 10: 155. PMID 23210687 DOI: 10.1186/1741-7015-10-155 |
0.343 |
|
| 2012 |
Smith JG, Avery CL, Evans DS, Nalls MA, Meng YA, Smith EN, Palmer C, Tanaka T, Mehra R, Butler AM, Young T, Buxbaum SG, Kerr KF, Berenson GS, Schnabel RB, ... ... Ellinor PT, et al. Impact of ancestry and common genetic variants on QT interval in African Americans. Circulation. Cardiovascular Genetics. 5: 647-55. PMID 23166209 DOI: 10.1161/Circgenetics.112.962787 |
0.378 |
|
| 2012 |
Butler AM, Yin X, Evans DS, Nalls MA, Smith EN, Tanaka T, Li G, Buxbaum SG, Whitsel EA, Alonso A, Arking DE, Benjamin EJ, Berenson GS, Bis JC, Chen W, ... ... Ellinor PT, et al. Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. Circulation. Cardiovascular Genetics. 5: 639-46. PMID 23139255 DOI: 10.1161/Circgenetics.112.963991 |
0.337 |
|
| 2012 |
Mahida S, Ellinor PT. New advances in the genetic basis of atrial fibrillation. Journal of Cardiovascular Electrophysiology. 23: 1400-6. PMID 23066792 DOI: 10.1111/j.1540-8167.2012.02445.x |
0.438 |
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| 2012 |
Sinner MF, Porthan K, Noseworthy PA, Havulinna AS, Tikkanen JT, Müller-Nurasyid M, Peloso G, Ulivi S, Beckmann BM, Brockhaus AC, Cooper RR, Gasparini P, Hengstenberg C, Hwang SJ, Iorio A, ... ... Ellinor PT, et al. A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 9: 1627-34. PMID 22683750 DOI: 10.1016/J.Hrthm.2012.06.008 |
0.336 |
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| 2012 |
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, Dörr M, Ozaki K, Roberts JD, et al. Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nature Genetics. 44: 670-5. PMID 22544366 DOI: 10.1038/Ng.2261 |
0.434 |
|
| 2012 |
Guo W, Schafer S, Greaser ML, Radke MH, Liss M, Govindarajan T, Maatz H, Schulz H, Li S, Parrish AM, Dauksaite V, Vakeel P, Klaassen S, Gerull B, Thierfelder L, ... ... Ellinor PT, et al. RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing. Nature Medicine. 18: 766-73. PMID 22466703 DOI: 10.1038/Nm.2693 |
0.323 |
|
| 2012 |
Rienstra M, Sun JX, Lubitz SA, Frankel DS, Vasan RS, Levy D, Magnani JW, Sullivan LM, Meigs JB, Ellinor PT, Benjamin EJ. Plasma resistin, adiponectin, and risk of incident atrial fibrillation: the Framingham Offspring Study. American Heart Journal. 163: 119-124.e1. PMID 22172445 DOI: 10.1016/j.ahj.2011.09.029 |
0.31 |
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| 2012 |
Schnabel RB, Baccarelli A, Lin H, Ellinor PT, Benjamin EJ. Next steps in cardiovascular disease genomic research - Sequencing, epigenetics, and transcriptomics Clinical Chemistry. 58: 113-126. PMID 22100807 DOI: 10.1373/clinchem.2011.170423 |
0.3 |
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| 2012 |
Rienstra M, Sun JX, Magnani JW, Sinner MF, Lubitz SA, Sullivan LM, Ellinor PT, Benjamin EJ. White blood cell count and risk of incident atrial fibrillation (from the Framingham Heart Study). The American Journal of Cardiology. 109: 533-7. PMID 22100030 DOI: 10.1016/j.amjcard.2011.09.049 |
0.315 |
|
| 2011 |
Magnani JW, Rienstra M, Lin H, Sinner MF, Lubitz SA, McManus DD, Dupuis J, Ellinor PT, Benjamin EJ. Atrial fibrillation: current knowledge and future directions in epidemiology and genomics. Circulation. 124: 1982-93. PMID 22042927 DOI: 10.1161/Circulationaha.111.039677 |
0.365 |
|
| 2011 |
Schnabel RB, Kerr KF, Lubitz SA, Alkylbekova EL, Marcus GM, Sinner MF, Magnani JW, Wolf PA, Deo R, Lloyd-Jones DM, Lunetta KL, Mehra R, Levy D, Fox ER, Arking DE, ... ... Ellinor PT, et al. Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) project. Circulation. Cardiovascular Genetics. 4: 557-64. PMID 21846873 DOI: 10.1161/Circgenetics.110.959197 |
0.365 |
|
| 2011 |
Estes NA, Sacco RL, Al-Khatib SM, Ellinor PT, Bezanson J, Alonso A, Antzelevitch C, Brockman RG, Chen PS, Chugh SS, Curtis AB, DiMarco JP, Ellenbogen KA, Epstein AE, Ezekowitz MD, et al. American Heart Association atrial fibrillation research summit: a conference report from the American Heart Association. Circulation. 124: 363-72. PMID 21709057 DOI: 10.1161/Cir.0B013E318224B037 |
0.344 |
|
| 2011 |
Smith JG, Magnani JW, Palmer C, Meng YA, Soliman EZ, Musani SK, Kerr KF, Schnabel RB, Lubitz SA, Sotoodehnia N, Redline S, Pfeufer A, Müller M, Evans DS, Nalls MA, ... ... Ellinor PT, et al. Genome-wide association studies of the PR interval in African Americans. Plos Genetics. 7: e1001304. PMID 21347284 DOI: 10.1371/Journal.Pgen.1001304 |
0.313 |
|
| 2011 |
Sinner MF, Ellinor PT, Meitinger T, Benjamin EJ, Kääb S. Genome-wide association studies of atrial fibrillation: past, present, and future Cardiovascular Research. 89: 701-709. PMID 21245058 DOI: 10.1093/Cvr/Cvr001 |
0.381 |
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| 2011 |
Mahida S, Lubitz SA, Rienstra M, Milan DJ, Ellinor PT. Monogenic atrial fibrillation as pathophysiological paradigms. Cardiovascular Research. 89: 692-700. PMID 21123219 DOI: 10.1093/cvr/cvq381 |
0.396 |
|
| 2011 |
Wirka RC, Gore S, Van Wagoner DR, Arking DE, Lubitz SA, Lunetta KL, Benjamin EJ, Alonso A, Ellinor PT, Barnard J, Chung MK, Smith JD. A common connexin-40 gene promoter variant affects connexin-40 expression in human atria and is associated with atrial fibrillation. Circulation. Arrhythmia and Electrophysiology. 4: 87-93. PMID 21076161 DOI: 10.1161/Circep.110.959726 |
0.38 |
|
| 2011 |
Sinner MF, Lubitz SA, Pfeufer A, Makino S, Beckmann BM, Lunetta KL, Steinbeck G, Perz S, Rahman R, Sonni A, Greenberg SM, Furie KL, Wichmann HE, Meitinger T, Peters A, ... ... Ellinor PT, et al. Lack of replication in polymorphisms reported to be associated with atrial fibrillation. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 8: 403-9. PMID 21056700 DOI: 10.1016/J.Hrthm.2010.11.003 |
0.333 |
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| 2010 |
Lubitz SA, Yin X, Fontes JD, Magnani JW, Rienstra M, Pai M, Villalon ML, Vasan RS, Pencina MJ, Levy D, Larson MG, Ellinor PT, Benjamin EJ. Association between familial atrial fibrillation and risk of new-onset atrial fibrillation. Jama. 304: 2263-9. PMID 21076174 DOI: 10.1001/Jama.2010.1690 |
0.303 |
|
| 2010 |
Yang Y, Yang Y, Liang B, Liu J, Li J, Grunnet M, Olesen SP, Rasmussen HB, Ellinor PT, Gao L, Lin X, Li L, Wang L, Xiao J, Liu Y, et al. Identification of a Kir3.4 mutation in congenital long QT syndrome. American Journal of Human Genetics. 86: 872-80. PMID 20560207 DOI: 10.1016/J.Ajhg.2010.04.017 |
0.384 |
|
| 2010 |
Thanassoulis G, Massaro JM, O'Donnell CJ, Hoffmann U, Levy D, Ellinor PT, Wang TJ, Schnabel RB, Vasan RS, Fox CS, Benjamin EJ. Pericardial fat is associated with prevalent atrial fibrillation: The framingham heart study Circulation: Arrhythmia and Electrophysiology. 3: 345-350. PMID 20558845 DOI: 10.1161/CIRCEP.109.912055 |
0.345 |
|
| 2010 |
Lubitz SA, Ozcan C, Magnani JW, Kääb S, Benjamin EJ, Ellinor PT. Genetics of atrial fibrillation implications for future research directions and personalized medicine Circulation: Arrhythmia and Electrophysiology. 3: 291-299. PMID 20551423 DOI: 10.1161/Circep.110.942441 |
0.392 |
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| 2010 |
Roberts JD, Davies RW, Lubitz SA, Thibodeau IL, Nery PB, Birnie DH, Benjamin EJ, Lemery R, Ellinor PT, Gollob MH. Evaluation of non-synonymous NPPA single nucleotide polymorphisms in atrial fibrillation. Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. 12: 1078-83. PMID 20543198 DOI: 10.1093/europace/euq161 |
0.33 |
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| 2010 |
Milan DJ, Lubitz SA, Kääb S, Ellinor PT. Genome-wide association studies in cardiac electrophysiology: recent discoveries and implications for clinical practice. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 7: 1141-8. PMID 20423731 DOI: 10.1016/J.Hrthm.2010.04.021 |
0.399 |
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| 2010 |
Lubitz SA, Yi BA, Ellinor PT. Genetics of atrial fibrillation. Heart Failure Clinics. 6: 239-47. PMID 20347792 DOI: 10.1016/j.hfc.2009.12.004 |
0.408 |
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| 2010 |
Lubitz SA, Benjamin EJ, Ellinor PT. Atrial fibrillation in congestive heart failure. Heart Failure Clinics. 6: 187-200. PMID 20347787 DOI: 10.1016/j.hfc.2009.11.001 |
0.311 |
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| 2010 |
Ellinor PT, Lunetta KL, Glazer NL, Pfeufer A, Alonso A, Chung MK, Sinner MF, de Bakker PI, Mueller M, Lubitz SA, Fox E, Darbar D, Smith NL, Smith JD, Schnabel RB, et al. Common variants in KCNN3 are associated with lone atrial fibrillation. Nature Genetics. 42: 240-4. PMID 20173747 DOI: 10.1038/Ng.537 |
0.447 |
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| 2010 |
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, Kao WH, Köttgen A, Coresh J, ... ... Ellinor PT, et al. Genome-wide association study of PR interval. Nature Genetics. 42: 153-9. PMID 20062060 DOI: 10.1038/Ng.517 |
0.443 |
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| 2009 |
Patton KK, Ellinor PT, Heckbert SR, Christenson RH, DeFilippi C, Gottdiener JS, Kronmal RA. N-terminal pro-B-type natriuretic peptide is a major predictor of the development of atrial fibrillation: the Cardiovascular Health Study. Circulation. 120: 1768-74. PMID 19841297 DOI: 10.1161/Circulationaha.109.873265 |
0.301 |
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| 2009 |
Watanabe H, Kaiser DW, Makino S, MacRae CA, Ellinor PT, Wasserman BS, Kannankeril PJ, Donahue BS, Roden DM, Darbar D. ACE I/D polymorphism associated with abnormal atrial and atrioventricular conduction in lone atrial fibrillation and structural heart disease: implications for electrical remodeling. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 6: 1327-32. PMID 19648063 DOI: 10.1016/J.Hrthm.2009.05.014 |
0.347 |
|
| 2009 |
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, D'Agostino RB, Lumley T, Ehret GB, ... ... Ellinor PT, et al. Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. Nature Genetics. 41: 879-81. PMID 19597492 DOI: 10.1038/Ng.416 |
0.351 |
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| 2009 |
Benjamin EJ, Chen PS, Bild DE, Mascette AM, Albert CM, Alonso A, Calkins H, Connolly SJ, Curtis AB, Darbar D, Ellinor PT, Go AS, Goldschlager NF, Heckbert SR, Jalife J, et al. Prevention of atrial fibrillation: report from a national heart, lung, and blood institute workshop. Circulation. 119: 606-18. PMID 19188521 DOI: 10.1161/Circulationaha.108.825380 |
0.335 |
|
| 2009 |
Kääb S, Darbar D, van Noord C, Dupuis J, Pfeufer A, Newton-Cheh C, Schnabel R, Makino S, Sinner MF, Kannankeril PJ, Beckmann BM, Choudry S, Donahue BS, Heeringa J, Perz S, ... ... Ellinor PT, et al. Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation. European Heart Journal. 30: 813-9. PMID 19141561 DOI: 10.1093/Eurheartj/Ehn578 |
0.31 |
|
| 2009 |
Lubitz SA, Yi BA, Ellinor PT. Genetics of atrial fibrillation. Cardiology Clinics. 27: 25-33, vii. PMID 19111761 DOI: 10.1016/j.ccl.2008.09.007 |
0.4 |
|
| 2008 |
Ellinor PT, Yi BA, MacRae CA. Genetics of atrial fibrillation. The Medical Clinics of North America. 92: 41-51, x. PMID 18060996 DOI: 10.1016/j.mcna.2007.09.005 |
0.418 |
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| 2007 |
Albert CM, Nam EG, Rimm EB, Jin HW, Hajjar RJ, Hunter DJ, MacRae CA, Ellinor PT. Cardiac sodium channel gene variants and sudden cardiac death in women. Circulation. 117: 16-23. PMID 18071069 DOI: 10.1161/CIRCULATIONAHA.107.736330 |
0.348 |
|
| 2007 |
Gudbjartsson DF, Arnar DO, Helgadottir A, Gretarsdottir S, Holm H, Sigurdsson A, Jonasdottir A, Baker A, Thorleifsson G, Kristjansson K, Palsson A, Blondal T, Sulem P, Backman VM, Hardarson GA, ... ... Ellinor PT, et al. Variants conferring risk of atrial fibrillation on chromosome 4q25. Nature. 448: 353-7. PMID 17603472 DOI: 10.1038/Nature06007 |
0.451 |
|
| 2006 |
Ellinor PT, Choudry S, Macrae CA. Genetics of atrial fibrillation. Future Cardiology. 2: 579-84. PMID 19804195 DOI: 10.2217/14796678.2.5.579 |
0.345 |
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| 2006 |
Heuser A, Plovie ER, Ellinor PT, Grossmann KS, Shin JT, Wichter T, Basson CT, Lerman BB, Sasse-Klaassen S, Thierfelder L, MacRae CA, Gerull B. Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy. American Journal of Human Genetics. 79: 1081-8. PMID 17186466 DOI: 10.1086/509044 |
0.314 |
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| 2005 |
Patton KK, Zacks ES, Chang JY, Shea MA, Ruskin JN, Macrae CA, Ellinor PT. Clinical subtypes of lone atrial fibrillation. Pacing and Clinical Electrophysiology : Pace. 28: 630-8. PMID 16008797 DOI: 10.1111/j.1540-8159.2005.00161.x |
0.323 |
|
| 2004 |
Ellinor PT, Macrae CA. The genetics of atrial fibrillation. Journal of Cardiovascular Electrophysiology. 14: 1007-9. PMID 12950549 DOI: 10.1046/j.1540-8167.2003.03307.x |
0.338 |
|
| 2003 |
Ellinor PT, Shin JT, Moore RK, Yoerger DM, MacRae CA. Locus for atrial fibrillation maps to chromosome 6q14-16. Circulation. 107: 2880-3. PMID 12782570 DOI: 10.1161/01.CIR.0000077910.80718.49 |
0.315 |
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