Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Patrick Thomas Ellinor, M.D.,Ph.D.

Co-Author

This page shows the publications co-authored by Patrick Ellinor and Sekar Kathiresan.
Connection Strength

2.162
  1. Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations. Nat Genet. 2018 09; 50(9):1219-1224.
    View in: PubMed
    Score: 0.193
  2. Multi-ethnic genome-wide association study for atrial fibrillation. Nat Genet. 2018 06 11; 50(9):1225-1233.
    View in: PubMed
    Score: 0.191
  3. Gene-gene Interaction Analyses for Atrial Fibrillation. Sci Rep. 2016 11 08; 6:35371.
    View in: PubMed
    Score: 0.171
  4. Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese. J Am Coll Cardiol. 2014 Apr 01; 63(12):1200-1210.
    View in: PubMed
    Score: 0.141
  5. Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat Genet. 2012 Apr 29; 44(6):670-5.
    View in: PubMed
    Score: 0.125
  6. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices. Nat Commun. 2021 04 12; 12(1):2182.
    View in: PubMed
    Score: 0.058
  7. Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes. Nature. 2021 Mar; 591(7851):E27.
    View in: PubMed
    Score: 0.058
  8. Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. Nat Commun. 2020 12 18; 11(1):6417.
    View in: PubMed
    Score: 0.057
  9. Transethnic Transferability of a Genome-Wide Polygenic Score for Coronary Artery Disease. Circ Genom Precis Med. 2021 02; 14(1):e003092.
    View in: PubMed
    Score: 0.057
  10. Lp(a) (Lipoprotein[a]) Concentrations and Incident Atherosclerotic Cardiovascular Disease: New Insights From a Large National Biobank. Arterioscler Thromb Vasc Biol. 2021 01; 41(1):465-474.
    View in: PubMed
    Score: 0.056
  11. Inherited causes of clonal haematopoiesis in 97,691 whole genomes. Nature. 2020 10; 586(7831):763-768.
    View in: PubMed
    Score: 0.056
  12. Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions. Nat Commun. 2020 08 20; 11(1):3635.
    View in: PubMed
    Score: 0.056
  13. Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery Disease. J Am Coll Cardiol. 2020 06 09; 75(22):2769-2780.
    View in: PubMed
    Score: 0.055
  14. Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy. Nat Commun. 2020 05 07; 11(1):2254.
    View in: PubMed
    Score: 0.055
  15. Association of Rare Pathogenic DNA Variants for Familial Hypercholesterolemia, Hereditary Breast and Ovarian Cancer Syndrome, and Lynch Syndrome With Disease Risk in Adults According to Family History. JAMA Netw Open. 2020 04 01; 3(4):e203959.
    View in: PubMed
    Score: 0.054
  16. Titin Truncating Variants in Adults Without Known Congestive Heart Failure. J Am Coll Cardiol. 2020 03 17; 75(10):1239-1241.
    View in: PubMed
    Score: 0.054
  17. Leveraging Human Genetics to Estimate Clinical Risk Reductions Achievable by Inhibiting Factor XI. Stroke. 2019 11; 50(11):3004-3012.
    View in: PubMed
    Score: 0.052
  18. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat Genet. 2019 Jul; 51(7):1191-1192.
    View in: PubMed
    Score: 0.051
  19. Response by Aragam et al to Letter Regarding Article, "Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery". Circulation. 2019 07 02; 140(1):e7-e8.
    View in: PubMed
    Score: 0.051
  20. Single-Cell Analysis of the Normal Mouse Aorta Reveals Functionally Distinct Endothelial Cell Populations. Circulation. 2019 07 09; 140(2):147-163.
    View in: PubMed
    Score: 0.051
  21. Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation. JAMA. 2018 12 11; 320(22):2354-2364.
    View in: PubMed
    Score: 0.049
  22. Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery. Circulation. 2018 Nov 11.
    View in: PubMed
    Score: 0.049
  23. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat Genet. 2018 05; 50(5):765-766.
    View in: PubMed
    Score: 0.047
  24. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat Genet. 2018 05; 50(5):766-767.
    View in: PubMed
    Score: 0.047
  25. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat Genet. 2018 01; 50(1):26-41.
    View in: PubMed
    Score: 0.046
  26. Heritability of Atrial Fibrillation. Circ Cardiovasc Genet. 2017 Dec; 10(6).
    View in: PubMed
    Score: 0.046
  27. Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat Genet. 2017 07 27; 49(8):1286.
    View in: PubMed
    Score: 0.045
  28. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat Genet. 2017 Jun; 49(6):946-952.
    View in: PubMed
    Score: 0.044
  29. Rare and low-frequency coding variants alter human adult height. Nature. 2017 02 09; 542(7640):186-190.
    View in: PubMed
    Score: 0.044
  30. Genetic Risk Prediction of Atrial Fibrillation. Circulation. 2017 Apr 04; 135(14):1311-1320.
    View in: PubMed
    Score: 0.043
  31. Twelve-single nucleotide polymorphism genetic risk score identifies individuals at increased risk for future atrial fibrillation and stroke. Stroke. 2014 Oct; 45(10):2856-2862.
    View in: PubMed
    Score: 0.037
  32. Aging syndrome genes and premature coronary artery disease. BMC Med Genet. 2005 Oct 31; 6:38.
    View in: PubMed
    Score: 0.020
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.