Harvard Catalyst Profiles

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

Co-Author

This page shows the publications co-authored by Patrick Ellinor and Amit Khera.
Connection Strength

2.585
  1. Association of the Interaction Between Familial Hypercholesterolemia Variants and Adherence to a Healthy Lifestyle With Risk of Coronary Artery Disease. JAMA Netw Open. 2022 Mar 01; 5(3):e222687.
    View in: PubMed
    Score: 0.247
  2. Machine learning enables new insights into genetic contributions to liver fat accumulation. Cell Genom. 2021 Dec 08; 1(3).
    View in: PubMed
    Score: 0.244
  3. Selection of 51 predictors from 13,782 candidate multimodal features using machine learning improves coronary artery disease prediction. Patterns (N Y). 2021 Dec 10; 2(12):100364.
    View in: PubMed
    Score: 0.241
  4. 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: 0.227
  5. 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: 0.226
  6. Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions. Nat Commun. 2020 08 20; 11(1):3635.
    View in: PubMed
    Score: 0.223
  7. 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: 0.217
  8. 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: 0.216
  9. Monogenic and Polygenic Contributions to Atrial Fibrillation Risk: Results From a National Biobank. Circ Res. 2020 01 17; 126(2):200-209.
    View in: PubMed
    Score: 0.211
  10. 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
  11. Association of Habitual Alcohol Intake With Risk of Cardiovascular Disease. JAMA Netw Open. 2022 Mar 01; 5(3):e223849.
    View in: PubMed
    Score: 0.062
  12. Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes. Am J Hum Genet. 2022 01 06; 109(1):81-96.
    View in: PubMed
    Score: 0.061
  13. Performance of Atrial Fibrillation Risk Prediction Models in Over 4 Million Individuals. Circ Arrhythm Electrophysiol. 2021 01; 14(1):e008997.
    View in: PubMed
    Score: 0.057
  14. 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
  15. 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
  16. 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
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.