Harvard Catalyst Profiles

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

Sekar Kathiresan, M.D.

Co-Author

This page shows the publications co-authored by Sekar Kathiresan and Connor Emdin.
Connection Strength

9.812
  1. Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease. PLoS Genet. 2021 Apr; 17(4):e1009503.
    View in: PubMed
    Score: 0.930
  2. A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease. PLoS Genet. 2020 04; 16(4):e1008629.
    View in: PubMed
    Score: 0.869
  3. DNA Sequence Variation in ACVR1C Encoding the Activin Receptor-Like Kinase 7 Influences Body Fat Distribution and Protects Against Type 2 Diabetes. Diabetes. 2019 01; 68(1):226-234.
    View in: PubMed
    Score: 0.786
  4. Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease. Nat Commun. 2018 04 24; 9(1):1613.
    View in: PubMed
    Score: 0.758
  5. Mendelian Randomization. JAMA. 2017 Nov 21; 318(19):1925-1926.
    View in: PubMed
    Score: 0.736
  6. Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide Signaling. Circulation. 2018 01 16; 137(3):222-232.
    View in: PubMed
    Score: 0.729
  7. Genetic Predisposition to Abdominal Obesity and Cardiometabolic Risk-Reply. JAMA. 2017 06 13; 317(22):2334-2335.
    View in: PubMed
    Score: 0.714
  8. Genetic Association of Waist-to-Hip Ratio With Cardiometabolic Traits, Type 2 Diabetes, and Coronary Heart Disease. JAMA. 2017 02 14; 317(6):626-634.
    View in: PubMed
    Score: 0.698
  9. Evaluation of the Pooled Cohort Equations for Prediction of Cardiovascular Risk in a Contemporary Prospective Cohort. Am J Cardiol. 2017 Mar 15; 119(6):881-885.
    View in: PubMed
    Score: 0.690
  10. Association of Genetic Variation With Cirrhosis: A Multi-Trait Genome-Wide Association and Gene-Environment Interaction Study. Gastroenterology. 2021 04; 160(5):1620-1633.e13.
    View in: PubMed
    Score: 0.227
  11. Heterozygous ABCG5 Gene Deficiency and Risk of Coronary Artery Disease. Circ Genom Precis Med. 2020 10; 13(5):417-423.
    View in: PubMed
    Score: 0.223
  12. Genome-Wide Polygenic Score and Cardiovascular Outcomes With Evacetrapib in Patients With High-Risk Vascular Disease: A Nested Case-Control Study. Circ Genom Precis Med. 2020 02; 13(1):e002767.
    View in: PubMed
    Score: 0.213
  13. Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. Am J Hum Genet. 2018 10 04; 103(4):461-473.
    View in: PubMed
    Score: 0.195
  14. Exome-wide association study of plasma lipids in >300,000 individuals. Nat Genet. 2017 Dec; 49(12):1758-1766.
    View in: PubMed
    Score: 0.183
  15. A Genetic Variant Associated with Five Vascular Diseases Is a Distal Regulator of Endothelin-1 Gene Expression. Cell. 2017 Jul 27; 170(3):522-533.e15.
    View in: PubMed
    Score: 0.180
  16. Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease. Nat Genet. 2017 Sep; 49(9):1392-1397.
    View in: PubMed
    Score: 0.180
  17. Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease. Circ Res. 2017 Jun 23; 121(1):81-88.
    View in: PubMed
    Score: 0.177
  18. Genetic Variation at the Sulfonylurea Receptor, Type 2 Diabetes, and Coronary Heart Disease. Diabetes. 2017 08; 66(8):2310-2315.
    View in: PubMed
    Score: 0.176
  19. Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor. Circ Cardiovasc Genet. 2017 Apr; 10(2).
    View in: PubMed
    Score: 0.176
  20. Genetic Risk, Lifestyle, and Coronary Artery Disease. N Engl J Med. 2017 03 23; 376(12):1194-5.
    View in: PubMed
    Score: 0.176
  21. Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels. J Am Coll Cardiol. 2016 Dec 27; 68(25):2761-2772.
    View in: PubMed
    Score: 0.173
  22. Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease. N Engl J Med. 2016 12 15; 375(24):2349-2358.
    View in: PubMed
    Score: 0.171
  23. Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia. J Am Coll Cardiol. 2016 06 07; 67(22):2578-89.
    View in: PubMed
    Score: 0.164
  24. Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells. Nature. 2020 10; 586(7831):769-775.
    View in: PubMed
    Score: 0.056
  25. Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. Nat Genet. 2018 11; 50(11):1514-1523.
    View in: PubMed
    Score: 0.049
  26. Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes. Nat Commun. 2018 06 13; 9(1):2252.
    View in: PubMed
    Score: 0.048
  27. Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum. Am J Hum Genet. 2018 06 07; 102(6):1204-1211.
    View in: PubMed
    Score: 0.048
  28. ANGPTL3 Deficiency and Protection Against Coronary Artery Disease. J Am Coll Cardiol. 2017 Apr 25; 69(16):2054-2063.
    View in: PubMed
    Score: 0.044
  29. Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease. JAMA. 2017 03 07; 317(9):937-946.
    View in: PubMed
    Score: 0.044
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.