Harvard Catalyst Profiles

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

Amit Vikram Khera, M.D.

Co-Author

This page shows the publications co-authored by Amit Khera and Connor Emdin.
Connection Strength

6.088
  1. 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: 0.909
  2. 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: 0.852
  3. Genetic Variation at the Sulfonylurea Receptor, Type 2 Diabetes, and Coronary Heart Disease. Diabetes. 2017 08; 66(8):2310-2315.
    View in: PubMed
    Score: 0.706
  4. 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
  5. 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
  6. 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: 0.232
  7. 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: 0.217
  8. 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: 0.196
  9. 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: 0.189
  10. Mendelian Randomization. JAMA. 2017 Nov 21; 318(19):1925-1926.
    View in: PubMed
    Score: 0.184
  11. Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide Signaling. Circulation. 2018 01 16; 137(3):222-232.
    View in: PubMed
    Score: 0.182
  12. Genetic Predisposition to Abdominal Obesity and Cardiometabolic Risk-Reply. JAMA. 2017 06 13; 317(22):2334-2335.
    View in: PubMed
    Score: 0.178
  13. Genetic Risk, Lifestyle, and Coronary Artery Disease. N Engl J Med. 2017 03 23; 376(12):1194-5.
    View in: PubMed
    Score: 0.176
  14. 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: 0.175
  15. 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: 0.174
  16. 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
  17. 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: 0.173
  18. 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
  19. 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
  20. 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
  21. Electronic health record-based genome-wide meta-analysis provides insights on the genetic architecture of non-alcoholic fatty liver disease. Cell Rep Med. 2021 11 16; 2(11):100437.
    View in: PubMed
    Score: 0.060
  22. Heterozygous ABCG5 Gene Deficiency and Risk of Coronary Artery Disease. Circ Genom Precis Med. 2020 10; 13(5):417-423.
    View in: PubMed
    Score: 0.056
  23. Genetic Association of Finger Photoplethysmography-Derived Arterial Stiffness Index With Blood Pressure and Coronary Artery Disease. Arterioscler Thromb Vasc Biol. 2019 06; 39(6):1253-1261.
    View in: PubMed
    Score: 0.051
  24. 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
  25. 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
  26. Exome-wide association study of plasma lipids in >300,000 individuals. Nat Genet. 2017 Dec; 49(12):1758-1766.
    View in: PubMed
    Score: 0.046
  27. 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: 0.045
  28. 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: 0.045
  29. 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: 0.044
  30. 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
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.