Harvard Catalyst Profiles

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Dan Chasman, Ph.D.

Co-Author

This page shows the publications co-authored by Dan Chasman and Julie Buring.
Connection Strength

4.026
  1. Association of Genetic Variants With Migraine Subclassified by Clinical Symptoms in Adult Females. Front Neurol. 2020; 11:617472.
    View in: PubMed
    Score: 0.223
  2. COMT and Alpha-Tocopherol Effects in Cancer Prevention: Gene-Supplement Interactions in Two Randomized Clinical Trials. J Natl Cancer Inst. 2019 07 01; 111(7):684-694.
    View in: PubMed
    Score: 0.199
  3. Family History of MI, Smoking, and Risk of Periodontal Disease. J Dent Res. 2018 09; 97(10):1106-1113.
    View in: PubMed
    Score: 0.186
  4. Homocysteine, B Vitamins, MTHFR Genotype, and Incident Age-related Macular Degeneration. Ophthalmol Retina. 2018 May; 2(5):508-510.
    View in: PubMed
    Score: 0.184
  5. Correction: Selectivity in Genetic Association with Sub-classified Migraine in Women. PLoS Genet. 2015 Jun; 11(6):e1005330.
    View in: PubMed
    Score: 0.151
  6. Polymorphisms in catechol-O-methyltransferase modify treatment effects of aspirin on risk of cardiovascular disease. Arterioscler Thromb Vasc Biol. 2014 Sep; 34(9):2160-7.
    View in: PubMed
    Score: 0.141
  7. Selectivity in genetic association with sub-classified migraine in women. PLoS Genet. 2014 May; 10(5):e1004366.
    View in: PubMed
    Score: 0.140
  8. Catechol-O-methyltransferase Associated Risk of Cardiovascular Disease Is Modified by Treatment with Vitamin E. J Altern Complement Med. 2014 May; 20(5):A3.
    View in: PubMed
    Score: 0.139
  9. Genome-wide association study reveals three susceptibility loci for common migraine in the general population. Nat Genet. 2011 Jun 12; 43(7):695-8.
    View in: PubMed
    Score: 0.114
  10. Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. Circulation. 2011 Feb 22; 123(7):731-8.
    View in: PubMed
    Score: 0.111
  11. Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. Nat Genet. 2009 Jun; 41(6):724-8.
    View in: PubMed
    Score: 0.099
  12. Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and Apolipoprotein B among 6382 white women in genome-wide analysis with replication. Circ Cardiovasc Genet. 2008 Oct; 1(1):21-30.
    View in: PubMed
    Score: 0.095
  13. Polymorphism in the apolipoprotein(a) gene, plasma lipoprotein(a), cardiovascular disease, and low-dose aspirin therapy. Atherosclerosis. 2009 Apr; 203(2):371-6.
    View in: PubMed
    Score: 0.093
  14. Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study. Am J Hum Genet. 2008 May; 82(5):1185-92.
    View in: PubMed
    Score: 0.092
  15. Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles. Nat Genet. 2022 02; 54(2):152-160.
    View in: PubMed
    Score: 0.060
  16. The power of genetic diversity in genome-wide association studies of lipids. Nature. 2021 12; 600(7890):675-679.
    View in: PubMed
    Score: 0.059
  17. Genetic insights into biological mechanisms governing human ovarian ageing. Nature. 2021 08; 596(7872):393-397.
    View in: PubMed
    Score: 0.058
  18. Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Nat Genet. 2021 May; 53(5):762.
    View in: PubMed
    Score: 0.057
  19. Effect of Vitamin D and ?-3 Fatty Acid Supplementation on Risk of Age-Related Macular Degeneration: An Ancillary Study of the VITAL Randomized Clinical Trial. JAMA Ophthalmol. 2020 12 01; 138(12):1280-1289.
    View in: PubMed
    Score: 0.055
  20. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Nat Genet. 2020 12; 52(12):1314-1332.
    View in: PubMed
    Score: 0.055
  21. Circulating branched-chain amino acids and long-term risk of obesity-related cancers in women. Sci Rep. 2020 10 06; 10(1):16534.
    View in: PubMed
    Score: 0.054
  22. Genetic variation at the coronary artery disease risk locus GUCY1A3 modifies cardiovascular disease prevention effects of aspirin. Eur Heart J. 2019 11 01; 40(41):3385-3392.
    View in: PubMed
    Score: 0.051
  23. Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nat Commun. 2019 10 24; 10(1):4857.
    View in: PubMed
    Score: 0.051
  24. Quality of dietary fat and genetic risk of type 2 diabetes: individual participant data meta-analysis. BMJ. 2019 07 25; 366:l4292.
    View in: PubMed
    Score: 0.050
  25. Analysis of shared heritability in common disorders of the brain. Science. 2018 06 22; 360(6395).
    View in: PubMed
    Score: 0.046
  26. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nat Genet. 2018 04; 50(4):524-537.
    View in: PubMed
    Score: 0.046
  27. Association between Vitamin D Genetic Risk Score and Cancer Risk in a Large Cohort of U.S. Women. Nutrients. 2018 Jan 09; 10(1).
    View in: PubMed
    Score: 0.045
  28. Genome-wide association meta-analysis of fish and EPA+DHA consumption in 17 US and European cohorts. PLoS One. 2017; 12(12):e0186456.
    View in: PubMed
    Score: 0.045
  29. Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry. Sci Rep. 2017 09 12; 7(1):11380.
    View in: PubMed
    Score: 0.044
  30. Cumulative psychological stress and cardiovascular disease risk in middle aged and older women: Rationale, design, and baseline characteristics. Am Heart J. 2017 Oct; 192:1-12.
    View in: PubMed
    Score: 0.043
  31. Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism. Nat Commun. 2017 05 24; 8:15539.
    View in: PubMed
    Score: 0.043
  32. Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nat Genet. 2017 Jun; 49(6):834-841.
    View in: PubMed
    Score: 0.043
  33. Discordance between Circulating Atherogenic Cholesterol Mass and Lipoprotein Particle Concentration in Relation to Future Coronary Events in Women. Clin Chem. 2017 04; 63(4):870-879.
    View in: PubMed
    Score: 0.042
  34. Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nat Genet. 2016 12; 48(12):1462-1472.
    View in: PubMed
    Score: 0.041
  35. Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nat Genet. 2016 09 28; 48(10):1296.
    View in: PubMed
    Score: 0.041
  36. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nat Genet. 2016 08; 48(8):856-66.
    View in: PubMed
    Score: 0.040
  37. Physical and neurobehavioral determinants of reproductive onset and success. Nat Genet. 2016 06; 48(6):617-623.
    View in: PubMed
    Score: 0.040
  38. Corrigendum: Rare coding variants and X-linked loci associated with age at menarche. Nat Commun. 2015 Dec 17; 6:10257.
    View in: PubMed
    Score: 0.039
  39. Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nat Genet. 2015 Nov; 47(11):1294-1303.
    View in: PubMed
    Score: 0.038
  40. A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. Nat Genet. 2015 Oct; 47(10):1121-1130.
    View in: PubMed
    Score: 0.038
  41. Rare coding variants and X-linked loci associated with age at menarche. Nat Commun. 2015 Aug 04; 6:7756.
    View in: PubMed
    Score: 0.038
  42. Cardiovascular risks associated with incident and prevalent periodontal disease. J Clin Periodontol. 2015 Jan; 42(1):21-8.
    View in: PubMed
    Score: 0.037
  43. Vitamin D-associated genetic variation and risk of breast cancer in the breast and prostate cancer cohort consortium (BPC3). Cancer Epidemiol Biomarkers Prev. 2015 Mar; 24(3):627-30.
    View in: PubMed
    Score: 0.036
  44. Inactivating mutations in NPC1L1 and protection from coronary heart disease. N Engl J Med. 2014 Nov 27; 371(22):2072-82.
    View in: PubMed
    Score: 0.036
  45. Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. Nature. 2014 Oct 02; 514(7520):92-97.
    View in: PubMed
    Score: 0.035
  46. Common genetic variations in the vitamin D pathway in relation to blood pressure. Am J Hypertens. 2014 Nov; 27(11):1387-95.
    View in: PubMed
    Score: 0.035
  47. DNA mismatch repair gene MSH6 implicated in determining age at natural menopause. Hum Mol Genet. 2014 May 01; 23(9):2490-7.
    View in: PubMed
    Score: 0.034
  48. Genome-wide meta-analysis identifies new susceptibility loci for migraine. Nat Genet. 2013 Aug; 45(8):912-917.
    View in: PubMed
    Score: 0.033
  49. Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. Am J Epidemiol. 2013 Aug 01; 178(3):451-60.
    View in: PubMed
    Score: 0.032
  50. Genome-wide association studies identify four ER negative-specific breast cancer risk loci. Nat Genet. 2013 Apr; 45(4):392-8, 398e1-2.
    View in: PubMed
    Score: 0.032
  51. A genome-wide association study of early menopause and the combined impact of identified variants. Hum Mol Genet. 2013 Apr 01; 22(7):1465-72.
    View in: PubMed
    Score: 0.032
  52. Lipoprotein(a), polymorphisms in the LPA gene, and incident venous thromboembolism among 21483 women. J Thromb Haemost. 2013 Jan; 11(1):205-8.
    View in: PubMed
    Score: 0.032
  53. Genome-wide linkage and association analyses implicate FASN in predisposition to Uterine Leiomyomata. Am J Hum Genet. 2012 Oct 05; 91(4):621-8.
    View in: PubMed
    Score: 0.031
  54. A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. Hum Mol Genet. 2012 Dec 15; 21(24):5373-84.
    View in: PubMed
    Score: 0.031
  55. An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12. PLoS One. 2012; 7(5):e37903.
    View in: PubMed
    Score: 0.031
  56. Reproductive aging-associated common genetic variants and the risk of breast cancer. Breast Cancer Res. 2012 Mar 20; 14(2):R54.
    View in: PubMed
    Score: 0.030
  57. Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nat Genet. 2012 Jan 22; 44(3):260-8.
    View in: PubMed
    Score: 0.030
  58. A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer. Nat Genet. 2011 Oct 30; 43(12):1210-4.
    View in: PubMed
    Score: 0.029
  59. Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study. PLoS One. 2011; 6(7):e22106.
    View in: PubMed
    Score: 0.029
  60. Physical activity modifies the effect of LPL, LIPC, and CETP polymorphisms on HDL-C levels and the risk of myocardial infarction in women of European ancestry. Circ Cardiovasc Genet. 2011 Feb; 4(1):74-80.
    View in: PubMed
    Score: 0.028
  61. Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nat Genet. 2010 Dec; 42(12):1077-85.
    View in: PubMed
    Score: 0.028
  62. The fat-mass and obesity-associated (FTO) gene, physical activity, and risk of incident cardiovascular events in white women. Am Heart J. 2010 Dec; 160(6):1163-9.
    View in: PubMed
    Score: 0.028
  63. A large-scale candidate gene association study of age at menarche and age at natural menopause. Hum Genet. 2010 Nov; 128(5):515-27.
    View in: PubMed
    Score: 0.027
  64. Common variants in cardiac ion channel genes are associated with sudden cardiac death. Circ Arrhythm Electrophysiol. 2010 Jun; 3(3):222-9.
    View in: PubMed
    Score: 0.026
  65. Association between a literature-based genetic risk score and cardiovascular events in women. JAMA. 2010 Feb 17; 303(7):631-7.
    View in: PubMed
    Score: 0.026
  66. Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3. Ann Intern Med. 2009 Jan 20; 150(2):65-72.
    View in: PubMed
    Score: 0.024
  67. Rationale, design, and methodology of the Women's Genome Health Study: a genome-wide association study of more than 25,000 initially healthy american women. Clin Chem. 2008 Feb; 54(2):249-55.
    View in: PubMed
    Score: 0.022
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.