Harvard Catalyst Profiles

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Jonathan Rosand, M.D.

Co-Author

This page shows the publications co-authored by Jonathan Rosand and Farid Radmanesh.
Connection Strength

1.635
  1. Rare Coding Variation and Risk of Intracerebral Hemorrhage. Stroke. 2015 Aug; 46(8):2299-301.
    View in: PubMed
    Score: 0.639
  2. Risk factors for computed tomography angiography spot sign in deep and lobar intracerebral hemorrhage are shared. Stroke. 2014 Jun; 45(6):1833-5.
    View in: PubMed
    Score: 0.148
  3. Accuracy of imputation to infer unobserved APOE epsilon alleles in genome-wide genotyping data. Eur J Hum Genet. 2014 Oct; 22(10):1239-42.
    View in: PubMed
    Score: 0.145
  4. Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6. Genome Biol. 2018 07 17; 19(1):87.
    View in: PubMed
    Score: 0.049
  5. 17p12 Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage. Stroke. 2018 07; 49(7):1618-1625.
    View in: PubMed
    Score: 0.049
  6. Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval. Circ Genom Precis Med. 2018 05; 11(5):e002037.
    View in: PubMed
    Score: 0.049
  7. ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals. Circ Genom Precis Med. 2018 01; 11(1):e001758.
    View in: PubMed
    Score: 0.048
  8. COL4A2 is associated with lacunar ischemic stroke and deep ICH: Meta-analyses among 21,500 cases and 40,600 controls. Neurology. 2017 Oct 24; 89(17):1829-1839.
    View in: PubMed
    Score: 0.047
  9. 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: 0.046
  10. Discovery of novel heart rate-associated loci using the Exome Chip. Hum Mol Genet. 2017 06 15; 26(12):2346-2363.
    View in: PubMed
    Score: 0.046
  11. 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: 0.045
  12. Genetic variation at 16q24.2 is associated with small vessel stroke. Ann Neurol. 2017 Mar; 81(3):383-394.
    View in: PubMed
    Score: 0.045
  13. Genetic variants in CETP increase risk of intracerebral hemorrhage. Ann Neurol. 2016 11; 80(5):730-740.
    View in: PubMed
    Score: 0.044
  14. GENOME-WIDE ASSOCIATION STUDY (GWAS) AND GENOME-WIDE BY ENVIRONMENT INTERACTION STUDY (GWEIS) OF DEPRESSIVE SYMPTOMS IN AFRICAN AMERICAN AND HISPANIC/LATINA WOMEN. Depress Anxiety. 2016 Apr; 33(4):265-80.
    View in: PubMed
    Score: 0.042
  15. Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke. Neurology. 2016 Jan 12; 86(2):146-53.
    View in: PubMed
    Score: 0.041
  16. Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease. Neurology. 2015 Mar 03; 84(9):918-26.
    View in: PubMed
    Score: 0.039
  17. Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke. Stroke. 2015 Feb; 46(2):348-53.
    View in: PubMed
    Score: 0.039
  18. APOE e variants increase risk of warfarin-related intracerebral hemorrhage. Neurology. 2014 Sep 23; 83(13):1139-46.
    View in: PubMed
    Score: 0.038
  19. Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. Am J Hum Genet. 2014 Apr 03; 94(4):511-21.
    View in: PubMed
    Score: 0.037
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.