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Natalia Sana Rost, M.D.

Co-Author

This page shows the publications co-authored by Natalia Rost and Christopher Anderson.
Connection Strength

1.734
  1. Common variants within oxidative phosphorylation genes influence risk of ischemic stroke and intracerebral hemorrhage. Stroke. 2013 Mar; 44(3):612-9.
    View in: PubMed
    Score: 0.135
  2. Statin treatment and functional outcome after ischemic stroke: case-control and meta-analysis. Stroke. 2011 May; 42(5):1314-9.
    View in: PubMed
    Score: 0.119
  3. The effect of survival bias on case-control genetic association studies of highly lethal diseases. Circ Cardiovasc Genet. 2011 Apr; 4(2):188-96.
    View in: PubMed
    Score: 0.118
  4. White matter hyperintensity burden and susceptibility to cerebral ischemia. Stroke. 2010 Dec; 41(12):2807-11.
    View in: PubMed
    Score: 0.115
  5. Common mitochondrial sequence variants in ischemic stroke. Ann Neurol. 2011 Mar; 69(3):471-80.
    View in: PubMed
    Score: 0.115
  6. Chromosome 9p21 in ischemic stroke: population structure and meta-analysis. Stroke. 2010 Jun; 41(6):1123-31.
    View in: PubMed
    Score: 0.112
  7. Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies. Lancet Neurol. 2021 05; 20(5):351-361.
    View in: PubMed
    Score: 0.060
  8. Automated Electronic Phenotyping of Cardioembolic Stroke. Stroke. 2021 01; 52(1):181-189.
    View in: PubMed
    Score: 0.058
  9. Atrial Fibrillation Risk and Discrimination of Cardioembolic From Noncardioembolic Stroke. Stroke. 2020 05; 51(5):1396-1403.
    View in: PubMed
    Score: 0.056
  10. Trends in Telestroke Care Delivery: A 15-Year Experience of an Academic Hub and Its Network of Spokes. Circ Cardiovasc Qual Outcomes. 2020 03; 13(3):e005903.
    View in: PubMed
    Score: 0.055
  11. Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nat Genet. 2019 Jul; 51(7):1192-1193.
    View in: PubMed
    Score: 0.053
  12. Multi-ethnic genome-wide association study for atrial fibrillation. Nat Genet. 2018 06 11; 50(9):1225-1233.
    View in: PubMed
    Score: 0.049
  13. 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: 0.048
  14. Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke. Brain. 2017 Oct 01; 140(10):2663-2672.
    View in: PubMed
    Score: 0.047
  15. 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
  16. 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
  17. 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
  18. 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
  19. Genetic Risk Prediction of Atrial Fibrillation. Circulation. 2017 Apr 04; 135(14):1311-1320.
    View in: PubMed
    Score: 0.044
  20. 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
  21. Warfarin and statins are associated with hematoma volume in primary infratentorial intracerebral hemorrhage. Neurocrit Care. 2014 Oct; 21(2):192-9.
    View in: PubMed
    Score: 0.038
  22. 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
  23. Predictors of hematoma volume in deep and lobar supratentorial intracerebral hemorrhage. JAMA Neurol. 2013 Aug; 70(8):988-94.
    View in: PubMed
    Score: 0.035
  24. Heritability estimates identify a substantial genetic contribution to risk and outcome of intracerebral hemorrhage. Stroke. 2013 Jun; 44(6):1578-83.
    View in: PubMed
    Score: 0.034
  25. Burden of blood pressure-related alleles is associated with larger hematoma volume and worse outcome in intracerebral hemorrhage. Stroke. 2013 Feb; 44(2):321-6.
    View in: PubMed
    Score: 0.034
  26. Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke? Stroke. 2012 Apr; 43(4):980-6.
    View in: PubMed
    Score: 0.032
  27. Genome-wide association analysis of ischemic stroke in young adults. G3 (Bethesda). 2011 Nov; 1(6):505-14.
    View in: PubMed
    Score: 0.031
  28. APOE genotype and extent of bleeding and outcome in lobar intracerebral haemorrhage: a genetic association study. Lancet Neurol. 2011 Aug; 10(8):702-9.
    View in: PubMed
    Score: 0.030
  29. Variants at APOE influence risk of deep and lobar intracerebral hemorrhage. Ann Neurol. 2010 Dec; 68(6):934-43.
    View in: PubMed
    Score: 0.029
  30. Principal-component analysis for assessment of population stratification in mitochondrial medical genetics. Am J Hum Genet. 2010 Jun 11; 86(6):904-17.
    View in: PubMed
    Score: 0.028
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.