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Susan Redline, M.D.

Co-Author

This page shows the publications co-authored by Susan Redline and Heming Wang.
Connection Strength

4.024
  1. Cutting the fat: advances and challenges in sleep apnoea genetics. Eur Respir J. 2021 05; 57(5).
    View in: PubMed
    Score: 0.960
  2. Non-REM Apnea and Hypopnea Duration Varies across Population Groups and Physiologic Traits. Am J Respir Crit Care Med. 2021 05 01; 203(9):1173-1182.
    View in: PubMed
    Score: 0.240
  3. Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure. Mol Psychiatry. 2021 Apr 15.
    View in: PubMed
    Score: 0.239
  4. Local Ancestry Inference in Large Pedigrees. Sci Rep. 2020 01 13; 10(1):189.
    View in: PubMed
    Score: 0.219
  5. Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. Nat Commun. 2019 11 12; 10(1):5121.
    View in: PubMed
    Score: 0.217
  6. Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes. Nat Commun. 2019 08 13; 10(1):3503.
    View in: PubMed
    Score: 0.213
  7. Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep. PLoS Genet. 2019 04; 15(4):e1007739.
    View in: PubMed
    Score: 0.208
  8. Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino Americans. Hum Mol Genet. 2019 02 15; 28(4):675-687.
    View in: PubMed
    Score: 0.206
  9. Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in Men. Am J Respir Cell Mol Biol. 2018 03; 58(3):391-401.
    View in: PubMed
    Score: 0.193
  10. Genome-wide survey in African Americans demonstrates potential epistasis of fitness in the human genome. Genet Epidemiol. 2017 Feb; 41(2):122-135.
    View in: PubMed
    Score: 0.177
  11. Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level. Hum Mol Genet. 2016 12 01; 25(23):5244-5253.
    View in: PubMed
    Score: 0.177
  12. Presence and transmission of mitochondrial heteroplasmic mutations in human populations of European and African ancestry. Mitochondrion. 2021 Sep; 60:33-42.
    View in: PubMed
    Score: 0.061
  13. The trans-ancestral genomic architecture of glycemic traits. Nat Genet. 2021 06; 53(6):840-860.
    View in: PubMed
    Score: 0.060
  14. Detecting fitness epistasis in recently admixed populations with genome-wide data. BMC Genomics. 2020 Jul 11; 21(1):476.
    View in: PubMed
    Score: 0.057
  15. Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels. Circ Genom Precis Med. 2020 08; 13(4):e002772.
    View in: PubMed
    Score: 0.056
  16. Low oxygen saturation during sleep reduces CD1D and RAB20 expressions that are reversed by CPAP therapy. EBioMedicine. 2020 Jun; 56:102803.
    View in: PubMed
    Score: 0.056
  17. De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population. Proc Natl Acad Sci U S A. 2020 02 04; 117(5):2560-2569.
    View in: PubMed
    Score: 0.055
  18. Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level. Am J Hum Genet. 2019 11 07; 105(5):1057-1068.
    View in: PubMed
    Score: 0.054
  19. A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. Hum Mol Genet. 2019 08 01; 28(15):2615-2633.
    View in: PubMed
    Score: 0.053
  20. Epigenome-wide association analysis of daytime sleepiness in the Multi-Ethnic Study of Atherosclerosis reveals African-American-specific associations. Sleep. 2019 08 01; 42(8).
    View in: PubMed
    Score: 0.053
  21. Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Nat Genet. 2019 04; 51(4):636-648.
    View in: PubMed
    Score: 0.052
  22. Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates. Nat Commun. 2019 03 07; 10(1):1100.
    View in: PubMed
    Score: 0.052
  23. Biological and clinical insights from genetics of insomnia symptoms. Nat Genet. 2019 03; 51(3):387-393.
    View in: PubMed
    Score: 0.052
  24. Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. Nat Commun. 2019 01 22; 10(1):376.
    View in: PubMed
    Score: 0.051
  25. Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. PLoS Genet. 2018 05; 14(5):e1007345.
    View in: PubMed
    Score: 0.049
  26. A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Am J Hum Genet. 2018 03 01; 102(3):375-400.
    View in: PubMed
    Score: 0.048
  27. Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. PLoS Genet. 2017 May; 13(5):e1006728.
    View in: PubMed
    Score: 0.046
  28. Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure. PLoS Genet. 2017 03; 13(3):e1006678.
    View in: PubMed
    Score: 0.045
  29. Comparison of Heritability Estimation and Linkage Analysis for Multiple Traits Using Principal Component Analyses. Genet Epidemiol. 2016 Apr; 40(3):222-32.
    View in: PubMed
    Score: 0.042
  30. Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. Am J Hum Genet. 2013 Sep 05; 93(3):545-54.
    View in: PubMed
    Score: 0.035
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.