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Susan Redline, M.D.

Co-Author

This page shows the publications co-authored by Susan Redline and Brian Cade.
Connection Strength

5.235
  1. 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: 0.833
  2. Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans. Am J Respir Crit Care Med. 2016 Oct 01; 194(7):886-897.
    View in: PubMed
    Score: 0.698
  3. Associations of sleep duration and sleep-wake rhythm with lung parenchymal abnormalities on computed tomography: The MESA study. J Sleep Res. 2021 Sep 09; e13475.
    View in: PubMed
    Score: 0.246
  4. Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Genome Med. 2021 Aug 26; 13(1):136.
    View in: PubMed
    Score: 0.245
  5. Reply to Mulla and Pathak: Sleep Apnea and Poor COVID-19 Outcomes: Beware of Causal Intermediates and Colliders. Am J Respir Crit Care Med. 2021 05 15; 203(10):1326-1327.
    View in: PubMed
    Score: 0.240
  6. Sleep Apnea and COVID-19 Mortality and Hospitalization. Am J Respir Crit Care Med. 2020 11 15; 202(10):1462-1464.
    View in: PubMed
    Score: 0.232
  7. 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
  8. 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
  9. Common variants in DRD2 are associated with sleep duration: the CARe consortium. Hum Mol Genet. 2016 Jan 01; 25(1):167-79.
    View in: PubMed
    Score: 0.163
  10. Association of genetic loci with sleep apnea in European Americans and African-Americans: the Candidate Gene Association Resource (CARe). PLoS One. 2012; 7(11):e48836.
    View in: PubMed
    Score: 0.133
  11. Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis. Circ Genom Precis Med. 2021 08; 14(4):e003300.
    View in: PubMed
    Score: 0.061
  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. Genome-wide association study of neck circumference identifies sex-specific loci independent of generalized adiposity. Int J Obes (Lond). 2021 07; 45(7):1532-1541.
    View in: PubMed
    Score: 0.060
  15. Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure. Mol Psychiatry. 2021 Apr 15.
    View in: PubMed
    Score: 0.060
  16. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices. Nat Commun. 2021 04 12; 12(1):2182.
    View in: PubMed
    Score: 0.060
  17. Sleep health, diseases, and pain syndromes: findings from an electronic health record biobank. Sleep. 2021 03 12; 44(3).
    View in: PubMed
    Score: 0.059
  18. Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. Am J Hum Genet. 2021 04 01; 108(4):564-582.
    View in: PubMed
    Score: 0.059
  19. Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes. Nature. 2021 Mar; 591(7851):E27.
    View in: PubMed
    Score: 0.059
  20. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program. Nature. 2021 02; 590(7845):290-299.
    View in: PubMed
    Score: 0.059
  21. Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants. Nat Commun. 2020 10 14; 11(1):5182.
    View in: PubMed
    Score: 0.058
  22. Inherited causes of clonal haematopoiesis in 97,691 whole genomes. Nature. 2020 10; 586(7831):763-768.
    View in: PubMed
    Score: 0.058
  23. 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
  24. 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
  25. 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
  26. 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
  27. 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: 0.053
  28. 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
  29. 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
  30. 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
  31. 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
  32. Biological and clinical insights from genetics of insomnia symptoms. Nat Genet. 2019 03; 51(3):387-393.
    View in: PubMed
    Score: 0.052
  33. 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: 0.051
  34. 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
  35. Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data. Hum Genet. 2019 Feb; 138(2):199-210.
    View in: PubMed
    Score: 0.051
  36. Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies. Am J Hum Genet. 2019 02 07; 104(2):260-274.
    View in: PubMed
    Score: 0.051
  37. 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
  38. Evaluation of an automated pipeline for large-scale EEG spectral analysis: the National Sleep Research Resource. Sleep Med. 2018 07; 47:126-136.
    View in: PubMed
    Score: 0.047
  39. Characterizing sleep spindles in 11,630 individuals from the National Sleep Research Resource. Nat Commun. 2017 06 26; 8:15930.
    View in: PubMed
    Score: 0.046
  40. 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
  41. 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: 0.044
  42. Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees. Am J Hum Genet. 2016 Oct 06; 99(4):846-859.
    View in: PubMed
    Score: 0.044
  43. Beyond type 2 diabetes, obesity and hypertension: an axis including sleep apnea, left ventricular hypertrophy, endothelial dysfunction, and aortic stiffness among Mexican Americans in Starr County, Texas. Cardiovasc Diabetol. 2016 Jun 08; 15:86.
    View in: PubMed
    Score: 0.043
  44. 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
  45. Impact of Common Diabetes Risk Variant in MTNR1B on Sleep, Circadian, and Melatonin Physiology. Diabetes. 2016 06; 65(6):1741-51.
    View in: PubMed
    Score: 0.042
  46. Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study. Mol Psychiatry. 2015 Oct; 20(10):1232-9.
    View in: PubMed
    Score: 0.038
  47. Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations. Hum Mol Genet. 2014 May 01; 23(9):2498-510.
    View in: PubMed
    Score: 0.036
  48. Sleep duration does not mediate or modify association of common genetic variants with type 2 diabetes. Diabetologia. 2014 Feb; 57(2):339-46.
    View in: PubMed
    Score: 0.036
  49. Common variants in CLOCK are not associated with measures of sleep duration in people of european ancestry from the sleep heart health study. Biol Psychiatry. 2013 Dec 15; 74(12):e33-5.
    View in: PubMed
    Score: 0.035
  50. Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource. Diabetologia. 2012 Nov; 55(11):2970-84.
    View in: PubMed
    Score: 0.033
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.