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Connection

Marcelo A. Nobrega to Humans

This is a "connection" page, showing publications Marcelo A. Nobrega has written about Humans.
Connection Strength

0.403
  1. Extensive pleiotropism and allelic heterogeneity mediate metabolic effects of IRX3 and IRX5. Science. 2021 06 04; 372(6546):1085-1091.
    View in: PubMed
    Score: 0.027
  2. Gene therapy for pathologic gene expression. Science. 2019 01 18; 363(6424):231-232.
    View in: PubMed
    Score: 0.023
  3. A promoter interaction map for cardiovascular disease genetics. Elife. 2018 07 10; 7.
    View in: PubMed
    Score: 0.022
  4. Editorial. Semin Cell Dev Biol. 2016 09; 57:1.
    View in: PubMed
    Score: 0.019
  5. Evidence of non-pancreatic beta cell-dependent roles of Tcf7l2 in the regulation of glucose metabolism in mice. Hum Mol Genet. 2015 Mar 15; 24(6):1646-54.
    View in: PubMed
    Score: 0.017
  6. In vitro scan for enhancers at the TCF7L2 locus. Diabetologia. 2013 Jan; 56(1):121-5.
    View in: PubMed
    Score: 0.015
  7. Transcriptional enhancers in development and disease. Genome Biol. 2012 Jan 23; 13(1):238.
    View in: PubMed
    Score: 0.014
  8. Alterations in TCF7L2 expression define its role as a key regulator of glucose metabolism. Genome Res. 2011 Sep; 21(9):1417-25.
    View in: PubMed
    Score: 0.013
  9. An 8q24 gene desert variant associated with prostate cancer risk confers differential in vivo activity to a MYC enhancer. Genome Res. 2010 Sep; 20(9):1191-7.
    View in: PubMed
    Score: 0.012
  10. Genome-wide maps of transcription regulatory elements. Wiley Interdiscip Rev Syst Biol Med. 2010 Jul-Aug; 2(4):422-437.
    View in: PubMed
    Score: 0.012
  11. Identifying synonymous regulatory elements in vertebrate genomes. Nucleic Acids Res. 2005 Jul 01; 33(Web Server issue):W403-7.
    View in: PubMed
    Score: 0.009
  12. Exploiting human--fish genome comparisons for deciphering gene regulation. Hum Mol Genet. 2004 Oct 01; 13 Spec No 2:R261-6.
    View in: PubMed
    Score: 0.008
  13. Paternal dietary macronutrient balance and energy intake drive metabolic and behavioral differences among offspring. Nat Commun. 2024 Apr 06; 15(1):2982.
    View in: PubMed
    Score: 0.008
  14. Mechanosensitive super-enhancers regulate genes linked to atherosclerosis in endothelial cells. J Cell Biol. 2024 03 04; 223(3).
    View in: PubMed
    Score: 0.008
  15. Comparative genomic analysis as a tool for biological discovery. J Physiol. 2004 Jan 01; 554(Pt 1):31-9.
    View in: PubMed
    Score: 0.008
  16. Scanning human gene deserts for long-range enhancers. Science. 2003 Oct 17; 302(5644):413.
    View in: PubMed
    Score: 0.008
  17. A non-coding variant linked to metabolic obesity with normal weight affects actin remodelling in subcutaneous adipocytes. Nat Metab. 2023 05; 5(5):861-879.
    View in: PubMed
    Score: 0.008
  18. Single cell profiling at the maternal-fetal interface reveals a deficiency of PD-L1+?non-immune cells in human spontaneous preterm labor. Sci Rep. 2023 05 16; 13(1):7903.
    View in: PubMed
    Score: 0.008
  19. Upregulation of SYNGAP1 expression in mice and human neurons by redirecting alternative splicing. Neuron. 2023 05 17; 111(10):1637-1650.e5.
    View in: PubMed
    Score: 0.008
  20. African-specific alleles modify risk for asthma at the 17q12-q21 locus in African Americans. Genome Med. 2022 09 29; 14(1):112.
    View in: PubMed
    Score: 0.007
  21. Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries. Circ Res. 2022 01 21; 130(2):166-180.
    View in: PubMed
    Score: 0.007
  22. Establishment of human induced trophoblast stem-like cells from term villous cytotrophoblasts. Stem Cell Res. 2021 10; 56:102507.
    View in: PubMed
    Score: 0.007
  23. Pluripotent stem cell-derived endometrial stromal fibroblasts in a cyclic, hormone-responsive, coculture model of human decidua. Cell Rep. 2021 05 18; 35(7):109138.
    View in: PubMed
    Score: 0.007
  24. Genetic Variation in Enhancers Modifies Cardiomyopathy Gene Expression and Progression. Circulation. 2021 03 30; 143(13):1302-1316.
    View in: PubMed
    Score: 0.006
  25. Altered transcriptional and chromatin responses to rhinovirus in bronchial epithelial cells from adults with asthma. Commun Biol. 2020 11 13; 3(1):678.
    View in: PubMed
    Score: 0.006
  26. Altered Enhancer and Promoter Usage Leads to Differential Gene Expression in the Normal and Failed Human Heart. Circ Heart Fail. 2020 10; 13(10):e006926.
    View in: PubMed
    Score: 0.006
  27. Advancing human health in the decade ahead: pregnancy as a key window for discovery: A Burroughs Wellcome Fund Pregnancy Think Tank. Am J Obstet Gynecol. 2020 09; 223(3):312-321.
    View in: PubMed
    Score: 0.006
  28. Transcriptional Patterning of the Ventricular Cardiac Conduction System. Circ Res. 2020 07 17; 127(3):e94-e106.
    View in: PubMed
    Score: 0.006
  29. Identification of atrial fibrillation associated genes and functional non-coding variants. Nat Commun. 2019 10 18; 10(1):4755.
    View in: PubMed
    Score: 0.006
  30. Reducing mitochondrial reads in ATAC-seq using CRISPR/Cas9. Sci Rep. 2017 05 26; 7(1):2451.
    View in: PubMed
    Score: 0.005
  31. DNA methylation in lung cells is associated with asthma endotypes and genetic risk. JCI Insight. 2016 12 08; 1(20):e90151.
    View in: PubMed
    Score: 0.005
  32. Probing chromatin landscape reveals roles of endocardial TBX20 in septation. J Clin Invest. 2016 08 01; 126(8):3023-35.
    View in: PubMed
    Score: 0.005
  33. Evolutionary comparison reveals that diverging CTCF sites are signatures of ancestral topological associating domains borders. Proc Natl Acad Sci U S A. 2015 Jun 16; 112(24):7542-7.
    View in: PubMed
    Score: 0.004
  34. A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancer. J Clin Endocrinol Metab. 2015 Jan; 100(1):E173-81.
    View in: PubMed
    Score: 0.004
  35. TCF7L2 is a master regulator of insulin production and processing. Hum Mol Genet. 2014 Dec 15; 23(24):6419-31.
    View in: PubMed
    Score: 0.004
  36. A common genetic variant within SCN10A modulates cardiac SCN5A expression. J Clin Invest. 2014 Apr; 124(4):1844-52.
    View in: PubMed
    Score: 0.004
  37. PU.1 is essential for MLL leukemia partially via crosstalk with the MEIS/HOX pathway. Leukemia. 2014 Jul; 28(7):1436-48.
    View in: PubMed
    Score: 0.004
  38. Regulation of MEIS1 by distal enhancer elements in acute leukemia. Leukemia. 2014 Jan; 28(1):138-46.
    View in: PubMed
    Score: 0.004
  39. Enhancers: five essential questions. Nat Rev Genet. 2013 04; 14(4):288-95.
    View in: PubMed
    Score: 0.004
  40. FTO-mediated formation of N6-hydroxymethyladenosine and N6-formyladenosine in mammalian RNA. Nat Commun. 2013; 4:1798.
    View in: PubMed
    Score: 0.004
  41. Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease. Hum Mol Genet. 2012 Jul 15; 21(14):3255-63.
    View in: PubMed
    Score: 0.004
  42. A fine-scale chimpanzee genetic map from population sequencing. Science. 2012 Apr 13; 336(6078):193-8.
    View in: PubMed
    Score: 0.004
  43. Tbx20 regulates a genetic program essential to adult mouse cardiomyocyte function. J Clin Invest. 2011 Dec; 121(12):4640-54.
    View in: PubMed
    Score: 0.003
  44. Appendage expression driven by the Hoxd Global Control Region is an ancient gnathostome feature. Proc Natl Acad Sci U S A. 2011 Aug 02; 108(31):12782-6.
    View in: PubMed
    Score: 0.003
  45. Genome-wide identification of conserved regulatory function in diverged sequences. Genome Res. 2011 Jul; 21(7):1139-49.
    View in: PubMed
    Score: 0.003
  46. The emerging genetic landscape underlying cardiac conduction system function. Birth Defects Res A Clin Mol Teratol. 2011 Jun; 91(6):578-85.
    View in: PubMed
    Score: 0.003
  47. Homotypic clusters of transcription factor binding sites are a key component of human promoters and enhancers. Genome Res. 2010 May; 20(5):565-77.
    View in: PubMed
    Score: 0.003
  48. Genome-wide discovery of human heart enhancers. Genome Res. 2010 Mar; 20(3):381-92.
    View in: PubMed
    Score: 0.003
  49. Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome. J Med Genet. 2009 Aug; 46(8):511-23.
    View in: PubMed
    Score: 0.003
  50. Predicting tissue-specific enhancers in the human genome. Genome Res. 2007 Feb; 17(2):201-11.
    View in: PubMed
    Score: 0.002
  51. In vivo enhancer analysis of human conserved non-coding sequences. Nature. 2006 Nov 23; 444(7118):499-502.
    View in: PubMed
    Score: 0.002
  52. In vivo characterization of a vertebrate ultraconserved enhancer. Genomics. 2005 Jun; 85(6):774-81.
    View in: PubMed
    Score: 0.002
  53. Evolution and functional classification of vertebrate gene deserts. Genome Res. 2005 Jan; 15(1):137-45.
    View in: PubMed
    Score: 0.002
  54. ECR Browser: a tool for visualizing and accessing data from comparisons of multiple vertebrate genomes. Nucleic Acids Res. 2004 Jul 01; 32(Web Server issue):W280-6.
    View in: PubMed
    Score: 0.002
  55. Comparative genomics at the vertebrate extremes. Nat Rev Genet. 2004 Jun; 5(6):456-65.
    View in: PubMed
    Score: 0.002
  56. Gene expression profiling leads to identification of GLI1-binding elements in target genes and a role for multiple downstream pathways in GLI1-induced cell transformation. J Biol Chem. 2002 Feb 15; 277(7):5548-55.
    View in: PubMed
    Score: 0.002
  57. Automated construction of high-density comparative maps between rat, human, and mouse. Genome Res. 2001 Nov; 11(11):1935-43.
    View in: PubMed
    Score: 0.002
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.