Connection

SCOTT LEMAIRE to Phenotype

This is a "connection" page, showing publications SCOTT LEMAIRE has written about Phenotype.
Connection Strength

0.368
  1. Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations. Nat Med. 2021 01; 27(1):66-72.
    View in: PubMed
    Score: 0.091
  2. Ciprofloxacin accelerates aortic enlargement and promotes dissection and rupture in Marfan mice. J Thorac Cardiovasc Surg. 2022 03; 163(3):e215-e226.
    View in: PubMed
    Score: 0.090
  3. NLRP3 (Nucleotide Oligomerization Domain-Like Receptor Family, Pyrin Domain Containing 3)-Caspase-1 Inflammasome Degrades Contractile Proteins: Implications for Aortic Biomechanical Dysfunction and Aneurysm and Dissection Formation. Arterioscler Thromb Vasc Biol. 2017 04; 37(4):694-706.
    View in: PubMed
    Score: 0.070
  4. Epigenetic Induction of Smooth Muscle Cell Phenotypic Alterations in Aortic Aneurysms and Dissections. Circulation. 2023 09 19; 148(12):959-977.
    View in: PubMed
    Score: 0.027
  5. Cholesterol-Induced Phenotypic Modulation of Smooth Muscle Cells to Macrophage/Fibroblast-like Cells Is Driven by an Unfolded Protein Response. Arterioscler Thromb Vasc Biol. 2021 01; 41(1):302-316.
    View in: PubMed
    Score: 0.022
  6. Associations of Age and Sex With Marfan Phenotype: The National Heart, Lung, and Blood Institute GenTAC (Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions) Registry. Circ Cardiovasc Genet. 2017 Jun; 10(3).
    View in: PubMed
    Score: 0.018
  7. International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium). Circ Cardiovasc Genet. 2016 Dec; 9(6):548-558.
    View in: PubMed
    Score: 0.017
  8. Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections. PLoS Genet. 2011 Jun; 7(6):e1002118.
    View in: PubMed
    Score: 0.012
  9. FBN1 mutations in patients with descending thoracic aortic dissections. Am J Med Genet A. 2010 Feb; 152A(2):413-6.
    View in: PubMed
    Score: 0.011
  10. Paucity of skeletal manifestations in Hispanic families with FBN1 mutations. Eur J Med Genet. 2010 Mar-Apr; 53(2):80-4.
    View in: PubMed
    Score: 0.011
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.