Connection

OSSAMA ABOU HASSAN to Male

This is a "connection" page, showing publications OSSAMA ABOU HASSAN has written about Male.
Connection Strength

0.115
  1. Novel EIF2AK4 mutations in histologically proven pulmonary capillary hemangiomatosis and hereditary pulmonary arterial hypertension. BMC Med Genet. 2019 11 11; 20(1):176.
    View in: PubMed
    Score: 0.025
  2. Clinical and genetic characteristics of pulmonary arterial hypertension in Lebanon. BMC Med Genet. 2018 05 30; 19(1):89.
    View in: PubMed
    Score: 0.022
  3. NKX2-5 mutations in an inbred consanguineous population: genetic and phenotypic diversity. Sci Rep. 2015 Mar 06; 5:8848.
    View in: PubMed
    Score: 0.018
  4. Imaging and haemodynamic parameters associated with clinical outcomes following isolated tricuspid valve surgery. Open Heart. 2022 12; 9(2).
    View in: PubMed
    Score: 0.008
  5. Impact of elevated left ventricular filling pressure on long-term outcomes after transcatheter aortic valve replacement. Open Heart. 2022 06; 9(1).
    View in: PubMed
    Score: 0.007
  6. Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy. Circ Genom Precis Med. 2020 10; 13(5):444-452.
    View in: PubMed
    Score: 0.007
  7. AUB-HAS2 Cardiovascular Risk Index: Performance in Surgical Subpopulations and Comparison to the Revised Cardiac Risk Index. J Am Heart Assoc. 2020 05 18; 9(10):e016228.
    View in: PubMed
    Score: 0.006
  8. A speckle-tracking strain-based artificial neural network model to differentiate cardiomyopathy type. Scand Cardiovasc J. 2020 Apr; 54(2):92-99.
    View in: PubMed
    Score: 0.006
  9. A New Index for Pre-Operative Cardiovascular Evaluation. J Am Coll Cardiol. 2019 06 25; 73(24):3067-3078.
    View in: PubMed
    Score: 0.006
  10. Mutations in the ABCG8 gene are associated with sitosterolaemia in the homozygous form and xanthelasmas in the heterozygous form. Eur J Dermatol. 2017 Oct 01; 27(5):519-523.
    View in: PubMed
    Score: 0.005
  11. Identification of several mutations in ATP2C1 in Lebanese families: insight into the pathogenesis of Hailey-Hailey disease. PLoS One. 2015; 10(2):e0115530.
    View in: PubMed
    Score: 0.004
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.