Connection

SHAINE MORRIS to Mutation

This is a "connection" page, showing publications SHAINE MORRIS has written about Mutation.
Connection Strength

0.691
  1. Arterial tortuosity in genetic arteriopathies. Curr Opin Cardiol. 2015 Nov; 30(6):587-93.
    View in: PubMed
    Score: 0.195
  2. Fetal Diagnosis of Supravalvular Aortic Stenosis and Pulmonary Stenosis in a Family with Non-Syndromic Elastin Mutation. Pediatr Cardiol. 2024 Jun; 45(5):1154-1156.
    View in: PubMed
    Score: 0.086
  3. Evaluating perinatal and neonatal outcomes among children with vascular Ehlers-Danlos syndrome. Genet Med. 2022 10; 24(10):2134-2143.
    View in: PubMed
    Score: 0.078
  4. The first reported case of Loeys-Dietz syndrome in a patient with biallelic SMAD3 variants. Am J Med Genet A. 2020 11; 182(11):2755-2760.
    View in: PubMed
    Score: 0.068
  5. Obstetric Management of Loeys-Dietz Syndrome. Obstet Gynecol. 2018 06; 131(6):1080-1084.
    View in: PubMed
    Score: 0.058
  6. 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: 0.052
  7. Disrupted nitric oxide signaling due to GUCY1A3 mutations increases risk for moyamoya disease, achalasia and hypertension. Clin Genet. 2016 10; 90(4):351-60.
    View in: PubMed
    Score: 0.050
  8. Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016-2023). Am J Med Genet A. 2024 Oct; 194(10):e63638.
    View in: PubMed
    Score: 0.022
  9. Comparative Risks of Initial Aortic Events Associated With Genetic Thoracic Aortic?Disease. J Am Coll Cardiol. 2022 08 30; 80(9):857-869.
    View in: PubMed
    Score: 0.020
  10. A clinical scoring system for early onset (neonatal) Marfan syndrome. Genet Med. 2022 07; 24(7):1503-1511.
    View in: PubMed
    Score: 0.019
  11. Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort. Genet Med. 2022 05; 24(5):1045-1053.
    View in: PubMed
    Score: 0.019
  12. Marfan syndrome. Nat Rev Dis Primers. 2021 09 02; 7(1):64.
    View in: PubMed
    Score: 0.018
  13. Genetic and comparative mapping of genes dysregulated in mouse hearts lacking the Hand2 transcription factor gene. Genomics. 2002 Dec; 80(6):593-600.
    View in: PubMed
    Score: 0.005
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.