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Connection

SHAINE MORRIS to Heterotaxy Syndrome

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This is a "connection" page, showing publications SHAINE MORRIS has written about Heterotaxy Syndrome.
SHAINE MORRIS
Connection Strength
1.876
Heterotaxy Syndrome
  1. NODAL variants are associated with a continuum of laterality defects from simple D-transposition of the great arteries to heterotaxy. Genome Med. 2024 04 03; 16(1):53.
    View in: PubMed
    Score: 0.869
  2. Trends in Infant Mortality After TAPVR Repair over 18?Years in Texas and Impact of Hospital Surgical Volume. Pediatr Cardiol. 2020 Jan; 41(1):77-87.
    View in: PubMed
    Score: 0.642
  3. Non-coding cause of congenital heart defects: Abnormal RNA splicing with multiple isoforms as a mechanism for heterotaxy. HGG Adv. 2024 Oct 10; 5(4):100353.
    View in: PubMed
    Score: 0.224
  4. Heterotaxy syndrome and associated arrhythmias in pediatric patients. Heart Rhythm. 2018 04; 15(4):548-554.
    View in: PubMed
    Score: 0.140
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.