Connection

Co-Authors

This is a "connection" page, showing publications co-authored by DARYL SCOTT and PAMELA LUNA.
Connection Strength

1.501
  1. WNT4 deficiency impacts heart, diaphragm, and palate development: Insights from human genetics, machine learning, and mouse models. Dev Biol. 2026 Jan; 529:66-80.
    View in: PubMed
    Score: 0.235
  2. Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+). Eur J Hum Genet. 2025 12; 33(12):1606-1615.
    View in: PubMed
    Score: 0.234
  3. Non-isolated tetralogy of fallot (TOF+): exome sequencing efficacy and phenotypic expansions. Eur J Hum Genet. 2026 03; 34(3):333-339.
    View in: PubMed
    Score: 0.233
  4. High Clinical Exome Sequencing Diagnostic Rates and Novel Phenotypic Expansions for Nonisolated Microphthalmia, Anophthalmia, and Coloboma. Invest Ophthalmol Vis Sci. 2024 03 05; 65(3):25.
    View in: PubMed
    Score: 0.211
  5. Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return. Eur J Hum Genet. 2023 12; 31(12):1430-1439.
    View in: PubMed
    Score: 0.204
  6. High molecular diagnostic yields and novel phenotypic expansions involving syndromic anorectal malformations. Eur J Hum Genet. 2023 03; 31(3):296-303.
    View in: PubMed
    Score: 0.193
  7. Exome sequencing efficacy and phenotypic expansions involving esophageal atresia/tracheoesophageal fistula plus. Am J Med Genet A. 2022 12; 188(12):3492-3504.
    View in: PubMed
    Score: 0.191
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.