Connection

PRZEMYSLAW SZAFRANSKI to Mutation, Missense

This is a "connection" page, showing publications PRZEMYSLAW SZAFRANSKI has written about Mutation, Missense.
Connection Strength

1.068
  1. Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype. Hum Genet. 2019 Dec; 138(11-12):1301-1311.
    View in: PubMed
    Score: 0.484
  2. The Glu86 Residue in TBX4 Proves Critical for Human Lung Development. Am J Med Genet A. 2025 Mar; 197(3):e63936.
    View in: PubMed
    Score: 0.172
  3. Diminished TMEM100 Expression in a Newborn With Acinar Dysplasia and a Novel TBX4 Variant: A Case Report. Pediatr Dev Pathol. 2024 May-Jun; 27(3):255-259.
    View in: PubMed
    Score: 0.160
  4. Lung-specific distant enhancer cis regulates expression of FOXF1 and lncRNA FENDRR. Hum Mutat. 2021 06; 42(6):694-698.
    View in: PubMed
    Score: 0.133
  5. Variable phenotypic presentation of a novel FOXF1 missense mutation in a single family. Pediatr Pulmonol. 2016 09; 51(9):921-7.
    View in: PubMed
    Score: 0.095
  6. CAV3 mutation in a patient with transient hyperCKemia and myalgia. Neurol Neurochir Pol. 2016 Nov - Dec; 50(6):468-473.
    View in: PubMed
    Score: 0.024
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.