Connection

JONATHAN FLANAGAN to Genetic Variation

This is a "connection" page, showing publications JONATHAN FLANAGAN has written about Genetic Variation.
Connection Strength

0.460
  1. The genetic basis of human erythrocyte pyridoxal kinase activity variation. Haematologica. 2006 Jun; 91(6):801-4.
    View in: PubMed
    Score: 0.166
  2. Identification of sequence variation in the galactose-1-phosphate uridyl transferase gene by dHPLC. Mol Genet Metab. 2004 Feb; 81(2):133-6.
    View in: PubMed
    Score: 0.142
  3. Whole-exome sequencing of sickle cell disease patients with hyperhemolysis syndrome suggests a role for rare variation in disease predisposition. Transfusion. 2018 03; 58(3):726-735.
    View in: PubMed
    Score: 0.093
  4. Genetic variants in canonical Wnt signaling pathway associated with pediatric immune thrombocytopenia. Blood Adv. 2024 11 12; 8(21):5529-5538.
    View in: PubMed
    Score: 0.037
  5. Genetic Modifiers of White Blood Cell Count, Albuminuria and Glomerular Filtration Rate in Children with Sickle Cell Anemia. PLoS One. 2016; 11(10):e0164364.
    View in: PubMed
    Score: 0.021
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.