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Connection

Timothy Wood to Humans

This is a "connection" page, showing publications Timothy Wood has written about Humans.

 
Connection Strength
 
 
 
0.054
 
  1. Wood TC. Commentary on A Patient with Coarse Facial Features and Molecular Odyssey: Lessons Learned and Best Practice. Clin Chem. 2023 01 04; 69(1):22.
    View in: PubMed
    Score: 0.019
  2. Wood TC, Harvey K, Beck M, Burin MG, Chien YH, Church HJ, D'Almeida V, van Diggelen OP, Fietz M, Giugliani R, Harmatz P, Hawley SM, Hwu WL, Ketteridge D, Lukacs Z, Miller N, Pasquali M, Schenone A, Thompson JN, Tylee K, Yu C, Hendriksz CJ. Diagnosing mucopolysaccharidosis IVA. J Inherit Metab Dis. 2013 Mar; 36(2):293-307.
    View in: PubMed
    Score: 0.009
  3. Pollard LM, Jones JR, Wood TC. Molecular characterization of 355 mucopolysaccharidosis patients reveals 104 novel mutations. J Inherit Metab Dis. 2013 Mar; 36(2):179-87.
    View in: PubMed
    Score: 0.009
  4. Swanson MA, Jiang H, Kolora LD, Molino R, Reisdorph R, Michel CR, Doenges KA, Leung KY, Lin X, Wong F, Lancaster S, Michael B, Snyder M, Hock DH, Stroud DA, Wood T, Binard R, Anderson-Lehman L, Christians U, Arning E, Friederich MW, Van Hove RA, MacLean KN, Greene NDE, Van Hove JLK. A Nonketotic Hyperglycinemia Mouse Shows Wide-Ranging Biochemical Consequences of Elevated Glycine, Reduced Folate One-Carbon Charging, and Serine Deficiency. J Inherit Metab Dis. 2026 Jan; 49(1):e70137.
    View in: PubMed
    Score: 0.006
  5. D'Annibale O, Phinney W, Crenshaw M, LoPiccolo MK, Elsharkawi I, Shelkowitz E, Pique D, Starosta RT, Larson A, Van Hove JLK, Wood T, Kochhar A. Differentiation of neonatal and infantile onset ECHS1 deficiency using SCEH enzyme activity and plasma acylcarnitine analysis. Mol Genet Metab. 2025 Aug; 145(4):109156.
    View in: PubMed
    Score: 0.006
  6. Oglesbee D, Cowan TM, Pasquali M, Wood TC, Weck KE, Long T, Palomaki GE. CAP/ACMG proficiency testing for biochemical genetics laboratories: a summary of performance. Genet Med. 2018 Jan; 20(1):83-90.
    View in: PubMed
    Score: 0.003
  7. Schimmenti LA, Crombez EA, Schwahn BC, Heese BA, Wood TC, Schroer RJ, Bentler K, Cederbaum S, Sarafoglou K, McCann M, Rinaldo P, Matern D, di San Filippo CA, Pasquali M, Berry SA, Longo N. Expanded newborn screening identifies maternal primary carnitine deficiency. Mol Genet Metab. 2007 Apr; 90(4):441-5.
    View in: PubMed
    Score: 0.002
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.

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