Header Logo

Connection

Edward Ginns to DNA Mutational Analysis

This is a "connection" page, showing publications Edward Ginns has written about DNA Mutational Analysis.
Connection Strength

0.211
  1. Sidransky E, Bottler A, Stubblefield B, Ginns EI. DNA mutational analysis of type 1 and type 3 Gaucher patients: how well do mutations predict phenotype? Hum Mutat. 1994; 3(1):25-8.
    View in: PubMed
    Score: 0.107
  2. Moya PR, Dodman NH, Timpano KR, Rubenstein LM, Rana Z, Fried RL, Reichardt LF, Heiman GA, Tischfield JA, King RA, Galdzicka M, Ginns EI, Wendland JR. Rare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypes. Eur J Hum Genet. 2013 Aug; 21(8):850-4.
    View in: PubMed
    Score: 0.025
  3. Sidransky E, Tsuji S, Martin BM, Stubblefield B, Ginns EI. DNA mutation analysis of Gaucher patients. Am J Med Genet. 1992 Feb 01; 42(3):331-6.
    View in: PubMed
    Score: 0.024
  4. Sidransky E, Tsuji S, Stubblefield BK, Currie J, FitzGibbon EJ, Ginns EI. Gaucher patients with oculomotor abnormalities do not have a unique genotype. Clin Genet. 1992 Jan; 41(1):1-5.
    View in: PubMed
    Score: 0.023
  5. Sidransky E, Maysak K, Ginns EI. Mutations in Gaucher's disease detected by MspI. Lancet. 1990 Sep 08; 336(8715):628-9.
    View in: PubMed
    Score: 0.021
  6. Lau EK, Tayebi N, Ingraham LJ, Winfield SL, Koprivica V, Stone DL, Zimran A, Ginns EI, Sidransky E. Two novel polymorphic sequences in the glucocerebrosidase gene region enhance mutational screening and founder effect studies of patients with Gaucher disease. Hum Genet. 1999 Apr; 104(4):293-300.
    View in: PubMed
    Score: 0.010
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.