 Connection
Laura Saba to Mutation
This is a "connection" page, showing publications Laura Saba has written about Mutation.
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Connection Strength |
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0.067 |
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Sacconi B, Anzidei M, Leonardi A, Boni F, Saba L, Scipione R, Anile M, Rengo M, Longo F, Bezzi M, Venuta F, Napoli A, Laghi A, Catalano C. Analysis of CT features and quantitative texture analysis in patients with lung adenocarcinoma: a correlation with EGFR mutations and survival rates. Clin Radiol. 2017 Jun; 72(6):443-450.
Score: 0.060
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Rosatelli MC, Meloni A, Faa V, Saba L, Crisponi G, Clemente MG, Meloni G, Piga MT, Cao A. Molecular analysis of patients of Sardinian descent with Crigler-Najjar syndrome type I. J Med Genet. 1997 Feb; 34(2):122-5.
Score: 0.004
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Rosatelli MC, Pischedda A, Meloni A, Saba L, Pomo A, Travi M, Fattore S, Cao A. Homozygous beta-thalassaemia resulting in the beta-thalassaemia carrier state phenotype. Br J Haematol. 1994 Nov; 88(3):562-5.
Score: 0.003
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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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