Nancy Jean Cox to Genetic Diseases, Inborn
This is a "connection" page, showing publications Nancy Jean Cox has written about Genetic Diseases, Inborn.
Connection Strength
0.647
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Phenotypic signatures in clinical data enable systematic identification of patients for genetic testing. Nat Med. 2021 06; 27(6):1097-1104.
Score: 0.190
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Phenotype risk scores identify patients with unrecognized Mendelian disease patterns. Science. 2018 03 16; 359(6381):1233-1239.
Score: 0.152
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Genetic Analysis in Translational Medicine: The 2010 GOLDEN HELIX Symposium. Hum Mutat. 2011 Jun; 32(6):698-703.
Score: 0.094
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Finding the missing heritability of complex diseases. Nature. 2009 Oct 08; 461(7265):747-53.
Score: 0.085
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Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases? Eur J Hum Genet. 2007 Mar; 15(3):260-3.
Score: 0.070
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MERLIN...and the geneticist's stone? Nat Genet. 2002 Jan; 30(1):3-4.
Score: 0.050
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Sequential imputation and multipoint linkage analysis. Genet Epidemiol. 1993; 10(6):483-8.
Score: 0.007