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Times Cited: 304
Times Cited
Times Co-cited
Similarity
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The Congenital Heart Disease Genetic Network Study: rationale, design, and early results.
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Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy.
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Advances in the Genetics of Congenital Heart Disease: A Clinician's Guide.
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GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling.
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Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients.
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Frequency of 22q11 deletions in patients with conotruncal defects.
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Targeted next-generation sequencing identifies pathogenic variants in familial congenital heart disease.
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Global genetic analysis in mice unveils central role for cilia in congenital heart disease.
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20
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.