Shared genetic causes of cardiac hypertrophy in children and adults.

By H. Morita, H. Rehm, Andres Menesses, B. McDonough, A. Roberts, R. Kucherlapati, J. Towbin, J. Seidman, C. Seidman. 2008

406 citations recorded by the source corpus.

Subfields: Cardiology and Cardiovascular Medicine, Molecular Biology

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Cardiology and Cardiovascular Medicine

1. Birgit Funke
2. C. Seidman

In Molecular Biology

1. Karl V. Voelkerding
2. Jacob Durtschi
3. S. Dames
4. James M. Heather
5. B. Chain

Citations in the corpus

• Next-generation sequencing: from basic research to diagnostics. (2009, background): “For example, 16 different genes are implicated in the pathogenesis of hypertrophic cardiomyopathy (85, 86 ).”
• Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity (2015, background): “Although a rigorous cost-effectiveness analysis is outside the scope of this study, our findings are consistent with two prior cost-effectiveness studies examining the clinical and economic utility of genetic testing for HCM.31,32 The inability to identify a genetic etiology in a substantial proport”