Stephanie W Cox

Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity

Matthew S. Lebo, J. Seidman, H. Rehm, 2015, Genetics in Medicine.

High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays

H. Rehm, B. Aronow, P. Kothiyal, 2010, BMC biotechnology.

Targeted Sequencing Using Affymetrix CustomSeq Arrays

H. Rehm, B. Funke, Stephanie W Cox, 2011, Current protocols in human genetics.

A novel custom resequencing array for dilated cardiomyopathy

J. Seidman, H. Rehm, C. Seidman, 2010, Genetics in Medicine.

Evaluation of second-generation sequencing of 19 dilated cardiomyopathy genes for clinical applications.

Sivakumar Gowrisankar, Megan Manion, Heidi L Rehm, 2010, The Journal of molecular diagnostics : JMD.

An Overview of Custom Array Sequencing

H. Rehm, Stephanie W Cox, J. Greinwald, 2009, Current protocols in human genetics.

OSIRIS: A Minimum Data Set for Data Sharing and Interoperability in Oncology

Y. Laizet, M. Toulmonde, B. Rance, 2021, JCO clinical cancer informatics.

Data sharing in the era of precision medicine: a scientometric analysis

Vincent Le Texier, Nesrine Henda, Stéphanie Cox, 2019, Precision Cancer Medicine.

CORRIGENDUM: Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity

Matthew S. Lebo, J. Seidman, H. Rehm, 2015, Genetics in Medicine.