Christine M. Eng
Illumina (United States)(US)Baylor College of Medicine(US)The Coordinating Center(US)Baylor Genetics(US)
Publications by Year
Research Areas
Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Lysosomal Storage Disorders Research, Cancer Genomics and Diagnostics
Most-Cited Works
- → Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders(2013)1,960 cited
- → Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics(2016)1,687 cited
- → Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis(2012)1,410 cited
- → Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing(2014)1,387 cited
- → Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation(2016)762 cited
- → Fabry disease revisited: Management and treatment recommendations for adult patients(2018)626 cited