Grant Hogg
LabCorp (United States)(US)
Publications by Year
Research Areas
Prenatal Screening and Diagnostics, Genomic variations and chromosomal abnormalities, Fetal and Pediatric Neurological Disorders, Mitochondrial Function and Pathology, Acute Myeloid Leukemia Research
Most-Cited Works
- → Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts(2015)238 cited
- → Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants(2016)203 cited
- → Somatic instability of the expanded CTG triplet repeat in myotonic dystrophy type 1 is a heritable quantitative trait and modifier of disease severity(2012)181 cited
- → Dystrophin deficiency in Drosophila reduces lifespan and causes a dilated cardiomyopathy phenotype(2008)110 cited
- → Clinical Validation of a Non-Invasive Prenatal Test for Genome-Wide Detection of Fetal Copy Number Variants(2015)19 cited
- → Mutation profiling in tumor samples using the Sequenom OncoCarta™ Panel(2009)12 cited
- → Clinical characterization of the mutational landscape of 24,639 real-world samples from patients with myeloid malignancies(2023)9 cited
- → Using Targeted Sequencing of Paralogous Sequences for Noninvasive Detection of Selected Fetal Aneuploidies(2016)8 cited
- → Mutational landscape and clinical characterization of over 17,000 patients with myeloid malignancies using real-world data.(2022)
- Understanding Somatic Mosaicism in Myotonic Dystrophy Type 1(2000)