Parents
Sign in to add mentor| Man-Wah Tan | grad student | 2008 | Stanford | |
| (The role of the Daf-2 insulin -like signaling pathway in Caenorhabditis elegans innate immunity.) | ||||
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Publications
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| Hancock S, Ben-Shachar R, Adusei C, et al. (2019) Clinical experience across the fetal-fraction spectrum for a non-invasive prenatal screen with low test-failure rate. Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology |
| Hogan GJ, Vysotskaia VS, Beauchamp KA, et al. (2018) Validation of an Expanded Carrier Screen that Optimizes Sensitivity via Full-Exon Sequencing and Panel-wide Copy Number Variant Identification. Clinical Chemistry |
| Muzzey D, Beauchamp KA, Grauman P, et al. (2018) 259: Copy number variant calling on a 176-disease expanded carrier screening panel American Journal of Obstetrics and Gynecology. 218 |
| Beauchamp KA, Muzzey D, Wong KK, et al. (2017) Systematic design and comparison of expanded carrier screening panels. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Artieri CG, Haverty C, Evans EA, et al. (2017) Noninvasive Prenatal Screening at Low Fetal Fraction: Comparing Whole-Genome Sequencing and Single-Nucleotide Polymorphism Methods. Prenatal Diagnosis |
| Vysotskaia VS, Hogan GJ, Gould GM, et al. (2017) Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment. Peerj. 5: e3046 |
| Artieri CG, Beauchamp KA, Vysotskaia VS, et al. (2017) Abstract 5690: Optimized molecular barcoding enables accurate targeted mutation detection in circulating cell-free DNA (cfDNA) Cancer Research. 77: 5690-5690 |
| Beauchamp KA, Grauman P, Hogan GJ, et al. (2017) Copy number variant calling on a 177 gene expanded carrier screening panel reveals impact of hbb deletions Fertility and Sterility. 108 |
| Kaseniit KE, Theilmann MR, Robertson A, et al. (2016) Group Testing Approach for Trinucleotide Repeat Expansion Disorder Screening. Clinical Chemistry |
| Haque IS, Lazarin GA, Kang HP, et al. (2016) Modeled Fetal Risk of Genetic Diseases Identified by Expanded Carrier Screening. Jama. 316: 734-742 |