Zachary P. Demko, Ph.D.
Affiliations: | 2002 | Scripps Research Institute, La Jolla, La Jolla, CA, United States |
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"Zachary Demko"Parents
Sign in to add mentor| K. Barry Sharpless | grad student | 2002 | Scripps Institute | |
| (Expedient syntheses of tetrazoles using [2+3] dipolar cycloadditions.) | ||||
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Publications
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| Hedriana H, Martin K, Saltzman D, et al. (2019) Cell Free DNA fetal fraction in twin gestations in single nucleotide polymorphism-based non-invasive prenatal screening. Prenatal Diagnosis |
| DiNonno W, Demko Z, Martin K, et al. (2019) Quality Assurance of Non-Invasive Prenatal Screening (NIPS) for Fetal Aneuploidy Using Positive Predictive Values as Outcome Measures. Journal of Clinical Medicine. 8 |
| Norwitz ER, McNeill G, Kalyan A, et al. (2019) Validation of a Single-Nucleotide Polymorphism-Based Non-Invasive Prenatal Test in Twin Gestations: Determination of Zygosity, Individual Fetal Sex, and Fetal Aneuploidy. Journal of Clinical Medicine. 8 |
| Benn P, Valenti E, Shah S, et al. (2018) Factors Associated With Informative Redraw After an Initial No Result in Noninvasive Prenatal Testing. Obstetrics and Gynecology |
| Simon AL, Kiehl M, Fischer E, et al. (2018) Pregnancy outcomes from more than 1,800 in vitro fertilization cycles with the use of 24-chromosome single-nucleotide polymorphism-based preimplantation genetic testing for aneuploidy. Fertility and Sterility |
| McCoy RC, Newnham LJ, Ottolini CS, et al. (2018) Tripolar chromosome segregation drives the association between maternal genotype at variants spanning PLK4 and aneuploidy in human preimplantation embryos. Human Molecular Genetics |
| Ravi H, McNeill G, Goel S, et al. (2018) Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples. Plos One. 13: e0193476 |
| Ryan A, Iyengar S, Demko Z. (2018) Increased Positive Predictive Value for a Single-Nucleotide Polymorphism-Based Non-invasive Prenatal Test for the 22q11.2 Deletion Journal of Fetal Medicine. 5: 65-67 |
| Martin K, Iyengar S, Kalyan A, et al. (2017) Clinical Experience with a Single-Nucleotide Polymorphism-Based Noninvasive Prenatal Test for Five Clinically Significant Microdeletions. Clinical Genetics |
| Ryan A, Hunkapiller N, Banjevic M, et al. (2016) Validation of an Enhanced Version of a Single-Nucleotide Polymorphism-Based Noninvasive Prenatal Test for Detection of Fetal Aneuploidies. Fetal Diagnosis and Therapy |