Dale Muzzey (D Muzzey)

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 12

Top Topics

Body Mass Index

Dna Methylation

Liquid Chromatography

Top Venues

Genetics in medicine : official journal of the American College of Medical Genetics

Prenatal diagnosis

Molecular genetics & genomic medicine

BMC medical genomics

This page only lists publications with an associated author ORCID identifier.

Publications

Manesha Putra, Kristjan Eerik Kaseniit, Melissa A Hicks, Dale Muzzey, David Hackney
The impact of HBB-related hemoglobinopathies carrier status on fetal fraction in noninvasive prenatal screening. Prenatal diagnosis 42 (4) (2022)
S Hancock, R Ben-Shachar, C Adusei, C B Oyolu, E A Evans, H P Kang, C Haverty, Dale Muzzey
Clinical experience across the fetal-fraction spectrum of a non-invasive prenatal screening approach with low test-failure rate. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 56 (3) (2021)
Noah C Welker, Albert K Lee, Rachel A S Kjolby, Helen Y Wan, Mark R Theilmann, Diana Jeon, James D Goldberg, Kevin R Haas, Dale Muzzey, Clement S Chu
High-throughput fetal fraction amplification increases analytical performance of noninvasive prenatal screening. Genetics in medicine : official journal of the American College of Medical Genetics 23 (3) (2020)
Kristjan E Kaseniit, Imran S Haque, James D Goldberg, Lee P Shulman, Dale Muzzey
Genetic ancestry analysis on >93,000 individuals undergoing expanded carrier screening reveals limitations of ethnicity-based medical guidelines. Genetics in medicine : official journal of the American College of Medical Genetics 22 (10) (2020)
Marie Balzotti, Linyan Meng, Dale Muzzey, Katherine Johansen Taber, Kyle A Beauchamp, Myriad Genetics Curation Team, Baylor Genetics Curation Team, Rebecca Mar-Heyming, Bethany Buckley, Krista Moyer
Clinical validity of expanded carrier screening: Evaluating the gene-disease relationship in more than 200 conditions. Human mutation 41 (8) (2020)
Dale Muzzey, James D Goldberg, Carrie Haverty
Noninvasive prenatal screening for patients with high body mass index: Evaluating the impact of a customized whole genome sequencing workflow on sensitivity and residual risk. Prenatal diagnosis 40 (3) (2019)
Alana C Cecchi, Elizabeth S Vengoechea, Kristjan E Kaseniit, Melanie W Hardy, Laura A Kiger, Nikita Mehta, Imran S Haque, Krista Moyer, Patricia Z Page, Dale Muzzey, Karen A Grinzaid
Screening for Tay-Sachs disease carriers by full-exon sequencing with novel variant interpretation outperforms enzyme testing in a pan-ethnic cohort. Molecular genetics & genomic medicine 7 (8) (2019)
Kyle A Beauchamp, Katherine A Johansen Taber, Peter V Grauman, Lindsay Spurka, Jeraldine Lim-Harashima, Ashley Svenson, James D Goldberg, Dale Muzzey
Sequencing as a first-line methodology for cystic fibrosis carrier screening. Genetics in medicine : official journal of the American College of Medical Genetics 21 (11) (2019)
Kristjan E Kaseniit, Elizabeth Collins, Christine Lo, Krista Moyer, Rebecca Mar-Heyming, Hyunseok P Kang, Dale Muzzey
Inter-lab concordance of variant classifications establishes clinical validity of expanded carrier screening. Clinical genetics 96 (3) (2019)
Kristjan Eerik Kaseniit, Gregory J Hogan, Kevin M D'Auria, Carrie Haverty, Dale Muzzey
Strategies to minimize false positives and interpret novel microdeletions based on maternal copy-number variants in 87,000 noninvasive prenatal screens. BMC medical genomics 11 (1) (2018)
Genevieve M Gould, Peter V Grauman, Mark R Theilmann, Lindsay Spurka, Irving E Wang, Laura M Melroy, Robert G Chin, Dustin H Hite, Clement S Chu, Jared R Maguire, Gregory J Hogan, Dale Muzzey
Detecting clinically actionable variants in the 3' exons of PMS2 via a reflex workflow based on equivalent hybrid capture of the gene and its pseudogene. BMC medical genetics 19 (1) (2018)
Dale Muzzey, Carrie Haverty, Eric A Evans, James D Goldberg
Response to "Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods". Prenatal diagnosis 37 (7) (2017)