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Melody Menezes

Showing results (21-30 of 32) with videos related to

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American Journal of Obstetrics and Gynecology|November 26, 2023
Placental, maternal, fetal, and technical origins of false-positive cell-free DNA screening resultsYvette Raymond, Shavi Fernando, Melody Menezes, et al.
Archives of Gynecology and Obstetrics|August 31, 2025
Repeat cell-free DNA screening after initial false-positive results and term placental analysis for confined mosaicism: a prospective cohort studyYvette C Raymond, Shavi Fernando, Melody Menezes, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|January 19, 2023
The accuracy of cell-free DNA screening for fetal segmental copy number variants: A systematic review and meta-analysisYvette C Raymond, Melissa L Acreman, Sofia Bussolaro, et al.
Frontiers in Genetics|September 15, 2022
Multisite assessment of the impact of cell-free DNA-based screening for rare autosomal aneuploidies on pregnancy management and outcomesTamara Mossfield, Erica Soster, Melody Menezes, et al.
Prenatal Diagnosis|September 7, 2022
Cell-free DNA screening for rare autosomal trisomies and segmental chromosome imbalancesYvette C Raymond, Shavi Fernando, Melody Menezes, et al.
European Journal of Human Genetics : EJHG|January 10, 2026
Unexpected genotypes associated with severe paediatric conditions identified in a healthy population cohortYasmin Bylstra, Weng Khong Lim, Jing Xian Teo, et al.
Frontiers in Genetics|April 9, 2026
Concordance between genome-wide cfDNA screening and diagnostic test results for large copy-number variants: a multi-site study from the Global Expanded NIPT ConsortiumErica Soster, Kristin Dalton, Michael Bonifacio, et al.
NPJ Genomic Medicine|December 26, 2025
Expanding carrier screening: beyond the genes, to include underrepresented ancestriesYasmin Bylstra, Pua Chee Jian, Sui Lin, et al.
European Journal of Human Genetics : EJHG|February 8, 2018
Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective studyJane L Halliday, Cecile Muller, Taryn Charles, et al.
Human Reproduction (Oxford, England)|March 25, 2020
A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohortLisa Hui, Alice Poulton, Eliza Kluckow, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
American Journal of Obstetrics and Gynecology|November 26, 2023
Placental, maternal, fetal, and technical origins of false-positive cell-free DNA screening resultsYvette Raymond, Shavi Fernando, Melody Menezes, et al.
Archives of Gynecology and Obstetrics|August 31, 2025
Repeat cell-free DNA screening after initial false-positive results and term placental analysis for confined mosaicism: a prospective cohort studyYvette C Raymond, Shavi Fernando, Melody Menezes, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|January 19, 2023
The accuracy of cell-free DNA screening for fetal segmental copy number variants: A systematic review and meta-analysisYvette C Raymond, Melissa L Acreman, Sofia Bussolaro, et al.
Frontiers in Genetics|September 15, 2022
Multisite assessment of the impact of cell-free DNA-based screening for rare autosomal aneuploidies on pregnancy management and outcomesTamara Mossfield, Erica Soster, Melody Menezes, et al.
Prenatal Diagnosis|September 7, 2022
Cell-free DNA screening for rare autosomal trisomies and segmental chromosome imbalancesYvette C Raymond, Shavi Fernando, Melody Menezes, et al.
European Journal of Human Genetics : EJHG|January 10, 2026
Unexpected genotypes associated with severe paediatric conditions identified in a healthy population cohortYasmin Bylstra, Weng Khong Lim, Jing Xian Teo, et al.
Frontiers in Genetics|April 9, 2026
Concordance between genome-wide cfDNA screening and diagnostic test results for large copy-number variants: a multi-site study from the Global Expanded NIPT ConsortiumErica Soster, Kristin Dalton, Michael Bonifacio, et al.
NPJ Genomic Medicine|December 26, 2025
Expanding carrier screening: beyond the genes, to include underrepresented ancestriesYasmin Bylstra, Pua Chee Jian, Sui Lin, et al.
European Journal of Human Genetics : EJHG|February 8, 2018
Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective studyJane L Halliday, Cecile Muller, Taryn Charles, et al.
Human Reproduction (Oxford, England)|March 25, 2020
A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohortLisa Hui, Alice Poulton, Eliza Kluckow, et al.
Pageof 4