Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Melody Menezes"'
Autor:
Erica Soster, Tamara Mossfield, Melody Menezes, Gloudi Agenbag, Marie-Line Dubois, Jean Gekas, Tristan Hardy, Kelly Loggenberg, on behalf of the Global Expanded NIPT Consortium
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-7 (2024)
Abstract Trisomy 20 has been shown to be one of the most frequent rare autosomal trisomies in patients that undergo genome-wide noninvasive prenatal testing. Here, we describe the clinical outcomes of cases that screened positive for trisomy 20 follo
Externí odkaz:
https://doaj.org/article/634db5f3cfe74ed4a291f924099049a6
Autor:
Melody Menezes
Publikováno v:
Fertility & Reproduction, Vol 05, Iss 04, Pp 226-226 (2023)
Preimplantation Genetic Testing for Monogenic Conditions (PGT-M) is increasingly becoming an important reproductive option for individuals and couples planning a pregnancy. In Australia, government funding for PGT-M came into effect in November 2021
Externí odkaz:
https://doaj.org/article/b26756c4f3d546b595694a083853f2f2
Autor:
Tamara Mossfield, Erica Soster, Melody Menezes, Gloudi Agenbag, Marie-Line Dubois, Jean Gekas, Tristan Hardy, Monika Jurkowska, Pascale Kleinfinger, Kelly Loggenberg, Pablo Marchili, Roberto Sirica, on behalf of the Global Expanded NIPT Consortium
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Cell-free (cf) DNA screening is a noninvasive prenatal screening approach that is typically used to screen for common fetal trisomies, with optional screening for sex chromosomal aneuploidies and fetal sex. Genome-wide cfDNA screening can screen for
Externí odkaz:
https://doaj.org/article/563126c106e74772acf05d567fbd0f6f
Publikováno v:
Revista Brasileira de Ginecologia e Obstetrícia, Vol 35, Iss 5, Pp 195-198 (2013)
Externí odkaz:
https://doaj.org/article/b010fcc16c43460da7f3d47aa7568a7f
Autor:
Yvette C. Raymond, Melissa L. Acreman, Sofia Bussolaro, Ben W. Mol, Shavi Fernando, Melody Menezes, Fabricio Da Silva Costa, Ilaria Fantasia, Daniel Lorber Rolnik
Publikováno v:
BJOG: An International Journal of Obstetrics & Gynaecology. 130:549-559
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa39742a57c0e39b0ca19eb8d32b4dc9
https://doi.org/10.1111/1471-0528.17386
https://doi.org/10.1111/1471-0528.17386
Autor:
Miranda F. Lewit‐Mendes, Hazel Robson, Joanne Kelley, Justine Elliott, Erica Brown, Melody Menezes, Alison D. Archibald
Publikováno v:
Journal of Genetic Counseling. 32:213-223
Many non-invasive prenatal testing (NIPT) platforms screen for sex chromosome aneuploidy (SCA) and SCA analysis is generally included in Australia where NIPT is available as a self-funded test. Little is known about the experience of receiving an NIP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eedf12f01a570d613ec3a24d76cfba9c
https://doi.org/10.1002/jgc4.1635
https://doi.org/10.1002/jgc4.1635
Publikováno v:
Molecular Diagnosis & Therapy. 25:683-690
Genetic assessment of an embryo via preimplantation genetic testing (PGT) represents an important reproductive option for couples wanting to try and improve success rates from in vitro fertilisation (IVF) cycles, as well as reduce their risk of havin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::585892851e2e6acfcddfd7a923c42589
https://doi.org/10.1007/s40291-021-00556-0
https://doi.org/10.1007/s40291-021-00556-0
Autor:
Yvette C. Raymond, Shavi Fernando, Melody Menezes, Simon Meagher, Ben W. Mol, Andrew McLennan, Fergus Scott, Karen Mizia, Karen Carey, Gabrielle Fleming, Daniel Lorber Rolnik
Publikováno v:
Prenatal diagnosisREFERENCES. 42(11)
To assess the outcomes of pregnancies at high-risk for rare autosomal trisomies (RATs) and segmental imbalances (SIs) on cell-free DNA (cfDNA) screening.A retrospective study of women who underwent cfDNA screening between September 2019 and July 2021
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6030ccec66b06a50bb8d25f2f02bdd0f
https://pubmed.ncbi.nlm.nih.gov/36068932
https://pubmed.ncbi.nlm.nih.gov/36068932
Autor:
Andrew McLennan, Melody Menezes, Rhiannon Sandow, Fergus Scott, Deborah Nisbet, Daniel L. Rolnik, Philip J. Schluter
Publikováno v:
Prenatal Diagnosis. 40:1466-1473
Objective The accuracy of cell-free DNA aneuploidy screening varies by the chromosome assessed. The positive predictive value is consistently low for monosomy X (MX), at less than 30%. This study aims to investigate maternal age and other possible pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d624094eb737ce378c2ad788af893f5e
https://doi.org/10.1002/pd.5790
https://doi.org/10.1002/pd.5790
Autor:
Melody Menezes, Imogen Brown, Simon Meagher, Daniel L. Rolnik, Shavi Fernando, Jayshree Ramkrishna, Fabricio da Silva Costa
Publikováno v:
Prenatal Diagnosis. 40:1439-1446
Objective This study aims to determine the incidence of ultrasound findings that may change clinical management on the day of blood-sampling for cell-free DNA (cfDNA) screening. Methods A retrospective study was conducted at a tertiary provider of ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c86e3b06667a8f2007c4f59c384221e7
https://doi.org/10.1002/pd.5788
https://doi.org/10.1002/pd.5788