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The Journal of Maternal-Fetal & Neonatal Medicine Volume 27, 2014 - Issue 13
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Research Article

Clinical utility of chromosomal microarray analysis in prenatal diagnosis: report of first 6 months in clinical practice

Susan KlugmanDepartment of Obstetrics & Gynecology and Women’s Health Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, NYUSACorrespondence[email protected]
,
Barrie SuskinDepartment of Obstetrics & Gynecology and Women’s Health Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, NYUSA
,
Brianna L. SpencerDepartment of Obstetrics & Gynecology and Women’s Health Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, NYUSA
,
Pe’er DarDepartment of Obstetrics & Gynecology and Women’s Health Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, NYUSA
,
Komal BajajDepartment of Obstetrics & Gynecology, North Bronx Health Network Bronx, NYUSA
,
Judith PowersDepartment of Obstetrics & Gynecology and Women’s Health Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, NYUSA
,
Julie ReichlingDepartment of Obstetrics & Gynecology and Women’s Health Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, NYUSA
,
David WassermanCenter for Ethics at Yeshiva University Bronx, NYUSA
,
Siobhan M. DolanDepartment of Obstetrics & Gynecology and Women’s Health Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, NYUSA
&
Irwin R. MerkatzDepartment of Obstetrics & Gynecology and Women’s Health Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, NYUSA
 show all
Pages 1333-1338 | Received 12 Aug 2013, Accepted 19 Oct 2013, Published online: 26 Nov 2013

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Karin EM Diderich, Jasmijn E Klapwijk, Vyne van der Schoot, Hennie T Brüggenwirth, Marieke Joosten & Malgorzata I Srebniak. (2023) Challenges and Pragmatic Solutions in Pre-Test and Post-Test Genetic Counseling for Prenatal Exome Sequencing. The Application of Clinical Genetics 16, pages 89-97.
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Dong-Zhi Li & Hai-Shen Tang. (2021) Chromosomal microarray analysis in pregnancies at risk for a molecular disorder. The Journal of Maternal-Fetal & Neonatal Medicine 34:1, pages 159-162.
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Articles from other publishers (15)

Kate Swanson, Kelsey B. Loeliger, Shilpa P. Chetty, Teresa N. Sparks & Mary E. Norton. (2022) Disparities in the acceptance of chromosomal microarray at the time of prenatal genetic diagnosis. Prenatal Diagnosis 42:5, pages 611-616.
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Gioia Mastromoro, Daniele Guadagnolo, Nader Khaleghi Hashemian, Enrica Marchionni, Alice Traversa & Antonio Pizzuti. (2022) Molecular Approaches in Fetal Malformations, Dynamic Anomalies and Soft Markers: Diagnostic Rates and Challenges—Systematic Review of the Literature and Meta-Analysis. Diagnostics 12:3, pages 575.
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Karin E.M. Diderich, Jasmijn E. Klapwijk, Marieke Joosten, Hennie T. Brüggenwirth & Malgorzata I. Srebniak. 2022. Prenatal Genetic Counseling. Prenatal Genetic Counseling 39 67 .
AH Mardy, AP Wiita, BV Wayman, K Drexler, TN Sparks & ME Norton. (2020) Variants of uncertain significance in prenatal microarrays: a retrospective cohort study. BJOG: An International Journal of Obstetrics & Gynaecology 128:2, pages 431-438.
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Yan Wang, Min Zhang, Lingji Chen, Hailong Huang & Liangpu Xu. (2020) Prenatal diagnosis of BACs‐on‐Beads assay in 1520 cases from Fujian Province, China. Molecular Genetics & Genomic Medicine 8:10.
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Wei-Ju Chen, Shixi Zhao, Tse-Yang Huang, Oi-Man Kwok & Lei-Shih Chen. (2020) Autism Spectrum Disorders: Prenatal Genetic Testing and Abortion Decision-Making among Taiwanese Mothers of Affected Children. International Journal of Environmental Research and Public Health 17:2, pages 476.
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Claire N. Singletary, Nevena Cvjetkovic Krstic, Jennifer L. Czerwinski, Meagan Giles Choates & Chelsea Wagner. (2018) Prenatal chromosomal microarray uptake with invasive prenatal diagnosis: How many patients take the leap?. Prenatal Diagnosis 38:10, pages 748-754.
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M. I. Srebniak, M. Joosten, M. F. C. M. Knapen, L. R. Arends, M. Polak, S. van Veen, A. T. J. I. Go & D. Van Opstal. (2018) Frequency of submicroscopic chromosomal aberrations in pregnancies without increased risk for structural chromosomal aberrations: systematic review and meta‐analysis. Ultrasound in Obstetrics & Gynecology 51:4, pages 445-452.
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Beatrice Oneda & Anita Rauch. (2017) Microarrays in prenatal diagnosis. Best Practice & Research Clinical Obstetrics & Gynaecology 42, pages 53-63.
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Allison Werner-Lin, Sarah Walser, Frances K. Barg & Barbara A. Bernhardt. (2017) “ They Can't Find Anything Wrong with Him, Yet ”: Mothers’ experiences of parenting an infant with a prenatally diagnosed copy number variant (CNV) . American Journal of Medical Genetics Part A 173:2, pages 444-451.
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Mariam Naqvi, Ilona T. Goldfarb, Kaitlin J. Hanmer & Allison Bryant. (2016) Chromosomal microarray use among women undergoing invasive prenatal diagnosis. Prenatal Diagnosis 36:7, pages 656-661.
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Hagit Shani, Tamar Goldwaser, Jennifer Keating & Susan Klugman. (2016) Chromosomal abnormalities not currently detected by cell-free fetal DNA: a retrospective analysis at a single center. American Journal of Obstetrics and Gynecology 214:6, pages 729.e1-729.e11.
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M. I. Srebniak, D. Van Opstal, M. Joosten, K. E. M. Diderich, F. A. T. de Vries, S. Riedijk, M. F. C. M. Knapen, A. T. J. I. Go, L. C. P. Govaerts & R.-J. H. Galjaard. (2015) Whole-genome array as a first-line cytogenetic test in prenatal diagnosis. Ultrasound in Obstetrics & Gynecology 45:4, pages 363-372.
Crossref
Barbara A. Bernhardt, Katherine Kellom, Alexandra Barbarese, W. Andrew Faucett & Ronald J. Wapner. (2014) An Exploration of Genetic Counselors’ Needs and Experiences with Prenatal Chromosomal Microarray Testing. Journal of Genetic Counseling 23:6, pages 938-947.
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Sam Riedijk, Karin Diderich, Sanne van der Steen, Lutgarde Govaerts, Marieke Joosten, Maarten Knapen, Femke de Vries, Diane van Opstal, Aad Tibben & Robert-Jan Galjaard. (2014) The Psychological Challenges of Replacing Conventional Karyotyping with Genomic SNP Array Analysis in Prenatal Testing. Journal of Clinical Medicine 3:3, pages 713-723.
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