Rebecca Reimers

4PUBLICATIONS
15CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)NeonatologyForensic epidemiologyFoetal development and medicine
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Publications (4)

|Feb 26, 2024
Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations.

Shilpa Nadimpalli Kobren, Mikhail A Moldovan, Rebecca Reimers

|Apr 20, 2023
Position statement from the International Society for Prenatal Diagnosis on the use of non-invasive prenatal testing for the detection of fetal chromosomal conditions in singleton pregnancies.

Lisa Hui, Katie Ellis, Dora Mayen

|Nov 01, 2022
Prenatal diagnosis of sex chromosome aneuploidy-What do we tell the prospective parents?

Rebecca Reimers, Frances High, Jessica Kremen

|Feb 14, 2018
When ultrasound anomalies are present: An estimation of the frequency of chromosome abnormalities not detected by cell-free DNA aneuploidy screens.

Rebecca M Reimers, Heather Mason-Suares, Sarah E Little

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Frequent Collaborators

2 joint publications

Louise Wilkins-Haug

1 joint publications

Lisa Hui

1 joint publications

Mark D Pertile

1 joint publications

Luming Sun