F
Françoise Rypens
Researcher at Université de Montréal
Publications - 26
Citations - 725
Françoise Rypens is an academic researcher from Université de Montréal. The author has contributed to research in topics: Magnetic resonance imaging & Prenatal diagnosis. The author has an hindex of 13, co-authored 26 publications receiving 644 citations.
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Journal ArticleDOI
Prenatal prognosis of congenital diaphragmatic hernia using magnetic resonance imaging measurement of fetal lung volume
Guillaume Gorincour,J. Bouvenot,M.G. Mourot,Pascale Sonigo,Kathia Chaumoitre,Catherine Garel,Laurent Guibaud,Françoise Rypens,Fred E. Avni,Marie Cassart,B. Maugey-Laulom,B. Bourlière-Najean,Francis Brunelle,C. Durand,D. Eurin +14 more
TL;DR: To investigate the correlation between fetal lung volume (FLV), measured with magnetic resonance imaging (MRI), and postnatal mortality in newborns with prenatally diagnosed isolated congenital diaphragmatic hernia (CDH), MRI is used.
Journal ArticleDOI
Imaging characteristics of two subtypes of congenital hemangiomas: rapidly involuting congenital hemangiomas and non-involuting congenital hemangiomas.
TL;DR: Distinctive imaging characteristics are observed in cases of CH with US findings of visible vessels and calcifications statistically significant, and compared with COMMON.
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Loss of the proprioception and touch sensation channel PIEZO2 in siblings with a progressive form of contractures
Abdullah Al Mahmud,Noor Ahmed Nahid,Christina Nassif,Muhammad Shahdaat Bin Sayeed,Maizbha Uddin Ahmed,Monowara Parveen,Mohammad Ibrahim Khalil,Mohammad Mohinul Islam,Zabun Nahar,Françoise Rypens,Fadi F. Hamdan,Guy A. Rouleau,Abul Hasnat,Jacques L. Michaud +13 more
TL;DR: Recessive mutations in PIEZO2 thus appear to cause a progressive phenotype that overlaps with, while being mostly distinct from that associated with dominant mutations in the same gene.
Journal ArticleDOI
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis.
Sarah Boissel,Catherine Fallet-Bianco,David Chitayat,Valérie Kremer,Christina Nassif,Françoise Rypens,Marie-Ange Delrue,Dorothée Dal Soglio,Luc L. Oligny,Natalie Patey,Elisabeth Flori,Mireille Cloutier,David A. Dyment,Philippe M. Campeau,Aspasia Karalis,Sonia Nizard,William D. Fraser,François Audibert,Emmanuelle Lemyre,Guy A. Rouleau,Fadi F. Hamdan,Zoha Kibar,Jacques L. Michaud +22 more
TL;DR: This study opens a window on the distinctive genetic landscape associated with fetal anomalies and highlights the power—but also the challenges— of WES in prenatal diagnosis.
Journal ArticleDOI
Obstetric US: Watch the Fetal Hands
Françoise Rypens,Josée Dubois,Laurent Garel,Jean-Christophe Fournet,Jacques L. Michaud,Andrée Grignon +5 more
TL;DR: The detection of a fetal hand malformation warrants a complete work-up, including complete fetal and cardiac US examinations, as well as genetic counseling to determine whether familial inquiry and karyotype analysis are necessary.