Publications by authors named "Louise Devisme"

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Caracteristics of women presenting with chronic histiocytic intervillositis during pregnancy: A case-control study.
Amandine Mawa, Gabriel Bizet, Morgane Stichelbout, Louise Devisme, Myrtille Pauchet

J Gynecol Obstet Hum Reprod· February 2025

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Fetal Presentation of MYRF-Related Cardiac Urogenital Syndrome: An Emerging and Challenging Prenatal Diagnosis.
Maud Favier, Elise Brischoux-Boucher, Louise C Pyle, Nicolas Mottet, Marion Auber-Lenoir, Louise Devisme

Prenat Diagn· December 2024

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Cardiac rhabdomyoma: a rare feature of Birt-Hogg-Dubé syndrome.
Florence Petit, Louise Devisme, Dimitri Tchernitchko, Olivia Domanski, Cecilia Gonzalez-Corcia

J Med Genet· November 2024

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PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects.
Florence Petit, Mauro Longoni, Julie Wells, Richard S Maser, Eric L Bogenschutz, Louise Devisme

Am J Hum Genet· October 2023

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COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage.
Thibault Coste, Catherine Vincent-Delorme, Morgane Stichelbout, Louise Devisme, Antoinette Gelot

Prenat Diagn· May 2022

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Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract.
Johannes Münch, Marie Engesser, Ria Schönauer, J Austin Hamm, Christin Hartig, Louise Devisme

Kidney Int· May 2022

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The first two non-Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome.
Leïla Ghesh, Marie Denis Musquer, Louise Devisme, Morgane Stichelbout, Lucile Boutaud

Clin Genet· October 2021

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Risk factors for spontaneous hematoma of the umbilical cord: A case-control study.
Yasmine Clermont-Hama, Kathleen Thibouw, Louise Devisme, Hélène Franquet-Ansart, Morgane Stichelbout

Placenta· September 2020

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TAR syndrome: Clinical and molecular characterization of a cohort of 26 patients and description of novel noncoding variants of RBM8A.
Simon Boussion, Fabienne Escande, Anne-Sophie Jourdain, Thomas Smol, Perrine Brunelle, Louise Devisme

Hum Mutat· July 2020

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p57-discordant villi in hydropic products of conception: a clinicopathological study of 70 cases.
Lucie Gaillot-Durand, Sophie Patrier, Jacqueline Aziza, Louise Devisme, Anne-Claude Riera

Hum Pathol· July 2020

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Association of Chorioamnionitis with Cerebral Palsy at Two Years after Spontaneous Very Preterm Birth: The EPIPAGE-2 Cohort Study.
Emeline Maisonneuve, Elsa Lorthe, Héloïse Torchin, Pierre Delorme, Louise Devisme

J Pediatr· July 2020

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Exome sequencing identifies the first genetic determinants of sirenomelia in humans.
François Lecoquierre, Anne-Claire Brehin, Sophie Coutant, Juliette Coursimault, Anne Bazin, Louise Devisme

Hum Mutat· May 2020

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Histoanatomical structures of laryngeal atresia: Functional considerations.
Pierre Fayoux, Louise Devisme

Laryngoscope· January 2020

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Bardet-Biedl syndrome: Antenatal presentation of forty-five fetuses with biallelic pathogenic variants in known Bardet-Biedl syndrome genes.
Laura Mary, Kirsley Chennen, Corinne Stoetzel, Manuela Antin, Anne Leuvrey, Louise Devisme

Clin Genet· March 2019

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Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF Pathway.
Justyna A Karolak, Marie Vincent, Gail Deutsch, Tomasz Gambin, Benjamin Cogné, Louise Devisme

Am J Hum Genet· February 2019

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Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome.
Carine Bonnard, Mohammad Shboul, Seyed Hassan Tonekaboni, Alvin Yu Jin Ng, Sumanty Tohari, Louise Devisme

Eur J Med Genet· October 2018

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Histologic Chorioamnionitis and Bronchopulmonary Dysplasia in Preterm Infants: The Epidemiologic Study on Low Gestational Ages 2 Cohort.
Héloïse Torchin, Elsa Lorthe, François Goffinet, Gilles Kayem, Damien Subtil, Louise Devisme

J Pediatr· August 2017

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Perinatal outcome of placental massive perivillous fibrin deposition: a case-control study.
Louise Devisme, Claire Chauvière, Hélène Franquet-Ansart, Anastasia Chudzinski, Morgane Stichelbout

Prenat Diagn· April 2017

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SALL4 expression in gestational trophoblastic tumors: a useful tool to distinguish choriocarcinoma from placental site trophoblastic tumor and epithelioid trophoblastic tumor.
Morgane Stichelbout, Louise Devisme, Hélène Franquet-Ansart, Jérôme Massardier, Denis Vinatier

Hum Pathol· August 2016

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Novel NEK8 Mutations Cause Severe Syndromic Renal Cystic Dysplasia through YAP Dysregulation.
Valentina Grampa, Marion Delous, Mohamad Zaidan, Gweltas Odye, Sophie Thomas, Louise Devisme

PLoS Genet· March 2016

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[Cardiac fibroma: A rare cause of sudden child death].
Sarah Humez, Jean-Baptiste Gibier, Morgan Recher, Stéphane Leteurtre, Xavier Leroy, Louise Devisme

Ann Pathol· October 2015

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Curative surgery for placental site trophoblastic tumors.
Florence Renaud, Karine Llinares, François Golfier, Louise Devisme

Int J Gynaecol Obstet· July 2015

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Clinical and molecular delineation of Tetrasomy 9p syndrome: report of 12 new cases and literature review.
Laïla El Khattabi, Sylvie Jaillard, Joris Andrieux, Laurent Pasquier, Laurence Perrin, Louise Devisme

Am J Med Genet A· June 2015

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New insights into genotype-phenotype correlation for GLI3 mutations.
Florence Démurger, Amale Ichkou, Soumaya Mougou-Zerelli, Martine Le Merrer, Géraldine Goudefroye, Louise Devisme

Eur J Hum Genet· January 2015

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Fetal phenotype associated with the 22q11 deletion.
Anne-Claire Noël, Fanny Pelluard, Anne-Lise Delezoide, Louise Devisme, Laurence Loeuillet

Am J Med Genet A· November 2014

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