Publications by authors named "Luc Oligny"

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Self-supervised deep metric learning for prototypical zero-shot lesion retrieval in placenta whole-slide images.
Gaspar Faure, Dorothée Dal Soglio, Natalie Patey, Luc Oligny, Sylvie Girard

Comput Biol Med· September 2025

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Low TTG-IgA associated with isolated bulb pathology in pediatric celiac disease: Implications in a no-biopsy approach era.
Qing Yin Wang, Prévost Jantchou, Martha Dirks, Sébastien B Lavoie, Luc L Oligny

J Pediatr Gastroenterol Nutr· April 2025

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Workload Measurement in Subspecialty Placental Pathology in Canada.
James R Wright, Suzanne Chan, Eric K Morgen, Raymond T A Maung, , Luc L Oligny

Pediatr Dev Pathol· December 2022

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Multicentric Castleman disease revealing complete signal transducer and activator of transcription 1 deficiency treated by JAK1/2 inhibition.
Camille Beaufils, Isabel Fernandez, Lorie Marchitto, Marie-Paule Morin, Jean-Jacques De Bruycker, Luc Oligny

J Allergy Clin Immunol Pract· October 2021

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Prenatal presentation of glutaric aciduria type II: A case report with radiologic, clinical, biochemical, molecular, and pathological phenotyping.
Laurence Carmant, Aspasia Karalis, Françoise Rypens, Luc Oligny, Sandrine Wavrant

Clin Case Rep· March 2021

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Fulminant Necrotizing Enterocolitis and Multiple Organ Dysfunction in a Toddler with Mitochondrial DNA Depletion Syndrome-13.
Nicolas Nardi, François Proulx, Catherine Brunel-Guiton, Luc L Oligny, Nelson Piché

J Pediatr Intensive Care· March 2020

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Cryptic recurrent ACIN1-NUTM1 fusions in non-KMT2A-rearranged infant acute lymphoblastic leukemia.
Thomas Pincez, Josette-Renée Landry, Mathieu Roussy, Loubna Jouan, Mélanie Bilodeau, Luc Oligny

Genes Chromosomes Cancer· February 2020

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Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype.
Przemyslaw Szafranski, Qian Liu, Justyna A Karolak, Xiaofei Song, Nicole de Leeuw, Luc L Oligny

Hum Genet· December 2019

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Ossifying Renal Tumor of Infancy: Report of a Case With Positive WT1 Immunohistochemistry and High Mitotic Index and Review of the Literature.
Benoit Vaillancourt, Luc Oligny, Julie Déry, Julie Franc-Guimond, Dorothée Bouron-Dal Soglio

Pediatr Dev Pathol· May 2019

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LINE- and Alu-containing genomic instability hotspot at 16q24.1 associated with recurrent and nonrecurrent CNV deletions causative for ACDMPV.
Przemyslaw Szafranski, Ewelina Kośmider, Qian Liu, Justyna A Karolak, Lauren Currie, Luc Oligny

Hum Mutat· December 2018

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No. 365-Fetal and Perinatal Autopsy in Prenatally Diagnosed Fetal Abnormalities with Normal Chromosome Analysis.
Catherine Fallet-Bianco, Isabelle De Bie, Valérie Désilets, Luc Laurier Oligny

J Obstet Gynaecol Can· October 2018

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N° 365 -Autopsies fœtales et périnatales en cas d'anomalies fœtales diagnostiquées avant la naissance avec une analyse chromosomique normale.
Catherine Fallet-Bianco, Isabelle De Bie, Valérie Désilets, Luc Laurier Oligny

J Obstet Gynaecol Can· October 2018

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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, Luc L Oligny

Genet Med· July 2018

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Liver mass containing normal bile ducts in an Alagille patient: a case report.
Stefanie Parisien-La Salle, Justin Côté-Daigneault, Laurent Garel, Luc Laurier Oligny, Fernando Álvarez

Arch Argent Pediatr· August 2015

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Assessment of correlation between p16INK4a staining, specific subtype of human papillomavirus, and progression of LSIL/CIN1 lesions: first comparative study.
Maryam Razmpoosh, Andrée Sansregret, Luc L Oligny, Natalie Patey, Virginie Dormoy-Raclet

Am J Clin Pathol· July 2014

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Fetal and perinatal autopsy in prenatally diagnosed fetal abnormalities with normal karyotype.
Valérie Désilets, Luc Laurier Oligny, , ,

J Obstet Gynaecol Can· October 2011

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Development and description of GETT: a genetic testing evidence tracking tool.
François Rousseau, Carmen Lindsay, Marc Charland, Yves Labelle, Jean Bergeron, Luc Oligny

Clin Chem Lab Med· October 2010

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[Juvenile xanthogranuloma of the nasal cavity].
Rose Chami, Olga Aleynikova, Antony Abela, Martine Blais, Luc Oligny

Ann Pathol· October 2010

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High level of apoptosis and low AKT activation in mass screening as opposed to standard neuroblastoma.
Hervé Sartelet, Shigeru Ohta, Stephane Barrette, Anne-Laure Rougemont, Marie Brevet, Luc L Oligny

Histopathology· April 2010

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Lethal respiratory failure and mild primary hypothyroidism in a term girl with a de novo heterozygous mutation in the TITF1/NKX2.1 gene.
Emilie Maquet, Sabine Costagliola, Jasmine Parma, Christiane Christophe-Hobertus, Luc L Oligny

J Clin Endocrinol Metab· January 2009

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Collapsing glomerulopathy in Galloway-Mowat syndrome: a case report and review of the literature.
Hervé Sartelet, Christine Pietrement, Laure-Hélène Noel, Pascal Sabouraud, Philippe Birembaut, Luc Laurier Oligny

Pathol Res Pract· August 2008

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Presence of autoantibodies against tubular and uveal cells in a patient with tubulointerstitial nephritis and uveitis (TINU) syndrome.
Lynda Abed, Aicha Merouani, Elie Haddad, Genevieve Benoit, Luc Laurier Oligny

Nephrol Dial Transplant· April 2008

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A B-cell lymphoma-associated chromosomal translocation in a progressive transformation of germinal center.
Dorothée Bouron-Dal Soglio, Françoise Truong, Raouf Fetni, Sawcene Hazourli, Josette Champagne, Luc Laurier Oligny

Hum Pathol· February 2008

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Accessory liver lobe with mesothelial inclusion cysts in an omphalocele: a new malformative association.
Anne-Laure Rougemont, Hervé Sartelet, Luc L Oligny, Arie Bensoussan, Salam Yazbeck

Pediatr Dev Pathol· July 2007

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A dire finding.
Guillaume Gorincour, Andrée Grignon, Luc Oligny

Am J Obstet Gynecol· May 2007

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