Alexandre Fabre

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 6

Top Topics

Duchenne Muscular Dystrophy

Intellectual Disability

Endothelial Cells

Top Venues

Pediatric radiology

American journal of medical genetics. Part A

Clinical case reports

European journal of human genetics : EJHG

This page only lists publications with an associated author ORCID identifier.

Publications

Paul Knebelmann, Antoine Martin-Champetier, Anderson Loundou, Alexandre Fabre, Philippe Petit, Alexia Dabadie
Weight-specific normal liver stiffness values in children. Pediatric radiology (2024)
Alexandre Fabre, Paul Guerry
Goldilocks principle and recessive disease. European journal of human genetics : EJHG (2023)
Marion Almes, Anne Spraul, Mathias Ruiz, Muriel Girard, Bertrand Roquelaure, Nolwenn Laborde, Fréderic Gottrand, Anne Turquet, Thierry Lamireau, Alain Dabadie, Marjorie Bonneton, Alice Thebaut, Babara Rohmer, Florence Lacaille, Pierre Broué, Alexandre Fabre, Karine Mention-Mulliez, Jérôme Bouligand, Emmanuel Jacquemin, Emmanuel M Gonzales
Targeted-Capture Next-Generation Sequencing in Diagnosis Approach of Pediatric Cholestasis. Diagnostics (Basel, Switzerland) 12 (5) (2022)
Laure Segurel, Perle Guarino-Vignon, Nina Marchi, Sophie Lafosse, Romain Laurent, Céline Bon, Alexandre Fabre, Tatyana Hegay, Evelyne Heyer
Why and when was lactase persistence selected for? Insights from Central Asian herders and ancient DNA. PLoS biology 18 (6) (2020)
Coline Mejean, Daniel Bertin, Kim Guetta, Cécile Desaldeleer, Mathilde Butori, Bertrand Roquelaure, Alexandre Fabre
Chronic hepatitis associated with antiribosomal-P autoantibodies in a 14-year-old girl. Clinical case reports 7 (10) (2019)
Alexandre Fabre, Laetitia-Marie Petit, Lars F Hansen, Anne V Wewer, Clothilde Esteve, Charlène Chaix, Patrice Bourgeois, Catherine Badens, Anders Paerregaard
A new mutation in the C-terminal end of TTC37 leading to a mild form of syndromic diarrhea/tricho-hepato-enteric syndrome in seven patients from two families. American journal of medical genetics. Part A 176 (3) (2018)