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Annales De Biologie Clinique|September 30, 2017
Study of two comparison procedures applied to biochemical results from twin analyzersLise Larcher, Laurence Pacot, Sophie Bailleul, et al.
Annales De Biologie Clinique|September 30, 2017
Importance of pre-analytical for urinalysis with urinary crystalsLise Larcher, Guillaume Lefevre, Sophie Bailleul, et al.
Clinical Genetics|December 18, 2019
New evidence that biallelic loss of function in EEF1B2 gene leads to intellectual disabilityLise Larcher, Julien Buratti, Bénédicte Héron-Longe, et al.
Emerging Infectious Diseases|December 19, 2018
Orogenital Transmission of Neisseria meningitidis Causing Acute Urethritis in Men Who Have Sex with MenArnaud Jannic, Hedi Mammeri, Lise Larcher, et al.
European Journal of Medical Genetics|October 4, 2019
The complete loss of function of the SMS gene results in a severe form of Snyder-Robinson syndromeLise Larcher, Joy W Norris, Elodie Lejeune, et al.
British Journal of Haematology|May 19, 2026
From a novel pathogenic SAMD9L variant to cohort-wide insights: Whole-genome sequencing highlights somatic genetic rescue and phenotypic heterogeneityHadjer Dellal, Roman Klifa, Lise Larcher, et al.
Human Molecular Genetics|February 1, 2023
A novel cancer risk prediction score for the natural course of FA patients with biallelic BRCA2/FANCD1 mutationsIvana Radulovic, Michael M Schündeln, Lisa Müller, et al.
Nucleic Acids Research|July 3, 2023
A clickable melphalan for monitoring DNA interstrand crosslink accumulation and detecting ICL repair defects in Fanconi anemia patient cellsSara Berrada, Elena Martínez-Balsalobre, Lise Larcher, et al.
American Journal of Hematology|September 16, 2025
Recursive Partitioning to Differentiate Acquired From Inherited Bone Marrow Failure SyndromesEléonore Kaphan, Anouk Walter-Petrich, Lise Larcher, et al.
Blood|January 10, 2023
Rare germline complement factor H variants in patients with paroxysmal nocturnal hemoglobinuriaPedro Henrique Prata, Jacques-Emmanuel Galimard, Flore Sicre de Fontbrune, et al.
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