Lara Reichman

12PUBLICATIONS
25CO-AUTHORS
Haematological tumoursMolecular targetsGene expression (incl. microarray and other genome-wide approaches)Predictive and prognostic markersCancer genetics
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Publications (12)

|Mar 31, 2026
Rare solid tumours as indicators of hereditary cancer syndromes.

Barbara Rivera, Giovana Tardin Torrezan, Carla Roca

|Mar 03, 2026
Tumor patterns and cancer risk in carriers of TP53 exonic germline variants that alter mRNA splicing.

Deborah Schönegger, Emilie Montellier, Sandrine Blanchet

|Mar 12, 2025
Germline analysis of an international cohort of pediatric diffuse midline glioma patients.

Marion K Mateos, Pamela Ajuyah, Noemi Fuentes-Bolanos

|May 24, 2024
Cost-effectiveness of the McGill interactive pediatric oncogenetic guidelines in identifying Li-Fraumeni syndrome in female patients with osteosarcoma.

Juan David Rios, Frances Simbulan, Lara Reichman

|Aug 28, 2023
A systematic review of the prevalence of pathogenic or likely pathogenic germline variants in individuals with FOXO1 fusion-positive rhabdomyosarcoma.

Claire Freycon, Philip J Lupo, Leora Witkowski

|Jul 17, 2023
Performance of the eHealth decision support tool, MIPOGG, for recognising children with Li-Fraumeni, DICER1, Constitutional mismatch repair deficiency and Gorlin syndromes.

Robyn Hebert, Noelle Cullinan, Linlea Armstrong

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Frequent Collaborators

4 joint publications

William D Foulkes

2 joint publications

Nada Jabado

1 joint publications

Noelle Cullinan

1 joint publications

Kalene van Engelen