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Genetic evaluation of patients with multiple primary cancers.
Freire MV, Thissen R, Martin M, Fasquelle C, Helou L, Durkin K, Artesi M, Lumaka A, Leroi N, Segers K, Deberg M, Gatot JS, Habran L, Palmeira L, Josse C, Bours V. Freire MV, et al. Among authors: martin m. Oncol Lett. 2024 Oct 15;29(1):4. doi: 10.3892/ol.2024.14750. eCollection 2025 Jan. Oncol Lett. 2024. PMID: 39492936 Free PMC article.
Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants.
Gallon R, Brekelmans C, Martin M, Bours V, Schamschula E, Amberger A, Muleris M, Colas C, Dekervel J, De Hertogh G, Coupier J, Colleye O, Sepulchre E, Burn J, Brems H, Legius E, Wimmer K. Gallon R, et al. Among authors: martin m. NPJ Precis Oncol. 2024 May 24;8(1):119. doi: 10.1038/s41698-024-00603-z. NPJ Precis Oncol. 2024. PMID: 38789506 Free PMC article.
Case Report Series: Aggressive HR Deficient Colorectal Cancers Related to BRCA1 Pathogenic Germline Variants.
Freire MV, Martin M, Thissen R, Van Marcke C, Segers K, Sépulchre E, Leroi N, Lété C, Fasquelle C, Radermacher J, Gokburun Y, Collignon J, Sacré A, Josse C, Palmeira L, Bours V. Freire MV, et al. Among authors: martin m. Front Oncol. 2022 Feb 24;12:835581. doi: 10.3389/fonc.2022.835581. eCollection 2022. Front Oncol. 2022. PMID: 35280729 Free PMC article.
Dementia Care Research and Psychosocial Factors.
Martin ME, Martinez C, Worff I, Belucci MA, Keller G, Arruabarrena MM, Corvalan N, Clarens MF, Allegri R, Crivelli L. Martin ME, et al. Alzheimers Dement. 2024 Dec;20 Suppl 4:e091916. doi: 10.1002/alz.091916. Alzheimers Dement. 2024. PMID: 39782293
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