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MARTIN Marie

Unilab > Consultation Génétique

See author's contact details
Main Referenced Co-authors
Bours, Vincent  (8)
Sautois, Brieuc  (4)
Demez, Pierre  (3)
Docampo Martínez, Elisa  (3)
Freire Chadrina, Maria  (3)
Main Referenced Keywords
Humans (5); Female (3); chimiothérapie (2); Genetic Predisposition to Disease (2); Head and neck cancer (2);
Main Referenced Unit & Research Centers
GIGA-I3 - Giga-Infection, Immunity and Inflammation - ULiège (1)
Main Referenced Disciplines
Oncology (6)
Genetics & genetic processes (5)
Cardiovascular & respiratory systems (2)
Dermatology (1)
Immunology & infectious disease (1)

Publications (total 16)

The most downloaded
821 downloads
SIBILLE, A., PAULUS, A., MARTIN, M., BOURHABA, M., Barthélemy, N., Radermecker, M., CORHAY, J.-L., LOUIS, R., & DUYSINX, B. (2015). Prise en charge du cancer bronchique non à petites cellules. Revue Médicale de Liège, 70 (9), 432-41. https://hdl.handle.net/2268/195381

The most cited

13 citations (OpenAlex)

SIBILLE, A., PAULUS, A., MARTIN, M., BOURHABA, M., Barthélemy, N., Radermecker, M., CORHAY, J.-L., LOUIS, R., & DUYSINX, B. (2015). Prise en charge du cancer bronchique non à petites cellules. Revue Médicale de Liège, 70 (9), 432-41. https://hdl.handle.net/2268/195381

Freire Chadrina, M., Martin, M., Segers, K., Sépulchre, E., LEROI, N., COUPIER, J., Kalantari, H. R., Wolter, P., Collignon, J., Polus, M., Plomteux, O., Josse, C., & Bours, V. (29 May 2024). Digenic Inheritance of Mutations in Homologous Recombination Genes in Cancer Patients. Journal of Personalized Medicine, 14 (6), 584. doi:10.3390/jpm14060584
Peer Reviewed verified by ORBi

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., Sépulchre, E., Burn, J., Brems, H., Legius, E., & Wimmer, K. (24 May 2024). Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants. npj Precision Oncology, 8 (1), 119. doi:10.1038/s41698-024-00603-z
Peer Reviewed verified by ORBi

Harvengt, J., Docampo Martínez, E., Jacquinet, A., Alkan, S., Martin, M., Debray, F.-G., BULK, S., & Bours, V. (12 April 2024). New paradigms in clinical geneticist practice in the era of emerging therapies: examples of two pediatric syndromes [Poster presentation]. BESHG Annual Symposium 2024.
Peer reviewed

CREVECOEUR, J., Docampo, E., Martin, M., & Bours, V. (2024). INTÉRÊT DE L’UTILISATION DES SCORES DE RISQUES POLYGÉNIQUES DANS LE DÉPISTAGE DU CANCER DU SEIN ET LA MÉDECINE DE PRÉVENTION. Revue Médicale de Liège, 79 (6), 372 - 378.
Editorial Reviewed verified by ORBi

Bailleux, S., SOMJA, J., MARTIN, M., DE PRIJCK, B., & NIKKELS, A. (2022). HEREDITARY LEIOMYOMATOSIS AND ACUTE LYMPHOBLASTIC LEUKEMIA: a LINK THROUGH FUMARATE DYSHYDRATASE MUTATION? Acta Clinica Belgica, 77, 778-781. doi:10.1080/17843286.2021.1980669
Peer Reviewed verified by ORBi

Freire, M. V., MARTIN, M., Thissen, R., Van Marcke, C., SEGERS, K., SEPULCHRE, E., LEROI, N., LETE, C., FASQUELLE, C., Radermacher, J., Gokburun, Y., COLLIGNON, J., Sacré, A., JOSSE, C., PALMEIRA, L., & BOURS, V. (2022). Case Report Series: Aggressive HR Deficient Colorectal Cancers Related to BRCA1 Pathogenic Germline Variants. Frontiers in Oncology, 12, 835581. doi:10.3389/fonc.2022.835581
Peer Reviewed verified by ORBi

Martin, M., & SAUTOIS, B. (January 2021). Early onset of head and neck squamous-cell carcinoma and fatal toxicity with concurrent chemoradiotherapy in a patient compound heterozygote for FANCA gene [letter to the editor]. Oral Oncology, 112, 104989. doi:10.1016/j.oraloncology.2020.104989
Peer Reviewed verified by ORBi

DOCAMPO MARTINEZ, E., MARTIN, M., GANGOLF, M., HARVENGT, J., BULK, S., SEGERS, K., LEROI, N., LETE, C., PALMARICCIOTTI, V., Freire Chadrina, M., LAMBERT, F., & Bours, V. (2021). Hérédité et cancer. Revue Médicale de Liège, 76 (5-6), 327-336.
Peer reviewed

DOCAMPO MARTINEZ, E., MARTIN, M., Marnette, J., & Bours, V. (06 March 2020). LTBP3 mutation identified in a patient with a severe valvular disease [Poster presentation]. 20th Annual Meeting of the Belgian Society of Human Genetics.

JADOT, V., SEGERS, K., Bours, V., KOHNEN, L., HONORE, P., MARTIN, M., DE FLINES, J., MUTIJIMA NZARAMBA, E., & LECLERCQ, P. (2019). Cancer gastrique diffus héréditaire Série de 8 patients appartenant à une même famille et revue de la littérature. Revue Médicale de Liège, 74 (3), 134-138.

SAUTOIS, B., SCHROEDER, H., MARTIN, M., PIRET, P., DEMEZ, P., BOUCHAIN, O., MUTIJIMA NZARAMBA, E., & MOREAU, P. (2016). Weekly cisplatin with radiotherapy for locally advanced head and neck squamous cell carcinoma. Journal of Balkan Union of Oncology, 21 (4), 979-988.
Peer Reviewed verified by ORBi

PAULUS, A., SIBILLE, A., BOURHABA, M., MARTIN, M., LOUIS, R., & DUYSINX, B. (December 2015). PRISE EN CHARGE DES TUMEURS EPITHELIALES THYMIQUES. Revue Médicale de Liège, 70 (12), 623-8.
Peer reviewed

SIBILLE, A., PAULUS, A., MARTIN, M., BOURHABA, M., Barthélemy, N., Radermecker, M., CORHAY, J.-L., LOUIS, R., & DUYSINX, B. (2015). Prise en charge du cancer bronchique non à petites cellules. Revue Médicale de Liège, 70 (9), 432-41.
Peer reviewed

Amand, M., Erpicum, C., BAJOU, K., Cerignoli, F., Blacher, S., MARTIN, M., Dequiedt, F., Drion, P., Singh, P., Vandereyken, M., Musumeci, L., Moutschen, M., Gilles, C., Noël, A., & Rahmouni, S. (27 January 2014). DUSP3/VHR is a pro-angiogenic atypical dual-specificity phosphatase [Poster presentation]. GIGA Day 2014, Liège, Belgium.

Martin, M., Demez, P., MOREAU, P., Devillers, D., PIRET, P., & Sautois, B. (January 2010). Chimiothérapie néoadjuvante dans les cancers "tête et cou". Revue Médicale de Liège, 65 (1), 15-17.
Peer reviewed

Sautois, B., Martin, M., Demez, P., Piret, P., Devillers, D., & Moreau, P. (2009). Place des anticorps monoclonaux dans le traitement des tumeurs de la tete et du cou. Revue Médicale de Liège, 64 (5-6), 284-6.
Peer reviewed

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