Increased prevalence of the founder BRCA1 c.5309G>T and recurrent BRCA2 c.1310_1313delAAGA mutations in breast cancer families from Northerstern region of Morocco: evidence of geographical specificity and high relevance for genetic counseling
Melki, Rahma, Melloul, Marouane, Aissaoui, Souria, El Harroudi, Tijani, Boukhatem, Noureddine
Published in BMC cancer (13.04.2023)
Published in BMC cancer (13.04.2023)
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Significant association between ERCC2 and MTHR polymorphisms and breast cancer susceptibility in Moroccan population: genotype and haplotype analysis in a case-control study
Hardi, Hanaa, Melki, Rahma, Boughaleb, Zouhour, El Harroudi, Tijani, Aissaoui, Souria, Boukhatem, Noureddine
Published in BMC cancer (15.03.2018)
Published in BMC cancer (15.03.2018)
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Increased prevalence of the founder BRCA1 c.5309GT and recurrent BRCA2 c.1310_1313delAAGA mutations in breast cancer families from Northerstern region of Morocco: evidence of geographical specificity and high relevance for genetic counseling
Melki, Rahma, Melloul, Marouane, Aissaoui, Souria, EL Harroudi, Tijani, Boukhatem, Noureddine
Published in BMC cancer (13.04.2023)
Published in BMC cancer (13.04.2023)
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Retroperitoneal liposarcoma and craniosynostosis: possible genomic relationship, case report, and literature review
Sguinzi, Raffaella Maria, Aissaoui, Souria, Genevay-Infante, Muriel, Breguet, Romain, Charbonnet, Pierre, Francis, Karim, Kini, Riad, Bühler, Leo
Published in Functional & integrative genomics (01.03.2023)
Published in Functional & integrative genomics (01.03.2023)
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Intention to Inform Relatives, Rates of Cascade Testing, and Preference for Patient-Mediated Communication in Families Concerned with Hereditary Breast and Ovarian Cancer and Lynch Syndrome: The Swiss CASCADE Cohort
Sarki, Mahesh, Ming, Chang, Aissaoui, Souria, Bürki, Nicole, Caiata-Zufferey, Maria, Erlanger, Tobias Ephraim, Graffeo-Galbiati, Rossella, Heinimann, Karl, Heinzelmann-Schwarz, Viola, Monnerat, Christian, Probst-Hensch, Nicole, Rabaglio, Manuela, Zürrer-Härdi, Ursina, Chappuis, Pierre Olivier, Katapodi, Maria C, On Behalf Of The Cascade Consortium
Published in Cancers (23.03.2022)
Published in Cancers (23.03.2022)
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Relatives from Hereditary Breast and Ovarian Cancer and Lynch Syndrome Families Forgoing Genetic Testing: Findings from the Swiss CASCADE Cohort
Sarki, Mahesh, Ming, Chang, Aceti, Monica, Fink, Günther, Aissaoui, Souria, Bürki, Nicole, Graffeo, Rossella, Heinimann, Karl, Caiata Zufferey, Maria, Monnerat, Christian, Rabaglio, Manuela, Zürrer-Härdi, Ursina, Chappuis, Pierre O., Katapodi, Maria C.
Published in Journal of personalized medicine (19.10.2022)
Published in Journal of personalized medicine (19.10.2022)
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Elaboration of EQID tool for digestive cancer predisposition
Aissaoui, Souria, Pinson, Stéphane, Giraud, Sophie, Raymond, Marisa, Sobol, Hagay, Calender, Alain
Published in Cancer Archives (2019)
Published in Cancer Archives (2019)
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Predicting Openness of Communication in Families With Hereditary Breast and Ovarian Cancer Syndrome: Natural Language Processing Analysis
Baroutsou, Vasiliki, Cerqueira Gonzalez Pena, Rodrigo, Schweighoffer, Reka, Caiata-Zufferey, Maria, Kim, Sue, Hesse-Biber, Sharlene, Ciorba, Florina M, Lauer, Gerhard, Katapodi, Maria
Published in JMIR formative research (19.01.2023)
Published in JMIR formative research (19.01.2023)
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Development of multidisciplinary committees for decision making and care management in hereditary colon cancer: the French state of the art
Aissaoui, Souria, Aissaoui, Hanaa, Giraud, Sophie, Pinson, Stéphane, Calender, Alain
Published in Journal of community genetics (01.04.2014)
Published in Journal of community genetics (01.04.2014)
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Genetic mutation risk calculation in Lynch syndrome inheritance: Evaluating the utility of the PREMM 1,2,6 model in Lyon: The first French study
Aissaoui, Souria, Cartellier, Charline, Seytier, Thomas, Giraud, Sophie, Calender, Alain
Published in Bulletin du cancer (01.03.2017)
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Published in Bulletin du cancer (01.03.2017)
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