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Page 1
Homozygous variant rs2076530 of BTNL2 and familial sarcoidosis.
Coudurier M, Freymond N, Aissaoui S, Calender A, Pacheco Y, Devouassoux G. Coudurier M, et al. Among authors: aissaoui s. Sarcoidosis Vasc Diffuse Lung Dis. 2009 Jul;26(2):162-6. Sarcoidosis Vasc Diffuse Lung Dis. 2009. PMID: 20560297
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 R, Melloul M, Aissaoui S, El Harroudi T, Boukhatem N. Melki R, et al. Among authors: aissaoui s. BMC Cancer. 2023 Apr 13;23(1):339. doi: 10.1186/s12885-023-10822-5. BMC Cancer. 2023. PMID: 37055759 Free PMC article.
Relatives from Hereditary Breast and Ovarian Cancer and Lynch Syndrome Families Forgoing Genetic Testing: Findings from the Swiss CASCADE Cohort.
Sarki M, Ming C, Aceti M, Fink G, Aissaoui S, Bürki N, Graffeo R, Heinimann K, Caiata Zufferey M, Monnerat C, Rabaglio M, Zürrer-Härdi U, Chappuis PO, Katapodi MC, The Cascade Consortium. Sarki M, et al. Among authors: aissaoui s. J Pers Med. 2022 Oct 19;12(10):1740. doi: 10.3390/jpm12101740. J Pers Med. 2022. PMID: 36294879 Free PMC article.
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 M, Ming C, Aissaoui S, Bürki N, Caiata-Zufferey M, Erlanger TE, Graffeo-Galbiati R, Heinimann K, Heinzelmann-Schwarz V, Monnerat C, Probst-Hensch N, Rabaglio M, Zürrer-Härdi U, Chappuis PO, Katapodi MC, On Behalf Of The Cascade Consortium. Sarki M, et al. Among authors: aissaoui s. Cancers (Basel). 2022 Mar 23;14(7):1636. doi: 10.3390/cancers14071636. Cancers (Basel). 2022. PMID: 35406409 Free PMC article.
15 results