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Clinical Case Reports|September 15, 2018
Identification of a BRCA2 mutation in a Turkish family with early-onset breast cancerElifnaz Celik, Kubra Ermis Tekkus, Izzet Mehmet Akcay, et al.
Investigative Ophthalmology & Visual Science|January 29, 2026
Downregulation of Cyclin Kinase Inhibitors p16INK4a and p27 in Conjunctival MelanomasEmerentienne Sarrasin, Elea Lalys, Katya Nardou, et al.
Cancers|March 25, 2022
Identification of New Vulnerabilities in Conjunctival Melanoma Using Image-Based High Content Drug ScreeningKatya Nardou, Michael Nicolas, Fabien Kuttler, et al.
International Journal of Cancer|July 14, 2020
Germline pathogenic variant spectrum in 25 cancer susceptibility genes in Turkish breast and colorectal cancer patients and elderly controlsIzzet Mehmet Akcay, Elifnaz Celik, Nihat Bugra Agaoglu, et al.
American Journal of Human Genetics|January 25, 2024
Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunctionMiriam Bauwens, Elifnaz Celik, Dinah Zur, et al.
American Journal of Human Genetics|March 26, 2024
Detection of elusive DNA copy-number variations in hereditary disease and cancer through the use of noncoding and off-target sequencing readsMathieu Quinodoz, Karolina Kaminska, Francesca Cancellieri, et al.
Biorxiv : the Preprint Server for Biology|July 15, 2025
RetiGene, a comprehensive gene atlas for inherited retinal diseases (IRDs)Mathieu Quinodoz, Elifnaz Celik, Dhryata Kamdar, et al.
American Journal of Human Genetics|September 17, 2025
RetiGene, a comprehensive gene atlas for inherited retinal diseasesCarlo Rivolta, Elifnaz Celik, Dhryata Kamdar, et al.
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