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Ayca Yigit

Showing results (1-10 of 6) with videos related to

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American Journal of Medical Genetics. Part A|April 6, 2026
Grange-Like Phenotype Associated With an RNF213 Pathogenic Variant: Expanding the Vasculopathy SpectrumSerife Ozturk Yilmaz, Ayca Yigit, Sevcan Hatipoglu, et al.
Frontiers in Public Health|February 6, 2025
Management of rare and undiagnosed diseases: insights from researchers and healthcare professionals in TürkiyeSinem Durmus, Emrah Yucesan, Sinem Aktug, et al.
European Journal of Human Genetics : EJHG|July 9, 2026
Integrative and systematic genomic approaches to improve diagnosis in rare and undiagnosed diseases: results from the RareBoost projectAyca Yigit, Mert Pekerbas, Baris Salman, et al.
Frontiers in Genetics|April 1, 2024
Impact of deep phenotyping: high diagnostic yield in a diverse pediatric population of 172 patients through clinical whole-genome sequencing at a single centerOzlem Akgun-Dogan, Ecenur Tuc Bengur, Beril Ay, et al.
Frontiers in Neurology|March 16, 2026
Unmasking genetic etiologies in neurodevelopmental disorders characterized by Cerebral Palsy: insights from integrative genomic approachesAyca Yigit, Ozlem Akgun-Dogan, Zeynep Ozkeserli, et al.
Frontiers in Pediatrics|July 19, 2024
Rapid genome sequencing for critically ill infants: an inaugural pilot study from TurkeyBengisu Guner Yilmaz, Ozlem Akgun-Dogan, Ozkan Ozdemir, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|April 6, 2026
Grange-Like Phenotype Associated With an RNF213 Pathogenic Variant: Expanding the Vasculopathy SpectrumSerife Ozturk Yilmaz, Ayca Yigit, Sevcan Hatipoglu, et al.
Frontiers in Public Health|February 6, 2025
Management of rare and undiagnosed diseases: insights from researchers and healthcare professionals in TürkiyeSinem Durmus, Emrah Yucesan, Sinem Aktug, et al.
European Journal of Human Genetics : EJHG|July 9, 2026
Integrative and systematic genomic approaches to improve diagnosis in rare and undiagnosed diseases: results from the RareBoost projectAyca Yigit, Mert Pekerbas, Baris Salman, et al.
Frontiers in Genetics|April 1, 2024
Impact of deep phenotyping: high diagnostic yield in a diverse pediatric population of 172 patients through clinical whole-genome sequencing at a single centerOzlem Akgun-Dogan, Ecenur Tuc Bengur, Beril Ay, et al.
Frontiers in Neurology|March 16, 2026
Unmasking genetic etiologies in neurodevelopmental disorders characterized by Cerebral Palsy: insights from integrative genomic approachesAyca Yigit, Ozlem Akgun-Dogan, Zeynep Ozkeserli, et al.
Frontiers in Pediatrics|July 19, 2024
Rapid genome sequencing for critically ill infants: an inaugural pilot study from TurkeyBengisu Guner Yilmaz, Ozlem Akgun-Dogan, Ozkan Ozdemir, et al.
Pageof 1