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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.
Scandinavian Journal of Clinical and Laboratory Investigation|April 8, 2023
Impact of <i>TP53</i> gene variants on prognosis and survival of childhood acute lymphoblastic leukemiaSinem Firtina, Yucel Erbilgin, Ozden Hatirnaz Ng, et al.
Epilepsy Research|January 17, 2016
Screening LGI1 in a cohort of 26 lateral temporal lobe epilepsy patients with auditory aura from Turkey detects a novel de novo mutationYesim F Kesim, Gunes Altiokka Uzun, Emrah Yucesan, et al.
Genetic Testing and Molecular Biomarkers|February 21, 2012
Evaluation of glutathione S-transferase P1 polymorphisms (Ile105Val and Ala114Val) in patients with small cell lung cancerBurcak Vural, Fatih Yakar, Duygu Derin, et al.
Immunogenetics|June 10, 2017
A novel pathogenic frameshift variant of CD3E gene in two T-B+ NK+ SCID patients from TurkeySinem Firtina, Yuk Yin Ng, Ozden Hatirnaz Ng, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 11, 2002
Preclinical validation of a monochrome real-time multiplex assay for translocations in childhood acute lymphoblastic leukemiaAbdul K Siraj, Ugur Ozbek, Sudha Sazawal, et al.
Molecular and Cellular Biology|March 4, 2005
The novel ETS factor TEL2 cooperates with Myc in B lymphomagenesisMonica Cardone, Ayten Kandilci, Cintia Carella, 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.
American Journal of Medical Genetics. Part A|October 11, 2024
Managing CDH1 Cancer Risks in a Child: Complex Decision Making in a Family With Hereditary Diffuse Gastric CancerNihat Bugra Agaoglu, Ozden Hatirnaz Ng, Itir Ebru Zemheri, 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.
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