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Sezin Yakut

Observed names: S Yakut, S. Yakut, SEZİN YAKUT, Sezin Yakut Uzuner, Sezin Yakut-Uzuner, Yakut, S
ORCID: 0000-0002-9540-5099
Observed ORCID: 0000-0002-9540-5099
OpenAlex ID: A5081092338
A familial interstitial 4q35 deletion with no discernible clinical effects
2015 · Sezin Yakut, Ozden Altiok Clarck, et al. · American Journal of Medical Genetics Part A · 44
Pure and complete 12p trisomy due to a maternal centric fission of chromosome 12
2011 · Zafer Cetin, Ercan Mihci, et al. · American Journal of Medical Genetics Part A · 38
Prenatal management, pregnancy and pediatric outcomes in fetuses with septated cystic hygroma
2014 · C.Y. Sanhal, I. Mendilcioglu, et al. · Brazilian Journal of Medical and Biological Research · 27
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Chromosome abnormalities identified in 457 spontaneous abortions and their histopathological findings
2015 · Sezin Yakut, Havva Serap Toru, et al. · Turkish Journal of Pathology · 16
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Prenatal Diagnosis of β-Thalassemia and Other Hemoglobinopathies in Southwestern Turkey
2011 · Inanc Mendilcioglu, Sezin Yakut, et al. · Hemoglobin · 15
Microwave-assisted biofabrication of silver nanoparticles using Helichrysum arenarium flower extract: characterization and biomedical applications
2023 · Cigdem Aydin Acar, Suray Pehlivanoglu, et al. · Biomass Conversion and Biorefinery · 13
Telomere‐specific fluorescence in situ hybridization analysis of couples with five or more recurrent miscarriages
2002 · S Yakut, S Berker‐Karaüzüm, et al. · Clinical Genetics · 12
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A 5q12.1–5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement
2012 · Zafer Cetin, Sezin Yakut, et al. · Gene · 11
Exceptional complex chromosomal rearrangement and microdeletions at the 4q22.3q23 and 14q31.1q31.3 regions in a patient with azoospermia
2012 · Sezin Yakut, Zafer Cetin, et al. · Gene · 10
Effect of Ultrasound Therapy on Expression of Vascular Endothelial Growth Factor, Vascular Endothelial Growth Factor Receptors, CD31 and Functional Recovery After Facial Nerve Injury
2022 · Arzu Hizay, Umut Ozsoy, et al. · Ultrasound in Medicine & Biology · 8
We can diagnose it if we consider it. diagnostic pitfall for placenta: placental mesenchymal dysplasia
2015 · Havva Serap Toru, Esra Cobankent Aytekin, et al. · Turkish Journal of Pathology · 7
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A patient with Down syndrome with a de novo derivative chromosome 21
2012 · Zafer Cetin, Sezin Yakut, et al. · Gene · 7
Investigation of the relationship between reproductive disorders and chromosomal abnormalities in a large-scale, single-center 10-year retrospective study
2022 · Mustafa Gokhan Ertosun, Duygu Gamze Araci, et al. · Journal of Gynecology Obstetrics and Human Reproduction · 6
Rare structural chromosomal abnormalities in prenatal diagnosis; clinical and cytogenetic findings on 10125 prenatal cases
2014 · Sezin Yakut, Zafer Cetin, et al. · Turkish Journal of Pathology · 6
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Mosaic Intrachromosomal Triplication of (12)(p11.2p13) in a Patient with Pallister-Killian Syndrome
2012 · S Yakut, E Mıhcı, et al. · Balkan Journal of Medical Genetics · 6
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Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)
2011 · Z Cetin, I Mendilcioglu, et al. · Balkan Journal of Medical Genetics · 5
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Maternal origin and clinical findings in a case with trisomy 22
2007 · Ercan Mıhçı, Şükran Taçoy, et al. · The Turkish Journal of Pediatrics · 5
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M-FISH applications in clinical genetics.
2005 · Z Cetin, S Berker Karaüzüm, et al. · PubMed · 5
Aberrations of Chromosomes 9 and 22 in Acute Lymphoblastic Leukemia Cases Detected by ES-Fluorescence In Situ Hybridization
2012 · Zafer Cetin, Sezin Yakut, et al. · Genetic Testing and Molecular Biomarkers · 4
Del (18p) syndrome with increased nuchal translucency revealed in prenatal diagnosis
2011 · Yakut, S, Simsek, M, et al. · PubMed · 4
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Prenatal diagnosis of a de novo supernumerary marker chromosome originating from chromosome 16.
2009 · S Yakut, Z Cetin, et al. · PubMed · 4
A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOMPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES.
2016 · Z Cetin, O Altiok-Clark, et al. · PubMed · 3
Is intermediate risk really intermediate? Comparison of karyotype and non‐invasive prenatal testing results of pregnancies at intermediate risk of trisomy 21 on maternal serum screening
2024 · Gul Alkan Bulbul, Emine Kirtis, et al. · Journal of Genetic Counseling · 2
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Absence of the SLC22A12 gene mutation in Turkish population with primary gout disease
2012 · Sezin Yakut, Zafer Cetin, et al. · Rheumatology International · 2
The prenatal diagnosis of familial satellited Yq chromosomes
2011 · SEZİN YAKUT, SAFFET ÖZTÜRK, et al. · TURKISH JOURNAL OF MEDICAL SCIENCES · 2
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Works count: 45
Citation count: 275
H-index: 9
I10-index: 9
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