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Gülay Ceylaner

Observed names: Ceylaner, Gülay, G Ceylaner, G. Ceylaner, Gulay CEYLANER, Gulay Ceylaner
ORCID: 0000-0003-0648-9831
Observed ORCID: 0000-0003-0648-9831
OpenAlex ID: A5035349447
Genetic abnormalities in Turkish women with premature ovarian failure
2010 · Gulay Ceylaner, Sunduz Ozlem Altinkaya, et al. · International Journal of Gynecology & Obstetrics · 34
A Novel Mutation in the Lysyl Hydroxylase 1 Gene Causes Decreased Lysyl Hydroxylase Activity in an Ehlers–Danlos VIA Patient
2005 · Linda C. Walker, Mayra A. Overstreet, et al. · Journal of Investigative Dermatology · 23
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Extremely skewed X‐chromosome inactivation patterns in women with recurrent spontaneous abortion
2006 · Sevgi BAGISLAR, Isik USTUNER, et al. · Australian and New Zealand Journal of Obstetrics and Gynaecology · 22
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GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals
2008 · Elif Baysal, Yildirim A. Bayazit, et al. · Journal of Genetics · 19
Evaluation of 2407 fetuses in a Turkish population
2007 · Gülay Ceylaner, Serdar Ceylaner, et al. · Prenatal Diagnosis · 19
Postmortem evaluation of 220 prenatally diagnosed fetuses with neural tube defects: detection of associated anomalies in a Turkish population
2006 · Serdar Ceylaner, Gülay Ceylaner, et al. · Prenatal Diagnosis · 17
A prenatally diagnosed case of sirenomelia with polydactyly and vestigial tail.
2008 · M A Guven, M Uzel, et al. · PubMed · 13
A case of fetal anticonvulsant syndrome with severe bilateral upper limb defect
2006 · Meli˙h Atahan Guven, Cem Batukan, et al. · The Journal of Maternal-Fetal & Neonatal Medicine · 13
Fabry Disease Screening in Patients With Kidney Transplant: A Single-Center Study in Turkey
2020 · Siyar Erdogmus, Sim Kutlay, et al. · Experimental and Clinical Transplantation · 12
Nephron-sparing Surgery for Renal Cell Carcinoma of the Allograft After Renal Transplantation: Report of Two Cases
2013 · A. Tuzuner, F. Çakir, et al. · Transplantation Proceedings · 12
A new family with autosomal dominant porencephaly with a novel Col4A1 mutation. Are arachnoid cysts related to Col4A1 mutations?
2012 · A Değerliyurt, G Ceylaner, et al. · PubMed · 9
Partial trisomy due to a de novo duplication 22q11.1-22q13.1: a cat-eye syndrome variant with brain anomalies.
2010 · D Karcaaltincaba, S Ceylaner, et al. · PubMed · 8
Specific Granule Deficiency Due To Novel Homozygote SMARCD2 Variant
2022 · Zeynep Kihtir, Kıymet Çelik, et al. · Pediatric Allergy Immunology and Pulmonology · 6
The outcome of 41 Late-Diagnosed Turkish GA-1 Patients: A Candidate for the Turkish NBS
2021 · Sebile Kılavuz, Derya Bulut, et al. · Neuropediatrics · 6
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Prenatal diagnosis of a case with anencephaly-omphalocele-unilateral absent radial ray.
2009 · S Ceylaner, G Ceylaner, et al. · PubMed · 3
Neu-Laxova syndrome in an appropriate for gestational age newborn
2008 · Dilek Dilli, Handan Yasar, et al. · Indian Journal of Dermatology Venereology and Leprology · 3
Prenatal diagnosis of a Turkish Bartsocas–Papas syndrome case with upper limb pterigia
2007 · Gülay Ceylaner, Melih A. Güven, et al. · Prenatal Diagnosis · 3
Mitral valve prolapse in two siblings with pyknodysostosis.
2009 · S Senel, C Karacan, et al. · PubMed · 2
P01.43: Prenatal diagnosis of a case with EMANUEL syndrome (supernumary der (22) syndrome)
2006 · M. A. Guven, G. Ceylaner, et al. · Ultrasound in Obstetrics and Gynecology · 2
Craniosynostosis and ectopia lentis in a propositus whose parents are cousins
2005 · Dilek Güven, Defne Kalaycı, et al. · American Journal of Medical Genetics Part A · 2
Analyzing the Distribution of Mutations for Glycogen Storage Disease Type 1a in Turkey and Suggested Gene Therapy Methods for Its Treatment
2020 · Aysun Mantas, Cemre Ucaryilmaz, et al. · Preprints.org · 1
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A novel mutation in the RPS6KA3 gene in a patient with Coffin-Lowry syndrome.
2011 · S Senel, S Ceylaner, et al. · PubMed · 1
Prenatal diagnosis of a case probably with Oral-Facial-Digital Syndrome--Gabrielli type.
2009 · M A Güven, G Ceylaner, et al. · PubMed · 1
Chromosomal heteromorphisms may help for the diagnosis of uniparental disomy (UPD): a case report
2007 · Gülay Ceylaner, Serdar Ceylaner, et al. · Prenatal Diagnosis · 1
Prenatal diagnosis of Meckel Gruber syndrome presenting with renal agenesis: report of a case.
2006 · M A Guven, S Ceylaner, et al. · PubMed · 1
Works count: 44
Citation count: 235
H-index: 10
I10-index: 10
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