Güven Lüleci

Akdeniz University — Turkey

Biochemistry, Genetics and Molecular Biology · Life Sciences

26h-index2.4kcitations134works0.02yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(33), Prenatal Screening and Diagnostics(22), Hemoglobinopathies and Related Disorders(16), Chromosomal and Genetic Variations(12), Iron Metabolism and Disorders(12)

Publications134 total

Turkish population-based screening for first identified changes of BRCA1 and BRCA2 genes in breast and/or ovarian cancer patients
Egyptian Journal of Medical Human Genetics·2024Open Access
Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia
Molecular Cytogenetics·2018· 23 citedOpen Access
17P PERİSENTRİK İNVERSİYONLU BİR AİLE: TAŞIYICILARA UYARILAR
DergiPark (Istanbul University)·2015
The association of Klinefelter syndrome and multiple pterygium syndrome: an unusual presentation.
PubMed·2015· 2 cited
Chromosome abnormalities identified in 457 spontaneous abortions and their histopathological findings
Turkish Journal of Pathology·2015· 16 citedOpen Access
Mitochondrial ATPase Subunit 6 and Cytochrome B Gene Variations in Obese Turkish Children
Journal of Clinical Research in Pediatric Endocrinology·2014· 10 citedOpen Access
A family with a 17p: pericentric inversion: implications for carriers (Olgu Sunumu)
Dspace Repository (Marmara Üniversitesi)·2014
Assessment of women who applied for the uterine transplant project as potential candidates for uterus transplantation
Journal of obstetrics and gynaecology research·2014· 18 cited
Prenatal management, pregnancy and pediatric outcomes in fetuses with septated cystic hygroma
Brazilian Journal of Medical and Biological Research·2014· 27 citedOpen Access
Clinicogenetic Study of Turkish Patients With Syndromic Craniosynostosis and Literature Review
Pediatric Neurology·2014· 25 cited
Rare structural chromosomal abnormalities in prenatal diagnosis; clinical and cytogenetic findings on 10125 prenatal cases
Turkish Journal of Pathology·2014· 6 citedOpen Access
Mixed gonadal dysgenesis in a patient with de novo tas(Y;19)(p11.3;q13.4) and 45,X mosaicism
European Journal of Pediatrics·2013· 1 cited
Abstract 3166: Clinopathologic correlation with the LCM based instability profiles for the mitochondrial microsatellite regions in the benign to metastatic transitions of surface epithelium ovarian tumor subtypes.
Cancer Research·2013
A 5q12.1–5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement
Gene·2012· 17 cited
Novel and rare<i>CFTR</i>gene mutations in Turkish patients with congenital aplasia of vas deferens
Andrologia·2012· 1 cited
Absence of the SLC22A12 gene mutation in Turkish population with primary gout disease
Rheumatology International·2012· 2 cited
Exceptional complex chromosomal rearrangement and microdeletions at the 4q22.3q23 and 14q31.1q31.3 regions in a patient with azoospermia
Gene·2012· 15 cited
P06.05: Prenatal management, pregnancy and pediatric outcome in fetuses with septated cystic hygroma
Ultrasound in Obstetrics and Gynecology·2012· 1 citedOpen Access
A patient with Down syndrome with a de novo derivative chromosome 21
Gene·2012· 6 cited
Aberrations of Chromosomes 9 and 22 in Acute Lymphoblastic Leukemia Cases Detected by ES-Fluorescence <i>In Situ</i> Hybridization
Genetic Testing and Molecular Biomarkers·2012· 3 cited
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Frequent Co-authors

Özgül M. Alper(7), Mehmet Baykara(7), Zafer Çetin(7), Sezin Yakut(7), Salih Şanlıoğlu(6), Sibel Berker-Karaüzüm(5), İbrahim Keser(5), Sibel Berker Karaüzüm(5), Ozlem Guzeloglu‐Kayisli(4), Türker Bilgen(4), I Keser(4), İsmail Türker Köksal(4), Ahter Dilşad Şanlioğlu(4), Mehmet Şimşek(4), İnanç Mendilcioğlu(4), Umit A. Kayisli(3), Duygu Yasar(3), Esra Manguoğlu(3), Ercan Mıhçı(3), Mehmet Şımşek(3)