Prof. Dr. SULTAN CİNGÖZ

Yayın Ağı

Makaleler 29

1. WCN23-0159 ENPP6 IS A POTENTIAL NOVEL CANDIDATE GENE FOR MONOGENIC CONGENITAL ANOMALIES OF THE KIDNEYS AND URINARY TRACT

Mertens N., Kano K., Merz L., El Desoky S., A Kari J., Gyung Kang H., et al.

KIDNEY INTERNATIONAL REPORTS , cilt.8, sa.3, ss.242, 2023 (SCI-Expanded, Scopus)

2. Functional divergence of the two Elongator subcomplexes during neurodevelopment

Gaik M., Kojic M., Stegeman M. R., Öncü-Öner T., Kościelniak A., Jones A., et al.

EMBO MOLECULAR MEDICINE , cilt.14, sa.7, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

3. Novel biallelic variants affecting the OTU domain of the gene OTUD6B associate with severe intellectual disability syndrome and molecular dynamics simulations

Cingöz S., Soydemir D., Öner T. Ö., Karaca E., Özden B., Kurul S. H., et al.

European Journal of Medical Genetics , cilt.65, sa.6, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

4. Mutation Analysis of the AGXT Gene in Combined Liver-Kidney and Isolated Liver Transplanted Children for Primary Hyperoxaluria Type 1: a Single Center Experience

TÜRKMEN M. A., ALAYGUT D., Agilkaya S., BAYRAM M. T., DEMİR B., SOYLU A., et al.

Turkish Journal of Nephrology , cilt.31, sa.4, ss.355-362, 2022 (Scopus, TRDizin)

5. OCLN gene variants identified in three patients with severe neurodevelopmental disorder associated with epilepsy, intellectual disability and malformation of cortical development

Oner T. O., Unalp A., Hiz S., Bayram E., Kaytan I., Cingoz S.

EPILEPTIC DISORDERS , cilt.23, sa.6, ss.843-853, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

6. **GPR56 homozygous nonsense mutation p.R271*associated with phenotypic variability in bilateral frontoparietal polymicrogyria**

Oncu-Oner T., Unalp A., Porsuk-Doru I., Agilkaya S., Güleryüz Uçar H., Sarac A., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.60, sa.3, ss.229-237, 2018 (SCI-Expanded)

7. Exercise increases leptin levels correlated with IGF-1 in hippocampus and prefrontal cortex of adolescent male and female rats

Uysal Harzadın N., Agilkaya S., Sisman A., Camsari U. M., Gençoğlu C., Dayı A., et al.

JOURNAL OF CHEMICAL NEUROANATOMY , cilt.81, ss.27-33, 2017 (SCI-Expanded, Scopus)

8. Anxiety- and depression-like behavior are correlated with leptin and leptin receptor expression in prefrontal cortex of streptozotocin-induced diabetic rats

Ateş M., Dayı A., Kiray M., Sisman A., Agilkaya S., Aksu İ., et al.

BIOTECHNIC & HISTOCHEMISTRY , cilt.89, sa.3, ss.161-171, 2014 (SCI-Expanded, Scopus)

9. **Identification of the Variations in the CPT1B and CHKB Genes Along with the HLA-DQB1*06:02 Allele in Turkish Narcolepsy Patients and Healthy Persons**

CİNGÖZ S., Agilkaya S., ÖZTURA İ., Eroglu S., KARADENİZ D., Evlice A., et al.

GENETIC TESTING AND MOLECULAR BIOMARKERS , cilt.18, sa.4, ss.261-268, 2014 (SCI-Expanded, Scopus)

10. The effect of the alternative solutions to formaldehyde and xylene on tissue processing

Aydin I., YÖRÜKOĞLU K., CİNGÖZ S., Agilkaya S.

INDIAN JOURNAL OF PATHOLOGY AND MICROBIOLOGY , cilt.56, sa.3, ss.221-230, 2013 (SCI-Expanded, Scopus)

11. A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts

CİNGÖZ S., van der Luijt R. B., Kurt E., Apaydin M., Akkol I., Ozgen M. H.

FAMILIAL CANCER , cilt.12, sa.1, ss.111-117, 2013 (SCI-Expanded, Scopus)

12. Novel anti-HER2 monoclonal antibodies: synergy and antagonism with tumor necrosis factor-alpha

Ceran C., Çokol M., Cingöz S., Tasan I., Ozturk M., Yagci T.

BMC CANCER , cilt.12, 2012 (SCI-Expanded, Scopus)

13. Maternal Aerobic Exercise during Pregnancy Can Increase Spatial Learning by Affecting Leptin Expression on Offspring's Early and Late Period in Life Depending on Gender

Dayı A., Agilkaya S., Özbal S., Cetin F., Aksu İ., Gençoğlu C., et al.

SCIENTIFIC WORLD JOURNAL , 2012 (SCI-Expanded)

14. TLR Polymorphisms in FMF: Association of TLR-2 (Arg753Gln) and TLR-4 (Asp299Gly, Thre399Ile) Polymorphisms and Myeloid Cell TLR-2 and TLR-4 Expression with the Development of Secondary Amyloidosis in FMF

Soylu A., Ateş H., Cingöz S., Turkmen M., Demir B. K., Tunca M., et al.

INFLAMMATION , cilt.34, sa.5, ss.379-387, 2011 (SCI-Expanded, Scopus)

15. Interstitial Deletion of 14q24.3-q32.2 in a Male Patient With Plagiocephaly, BPES Features, Developmental Delay, and Congenital Heart Defects

CİNGÖZ S., Bache I., Bjerglund L., Ropers H., Tommerup N., Jensen H., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.155A, sa.1, ss.203-206, 2011 (SCI-Expanded, Scopus)

16. TLR-2 Arg753Gln, TLR-4 Asp299Gly, and TLR-4 Thr399Ile polymorphisms in Henoch Schonlein purpura with and without renal involvement

SOYLU A., KIZILDAĞ S., KAVUKÇU S., CİNGÖZ S., Turkmen M., Demir B. K., et al.

RHEUMATOLOGY INTERNATIONAL , cilt.30, sa.5, ss.667-670, 2010 (SCI-Expanded, Scopus)

17. A Novel Subtype of Distal Symphalangism Affecting Only the 4th Finger

Kjaer K. W., Tiner M., CİNGÖZ S., Karatosun V. A., Tommerup N., Mundlos S., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.149A, sa.7, ss.1571-1573, 2009 (SCI-Expanded, Scopus)

18. TLR-2 and TLR-4 polymorphisms and TLR-2 and TLR-4 expression in leukocytes in FMF patients with and without amyloidosis

Soylu A., Ateş H., Cingöz S., Turkmen M. A., Kasap B., Tunca M., et al.

PEDIATRIC NEPHROLOGY , cilt.23, sa.9, ss.1624, 2008 (SCI-Expanded, Scopus)

19. Evaluation of TLR-2 and TLR-4 polymorphisms in Henoch Schonlein vasculitis with and without renal involvement

SOYLU A., Kizildag S., Kavukcu S., CİNGÖZ S., Turkmen M. A., Demir B. K., et al.

PEDIATRIC NEPHROLOGY , cilt.23, sa.9, ss.1707, 2008 (SCI-Expanded, Scopus)

20. Familial pericentric inversion chromosome 3 and R448C mutation of CYP11B1 gene in Turkish kindred with 11 beta-hydroxylase deficiency

Cingöz S., Ozkan B., Doneray H., Sakizli M.

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , cilt.30, sa.4, ss.285-291, 2007 (SCI-Expanded, Scopus)

21. 4q35 deletion and 10p15 duplication associated with immunodeficiency

CİNGÖZ S., Bisgaard A. M., Bache I., Bryndorf T., Kirchoff M., Petersen W., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.140A, sa.20, ss.2231-2235, 2006 (SCI-Expanded, Scopus)

22. Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter

Sogaard M., Tumer Z., Hjalgrim H., Hahnemann J., Friis B., Ledaal P., et al.

BMC MEDICAL GENETICS , cilt.6, 2005 (SCI-Expanded, Scopus)

23. An excess of chromosome 1 breakpoints in male infertility

Bache I., Van Assche E., CİNGÖZ S., Bugge M., Tumer Z., Hjorth M., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.12, sa.12, ss.993-1000, 2004 (SCI-Expanded, Scopus)

24. DNA copy number changes detected by comparative genomic hybridization and their association with clinicopathologic parameters in breast tumors

CİNGÖZ S., Altungoz O., Canda T., Saydam S., Aksakoglu G., Sakizli M.

CANCER GENETICS AND CYTOGENETICS , cilt.145, sa.2, ss.108-114, 2003 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

25. Prognostic parameters in astrocytoma: p53 and c-erbB-2 immunoreactivity, PCNA, and AgNOR count

Koyuncuoglu M., YÜCESOY K., CİNGÖZ S., Canda M., ÇABUK M., AKTAŞ S.

Turkish Neurosurgery , cilt.9, sa.3-4, ss.85-91, 1999 (Scopus)

26. Investigation of p53, c-erbB-2, PCNA immunoreactivity, DNA content, AgNOR and apoptosis in bladder carcinoma as prognostic parameters

KOYUNCUOĞLU ÜLGÜN M., Kargi A., CİNGÖZ S., Kirkali Z.

CANCER LETTERS , cilt.126, sa.2, ss.143-148, 1998 (SCI-Expanded, Scopus)

27. Proliferating cell nuclear antigen expression in normal squamous epithelia, premalignant lesions and squamous cell carcinoma of the uterine cervix

YÖRÜKOĞLU K., Atac G., CİNGÖZ S., ÖZEN E., Koyuncuoglu M., USLU T., et al.

Annals of Medical Sciences , cilt.6, sa.1, ss.7-11, 1997 (Scopus)

28. Meme Kanserli Hastalarda CD44, P-Glikoproteini, ve P-53 Metastaz Gelişimini Yansıtabilir mi?

ALAKAVUKLAR M., KOYUNCUOĞLU ÜLGÜN M., CİNGÖZ S., DEMİRKAN H. M. B., CANDA T., ALANYALI H., et al.

Uhod-Uluslararasi Hematoloji-Onkoloji Dergisi , cilt.7, sa.2, ss.73-79, 1997 (SCI-Expanded, Scopus, TRDizin) Sürdürülebilir Kalkınma

29. Epitope retrieval technique: A simple modification that reduces staining time

Yorukoglu K., CİNGÖZ S.

APPLIED IMMUNOHISTOCHEMISTRY , cilt.5, sa.1, ss.71, 1997 (SCI-Expanded)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 14

1. OCLN GENE VARIANTS IDENTIFIED BY EXOME SEQUENCING AMONG CASES WITH NEURODEVELOPMENTAL DISORDERS

ÖNCÜ ÖNER T., ÜNALP A., BAYRAM E., HIZ A. S., Kaytan İ., CİNGÖZ S.

13. “Uluslararası Katılımlı” Ulusal Tıbbi Genetik Kongresi, 7 - 11 Kasım 2018, (Tam Metin Bildiri)

2. Nörogelişimsel bozukluğu olan olgularda tüm exom dizileme ile saptanan OCLN gen varyantları

ÖNCÜ ÖNER T., ÜNALP A., BAYRAM E., HIZ A. S., Kaytan İ., CİNGÖZ S.

Uluslararası Katılımlı XIII. Ulusal Tıbbi Genetik Kongresi, 7 - 11 Kasım 2018

3. MATERNAL INHERITED SUBMICROSCOPIC DUPLICATION IN CHROMOSOME Xq22.2 INCLUDING PLP1, GLRA4 AND MORF4L2 GENES IDENTIFIED BY ARRAY-CGH IN MALE PATIENT WITH NEURODEVELOPMENTAL DISORDERS

BAYRAM E., AĞILKAYA S., HIZ A. S., CİNGÖZ S.

13. “Uluslararası Katılımlı” Ulusal Tıbbi Genetik Kongresi, 7 - 11 Kasım 2018, (Özet Bildiri)

4. ZBTB18 Genindeki Nonsinonim SNP’lerin In Silico Analizi

ÖNCÜ ÖNER T., CİNGÖZ S.

International Conference on Data Science and Applications (ICONDATA), 4 - 07 Ekim 2018, (Özet Bildiri)

5. Bilateral frontoparietal polimikrogride fenotipik değişkenlik ile ilişkili GPR56 homozigot nonsense mutasyonu p.R271

Öner T. Ö., ÜNALP A., Doru İ. P., Ağılkaya S., GÜLERYÜZ H., Saraç A., et al.

XV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, 26 - 29 Ekim 2017, (Özet Bildiri)

6. Bilateral frontoparietal polimikrogiride fenotipik değişkenlik ile ilişkili GPR56 homozigot nonsense mutasyonu p.R271’

ÖNCÜ ÖNER T., ÜNALP A., PORSUK İ., AĞILKAYA S., GÜLERYÜZ H., SARAÇ A., et al.

XV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi (Uluslararası Katılımlı), Türkiye, 26 - 29 Ekim 2017, (Özet Bildiri)

7. Nörogelişimsel Bozukluğu Olan Hastada CLP1 Geninde Saptanan Homozigot Missense Mutasyon

ÖNCÜ ÖNER T., ÜNALP A., CİNGÖZ S.

XV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi (Uluslararası Katılımlı), Türkiye, 26 - 29 Ekim 2017, (Özet Bildiri)

8. Korpus kallozum Anormalliği Saptanan Olguların Klinik Bulgular ve Kromozomal Değişiklikler Açısından Değerlendirilmesi

BAYRAM E., Agilkaya S., Yasemin T., Pakize k., uluc y., CİNGÖZ S., et al.

16. Ulusal Çocuk Nörolojisi Kongresi, Türkiye, 22 - 27 Haziran 2015

9. MOLECULAR CHARACTERIZATION OF A FAMILIAL CHROMOSOME 9Q22.2-22.32 DELETION IN A PATIENT WITH CORPUS CALLOSUM AGENESIS AND INTRACTABLE EPILEPSY

HIZ A. S., Agilkaya S., Bayram E., CİNGÖZ S.

11th European Congress on Epileptology, Stockholm, İsveç, 29 Haziran - 03 Temmuz 2014, cilt.55, ss.79, (Özet Bildiri)

10. Human epidermal growth factor receptor 2 (HER2) testing in operable breast cancer: comparison of immunohistochemistry (IHC), fluorescent in situ hybridization (FISH), chromogenic in situ hybridization (CISH), and quantitative real-time polymerase chain reaction (qRT-PCR)

Demirkan B., CİNGÖZ S., Cavusoglu A., Kilic Y., Canda T., Sakizli M., et al.

15th Congress of the European-Cancer-Organization/34th Multidisciplinary Congress of the European-Society-for-Medical-Oncology, Berlin, Almanya, 20 - 24 Eylül 2009, cilt.7, ss.99-100, (Özet Bildiri) Sürdürülebilir Kalkınma

11. Low frequency of favorable genotypes in pediatric precursor B-cell acute lymphoblastic leukemia patients in western Turkey

Sercan H. O., Yuksel E., Kizildag S., CİNGÖZ S., Vergin C., Oren H., et al.

6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, cilt.15, ss.203, (Özet Bildiri)

Metrikler

Yayın

Yayın (WoS)

Yayın (Scopus)

Atıf (WoS)

345

H-İndeks (WoS)

Atıf (Scopus)

384

H-İndeks (Scopus)

Atıf (Scholar)

605

H-İndeks (Scholar)

Atıf (Sobiad)

H-İndeks (Sobiad)

Proje

Tez Danışmanlığı

Açık Erişim

BM Sürdürülebilir Kalkınma Amaçları

Yayınlar & Eserler