Serdar Ceylaner (Atil Bisgin, Atıl Bisgin, Atıl Bişgin)

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 27

Top Topics

Walled Carbon Nanotubes

Genome Wide Analysis

Top Venues

Medicina (Kaunas, Lithuania)

Journal of clinical research in pediatric endocrinology

Pediatric hematology and oncology

This page only lists publications with an associated author ORCID identifier.

Publications

Alakesh Das, Suman Adhikari, Dikshita Deka, Nabajyoti Baildya, Padmavati Sahare, Antara Banerjee, Sujay Paul, Serdar Ceylaner, Surajit Pathak
An Updated Review on the Role of Nanoformulated Phytochemicals in Colorectal Cancer. Medicina (Kaunas, Lithuania) 59 (4) (2023)
Orcun Yalav, Ozge Sonmezler, Kivilcim Eren Erdogan, Ahmet Rencuzogullari, Figen Doran, Serdar Ceylaner, Ibrahim Boga
Pre-operative Neo-adjuvant Chemotherapy Related miRNAs as Key Regulators and Therapeutic Targets in Colorectal Cancer. Current aging science (2023)
Irfan Cicin, Nuri Karadurmus, Ahmet Bilici, Taha Bahsi, Mehmet Ali Nahit Şendur, Umut Demirci, Sema Sezgin Goksu, Ozlem Er, Serdar Ceylaner, Ozge Fulya Ozturk Saglam, Birkan Aver, Saadettin Kılıçkap
Genetic testing and counseling challenges in personalized breast cancer care: review article with insights from Türkiye. Future oncology (London, England) (2023)
Alakesh Das, Suman Adhikari, Dikshita Deka, Nabajyoti Baildya, Padmavati Sahare, Antara Banerjee, Sujay Paul, Serdar Ceylaner, Surajit Pathak
An Updated Review on the Role of Nanoformulated Phytochemicals in Colorectal Cancer. Medicina (Kaunas, Lithuania) 59 (4) (2023)
Şeyda Besen, Yasemin Özkale, Serdar Ceylaner, Aytul Noyan, İlknur Erol
Clinical and laboratory findings and etiologies of genetic homocystinemia: a single-center experience. Acta neurologica Belgica (2023)
Antara Banerjee, Indumathi Somasundaram, Diptimayee Das, Samatha Jain Manoj, Husaina Banu, Pavane Mitta Suresh, Sujay Paul, Serdar Ceylaner, Hong Zhang, Xiao-Feng Sun, Asim K Duttaroy, Surajit Pathak
Functional Foods: A Promising Strategy for Restoring Gut Microbiota Diversity Impacted by SARS-CoV-2 Variants. Nutrients 15 (11) (2023)
Ibrahim Boga, Sebnem Ozemri Sag, Nilgun Duman, Sevda Yesim Ozdemir, Mahmut Çerkez Ergoren, Kubilay Dalcı, Cem Mujde, Cem Kaan Parsak, Cagla Rencuzogullari, Ozge Sonmezler, Orçun Yalav, Adem Alemdar, Lamiya Aliyeva, Özlem Bozkurt, Sibel Cetintas, Erdem Cubukcu, Adem Deligonul, Berkcan Dogan, Cemre Ornek Erguzeloglu, Türkkan Evrensel, Mustafa Şehsuvar Gökgöz, Kazım Şenol, Sahsine Tolunay, Esra Akyurek, Neslihan Basgoz, Nuriye Coskun, Bilge Dundar, Figen Öztürk, Duygu Taskin, Mercan Demirtas, Murat Cag, Omer Diker, Polat Olgun, Munis Dündar, Serdar Ceylaner, Sehime Gulsun Temel
A Multicenter Study of Genotype Variation/Demographic Patterns in 2475 Individuals Including 1444 Cases With Breast Cancer in Turkey. European journal of breast health 19 (3) (2023)
Alakesh Das, Suman Adhikari, Dikshita Deka, Nabajyoti Baildya, Padmavati Sahare, Antara Banerjee, Sujay Paul, Serdar Ceylaner, Surajit Pathak
An Updated Review on the Role of Nanoformulated Phytochemicals in Colorectal Cancer. Medicina (Kaunas, Lithuania) 59 (4) (2023)
Alakesh Das, Suman Adhikari, Dikshita Deka, Nabajyoti Baildya, Padmavati Sahare, Antara Banerjee, Sujay Paul, Serdar Ceylaner, Surajit Pathak
An Updated Review on the Role of Nanoformulated Phytochemicals in Colorectal Cancer. Medicina (Kaunas, Lithuania) 59 (4) (2023)
Veysel Gök, Alper Ozcan, Sinem Ozer, Filiz Karaman, Esra Aykutlu, Ebru Yilmaz, Musa Karakukcu, Serdar Ceylaner, Ekrem Ünal
Aceruloplasminemia presenting with microcytic anemia in a Turkish boy due to a novel pathogenic variant. Pediatric hematology and oncology (2022)
Ahmet Umit Sabancı, Perihan Erkan Alkan, Cem Mujde, Hivda Ulbeği Polat, Cemre Ornek Erguzeloglu, Serdar Ceylaner, Cüneyt Özakın, Sehime Gulsun Temel
Nanobubble Ozone Stored in Hyaluronic Acid Decorated Liposomes: Antibacterial, Anti-SARS-CoV-2 Effect and Biocompatibility Tests. International journal of nanomedicine 17 (2022)
Sebile Kılavuz, Sibel Basaran, Deniz Kor, Fatma Derya Bulut, Sevcan Erdem, Hüseyin Tuğsan Ballı, Muhammed Dağkıran, Serdar Ceylaner, Halise Neslihan Onenli Mungan
Morquio A syndrome and effect of enzyme replacement therapy in different age groups of Turkish patients: a case series. Orphanet journal of rare diseases 16 (1) (2021)
Sevcan Tuğ Bozdoğan, Selim Buyukkurt, Sinem Özer, Serdar Ceylaner
Evaluation of the results of patients who applied to the Çukurova University, Medical Genetics Department for prenatal diagnosis and determination of genetic counseling principles Turkish journal of medical sciences 51 (2) (2021)
Sevcan Tug Bozdogan, Cem Mujde, Ibrahim Boga, Ozge Sonmezler, Abdullah Hanta, Cagla Rencuzogullari, Dilek Ozcan, Derya Ufuk Altintas, Serdar Ceylaner
Current Status of Genetic Diagnosis Laboratories and Frequency of Genetic Variants Associated with Cystic Fibrosis through a Newborn-Screening Program in Turkey. Genes 12 (2) (2021)
Ihsan Turan, Sevcan Erdem, Leman Damla Kotan, Semine Özdemir Dilek, Mehmet Tastan, Fatih Gurbuz, Serdar Ceylaner, Aysun Karabay Bayazıt, Ali Kemal Topaloğlu, Bilgin Yuksel
Experience with the targeted next-generation sequencing in the diagnosis of hereditary hypophosphatemic rickets. Journal of pediatric endocrinology & metabolism : JPEM 34 (5) (2021)
Mehmet Satar, Ahmet İbrahim Kurtoğlu, Hacer Yapıcıoğlu Yıldızdaş, Halise Neslihan Onenli Mungan, Ferda Ozlü, Serdar Ceylaner
Coexistence of molybdenum cofactor deficiency type A and hypertrophic pyloric stenosis, a new case. Turkish archives of pediatrics 56 (1) (2021)
Rabia Miray Kisla Ekinci, Sibel Balcı, Ahmet Hakan Erol, Dilek Karagoz, Derya Ufuk Altintas, Serdar Ceylaner
Differentiating children with familial Mediterranean fever from other recurrent fever syndromes: The utility of new Eurofever/PRINTO classification criteria. Archives of rheumatology 36 (4) (2021)
Serdar Ceylaner, Ibrahim Boga, Cihan Cetin, Selim Buyukkurt
Identification of a novel homozygous variant in the alkaline phosphate (ALPL) gene associated with hypophosphatasia. Clinical case reports 8 (9) (2020)
Rabia Miray Kisla Ekinci, İbrahim Altun, Serdar Ceylaner, Bahriye Atmis, Derya Ufuk Altintas, Sibel Balcı
Recurrent macroscopic hematuria in a pediatric patient: is it early to diagnose as having type I hereditary C2 deficiency? CEN case reports 9 (4) (2020)
Fatih Gurbuz, Murat Alkan, Gonca Çelik, Serdar Ceylaner, Necmi Çekin, Ali Kemal Topaloğlu, Ünal Zorludemir, Ayşe Avcı, Bilgin Yuksel
Gender Identity and Assignment Recommendations in Disorders of Sex Development Patients: 20 Years’ Experience and Challenges Journal of clinical research in pediatric endocrinology 12 (4) (2020)
Serdar Ceylaner, Ibrahim Boga, Orcun Yalav, Ozge Sonmezler, Sevcan Tug Bozdogan
BRCA mutation characteristics in a series of index cases of breast cancer selected independent of family history. The breast journal 25 (5) (2019)
Rabia Miray Kisla Ekinci, Sibel Balcı, Serdar Ceylaner, Hatice Ilgen Sasmaz, Goksel Leblebisatan, Faruk Incecik, Mustafa Yilmaz
A homozygote novel L451W mutation in CECR1 gene causes deficiency of adenosine deaminase 2 in a pediatric patient representing with chronic lymphoproliferation and cytopenia. Pediatric hematology and oncology 36 (6) (2019)
Serdar Ceylaner, Wen-Jian Meng, Gunnar Adell, Xiao-Feng Sun
Interaction of CD200 Overexpression on Tumor Cells with CD200R1 Overexpression on Stromal Cells: An Escape from the Host Immune Response in Rectal Cancer Patients. Journal of oncology 2019 (2019)
Volkan Çiftçi, Sebile Kılavuz, Fatma Derya Bulut, Halise Neslihan Onenli Mungan, Serdar Ceylaner, Muharrem Cem Dogan
Congenital erythropoietic porphyria with erythrodontia: A case report. International journal of paediatric dentistry 29 (4) (2019)
Rabia Miray Kisla Ekinci, Sibel Balcı, Serdar Ceylaner, Bahriye Atmis, Dilek Karagoz, Derya Ufuk Altintas, Mustafa Yilmaz
MEFV gene variants in children with Henoch-Schönlein purpura and association with clinical manifestations: a single-center Mediterranean experience. Postgraduate medicine 131 (1) (2018)
Serdar Ceylaner, Ibrahim Boga, Mustafa Yilmaz, Gulbin Bingol, Derya Altintas
The Utility of Next-Generation Sequencing for Primary Immunodeficiency Disorders: Experience from a Clinical Diagnostic Laboratory. BioMed research international 2018 (2018)
Rabia Miray Kisla Ekinci, Fatih Gurbuz, Sibel Balcı, Serdar Ceylaner, Mehmet Taştan, Bilgin Yuksel, Mustafa Yilmaz
Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in GALNT3 Gene: Experience from Southern Turkey Journal of clinical research in pediatric endocrinology 11 (1) (2018)