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A. Berdeli · SciRah

Researcher profile · Semantic Scholar

A. Berdeli

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A. Berdeli — researcher profile on SciRah

h-index: 35
Works: 276
Citations: 4,233

Most-cited papers

Inflammasomes and their regulation in periodontal disease: A review.
K. Aral, M. Milward, Y. Kapila, A. Berdeli +1 more
2020Journal of Periodontal Research57 citations Open access
Semantic Scholar
University of Birmingham Differential expression of inflammasome regulatory transcripts in periodontal disease
K. Aral, Eynar Berdeli, Paul R. Cooper, Michael R. Milward +4 more
201951 citations
Semantic Scholar
Advillin acts upstream of phospholipase C ε1 in steroid-resistant nephrotic syndrome
Jia Rao, S. Ashraf, Wei-Zhen Tan, A. T. van der Ven +33 more
2017Journal of Clinical Investigation51 citations Open access
Semantic Scholar
Matrix metalloproteinase (MMP)-8 and tissue inhibitor of MMP-1 (TIMP-1) gene polymorphisms in generalized aggressive periodontitis: gingival crevicular fluid MMP-8 and TIMP-1 levels and outcome of periodontal therapy.
G. Emingil, B. Han, Ali Gürkan, A. Berdeli +6 more
2014The Journal of Periodontology36 citations
Semantic Scholar
TBC1D8B Mutations Implicate RAB11-Dependent Vesicular Trafficking in the Pathogenesis of Nephrotic Syndrome.
Lina L. Kampf, Ronen Schneider, Lea Gerstner, Roland Thünauer +19 more
2019Journal of the American Society of Nephrology33 citations Open access
Semantic Scholar
Prevalence and risk factors of sarcopenia in elderly nursing home residents
P. Tasar, S. Şahin, E. Karaman, M. Ulusoy +3 more
201528 citations
Semantic Scholar
Association of Interleukin-6 −174 G>C Promoter Polymorphism with Increased Risk of Type 2 Diabetes Mellitus Patients with Diabetic Nephropathy in Turkey
M. Karadeniz, M. Erdoğan, A. Berdeli, C. Yılmaz
2014Genetic Testing and Molecular Biomarkers28 citations
Semantic Scholar
Blau Syndrome and Early-Onset Sarcoidosis: A Six Case Series and Review of the Literature.
A. Kısaarslan, B. Sözeri, Nihal Şahin, S. Çiçek +6 more
2020Archives of Rheumatology25 citations Open access
Semantic Scholar
Effects of colchicine on gingival inflammation, apoptosis, and alveolar bone loss in experimental periodontitis
Cüneyt Asım Aral, K. Aral, A. Yay, Özge Özçoban +2 more
2018The Journal of Periodontology24 citations
Semantic Scholar
A novel mutation of interleukin-1 receptor antagonist (IL1RN) in a DIRA patient from Turkey: Diagnosis and treatment.
B. Sözeri, B. Gerceker-Turk, Başak Yıldız-Atıkan, S. Mir +1 more
2018Turkish Journal of Pediatrics22 citations Open access
Semantic Scholar
Treatment of familial mediterranean fever with canakinumab in patients who are unresponsive to colchicine
A. Berdeli, Özgür Şenol, Gamze Talay
2019European Journal of Rheumatology20 citations Open access
Semantic Scholar
Development of a medication adherence scale for familial Mediterranean fever (MASIF) in a cohort of Turkish children.
Ş. Yeşilkaya, C. Acikel, B. Fidanci, A. Polat +28 more
2015Clinical and Experimental Rheumatology19 citations
Semantic Scholar
MEFV gene allele frequency and genotype distribution in 3230 patients' analyses by next generation sequencing methods.
Berkay Kırnaz, Y. Gezgin, A. Berdeli
2022Gene17 citations
Semantic Scholar
Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA‐2; PLCG2): Striking clinical phenotypic overlap and difference
N. Kutukculer, E. Topyıldız, A. Berdeli, Burcu Guven Bilgin +5 more
2020Clinical Case Reports16 citations Open access
Semantic Scholar
Familial Mediterranean fever in children from the Aegean region of Turkey: gene mutation frequencies and phenotype-genotype correlation.
E. Yılmaz, N. Dinçel, B. Sözeri, K. Ozdemir +3 more
2015Turkish Journal of Medical Sciences16 citations
Semantic Scholar
Can Urinary Nerve Growth Factor and Brain-Derived Neurotrophic Factor be used in the Diagnosis and Follow-Up of Voiding Dysfunction in Children?
Kadriye Özdemir, N. Dinçel, A. Berdeli, S. Mir
2016Urologia Journal14 citations
Semantic Scholar
Fas/FasL gene polymorphism in patients with Hashimoto’s thyroiditis in Turkish population
Mehmet Erdogan, Mustafa Kulaksizoglu, Sencer Ganidağlı, A. Berdeli
2016Journal of Endocrinological Investigation14 citations
Semantic Scholar
Effects of bodybuilding and protein supplements in saliva, gingival crevicular fluid, and serum.
K. Aral, Eynar Berdeli, Cüneyt Asım Aral, A. Berdeli +1 more
2017Journal of Oral Science11 citations Open access
Semantic Scholar
The relationship of Interleukin-6 -174 G>C gene polymorphism in type 2 diabetic patients with and without diabetic foot ulcers in Turkish population.
M. Erdoğan, M. Kulaksızoğlu, S. Solmaz, A. Berdeli
2017The Foot10 citations
Semantic Scholar
Efficacy and safety of eculizumab in adult patients with atypical hemolytic uremic syndrome: A single center experience from Turkey.
F. Gediz, B. Payzin, S. Ecemiş, Naile Güler +3 more
2016Transfusion and Apheresis Science10 citations
Semantic Scholar
Prevalence and significance of MEFV gene mutations in patients with gouty arthritis
A. Karaarslan, Ş. Kobak, I. Kaya, Nazım Intepe +2 more
2016Rheumatology International8 citations
Semantic Scholar
Val2Ala mutation in the Atp6v0a4 gene causes early-onset sensorineural hearing loss in children with recessive distal renal tubular acidosis: a case report
Engin Kose, Seda Sirin Kose, C. Alparslan, Belde Kasap Demir +4 more
2014Renal Failure8 citations Open access
Semantic Scholar
Effects of 15-Lipoxygenase Overexpressing Adipose Tissue Mesenchymal Stem Cells on The Th17 / Treg Plasticity.
Alper Tunga Özdemir, A. Nalbantsoy, Rabia Bilge Özgül Özdemir, A. Berdeli
2021Prostaglandins & other lipid mediators7 citations
Semantic Scholar
FAS/FASL gene polymorphisms in Turkish patients with chronic myeloproliferative disorders
Fusun Ozdemirkiran, S. Nalbantoğlu, Z. Gokgoz, B. Payzin +3 more
2016Archives of medical science : AMS7 citations Open access
Semantic Scholar
Myostatin Gene Polymorphism in an Elderly Sarcopenic Turkish Population
Pınar Tosun Taşar, S. Şahin, Emine Karaman, A. Oz +4 more
2015Genetic Testing and Molecular Biomarkers7 citations
Semantic Scholar
MAPK pathway and NIS in B-CPAP human papillary thyroid carcinoma cells treated with resveratrol.
Gokcen Unal Kocabas, Asli Kisim Blatti, A. Berdeli, A. Ozgen +1 more
2024Pathology, Research and Practice6 citations
Semantic Scholar
Next-Generation Sequencing Analysis of MVK, NLRP3, TNFRSF1A, and PSTPIP1 Genes in Patients without MEFV Gene Variation and Genotype–Phenotype Correlation
Gamze Vuran, A. Berdeli
2022European Journal of Rheumatology6 citations Open access
Semantic Scholar
NPHS2 gene mutations in azerbaijani children with steroid-resistant nephrotic syndrome
R. Baylarov, O. Senol, M. Atan, A. Berdeli
2020Saudi Journal of Kidney Diseases and Transplantation6 citations Open access
Semantic Scholar
Prevalence and significance of MEFV gene mutations in patients with sarcoidosis
F. Sever, Ş. Kobak, O. Goksel, T. Goksel +2 more
2016Scandinavian Journal of Rheumatology6 citations
Semantic Scholar
Congenital nephrotic syndrome of NPHS1 associated with cardiac malformation
Berfin Uysal, O. Dönmez, F. Uysal, Okan Akacı +2 more
2015Pediatrics International6 citations
Semantic Scholar
Evaluation of development of subclinical atherosclerosis in children with uveitis
S. Conkar, Suzan Guvenyilmaz, I. Ö. Koska, A. Berdeli +1 more
2018Clinical Rheumatology5 citations
Semantic Scholar
A newborn with pertussis accompanying nephrotic syndrome.
Münevver Kaynak-Türkmen, Fulya Cengiz-Erdem, F. Sönmez, I. Girisgen +2 more
2014Turkish Journal of Pediatrics5 citations Open access
Semantic Scholar
The effects of mesenchymal stem cells on the IDO, HLA-G and PD-L1 expression of breast tumor cells MDA-MB-231 and MCF-7
Rabia Bilge Özgül Özdemir, Alper Tunga Özdemir, C. Kırmaz, M. Tuğlu +3 more
2019Archives of Clinical and Experimental Medicine4 citations Open access
Semantic Scholar
Recombinase Activating Gene 1 Deficiencies Without Omenn Syndrome May Also Present With Eosinophilia and Bone Marrow Fibrosis
Ezgi Ulusoy, N. Karaca, E. Azarsız, A. Berdeli +2 more
2016Journal of Clinical Medicine Research4 citations Open access
Semantic Scholar
Demographic and clinical characteristics of children with autosomal dominant polycystic kidney disease: a single center experience
Belde Kasap Demir, Fatma Mutlubaş, Eren Soyaltın, C. Alparslan +5 more
2020Turkish Journal of Medical Sciences3 citations Open access
Semantic Scholar
Genetics and outcome of atypical hemolytic-uremic syndrome in Turkish children: a retrospective study between 2010 and 2017, a single-center experience.
S. Conkar, S. Mir, A. Berdeli
2019Iranian Journal of Kidney Diseases3 citations
Semantic Scholar
NPHS2 gene sequencing results in children of the Azerbaijani population with different types of nephrotic syndrome caused by chronic glomerulonephritis
R. Baylarov, R. Baylarova, A. Berdeli, R. Bayramov +1 more
2019Bratislava Medical Journal3 citations Open access
Semantic Scholar
Distribution of nucleotide variants in the DNA sequence of ERCC1 and XRCC1 genes and the effect of phenotype in patients with gastric cancer.
Elmir Asgerov, Özgür Şenol, Adem Güler, A. Berdeli
2019The Turkish Journal of Gastroenterology3 citations Open access
Semantic Scholar
Novel HCK-associated mutation causing autoinflammatory disorder with pulmonary manifestations in a pediatric patient
A. Berdeli, S. Ismayilova, Nida Gürbüz
2025Pediatric Rheumatology Online Journal2 citations Open access
Semantic Scholar
Analysis of IL-1β, TGF-β, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis
Raziye Burcu Taşkın, İlyas Aydın, G. Aytaç, Süleyman İmamoğlu +6 more
2023Molecular Biology Reports2 citations Open access
Semantic Scholar
Long-term follow-up of alkaptonuria patients: single center experience
A. E. Bozacı, Havva Yazıcı, E. Canda, S. K. Uçar +4 more
2022Journal of Pediatric Endocrinology & Metabolism (JPEM)2 citations
Semantic Scholar
Fever-induced Brugada syndrome in a 9-year-old boy presenting with acute chest pain.
G. E. Besli, S. Yıldırım, I. Akalın, Y. Ayhan +2 more
2018Turkish Journal of Pediatrics2 citations Open access
Semantic Scholar
Severe Hyper IgD Syndrome Associated with Heterozygote S52N Mevalonate Kinase Mutation
M. Çeliksoy, A. Berdeli, A. Comba, G. Çaltepe +1 more
20172 citations
Semantic Scholar
Significant Association of Mediterranean Fever Gene Mutations with Acute Rheumatic Fever International Journal of Autoimmune Disorders & Therapy
S. Nalbantoğlu, Buket Dogrusöz, E. Levent, Ruhi Özyurek +1 more
20162 citations
Semantic Scholar
Role of Toll-Like Receptors in Tuberculosis Infection
Oguz Oben Biyikli, A. Baysak, G. Ece, A. Oz +2 more
2016Jundishapur Journal of Microbiology2 citations Open access
Semantic Scholar
MEFV gene mutation distrubution in Azerbaijan population
A. Berdeli, G. Mukhtarova, A. Oz, S. Musayev
2015Pediatric Rheumatology Online Journal2 citations Open access
Semantic Scholar
The predictive value of urinary UPIb mRNA levels in VUR and recurrent urinary tract infections.
I. Bulut, S. Mir, A. Berdeli, B. Sozeri
2014Clinical Nephrology2 citations
Semantic Scholar
Validity and reliability of medication adherence scale in FMF (adult version)
B. Fidanci, Ş. Yeşilkaya, C. Acikel, A. Ozden +20 more
2014Pediatric Rheumatology Online Journal2 citations Open access
Semantic Scholar
A Case With Congenital Nephrotic Syndrome Having E117K Mutation: Is This a Polymorphism? or Mutation?
Ebru YÄ-lmaz, N. Dinçel, Gözde Gözüolu, Kadriye Özdemir +2 more
20142 citations Open access
Semantic Scholar
Exploring the role of NOD2 variants in pediatric undifferentiated recurrent fever: a clinical and functional perspective
Raziye Burcu Taşkın, Arzum Hande Kamiloğlu, Busra Bara, G. Akyol +7 more
2025Frontiers in Immunology1 citations
Semantic Scholar

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