| Interleukin 1 activates STAT3/nuclear factor-κB cross-talk via a unique TRAF6-and p65-dependent mechanism Y Yoshida, A Kumar, Y Koyama, H Peng, A Arman, JA Boch, PE Auron Journal of Biological Chemistry 279 (3), 1768-1776, 2004 | 164 | 2004 |
| Interleukin-1 receptor antagonist (IL-1RN) and interleukin-1B gene polymorphisms in Turkish patients with rheumatoid arthritis A Arman, B Yilmaz, A Coker, N Inanc, H Direskeneli Clin Exp Rheumatol 24 (6), 643-8, 2006 | 52 | 2006 |
| Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features A Arman, A Bereket, A Coker, PÖŞ Kiper, T Güran, B Özkan, Z Atay, ... Orphanet journal of rare diseases 9, 1-8, 2014 | 49 | 2014 |
| Interleukin-1 receptor antagonist gene VNTR polymorphism is associated with coronary artery disease A Arman, O Soylu, A Yildirim, A Furman, N Ercelen, H Aydogan, A Coker, ... Arquivos brasileiros de cardiologia 91, 293-298, 2008 | 44 | 2008 |
| Assessment of Interleukin‐1 Gene Cluster Polymorphisms in Lone Atrial Fibrillation: New Insight into the Role of Inflammation in Atrial Fibrillation B Gungor, A Ekmekci, A Arman, KS Ozcan, E Ucer, AT Alper, N Calik, ... Pacing and Clinical Electrophysiology 36 (10), 1220-1227, 2013 | 43 | 2013 |
| Lack of association between IL-6 gene polymorphisms and rheumatoid arthritis in Turkish population A Arman, A Coker, O Sarioz, N Inanc, H Direskeneli Rheumatology international 32, 2199-2201, 2012 | 31 | 2012 |
| Multiple sclerosis: association with the interleukin-1 gene family polymorphisms in the Turkish population N Isik, A Arman, IA Canturk, AC Gurkan, F Candan, S Aktan, N Erzaim, ... International Journal of Neuroscience 123 (10), 711-718, 2013 | 24 | 2013 |
| Association between sporadic Parkinson disease and interleukin-1β-511 gene polymorphisms in the Turkish population A Arman, N Isık, A Coker, F Candan, KS Becit, EO List European cytokine network 21 (2), 116-121, 2010 | 23 | 2010 |
| Interleukin-1B (-511) gene polymorphism is associated with acute coronary syndrome in the Turkish population O Soylu, A Yildirim, A Coker, T Tezel, EO List, A Arman European cytokine network 19 (1), 42-48, 2008 | 20 | 2008 |
| Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency A Turkyilmaz, C Alavanda, EA Ates, BB Geckinli, H Polat, M Gokcu, ... Journal of Assisted Reproduction and Genetics 39 (3), 695-710, 2022 | 14 | 2022 |
| Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium M Dundar, U Fahrioglu, SH Yildiz, B Bakir-Gungor, SG Temel, H Akin, ... Functional & integrative genomics 22 (3), 291-315, 2022 | 12 | 2022 |
| Novel growth hormone-releasing hormone receptor gene mutations in Turkish children with isolated growth hormone deficiency A Arman, BN Dündar, E Çetinkaya, N Erzaim, A Büyükgebiz Journal of Clinical Research in Pediatric Endocrinology 6 (4), 202, 2014 | 10 | 2014 |
| Novel growth hormone receptor gene mutation in a patient with Laron syndrome A Arman, B Yüksel, A Coker, O Sarioz, F Temiz, AK Topaloglu Walter de Gruyter GmbH & Co. KG 23 (4), 407-414, 2010 | 10 | 2010 |
| Novel splice site mutation in the growth hormone receptor gene in Turkish patients with Laron-type dwarfism A Arman, A Ozon, PS Isguven, A Coker, I Peker, N Yordam Journal of Pediatric Endocrinology and Metabolism 21 (1), 47-58, 2008 | 10 | 2008 |
| Interleukin 1 (IL-1) induces the activation of Stat3 A Arman, PE Auron Tissue Engineering, Stem Cells, and Gene Therapies, 297-307, 2003 | 10 | 2003 |
| Secondary findings in 622 Turkish clinical exome sequencing data E Arslan Ateş, A Türkyilmaz, Ö Yıldırım, C Alavanda, H Polat, Ş Demir, ... Journal of Human Genetics 66 (11), 1113-1119, 2021 | 9 | 2021 |
| Association between IL7R promoter polymorphisms and multiple sclerosis in turkish population H Simsek, H Geckin, NP Sensoz, EO List, A Arman Journal of Molecular Neuroscience 67, 38-47, 2019 | 8 | 2019 |
| Array-based comparative genomic hybridization analysis in children with developmental delay/intellectual disability A Türkyılmaz, BB Geckinli, E Tekin, EA Ates, O Yarali, AH Cebi, A Arman Balkan Journal of Medical Genetics 24 (2), 15-24, 2022 | 7 | 2022 |
| Biallelic mutations in DNAJB11 are associated with prenatal polycystic kidney disease in a Turkish family EA Ateş, A Turkyilmaz, K Delil, C Alavanda, MA Söylemez, BB Geçkinli, ... Molecular Syndromology 12 (3), 179-185, 2021 | 6 | 2021 |
| Meckel-Gruber syndrome: clinical and molecular genetic profiles in two fetuses and review of the current literature A Turkyilmaz, BB Geckinli, C Alavanda, E Arslan Ates, EE Buyukbayrak, ... Genetic testing and molecular biomarkers 25 (6), 445-451, 2021 | 6 | 2021 |
