| A dystroglycan mutation associated with limb-girdle muscular dystrophy Y Hara, B Balci-Hayta, T Yoshida-Moriguchi, M Kanagawa, ... New England Journal of Medicine 364 (10), 939-946, 2011 | 286 | 2011 |
| Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophy H Gundesli, B Talim, P Korkusuz, B Balci-Hayta, S Cirak, NA Akarsu, ... The American Journal of Human Genetics 87 (6), 834-841, 2010 | 127 | 2010 |
| Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: a novel gene related to nuclear envelopathies G Kayman-Kurekci, B Talim, P Korkusuz, N Sayar, T Sarioglu, I Oncel, ... Neuromuscular Disorders 24 (7), 624-633, 2014 | 83 | 2014 |
| A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathies N Cetin, B Balci-Hayta, H Gundesli, P Korkusuz, N Purali, B Talim, E Tan, ... Journal of medical genetics 50 (7), 437-443, 2013 | 81 | 2013 |
| Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2H M Cossée, C Lagier-Tourenne, C Seguela, M Mohr, F Leturcq, H Gundesli, ... Neuromuscular Disorders 19 (4), 255-260, 2009 | 40 | 2009 |
| Eosinophilic myositis in calpainopathy: Could immunosuppression of the eosinophilic myositis alter the early natural course of the dystrophic disease? PS Oflazer, H Gundesli, S Zorludemir, T Sabuncu, P Dincer Neuromuscular Disorders 19 (4), 261-263, 2009 | 19 | 2009 |
| Distribution of Enterobius vermicularis among the schoolchildren of two primary schools with different social-economic status in the Ankara province C Hazir, H Gündeşli, A Ozkirim, N Keskin Turkiye Parazitolojii Dergisi 33 (1), 54-58, 2009 | 15 | 2009 |
| Ankara’da Farklı Sosyoekonomik Düzeye Sahip İki İlköğretim Okulu Öğrencileri Arasında Enterobius vermicularis’ in Dağılımı C Hazır, H Gündeşli, A Özkırım, N Keskin Turkiye Parazitol Derg 33 (1), 54-58, 2009 | 12 | 2009 |
| Pitfall of identifying a disease locus by using low-resolution SNP arrays H Gundesli, S Cirak, P Dincer Journal of molecular and genetic medicine: an international journal of …, 2011 | 4 | 2011 |
| Lithium Has Neuroprotective Effect On Neuroblastoma Cell Line In Low Dosages Ş Güran, Z Çoban, H Gündeşli, Ö Kılıçarslan Cumhuriyet Medical Journal 45 (1), 17-24, 2023 | 1 | 2023 |
| The Versatility of Plectin in Cancer: A Pan-Cancer Analysis on Potential Diagnostic and Prognostic Impacts of Plectin Isoforms H Gundesli, M Kori, KY Arga OMICS: A Journal of Integrative Biology 27 (6), 281-296, 2023 | | 2023 |
| 11. EVALUATION OF ENDOMETRIAL Bcl-2 EXPRESSION AND Ki-67 PROLIFERATIVE INDEX IN INFERTILE PATIENTS WITH AND WITHOUT POLYCYSTIC OVARY SYNDROME A Çalı, R Aslan, C Çelik, A Alim, Ş Güran, Z Çoban, H Gündeşli, ... | | 2023 |
| Uptake of high-dose folic acid decreases cell viability and proliferation via JAK/STAT pathway in human prostate cancer cells Ş Güran, ZD Çoban, H Gündeşli | | 2023 |
| O. 23 A novel desmin mutation causes autosomal recessive limb girdle muscular dystrophy without features of myofibrillar myopathy N Cetin, B Balci-Hayta, H Gundesli, P Korkusuz, N Purali, B Talim, E Tan, ... Neuromuscular Disorders 23 (9), 851-852, 2013 | | 2013 |
| D/BMD, LGMD2 ve Distroglikanopatilerde Moleküler Genetik Çalışmalar BB HAYTA, H GÜNDEŞLİ, P DİNÇER Turkiye Klinikleri Neurology-Special Topics 3 (2), 22-27, 2010 | | 2010 |
| GP 4.13 Mutation screening of CAPN3 gene in 13 Turkish LGMD2A patients H Gündesli, B Balci, B Talim, H Topaloglu, P Dincer Neuromuscular Disorders 17 (9), 791, 2007 | | 2007 |
