| 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 | 285 | 2011 |
| An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker–Warburg syndrome (WWS) caused by a mutation in the POMT1 gene B Balci, G Uyanik, P Dincer, C Gross, T Willer, B Talim, G Haliloglu, ... Neuromuscular Disorders 15 (4), 271-275, 2005 | 201 | 2005 |
| Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins. I Richard, L Brenguier, P Dincer, C Roudaut, B Bady, JM Burgunder, ... American journal of human genetics 60 (5), 1128, 1997 | 141 | 1997 |
| A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey P Dincer, F Leturcq, I Richard, F Piccolo, D Yalnizoàlu, C De Toma, ... Annals of Neurology: Official Journal of the American Neurological …, 1997 | 133 | 1997 |
| 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 |
| A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of α-dystroglycan P Dinçer, B Balcı, Y Yuva, B Talim, M Brockington, D Dinçel, S Torelli, ... Neuromuscular Disorders 13 (10), 771-778, 2003 | 64 | 2003 |
| Calpain-3 deficiency causes a mild muscular dystrophy in childhood H Topaloǧlu, P Dincer, I Richard, Z Akçören, D Alehan, Ş Özme, ... Neuropediatrics 28 (04), 212-216, 1997 | 56 | 1997 |
| Calpain-3 mutations in Turkey B Balci, S Aurino, G Haliloglu, B Talim, S Erdem, Z Akcören, E Tan, ... European journal of pediatrics 165, 293-298, 2006 | 55 | 2006 |
| A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families P Dinçer, Z Akçören, E Demir, I Richard, Ö Sancak, G Kale, S Özme, ... Journal of medical genetics 37 (5), 361-367, 2000 | 42 | 2000 |
| A homozygous nonsense mutation in δ-sarcoglycan exon 3 in a case of LGMD2F P Dincer, CG Bönnemann, ÖE Aker, Z Akçören, V Nigro, LM Kunkel, ... Neuromuscular Disorders 10 (4-5), 247-250, 2000 | 28 | 2000 |
| Efficient transfection of mouse‐derived C2C12 myoblasts using a matrigel basement membrane matrix B Balcı, P Dinçer Biotechnology Journal: Healthcare Nutrition Technology 4 (7), 1042-1045, 2009 | 23 | 2009 |
| Tedavi yaklaşımlarında yeni bir dönem: Kodlamayan RNA’lar ve hastalıklar Z AKKAYA, P DİnÇer Marmara Medical Journal 26 (1), 5-10, 2013 | 19 | 2013 |
| 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 |
| Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients P Dinçer, H Topalogˇlu, Ş Ayter, M Özgüç, HA Tas, Y Renda Brain and Development 18 (2), 91-94, 1996 | 19 | 1996 |
| Knockout of zebrafish desmin genes does not cause skeletal muscle degeneration but alters calcium flux G Kayman Kürekçi, E Kural Mangit, C Koyunlar, S Unsal, B Saglam, ... Scientific reports 11 (1), 7505, 2021 | 18 | 2021 |
| Identification of muscle-specific calpain and β-sarcoglycan genes in progressive autosomal recessive muscular dystrophies JS Beckmann, I Richard, O Broux, F Fougerousse, V Allamand, ... Neuromuscular Disorders 6 (6), 455-462, 1996 | 18 | 1996 |
| Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6 FY Tuncay, GK Kurekci, SG Ergun, OT Pasaoglu, RF Akata, PR Dincer Molecular Vision 22, 1267, 2016 | 17 | 2016 |
| Higher angiotensin II type 1 receptor levels and activity in the postmortem brains of older persons with Alzheimer’s dementia C Cosarderelioglu, LS Nidadavolu, CJ George, R Marx-Rattner, L Powell, ... The Journals of Gerontology: Series A 77 (4), 664-672, 2022 | 14 | 2022 |
