| 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 | 287 | 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 |
| 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 | 129 | 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 |
| Reprogramming of human umbilical cord stromal mesenchymal stem cells for myogenic differentiation and muscle repair Ç Kocaefe, D Balcı, B Balcı Hayta, A Can Stem cell reviews and reports 6, 512-522, 2010 | 70 | 2010 |
| 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 |
| A Spectrum of Clinical Findings from ALPS to CVID: Several Novel LRBA Defects D Cagdas, SO Halaçlı, Ç Tan, B Lo, PG Çetinkaya, S Esenboğa, ... Journal of clinical immunology 39, 726-738, 2019 | 56 | 2019 |
| 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 |
| Is there a heterozygote advantage for familial Mediterranean fever carriers against tuberculosis infections: speculations remain? S Ozen, B Balci, S Ozkara, A Ozcan, E Yilmaz, N Besbas, M Ozguc, ... Clinical and experimental rheumatology 20 (4; SUPP/26), S-57, 2002 | 33 | 2002 |
| Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders T Geis, T Rödl, H Topaloğlu, B Balci-Hayta, S Hinreiner, W Müller-Felber, ... Orphanet Journal of Rare Diseases 14, 1-17, 2019 | 25 | 2019 |
| 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 |
| Autoinflammation in addition to combined immunodeficiency: SLC29A3 gene defect D Çağdaş, N Sürücü, Ç Tan, B Kayaoğlu, RK Özgül, YZ Akkaya-Ulum, ... Molecular immunology 121, 28-37, 2020 | 20 | 2020 |
| Amyloidosis in Behcet's disease and familial Mediterranean fever T Akpolat, E Yilmaz, I Akpolat, M Dilek, F Karagoz, B Balci, S Ozen Rheumatology 41 (5), 592-593, 2002 | 19 | 2002 |
| Diversity in serine/threonine protein kinase-4 deficiency and review of the literature D Cagdas, SO Halacli, C Tan, S Esenboga, B Karaatmaca, PG Cetinkaya, ... The Journal of Allergy and Clinical Immunology: In Practice 9 (10), 3752 …, 2021 | 18 | 2021 |
| Microtubule-associated protein 1B dysregulates microtubule dynamics and neuronal mitochondrial transport in spinal muscular atrophy G Bora, N Hensel, S Rademacher, D Koyunoğlu, M Sunguroğlu, ... Human molecular genetics 29 (24), 3935-3944, 2020 | 18 | 2020 |
| The common miRNA signatures associated with mitochondrial dysfunction in different muscular dystrophies E Aksu-Menges, YZ Akkaya-Ulum, D Dayangac-Erden, ... The American Journal of Pathology 190 (10), 2136-2145, 2020 | 14 | 2020 |
| Identification of an ancestral haplotype of the 35delG mutation in the GJB2 (connexin 26) gene responsible for autosomal recessive non-syndromic hearing loss in families from … B Balci, FO Gerçeker, S Aksoy, G Sennaroğlu, E Kalay, L Sennaroğlu, ... The Turkish Journal of Pediatrics 47 (3), 213-221, 2005 | 13 | 2005 |
| Prenatal diagnosis of muscle‐eye‐brain disease B Balci, DJ Morris‐Rosendahl, A Celebi, B Talim, H Topaloǧlu, P Dinçer Prenatal Diagnosis: Published in Affiliation With the International Society …, 2007 | 12 | 2007 |
| Analgesic intolerance with or without bronchial asthma: is there a marker? AF Kalyoncu, G Karakaya, E Yilmaz, B Balci, A Karaduman, U Yasavul Journal of Investigational Allergology & Clinical Immunology 13 (3), 162-169, 2003 | 12 | 2003 |
