H. Gundesli

Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2H

M. Koenig, M. Cossée, J. Mandel, 2009, Neuromuscular Disorders.

Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophy.

P. Korkusuz, H. Topaloglu, S. Çırak, 2010, American journal of human genetics.

Eosinophilic myositis in calpainopathy: Could immunosuppression of the eosinophilic myositis alter the early natural course of the dystrophic disease?

T. Sabuncu, P. Oflazer, P. Dincer, 2009, Neuromuscular Disorders.

Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: A novel gene related to nuclear envelopathies

P. Sharafi, P. Korkusuz, H. Topaloglu, 2014, Neuromuscular Disorders.

A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathies

P. Korkusuz, E. Tan, B. Talim, 2013, Journal of Medical Genetics.

Pitfall of identifying a disease locus by using low-resolution SNP arrays

S. Çırak, H. Gundesli, P. Dinçer, 2011, Journal of molecular and genetic medicine : an international journal of biomedical research.

The Versatility of Plectin in Cancer: A Pan-Cancer Analysis on Potential Diagnostic and Prognostic Impacts of Plectin Isoforms.

Medi Kori, K. Arğa, H. Gundesli, 2023, Omics : a journal of integrative biology.