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International Journal of Molecular Sciences|March 28, 2009
Thick and thin filament gene mutations in striated muscle diseasesHoma TajsharghiActa Neuropathologica|August 25, 2012
Myosinopathies: pathology and mechanismsHoma Tajsharghi, Anders OldforsScandinavian Cardiovascular Journal : SCJ|March 28, 2008
Structural effects of the slow/b-cardiac myosin heavy chain R453C mutation in cardiac and skeletal muscleHoma Tajsharghi, Ing-Marie FyhrAnnals of Neurology|September 1, 2005
A Caenorhabditis elegans model of the myosin heavy chain IIa E706K [corrected] mutationHoma Tajsharghi, Marc Pilon, Anders OldforsArchives of Neurology|September 12, 2007
Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2)Homa Tajsharghi, Monica Ohlsson, Christopher Lindberg, et al.Neuromuscular Disorders : NMD|March 29, 2005
Early onset myopathy with a novel mutation in the Selenoprotein N gene (SEPN1)Homa Tajsharghi, Niklas Darin, Mar Tulinius, et al.Plos One|September 17, 2013
Phenotypes of myopathy-related beta-tropomyosin mutants in human and mouse tissue culturesSaba Abdul-Hussein, Karin Rahl, Ali-Reza Moslemi, et al.Acta Paediatrica (Oslo, Norway : 1992)|April 24, 2012
Distal arthrogryposis: clinical and genetic findingsEva Kimber, Homa Tajsharghi, Anna-Karin Kroksmark, et al.Journal of Neurology|March 3, 2004
Induced shift in myosin heavy chain expression in myosin myopathy by endurance trainingHoma Tajsharghi, Katharina Stibrant Sunnerhagen, Niklas Darin, et al.BMC Musculoskeletal Disorders|January 1, 2013
Expression profiles of muscle disease-associated genes and their isoforms during differentiation of cultured human skeletal muscle cellsSaba Abdul-Hussein, Peter F M van der Ven, Homa TajsharghiPageof 6