Monica Ohlsson

Hereditary myopathy with early respiratory failure associated with a mutation in A-band titin

Monica Ohlsson, Carola Hedberg, Björn Brådvik et al. · Brain · 2012 · 108 citations · Full text

Medicine, Genetics, Molecular Genetics +15

Congenital Myopathy With Nemaline Rods and Cap Structures Caused by a Mutation in the β-Tropomyosin Gene (TPM2)

Homa Tajsharghi, Monica Ohlsson, Christopher Lindberg et al. · Archives of Neurology · 2007 · 101 citations

Medicine, Genetics, Molecular Genetics +15

Defective regulation of contractile function in muscle fibres carrying an E41K β‐tropomyosin mutation

Julien Ochala, Meishan Li, Monica Ohlsson et al. · The Journal of Physiology · 2008 · 53 citations · Full text

Medicine, Genetics, Physiology +17

Clinical Frailty Scale classes are independently associated with 6-month mortality for patients after acute myocardial infarction

Niklas Ekerstad, Dariush Javadzadeh, Karen P. Alexander et al. · European Heart Journal Acute Cardiovascular Care · 2021 · 49 citations · Full text

Medicine, Cardiology, Internal Medicine +12

<i>TPM3</i> mutation in one of the original cases of cap disease

Monica Ohlsson, Anna Fidziańska, Homa Tajsharghi et al. · Neurology · 2009 · 47 citations

Medicine, Genetics, Molecular Genetics +15