Researchclopedia

Research Researchers Institutions Topics Submit About

Command Palette

Search for a command to run...

Researchclopedia

Research Researchers Institutions About

© 2026 Researchclopedia. Powered by OpenAlex under CC0 license.

Carina Wallgren‐Pettersson | Researchclopedia

Back to researchers

Carina Wallgren‐Pettersson

University of Helsinki ORCID

893

Works

10,136

Citations

53

h-index

128

i10-index

Research Topics

Cardiomyopathy and Myosin Studies Muscle Physiology and Disorders Neurogenetic and Muscular Disorders Research

Affiliations

University of Helsinki1982–2025

Inserm2009–2009

University of Turku2007–2007

University of Michigan–Ann Arbor2014–2014

Hammersmith Hospital2007–2007

Top Works

Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy

Anne-Sophie Nicot,Anne Toussaint,et al.

2007431 citations

Cellular Mechanics and Interactions

Microtubule and mitosis dynamics

Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy

Kristen L. Nowak,Duangrurdee Wattanasirichaigoon,et al.

1999399 citations

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

Katarina Pelin,Pirta Hilpelä,et al.

1999329 citations

Centronuclear (myotubular) myopathy

Heinz Jungbluth,Carina Wallgren‐Pettersson,et al.

2008308 citations

Mutations and polymorphisms of the skeletal muscle Î±-actin gene (<i>ACTA1</i>)

Nigel G. Laing,Danielle E. Dye,et al.

2009242 citations

Nemaline Myopathy with Minicores Caused by Mutation of the CFL2 Gene Encoding the Skeletal Muscle Actin–Binding Protein, Cofilin-2

Pankaj B. Agrawal,Rebecca S. Greenleaf,et al.

2006235 citations

MTM1 mutations in X-linked myotubular myopathy

Jocelyn Laporte,Val�rie Biancalana,et al.

2000227 citations

Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy

Kati Donner,Miina Ollikainen,et al.

2002225 citations

Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy

Gianina Ravenscroft,Satoko Miyatake,et al.

2013221 citations