William Wallefeld - Concepedia

Author

William Wallefeld

The University of Western Australia

Also Known As

W. Wallefeld, William Wallefeld

Publications

612

Citations

H-Index

Concepts

All Affiliations

The University of Western Australia Harry Perkins Institute of Medical Research Queen Elizabeth II Medical Centre Royal Perth Hospital University of Helsinki

About

William Wallefeld is an author at The University of Western Australia specializing in medicine, pathology, and neuromuscular pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	578
2	Health Sciences	4	4	430
3	Cell Biology	1	1	52
4	Cellular Physiology	1	1	52
5	Exercise Physiology	1	1	48

William Wallefeld

Publications

592

Citations

H-Index

Page 1

	Year	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, Kinga K. Tomczak, The American Journal of Human Genetics Mitochondrial MyopathyMuscle PhysiologyMuscle FunctionMolecular PhysiologyHealth Sciences	2006	234
Novel Mutations Widen the Phenotypic Spectrum of Slow Skeletal/β-Cardiac Myosin (<i>MYH7</i>) Distal Myopathy Phillipa J. Lamont, William Wallefeld, David Hilton‐Jones, Human Mutation Cardiac MuscleSkeletal Muscle DiseasesGeneticsDistal MyopathyPathology	2014	96
Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvement Thomas Cullup, Phillipa J. Lamont, Sebahattin Çirak, Neuromuscular Disorders Cardiac MuscleCardiomyopathyHeart FailureCardiovascular DiseaseVariable Cardiac Involvement	2012	86
Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in <i>TPM2</i>-related nemaline and cap myopathy M. Marttila, Elina Lemola, William Wallefeld, Biochemical Journal Muscle FunctionPathologyCytoskeletonMechanotransductionCap Myopathy	2011	52
CAV3 mutations causing exercise intolerance, myalgia and rhabdomyolysis: Expanding the phenotypic spectrum of caveolinopathies R. Scalco, A. Gardiner, Robert D. S. Pitceathly, Neuromuscular Disorders MedicineExercise PhysiologyPhysiologyExercise IntolerancePathology	2016	48
Severe nemaline myopathy caused by mutations of the stop codon of the skeletal muscle alpha actin gene (ACTA1) William Wallefeld, Sabine Krause, Kristen L. Nowak, Neuromuscular Disorders Muscle FunctionMuscle InjurySkeletal MuscleMedicineGenetics	2006	37
A novel ACTA1 mutation resulting in a severe congenital myopathy with nemaline bodies, intranuclear rods and type I fibre predominance Gianina Ravenscroft, Jo M. Wilmshurst, Komala Pillay, Neuromuscular Disorders Mendelian DisorderGenetic DisorderMedicinePathologySevere Congenital Myopathy	2010	25
Distal myosin heavy chain-7 myopathy due to the novel transition c.5566G > A (p.E1856K) with high interfamilial cardiac variability and putative anticipation Josef Finsterer, Oliver Brandau, Claudia Stöllberger, Neuromuscular Disorders	2014	14

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