P. Anthony Akkari - Concepedia

Author

P. Anthony Akkari

The University of Western Australia ORCID

Also Known As

A. Akkari, AP Akkari, Anthony Akkari, P A Akkari, P Akkari, P Anthony Akkari, P. A. Akkari, P. Akkari, P. Anthony Akkari, P.A Akkari

Publications

2.7K

Citations

H-Index

Concepts

All Affiliations

The University of Western Australia Perron Institute for Neurological and Translational Science Murdoch University The University of Notre Dame Australia Queen Elizabeth II Medical Centre

About

P. Anthony Akkari is an author at The University of Western Australia specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	547
2	Immunology	2	2	48
3	Public Health	1	1	14
4	Allergy	1	1	14
5	Molecular Biology	1	1	17

P. Anthony Akkari

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy Nigel G. Laing, Steve D. Wilton, P. Anthony Akkari, Nature Genetics Autoimmune DiseaseGenetic DisorderMedicineGeneticsPathology	1995	355
Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy Katarina Pelin, Pirta Hilpelä, Kati Donner, Proceedings of the National Academy of Sciences	1999	328
Altered Gut Microbiome in Parkinson’s Disease and the Influence of Lipopolysaccharide in a Human α-Synuclein Over-Expressing Mouse Model Anastazja M. Gorecki, Leah Preskey, Megan C. Bakeberg, Frontiers in Neuroscience	2019	182
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families Lianna Ishihara, Rachel A. Gibson, Liling Warren, Movement Disorders	2006	91
Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome I. Nigel G. Laing, Bernadette T. Majda, P. Anthony Akkari, PubMed	1992	70
A splice-site mutation causing ovine McArdle's disease P. Tan, J Garrott Allen, Steve D. Wilton, Neuromuscular Disorders Somatic VariantMedicineGeneticsPathogenesisPathology	1997	70
Structural Variants May Be a Source of Missing Heritability in sALS Frances Theunissen, Loren L. Flynn, Ryan S. Anderton, Frontiers in Neuroscience	2020	65
An αtropomyosin mutation alters dimer preference in nemaline myopathy Mark Corbett, P. Anthony Akkari, Ana Domazetovska, Annals of Neurology	2004	64
Novel STMN2 Variant Linked to Amyotrophic Lateral Sclerosis Risk and Clinical Phenotype Frances Theunissen, Ryan S. Anderton, Frank Mastaglia, Frontiers in Aging Neuroscience	2021	47
Early onset chromosome 14-linked distal myopathy (Laing) F.L. Mastaglia, Beverley A. Phillips, Lesley Cala, Neuromuscular Disorders Genetic DisorderGeneticsHistopathologyPathologyMolecular Genetics	2002	36

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