David P. Dimasi - Concepedia

Author

David P. Dimasi

Flinders University ORCID

Also Known As

D P Dimasi, D. P. Dimasi, David Dimasi, David P Dimasi, David P. Dimasi

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

Flinders University Centre for Eye Research Australia Flinders Medical Centre South Australia Pathology University of Tasmania

About

David P. Dimasi is an author at Flinders University specializing in medicine, ophthalmology, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	11	296
2	Cell Biology	3	3	37
3	Natural Sciences	2	2	35
4	Allergy	1	1	14
5	Allergy Medicine	1	1	14

David P. Dimasi

Publications

962

Citations

H-Index

Page 1

	Year	Citations
Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people Alex W. Hewitt, Shiwani Sharma, Kathryn P. Burdon, Human Molecular Genetics	2007	159
Common Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal Thickness Yi Lu, David P. Dimasi, Pirro G. Hysi, PLoS Genetics	2010	153
Functional and Structural Implications of the Complement Factor H Y402H Polymorphism Associated with Age-Related Macular Degeneration Rebecca J. Ormsby, Shoba Ranganathan, Joo Chuan Tong, Investigative Ophthalmology & Visual Science	2008	84
A Glaucoma Case-control Study of the WDR36 Gene D658G Sequence Variant Alex W. Hewitt, David P. Dimasi, David A. Mackey, American Journal of Ophthalmology OphthalmologyGenetic DisorderGeneticsGenetic EpidemiologyMolecular Genetics	2006	67
Heritability of Central Corneal Thickness in Nuclear Families John A. Landers, Alex W. Hewitt, David P. Dimasi, Investigative Ophthalmology & Visual Science	2009	57
The p53 Codon 72 PRO/PRO Genotype May Be Associated with Initial Central Visual Field Defects in Caucasians with Primary Open Angle Glaucoma Janey L. Wiggs, Alex W. Hewitt, Baojian Fan, PLoS ONE	2012	55
Association of Genetic Variants in the<i>TMCO1</i>Gene with Clinical Parameters Related to Glaucoma and Characterization of the Protein in the Eye Shiwani Sharma, Kathryn P. Burdon, Glyn Chidlow, Investigative Ophthalmology & Visual Science	2012	46
The PITX3 gene in posterior polar congenital cataract in Australia. Kathryn P. Burdon, James McKay, Manuel Wirth, PubMed	2006	45
Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes David P. Dimasi, Jern Y. Chen, Alex W. Hewitt, Human Genetics Osteogenesis Imperfecta GenesAllelic VariantDevelopmental BiologyQuantitative GeneticsOphthalmology	2009	39
Dengue Virus Infection of Primary Endothelial Cells Induces Innate Immune Responses, Changes in Endothelial Cells Function and Is Restricted by Interferon-Stimulated Responses Julie K. Calvert, Karla J. Helbig, David P. Dimasi, Journal of Interferon & Cytokine Research Innate Immune SystemImmunologyViral PathogenesisPathologyInnate Immunity	2015	35

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