Denis Crimmins - Concepedia

Author

Denis Crimmins

Also Known As

Brian Costell, C. Bladin, D Crimmins, D S Crimmins, D. Crimmins, D. S. Crimmins, D.S Crimmins, D.S. Crimmins, Denis Crimmins, Denis S. Crimmins

Publications

3.9K

Citations

H-Index

Concepts

All Affiliations

Westmead Hospital Gosford Hospital The University of Sydney The University of Melbourne Women's and Children's Hospital

About

Denis Crimmins is an author at Westmead Hospital specializing in medicine, neurology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	834
2	Diabetes	2	2	105
3	Natural Sciences	1	1	58
4	Social Sciences	1	1	12
5	Molecular Biology	1	1	58

Denis Crimmins

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Mutations in DEPDC5 cause familial focal epilepsy with variable foci Leanne M. Dibbens, Boukje de Vries, Simona Donatello, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsNeurogeneticsVariable Foci	2013	358
Cause of Death and Predictors of All‐Cause Mortality in Anticoagulated Patients With Nonvalvular Atrial Fibrillation: Data From ROCKET AF Sean D. Pokorney, Jonathan P. Piccini, Susanna R. Stevens, Journal of the American Heart Association	2016	196
Neuroradiological features of six kindreds with MELAS tRNALeu A3243G point mutation: implications for pathogenesis Carolyn M. Sue, Denis Crimmins, Young Soo, Journal of Neurology Neurosurgery & Psychiatry	1998	141
Longitudinal prevalence and determinants of early mood disorder post-stroke Bradley Scott Townend, Scott Whyte, T. Desborough, Journal of Clinical Neuroscience PsychiatryMood SymptomMedicineDepressionNeurology	2007	92
Detection of MELAS A3243G point mutation in muscle, blood and hair follicles Carolyn M. Sue, Anita Quigley, Sophie Katsabanis, Journal of the Neurological Sciences	1998	80
Perimetric homonymous visual field loss post-stroke Bradley Scott Townend, Jonathan Sturm, Con Petsoglou, Journal of Clinical Neuroscience OphthalmologyMedicineVision ResearchNeurologyVisual Pathway	2007	76
Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM Kathryn Friend, Denis Crimmins, Thanh G. Phan, Human Genetics Cacna1a GeneGenetic DisorderMedicineGeneticsSecond Recurrent Mutation	1999	70
Pigmentary retinopathy associated with the mitochondrial DNA 3243 point mutation Carolyn M. Sue, Paul Mitchell, Denis Crimmins, Neurology Ocular DiseaseGeneticsMolecular BiologyPathologyMolecular Genetics	1997	58
Mitochondrial encephalomyopathy: variable clinical expression within a single kindred. Denis Crimmins, John G. Morris, G. Walker, Journal of Neurology Neurosurgery & Psychiatry Mitochondrial MyopathyNeurodegenerative DiseasesMendelian DisorderMitochondrial FunctionShort Stature	1993	52
Mitochondrial gene mutations and diabetes mellitus Carolyn M. Sue, D. Jane Holmes–Walker, John G. Morris, The Lancet Mitochondrial BiogenesisMitochondrial FunctionGeneticsDiabetesMolecular Genetics	1993	47

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