Denis A. Akkad - Concepedia

Author

Denis A. Akkad

Also Known As

Akkad, Denis, D A Akkad, D. A. Akkad, D.A. Akkad, Denis A Akkad, Denis A. Akkad, Denis Akkad, Denis Amer Akkad, Denis A. Akkad, Dilara Akkad

Publications

2.3K

Citations

H-Index

Concepts

All Affiliations

Ruhr University Bochum St. Josef-Hospital University of Rostock University Medical Center of the Johannes Gutenberg University Mainz Centre National de la Recherche Scientifique

About

Denis A. Akkad is an author at Ruhr University Bochum specializing in medicine, genetics, and multiple sclerosis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	18	1.5K
2	Public Health	4	4	130
3	Health Sciences	1	1	47
4	Social Sciences	1	1	73
5	Allergy	1	1	58

Denis A. Akkad

Publications

Citations

H-Index

Page 1

	Year	Citations
Dietary Fatty Acids Directly Impact Central Nervous System Autoimmunity via the Small Intestine Aiden Haghikia, Stefanie Jörg, Alexander Duscha, Immunity InflammationNutritionAutoimmune DiseaseSmall IntestineMedicine	2015	893
PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease Elahe Taherzadeh-Fard, Carsten Saft, Denis A. Akkad, Molecular Neurodegeneration	2011	130
A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis Ben J. Gu, Judith Field, Sébastien Dutertre, Human Molecular Genetics InflammationNeurodegenerative DiseasesMolecular NeuroscienceAutoimmune DiseaseNeurological Disorder	2015	73
mtDNA nt13708A Variant Increases the Risk of Multiple Sclerosis Xinhua Yu, Dirk Koczan, Anna-Maija Sulonen, PLoS ONE	2008	72
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis Christina M. Lill, Brit‐Maren M. Schjeide, Christiane Graetz, Brain NeurogenomicsNeurological DisorderGeneticsImmunologyGenetic Epidemiology	2013	69
Mitochondrial haplogroup H correlates with ATP levels and age at onset in Huntington disease Larissa Arning, Aiden Haghikia, Elahe Taherzadeh-Fard, Journal of Molecular Medicine Alzheimer's DiseaseAgingMitochondrial FunctionMitochondrial DynamicDementia	2010	59
Variation in the IL7RA and IL2RA genes in German multiple sclerosis patients Denis A. Akkad, Sabine Hoffjan, Elisabeth Petrasch‐Parwez, Journal of Autoimmunity ImmunogeneticsAutoimmune DiseaseAllergyImmune Cell DevelopmentMedicine	2009	58
Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene Gabriele Dekomien, Conni Vollrath, Elisabeth Petrasch‐Parwez, Neurogenetics Ocular DiseaseRetinaProgressive Retinal AtrophyOphthalmologyExperimental Ophthalmology	2009	50
ASK1 and MAP2K6 as modifiers of age at onset in Huntington’s disease Larissa Arning, Didier Monté, Wiebke Hansen, Journal of Molecular Medicine Neurodegenerative DiseasesHuntington ’Genetic DisorderGeneticsDegenerative Disease	2008	47
Ccdc66 null mutation causes retinal degeneration and dysfunction Wanda M. Gerding, Sabrina Schreiber, Tobias Schulte-Middelmann, Human Molecular Genetics Protein Ccdc66Developmental BiologyRetinaOphthalmologyExperimental Ophthalmology	2011	47

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